<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://wiki.tripsit.me/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=MDMQualone</id>
	<title>TripSit Wiki - User contributions [en]</title>
	<link rel="self" type="application/atom+xml" href="https://wiki.tripsit.me/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=MDMQualone"/>
	<link rel="alternate" type="text/html" href="https://wiki.tripsit.me/wiki/Special:Contributions/MDMQualone"/>
	<updated>2026-05-27T22:15:47Z</updated>
	<subtitle>User contributions</subtitle>
	<generator>MediaWiki 1.44.0</generator>
	<entry>
		<id>https://wiki.tripsit.me/index.php?title=DOx&amp;diff=5053</id>
		<title>DOx</title>
		<link rel="alternate" type="text/html" href="https://wiki.tripsit.me/index.php?title=DOx&amp;diff=5053"/>
		<updated>2016-07-06T21:55:24Z</updated>

		<summary type="html">&lt;p&gt;MDMQualone: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[File:Dom.jpg|thumb|300px|left|5mg DOM blotters]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;DOx&#039;&#039;&#039; is a chemical class of substituted amphetamines that persists of many long lasting and very potent psychedelic drugs.&lt;br /&gt;
DOx not only includes [[DOB]], [[DOC]], [[DOI]] and [[DOM]], but also as number of lesser known substances, such as the [[Aleph]] and [[TMA]] series.&lt;br /&gt;
Almost all substances of the DOx series have a very long duration (12-30 hours), are extremely potent (active at just a few miligrams) and have a very slow onset.&lt;br /&gt;
They&#039;re often described as less spiritual and more stimulating compared to classic psychedelics.&lt;br /&gt;
&lt;br /&gt;
== History ==&lt;br /&gt;
&lt;br /&gt;
The DOx series was first researched by Alexander and Ann Shulgin, who rated [[DOM]] as one of the most important phenethylamine compounds, the so called &amp;quot;magical half-dozen&amp;quot;, in their book PiHKAL.&lt;br /&gt;
The most popular substance of this class is [[DOM]], also known as STP (Serenity, Tranquility, and Peace), which first appeared in tablet form in 1967.&lt;br /&gt;
As of 2014, drugs of the DOx series are sometimes mistakenly sold as &amp;quot;acid&amp;quot; on blotters, and once again [[DOM]] is the most widespread compound among users of psychedelic amphetamines.&lt;br /&gt;
&lt;br /&gt;
== Effects ==&lt;br /&gt;
=== Postive ===&lt;br /&gt;
&lt;br /&gt;
* Mood lift, euphoria, sense of well being&lt;br /&gt;
&lt;br /&gt;
* Tactile sensations&lt;br /&gt;
&lt;br /&gt;
* Introspection&lt;br /&gt;
&lt;br /&gt;
* Increased empathy, love and sociability&lt;br /&gt;
&lt;br /&gt;
* Visuals&lt;br /&gt;
&lt;br /&gt;
=== Neutral ===&lt;br /&gt;
&lt;br /&gt;
* Stimulation&lt;br /&gt;
&lt;br /&gt;
* Time distortion&lt;br /&gt;
&lt;br /&gt;
=== Negative ===&lt;br /&gt;
&lt;br /&gt;
* Nausea&lt;br /&gt;
&lt;br /&gt;
* Vasoconstriction&lt;br /&gt;
&lt;br /&gt;
* Anxiety, restlessness, confusion&lt;br /&gt;
&lt;br /&gt;
* Insomnia&lt;br /&gt;
&lt;br /&gt;
== Harm Reduction ==&lt;br /&gt;
&lt;br /&gt;
Due to DOx&#039; nature as substituted amphetamines, they pose some risk as  potent stimulants; take similar harm reduction precautions as one would  on [[stimulants]].&lt;br /&gt;
&lt;br /&gt;
See [[Psychedelics#Harm_Reduction|Psychedelic Harm Reduction]] for general information.&lt;br /&gt;
&lt;br /&gt;
=== WARNING ===&lt;br /&gt;
&lt;br /&gt;
DOx compounds have a very long duration and also a long comeup, redosing is not recommended, as it may take multiple hours to peak.&lt;br /&gt;
&lt;br /&gt;
=== Potentiators ===&lt;br /&gt;
&lt;br /&gt;
* [[Cannabis]]&lt;br /&gt;
&lt;br /&gt;
=== Interactions ===&lt;br /&gt;
&lt;br /&gt;
Check out our [[Drug Combinations]] page and chart for interactions and combinations of common drugs.&lt;br /&gt;
&lt;br /&gt;
Under no circumstances any DOx compound should be combined with a MAOI.&lt;br /&gt;
&lt;br /&gt;
== Chemistry and Pharmacology ==&lt;br /&gt;
&lt;br /&gt;
DOx is a chemical class of substituted amphetamine derivatives featuring methoxy groups at the 2- and 5-positions of the phenyl ring, and a substituent such as alkyl or halogen at the 4- position of the phenyl ring. The compounds of this class are  potent and long-lasting psychedelic drugs, and act as highly selective 5-HT2A, 5-HT2B, and 5-HT2C receptor partial agonists.&lt;br /&gt;
&lt;br /&gt;
== Legal status ==&lt;br /&gt;
&lt;br /&gt;
Most substances of the DOx class are controlled substances in almost every country. DOC and DOI are unscheduled in the US and a few other countries.&lt;br /&gt;
&lt;br /&gt;
== Images ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;gallery mode=&amp;quot;packed-hover&amp;quot;&amp;gt;&lt;br /&gt;
Image:Dom.jpg|&#039;&#039;DOM&#039;&#039;&lt;br /&gt;
Image:Dom2.png|&#039;&#039;&#039;DOM blotter art&#039;&#039;&#039;&lt;br /&gt;
&amp;lt;/gallery&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
[https://en.wikipedia.org/wiki/DOx Wikipedia]&lt;br /&gt;
&lt;br /&gt;
[https://www.erowid.org/chemicals/dob/dob.shtml Erowid DOB Vault]&lt;br /&gt;
&lt;br /&gt;
[https://www.erowid.org/chemicals/doc/doc.shtml Erowid DOC Vault]&lt;br /&gt;
&lt;br /&gt;
[https://www.erowid.org/chemicals/doi/doi.shtml Erowid DOI Vault]&lt;br /&gt;
&lt;br /&gt;
[https://www.erowid.org/chemicals/dom/dom.shtml Erowid DOM Vault]&lt;br /&gt;
&lt;br /&gt;
[https://www.erowid.org/chemicals/tma2/tma2.shtml Erowid TMA-2 Vault]&lt;br /&gt;
&lt;br /&gt;
[[Category:Drugs]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Psychedelic]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Research Chemical]]&lt;/div&gt;</summary>
		<author><name>MDMQualone</name></author>
	</entry>
	<entry>
		<id>https://wiki.tripsit.me/index.php?title=2C-X&amp;diff=4975</id>
		<title>2C-X</title>
		<link rel="alternate" type="text/html" href="https://wiki.tripsit.me/index.php?title=2C-X&amp;diff=4975"/>
		<updated>2016-05-13T15:38:55Z</updated>

		<summary type="html">&lt;p&gt;MDMQualone: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[File:2cc.jpg|thumb|150px|2C-C vial and powder]]&lt;br /&gt;
&lt;br /&gt;
The &#039;&#039;&#039;2C family&#039;&#039;&#039; is a group of [[Psychedelics|psychedelic]] phenethylamines that share the same basic 2C structure. The name &#039;2C&#039; is an acronym for the two carbons between the benzene ring and the amino group in all 2C chemicals. There are also two methoxy groups on the the 2 and 5 positions of the benzene ring. The -x denotes a number of different varieties of 2C&#039;s that differ in their substituents on the 3 and 4 positions of the benzene ring.&lt;br /&gt;
&lt;br /&gt;
== History ==&lt;br /&gt;
Alexander Shulgin coined this term and also synthesized the majority of the 2C&#039;s, publishing detailed information about their synthesis in his book PiHKAL (Phenethylamines i Have Known And Loved).&lt;br /&gt;
&lt;br /&gt;
== 2C Family ==&lt;br /&gt;
&lt;br /&gt;
* [[2C-B]] (Dimethoxybromophenethylamine)&lt;br /&gt;
* [[2C-B-FLY]] (Dihydrodifuran-2C-B)&lt;br /&gt;
* [[2C-BCB]] (Dimethoxybromo(cyclobutylphenyl)ethylamine)&lt;br /&gt;
* [[2C-C]] (Dimethoxychlorophenethylamine)&lt;br /&gt;
* [[2C-D]] (Dimethoxymethylphenethylamine)&lt;br /&gt;
* [[2C-E]] (Dimethoxyethylphenethylamine)&lt;br /&gt;
* [[2C-EF]] (Fluoroethylmethoxyphenethylamine)&lt;br /&gt;
* [[2C-G]] (Dimethyldimethoxyphenethylamine)&lt;br /&gt;
* [[2C-I]] (Dimethoxyiodophenethylamine)&lt;br /&gt;
* [[2C-N]] (Dimethoxynitrophenethylamine)&lt;br /&gt;
* [[2C-P]] (Dimethoxypropylphenethylamine)&lt;br /&gt;
* [[2C-iP]] (Dimethoxyisopropylphenethylamine)&lt;br /&gt;
* [[2C-T]] (Dimethoxymethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-2]] (Dimethoxyethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-3]] (Dimethoxymethylallylthiophenethylamine)&lt;br /&gt;
* [[2C-T-4]] (Dimethoxyisopropylthiophenethylamine)&lt;br /&gt;
* [[2C-T-5]] (Dimethoxycyclohexylthiophenethylamine)&lt;br /&gt;
* [[2C-T-6]] (Dimethoxyphenylthiophenethylamine)&lt;br /&gt;
* [[2C-T-7]] (Dimethoxypropylthiophenethylamine)&lt;br /&gt;
* [[2C-T-8]] (Dimethoxycyclopropylmethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-10]] (Dimethoxypyridylthiophenethylamine)&lt;br /&gt;
* [[2C-T-11]] (Dimethoxypara-bromophenylthiophenethylamine)&lt;br /&gt;
* [[2C-T-12]] (Dimethoxymorpholinothiophenethylamine)&lt;br /&gt;
* [[2C-T-13]] (Dimethoxy(beta-methoxy)ethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-14]] (Dimethoxymethylthioethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-15]] (Dimethoxycyclopropylthiophenethylamine)&lt;br /&gt;
* [[2C-T-16]] (Dimethoxyallylthiophenethylamine)&lt;br /&gt;
* [[2C-T-17]] (Dimethoxysec-butylthiophenethylamine)&lt;br /&gt;
* [[2C-T-19]] (Dimethoxybutylthiophenethylamine)&lt;br /&gt;
* [[2C-T-21]] (Dimethoxyfluoroethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-21.5]] (Dimethoxydifluuoroethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-22]] (Dimethoxytrifluoroethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-28]] (Dimethoxyfluoropropylthiophenethylamine)&lt;br /&gt;
* [[2C-T-30]] (Dimethoxyfluorobutylthiophenethylamine)&lt;br /&gt;
* [[2C-TFM]] (Dimethoxytrifluorophenethylamine)&lt;br /&gt;
* [[2C-YN]] (Dimethoxyethynylphenethylamine)&lt;br /&gt;
&lt;br /&gt;
== Images ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;gallery mode=&amp;quot;packed-hover&amp;quot; heights=&amp;quot;200px&amp;quot;&amp;gt;&lt;br /&gt;
Image:2cb.jpg|&#039;&#039;2C-B&#039;&#039;&lt;br /&gt;
Image:2cc.jpg|&#039;&#039;2C-C&#039;&#039;&lt;br /&gt;
Image:2ce.jpg|&#039;&#039;2C-E&#039;&#039;&lt;br /&gt;
&amp;lt;/gallery&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Psychedelic]]&lt;br /&gt;
[[Category:Drugs]]&lt;/div&gt;</summary>
		<author><name>MDMQualone</name></author>
	</entry>
	<entry>
		<id>https://wiki.tripsit.me/index.php?title=2C-X&amp;diff=4974</id>
		<title>2C-X</title>
		<link rel="alternate" type="text/html" href="https://wiki.tripsit.me/index.php?title=2C-X&amp;diff=4974"/>
		<updated>2016-05-13T15:34:20Z</updated>

		<summary type="html">&lt;p&gt;MDMQualone: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[File:2cc.jpg|thumb|150px|2C-C vial and powder]]&lt;br /&gt;
&lt;br /&gt;
The &#039;&#039;&#039;2C family&#039;&#039;&#039; is a group of [[Psychedelics|psychedelic]] phenethylamines that share the same basic 2C structure. The name &#039;2C&#039; is an acronym for the two carbons between the benzene ring and the amino group in all 2C chemicals. There are also two methoxy groups on the the 2 and 5 positions of the benzene ring. The -x denotes a number of different varieties of 2C&#039;s that differ in their substituents on the 3 and 4 positions of the benzene ring.&lt;br /&gt;
&lt;br /&gt;
== History ==&lt;br /&gt;
Alexander Shulgin coined this term and also synthesized the majority of the 2C&#039;s, publishing detailed information about their synthesis in his book PiHKAL (Phenethylamines i Have Known And Loved).&lt;br /&gt;
&lt;br /&gt;
== 2C Family ==&lt;br /&gt;
&lt;br /&gt;
* [[2C-B]] (Dimethoxybromophenethylamine)&lt;br /&gt;
* [[2C-B-FLY]] (Dihydrodifuran-2C-B)&lt;br /&gt;
* [[2C-C]] (Dimethoxychlorophenethylamine)&lt;br /&gt;
* [[2C-D]] (Dimethoxymethylphenethylamine)&lt;br /&gt;
* [[2C-E]] (Dimethoxyethylphenethylamine)&lt;br /&gt;
* [[2C-EF]] (Fluoroethylmethoxyphenethylamine)&lt;br /&gt;
* [[2C-G]] (Dimethyldimethoxyphenethylamine)&lt;br /&gt;
* [[2C-I]] (Dimethoxyiodophenethylamine)&lt;br /&gt;
* [[2C-N]] (Dimethoxynitrophenethylamine)&lt;br /&gt;
* [[2C-P]] (Dimethoxypropylphenethylamine)&lt;br /&gt;
* [[2C-iP]] (Dimethoxyisopropylphenethylamine)&lt;br /&gt;
* [[2C-T]] (Dimethoxymethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-2]] (Dimethoxyethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-3]] (Dimethoxymethylallylthiophenethylamine)&lt;br /&gt;
* [[2C-T-4]] (Dimethoxyisopropylthiophenethylamine)&lt;br /&gt;
* [[2C-T-5]] (Dimethoxycyclohexylthiophenethylamine)&lt;br /&gt;
* [[2C-T-6]] (Dimethoxyphenylthiophenethylamine)&lt;br /&gt;
* [[2C-T-7]] (Dimethoxypropylthiophenethylamine)&lt;br /&gt;
* [[2C-T-10]] (Dimethoxypyridylthiophenethylamine)&lt;br /&gt;
* [[2C-T-11]] (Dimethoxypara-bromophenylthiophenethylamine)&lt;br /&gt;
* [[2C-T-12]] (Dimethoxymorpholinothiophenethylamine)&lt;br /&gt;
* [[2C-T-13]] (Dimethoxy(beta-methoxy)ethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-14]] (Dimethoxymethylthioethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-15]] (Dimethoxycyclopropylthiophenethylamine)&lt;br /&gt;
* [[2C-T-16]] (Dimethoxyallylthiophenethylamine)&lt;br /&gt;
* [[2C-T-17]] (Dimethoxysec-butylthiophenethylamine)&lt;br /&gt;
* [[2C-T-19]] (Dimethoxybutylthiophenethylamine)&lt;br /&gt;
* [[2C-T-21]] (Dimethoxyfluoroethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-21.5]] (Dimethoxydifluuoroethylthiophenethylamine)&lt;br /&gt;
* [[2C-T-22]] (Dimethoxytrifluoroethylthiophenethylamine)&lt;br /&gt;
* [[2C-TFM]] (Dimethoxytrifluorophenethylamine)&lt;br /&gt;
* [[2C-YN]] (Dimethoxyethynylphenethylamine)&lt;br /&gt;
&lt;br /&gt;
== Images ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;gallery mode=&amp;quot;packed-hover&amp;quot; heights=&amp;quot;200px&amp;quot;&amp;gt;&lt;br /&gt;
Image:2cb.jpg|&#039;&#039;2C-B&#039;&#039;&lt;br /&gt;
Image:2cc.jpg|&#039;&#039;2C-C&#039;&#039;&lt;br /&gt;
Image:2ce.jpg|&#039;&#039;2C-E&#039;&#039;&lt;br /&gt;
&amp;lt;/gallery&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Psychedelic]]&lt;br /&gt;
[[Category:Drugs]]&lt;/div&gt;</summary>
		<author><name>MDMQualone</name></author>
	</entry>
</feed>