https://wiki.tripsit.me/api.php?action=feedcontributions&feedformat=atom&user=Dumbdumb123 2026-04-28T12:52:50Z User contributions MediaWiki 1.44.0 https://wiki.tripsit.me/index.php?title=Opioids&diff=5761 2018-10-09T22:05:06Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5760 2018-10-09T22:04:58Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5759 2018-10-09T22:04:50Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> = Chemistry and Pharmacology =<br /> <br /> An opioid is any psychoactive chemical that resembles an opiate in its pharmacological effects. They work by binding to the opioid receptors (Delta, Kappa, Mu) Which are found in the Central/Peripheral nervous system and in the GI tract. <br /> <br /> =Goodbye moonmen=<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5758 2018-10-09T22:04:43Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> = Addiction =<br /> <br /> Opiates also give us the classical model of addiction. Used regularly, they produce tolerance - a need to continue increasing the dose in order to get the same effect, and stopping after repeated use produces withdrawal symptoms that can reinforce the addiction - physical discomfort and a mental craving for the drug, driving the user to continue taking the drug despite negative consequences of behaviour.<br /> <br /> = Chemistry and Pharmacology =<br /> <br /> An opioid is any psychoactive chemical that resembles an opiate in its pharmacological effects. They work by binding to the opioid receptors (Delta, Kappa, Mu) Which are found in the Central/Peripheral nervous system and in the GI tract. <br /> <br /> =Goodbye moonmen=<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5757 2018-10-09T22:04:27Z

<p>Dumbdumb123: /* Effects */</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> = Addiction =<br /> <br /> Opiates also give us the classical model of addiction. Used regularly, they produce tolerance - a need to continue increasing the dose in order to get the same effect, and stopping after repeated use produces withdrawal symptoms that can reinforce the addiction - physical discomfort and a mental craving for the drug, driving the user to continue taking the drug despite negative consequences of behaviour.<br /> <br /> = Chemistry and Pharmacology =<br /> <br /> An opioid is any psychoactive chemical that resembles an opiate in its pharmacological effects. They work by binding to the opioid receptors (Delta, Kappa, Mu) Which are found in the Central/Peripheral nervous system and in the GI tract. <br /> <br /> = Harm Reduction =<br /> <br /> Avoid driving on higher doses.<br /> <br /> Opioid analgesics do not cause any specific organ toxicity, unlike many other drugs, such as aspirin and acetaminophen. They are not associated with upper gastrointestinal bleeding and renal toxicity, however, people seeking codeine experiences from medications that contain acetaminophen (paracetamol) may be putting themselves at risk for acetaminophen-related complications such as liver damage. In the case of Acetaminophen and aspirin-containing medications, [[Cold Water Extraction]] is useful to reduce the amount of non-opioid analgesics ingested<br /> <br /> If possible, having Naloxone available (especially when dealing with high doses) is a good idea. Naloxone is a pure opioid antagonist, which means it reverses the effects of opiate drugs and can reverse overdose symptoms.<br /> <br /> Some users have noted that following the &quot;3-day rule&quot; prevents chemical dependency with some opioids, meaning that using no more than 3 days in a row. (this has no medical basis, however, and should be taken as only a guideline at best)<br /> <br /> When preparing IV solutions for injection of street drugs, a wheel filter (micron filter) is essential for reducing particulate matter in the solution, as well as using sterile needles, and clean distilled water. Never re-use injection equipment<br /> <br /> == Interactions ==<br /> <br /> Don't mix any of the class with any other CNS [[Depressants]] as it increases the risk of an overdose and respiratory depression.<br /> <br /> [[Tramadol]] and [[Meperidine]] are affecting serotonin levels in the brain and might cause Serotonin Syndrome with some combinations. Check [[Drug Combinations]] for more information.<br /> <br /> ==Research Chemicals==<br /> <br /> Respiratory depression is one of the very common side effects with this class and puts users at a high risk of overdose. With research chemicals, this is a particular issue since there are some substances being openly sold for which a single microgram can be the difference between life and death. With the emerging research chemical market for opioids, most have been explored in-vivo (outside of a human) and also in-vitro (in human) - though there are some exceptions (e.g. W-18/Acryl-Fentanyl).<br /> <br /> It's suggested to start at the lowest possible dose; in the case of W-18, animal testing has shown it to be around 10,000x the potency of Morphine. So the logical way to start is either to volumetrically dose or use a precise scale with a +/- microgram amount. Titrating up to an active dose with this class might be the most difficult, due to the massively steep dosage curves.<br /> <br /> See the [[Research Chemicals]] page for more information.<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5756 2018-10-09T22:04:18Z

<p>Dumbdumb123: /* History */</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> = Effects =<br /> <br /> All opiate drugs have similar effects. At low doses, they relieve pain and anxiety, and if the dose is increased, they produce a sedative effect. The analgesic (painkiller) effects of opioids are due to decreased perception of pain, decreased reaction to pain as well as increased pain tolerance. Opioids can cause cough suppression, which can be both an indication of opioid administration or an unintended side effect.<br /> <br /> Opiates influence the pupils: they contract (miosis). This is an extremely reliable signal of opiate use. Besides this, when suffocation occurs (as a result of respiratory inhibition) in the case of an overdose, the pupils dilate (mydriasis).<br /> <br /> The most striking quality of painkilling effect of opiates is that it has virtually no effect whatever on the other sensory perceptions, consciousness or the motor functions. All other substances with a painkilling effect, such as laughing gas, alcohol, ether and barbiturates also have, in an effective dose, a definite effect on consciousness, motor coordination, the intellect and emotional control. The drowsiness which can be caused by opiates is experienced only at high dosage.<br /> <br /> Opiates are affecting respiratory center. Both frequency and the depth of breathing is reduced. In the case of overdose, respiration can come to a complete halt resulting in death.<br /> <br /> Dependence is characterised by unpleasant withdrawal symptoms that occur if opioid use is abruptly discontinued. The withdrawal symptoms for opiates include severe dysphoria, craving for another opiate dose, irritability, sweating, nausea, rhinorrhea, tremor, vomiting and myalgia.<br /> <br /> == Positive ==<br /> <br /> *Euphoria<br /> <br /> *Analgesic effect<br /> <br /> *Pain relief<br /> <br /> == Neutral ==<br /> <br /> *Itching<br /> <br /> == Negative ==<br /> <br /> *Opioid-induced hyperalgesia (More sensitive to pain after stopping the use)<br /> <br /> *Nausea<br /> <br /> *Vomiting<br /> <br /> *Constipation<br /> <br /> *Respiratory depression<br /> <br /> = Addiction =<br /> <br /> Opiates also give us the classical model of addiction. Used regularly, they produce tolerance - a need to continue increasing the dose in order to get the same effect, and stopping after repeated use produces withdrawal symptoms that can reinforce the addiction - physical discomfort and a mental craving for the drug, driving the user to continue taking the drug despite negative consequences of behaviour.<br /> <br /> = Chemistry and Pharmacology =<br /> <br /> An opioid is any psychoactive chemical that resembles an opiate in its pharmacological effects. They work by binding to the opioid receptors (Delta, Kappa, Mu) Which are found in the Central/Peripheral nervous system and in the GI tract. <br /> <br /> = Harm Reduction =<br /> <br /> Avoid driving on higher doses.<br /> <br /> Opioid analgesics do not cause any specific organ toxicity, unlike many other drugs, such as aspirin and acetaminophen. They are not associated with upper gastrointestinal bleeding and renal toxicity, however, people seeking codeine experiences from medications that contain acetaminophen (paracetamol) may be putting themselves at risk for acetaminophen-related complications such as liver damage. In the case of Acetaminophen and aspirin-containing medications, [[Cold Water Extraction]] is useful to reduce the amount of non-opioid analgesics ingested<br /> <br /> If possible, having Naloxone available (especially when dealing with high doses) is a good idea. Naloxone is a pure opioid antagonist, which means it reverses the effects of opiate drugs and can reverse overdose symptoms.<br /> <br /> Some users have noted that following the &quot;3-day rule&quot; prevents chemical dependency with some opioids, meaning that using no more than 3 days in a row. (this has no medical basis, however, and should be taken as only a guideline at best)<br /> <br /> When preparing IV solutions for injection of street drugs, a wheel filter (micron filter) is essential for reducing particulate matter in the solution, as well as using sterile needles, and clean distilled water. Never re-use injection equipment<br /> <br /> == Interactions ==<br /> <br /> Don't mix any of the class with any other CNS [[Depressants]] as it increases the risk of an overdose and respiratory depression.<br /> <br /> [[Tramadol]] and [[Meperidine]] are affecting serotonin levels in the brain and might cause Serotonin Syndrome with some combinations. Check [[Drug Combinations]] for more information.<br /> <br /> ==Research Chemicals==<br /> <br /> Respiratory depression is one of the very common side effects with this class and puts users at a high risk of overdose. With research chemicals, this is a particular issue since there are some substances being openly sold for which a single microgram can be the difference between life and death. With the emerging research chemical market for opioids, most have been explored in-vivo (outside of a human) and also in-vitro (in human) - though there are some exceptions (e.g. W-18/Acryl-Fentanyl).<br /> <br /> It's suggested to start at the lowest possible dose; in the case of W-18, animal testing has shown it to be around 10,000x the potency of Morphine. So the logical way to start is either to volumetrically dose or use a precise scale with a +/- microgram amount. Titrating up to an active dose with this class might be the most difficult, due to the massively steep dosage curves.<br /> <br /> See the [[Research Chemicals]] page for more information.<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5755 2018-10-09T22:04:05Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> = History =<br /> <br /> Opioids are among the world's oldest known drugs; the therapeutic use of the opium poppy predates recorded history. Excavations of the remains of Neolithic settlements in Switzerland (the Cortaillod culture, 3200-2600 B.C.), have shown that Papaver was already being cultivated then; perhaps for the food value in the seeds (45% oil), which we know as poppy seeds. The slightly narcotic property of this plant was undoubtedly already known then. <br /> <br /> [[Opium]] contains a considerable number of different substances, and in the nineteenth century, these were isolated. In 1806 Friedrich Serturner was the first to extract one of these substances in its pure form. He called morphine after Morpheus, the Greek god of sleep. Codeine (Robiquet, 1832) and papaverine (Merck, 1848) followed. These pure substances supplanted the use of raw opium for medical purposes. Like opium, they were frequently used as painkillers and as anti-diarrheal. The invention of the hypodermic needle in the mid-nineteenth century led to widespread use of morphine intravenously as a painkiller and recreational drug.<br /> <br /> = Effects =<br /> <br /> All opiate drugs have similar effects. At low doses, they relieve pain and anxiety, and if the dose is increased, they produce a sedative effect. The analgesic (painkiller) effects of opioids are due to decreased perception of pain, decreased reaction to pain as well as increased pain tolerance. Opioids can cause cough suppression, which can be both an indication of opioid administration or an unintended side effect.<br /> <br /> Opiates influence the pupils: they contract (miosis). This is an extremely reliable signal of opiate use. Besides this, when suffocation occurs (as a result of respiratory inhibition) in the case of an overdose, the pupils dilate (mydriasis).<br /> <br /> The most striking quality of painkilling effect of opiates is that it has virtually no effect whatever on the other sensory perceptions, consciousness or the motor functions. All other substances with a painkilling effect, such as laughing gas, alcohol, ether and barbiturates also have, in an effective dose, a definite effect on consciousness, motor coordination, the intellect and emotional control. The drowsiness which can be caused by opiates is experienced only at high dosage.<br /> <br /> Opiates are affecting respiratory center. Both frequency and the depth of breathing is reduced. In the case of overdose, respiration can come to a complete halt resulting in death.<br /> <br /> Dependence is characterised by unpleasant withdrawal symptoms that occur if opioid use is abruptly discontinued. The withdrawal symptoms for opiates include severe dysphoria, craving for another opiate dose, irritability, sweating, nausea, rhinorrhea, tremor, vomiting and myalgia.<br /> <br /> == Positive ==<br /> <br /> *Euphoria<br /> <br /> *Analgesic effect<br /> <br /> *Pain relief<br /> <br /> == Neutral ==<br /> <br /> *Itching<br /> <br /> == Negative ==<br /> <br /> *Opioid-induced hyperalgesia (More sensitive to pain after stopping the use)<br /> <br /> *Nausea<br /> <br /> *Vomiting<br /> <br /> *Constipation<br /> <br /> *Respiratory depression<br /> <br /> = Addiction =<br /> <br /> Opiates also give us the classical model of addiction. Used regularly, they produce tolerance - a need to continue increasing the dose in order to get the same effect, and stopping after repeated use produces withdrawal symptoms that can reinforce the addiction - physical discomfort and a mental craving for the drug, driving the user to continue taking the drug despite negative consequences of behaviour.<br /> <br /> = Chemistry and Pharmacology =<br /> <br /> An opioid is any psychoactive chemical that resembles an opiate in its pharmacological effects. They work by binding to the opioid receptors (Delta, Kappa, Mu) Which are found in the Central/Peripheral nervous system and in the GI tract. <br /> <br /> = Harm Reduction =<br /> <br /> Avoid driving on higher doses.<br /> <br /> Opioid analgesics do not cause any specific organ toxicity, unlike many other drugs, such as aspirin and acetaminophen. They are not associated with upper gastrointestinal bleeding and renal toxicity, however, people seeking codeine experiences from medications that contain acetaminophen (paracetamol) may be putting themselves at risk for acetaminophen-related complications such as liver damage. In the case of Acetaminophen and aspirin-containing medications, [[Cold Water Extraction]] is useful to reduce the amount of non-opioid analgesics ingested<br /> <br /> If possible, having Naloxone available (especially when dealing with high doses) is a good idea. Naloxone is a pure opioid antagonist, which means it reverses the effects of opiate drugs and can reverse overdose symptoms.<br /> <br /> Some users have noted that following the &quot;3-day rule&quot; prevents chemical dependency with some opioids, meaning that using no more than 3 days in a row. (this has no medical basis, however, and should be taken as only a guideline at best)<br /> <br /> When preparing IV solutions for injection of street drugs, a wheel filter (micron filter) is essential for reducing particulate matter in the solution, as well as using sterile needles, and clean distilled water. Never re-use injection equipment<br /> <br /> == Interactions ==<br /> <br /> Don't mix any of the class with any other CNS [[Depressants]] as it increases the risk of an overdose and respiratory depression.<br /> <br /> [[Tramadol]] and [[Meperidine]] are affecting serotonin levels in the brain and might cause Serotonin Syndrome with some combinations. Check [[Drug Combinations]] for more information.<br /> <br /> ==Research Chemicals==<br /> <br /> Respiratory depression is one of the very common side effects with this class and puts users at a high risk of overdose. With research chemicals, this is a particular issue since there are some substances being openly sold for which a single microgram can be the difference between life and death. With the emerging research chemical market for opioids, most have been explored in-vivo (outside of a human) and also in-vitro (in human) - though there are some exceptions (e.g. W-18/Acryl-Fentanyl).<br /> <br /> It's suggested to start at the lowest possible dose; in the case of W-18, animal testing has shown it to be around 10,000x the potency of Morphine. So the logical way to start is either to volumetrically dose or use a precise scale with a +/- microgram amount. Titrating up to an active dose with this class might be the most difficult, due to the massively steep dosage curves.<br /> <br /> See the [[Research Chemicals]] page for more information.<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5754 2018-10-09T22:03:49Z

<p>Dumbdumb123: </p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> = Common opioids =<br /> <br /> *[[Codeine]]<br /> <br /> *[[Heroin]]<br /> <br /> *[[Hydrocodone]]<br /> <br /> *[[Hydromorphone]]<br /> <br /> *[[Methadone]]<br /> <br /> *[[Oxycodone]]<br /> <br /> *[[Oxymorphone]]<br /> <br /> *[[Tramadol]]<br /> <br /> = History =<br /> <br /> Opioids are among the world's oldest known drugs; the therapeutic use of the opium poppy predates recorded history. Excavations of the remains of Neolithic settlements in Switzerland (the Cortaillod culture, 3200-2600 B.C.), have shown that Papaver was already being cultivated then; perhaps for the food value in the seeds (45% oil), which we know as poppy seeds. The slightly narcotic property of this plant was undoubtedly already known then. <br /> <br /> [[Opium]] contains a considerable number of different substances, and in the nineteenth century, these were isolated. In 1806 Friedrich Serturner was the first to extract one of these substances in its pure form. He called morphine after Morpheus, the Greek god of sleep. Codeine (Robiquet, 1832) and papaverine (Merck, 1848) followed. These pure substances supplanted the use of raw opium for medical purposes. Like opium, they were frequently used as painkillers and as anti-diarrheal. The invention of the hypodermic needle in the mid-nineteenth century led to widespread use of morphine intravenously as a painkiller and recreational drug.<br /> <br /> = Effects =<br /> <br /> All opiate drugs have similar effects. At low doses, they relieve pain and anxiety, and if the dose is increased, they produce a sedative effect. The analgesic (painkiller) effects of opioids are due to decreased perception of pain, decreased reaction to pain as well as increased pain tolerance. Opioids can cause cough suppression, which can be both an indication of opioid administration or an unintended side effect.<br /> <br /> Opiates influence the pupils: they contract (miosis). This is an extremely reliable signal of opiate use. Besides this, when suffocation occurs (as a result of respiratory inhibition) in the case of an overdose, the pupils dilate (mydriasis).<br /> <br /> The most striking quality of painkilling effect of opiates is that it has virtually no effect whatever on the other sensory perceptions, consciousness or the motor functions. All other substances with a painkilling effect, such as laughing gas, alcohol, ether and barbiturates also have, in an effective dose, a definite effect on consciousness, motor coordination, the intellect and emotional control. The drowsiness which can be caused by opiates is experienced only at high dosage.<br /> <br /> Opiates are affecting respiratory center. Both frequency and the depth of breathing is reduced. In the case of overdose, respiration can come to a complete halt resulting in death.<br /> <br /> Dependence is characterised by unpleasant withdrawal symptoms that occur if opioid use is abruptly discontinued. The withdrawal symptoms for opiates include severe dysphoria, craving for another opiate dose, irritability, sweating, nausea, rhinorrhea, tremor, vomiting and myalgia.<br /> <br /> == Positive ==<br /> <br /> *Euphoria<br /> <br /> *Analgesic effect<br /> <br /> *Pain relief<br /> <br /> == Neutral ==<br /> <br /> *Itching<br /> <br /> == Negative ==<br /> <br /> *Opioid-induced hyperalgesia (More sensitive to pain after stopping the use)<br /> <br /> *Nausea<br /> <br /> *Vomiting<br /> <br /> *Constipation<br /> <br /> *Respiratory depression<br /> <br /> = Addiction =<br /> <br /> Opiates also give us the classical model of addiction. Used regularly, they produce tolerance - a need to continue increasing the dose in order to get the same effect, and stopping after repeated use produces withdrawal symptoms that can reinforce the addiction - physical discomfort and a mental craving for the drug, driving the user to continue taking the drug despite negative consequences of behaviour.<br /> <br /> = Chemistry and Pharmacology =<br /> <br /> An opioid is any psychoactive chemical that resembles an opiate in its pharmacological effects. They work by binding to the opioid receptors (Delta, Kappa, Mu) Which are found in the Central/Peripheral nervous system and in the GI tract. <br /> <br /> = Harm Reduction =<br /> <br /> Avoid driving on higher doses.<br /> <br /> Opioid analgesics do not cause any specific organ toxicity, unlike many other drugs, such as aspirin and acetaminophen. They are not associated with upper gastrointestinal bleeding and renal toxicity, however, people seeking codeine experiences from medications that contain acetaminophen (paracetamol) may be putting themselves at risk for acetaminophen-related complications such as liver damage. In the case of Acetaminophen and aspirin-containing medications, [[Cold Water Extraction]] is useful to reduce the amount of non-opioid analgesics ingested<br /> <br /> If possible, having Naloxone available (especially when dealing with high doses) is a good idea. Naloxone is a pure opioid antagonist, which means it reverses the effects of opiate drugs and can reverse overdose symptoms.<br /> <br /> Some users have noted that following the &quot;3-day rule&quot; prevents chemical dependency with some opioids, meaning that using no more than 3 days in a row. (this has no medical basis, however, and should be taken as only a guideline at best)<br /> <br /> When preparing IV solutions for injection of street drugs, a wheel filter (micron filter) is essential for reducing particulate matter in the solution, as well as using sterile needles, and clean distilled water. Never re-use injection equipment<br /> <br /> == Interactions ==<br /> <br /> Don't mix any of the class with any other CNS [[Depressants]] as it increases the risk of an overdose and respiratory depression.<br /> <br /> [[Tramadol]] and [[Meperidine]] are affecting serotonin levels in the brain and might cause Serotonin Syndrome with some combinations. Check [[Drug Combinations]] for more information.<br /> <br /> ==Research Chemicals==<br /> <br /> Respiratory depression is one of the very common side effects with this class and puts users at a high risk of overdose. With research chemicals, this is a particular issue since there are some substances being openly sold for which a single microgram can be the difference between life and death. With the emerging research chemical market for opioids, most have been explored in-vivo (outside of a human) and also in-vitro (in human) - though there are some exceptions (e.g. W-18/Acryl-Fentanyl).<br /> <br /> It's suggested to start at the lowest possible dose; in the case of W-18, animal testing has shown it to be around 10,000x the potency of Morphine. So the logical way to start is either to volumetrically dose or use a precise scale with a +/- microgram amount. Titrating up to an active dose with this class might be the most difficult, due to the massively steep dosage curves.<br /> <br /> See the [[Research Chemicals]] page for more information.<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Opioids&diff=5753 2018-10-09T22:03:36Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Papaver_somniferum.jpg|250px|right|Close-up color photo of a Papaver somniferum pod]]<br /> <br /> Opiates and opioids are classes of depressant analgesics derived from or chemically similar to substances found in Papaver somniferum, the opium poppy. They include both naturally occurring and synthetic substances. The term opiate is often used interchangeably for the term opioid. Opiate is limited to the natural alkaloids found in the resin of the poppy. Opioid refers to both opiates and synthetic substances as well as opioid peptides. The analgesic effect of opioids are due to decreased perception of pain, decreased reaction to pain as well as increased pain tolerance. They can also be used as for their antitussive properties. <br /> <br /> =Goodbye moonmen=<br /> <br /> = Common opioids =<br /> <br /> *[[Codeine]]<br /> <br /> *[[Heroin]]<br /> <br /> *[[Hydrocodone]]<br /> <br /> *[[Hydromorphone]]<br /> <br /> *[[Methadone]]<br /> <br /> *[[Oxycodone]]<br /> <br /> *[[Oxymorphone]]<br /> <br /> *[[Tramadol]]<br /> <br /> = History =<br /> <br /> Opioids are among the world's oldest known drugs; the therapeutic use of the opium poppy predates recorded history. Excavations of the remains of Neolithic settlements in Switzerland (the Cortaillod culture, 3200-2600 B.C.), have shown that Papaver was already being cultivated then; perhaps for the food value in the seeds (45% oil), which we know as poppy seeds. The slightly narcotic property of this plant was undoubtedly already known then. <br /> <br /> [[Opium]] contains a considerable number of different substances, and in the nineteenth century, these were isolated. In 1806 Friedrich Serturner was the first to extract one of these substances in its pure form. He called morphine after Morpheus, the Greek god of sleep. Codeine (Robiquet, 1832) and papaverine (Merck, 1848) followed. These pure substances supplanted the use of raw opium for medical purposes. Like opium, they were frequently used as painkillers and as anti-diarrheal. The invention of the hypodermic needle in the mid-nineteenth century led to widespread use of morphine intravenously as a painkiller and recreational drug.<br /> <br /> = Effects =<br /> <br /> All opiate drugs have similar effects. At low doses, they relieve pain and anxiety, and if the dose is increased, they produce a sedative effect. The analgesic (painkiller) effects of opioids are due to decreased perception of pain, decreased reaction to pain as well as increased pain tolerance. Opioids can cause cough suppression, which can be both an indication of opioid administration or an unintended side effect.<br /> <br /> Opiates influence the pupils: they contract (miosis). This is an extremely reliable signal of opiate use. Besides this, when suffocation occurs (as a result of respiratory inhibition) in the case of an overdose, the pupils dilate (mydriasis).<br /> <br /> The most striking quality of painkilling effect of opiates is that it has virtually no effect whatever on the other sensory perceptions, consciousness or the motor functions. All other substances with a painkilling effect, such as laughing gas, alcohol, ether and barbiturates also have, in an effective dose, a definite effect on consciousness, motor coordination, the intellect and emotional control. The drowsiness which can be caused by opiates is experienced only at high dosage.<br /> <br /> Opiates are affecting respiratory center. Both frequency and the depth of breathing is reduced. In the case of overdose, respiration can come to a complete halt resulting in death.<br /> <br /> Dependence is characterised by unpleasant withdrawal symptoms that occur if opioid use is abruptly discontinued. The withdrawal symptoms for opiates include severe dysphoria, craving for another opiate dose, irritability, sweating, nausea, rhinorrhea, tremor, vomiting and myalgia.<br /> <br /> == Positive ==<br /> <br /> *Euphoria<br /> <br /> *Analgesic effect<br /> <br /> *Pain relief<br /> <br /> == Neutral ==<br /> <br /> *Itching<br /> <br /> == Negative ==<br /> <br /> *Opioid-induced hyperalgesia (More sensitive to pain after stopping the use)<br /> <br /> *Nausea<br /> <br /> *Vomiting<br /> <br /> *Constipation<br /> <br /> *Respiratory depression<br /> <br /> = Addiction =<br /> <br /> Opiates also give us the classical model of addiction. Used regularly, they produce tolerance - a need to continue increasing the dose in order to get the same effect, and stopping after repeated use produces withdrawal symptoms that can reinforce the addiction - physical discomfort and a mental craving for the drug, driving the user to continue taking the drug despite negative consequences of behaviour.<br /> <br /> = Chemistry and Pharmacology =<br /> <br /> An opioid is any psychoactive chemical that resembles an opiate in its pharmacological effects. They work by binding to the opioid receptors (Delta, Kappa, Mu) Which are found in the Central/Peripheral nervous system and in the GI tract. <br /> <br /> = Harm Reduction =<br /> <br /> Avoid driving on higher doses.<br /> <br /> Opioid analgesics do not cause any specific organ toxicity, unlike many other drugs, such as aspirin and acetaminophen. They are not associated with upper gastrointestinal bleeding and renal toxicity, however, people seeking codeine experiences from medications that contain acetaminophen (paracetamol) may be putting themselves at risk for acetaminophen-related complications such as liver damage. In the case of Acetaminophen and aspirin-containing medications, [[Cold Water Extraction]] is useful to reduce the amount of non-opioid analgesics ingested<br /> <br /> If possible, having Naloxone available (especially when dealing with high doses) is a good idea. Naloxone is a pure opioid antagonist, which means it reverses the effects of opiate drugs and can reverse overdose symptoms.<br /> <br /> Some users have noted that following the &quot;3-day rule&quot; prevents chemical dependency with some opioids, meaning that using no more than 3 days in a row. (this has no medical basis, however, and should be taken as only a guideline at best)<br /> <br /> When preparing IV solutions for injection of street drugs, a wheel filter (micron filter) is essential for reducing particulate matter in the solution, as well as using sterile needles, and clean distilled water. Never re-use injection equipment<br /> <br /> == Interactions ==<br /> <br /> Don't mix any of the class with any other CNS [[Depressants]] as it increases the risk of an overdose and respiratory depression.<br /> <br /> [[Tramadol]] and [[Meperidine]] are affecting serotonin levels in the brain and might cause Serotonin Syndrome with some combinations. Check [[Drug Combinations]] for more information.<br /> <br /> ==Research Chemicals==<br /> <br /> Respiratory depression is one of the very common side effects with this class and puts users at a high risk of overdose. With research chemicals, this is a particular issue since there are some substances being openly sold for which a single microgram can be the difference between life and death. With the emerging research chemical market for opioids, most have been explored in-vivo (outside of a human) and also in-vitro (in human) - though there are some exceptions (e.g. W-18/Acryl-Fentanyl).<br /> <br /> It's suggested to start at the lowest possible dose; in the case of W-18, animal testing has shown it to be around 10,000x the potency of Morphine. So the logical way to start is either to volumetrically dose or use a precise scale with a +/- microgram amount. Titrating up to an active dose with this class might be the most difficult, due to the massively steep dosage curves.<br /> <br /> See the [[Research Chemicals]] page for more information.<br /> <br /> = Links =<br /> <br /> [https://en.wikipedia.org/wiki/Opiod Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/opiates/ Erowid]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Dissociatives&diff=5752 2018-10-09T22:03:06Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> ==Common Dissociatives==<br /> <br /> * [[Ketamine]]<br /> * [[DXM]]<br /> * [[MXE]]<br /> * [[PCP]]<br /> * [[Nitrous]]<br /> * [[Diphenidine]]<br /> * [[Diethyl Ether]] <br /> <br /> ==Effects==<br /> <br /> ===Dissociation and detachment===<br /> [[File:RWY72.jpg|200px|thumb|right]]<br /> Feelings of detachment are the most noticeable component of a dissociative trip. Which is entirely triggered by the blocking of NMDA receptors. <br /> <br /> At lower states of dissociation, this essentially feels like an obvious but still difficult to pinpoint feeling of detachment from the external environment and body. The greatest analogy to depict this is that if we look at the world through a window during our day to day lives when a person becomes dissociated they are standing increasingly further back from this window proportionally to the dosage consumed. Creating a feeling of being mentally withdrawn from the environment, allowing people to look at their lives from an almost third-person perspective and analyse it without bias, surprisingly resulting in an enjoyable state of deep introspection and a profound drunkenness. These states are often described by people as:<br /> [[File:OtakQ.jpg|200px|thumb|right]]<br /> *Feeling generally separate from the external world.<br /> *Feeling physically and mentally autonomous.<br /> *Feeling as though life is being watched through a screen.<br /> *Feeling as though life is a film or a dream.<br /> *Feeling as though you are physically further from the external world.<br /> *Feeling as though you are looking through somebody else’s eyes.<br /> <br /> States of dissociation and detachment increase proportionally to dosage until they become completely detached from the external environment and eventually their own bodies causing them to slip into the famous dissociative hole. <br /> <br /> A process which can be broken down into three distinct levels of increasing intensity.<br /> <br /> 1. '''Partial detachment''' <br /> <br /> Feelings of surrealness and general detachment from the external environment. As described in detail above.<br /> detachment from the environment. <br /> <br /> As the detachment increases the environment becomes physically further away in distance and increasingly disconnected from a person's sensory perception. Blurred vision sets in while anaesthetic like effects and tactile numbness begin to take place. At this point, motor control and balance become moderately to completely suppressed in a way that is proportional to dosage. In terms of sound, the hearing also seems to become muffled and distant.<br /> <br /> 2. '''Detachment from body''' <br /> <br /> Complete disconnection from the body. It is here where the tripper finds themselves out of their body has slipped into a what can only be described as a hallucinatory hole or an empty void.<br /> <br /> 3. '''Detachment from mind and sense of self''' <br /> <br /> The final level of dissociation and detachment is a complete disconnection from a person's mind and sense of self-resulting in ego death. Giving the profound experience that there is no longer an “I” experiencing the intensity of the trip anymore, there is just the trip as it is and by itself.<br /> <br /> In terms of the thought patterns and general mental processes, dissociative ego death is very similar to its psychedelic equivalent in a number of ways. Characterised by an extreme loss or failure of a person’s short-term memory. This means that a person who is experiencing ego death cannot hold onto the memory of where they are and what they are doing for more than a second or two, instantly forgetting everything as soon as it happens to them. Long-term memory, however, seems to remain mostly intact, with people usually capable of remembering things like who they are and what they are unless they are experiencing ego death at a, particularly high level.<br /> <br /> ===Double vision=== <br /> [[File:Tumblr_mfv8dhHwqV1r7wwr6o1_1280.jpg|200px|thumb|right]]<br /> As a person begins to become disconnected and detached from their external environment. The visual field not only becomes blurred and indistinct but completely doubled onto itself as well. This feels as if you are seeing out of both of your eyes at once with the two images no longer being spliced and merged together into a unified whole. Forcing people to close one of their eyes if they want to perform any task which requires fine vision or reading.<br /> <br /> ===Perspective distortions===<br /> [[File:Aliceinwonderlandsyndrome.png|200px|thumb|right]]<br /> Another very common mental component of a classic dissociative trip is one of a profound shift in perspective; this generally consists of drastic changes in the size and distance attributed either to a person’s body or their external environment.<br /> <br /> Feelings of suddenly having an impossibly giant or tiny body are very common and can be quite an incredible experience. This feeling is already known by the scientific literature as “Alice in Wonderland Syndrome”. It is known as a temporary condition often associated with migraines, brain tumours, and of course the use of psychoactive drugs. With dissociatives at least it can also be more specifically attributed to the room around you or certain body parts. For example feelings of having a huge head or tiny limbs are quite common. This specific mental component has limitless potential in terms of size and the feeling of being simultaneously huge and tiny or having a body that feels larger than the entire universe is not unheard of.<br /> <br /> Perspective distortions can also affect distance, making specific objects or the entire external environment seem physically closer or further away.<br /> Another common manifestation of this effect changes in noise volume, making sounds seem extremely quiet or extremely loud.<br /> <br /> ===Scenery slicing=== <br /> [[File:slice.jpg|200px|thumb|right]]<br /> Scenery slicing is a fairly uncommon visual but appears across multiple people and regularly enough to make it worth mentioning. This effect usually happens spontaneously with no obvious trigger and makes the external environment appear as if it has been cut remarkably cleanly into separate slices with a razor blade Which then slides across each other in separate directions causing the visual field to split apart into sections.<br /> <br /> ===Closed eye visuals=== <br /> [[File:Vusr5.jpg|200px|thumb|right]]<br /> Visuals are an effect triggered by Dissociatives that can be described as the sensation of a person’s field of closed-eye vision being partially or completely encompassed by shifting geometric patterns, shapes, structures and colour. Whilst LSD and Mushrooms merely display visuals on a veil in front of your visual field with no sense of particular size attributed them. Dissociatives take you directly into the centre of them as if they are surrounding you. They also have a sense of physical size attributed to them.<br /> <br /> Dissociative visuals are more simplistic and less intricate than psychedelic visuals. They tend to be darker and slower in terms of how fast they change, only displaying themselves when the tripper has their eyes closed. Simply put, the visuals are more solid and realistic than psychedelic visuals with an actual sense of physical size and 3-Dimensional depth but never quite as detailed or complex.<br /> <br /> ===Spaces and holes===<br /> The spaces and holes encountered on Dissociatives are something that is experienced once the detachment has reached level 3. When you have finally become completely disconnected from your physical body. Causing you to undergo an out of body experience and be pulled into a place that feels as if it is outside of reality. <br /> <br /> A place that is commonly referenced to by the dissociative community as a hole. With drug-specific manifestations of this state being known as “the K-hole” for Ketamine and the “M-hole” for MXE. Commonly described as a complete loss of bodily awareness and sensations of floating or falling through a dark and infinite void over great physical distances. Often done on what feels like some sort of invisible rail. A feeling that is interpreted by many people as flying through space or the night sky. With many trippers stating that they feel as though their perceptions are located so deep inside the mind that the real world seems so distant that it might as well not exist. <br /> <br /> In terms of its appearance, a typical dissociative hole is usually completely dark with occasional clouds of slow-moving amorphous colour clouds in the background. At their lowest level they are completely empty, but as dosage is increased they are accompanied by and filled with a wide variety of elaborate and complex structures which are described in detail below.<br /> <br /> ===Hallucinatory structures===<br /> [[File:SI6XZ.png|200px|thumb|right]]<br /> Dissociative induced hallucinatory structures are the only feature found within what would otherwise be completely empty spaces and holes. They can generally be described as 3-Dimensional and monolithic shapes or structures of infinite variety and size that float above, below or in front of you as they gradually zoom, rotate or pan into focus and become unveiled before your eyes at a slow pace. These structures can take any static comprehensible shape possible but can commonly be experienced as vast and giant pillars, columns, blocks, teardrops, wheels and pyramids. Often fractal in nature and capable of being manifested in any variety of colours but usually following darker themes and tones. In terms of the materials that they appear to be comprised of and the complexity of detail in which they are perceived in, dissociative structures can be broken into 4 basic levels.<br /> <br /> '''1. 2-Dimensional Structures'''<br /> <br /> The most basic level of structural complexity confines it’s geometry to strictly 2-Dimensional shapes. These shapes are usually very flat and dark in their colour and often “felt” instead of seen in a way that cannot be described adequately to the uninitiated. In terms of their size, these structures take up the entirety of a person's visual field but do not appear to have any particular size attributed to them.<br /> <br /> '''2. Partially defined 3-Dimensional Structures'''<br /> <br /> Above this, the structures become better defined and 3-Dimensional in shape with basic detail in their lighting and shadow. Appearing to be made of semi-transparent condensed colour or solidified shimmering visuals that are seen as ill-defined, soft and out of focus around their edges. In terms of size, these structures appear to be extremely large, stretching out across hundreds and hundreds of metres.<br /> <br /> '''3. Fully defined 3-Dimensional Structures'''<br /> <br /> Once hallucinatory structures reach their third level of complexity they become fully defined in their shape, edges, lighting, shadow and detail. Often appearing to be made of solid and dense realistic materials such as stone and metal. They are capable of being thousands of miles across themselves and extremely complex in form.<br /> <br /> '''4. Self-transforming mechanistic structural universes'''<br /> [[File:WZah0.jpg|200px|thumb|right]]<br /> As dosage increases, the detail continues to complexity proportionally until the sensation of seeing the entire universe condensed into an infinitely vast and intricate self-transforming machine structure becomes present. Accompanied by the sudden realization that you are the structure that you are staring down upon and that the structure is also you. In terms of its appearance, this state is extremely hard to describe. The structure can take any form but usually appears to be consistently shaped machine-like structures or clouds that are infinite in size and felt at every point of detail across themselves. This is immediately interpreted through some sort of innate instinct as “the universe” or at least, “everything” by everybody who undergoes the experience.<br /> <br /> Structures typically last anywhere from 30 seconds to several minutes before the person slips back into reality or into the presence of another structure. There are three different methods through which these hallucinatory structures are shifted between.<br /> <br /> *'''Structural Transformations''' - structures can switch between each other by morphing around you in a static, comprehensible way. Something that usually unfolds in front of you in a rather slow, step by step morphing process.<br /> *'''Structural Panning''' - structures can switch between each other by remaining completely static in their shape but simply panning out of view until they are no longer within your field of vision. It’s from here that another structure usually comes into view from behind your physical body within a few seconds to a couple of minutes. Allowing the cycle of continuous spontaneous structures to go on undisturbed.<br /> *'''Travelling over great distances''' - The third method of transitioning is experienced when the structures appear to be stuck in place whilst you are floating silently between them over what feels like a huge and physical distance. This is often done on an invisible rail through the vast and infinite dissociative hole. A feeling that is interpreted by many people as flying through space or the night sky.<br /> <br /> ===Hallucinatory states=== <br /> Hallucinations and scenarios are only possible during very high dose trips and an intensely realistic component of the Dissociative experience. They could be anything but generally fall under common archetypes such as contact with autonomous entities, imagined landscapes, alternate dimensions, replayed memories and situations that seem so unlike anything previously experienced that they are in all probability, untranslatable into English. Starting out by following a feeling of detachment from the hallucination itself, for example watching autonomous people and entities going about their daily business oblivious to your existence, playing out as if it were a film. At higher doses of hallucinatory states they become increasingly involved, accessing distant memories from your past is also completely possible. Replayed memories can feel like weeks and weeks of real-time hallucinations and are perfect in every detail.<br /> <br /> In comparison to psychedelics, they are more solid and not made of a closed eye visual based material. The solidity and detachment from these scenarios are what separates them in my opinion from any entity contact or hallucinations experienced on drugs such as Mushrooms or LSD.<br /> <br /> ==Harm Reduction==<br /> <br /> *Driving or operating machinery under the influence of dissociatives is strongly discouraged. Your spatial awareness is extremely limited, even when mildly intoxicated.<br /> *On higher does coordination is imparted to the point that any movement should be as limited as possible. A safe environment without hazards is recommended (such as a bed). Most of the damage imparted by dissociatives are through users hurting themselves while attempting to move around while impaired.<br /> *Nausea can happen on many dissociatives, usually directly after dosing - usually only if there are stomach contents. It is best to not eat for 3-4 hours before dosing.<br /> *Dissociatives may be neurotoxic.&lt;ref&gt;http://dx.doi.org/10.1126%2Fscience.2660263&lt;/ref&gt; Moderation is advised.<br /> *Some dissociatives (such as ketamine) are known to have negative impacts on bladder health.&lt;ref&gt;http://www.hkmj.org/article_pdfs/hkm1002p6.pdf&lt;/ref&gt;, and it is suspected in others.<br /> *If using a new substance having a sober person available may limit the fallout from unexpected effects.<br /> *Doctors usually prescribe Ativan (Lorazepam/Benzodiazepine) and Haldol (anti-psychotic) to treat overdoses.<br /> *As always, contact emergency professionals if you think you are a danger to yourself or others.<br /> * Excessive use or overdose of dissociatives has been known to cause muscle breakdown (or [http://en.wikipedia.org/wiki/Rhabdomyolysis rhabdomyolysis]), which is a potentially fatal condition.<br /> <br /> ===Interactions===<br /> <br /> It is generally unwise to mix CNS depressants, such as benzodiazepines or alcohol, as it increases the risk of an overdose through respiratory depression. Certain dissociatives also carry particular constraints in terms of interactions. See the [[Drug combinations]] chart for more information.<br /> <br /> ===Research Chemicals===<br /> <br /> The dangers of research chemical dissociatives inherit many of the potential dangers of the more traditional dissociatives including overdose mania, muscle degradation etc and as with most well-established dissociatives, most of the new RCs carry a heavy risk of addiction. However, due to the new and unresearched nature of these drugs, the thresholds at which these negative effects occur is relatively unknown. [[MXE]] was created with the express intent of reducing the risk of urinary tract damage through higher potency, users with a high tolerance to the drug will take large amounts of material to experience effects, and there is no information about how it differs from other dissociatives with respect to such damage.<br /> <br /> As with some more well-established dissociatives, there is often a wide range of isomer configurations which lead to inconsistencies in effects from one batch to another.<br /> <br /> It is fairly common practice for vendors to misrepresent their product in various ways. There have been batches of RC dissos released which have been found to contain chemicals left-over from the manufacturer. There have also been many anecdotes reporting incidents of batches being sold with other active cuts. Since these drugs are all very new there have been very few actual laboratory analysis reports on the exact content of various RC dissos, and as such, there is a fair bit of speculation and misinformation circulating about all RCs. Furthermore, vendors and manufacturers have been known to make exaggerated claims that have never been actually proven (for example, the theory that MXE will be less physically destructive than its cousin [[Ketamine]] originated from one of the first vendors to carry the product)<br /> <br /> Consider the case of Methoxyphenidine, which was named as such and abbreviated as 'MXP' specifically to be marketed as an MXE replacement, where in reality MXP is closer to PCP than it is to MXE in chemical structure and effects.<br /> <br /> See the [[Research Chemicals]] page for more information.<br /> <br /> ==Links==<br /> http://en.wikipedia.org/wiki/Dissociative<br /> <br /> ==References==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=MDMA&diff=5751 2018-10-09T22:01:11Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>=Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=MDMA&diff=5750 2018-10-09T22:00:56Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Mdma.jpg|thumb|300px|MDMA Crystals]]<br /> <br /> '''MDMA''' (3,4-methylenedioxy-N-Methylamphetamine) is an popular drug of the phenethylamine and amphetamine class known for its empathogenic, euphoric, and stimulant effects, and has also been used in psychotherapy. It most frequently comes in tablet form, although it is also found in capsules or as powder. MDMA is also known as Ecstasy, Molly, XTC, E and several other names. <br /> <br /> Because MDMA is so popular and because it goes well with dance parties, the demand for it usually exceeds supply, especially at any given location on any given night. This creates an opening for unscrupulous individuals to sell virtually anything as 'ecstasy'. While 'ecstasy' is the popular name for MDMA, the functional definition of ecstasy is any pill represented as MDMA on the street. Ecstasy pills are notoriously unreliable in content, more so than most other street drugs, and commonly contain either caffeine, ephedrine, amphetamines, other MDXX's, DXM, or in rare cases DOX's, and don't necessarily contain MDMA or any psychoactive. They can also contain very neurotoxic substances (such as PMA, 4-CA, among many others). This problem has led to the development of simple MDMA [[Test Kits]] that may help give the user a general sense of the content of a pill.<br /> <br /> The experience is often called rolling.<br /> <br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=MDMA&diff=5749 2018-10-09T22:00:40Z

<p>Dumbdumb123: /* Goodbye moonmen */</p> <hr /> <div>[[File:Mdma.jpg|thumb|300px|MDMA Crystals]]<br /> <br /> '''MDMA''' (3,4-methylenedioxy-N-Methylamphetamine) is an popular drug of the phenethylamine and amphetamine class known for its empathogenic, euphoric, and stimulant effects, and has also been used in psychotherapy. It most frequently comes in tablet form, although it is also found in capsules or as powder. MDMA is also known as Ecstasy, Molly, XTC, E and several other names. <br /> <br /> Because MDMA is so popular and because it goes well with dance parties, the demand for it usually exceeds supply, especially at any given location on any given night. This creates an opening for unscrupulous individuals to sell virtually anything as 'ecstasy'. While 'ecstasy' is the popular name for MDMA, the functional definition of ecstasy is any pill represented as MDMA on the street. Ecstasy pills are notoriously unreliable in content, more so than most other street drugs, and commonly contain either caffeine, ephedrine, amphetamines, other MDXX's, DXM, or in rare cases DOX's, and don't necessarily contain MDMA or any psychoactive. They can also contain very neurotoxic substances (such as PMA, 4-CA, among many others). This problem has led to the development of simple MDMA [[Test Kits]] that may help give the user a general sense of the content of a pill.<br /> <br /> The experience is often called rolling.<br /> <br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> <br /> = Harm Reduction =<br /> <br /> * MDMA rapidly builds tolerance, depletes serotonin and compounds neurotoxicity issues. Look for other drugs and avoid using MDMA more than once every few months.<br /> <br /> * Ecstasy tablets are notoriously impure, often containing chemicals other than MDMA. Check out [http://www.ecstasydata.org/ EcstasyData] and [http://pillreports.com/ Pill Reports] for pill testing results. Buy a [[Test Kit]]!<br /> <br /> == Health risks ==<br /> <br /> As with many drugs, there are some serious risks associated with taking MDMA affecting people with existing health conditions, or in certain cases people who are otherwise very healthy. It is not advisable to take MDMA if any of the following apply to you:<br /> * Health issues with the Heart, Kidneys or Liver<br /> * High blood pressure<br /> * History of having a stroke or heart attack<br /> <br /> In rare cases MDMA can cause seizures, overheating, hypothermia, dehydration or water poisoning. It is important to keep an eye on body temperature and hydration while under the effects of MDMA.<br /> <br /> There are some studies which suggest that long-term overuse and abuse of MDMA can cause or increase depression.<br /> <br /> === Interactions ===<br /> <br /> * MDMA can cause [[Serotonin Syndrome]] when combined with MAOIs. Refer to [[Drug combinations]] for more information.<br /> <br /> * [http://www.erowid.org/chemicals/mdma/mdma_info9.shtml SSRIs and SNRIs block most effects of MDMA.]<br /> <br /> == Chemistry and Pharmacology ==<br /> <br /> === Neurotoxicity, by Borax ===<br /> <br /> * The neurotoxicity is [https://pay.reddit.com/r/drugs/wiki/mdmaneurotoxicity well established], but studies are largely on mice and rats with [http://www.bluelight.org/vb/threads/614514 higher dosages than humans tend to use].<br /> <br /> * There is an excellent run through of the pharmacodynamics of MDMA neurotoxicity [http://www.dancesafe.org/drug-information/is-mdma-neurotoxic/ here].<br /> <br /> * Overall what we know is that the neurotoxicity scales with dose, and is likely to do so exponentially as the body is caused to overheat more and has less anitoxidants to deal with metabolites. <br /> <br /> * We don't have any quantitative estimates about damage from normal human doses because it would not be ethical to dose people repeatedly just to see how much it damages them, and it's very hard to gather data from regular users because of the huge number of variables like alcohol and cannabis use, sleep deprivation, environment of MDMA use etc.<br /> <br /> * We know that long term users are not [http://jop.sagepub.com/content/24/2/175 mentally impaired] but those *abusing* the drug do show a reduced ability to enjoy it and suffer a more intense comedown, indicating that there is something going on at higher doses.<br /> <br /> * Another discussion about MDMA neurotoxicity can be found [https://pay.reddit.com/r/Drugs/comments/12v5f8/research_suggests_no_neurotoxicity_in_mdma/c6ye9xc here].<br /> <br /> === MDMA purity myths, by Borax ===<br /> <br /> The 84% claims are based around either a poor understanding of the science or are a deliberate attempt to pass off inferior product as high quality.<br /> <br /> You should read [https://pay.reddit.com/r/Drugs/comments/xihdo/rdrugs_ama_series_mdma_aka_ecstasy_e_x_molly/c5moa3i this discussion], but basically if anyone claims their MDMA is 84% pure then they have performed no analysis at all and should not be trusted. <br /> <br /> With almost all, the name is an abbreviation for Drug.salt. In the case of MDMA, it is MDMA.HCl, amphetamine is usually amphetamine.H2SO4 and LSD is LSD.tartrate. Because these forms are ubiquitous, nobody bothers to mention the second bit because it's irrelevant. All doses you see for MDMA are referring to the HCl salt, which means that MDMA which is sold as &quot;the purest you can get, 84%&quot;, is treated as 100% pure.<br /> <br /> The reason sellers do this is because they usually don't have very pure MDMA, and they want people to make the mistake you have made and take more to account for crappy product. It is dishonest, confusing and misleading and if you have a choice you should avoid this vendor.<br /> <br /> === Production ===<br /> <br /> MDMA is generally synthesised from naturally occurring safrole, extracted from the sassafras tree, making it a semi-synthetic drug.<br /> <br /> == Legal Status ==<br /> <br /> MDMA is legally controlled in most of the world under the UN Convention on Psychotropic Substances and other international agreements, although exceptions exist for research and limited medical use. In general, the unlicensed use, sale or manufacture of MDMA are all criminal offences.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Mdma.jpg|''MDMA Crystals''<br /> Image:Mdma2.jpg|''MDMA Crystals''<br /> Image:Bitcoin.png|''Bitcoin MDMA Pill''<br /> Image:Mdma3.png|''MDMA Crystals''<br /> Image:Mdma7.jpg|''MDMA Crystals''<br /> &lt;/gallery&gt;<br /> <br /> == Links ==<br /> <br /> [https://pay.reddit.com/r/Borax/comments/w5c1x/a_stepbystep_guide_to_reducing_mdma_neurotoxicity/ A step-by-step guide to reducing MDMA neurotoxicity]<br /> <br /> [https://pay.reddit.com/r/drugs/wiki/mdmaneurotoxicity Studies on MDMA neurotoxicity]<br /> <br /> [https://pay.reddit.com/r/DrugNerds/comments/15m9sf/mdma_supplementation/ MDMA Supplementation]<br /> <br /> [https://www.erowid.org/chemicals/mdma/ Erowid MDMA vault]<br /> <br /> [https://rollsafe.org/ RollSafe - MDMA Info]<br /> <br /> [[Category:Drugs]]<br /> <br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=MDMA&diff=5748 2018-10-09T22:00:07Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Mdma.jpg|thumb|300px|MDMA Crystals]]<br /> <br /> '''MDMA''' (3,4-methylenedioxy-N-Methylamphetamine) is an popular drug of the phenethylamine and amphetamine class known for its empathogenic, euphoric, and stimulant effects, and has also been used in psychotherapy. It most frequently comes in tablet form, although it is also found in capsules or as powder. MDMA is also known as Ecstasy, Molly, XTC, E and several other names. <br /> <br /> Because MDMA is so popular and because it goes well with dance parties, the demand for it usually exceeds supply, especially at any given location on any given night. This creates an opening for unscrupulous individuals to sell virtually anything as 'ecstasy'. While 'ecstasy' is the popular name for MDMA, the functional definition of ecstasy is any pill represented as MDMA on the street. Ecstasy pills are notoriously unreliable in content, more so than most other street drugs, and commonly contain either caffeine, ephedrine, amphetamines, other MDXX's, DXM, or in rare cases DOX's, and don't necessarily contain MDMA or any psychoactive. They can also contain very neurotoxic substances (such as PMA, 4-CA, among many others). This problem has led to the development of simple MDMA [[Test Kits]] that may help give the user a general sense of the content of a pill.<br /> <br /> The experience is often called rolling.<br /> <br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> <br /> == Dosage ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 40-75mg<br /> |-<br /> | Common || 75-125mg<br /> |-<br /> | Strong || 125-175mg<br /> |-<br /> | Heavy || 175mg+<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 20-70 minutes<br /> |-<br /> | Peak || 2-3 hours<br /> |-<br /> | Total || 3-5 hours<br /> |-<br /> | After-effects || 2-24 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Postive ===<br /> <br /> * Mild to extreme mood lift, euphoria<br /> <br /> * Increased willingness to communicate<br /> <br /> * Increase in energy (stimulation)<br /> <br /> * Ego softening<br /> <br /> * Decreased fear, anxiety, and insecurities<br /> <br /> * Feelings of comfort, belonging, and closeness to others<br /> <br /> * Feelings of love and empathy<br /> <br /> * Forgiveness of self and others<br /> <br /> * A sense of inner peace and acceptance of self, others, and the world<br /> <br /> * Increased awareness of senses (taste, smell, touch, hearing, vision)<br /> <br /> * Life-changing spiritual experiences<br /> <br /> * Analgesia, anti-nocioception, decreased pain perception<br /> <br /> === Neutral ===<br /> <br /> * Decreased appetite<br /> <br /> * Visual distortion<br /> <br /> * Rapid, involuntary eye jiggling (nystagmus)<br /> <br /> * Mild visual hallucinations (uncommon)<br /> <br /> * Moderately increased heart rate and blood pressure (increases with dose)<br /> <br /> * Restlessness, nervousness, shivering<br /> <br /> * Change in body temperature regulation<br /> <br /> * Upwellings of unexpected emotion, emotional lability<br /> <br /> * Strong desire to do or want more when coming down<br /> <br /> === Negative ===<br /> <br /> Negative side effects increase with higher doses and frequent use.<br /> <br /> * Inappropriate and/or unintended emotional bonding<br /> <br /> * Anxiety or paranoia (less common than opposite)<br /> <br /> * Agitation (less common than opposite)<br /> <br /> * Tendency to say things you might feel uncomfortable about later<br /> <br /> * Mild to extreme jaw clenching (trisma), tongue and cheek chewing, and teeth grinding (bruxia)<br /> <br /> * Short-term memory scramble or loss &amp; confusion<br /> <br /> * Short periods of swooning, or disconnection from the external world, usually at very high doses or during brief blasts of intense rushing while coming up.<br /> <br /> * Muscle tension (common)<br /> <br /> * Insomnia, inability to fall asleep when physically tired<br /> <br /> * Erectile disfunction and difficulty reaching orgasm<br /> <br /> * Increase in body temperature, hyperthermia, dehydration (drink water)<br /> <br /> * Hyponatremia (don't drink too much water)<br /> <br /> * Nausea and vomiting<br /> <br /> * Headaches, dizziness, loss of balance, and vertigo<br /> <br /> * Sadness on coming down, sense of loss or immediate nostalgia<br /> <br /> * Post-trip crash - unpleasantly harsh comedown from the peak effect<br /> <br /> * Hangover the next day, lasting days to weeks<br /> <br /> * Possible strong urge to repeat the experience, though not physically addictive<br /> <br /> * Possible psychological crisis requiring hospitalization (psychotic episodes, severe panic attacks, etc) (rare)<br /> <br /> * Possible liver toxicity (rare)<br /> <br /> * Neurotoxicity<br /> <br /> * Small risk of death; approximately 2 per 100,000 new users have extreme negative reactions resulting in death (very rare)<br /> <br /> ==== Hangover ====<br /> <br /> Many users [http://www.erowid.org/chemicals/mdma/mdma_effects_hangover1.shtml report feeling extremely drained the day after MDMA use]. This 'day after' effect means for many MDMA users that they need to plan 2 days for the experience: one for the peak experience and one recovery day, with very little planned. Many users also experience some level of post-MDMA depression, often starting on the second day after the experience and lasting for up to 5 days. A small percentage of users report depressive symptoms for weeks afterwards. Alternately, some users report feeling better than normal for a week or so after taking MDMA. The negative after-effects of taking MDMA appear to be worse with higher frequencies of use, higher dosages, and perhaps total lifetime usage.<br /> <br /> = Harm Reduction =<br /> <br /> * MDMA rapidly builds tolerance, depletes serotonin and compounds neurotoxicity issues. Look for other drugs and avoid using MDMA more than once every few months.<br /> <br /> * Ecstasy tablets are notoriously impure, often containing chemicals other than MDMA. Check out [http://www.ecstasydata.org/ EcstasyData] and [http://pillreports.com/ Pill Reports] for pill testing results. Buy a [[Test Kit]]!<br /> <br /> == Health risks ==<br /> <br /> As with many drugs, there are some serious risks associated with taking MDMA affecting people with existing health conditions, or in certain cases people who are otherwise very healthy. It is not advisable to take MDMA if any of the following apply to you:<br /> * Health issues with the Heart, Kidneys or Liver<br /> * High blood pressure<br /> * History of having a stroke or heart attack<br /> <br /> In rare cases MDMA can cause seizures, overheating, hypothermia, dehydration or water poisoning. It is important to keep an eye on body temperature and hydration while under the effects of MDMA.<br /> <br /> There are some studies which suggest that long-term overuse and abuse of MDMA can cause or increase depression.<br /> <br /> === Interactions ===<br /> <br /> * MDMA can cause [[Serotonin Syndrome]] when combined with MAOIs. Refer to [[Drug combinations]] for more information.<br /> <br /> * [http://www.erowid.org/chemicals/mdma/mdma_info9.shtml SSRIs and SNRIs block most effects of MDMA.]<br /> <br /> == Chemistry and Pharmacology ==<br /> <br /> === Neurotoxicity, by Borax ===<br /> <br /> * The neurotoxicity is [https://pay.reddit.com/r/drugs/wiki/mdmaneurotoxicity well established], but studies are largely on mice and rats with [http://www.bluelight.org/vb/threads/614514 higher dosages than humans tend to use].<br /> <br /> * There is an excellent run through of the pharmacodynamics of MDMA neurotoxicity [http://www.dancesafe.org/drug-information/is-mdma-neurotoxic/ here].<br /> <br /> * Overall what we know is that the neurotoxicity scales with dose, and is likely to do so exponentially as the body is caused to overheat more and has less anitoxidants to deal with metabolites. <br /> <br /> * We don't have any quantitative estimates about damage from normal human doses because it would not be ethical to dose people repeatedly just to see how much it damages them, and it's very hard to gather data from regular users because of the huge number of variables like alcohol and cannabis use, sleep deprivation, environment of MDMA use etc.<br /> <br /> * We know that long term users are not [http://jop.sagepub.com/content/24/2/175 mentally impaired] but those *abusing* the drug do show a reduced ability to enjoy it and suffer a more intense comedown, indicating that there is something going on at higher doses.<br /> <br /> * Another discussion about MDMA neurotoxicity can be found [https://pay.reddit.com/r/Drugs/comments/12v5f8/research_suggests_no_neurotoxicity_in_mdma/c6ye9xc here].<br /> <br /> === MDMA purity myths, by Borax ===<br /> <br /> The 84% claims are based around either a poor understanding of the science or are a deliberate attempt to pass off inferior product as high quality.<br /> <br /> You should read [https://pay.reddit.com/r/Drugs/comments/xihdo/rdrugs_ama_series_mdma_aka_ecstasy_e_x_molly/c5moa3i this discussion], but basically if anyone claims their MDMA is 84% pure then they have performed no analysis at all and should not be trusted. <br /> <br /> With almost all, the name is an abbreviation for Drug.salt. In the case of MDMA, it is MDMA.HCl, amphetamine is usually amphetamine.H2SO4 and LSD is LSD.tartrate. Because these forms are ubiquitous, nobody bothers to mention the second bit because it's irrelevant. All doses you see for MDMA are referring to the HCl salt, which means that MDMA which is sold as &quot;the purest you can get, 84%&quot;, is treated as 100% pure.<br /> <br /> The reason sellers do this is because they usually don't have very pure MDMA, and they want people to make the mistake you have made and take more to account for crappy product. It is dishonest, confusing and misleading and if you have a choice you should avoid this vendor.<br /> <br /> === Production ===<br /> <br /> MDMA is generally synthesised from naturally occurring safrole, extracted from the sassafras tree, making it a semi-synthetic drug.<br /> <br /> == Legal Status ==<br /> <br /> MDMA is legally controlled in most of the world under the UN Convention on Psychotropic Substances and other international agreements, although exceptions exist for research and limited medical use. In general, the unlicensed use, sale or manufacture of MDMA are all criminal offences.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Mdma.jpg|''MDMA Crystals''<br /> Image:Mdma2.jpg|''MDMA Crystals''<br /> Image:Bitcoin.png|''Bitcoin MDMA Pill''<br /> Image:Mdma3.png|''MDMA Crystals''<br /> Image:Mdma7.jpg|''MDMA Crystals''<br /> &lt;/gallery&gt;<br /> <br /> == Links ==<br /> <br /> [https://pay.reddit.com/r/Borax/comments/w5c1x/a_stepbystep_guide_to_reducing_mdma_neurotoxicity/ A step-by-step guide to reducing MDMA neurotoxicity]<br /> <br /> [https://pay.reddit.com/r/drugs/wiki/mdmaneurotoxicity Studies on MDMA neurotoxicity]<br /> <br /> [https://pay.reddit.com/r/DrugNerds/comments/15m9sf/mdma_supplementation/ MDMA Supplementation]<br /> <br /> [https://www.erowid.org/chemicals/mdma/ Erowid MDMA vault]<br /> <br /> [https://rollsafe.org/ RollSafe - MDMA Info]<br /> <br /> [[Category:Drugs]]<br /> <br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Methamphetamine&diff=5747 2018-10-09T21:58:57Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Crystal Meth.jpg|250px|right]]<br /> <br /> '''Methamphetamine''' is a strong physical and mental stimulant. It is legally prescribed as a treatment for ADD under the brand name Desoxyn, for both children and adults. Recreationally, methamphetamine is used to increase sexual drive, lift the mood, and increase energy, allowing some users to engage in sexual activity continuously for several days straight. Methamphetamine production is a relatively simple process, especially when compared to many other recreational drugs which has contributed to its widespread use. It is frequently reported on in the media when home meth-producing labs are busted.<br /> <br /> Methamphetamine exists as two [[Glossary#Enantiomer|enantiomers]], dextrorotary and levorotary. Dextromethamphetamine is a stronger central nervous system(CNS) stimulant than levomethamphetamine; however, both are addictive and produce the same toxicity symptoms at high doses. Methamphetamine may be sold illegally, either as pure dextromethamphetamine or in an equal parts mixture of the right and left handed molecules (i.e., 50% levomethamphetamine and 50% dextromethamphetamine). Both dextromethamphetamine and racemic methamphetamine are schedule II controlled substances in the United States. Similarly, the production, distribution, sale, and possession of methamphetamine is restricted or illegal in many other countries due to its placement in schedule II of the United Nations Convention on Psychotropic Substancestreaty. In contrast, levomethamphetamine is an over-the-counter drug in the United States.<br /> <br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> <br /> == Dosage ==<br /> <br /> <br /> {{#tdose: methamphetamine }}<br /> <br /> == Duration ==<br /> <br /> These durations are for users of somewhat moderate tolerance. Amphetamine naive users may not be able to sleep for 18+ hours after oral use and other routes will be lengthened as well. <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 20-70 minutes<br /> |-<br /> | Total || 8-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 5-10 minutes<br /> |-<br /> | Total || 2-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 1-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> == Effects ==<br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Methamphetamine&diff=5746 2018-10-09T21:58:11Z

<p>Dumbdumb123: /* Goodbye moonmen */</p> <hr /> <div>[[File:Crystal Meth.jpg|250px|right]]<br /> <br /> '''Methamphetamine''' is a strong physical and mental stimulant. It is legally prescribed as a treatment for ADD under the brand name Desoxyn, for both children and adults. Recreationally, methamphetamine is used to increase sexual drive, lift the mood, and increase energy, allowing some users to engage in sexual activity continuously for several days straight. Methamphetamine production is a relatively simple process, especially when compared to many other recreational drugs which has contributed to its widespread use. It is frequently reported on in the media when home meth-producing labs are busted.<br /> <br /> Methamphetamine exists as two [[Glossary#Enantiomer|enantiomers]], dextrorotary and levorotary. Dextromethamphetamine is a stronger central nervous system(CNS) stimulant than levomethamphetamine; however, both are addictive and produce the same toxicity symptoms at high doses. Methamphetamine may be sold illegally, either as pure dextromethamphetamine or in an equal parts mixture of the right and left handed molecules (i.e., 50% levomethamphetamine and 50% dextromethamphetamine). Both dextromethamphetamine and racemic methamphetamine are schedule II controlled substances in the United States. Similarly, the production, distribution, sale, and possession of methamphetamine is restricted or illegal in many other countries due to its placement in schedule II of the United Nations Convention on Psychotropic Substancestreaty. In contrast, levomethamphetamine is an over-the-counter drug in the United States.<br /> <br /> == History ==<br /> Amphetamine, discovered before methamphetamine, was first synthesized in 1887 in Germany by Romanian chemist Lazăr Edeleanu who named it phenylisopropylamine. Shortly after, methamphetamine was synthesized from ephedrine in 1893 by Japanesechemist Nagai Nagayoshi. Three decades later, in 1919, methamphetamine hydrochloride was synthesized by pharmacologist Akira Ogata via reduction of ephedrine using red phosphorus and iodine. During World War II, methamphetamine was used extensively by the Axis forces for its stimulant effects. Obetrol, patented by Obetrol Pharmaceuticals in the 1950s and indicated for treatment of obesity, was one of the first brands of pharmaceutical methamphetamine products. Due to the psychological and stimulant effects of methamphetamine, Obetrol became a popular diet pill in America in the 1950s and 1960s. Eventually, as the addictive properties of the drug became known, governments began to strictly regulate the production and distribution of methamphetamine. For example, during the early 1970s in the United States, methamphetamine became a schedule II controlled substance under the Controlled Substances Act. Currently, methamphetamine is sold under the trade name Desoxyn, trademarked by the Danish pharmaceutical company Lundbeck. As of January 2013, the Desoxyn trademark had been sold to Italian pharmaceutical company Recordati.<br /> <br /> == Dosage ==<br /> <br /> <br /> {{#tdose: methamphetamine }}<br /> <br /> == Duration ==<br /> <br /> These durations are for users of somewhat moderate tolerance. Amphetamine naive users may not be able to sleep for 18+ hours after oral use and other routes will be lengthened as well. <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 20-70 minutes<br /> |-<br /> | Total || 8-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 5-10 minutes<br /> |-<br /> | Total || 2-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 1-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> == Effects ==<br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=<br /> =Goodbye moonmen=</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Methamphetamine&diff=5745 2018-10-09T21:57:42Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Crystal Meth.jpg|250px|right]]<br /> <br /> '''Methamphetamine''' is a strong physical and mental stimulant. It is legally prescribed as a treatment for ADD under the brand name Desoxyn, for both children and adults. Recreationally, methamphetamine is used to increase sexual drive, lift the mood, and increase energy, allowing some users to engage in sexual activity continuously for several days straight. Methamphetamine production is a relatively simple process, especially when compared to many other recreational drugs which has contributed to its widespread use. It is frequently reported on in the media when home meth-producing labs are busted.<br /> <br /> Methamphetamine exists as two [[Glossary#Enantiomer|enantiomers]], dextrorotary and levorotary. Dextromethamphetamine is a stronger central nervous system(CNS) stimulant than levomethamphetamine; however, both are addictive and produce the same toxicity symptoms at high doses. Methamphetamine may be sold illegally, either as pure dextromethamphetamine or in an equal parts mixture of the right and left handed molecules (i.e., 50% levomethamphetamine and 50% dextromethamphetamine). Both dextromethamphetamine and racemic methamphetamine are schedule II controlled substances in the United States. Similarly, the production, distribution, sale, and possession of methamphetamine is restricted or illegal in many other countries due to its placement in schedule II of the United Nations Convention on Psychotropic Substancestreaty. In contrast, levomethamphetamine is an over-the-counter drug in the United States.<br /> <br /> == History ==<br /> Amphetamine, discovered before methamphetamine, was first synthesized in 1887 in Germany by Romanian chemist Lazăr Edeleanu who named it phenylisopropylamine. Shortly after, methamphetamine was synthesized from ephedrine in 1893 by Japanesechemist Nagai Nagayoshi. Three decades later, in 1919, methamphetamine hydrochloride was synthesized by pharmacologist Akira Ogata via reduction of ephedrine using red phosphorus and iodine. During World War II, methamphetamine was used extensively by the Axis forces for its stimulant effects. Obetrol, patented by Obetrol Pharmaceuticals in the 1950s and indicated for treatment of obesity, was one of the first brands of pharmaceutical methamphetamine products. Due to the psychological and stimulant effects of methamphetamine, Obetrol became a popular diet pill in America in the 1950s and 1960s. Eventually, as the addictive properties of the drug became known, governments began to strictly regulate the production and distribution of methamphetamine. For example, during the early 1970s in the United States, methamphetamine became a schedule II controlled substance under the Controlled Substances Act. Currently, methamphetamine is sold under the trade name Desoxyn, trademarked by the Danish pharmaceutical company Lundbeck. As of January 2013, the Desoxyn trademark had been sold to Italian pharmaceutical company Recordati.<br /> <br /> == Dosage ==<br /> <br /> <br /> {{#tdose: methamphetamine }}<br /> <br /> == Duration ==<br /> <br /> These durations are for users of somewhat moderate tolerance. Amphetamine naive users may not be able to sleep for 18+ hours after oral use and other routes will be lengthened as well. <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 20-70 minutes<br /> |-<br /> | Total || 8-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 5-10 minutes<br /> |-<br /> | Total || 2-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 1-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> == Effects ==<br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> == Harm Reduction ==<br /> When dealing with methamphetamine it's important to remember that a large number of the harms come not from the drug itself, but from the behaviors the drug causes individuals to exhibit. Loss of sleep, poor nutrition, and poor self care are the cause of many of the negative effects. <br /> <br /> *Methamphetamine lasts for a long time and will impair sleep. Dose early in the day and do not redose to avoid sleep disruption.<br /> <br /> *Oral ROA has less redose compulsion than other routes such as vaporization. <br /> <br /> *It is important to eat and stay hydrated, even if you do not feel the need for food. Even if you are not feeling like eating you can generally have some fruit or a bowl of cereal or yogurt with granola. <br /> <br /> *It is important to keep up on your self-care. &quot;Meth mouth&quot; is caused by poor oral hygiene combined with the habit of users to sip sugary beverages to relieve dry mouth symptoms. Use water and not soda to relieve dry mouth. Remember to brush your teeth after eating or consuming any caloric beverages.<br /> <br /> *Stimulant drugs can cause kidney damage and stroke in users with high blood pressure. If you have been diagnosed or told you have high blood pressure use with caution.<br /> <br /> == Chemistry and Pharmacology ==<br /> [[File:Meth molecule.jpg|150px|right]]<br /> <br /> Systematic name: N-methyl-1-phenylpropan-2-amine<br /> <br /> At room temperature, the free base of methamphetamine is a clear and colorless liquid with an odor characteristic of geranium leaves. It is soluble in diethyl ether and ethanol as well as miscible with chloroform. In contrast, the methampetamine hydrochloride salt is odorless with a bitter taste. It has a melting point between 170 to 175 °C (338 to 347 °F) and, at room temperature, occurs as white crystals or a white crystalline powder. The hydrochloride salt is also freely soluble in alcohol and water.<br /> <br /> Powder methamphetamine is the hydrochloride salt form which is strongly hygroscopic (absorbs water from the air quickly). The HCl salt is smokable as is. Crystal meth &quot;Crystal Meth&quot; or &quot;Ice&quot; refer to methamphetamine grown into crystals. Though many people believe that Crystal Meth is the freebase form of methamphetamie HCl, this is not true. Methamphetamine is smokable in its normal HCL form, but taking the time to grow it into crystals makes it easier to smoke. Meth in visible crystals (rather than powder) is likely to be relatively pure as it is difficult to grow crystals from impure material. Methamphetamine freebase is an oil and is uncommon on the street.<br /> <br /> == Links==<br /> <br /> [https://en.wikipedia.org/wiki/Methamphetamine Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/meth/meth.shtml Erowid]<br /> <br /> [http://reddit.com/r/Drugs/wiki/methamphetamine /r/Drugs Wiki]<br /> <br /> [http://science.howstuffworks.com/meth3.htm howstuffworks]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Methamphetamine&diff=5744 2018-10-09T21:57:25Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Crystal Meth.jpg|250px|right]]<br /> <br /> '''Methamphetamine''' is a strong physical and mental stimulant. It is legally prescribed as a treatment for ADD under the brand name Desoxyn, for both children and adults. Recreationally, methamphetamine is used to increase sexual drive, lift the mood, and increase energy, allowing some users to engage in sexual activity continuously for several days straight. Methamphetamine production is a relatively simple process, especially when compared to many other recreational drugs which has contributed to its widespread use. It is frequently reported on in the media when home meth-producing labs are busted.<br /> <br /> Methamphetamine exists as two [[Glossary#Enantiomer|enantiomers]], dextrorotary and levorotary. Dextromethamphetamine is a stronger central nervous system(CNS) stimulant than levomethamphetamine; however, both are addictive and produce the same toxicity symptoms at high doses. Methamphetamine may be sold illegally, either as pure dextromethamphetamine or in an equal parts mixture of the right and left handed molecules (i.e., 50% levomethamphetamine and 50% dextromethamphetamine). Both dextromethamphetamine and racemic methamphetamine are schedule II controlled substances in the United States. Similarly, the production, distribution, sale, and possession of methamphetamine is restricted or illegal in many other countries due to its placement in schedule II of the United Nations Convention on Psychotropic Substancestreaty. In contrast, levomethamphetamine is an over-the-counter drug in the United States.<br /> <br /> == History ==<br /> Amphetamine, discovered before methamphetamine, was first synthesized in 1887 in Germany by Romanian chemist Lazăr Edeleanu who named it phenylisopropylamine. Shortly after, methamphetamine was synthesized from ephedrine in 1893 by Japanesechemist Nagai Nagayoshi. Three decades later, in 1919, methamphetamine hydrochloride was synthesized by pharmacologist Akira Ogata via reduction of ephedrine using red phosphorus and iodine. During World War II, methamphetamine was used extensively by the Axis forces for its stimulant effects. Obetrol, patented by Obetrol Pharmaceuticals in the 1950s and indicated for treatment of obesity, was one of the first brands of pharmaceutical methamphetamine products. Due to the psychological and stimulant effects of methamphetamine, Obetrol became a popular diet pill in America in the 1950s and 1960s. Eventually, as the addictive properties of the drug became known, governments began to strictly regulate the production and distribution of methamphetamine. For example, during the early 1970s in the United States, methamphetamine became a schedule II controlled substance under the Controlled Substances Act. Currently, methamphetamine is sold under the trade name Desoxyn, trademarked by the Danish pharmaceutical company Lundbeck. As of January 2013, the Desoxyn trademark had been sold to Italian pharmaceutical company Recordati.<br /> <br /> == Dosage ==<br /> <br /> <br /> {{#tdose: methamphetamine }}<br /> <br /> == Duration ==<br /> <br /> These durations are for users of somewhat moderate tolerance. Amphetamine naive users may not be able to sleep for 18+ hours after oral use and other routes will be lengthened as well. <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 20-70 minutes<br /> |-<br /> | Total || 8-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 5-10 minutes<br /> |-<br /> | Total || 2-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 1-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> == Effects ==<br /> =Goodbye moonmen=<br /> <br /> =Goodbye moonmen=<br /> <br /> === Negative ===<br /> <br /> *Weight loss<br /> <br /> *Disturbed sleep patterns, Insomnia<br /> <br /> *Bruxia<br /> <br /> *Drying of oral mucosa<br /> <br /> *Loss of appetite<br /> <br /> *Visual and auditory hallucinations<br /> <br /> *Itchiness<br /> <br /> *Aggressiveness<br /> <br /> *Hyperthermia (Overheating)<br /> <br /> *Moodiness, Irritability, Anxiety<br /> <br /> *Increased heart rate, Irregular heart rhythm<br /> <br /> *Hypertension (High blood pressure)<br /> <br /> *Excessive sweating, Dehydration<br /> <br /> *Fatal kidney disorder<br /> <br /> *Possible brain damage<br /> <br /> *Liver damage<br /> <br /> == Harm Reduction ==<br /> When dealing with methamphetamine it's important to remember that a large number of the harms come not from the drug itself, but from the behaviors the drug causes individuals to exhibit. Loss of sleep, poor nutrition, and poor self care are the cause of many of the negative effects. <br /> <br /> *Methamphetamine lasts for a long time and will impair sleep. Dose early in the day and do not redose to avoid sleep disruption.<br /> <br /> *Oral ROA has less redose compulsion than other routes such as vaporization. <br /> <br /> *It is important to eat and stay hydrated, even if you do not feel the need for food. Even if you are not feeling like eating you can generally have some fruit or a bowl of cereal or yogurt with granola. <br /> <br /> *It is important to keep up on your self-care. &quot;Meth mouth&quot; is caused by poor oral hygiene combined with the habit of users to sip sugary beverages to relieve dry mouth symptoms. Use water and not soda to relieve dry mouth. Remember to brush your teeth after eating or consuming any caloric beverages.<br /> <br /> *Stimulant drugs can cause kidney damage and stroke in users with high blood pressure. If you have been diagnosed or told you have high blood pressure use with caution.<br /> <br /> == Chemistry and Pharmacology ==<br /> [[File:Meth molecule.jpg|150px|right]]<br /> <br /> Systematic name: N-methyl-1-phenylpropan-2-amine<br /> <br /> At room temperature, the free base of methamphetamine is a clear and colorless liquid with an odor characteristic of geranium leaves. It is soluble in diethyl ether and ethanol as well as miscible with chloroform. In contrast, the methampetamine hydrochloride salt is odorless with a bitter taste. It has a melting point between 170 to 175 °C (338 to 347 °F) and, at room temperature, occurs as white crystals or a white crystalline powder. The hydrochloride salt is also freely soluble in alcohol and water.<br /> <br /> Powder methamphetamine is the hydrochloride salt form which is strongly hygroscopic (absorbs water from the air quickly). The HCl salt is smokable as is. Crystal meth &quot;Crystal Meth&quot; or &quot;Ice&quot; refer to methamphetamine grown into crystals. Though many people believe that Crystal Meth is the freebase form of methamphetamie HCl, this is not true. Methamphetamine is smokable in its normal HCL form, but taking the time to grow it into crystals makes it easier to smoke. Meth in visible crystals (rather than powder) is likely to be relatively pure as it is difficult to grow crystals from impure material. Methamphetamine freebase is an oil and is uncommon on the street.<br /> <br /> == Links==<br /> <br /> [https://en.wikipedia.org/wiki/Methamphetamine Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/meth/meth.shtml Erowid]<br /> <br /> [http://reddit.com/r/Drugs/wiki/methamphetamine /r/Drugs Wiki]<br /> <br /> [http://science.howstuffworks.com/meth3.htm howstuffworks]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Methamphetamine&diff=5743 2018-10-09T21:57:06Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Crystal Meth.jpg|250px|right]]<br /> <br /> '''Methamphetamine''' is a strong physical and mental stimulant. It is legally prescribed as a treatment for ADD under the brand name Desoxyn, for both children and adults. Recreationally, methamphetamine is used to increase sexual drive, lift the mood, and increase energy, allowing some users to engage in sexual activity continuously for several days straight. Methamphetamine production is a relatively simple process, especially when compared to many other recreational drugs which has contributed to its widespread use. It is frequently reported on in the media when home meth-producing labs are busted.<br /> <br /> Methamphetamine exists as two [[Glossary#Enantiomer|enantiomers]], dextrorotary and levorotary. Dextromethamphetamine is a stronger central nervous system(CNS) stimulant than levomethamphetamine; however, both are addictive and produce the same toxicity symptoms at high doses. Methamphetamine may be sold illegally, either as pure dextromethamphetamine or in an equal parts mixture of the right and left handed molecules (i.e., 50% levomethamphetamine and 50% dextromethamphetamine). Both dextromethamphetamine and racemic methamphetamine are schedule II controlled substances in the United States. Similarly, the production, distribution, sale, and possession of methamphetamine is restricted or illegal in many other countries due to its placement in schedule II of the United Nations Convention on Psychotropic Substancestreaty. In contrast, levomethamphetamine is an over-the-counter drug in the United States.<br /> <br /> == History ==<br /> Amphetamine, discovered before methamphetamine, was first synthesized in 1887 in Germany by Romanian chemist Lazăr Edeleanu who named it phenylisopropylamine. Shortly after, methamphetamine was synthesized from ephedrine in 1893 by Japanesechemist Nagai Nagayoshi. Three decades later, in 1919, methamphetamine hydrochloride was synthesized by pharmacologist Akira Ogata via reduction of ephedrine using red phosphorus and iodine. During World War II, methamphetamine was used extensively by the Axis forces for its stimulant effects. Obetrol, patented by Obetrol Pharmaceuticals in the 1950s and indicated for treatment of obesity, was one of the first brands of pharmaceutical methamphetamine products. Due to the psychological and stimulant effects of methamphetamine, Obetrol became a popular diet pill in America in the 1950s and 1960s. Eventually, as the addictive properties of the drug became known, governments began to strictly regulate the production and distribution of methamphetamine. For example, during the early 1970s in the United States, methamphetamine became a schedule II controlled substance under the Controlled Substances Act. Currently, methamphetamine is sold under the trade name Desoxyn, trademarked by the Danish pharmaceutical company Lundbeck. As of January 2013, the Desoxyn trademark had been sold to Italian pharmaceutical company Recordati.<br /> <br /> == Dosage ==<br /> <br /> <br /> {{#tdose: methamphetamine }}<br /> <br /> == Duration ==<br /> <br /> These durations are for users of somewhat moderate tolerance. Amphetamine naive users may not be able to sleep for 18+ hours after oral use and other routes will be lengthened as well. <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 20-70 minutes<br /> |-<br /> | Total || 8-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 5-10 minutes<br /> |-<br /> | Total || 2-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 1-4 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || 0-2 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> == Effects ==<br /> =Goodbye moonmen=<br /> <br /> === Neutral ===<br /> <br /> *Excessive talking<br /> <br /> *Decreased appetite <br /> <br /> *Sweating<br /> <br /> *Dilated pupils<br /> <br /> === Negative ===<br /> <br /> *Weight loss<br /> <br /> *Disturbed sleep patterns, Insomnia<br /> <br /> *Bruxia<br /> <br /> *Drying of oral mucosa<br /> <br /> *Loss of appetite<br /> <br /> *Visual and auditory hallucinations<br /> <br /> *Itchiness<br /> <br /> *Aggressiveness<br /> <br /> *Hyperthermia (Overheating)<br /> <br /> *Moodiness, Irritability, Anxiety<br /> <br /> *Increased heart rate, Irregular heart rhythm<br /> <br /> *Hypertension (High blood pressure)<br /> <br /> *Excessive sweating, Dehydration<br /> <br /> *Fatal kidney disorder<br /> <br /> *Possible brain damage<br /> <br /> *Liver damage<br /> <br /> == Harm Reduction ==<br /> When dealing with methamphetamine it's important to remember that a large number of the harms come not from the drug itself, but from the behaviors the drug causes individuals to exhibit. Loss of sleep, poor nutrition, and poor self care are the cause of many of the negative effects. <br /> <br /> *Methamphetamine lasts for a long time and will impair sleep. Dose early in the day and do not redose to avoid sleep disruption.<br /> <br /> *Oral ROA has less redose compulsion than other routes such as vaporization. <br /> <br /> *It is important to eat and stay hydrated, even if you do not feel the need for food. Even if you are not feeling like eating you can generally have some fruit or a bowl of cereal or yogurt with granola. <br /> <br /> *It is important to keep up on your self-care. &quot;Meth mouth&quot; is caused by poor oral hygiene combined with the habit of users to sip sugary beverages to relieve dry mouth symptoms. Use water and not soda to relieve dry mouth. Remember to brush your teeth after eating or consuming any caloric beverages.<br /> <br /> *Stimulant drugs can cause kidney damage and stroke in users with high blood pressure. If you have been diagnosed or told you have high blood pressure use with caution.<br /> <br /> == Chemistry and Pharmacology ==<br /> [[File:Meth molecule.jpg|150px|right]]<br /> <br /> Systematic name: N-methyl-1-phenylpropan-2-amine<br /> <br /> At room temperature, the free base of methamphetamine is a clear and colorless liquid with an odor characteristic of geranium leaves. It is soluble in diethyl ether and ethanol as well as miscible with chloroform. In contrast, the methampetamine hydrochloride salt is odorless with a bitter taste. It has a melting point between 170 to 175 °C (338 to 347 °F) and, at room temperature, occurs as white crystals or a white crystalline powder. The hydrochloride salt is also freely soluble in alcohol and water.<br /> <br /> Powder methamphetamine is the hydrochloride salt form which is strongly hygroscopic (absorbs water from the air quickly). The HCl salt is smokable as is. Crystal meth &quot;Crystal Meth&quot; or &quot;Ice&quot; refer to methamphetamine grown into crystals. Though many people believe that Crystal Meth is the freebase form of methamphetamie HCl, this is not true. Methamphetamine is smokable in its normal HCL form, but taking the time to grow it into crystals makes it easier to smoke. Meth in visible crystals (rather than powder) is likely to be relatively pure as it is difficult to grow crystals from impure material. Methamphetamine freebase is an oil and is uncommon on the street.<br /> <br /> == Links==<br /> <br /> [https://en.wikipedia.org/wiki/Methamphetamine Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/meth/meth.shtml Erowid]<br /> <br /> [http://reddit.com/r/Drugs/wiki/methamphetamine /r/Drugs Wiki]<br /> <br /> [http://science.howstuffworks.com/meth3.htm howstuffworks]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=GHB&diff=5742 2018-10-09T21:56:34Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:GHB.jpg|right]]<br /> <br /> '''GHB''' (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.<br /> <br /> == History ==<br /> Synthesis of this chemical was first reported in 1874 by Alexander Zaytsev. But the first major research in humans was conducted in the early 1960's by Dr. Henri Laborit to use in studying the neurotransmitter GABA. <br /> <br /> Throughout most of the 1960's it was a popular anesthetic, then was abandoned by doctors, following discoveries of its poor analgesic effects. In the 1970's was recommended for the treatment of narcolepsy, though the euphoric side of GHB made that unfavourable. <br /> <br /> GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth, but problems with its abuse potential and development of newer drugs have led to a decrease in the medical use in recent times. <br /> <br /> In the 1980's It was marketed for a short time as a fat burner and muscle developer. However, in 1990, based off many reports of GHB-linked illness, the FDA declared GHB unsafe, and ordered it to be removed from stores shelves. Following this, many users switched to GBL and 1 4-butanediol.<br /> <br /> GHB (Xyrem) was approved by the FDA in 2002 for use in the treatment of narcolepsy/Cataplexy.<br /> <br /> == Dosage ==<br /> <br /> GBL dose: 1ml GBL is equal to 1.6ml GHB<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 0.5-1.5g<br /> |-<br /> | Common || 1-2.5g<br /> |-<br /> | Strong || 2-4g<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-40 minutes<br /> |-<br /> | Total || 1-3 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> Goodbye moonmen<br /> <br /> Goodbye moonmen<br /> <br /> == Negative == <br /> *Nausea<br /> *Restlessness<br /> *Unconsciousness<br /> *Amnesia<br /> <br /> Goodbye moonmen<br /> <br /> == Harm Reduction ==<br /> * The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression. <br /> *The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.<br /> * Avoid driving and operating heavy machinery<br /> * Don't mix it with [[alcohol]], or other [[depressants]]<br /> * 2-3 uses a week should be the maximum<br /> * High addiction potential<br /> <br /> == Chemistry and Pharmacology == <br /> GHB has at least two distinct binding sites in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory, and it is a weak agonist at the GABA-B receptor, which is inhibitory. GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain. GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.<br /> <br /> If taken orally, GABA itself does not effectively cross the blood-brain-barrier.<br /> <br /> Goodbye moonmen<br /> <br /> Goodbye moonmen<br /> <br /> == Legal status ==<br /> <br /> GHB is illegal in most parts of the world, GBL is legal in parts of Europe.<br /> <br /> == Links ==<br /> <br /> [http://en.wikipedia.org/wiki/Gamma-Hydroxybutyric_acid Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/ghb/ghb.shtml Erowid]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Depressant]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=GHB&diff=5741 2018-10-09T21:56:02Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:GHB.jpg|right]]<br /> <br /> '''GHB''' (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.<br /> <br /> == History ==<br /> Synthesis of this chemical was first reported in 1874 by Alexander Zaytsev. But the first major research in humans was conducted in the early 1960's by Dr. Henri Laborit to use in studying the neurotransmitter GABA. <br /> <br /> Throughout most of the 1960's it was a popular anesthetic, then was abandoned by doctors, following discoveries of its poor analgesic effects. In the 1970's was recommended for the treatment of narcolepsy, though the euphoric side of GHB made that unfavourable. <br /> <br /> GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth, but problems with its abuse potential and development of newer drugs have led to a decrease in the medical use in recent times. <br /> <br /> In the 1980's It was marketed for a short time as a fat burner and muscle developer. However, in 1990, based off many reports of GHB-linked illness, the FDA declared GHB unsafe, and ordered it to be removed from stores shelves. Following this, many users switched to GBL and 1 4-butanediol.<br /> <br /> GHB (Xyrem) was approved by the FDA in 2002 for use in the treatment of narcolepsy/Cataplexy.<br /> <br /> == Dosage ==<br /> <br /> GBL dose: 1ml GBL is equal to 1.6ml GHB<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 0.5-1.5g<br /> |-<br /> | Common || 1-2.5g<br /> |-<br /> | Strong || 2-4g<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-40 minutes<br /> |-<br /> | Total || 1-3 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> Goodbye moonmen<br /> <br /> Goodbye moonmen<br /> <br /> == Negative == <br /> *Nausea<br /> *Restlessness<br /> *Unconsciousness<br /> *Amnesia<br /> <br /> Goodbye moonmen<br /> <br /> == Harm Reduction ==<br /> * The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression. <br /> *The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.<br /> * Avoid driving and operating heavy machinery<br /> * Don't mix it with [[alcohol]], or other [[depressants]]<br /> * 2-3 uses a week should be the maximum<br /> * High addiction potential<br /> <br /> == Chemistry and Pharmacology == <br /> GHB has at least two distinct binding sites in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory, and it is a weak agonist at the GABA-B receptor, which is inhibitory. GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain. GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.<br /> <br /> If taken orally, GABA itself does not effectively cross the blood-brain-barrier.<br /> <br /> Goodbye moonmen<br /> <br /> === Production ===<br /> Production of GHB consists simply of mixing &quot;lactone&quot; (short for gamma butyrlactone) and lye (sodium hydroxide) in the proper amounts. It can also be converted from GBL.<br /> <br /> == Legal status ==<br /> <br /> GHB is illegal in most parts of the world, GBL is legal in parts of Europe.<br /> <br /> == Links ==<br /> <br /> [http://en.wikipedia.org/wiki/Gamma-Hydroxybutyric_acid Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/ghb/ghb.shtml Erowid]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Depressant]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=GHB&diff=5740 2018-10-09T21:55:40Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:GHB.jpg|right]]<br /> <br /> '''GHB''' (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.<br /> <br /> == History ==<br /> Synthesis of this chemical was first reported in 1874 by Alexander Zaytsev. But the first major research in humans was conducted in the early 1960's by Dr. Henri Laborit to use in studying the neurotransmitter GABA. <br /> <br /> Throughout most of the 1960's it was a popular anesthetic, then was abandoned by doctors, following discoveries of its poor analgesic effects. In the 1970's was recommended for the treatment of narcolepsy, though the euphoric side of GHB made that unfavourable. <br /> <br /> GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth, but problems with its abuse potential and development of newer drugs have led to a decrease in the medical use in recent times. <br /> <br /> In the 1980's It was marketed for a short time as a fat burner and muscle developer. However, in 1990, based off many reports of GHB-linked illness, the FDA declared GHB unsafe, and ordered it to be removed from stores shelves. Following this, many users switched to GBL and 1 4-butanediol.<br /> <br /> GHB (Xyrem) was approved by the FDA in 2002 for use in the treatment of narcolepsy/Cataplexy.<br /> <br /> == Dosage ==<br /> <br /> GBL dose: 1ml GBL is equal to 1.6ml GHB<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 0.5-1.5g<br /> |-<br /> | Common || 1-2.5g<br /> |-<br /> | Strong || 2-4g<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-40 minutes<br /> |-<br /> | Total || 1-3 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> Goodbye moonmen<br /> <br /> Goodbye moonmen<br /> <br /> == Negative == <br /> *Nausea<br /> *Restlessness<br /> *Unconsciousness<br /> *Amnesia<br /> <br /> Goodbye moonmen<br /> <br /> == Harm Reduction ==<br /> * The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression. <br /> *The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.<br /> * Avoid driving and operating heavy machinery<br /> * Don't mix it with [[alcohol]], or other [[depressants]]<br /> * 2-3 uses a week should be the maximum<br /> * High addiction potential<br /> <br /> == Chemistry and Pharmacology == <br /> GHB has at least two distinct binding sites in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory, and it is a weak agonist at the GABA-B receptor, which is inhibitory. GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain. GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.<br /> <br /> If taken orally, GABA itself does not effectively cross the blood-brain-barrier.<br /> <br /> === Dopamine Rebound ===<br /> <br /> GHB will reduce dopamine levels in high amounts, but increase dopamine levels in the brain in low amounts&lt;ref&gt;https://www.ncbi.nlm.nih.gov/pubmed/1847191&lt;/ref&gt;. This leads to what is known as dopamine rebound among users. Users can experience strong wakefullness about 4 hours after the last dose was consumed. This is often strong enough to wake the user up from sleep, and may be accompanied by a strong redose compulsion. The longer and higher the dose of GHB used, the more pronounced the effect may become. <br /> <br /> === Production ===<br /> Production of GHB consists simply of mixing &quot;lactone&quot; (short for gamma butyrlactone) and lye (sodium hydroxide) in the proper amounts. It can also be converted from GBL.<br /> <br /> == Legal status ==<br /> <br /> GHB is illegal in most parts of the world, GBL is legal in parts of Europe.<br /> <br /> == Links ==<br /> <br /> [http://en.wikipedia.org/wiki/Gamma-Hydroxybutyric_acid Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/ghb/ghb.shtml Erowid]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Depressant]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=GHB&diff=5739 2018-10-09T21:55:28Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:GHB.jpg|right]]<br /> <br /> '''GHB''' (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.<br /> <br /> == History ==<br /> Synthesis of this chemical was first reported in 1874 by Alexander Zaytsev. But the first major research in humans was conducted in the early 1960's by Dr. Henri Laborit to use in studying the neurotransmitter GABA. <br /> <br /> Throughout most of the 1960's it was a popular anesthetic, then was abandoned by doctors, following discoveries of its poor analgesic effects. In the 1970's was recommended for the treatment of narcolepsy, though the euphoric side of GHB made that unfavourable. <br /> <br /> GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth, but problems with its abuse potential and development of newer drugs have led to a decrease in the medical use in recent times. <br /> <br /> In the 1980's It was marketed for a short time as a fat burner and muscle developer. However, in 1990, based off many reports of GHB-linked illness, the FDA declared GHB unsafe, and ordered it to be removed from stores shelves. Following this, many users switched to GBL and 1 4-butanediol.<br /> <br /> GHB (Xyrem) was approved by the FDA in 2002 for use in the treatment of narcolepsy/Cataplexy.<br /> <br /> == Dosage ==<br /> <br /> GBL dose: 1ml GBL is equal to 1.6ml GHB<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 0.5-1.5g<br /> |-<br /> | Common || 1-2.5g<br /> |-<br /> | Strong || 2-4g<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-40 minutes<br /> |-<br /> | Total || 1-3 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> Goodbye moonmen<br /> <br /> Goodbye moonmen<br /> <br /> == Negative == <br /> *Nausea<br /> *Restlessness<br /> *Unconsciousness<br /> *Amnesia<br /> <br /> === After effects ===<br /> <br /> * Hangover (usually only occurs from high doses)<br /> * [[#Dopamine Rebound]]<br /> <br /> <br /> == Harm Reduction ==<br /> * The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression. <br /> *The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.<br /> * Avoid driving and operating heavy machinery<br /> * Don't mix it with [[alcohol]], or other [[depressants]]<br /> * 2-3 uses a week should be the maximum<br /> * High addiction potential<br /> <br /> == Chemistry and Pharmacology == <br /> GHB has at least two distinct binding sites in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory, and it is a weak agonist at the GABA-B receptor, which is inhibitory. GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain. GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.<br /> <br /> If taken orally, GABA itself does not effectively cross the blood-brain-barrier.<br /> <br /> === Dopamine Rebound ===<br /> <br /> GHB will reduce dopamine levels in high amounts, but increase dopamine levels in the brain in low amounts&lt;ref&gt;https://www.ncbi.nlm.nih.gov/pubmed/1847191&lt;/ref&gt;. This leads to what is known as dopamine rebound among users. Users can experience strong wakefullness about 4 hours after the last dose was consumed. This is often strong enough to wake the user up from sleep, and may be accompanied by a strong redose compulsion. The longer and higher the dose of GHB used, the more pronounced the effect may become. <br /> <br /> === Production ===<br /> Production of GHB consists simply of mixing &quot;lactone&quot; (short for gamma butyrlactone) and lye (sodium hydroxide) in the proper amounts. It can also be converted from GBL.<br /> <br /> == Legal status ==<br /> <br /> GHB is illegal in most parts of the world, GBL is legal in parts of Europe.<br /> <br /> == Links ==<br /> <br /> [http://en.wikipedia.org/wiki/Gamma-Hydroxybutyric_acid Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/ghb/ghb.shtml Erowid]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Depressant]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=GHB&diff=5738 2018-10-09T21:55:15Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:GHB.jpg|right]]<br /> <br /> '''GHB''' (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.<br /> <br /> == History ==<br /> Synthesis of this chemical was first reported in 1874 by Alexander Zaytsev. But the first major research in humans was conducted in the early 1960's by Dr. Henri Laborit to use in studying the neurotransmitter GABA. <br /> <br /> Throughout most of the 1960's it was a popular anesthetic, then was abandoned by doctors, following discoveries of its poor analgesic effects. In the 1970's was recommended for the treatment of narcolepsy, though the euphoric side of GHB made that unfavourable. <br /> <br /> GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth, but problems with its abuse potential and development of newer drugs have led to a decrease in the medical use in recent times. <br /> <br /> In the 1980's It was marketed for a short time as a fat burner and muscle developer. However, in 1990, based off many reports of GHB-linked illness, the FDA declared GHB unsafe, and ordered it to be removed from stores shelves. Following this, many users switched to GBL and 1 4-butanediol.<br /> <br /> GHB (Xyrem) was approved by the FDA in 2002 for use in the treatment of narcolepsy/Cataplexy.<br /> <br /> == Dosage ==<br /> <br /> GBL dose: 1ml GBL is equal to 1.6ml GHB<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 0.5-1.5g<br /> |-<br /> | Common || 1-2.5g<br /> |-<br /> | Strong || 2-4g<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-40 minutes<br /> |-<br /> | Total || 1-3 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> Goodbye moonmen<br /> <br /> === Neutral === <br /> *Dizziness<br /> <br /> == Negative == <br /> *Nausea<br /> *Restlessness<br /> *Unconsciousness<br /> *Amnesia<br /> <br /> === After effects ===<br /> <br /> * Hangover (usually only occurs from high doses)<br /> * [[#Dopamine Rebound]]<br /> <br /> <br /> == Harm Reduction ==<br /> * The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression. <br /> *The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.<br /> * Avoid driving and operating heavy machinery<br /> * Don't mix it with [[alcohol]], or other [[depressants]]<br /> * 2-3 uses a week should be the maximum<br /> * High addiction potential<br /> <br /> == Chemistry and Pharmacology == <br /> GHB has at least two distinct binding sites in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory, and it is a weak agonist at the GABA-B receptor, which is inhibitory. GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain. GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.<br /> <br /> If taken orally, GABA itself does not effectively cross the blood-brain-barrier.<br /> <br /> === Dopamine Rebound ===<br /> <br /> GHB will reduce dopamine levels in high amounts, but increase dopamine levels in the brain in low amounts&lt;ref&gt;https://www.ncbi.nlm.nih.gov/pubmed/1847191&lt;/ref&gt;. This leads to what is known as dopamine rebound among users. Users can experience strong wakefullness about 4 hours after the last dose was consumed. This is often strong enough to wake the user up from sleep, and may be accompanied by a strong redose compulsion. The longer and higher the dose of GHB used, the more pronounced the effect may become. <br /> <br /> === Production ===<br /> Production of GHB consists simply of mixing &quot;lactone&quot; (short for gamma butyrlactone) and lye (sodium hydroxide) in the proper amounts. It can also be converted from GBL.<br /> <br /> == Legal status ==<br /> <br /> GHB is illegal in most parts of the world, GBL is legal in parts of Europe.<br /> <br /> == Links ==<br /> <br /> [http://en.wikipedia.org/wiki/Gamma-Hydroxybutyric_acid Wikipedia]<br /> <br /> [https://www.erowid.org/chemicals/ghb/ghb.shtml Erowid]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Depressant]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Adderall&diff=5737 2018-10-09T21:54:44Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Adderall.jpg|thumb|400px|left|Several 10mg Adderall IR pills]]<br /> Adderall is a commonly prescribed stimulant to treat ADHD and ADD. Adderall is a 3:1 mixture of dextroamphetamine and levoamphetamine. Adderall is commonly found in two forms, IR and XR. IR is instant release, while XR is extended release. Adderall XR releases half of the dosage immediately, and the other half 4 hours later. Adderall, containing [[Amphetamine|amphetamine]], is exceedingly similar to other forms of the substance, though with Adderall the constitution and doses are known.<br /> <br /> == History ==<br /> <br /> Adderall was originally developed from an amphetamine blend drug called Obetrol, prescribed for obesity and weight loss. This drug was a mix of racemic amphetamine (dl-amphetamine), d-amphetamine, and racemic methamphetamine. This made sense, as it was for weight loss, so the peripheral effects of l-amphetamine were actually useful as an anorexic and as a thermogenic. It was later reformulated without the methamphetamine, but also without FDA approval. When Richwood Pharmaceuticals bought Rexar, the company making Obetrol, they rebranded the reformulated Obetrol (without the methamphetamine) as Adderall, and began marketing it for ADD/ADHD.<br /> <br /> == Dosage ==<br /> <br /> Adderall XR is extended release Around 50% of the dose is released instantly, the other half over the next four hours. Effects take a while to begin, and last much longer.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 5-15mg<br /> |-<br /> | Common || 15-40mg<br /> |-<br /> | Strong || 40-75mg<br /> |-<br /> | Heavy || 75-125+mg<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 5-10mg<br /> |-<br /> | Common || 10-30mg<br /> |-<br /> | Strong || 30-50mg<br /> |-<br /> | Heavy || 50-80+mg<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 15-30 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> Goodbye moonmen<br /> <br /> == Harm Reduction ==<br /> <br /> * Avoid driving and operating heavy machinery<br /> <br /> * Recommended time (pauses) between using the substance<br /> <br /> * Adderall can be extremely addictive, and abuse can lead to stimulant psychosis, a very dangerous disorder.<br /> <br /> Goodbye moonmen<br /> <br /> Goodbye moonmen<br /> <br /> == Legal status ==<br /> <br /> * Canada: Schedule I<br /> <br /> * UK: Class B<br /> <br /> * Thailand: Category 1<br /> <br /> * United States: Schedule II<br /> <br /> == Links ==<br /> <br /> * [[Amphetamine|Amphetamine]]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Adderall&diff=5736 2018-10-09T21:54:24Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Adderall.jpg|thumb|400px|left|Several 10mg Adderall IR pills]]<br /> Adderall is a commonly prescribed stimulant to treat ADHD and ADD. Adderall is a 3:1 mixture of dextroamphetamine and levoamphetamine. Adderall is commonly found in two forms, IR and XR. IR is instant release, while XR is extended release. Adderall XR releases half of the dosage immediately, and the other half 4 hours later. Adderall, containing [[Amphetamine|amphetamine]], is exceedingly similar to other forms of the substance, though with Adderall the constitution and doses are known.<br /> <br /> == History ==<br /> <br /> Adderall was originally developed from an amphetamine blend drug called Obetrol, prescribed for obesity and weight loss. This drug was a mix of racemic amphetamine (dl-amphetamine), d-amphetamine, and racemic methamphetamine. This made sense, as it was for weight loss, so the peripheral effects of l-amphetamine were actually useful as an anorexic and as a thermogenic. It was later reformulated without the methamphetamine, but also without FDA approval. When Richwood Pharmaceuticals bought Rexar, the company making Obetrol, they rebranded the reformulated Obetrol (without the methamphetamine) as Adderall, and began marketing it for ADD/ADHD.<br /> <br /> == Dosage ==<br /> <br /> Adderall XR is extended release Around 50% of the dose is released instantly, the other half over the next four hours. Effects take a while to begin, and last much longer.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 5-15mg<br /> |-<br /> | Common || 15-40mg<br /> |-<br /> | Strong || 40-75mg<br /> |-<br /> | Heavy || 75-125+mg<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 5-10mg<br /> |-<br /> | Common || 10-30mg<br /> |-<br /> | Strong || 30-50mg<br /> |-<br /> | Heavy || 50-80+mg<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 15-30 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> Goodbye moonmen<br /> <br /> == Harm Reduction ==<br /> <br /> * Avoid driving and operating heavy machinery<br /> <br /> * Recommended time (pauses) between using the substance<br /> <br /> * Adderall can be extremely addictive, and abuse can lead to stimulant psychosis, a very dangerous disorder.<br /> <br /> Goodbye moonmen<br /> <br /> === Interactions ===<br /> <br /> Adderall can interact negatively with many drugs mainly tramadol, APAP, buproprion, and many anti-depressants.<br /> <br /> Adderall mixed with downers like Benzodiazepines can also cause adverse reactions. <br /> <br /> == Legal status ==<br /> <br /> * Canada: Schedule I<br /> <br /> * UK: Class B<br /> <br /> * Thailand: Category 1<br /> <br /> * United States: Schedule II<br /> <br /> == Links ==<br /> <br /> * [[Amphetamine|Amphetamine]]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Adderall&diff=5735 2018-10-09T21:54:11Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Adderall.jpg|thumb|400px|left|Several 10mg Adderall IR pills]]<br /> Adderall is a commonly prescribed stimulant to treat ADHD and ADD. Adderall is a 3:1 mixture of dextroamphetamine and levoamphetamine. Adderall is commonly found in two forms, IR and XR. IR is instant release, while XR is extended release. Adderall XR releases half of the dosage immediately, and the other half 4 hours later. Adderall, containing [[Amphetamine|amphetamine]], is exceedingly similar to other forms of the substance, though with Adderall the constitution and doses are known.<br /> <br /> == History ==<br /> <br /> Adderall was originally developed from an amphetamine blend drug called Obetrol, prescribed for obesity and weight loss. This drug was a mix of racemic amphetamine (dl-amphetamine), d-amphetamine, and racemic methamphetamine. This made sense, as it was for weight loss, so the peripheral effects of l-amphetamine were actually useful as an anorexic and as a thermogenic. It was later reformulated without the methamphetamine, but also without FDA approval. When Richwood Pharmaceuticals bought Rexar, the company making Obetrol, they rebranded the reformulated Obetrol (without the methamphetamine) as Adderall, and began marketing it for ADD/ADHD.<br /> <br /> == Dosage ==<br /> <br /> Adderall XR is extended release Around 50% of the dose is released instantly, the other half over the next four hours. Effects take a while to begin, and last much longer.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 5-15mg<br /> |-<br /> | Common || 15-40mg<br /> |-<br /> | Strong || 40-75mg<br /> |-<br /> | Heavy || 75-125+mg<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 5-10mg<br /> |-<br /> | Common || 10-30mg<br /> |-<br /> | Strong || 30-50mg<br /> |-<br /> | Heavy || 50-80+mg<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 15-30 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> <br /> * Increased focus<br /> <br /> * Abundance of energy<br /> <br /> * Increased motivation<br /> <br /> Goodbye moonmen<br /> <br /> == Harm Reduction ==<br /> <br /> * Avoid driving and operating heavy machinery<br /> <br /> * Recommended time (pauses) between using the substance<br /> <br /> * Adderall can be extremely addictive, and abuse can lead to stimulant psychosis, a very dangerous disorder.<br /> <br /> Goodbye moonmen<br /> <br /> === Interactions ===<br /> <br /> Adderall can interact negatively with many drugs mainly tramadol, APAP, buproprion, and many anti-depressants.<br /> <br /> Adderall mixed with downers like Benzodiazepines can also cause adverse reactions. <br /> <br /> == Legal status ==<br /> <br /> * Canada: Schedule I<br /> <br /> * UK: Class B<br /> <br /> * Thailand: Category 1<br /> <br /> * United States: Schedule II<br /> <br /> == Links ==<br /> <br /> * [[Amphetamine|Amphetamine]]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Adderall&diff=5734 2018-10-09T21:54:02Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Adderall.jpg|thumb|400px|left|Several 10mg Adderall IR pills]]<br /> Adderall is a commonly prescribed stimulant to treat ADHD and ADD. Adderall is a 3:1 mixture of dextroamphetamine and levoamphetamine. Adderall is commonly found in two forms, IR and XR. IR is instant release, while XR is extended release. Adderall XR releases half of the dosage immediately, and the other half 4 hours later. Adderall, containing [[Amphetamine|amphetamine]], is exceedingly similar to other forms of the substance, though with Adderall the constitution and doses are known.<br /> <br /> == History ==<br /> <br /> Adderall was originally developed from an amphetamine blend drug called Obetrol, prescribed for obesity and weight loss. This drug was a mix of racemic amphetamine (dl-amphetamine), d-amphetamine, and racemic methamphetamine. This made sense, as it was for weight loss, so the peripheral effects of l-amphetamine were actually useful as an anorexic and as a thermogenic. It was later reformulated without the methamphetamine, but also without FDA approval. When Richwood Pharmaceuticals bought Rexar, the company making Obetrol, they rebranded the reformulated Obetrol (without the methamphetamine) as Adderall, and began marketing it for ADD/ADHD.<br /> <br /> == Dosage ==<br /> <br /> Adderall XR is extended release Around 50% of the dose is released instantly, the other half over the next four hours. Effects take a while to begin, and last much longer.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 5-15mg<br /> |-<br /> | Common || 15-40mg<br /> |-<br /> | Strong || 40-75mg<br /> |-<br /> | Heavy || 75-125+mg<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 5-10mg<br /> |-<br /> | Common || 10-30mg<br /> |-<br /> | Strong || 30-50mg<br /> |-<br /> | Heavy || 50-80+mg<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 15-30 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> <br /> * Increased focus<br /> <br /> * Abundance of energy<br /> <br /> * Increased motivation<br /> <br /> === Negative === <br /> <br /> * Racing thoughts<br /> <br /> * Reduced appetite<br /> <br /> * Flushing of the face<br /> <br /> * Increased body temperature<br /> <br /> * Tachycardia (Elevated heart rate)<br /> <br /> *Hypertension (High blood pressure)<br /> <br /> * Paranoia<br /> <br /> * Insomnia<br /> <br /> Goodbye moonmen<br /> <br /> == Harm Reduction ==<br /> <br /> * Avoid driving and operating heavy machinery<br /> <br /> * Recommended time (pauses) between using the substance<br /> <br /> * Adderall can be extremely addictive, and abuse can lead to stimulant psychosis, a very dangerous disorder.<br /> <br /> Goodbye moonmen<br /> <br /> === Interactions ===<br /> <br /> Adderall can interact negatively with many drugs mainly tramadol, APAP, buproprion, and many anti-depressants.<br /> <br /> Adderall mixed with downers like Benzodiazepines can also cause adverse reactions. <br /> <br /> == Legal status ==<br /> <br /> * Canada: Schedule I<br /> <br /> * UK: Class B<br /> <br /> * Thailand: Category 1<br /> <br /> * United States: Schedule II<br /> <br /> == Links ==<br /> <br /> * [[Amphetamine|Amphetamine]]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Adderall&diff=5733 2018-10-09T21:53:47Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:Adderall.jpg|thumb|400px|left|Several 10mg Adderall IR pills]]<br /> Adderall is a commonly prescribed stimulant to treat ADHD and ADD. Adderall is a 3:1 mixture of dextroamphetamine and levoamphetamine. Adderall is commonly found in two forms, IR and XR. IR is instant release, while XR is extended release. Adderall XR releases half of the dosage immediately, and the other half 4 hours later. Adderall, containing [[Amphetamine|amphetamine]], is exceedingly similar to other forms of the substance, though with Adderall the constitution and doses are known.<br /> <br /> == History ==<br /> <br /> Adderall was originally developed from an amphetamine blend drug called Obetrol, prescribed for obesity and weight loss. This drug was a mix of racemic amphetamine (dl-amphetamine), d-amphetamine, and racemic methamphetamine. This made sense, as it was for weight loss, so the peripheral effects of l-amphetamine were actually useful as an anorexic and as a thermogenic. It was later reformulated without the methamphetamine, but also without FDA approval. When Richwood Pharmaceuticals bought Rexar, the company making Obetrol, they rebranded the reformulated Obetrol (without the methamphetamine) as Adderall, and began marketing it for ADD/ADHD.<br /> <br /> == Dosage ==<br /> <br /> Adderall XR is extended release Around 50% of the dose is released instantly, the other half over the next four hours. Effects take a while to begin, and last much longer.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Light || 5-15mg<br /> |-<br /> | Common || 15-40mg<br /> |-<br /> | Strong || 40-75mg<br /> |-<br /> | Heavy || 75-125+mg<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 5-10mg<br /> |-<br /> | Common || 10-30mg<br /> |-<br /> | Strong || 30-50mg<br /> |-<br /> | Heavy || 50-80+mg<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 15-30 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total (IR) || 2-4 hours<br /> |-<br /> | Total (XR) || 6-10 hours<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> <br /> * Increased focus<br /> <br /> * Abundance of energy<br /> <br /> * Increased motivation<br /> <br /> === Negative === <br /> <br /> * Racing thoughts<br /> <br /> * Reduced appetite<br /> <br /> * Flushing of the face<br /> <br /> * Increased body temperature<br /> <br /> * Tachycardia (Elevated heart rate)<br /> <br /> *Hypertension (High blood pressure)<br /> <br /> * Paranoia<br /> <br /> * Insomnia<br /> <br /> === After effects ===<br /> <br /> * Hangover<br /> <br /> * Afterglow<br /> <br /> * Restlessness<br /> <br /> * Persisting stimulation (5-15 hours after last dose)<br /> <br /> == Harm Reduction ==<br /> <br /> * Avoid driving and operating heavy machinery<br /> <br /> * Recommended time (pauses) between using the substance<br /> <br /> * Adderall can be extremely addictive, and abuse can lead to stimulant psychosis, a very dangerous disorder.<br /> <br /> Goodbye moonmen<br /> <br /> === Interactions ===<br /> <br /> Adderall can interact negatively with many drugs mainly tramadol, APAP, buproprion, and many anti-depressants.<br /> <br /> Adderall mixed with downers like Benzodiazepines can also cause adverse reactions. <br /> <br /> == Legal status ==<br /> <br /> * Canada: Schedule I<br /> <br /> * UK: Class B<br /> <br /> * Thailand: Category 1<br /> <br /> * United States: Schedule II<br /> <br /> == Links ==<br /> <br /> * [[Amphetamine|Amphetamine]]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Stimulant]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5732 2018-10-09T21:53:24Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5731 2018-10-09T21:53:04Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5730 2018-10-09T21:52:50Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5729 2018-10-09T21:52:29Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Negative ===<br /> *Panic attack/Bad trip<br /> *(oral only) Nausea/Vomitting<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5728 2018-10-09T21:52:09Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> *Euphoria<br /> *Feeling of awe<br /> *Realizations about one's life<br /> <br /> === Negative ===<br /> *Panic attack/Bad trip<br /> *(oral only) Nausea/Vomitting<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5727 2018-10-09T21:51:51Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> === Intravenous ===<br /> <br /> Intravenous DMT comes on extremely fast and is the most efficient method of use. The effects are extremely similar to vaporized DMT, though IV administration is much more dangerous. It is advised that potential users avoid intravenous administration of DMT and stick to vaporization.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Light || 10-15mg<br /> |-<br /> | Common || 15-25mg<br /> |-<br /> | Strong || 25-40mg+<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> *Euphoria<br /> *Feeling of awe<br /> *Realizations about one's life<br /> <br /> === Negative ===<br /> *Panic attack/Bad trip<br /> *(oral only) Nausea/Vomitting<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=2C-E&diff=5726 2018-10-09T21:51:23Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:2ce.jpg|thumb|150px|Vial of 2C-E with powder]]<br /> <br /> '''2C-E''' is a chemical of the [[2C-X]] series which is characterised by its particularly intense visuals and higher potency when compared with other members of the family.<br /> <br /> == History ==<br /> <br /> 2C-E, like many of its close analogues, was first synthesized by Alexander Shulgin and published in PiHKAL. He was quite fond of it, granting it a place in his &quot;Magical Half Dozen&quot; alongside of [[DOM]], [[2C-B]], [[2C-T-2]] &amp; 7 and [[mescaline]]. <br /> <br /> == Usage ==<br /> <br /> 2C-E is mainly a recreational entheogen. It can be quite introspective in appropriate doses and settings. It doesn't lend itself well to intense party-like surroundings, much like LSD or similarly intense psychedelics.<br /> <br /> == Dosage ==<br /> <br /> {{#tdose: 2ce }}<br /> <br /> == Duration ==<br /> <br /> Note: Duration can be significantly longer with higher doses.<br /> <br /> Anecdotal evidence has shown the oral onset of 2C-E may vary wildly for some users, taking up to three hours before first effects in some cases. <br /> <br /> {| class=&quot;wikitable&quot;<br /> <br /> |+ Oral<br /> <br /> | Onset || 60-90 minutes<br /> <br /> |-<br /> <br /> | Total || 9-14 hours<br /> <br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> <br /> |+ Insufflated<br /> <br /> | Onset || 20-40 minutes<br /> <br /> |-<br /> <br /> | Total || 6-9 hours<br /> <br /> |}<br /> <br /> == Effects ==<br /> <br /> 2C-E is a psychedelic phenethylamine and as such has psychedelic and stimulant effects. As with all psychedelics, different users are likely to experience different sets of effects, which usually include some however very rarely would include all of the following effects.<br /> <br /> Compared to other members of the 2C-X family, 2C-E is generally considered to have a heavier body load and to be more visual than its counterparts.<br /> <br /> Note: The prevalence of negative effects increases with higher doses.<br /> <br /> === Negative ===<br /> <br /> * Tension<br /> <br /> * Anxiety, restlessness, confusion<br /> <br /> * Dizziness<br /> <br /> * Nausea, gastrointestinal discomfort, possible vomiting<br /> <br /> * Over-sensitivity to music or other sensory stimuli<br /> <br /> * Unwanted 'spiritual' experiences<br /> <br /> * Racing thoughts<br /> <br /> == Harm Reduction ==<br /> <br /> * As with all psychedelic drugs 2C-E carries with it the potential for a very powerful experience, and as such has the potential to create a very difficult experience ('bad' trip). Mindset and setting play important roles in governing the nature of a psychedelic experience, among other things. <br /> <br /> See [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for more information.<br /> <br /> * As with all stimulants, care should be taken when dosing via different ROAs. The oral route has a much lower bioavailabity than those that bypass first pass metabolism i.e. Insufflated, rectal, intramuscular, intravenous and subcutaneous. <br /> <br /> See [[Stimulants#Harm Reduction|Stimulant Harm Reduction]] for more information.<br /> <br /> === Interactions ===<br /> <br /> See the [[Drug combinations]] chart for more information.<br /> <br /> == Chemistry and Pharmacology ==<br /> <br /> === Chemistry ===<br /> <br /> 2,5-Dimethoxy-4-ethylphenethylamine is a colorless oil and analogue of mescaline. Similarly it is classified as a psychedelic phenethylamine. It shares the substituted amphetamine core found in the structure of many entactogens. Crystalline forms are obtained as the amine salt by reacting the free base with a mineral acid, typically HCl. It is soluble in both water and ethanol. Maximum concentration in H2O is reported at ~50mg/ml and it is said to be relatively stable in solution. A drop below normal ambient temperatures can cause particles to crystalize out. <br /> <br /> Shulgin does not report an exact boiling point for the free base, stating only that during one synthesis the fraction boiling between 90-100 °C at 0.25 mmHg pressure was collected and converted to the hydrochloride salt. Shulgin reports the melting point of the hydrochloride salt as 208.5-210.5 °C. <br /> <br /> A full write up on Shulgin's synthesis for 2C-E can be found [https://www.erowid.org/library/books_online/pihkal/pihkal024.shtml here].<br /> <br /> === Pharmacology ===<br /> <br /> Like most psychedelic drugs, 2C-E is a 5-HT2a Agonist; from that, we can presume the concurrent or pre-administration of SSRIs may reduce the effects of 2C-E. 2C-E is one of the most potent of the 2C-X family, behind only 2C-P and 2C-T-4. The 2C-X family, specifically, 2C-E, 2C-I, and 2C-C all stimulated G protein binding, suggesting more of an activity similar to tryptamines such as 5-MeO-DMT and, interestingly, DPT. G Proteins are membrane proteins that effectively mediate interaction between hormone receptors and enzymes responsible for changes of metabolism as a result of hormonal changes.<br /> <br /> In rats, Stage I metabolism involved deamination and O-Demthylation, which are related to the Monoamine oxidase (MAO) and cytochrome P450 (CYP) enzymes. For virtually all the 2C’s, (B,I,D,E,T-2, and T-7), MAO-A and MAO-B were reacted upon; interestingly, ½ of the molecules in Shulgin’s Magical Half Dozen (2C-E, 2C-T-2, 2C-T-7, with the addition of 2C-D) also act to a small extent on the CYP2D6 enzyme. Because of the commonality of these receptors, the 2C-X family is likely to be more reactive with other concurrently administered chemicals.<br /> <br /> === LD50 ===<br /> <br /> The LD50 in humans is not currently known. Use caution when exploring high doses of this compound. <br /> <br /> == Legal status ==<br /> <br /> * In Australia, 2C-E was added to the 'Dangerous Drugs' list of the 'Drugs Misuse Amendment Act 2008. <br /> <br /> * In Denmark, 2C-E has been added to the list of Schedule B controlled substances.<br /> <br /> * In New Zealand, 2C-E is illegal under the Analogues section of Schedule 3 / Class C, along with 2C-I, DOI, ephedrine and pseudoephedrine.<br /> <br /> * In Sweden, 2C-E has been made illegal to sell or possess under their Act on the Prohibition of Certain Goods Dangerous to Health (''lagen om förbud mot vissa hälsofarliga varor'').<br /> <br /> * In the UK, 2C-E is a Class A controlled Substance under the Misuse of Drugs Act's 2002 amendments and as such is illegal to possess to supply.<br /> <br /> * In Germany, 2C-E is a Schedule I drug as of late 2014.<br /> <br /> * In the USA, 2C-E is a Schedule I substance under the FDA Safety and Innovation act of 2012, and is illegal to possess, distribute or manufacture.<br /> <br /> == Links ==<br /> <br /> * [https://www.erowid.org/chemicals/2ce/ Erowid]<br /> <br /> * [https://www.erowid.org/library/books_online/pihkal/pihkal024.shtml PiHKAL Entry]<br /> <br /> * [https://www.wikipedia.org/wiki/2C-E/ Wikipedia]<br /> <br /> [[Category:Stimulant]]<br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]<br /> [[Category:Research Chemical]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5725 2018-10-09T21:51:09Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> === Intravenous ===<br /> <br /> Intravenous DMT comes on extremely fast and is the most efficient method of use. The effects are extremely similar to vaporized DMT, though IV administration is much more dangerous. It is advised that potential users avoid intravenous administration of DMT and stick to vaporization.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Light || 10-15mg<br /> |-<br /> | Common || 15-25mg<br /> |-<br /> | Strong || 25-40mg+<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> *Euphoria<br /> *Feeling of awe<br /> *Realizations about one's life<br /> <br /> === Neutral ===<br /> *Time dilation<br /> *Intense hallucinations<br /> *Dissociation<br /> *Loss of comprehension of basic concepts such as ego, language or one's own body.<br /> *Out-of-body experiences<br /> *Unconventional thought patterns<br /> <br /> === Negative ===<br /> *Panic attack/Bad trip<br /> *(oral only) Nausea/Vomitting<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5724 2018-10-09T21:50:54Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> === Insufflated ===<br /> <br /> Insufflated doses vary wildly, start low. Dosages given are for freebase DMT, dosage for salt form may be a little bit higher.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 10-25mg<br /> |-<br /> | Common || 25-50mg<br /> |-<br /> | Strong || 50-125mg+<br /> |}<br /> <br /> Insufflation of DMT is a less popular method of administration because it can cause extreme physical discomfort. DMT can be snorted in both freebase and salt forms. The most common salt utilized for insufflation is DMT Fumarate. Note that highly basic substances can damage the nasal passageway so the potential user is advised to proceed with caution.<br /> '''[https://wiki.dmt-nexus.me/Ingestion_Methods#Hyperspace_Fool.27s_COCO_Tek_For_Insufflation_Of_DMT: Preparations to make DMT insuflation more tolerable]''' from '''[https://www.dmt-nexus.me DMT-Nexus]<br /> <br /> === Intravenous ===<br /> <br /> Intravenous DMT comes on extremely fast and is the most efficient method of use. The effects are extremely similar to vaporized DMT, though IV administration is much more dangerous. It is advised that potential users avoid intravenous administration of DMT and stick to vaporization.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Light || 10-15mg<br /> |-<br /> | Common || 15-25mg<br /> |-<br /> | Strong || 25-40mg+<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> *Euphoria<br /> *Feeling of awe<br /> *Realizations about one's life<br /> <br /> === Neutral ===<br /> *Time dilation<br /> *Intense hallucinations<br /> *Dissociation<br /> *Loss of comprehension of basic concepts such as ego, language or one's own body.<br /> *Out-of-body experiences<br /> *Unconventional thought patterns<br /> <br /> === Negative ===<br /> *Panic attack/Bad trip<br /> *(oral only) Nausea/Vomitting<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=2C-B&diff=5723 2018-10-09T21:50:38Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:2cb.jpg|thumb|150px|2C-B vial and powder]]<br /> <br /> '''2C-B''' is a [[Psychedelics|psychedelic]] drug of the [[2C-X|2C-X family]].<br /> Effects are often described as being more easily managed than other psychedelics; it is often compared to a mixture of a LSD and MDMA.<br /> 2C-B is also known for the strong body component of its effects which are alternately described as pleasurable energy or a 'sense of being in the body,' and by others as an unpleasant 'buzzing' or body-load, which is mostly occurring during onset. Users also report open eye visuals in the form of colour distortions, melting like hallucinations, and other minor visual psychedelic effects.<br /> <br /> == History ==<br /> 2C-B was first synthesized in 1974 by Alexander Shulgin, and it first saw use among the psychiatric community as an aid during therapy. It was considered one of the best drugs for this purpose because of its short duration, relative absence of side effects, and comparably mild nature. Shortly after becoming popular in the medical community, it became popular recreationally. 2C-B was first sold commercially as an aphrodisiac under the trade name &quot;Eros&quot;, which was manufactured by the German pharmaceutical company Drittewelle. From many years after it was available as tablets in Dutch smart shops under the name &quot;Nexus&quot;.<br /> <br /> == Dosage ==<br /> '''NOTE: DO NOT TAKE THE BELOW DOSING INFORMATION AS A KNOW ALL, PLEASE TAKE CAUTION, AND REMEMBER THAT YOU CAN ALWAYS TAKE MORE, BUT NEVER LESS.'''<br /> <br /> {{#tdose: 2cb }}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 20-75 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-15 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Rectal<br /> |-<br /> | Onset || 5-20 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |}<br /> <br /> == Effects ==<br /> === Neutral ===<br /> <br /> * Decreased Appetite<br /> <br /> * Pupil Dilation<br /> <br /> * Time Dilation<br /> <br /> === Negative ===<br /> <br /> * Restlessness<br /> <br /> * Sweating/Chills<br /> <br /> * Nausea<br /> <br /> * Insomnia<br /> <br /> * Muscle Tension<br /> <br /> * Confusion<br /> <br /> *Vasoconstriction<br /> <br /> == Aliases ==<br /> <br /> * Bees<br /> <br /> * Nexus<br /> <br /> == Chemistry and Pharmacology ==<br /> Systematic name: 2-(4-bromo-2,5-dimethoxyphenyl)ethanamine<br /> <br /> Unlike most hallucinogens, 2C-B has been shown to be a low efficacy serotonin 5-HT2A receptor partial agonist or even full antagonist. This suggests that the 5-HT2C receptor is primarily responsible for mediating the effects experienced by users of 2C-B, although functional antagonism of 5-HT2A or activation of the 5-HT2A-coupled phospholipase D pathway may also play a role. The rank order of receptorantagonist potency for this family of drugs is 2C-I &gt; 2C-B &gt; 2C-D &gt; 2C-H.<br /> <br /> Research suggests that 2C-B increases dopamine levels in the brains of rats, which may contribute to its psychoactivity.<br /> <br /> == Harm Reduction ==<br /> <br /> 2C-B is known as one of the safer psychedelics, with several reported cases of users far exceeding commonly used dosing limits without lasting adverse physical effects. It is also observed to have a low addiction potential. It is a stimulating psychedelic, and therefore it's important to remain hydrated. Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for more information.<br /> <br /> Do not take heroic doses thinking that 2C-B is one of the &quot;safer psychedelics&quot;.<br /> <br /> === Interactions === <br /> <br /> 2C-B increases dopamine levels and also has an effect on serotonin. Therefore, 2C-B may react negatively with serotonic drugs like anti-depressants and tramadol.<br /> <br /> == Legal Status ==<br /> Internationally, 2C-B is a Schedule II drug under the Convention on Psychotropic Substances. In the Netherlands, 2C-B became a list I substance of the Opium Law despite no health incidents occurring. Following the ban, other phenethylamines were sold in place of 2C-B until the Netherlands became the first country in the world to ban 2C-I, 2C-T-2 and 2C-T-7 alongside 2C-B.<br /> <br /> * UK: Class A (Along with all the others in the [[2C-X|2C-X family]]. (Illegal to produce, supply, or possess.))<br /> <br /> * United States: [http://www.justice.gov/dea/druginfo/ds.shtml Schedule I] (Illegal to produce, supply, or possess.)<br /> <br /> == Links ==<br /> <br /> * [https://en.wikipedia.org/wiki/2C-B Wikipedia]<br /> * [https://www.erowid.org/chemicals/2cb/2cb.shtml 2C-B Erowid Vault]<br /> <br /> [[Category:Drugs]]<br /> [[Category:Psychedelic]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=2C-E&diff=5722 2018-10-09T21:50:27Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:2ce.jpg|thumb|150px|Vial of 2C-E with powder]]<br /> <br /> '''2C-E''' is a chemical of the [[2C-X]] series which is characterised by its particularly intense visuals and higher potency when compared with other members of the family.<br /> <br /> == History ==<br /> <br /> 2C-E, like many of its close analogues, was first synthesized by Alexander Shulgin and published in PiHKAL. He was quite fond of it, granting it a place in his &quot;Magical Half Dozen&quot; alongside of [[DOM]], [[2C-B]], [[2C-T-2]] &amp; 7 and [[mescaline]]. <br /> <br /> == Usage ==<br /> <br /> 2C-E is mainly a recreational entheogen. It can be quite introspective in appropriate doses and settings. It doesn't lend itself well to intense party-like surroundings, much like LSD or similarly intense psychedelics.<br /> <br /> == Dosage ==<br /> <br /> {{#tdose: 2ce }}<br /> <br /> == Duration ==<br /> <br /> Note: Duration can be significantly longer with higher doses.<br /> <br /> Anecdotal evidence has shown the oral onset of 2C-E may vary wildly for some users, taking up to three hours before first effects in some cases. <br /> <br /> {| class=&quot;wikitable&quot;<br /> <br /> |+ Oral<br /> <br /> | Onset || 60-90 minutes<br /> <br /> |-<br /> <br /> | Total || 9-14 hours<br /> <br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> <br /> |+ Insufflated<br /> <br /> | Onset || 20-40 minutes<br /> <br /> |-<br /> <br /> | Total || 6-9 hours<br /> <br /> |}<br /> <br /> == Effects ==<br /> <br /> 2C-E is a psychedelic phenethylamine and as such has psychedelic and stimulant effects. As with all psychedelics, different users are likely to experience different sets of effects, which usually include some however very rarely would include all of the following effects.<br /> <br /> Compared to other members of the 2C-X family, 2C-E is generally considered to have a heavier body load and to be more visual than its counterparts.<br /> <br /> Note: The prevalence of negative effects increases with higher doses.<br /> <br /> === Neutral ===<br /> <br /> * Time dilation<br /> <br /> * Slight increase in heart-rate and body temperature<br /> <br /> * Inability to focus or difficulty focusing<br /> <br /> === Negative ===<br /> <br /> * Tension<br /> <br /> * Anxiety, restlessness, confusion<br /> <br /> * Dizziness<br /> <br /> * Nausea, gastrointestinal discomfort, possible vomiting<br /> <br /> * Over-sensitivity to music or other sensory stimuli<br /> <br /> * Unwanted 'spiritual' experiences<br /> <br /> * Racing thoughts<br /> <br /> == Harm Reduction ==<br /> <br /> * As with all psychedelic drugs 2C-E carries with it the potential for a very powerful experience, and as such has the potential to create a very difficult experience ('bad' trip). Mindset and setting play important roles in governing the nature of a psychedelic experience, among other things. <br /> <br /> See [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for more information.<br /> <br /> * As with all stimulants, care should be taken when dosing via different ROAs. The oral route has a much lower bioavailabity than those that bypass first pass metabolism i.e. Insufflated, rectal, intramuscular, intravenous and subcutaneous. <br /> <br /> See [[Stimulants#Harm Reduction|Stimulant Harm Reduction]] for more information.<br /> <br /> === Interactions ===<br /> <br /> See the [[Drug combinations]] chart for more information.<br /> <br /> == Chemistry and Pharmacology ==<br /> <br /> === Chemistry ===<br /> <br /> 2,5-Dimethoxy-4-ethylphenethylamine is a colorless oil and analogue of mescaline. Similarly it is classified as a psychedelic phenethylamine. It shares the substituted amphetamine core found in the structure of many entactogens. Crystalline forms are obtained as the amine salt by reacting the free base with a mineral acid, typically HCl. It is soluble in both water and ethanol. Maximum concentration in H2O is reported at ~50mg/ml and it is said to be relatively stable in solution. A drop below normal ambient temperatures can cause particles to crystalize out. <br /> <br /> Shulgin does not report an exact boiling point for the free base, stating only that during one synthesis the fraction boiling between 90-100 °C at 0.25 mmHg pressure was collected and converted to the hydrochloride salt. Shulgin reports the melting point of the hydrochloride salt as 208.5-210.5 °C. <br /> <br /> A full write up on Shulgin's synthesis for 2C-E can be found [https://www.erowid.org/library/books_online/pihkal/pihkal024.shtml here].<br /> <br /> === Pharmacology ===<br /> <br /> Like most psychedelic drugs, 2C-E is a 5-HT2a Agonist; from that, we can presume the concurrent or pre-administration of SSRIs may reduce the effects of 2C-E. 2C-E is one of the most potent of the 2C-X family, behind only 2C-P and 2C-T-4. The 2C-X family, specifically, 2C-E, 2C-I, and 2C-C all stimulated G protein binding, suggesting more of an activity similar to tryptamines such as 5-MeO-DMT and, interestingly, DPT. G Proteins are membrane proteins that effectively mediate interaction between hormone receptors and enzymes responsible for changes of metabolism as a result of hormonal changes.<br /> <br /> In rats, Stage I metabolism involved deamination and O-Demthylation, which are related to the Monoamine oxidase (MAO) and cytochrome P450 (CYP) enzymes. For virtually all the 2C’s, (B,I,D,E,T-2, and T-7), MAO-A and MAO-B were reacted upon; interestingly, ½ of the molecules in Shulgin’s Magical Half Dozen (2C-E, 2C-T-2, 2C-T-7, with the addition of 2C-D) also act to a small extent on the CYP2D6 enzyme. Because of the commonality of these receptors, the 2C-X family is likely to be more reactive with other concurrently administered chemicals.<br /> <br /> === LD50 ===<br /> <br /> The LD50 in humans is not currently known. Use caution when exploring high doses of this compound. <br /> <br /> == Legal status ==<br /> <br /> * In Australia, 2C-E was added to the 'Dangerous Drugs' list of the 'Drugs Misuse Amendment Act 2008. <br /> <br /> * In Denmark, 2C-E has been added to the list of Schedule B controlled substances.<br /> <br /> * In New Zealand, 2C-E is illegal under the Analogues section of Schedule 3 / Class C, along with 2C-I, DOI, ephedrine and pseudoephedrine.<br /> <br /> * In Sweden, 2C-E has been made illegal to sell or possess under their Act on the Prohibition of Certain Goods Dangerous to Health (''lagen om förbud mot vissa hälsofarliga varor'').<br /> <br /> * In the UK, 2C-E is a Class A controlled Substance under the Misuse of Drugs Act's 2002 amendments and as such is illegal to possess to supply.<br /> <br /> * In Germany, 2C-E is a Schedule I drug as of late 2014.<br /> <br /> * In the USA, 2C-E is a Schedule I substance under the FDA Safety and Innovation act of 2012, and is illegal to possess, distribute or manufacture.<br /> <br /> == Links ==<br /> <br /> * [https://www.erowid.org/chemicals/2ce/ Erowid]<br /> <br /> * [https://www.erowid.org/library/books_online/pihkal/pihkal024.shtml PiHKAL Entry]<br /> <br /> * [https://www.wikipedia.org/wiki/2C-E/ Wikipedia]<br /> <br /> [[Category:Stimulant]]<br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]<br /> [[Category:Research Chemical]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5721 2018-10-09T21:50:10Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> === Insufflated ===<br /> <br /> Insufflated doses vary wildly, start low. Dosages given are for freebase DMT, dosage for salt form may be a little bit higher.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 10-25mg<br /> |-<br /> | Common || 25-50mg<br /> |-<br /> | Strong || 50-125mg+<br /> |}<br /> <br /> Insufflation of DMT is a less popular method of administration because it can cause extreme physical discomfort. DMT can be snorted in both freebase and salt forms. The most common salt utilized for insufflation is DMT Fumarate. Note that highly basic substances can damage the nasal passageway so the potential user is advised to proceed with caution.<br /> '''[https://wiki.dmt-nexus.me/Ingestion_Methods#Hyperspace_Fool.27s_COCO_Tek_For_Insufflation_Of_DMT: Preparations to make DMT insuflation more tolerable]''' from '''[https://www.dmt-nexus.me DMT-Nexus]<br /> <br /> === Intravenous ===<br /> <br /> Intravenous DMT comes on extremely fast and is the most efficient method of use. The effects are extremely similar to vaporized DMT, though IV administration is much more dangerous. It is advised that potential users avoid intravenous administration of DMT and stick to vaporization.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Light || 10-15mg<br /> |-<br /> | Common || 15-25mg<br /> |-<br /> | Strong || 25-40mg+<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> *Euphoria<br /> *Feeling of awe<br /> *Realizations about one's life<br /> <br /> === Neutral ===<br /> *Time dilation<br /> *Intense hallucinations<br /> *Dissociation<br /> *Loss of comprehension of basic concepts such as ego, language or one's own body.<br /> *Out-of-body experiences<br /> *Unconventional thought patterns<br /> <br /> === Negative ===<br /> *Panic attack/Bad trip<br /> *(oral only) Nausea/Vomitting<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> === Production ===<br /> There are a number of ways to acquire this entheogen. The first and most difficult way is to have some substantial chemistry knowledge and experience and actually synthesize pure DMT in a laboratory. This a rather tricky and time consuming process and requires access to some rather obscure and hard to acquire chemicals. The most common and easiest method to acquire DMT is to extract it from the various plant species that contain the compound.<br /> DMT occurs naturally in several plants and may therefore be extracted from them with little chemistry knowledge, requiring no actual synthesis.<br /> <br /> Plants containing DMT include Mimosa hostilis/tenuflora, Psychotria viridis, Codariocalyx motorius, Diplopterys cabrerana, Acacia species, and Phalaris species.<br /> <br /> ==== Extraction Teks ====<br /> * [[Zim's Clarified ATB Hybrid Salt Tek]]<br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=DMT&diff=5720 2018-10-09T21:49:47Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>[[File:SpiceCrystal001.jpg|right|300px|Opaque DMT crystal]]<br /> '''N,N-Dimethyltryptamine''' (or '''DMT''' for short) is a short acting psychedelic entheogen which allows a person's consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable. It is most commonly classified as a psychedelic but also possesses some properties inherent to dissociatives. It is one of the most powerful yet mysterious psychedelics in existence, but in the opinion of many users, to classify DMT as merely a drug would be doing it a great injustice as DMT seems to some as a transdimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it. Nevertheless, it is important to realize that the experience may be very difficult for some to integrate, and great care and respect is necessary to use it.<br /> <br /> DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.<br /> <br /> == Plants Containing DMT ==<br /> (from Block 1994*; Smith 1977; Montgomery, pers. comm.; Ott 1993*; Schultes and Hofman 1980, 155*; supplemented)<br /> &lt;table style=&quot;font-family: Arial, Helvetica, sans-serif; font-size: 9pt;&quot; cellspacing=&quot;0&quot; cellpadding=&quot;0&quot;&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Species&lt;/strong&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;strong&gt;Demonstrated Tryptamines&lt;/strong&gt;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AGARICACEAE (FuNGI)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita citrina &lt;/em&gt;Gray&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita porphyria &lt;/em&gt;(Fries) Secretan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Amanita &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;AIZOACEAE/MESEMBRYANTHEMACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Delosperma &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,MMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mesembryanthemum &lt;/em&gt;spp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;GRAMINEAE (POACEAE)&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Arundo donax &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris arundinacea &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phalaris tuberosa &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phragmites australis &lt;/em&gt;(Cav.) Trin. ex Steud.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LAURACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Umbellularia californica &lt;/em&gt;(Hook. et A.) Nutt.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;LEGUMINOSAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia confusa &lt;/em&gt;Merr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia maidenii &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (0.360/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia nubica &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia phlebophylla &lt;/em&gt;F. von Mue1!.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.30/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acacia simpIicifolia &lt;/em&gt;Druce&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.810/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Acaciaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera colubrina &lt;/em&gt;(VeIl.) Bren.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Anadenanthera peregrina &lt;/em&gt;(1.) Spag.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmanthus illinoensis &lt;/em&gt;(Michx.) MacMillan&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (to 0.340/0)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium adscendens &lt;/em&gt;(Sw.) DC. var. &lt;em&gt;adscendens&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT (?)&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium caudatum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gangeticum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium gyrans &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium pulchellum &lt;/em&gt;Benth. ex Bak.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium racemosum &lt;/em&gt;Thunb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium tiliaefolium &lt;/em&gt;G. Don&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Desmodium triflorum &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, bufotenine, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;Turcz.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza bicolor &lt;/em&gt;var. &lt;em&gt;japonica &lt;/em&gt;Nakai&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Lespedeza capitata &lt;/em&gt;Michx.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa scabrella &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa tenuiflora &lt;/em&gt;(Willd.) Pair. [syn. &lt;em&gt;Mimosa hostilis&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.570/0 DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;Benth., &lt;em&gt;Mimosa nigra]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosa verrucosa&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mimosaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucuna pruriens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, bufotenine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Mucunaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis cassioides &lt;/em&gt;Pritze1&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tetrahydroharmane&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Petalostylis labicheoides &lt;/em&gt;R. Brown&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, tryptamine&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Phyllodium pulchellum &lt;/em&gt;(1.) Desv.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MALPIGHIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Banisteriopsis argentea &lt;/em&gt;Spring. [syn. &lt;em&gt;B. muricata &lt;/em&gt;(Cav.) Cuatr.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Diplopterys cabrerana &lt;/em&gt;(Cuatr.) Gates&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;[syn. &lt;em&gt;Banisteriopsis rusbyana]&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;MYRISTICACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Iryanthera ulei &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Osteophloeum platyspermum &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Viroia calophylla &lt;/em&gt;Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola calophylloidea &lt;/em&gt;Markgr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola carinata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola divergens &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola elongata &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola melinonii &lt;/em&gt;(Benoist) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola multinerva &lt;/em&gt;Ducke&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola pavonis &lt;/em&gt;(DC.) A.C. Smith&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola peruviana &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola rufula &lt;/em&gt;(DC.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola sebifera &lt;/em&gt;Aubi.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola theiodora &lt;/em&gt;(Spruce ex Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT,5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virola venosa &lt;/em&gt;(Benth.) Warb.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT, 5-MeO-DMT, and others&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Virolaspp.&lt;/em&gt;&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;OCHNACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Testulea gabonensis &lt;/em&gt;Pellegr.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;POLYGONACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Eriogonum &lt;/em&gt;sp.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUBIACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria carthaginensis &lt;/em&gt;Jacq.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria poeppigiana &lt;/em&gt;Mueli. Arg.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Psychotria viridis &lt;/em&gt;Ruiz et Pay. [syn. &lt;em&gt;P. &lt;/em&gt;&lt;em&gt;psychotriaefolia &lt;/em&gt;Stand!.]&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;RUTACEAE&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&amp;nbsp;&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dictyoloma incanescens &lt;/em&gt;DC.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea drupacea &lt;/em&gt;(Baill.) Hartley&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Dutaillyea oreophila &lt;/em&gt;(Baill.) Sevenet-Pusset&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Evodia rutaecarpa &lt;/em&gt;Benth.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Limonia acidissima &lt;/em&gt;1.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Melicope leptococca &lt;/em&gt;(Baill.) Guill.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;0.21% DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Pilocarpus organensis &lt;/em&gt;Rizzini et Occhioni&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;5-MeO-DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Vepris ampody &lt;/em&gt;H. Perro&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum arborescens &lt;/em&gt;Rose&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT traces&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;tr&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;&lt;em&gt;Zanthoxylum procerum &lt;/em&gt;Donn. Sm.&lt;/td&gt;<br /> &lt;td valign=&quot;top&quot; width=&quot;319&quot;&gt;DMT&lt;/td&gt;<br /> &lt;/tr&gt;<br /> &lt;/table&gt;<br /> <br /> == Dosage == <br /> === Smoked-Vaporized === <br /> <br /> '''Dosage given assumes 100% effective vaporization method.'''<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised<br /> |-<br /> | Light || 10-15mg<br /> |-<br /> | Common || 15-25mg<br /> |-<br /> | Strong || 25-40mg+<br /> |}<br /> <br /> Extracted DMT freebase can be vaporized for very potent effects that last around 10-15 minutes. DMT is ideally vaporized, as opposed to smoked. Vaporization is achieved by a controlled temperature that does not burn/combust DMT material (and potential impurities), but instead just makes DMT evaporate and be inhaled.<br /> <br /> Vaporization is much smoother than smoking. Smoking leads to break down of DMT (and impurity) molecules into potential toxic nitrogen oxides, so not only it is harsher but also there is a significant loss of actives.<br /> <br /> Vaporizing can be achieved with improvised vaporizers such as &quot;The Inspirator mk II&quot;,&quot;The Machine&quot; (both DIY) or commercially sold vaporizing pipes such as the Vapor Genie.<br /> <br /> === Insufflated ===<br /> <br /> Insufflated doses vary wildly, start low. Dosages given are for freebase DMT, dosage for salt form may be a little bit higher.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Light || 10-25mg<br /> |-<br /> | Common || 25-50mg<br /> |-<br /> | Strong || 50-125mg+<br /> |}<br /> <br /> Insufflation of DMT is a less popular method of administration because it can cause extreme physical discomfort. DMT can be snorted in both freebase and salt forms. The most common salt utilized for insufflation is DMT Fumarate. Note that highly basic substances can damage the nasal passageway so the potential user is advised to proceed with caution.<br /> '''[https://wiki.dmt-nexus.me/Ingestion_Methods#Hyperspace_Fool.27s_COCO_Tek_For_Insufflation_Of_DMT: Preparations to make DMT insuflation more tolerable]''' from '''[https://www.dmt-nexus.me DMT-Nexus]<br /> <br /> === Intravenous ===<br /> <br /> Intravenous DMT comes on extremely fast and is the most efficient method of use. The effects are extremely similar to vaporized DMT, though IV administration is much more dangerous. It is advised that potential users avoid intravenous administration of DMT and stick to vaporization.<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Light || 10-15mg<br /> |-<br /> | Common || 15-25mg<br /> |-<br /> | Strong || 25-40mg+<br /> |}<br /> <br /> == Duration ==<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Oral<br /> |-<br /> | Onset || 10-60 minutes<br /> |-<br /> | Total || 4-8 hours<br /> |-<br /> | After-effects || 2-3 hours<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Smoked &amp; Vapourised <br /> |-<br /> | Onset || 0-3 minutes<br /> |-<br /> | Peak || 10-15 minutes<br /> |-<br /> | Total || 15-30 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Insufflated<br /> |-<br /> | Onset || 1-5 minutes<br /> |-<br /> | Total || 45-60 minutes<br /> |}<br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Intravenous<br /> |-<br /> | Onset || &gt;1 minute<br /> |-<br /> | Total || 30-45 minutes<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Positive ===<br /> *Euphoria<br /> *Feeling of awe<br /> *Realizations about one's life<br /> <br /> === Neutral ===<br /> *Time dilation<br /> *Intense hallucinations<br /> *Dissociation<br /> *Loss of comprehension of basic concepts such as ego, language or one's own body.<br /> *Out-of-body experiences<br /> *Unconventional thought patterns<br /> <br /> === Negative ===<br /> *Panic attack/Bad trip<br /> *(oral only) Nausea/Vomitting<br /> <br /> === After effects ===<br /> *A lasting perspective shift is likely to occur.<br /> *Depersonalization/Derealization can occur after an experience and may last up to several months.<br /> *Some people experience long-term anxiety after an experience while others report a decrease in overall anxiety.<br /> <br /> == Harm Reduction ==<br /> <br /> If ingesting DMT orally with a MAOI, ensure that care is taken with the diet such that no food which may cause an interaction is ingested - as this is potentially deadly. Check [https://www.erowid.org/chemicals/maois/maois_info2.shtml Erowid's MAOI Foods To Avoid] page for more information. However, if using a reversible MAOI such as Syrian Rue, less care needs to be taken.<br /> <br /> Refer to [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information on psychedelic safety.<br /> <br /> == Images ==<br /> <br /> &lt;gallery mode=&quot;packed-hover&quot;&gt;<br /> Image:Dmtwaxy.png|''Waxy DMT crystals''<br /> Image:SpiceCrystal001.jpg|''DMT crystal''<br /> Image:DmtfreebaseMolecule.png|''Freebase DMT structure''<br /> Image:Changa.jpg|''Changa''<br /> Image:Nndmt.jpg|''DMT with vial''<br /> Image:Dmt3.jpg|''Crystallizing DMT''<br /> &lt;/gallery&gt;<br /> <br /> == Chemistry and Pharmacology ==<br /> DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, tissues, muscle, glands, and skin.<br /> <br /> <br /> === Production ===<br /> There are a number of ways to acquire this entheogen. The first and most difficult way is to have some substantial chemistry knowledge and experience and actually synthesize pure DMT in a laboratory. This a rather tricky and time consuming process and requires access to some rather obscure and hard to acquire chemicals. The most common and easiest method to acquire DMT is to extract it from the various plant species that contain the compound.<br /> DMT occurs naturally in several plants and may therefore be extracted from them with little chemistry knowledge, requiring no actual synthesis.<br /> <br /> Plants containing DMT include Mimosa hostilis/tenuflora, Psychotria viridis, Codariocalyx motorius, Diplopterys cabrerana, Acacia species, and Phalaris species.<br /> <br /> ==== Extraction Teks ====<br /> * [[Zim's Clarified ATB Hybrid Salt Tek]]<br /> <br /> == Legal status ==<br /> <br /> === Europe ===<br /> <br /> DMT is a class A substance in most European countries.<br /> <br /> === America ===<br /> <br /> DMT is a schedule I substance in the United States.<br /> <br /> [[Category:Psychedelic]]<br /> [[Category:Drugs]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Research_Chemicals&diff=5719 2018-10-09T21:49:10Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>'Research Chemical' is a term used to refer to any chemical that has not been well researched and does not have an established long-term safety profile.<br /> <br /> ==Definition==<br /> <br /> 'Research chemical' is a term used to indicate a chemical which has not had a history of research or human use, and is therefore considered to be at a 'research stage.' There is no official body which determines a research chemical, or when a research chemical has accrued enough history of use to cease its classification as one. Some have suggested that these chemicals should be called &quot;unresearched chemicals&quot; or another term &quot;Experimental Chemicals&quot;. Some are new, while others have been around for years; and little is known about most of them besides first-hand accounts of their use. There are research chemicals of many different types of drugs: while many drugs are qualified as research chemicals, the term itself is more of a flag than a category.<br /> <br /> The expression can be considered somewhat of a misnomer, as drugs in this category have often not actually been researched, or at least have almost no history of human use. Many research chemicals in use today were originally discovered and published by Alexander Shulgin in PiHKAL and TiHKAL, and a lot more have been found based on these works. The term partially came from the fact that substances in the recreational markets were drugs that had been discovered in labs and only examined in-vitro or low-level animal studies. However, the 'research' more readily applies to the fact that these drugs were usually found through a process of research - such as through exploring analogues of existing psychoactive substances. Very little to no research has been used to establish the toxicology or human pharmacology of these drugs.<br /> <br /> 'Legal highs' commonly sold on a grey-area market are usually one or more research chemicals made to mimic the effects of other illicit drugs. There is currently a very large market for the production, sale and use of research chemicals, driven by their implicit legality; vendors and users alike pursue research chemicals to avoid legal troubles encountered from being involved with the more traditional chemicals. Governments tend to ban research chemicals a short while after they become popular, and this, in turn, leads to more being discovered and sold. Some legal systems, such as that of the USA, have moved against research chemicals with acts of law implicitly banning analogues of drugs which are already banned.<br /> <br /> ==Risks==<br /> <br /> As many of these drugs are very new and may not have a well-established safety profile, there are a variety of stronger risk factors in using them. It is likely that many research chemicals have undocumented side-effects, interactions or contraindications.<br /> <br /> ==Harm Reduction Precautions==<br /> <br /> While there is a certain element of risk involved in all experimentation/use of research chemicals. There are some basic precautions one can take in an effort to make an inherently risky behaviour less dangerous than otherwise. <br /> <br /> ==Links==<br /> <br /> * [http://drugs.tripsit.me/category/research-chemical Research Chemical Factsheets]<br /> * [https://erowid.org/psychoactives/research_chems/research_chems.shtml Erowid Research Chemicals Vault]<br /> <br /> ==References==<br /> <br /> (1) * [http://www.fsijournal.org/article/S0379-0738(12)00434-3/abstract URB-754: A new class of designer drug and 12 synthetic cannabinoids detected in illegal products]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Research_Chemicals&diff=5718 2018-10-09T21:48:59Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>'Research Chemical' is a term used to refer to any chemical that has not been well researched and does not have an established long-term safety profile.<br /> <br /> ==Definition==<br /> <br /> 'Research chemical' is a term used to indicate a chemical which has not had a history of research or human use, and is therefore considered to be at a 'research stage.' There is no official body which determines a research chemical, or when a research chemical has accrued enough history of use to cease its classification as one. Some have suggested that these chemicals should be called &quot;unresearched chemicals&quot; or another term &quot;Experimental Chemicals&quot;. Some are new, while others have been around for years; and little is known about most of them besides first-hand accounts of their use. There are research chemicals of many different types of drugs: while many drugs are qualified as research chemicals, the term itself is more of a flag than a category.<br /> <br /> The expression can be considered somewhat of a misnomer, as drugs in this category have often not actually been researched, or at least have almost no history of human use. Many research chemicals in use today were originally discovered and published by Alexander Shulgin in PiHKAL and TiHKAL, and a lot more have been found based on these works. The term partially came from the fact that substances in the recreational markets were drugs that had been discovered in labs and only examined in-vitro or low-level animal studies. However, the 'research' more readily applies to the fact that these drugs were usually found through a process of research - such as through exploring analogues of existing psychoactive substances. Very little to no research has been used to establish the toxicology or human pharmacology of these drugs.<br /> <br /> 'Legal highs' commonly sold on a grey-area market are usually one or more research chemicals made to mimic the effects of other illicit drugs. There is currently a very large market for the production, sale and use of research chemicals, driven by their implicit legality; vendors and users alike pursue research chemicals to avoid legal troubles encountered from being involved with the more traditional chemicals. Governments tend to ban research chemicals a short while after they become popular, and this, in turn, leads to more being discovered and sold. Some legal systems, such as that of the USA, have moved against research chemicals with acts of law implicitly banning analogues of drugs which are already banned.<br /> <br /> ==Risks==<br /> <br /> As many of these drugs are very new and may not have a well-established safety profile, there are a variety of stronger risk factors in using them. It is likely that many research chemicals have undocumented side-effects, interactions or contraindications.<br /> <br /> ==Harm Reduction Precautions==<br /> <br /> While there is a certain element of risk involved in all experimentation/use of research chemicals. There are some basic precautions one can take in an effort to make an inherently risky behaviour less dangerous than otherwise. <br /> <br /> ===Preparation===<br /> <br /> When experimenting with any new drug a little forethought can go a long way, especially when it comes to drugs about which very little is actually known.<br /> <br /> Usually, if you're experimenting with a new drug (or even just a drug that is new to you) it's best practice to have a sober sitter with you, just in case something goes wrong. Some types of drugs produce effects that are more risky to go into alone than others but if you're using something new and you are unaware of how it will affect you, it's never a bad idea to be accompanied by a trustworthy person, such as a close friend, to help guide you through a difficult experience or just someone to keep an eye on how your body reacts to something.<br /> <br /> ==Links==<br /> <br /> * [http://drugs.tripsit.me/category/research-chemical Research Chemical Factsheets]<br /> * [https://erowid.org/psychoactives/research_chems/research_chems.shtml Erowid Research Chemicals Vault]<br /> <br /> ==References==<br /> <br /> (1) * [http://www.fsijournal.org/article/S0379-0738(12)00434-3/abstract URB-754: A new class of designer drug and 12 synthetic cannabinoids detected in illegal products]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Research_Chemicals&diff=5717 2018-10-09T21:48:49Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>'Research Chemical' is a term used to refer to any chemical that has not been well researched and does not have an established long-term safety profile.<br /> <br /> ==Definition==<br /> <br /> 'Research chemical' is a term used to indicate a chemical which has not had a history of research or human use, and is therefore considered to be at a 'research stage.' There is no official body which determines a research chemical, or when a research chemical has accrued enough history of use to cease its classification as one. Some have suggested that these chemicals should be called &quot;unresearched chemicals&quot; or another term &quot;Experimental Chemicals&quot;. Some are new, while others have been around for years; and little is known about most of them besides first-hand accounts of their use. There are research chemicals of many different types of drugs: while many drugs are qualified as research chemicals, the term itself is more of a flag than a category.<br /> <br /> The expression can be considered somewhat of a misnomer, as drugs in this category have often not actually been researched, or at least have almost no history of human use. Many research chemicals in use today were originally discovered and published by Alexander Shulgin in PiHKAL and TiHKAL, and a lot more have been found based on these works. The term partially came from the fact that substances in the recreational markets were drugs that had been discovered in labs and only examined in-vitro or low-level animal studies. However, the 'research' more readily applies to the fact that these drugs were usually found through a process of research - such as through exploring analogues of existing psychoactive substances. Very little to no research has been used to establish the toxicology or human pharmacology of these drugs.<br /> <br /> 'Legal highs' commonly sold on a grey-area market are usually one or more research chemicals made to mimic the effects of other illicit drugs. There is currently a very large market for the production, sale and use of research chemicals, driven by their implicit legality; vendors and users alike pursue research chemicals to avoid legal troubles encountered from being involved with the more traditional chemicals. Governments tend to ban research chemicals a short while after they become popular, and this, in turn, leads to more being discovered and sold. Some legal systems, such as that of the USA, have moved against research chemicals with acts of law implicitly banning analogues of drugs which are already banned.<br /> <br /> ==Risks==<br /> <br /> As many of these drugs are very new and may not have a well-established safety profile, there are a variety of stronger risk factors in using them. It is likely that many research chemicals have undocumented side-effects, interactions or contraindications.<br /> <br /> ==Harm Reduction Precautions==<br /> <br /> While there is a certain element of risk involved in all experimentation/use of research chemicals. There are some basic precautions one can take in an effort to make an inherently risky behaviour less dangerous than otherwise. <br /> <br /> ===Preparation===<br /> <br /> When experimenting with any new drug a little forethought can go a long way, especially when it comes to drugs about which very little is actually known.<br /> <br /> Usually, if you're experimenting with a new drug (or even just a drug that is new to you) it's best practice to have a sober sitter with you, just in case something goes wrong. Some types of drugs produce effects that are more risky to go into alone than others but if you're using something new and you are unaware of how it will affect you, it's never a bad idea to be accompanied by a trustworthy person, such as a close friend, to help guide you through a difficult experience or just someone to keep an eye on how your body reacts to something.<br /> <br /> ===Dosing===<br /> <br /> As these chemicals are generally very new, and little information exists as to their effect on humans, there is also a lack of information about recommended doses. Often, speculative doses can be found on the Internet. When a new research chemical is released, the first results can often be found on forums such as Bluelight or drugs-forum. These consist of anecdotal trip reports, and cannot be trusted very much since in the early days of a drug's release, vendors will often sell other drugs under the newer name. After a time, and once some verifiable reports about the drug have been collected, tiered summaries are compiled by resources such as [http://factsheet.tripsit.me/factsheet/ TripSit Factsheets] and [https://www.erowid.org Erowid], which can provide more conclusive dosage guidelines. However, even when speculative doses are published, they should not be fully trusted due to the lack of long-term testing a drug has received at this point. Drugs which do not have much reliable information pertaining to their dose will generally be tagged.<br /> <br /> With a chemical that has never been tested in vivo (animal subjects) for most substances, you would want to start around 25ug's and titrate your dosage up to 50ug's in increments of 25ug's Leaving a week minimum between the 25ug test and 50ug, and work your way up. But this isn't needed for every chemical, such as BK-2C-I. You can use BK-2C-B as a &quot;reference&quot; of sorts, of it being 10x weaker than the parent compound(BK-2C-B). It is much safer to start at a lower dose than what would be an active dose to see if your body can handle the drug.Some might say that you can gauge an activity with just SAR's (Structure-Activity relationship) which in the most part true, yet in cases such as Lophophine and IRIS, there is a very good reason why it should be active, yet it isn't. That can also go the other way, as IRIS is one of the &quot;Ten Classic Ladies&quot; or the ten possible homologues of DOM. While DOM is active around 3mg's, yet IRIS is inactive.<br /> <br /> Therefore, because of the importance of using sub-threshold tester-doses, and since many of these new chemicals are highly potent anyways it is imperative that one has a reliable way to accurately measure chemicals in low doses.<br /> <br /> It is not safe to assume any consumer-grade scale will be reliably accurate &lt;50mg, however, there is a way to measure accurately low doses of chemicals using a method known as 'volumetric dosing', [[Quick guide to volumetric dosing]]. While this technique is not particularly difficult it does require some planning and precision.<br /> <br /> If you intend to employ volumetric measuring techniques, or when working with new chemicals (or any chemicals for that matter) it is important to be sure to use the most accurate scale available on a consumer level. Unfortunately, there are no scales that are reliably accurate for weights under approximately 25 mg that are readily available to the average consumer. That being said, there are some scales for sale for under $100, which if used correctly, can be safely used to prepare a solution for volumetric dosing of a substance. For more information on how to correctly use a scale, and sources for reasonably reliable scales to buy, check [[Scales]].<br /> <br /> ==Links==<br /> <br /> * [http://drugs.tripsit.me/category/research-chemical Research Chemical Factsheets]<br /> * [https://erowid.org/psychoactives/research_chems/research_chems.shtml Erowid Research Chemicals Vault]<br /> <br /> ==References==<br /> <br /> (1) * [http://www.fsijournal.org/article/S0379-0738(12)00434-3/abstract URB-754: A new class of designer drug and 12 synthetic cannabinoids detected in illegal products]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Research_Chemicals&diff=5716 2018-10-09T21:48:37Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>'Research Chemical' is a term used to refer to any chemical that has not been well researched and does not have an established long-term safety profile.<br /> <br /> ==Definition==<br /> <br /> 'Research chemical' is a term used to indicate a chemical which has not had a history of research or human use, and is therefore considered to be at a 'research stage.' There is no official body which determines a research chemical, or when a research chemical has accrued enough history of use to cease its classification as one. Some have suggested that these chemicals should be called &quot;unresearched chemicals&quot; or another term &quot;Experimental Chemicals&quot;. Some are new, while others have been around for years; and little is known about most of them besides first-hand accounts of their use. There are research chemicals of many different types of drugs: while many drugs are qualified as research chemicals, the term itself is more of a flag than a category.<br /> <br /> The expression can be considered somewhat of a misnomer, as drugs in this category have often not actually been researched, or at least have almost no history of human use. Many research chemicals in use today were originally discovered and published by Alexander Shulgin in PiHKAL and TiHKAL, and a lot more have been found based on these works. The term partially came from the fact that substances in the recreational markets were drugs that had been discovered in labs and only examined in-vitro or low-level animal studies. However, the 'research' more readily applies to the fact that these drugs were usually found through a process of research - such as through exploring analogues of existing psychoactive substances. Very little to no research has been used to establish the toxicology or human pharmacology of these drugs.<br /> <br /> 'Legal highs' commonly sold on a grey-area market are usually one or more research chemicals made to mimic the effects of other illicit drugs. There is currently a very large market for the production, sale and use of research chemicals, driven by their implicit legality; vendors and users alike pursue research chemicals to avoid legal troubles encountered from being involved with the more traditional chemicals. Governments tend to ban research chemicals a short while after they become popular, and this, in turn, leads to more being discovered and sold. Some legal systems, such as that of the USA, have moved against research chemicals with acts of law implicitly banning analogues of drugs which are already banned.<br /> <br /> ==Risks==<br /> <br /> As many of these drugs are very new and may not have a well-established safety profile, there are a variety of stronger risk factors in using them. It is likely that many research chemicals have undocumented side-effects, interactions or contraindications.<br /> <br /> ==Harm Reduction Precautions==<br /> <br /> While there is a certain element of risk involved in all experimentation/use of research chemicals. There are some basic precautions one can take in an effort to make an inherently risky behaviour less dangerous than otherwise. <br /> <br /> ===Research===<br /> <br /> While most readily available anecdotal information on research chemicals cannot be entirely trusted (due to the nature of research chemicals most data available on RC's is just that, a series of anecdotes), even for very new drugs there is usually a fair amount of information available which can give a good idea of what to expect. It is important that you do your own research and carefully make your own informed decisions; don't take people's word for what a drug can/will do to/for you at face value as the same drug can affect people differently.<br /> <br /> * The TripSit [http://drugs.tripsit.me/ factsheets] often have data on new drugs, and our Wiki includes harm reduction information for research chemicals in each drug class on their respective pages.<br /> <br /> * While Erowid is usually slow to publish full vaults on research chemicals, there are usually a number of experience reports published for even very new drugs. These can give a good idea about what can be expected from the experience itself, as well as more anecdotal information about dosages and the like.<br /> <br /> * Forums such as Bluelight.org and drugs-forum.com often have the first discussions and experience reports for very new chemicals, however, reports can be somewhat dubious as in many cases very new drugs are often falsely sold, so the reports actually pertain to another chemical.<br /> <br /> ===Preparation===<br /> <br /> When experimenting with any new drug a little forethought can go a long way, especially when it comes to drugs about which very little is actually known.<br /> <br /> Usually, if you're experimenting with a new drug (or even just a drug that is new to you) it's best practice to have a sober sitter with you, just in case something goes wrong. Some types of drugs produce effects that are more risky to go into alone than others but if you're using something new and you are unaware of how it will affect you, it's never a bad idea to be accompanied by a trustworthy person, such as a close friend, to help guide you through a difficult experience or just someone to keep an eye on how your body reacts to something.<br /> <br /> ===Dosing===<br /> <br /> As these chemicals are generally very new, and little information exists as to their effect on humans, there is also a lack of information about recommended doses. Often, speculative doses can be found on the Internet. When a new research chemical is released, the first results can often be found on forums such as Bluelight or drugs-forum. These consist of anecdotal trip reports, and cannot be trusted very much since in the early days of a drug's release, vendors will often sell other drugs under the newer name. After a time, and once some verifiable reports about the drug have been collected, tiered summaries are compiled by resources such as [http://factsheet.tripsit.me/factsheet/ TripSit Factsheets] and [https://www.erowid.org Erowid], which can provide more conclusive dosage guidelines. However, even when speculative doses are published, they should not be fully trusted due to the lack of long-term testing a drug has received at this point. Drugs which do not have much reliable information pertaining to their dose will generally be tagged.<br /> <br /> With a chemical that has never been tested in vivo (animal subjects) for most substances, you would want to start around 25ug's and titrate your dosage up to 50ug's in increments of 25ug's Leaving a week minimum between the 25ug test and 50ug, and work your way up. But this isn't needed for every chemical, such as BK-2C-I. You can use BK-2C-B as a &quot;reference&quot; of sorts, of it being 10x weaker than the parent compound(BK-2C-B). It is much safer to start at a lower dose than what would be an active dose to see if your body can handle the drug.Some might say that you can gauge an activity with just SAR's (Structure-Activity relationship) which in the most part true, yet in cases such as Lophophine and IRIS, there is a very good reason why it should be active, yet it isn't. That can also go the other way, as IRIS is one of the &quot;Ten Classic Ladies&quot; or the ten possible homologues of DOM. While DOM is active around 3mg's, yet IRIS is inactive.<br /> <br /> Therefore, because of the importance of using sub-threshold tester-doses, and since many of these new chemicals are highly potent anyways it is imperative that one has a reliable way to accurately measure chemicals in low doses.<br /> <br /> It is not safe to assume any consumer-grade scale will be reliably accurate &lt;50mg, however, there is a way to measure accurately low doses of chemicals using a method known as 'volumetric dosing', [[Quick guide to volumetric dosing]]. While this technique is not particularly difficult it does require some planning and precision.<br /> <br /> If you intend to employ volumetric measuring techniques, or when working with new chemicals (or any chemicals for that matter) it is important to be sure to use the most accurate scale available on a consumer level. Unfortunately, there are no scales that are reliably accurate for weights under approximately 25 mg that are readily available to the average consumer. That being said, there are some scales for sale for under $100, which if used correctly, can be safely used to prepare a solution for volumetric dosing of a substance. For more information on how to correctly use a scale, and sources for reasonably reliable scales to buy, check [[Scales]].<br /> <br /> ==Links==<br /> <br /> * [http://drugs.tripsit.me/category/research-chemical Research Chemical Factsheets]<br /> * [https://erowid.org/psychoactives/research_chems/research_chems.shtml Erowid Research Chemicals Vault]<br /> <br /> ==References==<br /> <br /> (1) * [http://www.fsijournal.org/article/S0379-0738(12)00434-3/abstract URB-754: A new class of designer drug and 12 synthetic cannabinoids detected in illegal products]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Research_Chemicals&diff=5715 2018-10-09T21:48:26Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>'Research Chemical' is a term used to refer to any chemical that has not been well researched and does not have an established long-term safety profile.<br /> <br /> ==Definition==<br /> <br /> 'Research chemical' is a term used to indicate a chemical which has not had a history of research or human use, and is therefore considered to be at a 'research stage.' There is no official body which determines a research chemical, or when a research chemical has accrued enough history of use to cease its classification as one. Some have suggested that these chemicals should be called &quot;unresearched chemicals&quot; or another term &quot;Experimental Chemicals&quot;. Some are new, while others have been around for years; and little is known about most of them besides first-hand accounts of their use. There are research chemicals of many different types of drugs: while many drugs are qualified as research chemicals, the term itself is more of a flag than a category.<br /> <br /> The expression can be considered somewhat of a misnomer, as drugs in this category have often not actually been researched, or at least have almost no history of human use. Many research chemicals in use today were originally discovered and published by Alexander Shulgin in PiHKAL and TiHKAL, and a lot more have been found based on these works. The term partially came from the fact that substances in the recreational markets were drugs that had been discovered in labs and only examined in-vitro or low-level animal studies. However, the 'research' more readily applies to the fact that these drugs were usually found through a process of research - such as through exploring analogues of existing psychoactive substances. Very little to no research has been used to establish the toxicology or human pharmacology of these drugs.<br /> <br /> 'Legal highs' commonly sold on a grey-area market are usually one or more research chemicals made to mimic the effects of other illicit drugs. There is currently a very large market for the production, sale and use of research chemicals, driven by their implicit legality; vendors and users alike pursue research chemicals to avoid legal troubles encountered from being involved with the more traditional chemicals. Governments tend to ban research chemicals a short while after they become popular, and this, in turn, leads to more being discovered and sold. Some legal systems, such as that of the USA, have moved against research chemicals with acts of law implicitly banning analogues of drugs which are already banned.<br /> <br /> ==Risks==<br /> <br /> As many of these drugs are very new and may not have a well-established safety profile, there are a variety of stronger risk factors in using them. It is likely that many research chemicals have undocumented side-effects, interactions or contraindications.<br /> <br /> ===Analogue Misconception===<br /> <br /> Remember, just because it is an analogue of something, does not mean it will behave the same way.<br /> <br /> An example of this can be seen in the following comparison of two structurally related chemicals [[MDAI]] and [[MDMA]]. MDMA has been documented since the late 60's. MDAI is an analogue of MDMA, and while it produces some similar effects to MDMA it differs in that it's non-neurotoxic.<br /> <br /> Or we can take [[2C-B]] and its analogues such as [[BK-2C-B]], 25B-NBXXX, TCB-2, DOB, Bromo-Dragon-Fly, 2C-B-FLY. The parent drug in this example is much safer than the rest. There is no record of a death from 2C-B alone, with 25B-NBOMe there have been reports of multiple deaths during its short history of release.<br /> <br /> ==Harm Reduction Precautions==<br /> <br /> While there is a certain element of risk involved in all experimentation/use of research chemicals. There are some basic precautions one can take in an effort to make an inherently risky behaviour less dangerous than otherwise. <br /> <br /> ===Research===<br /> <br /> While most readily available anecdotal information on research chemicals cannot be entirely trusted (due to the nature of research chemicals most data available on RC's is just that, a series of anecdotes), even for very new drugs there is usually a fair amount of information available which can give a good idea of what to expect. It is important that you do your own research and carefully make your own informed decisions; don't take people's word for what a drug can/will do to/for you at face value as the same drug can affect people differently.<br /> <br /> * The TripSit [http://drugs.tripsit.me/ factsheets] often have data on new drugs, and our Wiki includes harm reduction information for research chemicals in each drug class on their respective pages.<br /> <br /> * While Erowid is usually slow to publish full vaults on research chemicals, there are usually a number of experience reports published for even very new drugs. These can give a good idea about what can be expected from the experience itself, as well as more anecdotal information about dosages and the like.<br /> <br /> * Forums such as Bluelight.org and drugs-forum.com often have the first discussions and experience reports for very new chemicals, however, reports can be somewhat dubious as in many cases very new drugs are often falsely sold, so the reports actually pertain to another chemical.<br /> <br /> ===Preparation===<br /> <br /> When experimenting with any new drug a little forethought can go a long way, especially when it comes to drugs about which very little is actually known.<br /> <br /> Usually, if you're experimenting with a new drug (or even just a drug that is new to you) it's best practice to have a sober sitter with you, just in case something goes wrong. Some types of drugs produce effects that are more risky to go into alone than others but if you're using something new and you are unaware of how it will affect you, it's never a bad idea to be accompanied by a trustworthy person, such as a close friend, to help guide you through a difficult experience or just someone to keep an eye on how your body reacts to something.<br /> <br /> ===Dosing===<br /> <br /> As these chemicals are generally very new, and little information exists as to their effect on humans, there is also a lack of information about recommended doses. Often, speculative doses can be found on the Internet. When a new research chemical is released, the first results can often be found on forums such as Bluelight or drugs-forum. These consist of anecdotal trip reports, and cannot be trusted very much since in the early days of a drug's release, vendors will often sell other drugs under the newer name. After a time, and once some verifiable reports about the drug have been collected, tiered summaries are compiled by resources such as [http://factsheet.tripsit.me/factsheet/ TripSit Factsheets] and [https://www.erowid.org Erowid], which can provide more conclusive dosage guidelines. However, even when speculative doses are published, they should not be fully trusted due to the lack of long-term testing a drug has received at this point. Drugs which do not have much reliable information pertaining to their dose will generally be tagged.<br /> <br /> With a chemical that has never been tested in vivo (animal subjects) for most substances, you would want to start around 25ug's and titrate your dosage up to 50ug's in increments of 25ug's Leaving a week minimum between the 25ug test and 50ug, and work your way up. But this isn't needed for every chemical, such as BK-2C-I. You can use BK-2C-B as a &quot;reference&quot; of sorts, of it being 10x weaker than the parent compound(BK-2C-B). It is much safer to start at a lower dose than what would be an active dose to see if your body can handle the drug.Some might say that you can gauge an activity with just SAR's (Structure-Activity relationship) which in the most part true, yet in cases such as Lophophine and IRIS, there is a very good reason why it should be active, yet it isn't. That can also go the other way, as IRIS is one of the &quot;Ten Classic Ladies&quot; or the ten possible homologues of DOM. While DOM is active around 3mg's, yet IRIS is inactive.<br /> <br /> Therefore, because of the importance of using sub-threshold tester-doses, and since many of these new chemicals are highly potent anyways it is imperative that one has a reliable way to accurately measure chemicals in low doses.<br /> <br /> It is not safe to assume any consumer-grade scale will be reliably accurate &lt;50mg, however, there is a way to measure accurately low doses of chemicals using a method known as 'volumetric dosing', [[Quick guide to volumetric dosing]]. While this technique is not particularly difficult it does require some planning and precision.<br /> <br /> If you intend to employ volumetric measuring techniques, or when working with new chemicals (or any chemicals for that matter) it is important to be sure to use the most accurate scale available on a consumer level. Unfortunately, there are no scales that are reliably accurate for weights under approximately 25 mg that are readily available to the average consumer. That being said, there are some scales for sale for under $100, which if used correctly, can be safely used to prepare a solution for volumetric dosing of a substance. For more information on how to correctly use a scale, and sources for reasonably reliable scales to buy, check [[Scales]].<br /> <br /> ==Links==<br /> <br /> * [http://drugs.tripsit.me/category/research-chemical Research Chemical Factsheets]<br /> * [https://erowid.org/psychoactives/research_chems/research_chems.shtml Erowid Research Chemicals Vault]<br /> <br /> ==References==<br /> <br /> (1) * [http://www.fsijournal.org/article/S0379-0738(12)00434-3/abstract URB-754: A new class of designer drug and 12 synthetic cannabinoids detected in illegal products]<br /> <br /> [[Category:Drug class]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Diethyl_Ether&diff=5714 2018-10-09T21:47:55Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>== Diethyl Ether ==<br /> [[File:Ether.jpeg|300px|thumbnail|left]]<br /> <br /> '''Diethyl Ether''' ((C2H5)2O) is a highly flammable solvent with anesthetic and dissociative effects when inhaled. It was synthesized first in the late 1200's and has been used recreationally among Polish peasants since the late 19th century. More recently, it gained popularity in the movie &quot;Fear and Loathing in Las Vegas&quot; which depicted Hunter S. Thompson experiencing the strange fiendishness of Diethyl Ether's intoxicating properties, sometimes called &quot;Ethermania&quot;. Liquid Diethyl Ether can be obtained in pure form which greatly reduces negative effects. <br /> <br /> '''Most negative effects result from impure diethyl ether being extracted from lighter fluid or other sources. The harmfulness and experiences related to these other unknown chemicals cannot distinguished from brain damage occurring. Avoid these awful effects by only obtaining pure chemical grade 99%+ pure Diethyl Ether'''.<br /> <br /> Also note that most pure Diethyl Ether contains some amount of BHT as a stabilizer to prevent explosions and fires. BHT's effects when inhaled are unclear as it is a FDA approved food additive but there is conflicting research on the substance.<br /> <br /> <br /> <br /> == Duration ==<br /> <br /> As Diethyl Ether is huffed continuously by its users, the effects are felt immediately <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Inhaled<br /> |-<br /> | Onset || immediatley<br /> |-<br /> | Total || 1 hour<br /> |-<br /> | After-effects || 2-48 hours (dose-dependent)<br /> |}<br /> <br /> == Effects ==<br /> <br /> == Harm Reduction ==<br /> * Huff only PURE diethyl ether as all self extractions contain harmful other chemicals.<br /> * Diethyl Ether is incredibly flammable so keep it away from flames <br /> * To avoid explosions store it in a dark colored bottle in a freezer/refrigerator.<br /> * The lethal dose is far beyond the dose that would cause one to vomit and lose consciousness, but huff slowly taking breaks frequently. <br /> * Don't inhale ether if you don't want to smell like gas for the following 24 hours. It seeps out of your skin and mouth. <br /> <br /> See [[Dissociatives#Harm_Reduction|Dissociative Harm Reduction]] for general information.<br /> <br /> == Legal status==<br /> <br /> == Links == <br /> <br /> [https://en.wikipedia.org/wiki/Ether Wikipedia]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Drugs]]<br /> [[Category:Dissociative]]<br /> [[Category:Research Chemical]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Diethyl_Ether&diff=5713 2018-10-09T21:47:37Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>== Diethyl Ether ==<br /> [[File:Ether.jpeg|300px|thumbnail|left]]<br /> <br /> '''Diethyl Ether''' ((C2H5)2O) is a highly flammable solvent with anesthetic and dissociative effects when inhaled. It was synthesized first in the late 1200's and has been used recreationally among Polish peasants since the late 19th century. More recently, it gained popularity in the movie &quot;Fear and Loathing in Las Vegas&quot; which depicted Hunter S. Thompson experiencing the strange fiendishness of Diethyl Ether's intoxicating properties, sometimes called &quot;Ethermania&quot;. Liquid Diethyl Ether can be obtained in pure form which greatly reduces negative effects. <br /> <br /> '''Most negative effects result from impure diethyl ether being extracted from lighter fluid or other sources. The harmfulness and experiences related to these other unknown chemicals cannot distinguished from brain damage occurring. Avoid these awful effects by only obtaining pure chemical grade 99%+ pure Diethyl Ether'''.<br /> <br /> Also note that most pure Diethyl Ether contains some amount of BHT as a stabilizer to prevent explosions and fires. BHT's effects when inhaled are unclear as it is a FDA approved food additive but there is conflicting research on the substance.<br /> <br /> <br /> <br /> == Duration ==<br /> <br /> As Diethyl Ether is huffed continuously by its users, the effects are felt immediately <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Inhaled<br /> |-<br /> | Onset || immediatley<br /> |-<br /> | Total || 1 hour<br /> |-<br /> | After-effects || 2-48 hours (dose-dependent)<br /> |}<br /> <br /> == Effects ==<br /> <br /> == Harm Reduction ==<br /> * Huff only PURE diethyl ether as all self extractions contain harmful other chemicals.<br /> * Diethyl Ether is incredibly flammable so keep it away from flames <br /> * To avoid explosions store it in a dark colored bottle in a freezer/refrigerator.<br /> * The lethal dose is far beyond the dose that would cause one to vomit and lose consciousness, but huff slowly taking breaks frequently. <br /> * Don't inhale ether if you don't want to smell like gas for the following 24 hours. It seeps out of your skin and mouth. <br /> <br /> See [[Dissociatives#Harm_Reduction|Dissociative Harm Reduction]] for general information.<br /> <br /> === Interactions ===<br /> <br /> == Legal status==<br /> <br /> == Links == <br /> <br /> [https://en.wikipedia.org/wiki/Ether Wikipedia]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Drugs]]<br /> [[Category:Dissociative]]<br /> [[Category:Research Chemical]]</div>

Dumbdumb123 https://wiki.tripsit.me/index.php?title=Diethyl_Ether&diff=5712 2018-10-09T21:47:24Z

<p>Dumbdumb123: Goodbye moonmen</p> <hr /> <div>== Diethyl Ether ==<br /> [[File:Ether.jpeg|300px|thumbnail|left]]<br /> <br /> '''Diethyl Ether''' ((C2H5)2O) is a highly flammable solvent with anesthetic and dissociative effects when inhaled. It was synthesized first in the late 1200's and has been used recreationally among Polish peasants since the late 19th century. More recently, it gained popularity in the movie &quot;Fear and Loathing in Las Vegas&quot; which depicted Hunter S. Thompson experiencing the strange fiendishness of Diethyl Ether's intoxicating properties, sometimes called &quot;Ethermania&quot;. Liquid Diethyl Ether can be obtained in pure form which greatly reduces negative effects. <br /> <br /> '''Most negative effects result from impure diethyl ether being extracted from lighter fluid or other sources. The harmfulness and experiences related to these other unknown chemicals cannot distinguished from brain damage occurring. Avoid these awful effects by only obtaining pure chemical grade 99%+ pure Diethyl Ether'''.<br /> <br /> Also note that most pure Diethyl Ether contains some amount of BHT as a stabilizer to prevent explosions and fires. BHT's effects when inhaled are unclear as it is a FDA approved food additive but there is conflicting research on the substance.<br /> <br /> <br /> <br /> == Duration ==<br /> <br /> As Diethyl Ether is huffed continuously by its users, the effects are felt immediately <br /> <br /> {| class=&quot;wikitable&quot;<br /> |+ Inhaled<br /> |-<br /> | Onset || immediatley<br /> |-<br /> | Total || 1 hour<br /> |-<br /> | After-effects || 2-48 hours (dose-dependent)<br /> |}<br /> <br /> == Effects ==<br /> <br /> === Negative ===<br /> * Smelling of gasoline for 24 hours<br /> * Risk of short term dependency <br /> * Intense desire to binge once started<br /> * Blacking out and forgetting one has taken a drug<br /> * Discomfort, pain or bitterness in taste and harshness<br /> * Severe confusion, disorganised thinking<br /> * Vertigo, spinning sensation (risk of injury)<br /> * Nausea, vomiting<br /> * Susceptibility to accidents (from incoordination and change in perception of body and time)<br /> * Severe dissociation, depersonalisation<br /> * Loss of consciousness<br /> * Depression of heart rate and respiration (risk increases with increased dose or when combined with depressants)<br /> <br /> == Harm Reduction ==<br /> * Huff only PURE diethyl ether as all self extractions contain harmful other chemicals.<br /> * Diethyl Ether is incredibly flammable so keep it away from flames <br /> * To avoid explosions store it in a dark colored bottle in a freezer/refrigerator.<br /> * The lethal dose is far beyond the dose that would cause one to vomit and lose consciousness, but huff slowly taking breaks frequently. <br /> * Don't inhale ether if you don't want to smell like gas for the following 24 hours. It seeps out of your skin and mouth. <br /> <br /> See [[Dissociatives#Harm_Reduction|Dissociative Harm Reduction]] for general information.<br /> <br /> === Interactions ===<br /> <br /> == Legal status==<br /> <br /> == Links == <br /> <br /> [https://en.wikipedia.org/wiki/Ether Wikipedia]<br /> <br /> == References ==<br /> <br /> &lt;references /&gt;<br /> <br /> [[Category:Drugs]]<br /> [[Category:Dissociative]]<br /> [[Category:Research Chemical]]</div>

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