
2C-T-x: Difference between revisions
>David Hedlund wording |
>Snowcyclone m Changed from R5 to RS for substitution. R5 would be a ring-substitute, RS is a substitution on the sulphur-atom of the molecule. |
||
(19 intermediate revisions by 9 users not shown) | |||
Line 1: | Line 1: | ||
{{headerpanel| | {{headerpanel|{{stub}}}} | ||
[[File:2C-T. | [[File:Substituted 2C-T-x.svg|250px|thumbnail|The general structure for a 2C-T-x compound]] | ||
'''2C-T-x''' is a | '''2C-T-x''' is a subset of the [[2C-x]] series. [[Alexander Shulgin]] has discovered over 25 2C-T-x compounds and more are currently being made by individual scientists such as Daniel Trachsel<ref>{{cite journal | vauthors=((Trachsel, D.)) | journal=Helvetica Chimica Acta | title=Synthese von neuen (Phenylalkyl)aminen zur Untersuchung von Struktur–Aktivitätsbeziehungen. Mitteilung 2: 4-Thio-substituierte[2-(2,5-Dimethoxyphenyl)ethyl]amine (=2,5-Dimethoxybenzolethanamine) | volume=86 | issue=7 | pages=2610–2619 | date= July 2003 | url=https://onlinelibrary.wiley.com/doi/10.1002/hlca.200390210 | issn=0018-019X | doi=10.1002/hlca.200390210}}</ref>.<ref>http://countyourculture.com/2011/01/15/shulgins-sulfur-symphony-part-i/</ref> | ||
The 2C-T-x series contains a very broad spectrum of compounds from barely active to fully psychedelic phenethylamines. It is theorized that all of the members are [[MAOI]]s, as it is seen within the [[ALEPH]] series{{citation needed}}. Many have not been synthesized yet. | |||
[[2C-T-2]] and [[2C-T-7]] are part of the so-called "magical half-dozen" which refers to Shulgin's self-rated most important phenethylamine compounds, all of which -- with the exception of [[mescaline]] -- he designed, synthesized and tested on himself. They can be found within the first book of PiHKAL, and are as follows: [[Mescaline]], [[DOM]], [[2C-B]], [[2C-E]], [[2C-T-2]] and [[2C-T-7]].<ref>https://erowid.org/library/books_online/pihkal/pihkal.shtml | Among the members, the most popular ones are [[2C-T-2]] and [[2C-T-7]], which are part of the so-called "magical half-dozen" which refers to Shulgin's self-rated most important phenethylamine compounds, all of which -- with the exception of [[mescaline]] -- he designed, synthesized and tested on himself. They can be found within the first book of PiHKAL, and are as follows: [[Mescaline]], [[DOM]], [[2C-B]], [[2C-E]], [[2C-T-2]] and [[2C-T-7]].<ref>{{Citation | title=Erowid Online Books : “PIHKAL” - The Chemical Story | url=https://erowid.org/library/books_online/pihkal/pihkal.shtml}}</ref> | ||
==List of 2C-x compunds== | ==List of 2C-T-x compunds== | ||
{| | |||
|- style="vertical-align:top;" | |||
|<!--Begin Table 1 --> | |||
{| class="wikitable" | {| class="wikitable" | ||
|- | |- | ||
! scope="col" | '''Compound''' | ! scope="col" |'''Compound''' | ||
! scope="col" style="width: 50px;" | '''R<sub> | ! scope="col" style="width: 50px;" |'''R<sub>S</sub>''' | ||
! scope="col" | '''Structure''' | ! scope="col" |'''Structure''' | ||
|- | |- | ||
| 2C-T | |[[2C-T]]||CH<sub>3</sub>||[[File:2C-T.svg|140px]] | ||
|- | |- | ||
| [[2C-T-2]] || | |[[2C-T-2]]||CH<sub>2</sub>CH<sub>3</sub>||[[File:2C-T-2.svg|140px]] | ||
|- | |- | ||
| 2C-T- | |2C-T-3 (2C-T-20)||CH<sub>2</sub>C(CH<sub>2</sub>)CH<sub>3</sub>||[[File:2C-T-3.svg|140px]] | ||
|- | |- | ||
| | |2C-T-4||CH(CH<sub>3</sub>)<sub>2</sub>||[[File:2C-T-4.svg|140px]] | ||
|- | |- | ||
| [[2C-T- | |2C-T-5||C<sub>6</sub>H<sub>11</sub>||[[File:2C-T-5.svg|140px]] | ||
|- | |||
|2C-T-6||C<sub>6</sub>H<sub>5</sub>||[[File:2C-T-6.svg|140px]] | |||
|- | |||
|[[2C-T-7]]||CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>||[[File:2C-T-7.svg|140px]] | |||
|- | |||
|2C-T-8||CH<sub>2</sub>C<sub>3</sub>H<sub>5</sub>||[[File:2C-T-8.svg|140px]] | |||
|- | |||
|2C-T-9||C(CH<sub>3</sub>)<sub>3</sub>||[[File:2C-T-9.svg|140px]] | |||
|- | |||
|2C-T-10||C<sub>5</sub>H<sub>4</sub>N||[[File:2C-T-10.svg|140px]] | |||
|- | |||
|2C-T-11||C<sub>6</sub>H<sub>4</sub>Br||[[File:2C-T-11.svg|140px]] | |||
|- | |||
|2C-T-12||NC<sub>4</sub>H<sub>8</sub>O||[[File:2C-T-12.svg|140px]] | |||
|- | |||
|2C-T-13||CH<sub>2</sub>CH<sub>2</sub>OCH<sub>3</sub>||[[File:2C-T-13.svg|140px]] | |||
|- | |||
|2C-T-14||CH<sub>2</sub>CH<sub>2</sub>SCH<sub>3</sub>||[[File:2C-T-14.svg|140px]] | |||
|- | |||
|2C-T-15||C<sub>3</sub>H<sub>5</sub>||[[File:2C-T-15.svg|140px]] | |||
|- | |||
|2C-T-16||CH<sub>2</sub>CH=CH<sub>2</sub>||[[File:2C-T-16.svg|140px]] | |||
|- | |||
|2C-T-17||CH(CH<sub>3</sub>)CH<sub>2</sub>CH<sub>3</sub>||[[File:2C-T-17.svg|140px]] | |||
|- | |||
|2C-T-18||C<sub>4</sub>H<sub>7</sub>||[[File:2C-T-18.svg|140px]] | |||
|- | |- | ||
|} | |||
|<!--Begin Table 2 --> | |||
{| class="wikitable" | |||
|- | |||
! scope="col" |'''Compound''' | |||
! scope="col" style="width: 50px;" |'''R<sub>S</sub>''' | |||
! scope="col" |'''Structure''' | |||
|- | |||
|2C-T-19||CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>||[[File:2C-T-19.svg|140px]] | |||
|- | |||
|[[2C-T-21]]||CH<sub>2</sub>CH<sub>2</sub>F||[[File:2C-T-21.svg|140px]] | |||
|- | |||
|2C-T-21.5||CH<sub>2</sub>CHF<sub>2</sub>||[[File:2C-T-21.5.svg|140px]] | |||
|- | |||
|2C-T-22||CH<sub>2</sub>CF<sub>3</sub>||[[File:2C-T-22.svg|140px]] | |||
|- | |||
|2C-T-23||C<sub>5</sub>H<sub>9</sub>||[[File:2C-T-23.svg|140px]] | |||
|- | |||
|2C-T-24||N(CH<sub>2</sub>CH<sub>3</sub>)<sub>2</sub>||[[File:2C-T-24.svg|140px]] | |||
|- | |||
|2C-T-25||CH<sub>2</sub>CH(CH<sub>3</sub>)<sub>2</sub>||[[File:2C-T-25.svg|140px]] | |||
|- | |||
|2C-T-26||CH(CH<sub>2</sub>F)<sub>2</sub>||[[File:2C-T-26.svg|140px]] | |||
|- | |||
|2C-T-27||CH<sub>2</sub>C<sub>6</sub>H<sub>5</sub>||[[File:2C-T-27.svg|140px]] | |||
|- | |||
|2C-T-28||CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>F||[[File:2C-T-28.svg|140px]] | |||
|- | |||
|2C-T-29||CH<sub>2</sub>C≡CH||[[File:2C-T-29.svg|140px]] | |||
|- | |||
|2C-T-30||CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>F||[[File:2C-T-30.svg|140px]] | |||
|- | |||
|2C-T-31||CH<sub>2</sub>C<sub>6</sub>H<sub>4</sub>CF<sub>3</sub>||[[File:2C-T-31.svg|140px]] | |||
|- | |||
|2C-T-32||CH<sub>2</sub>C<sub>6</sub>F<sub>5</sub>||[[File:2C-T-32.svg|140px]] | |||
|- | |||
|2C-T-33||CH<sub>2</sub>C<sub>6</sub>H<sub>4</sub>OCH<sub>3</sub>||[[File:2C-T-33.svg|140px]] | |||
|- | |||
|2C-T-34||CH<sub>2</sub>F||[[File:2C-T-34.svg|140px]] | |||
|- | |||
|2C-T-35||CHF<sub>2</sub>||[[File:2C-T-35.svg|140px]] | |||
|- | |||
|2C-T-36||CF<sub>3</sub>||[[File:2C-T-36.svg|140px]] | |||
|- | |||
|} | |||
|} | |} | ||
== | ==Toxicity and harm potential== | ||
The 2C-x chemicals, as with many other serotonergic psychedelics, should not be taken in combination with SSRIs (selective [[serotonin]] [[reuptake Inhibitor]]) or [[tricyclic antidepressants]] in general to avoid [[ | The 2C-T-x chemicals, as with many other serotonergic psychedelics, should not be taken in combination with SSRIs (selective [[serotonin]] [[reuptake Inhibitor]]) or [[tricyclic antidepressants]] in general to avoid [[serotonin syndrome]], a potentially life-threatening condition in which an abundance of serotonin is built up the body, causing many physical and cognitive health problems. | ||
==See also== | ==See also== | ||
*[[Responsible use]] | *[[Responsible use]] | ||
*[[DOx]] | *[[DOx]] | ||
Line 39: | Line 114: | ||
==External links== | ==External links== | ||
*[https://en.wikipedia.org/wiki/2C_(psychedelics) 2C (Wikipedia)] | *[https://en.wikipedia.org/wiki/2C_(psychedelics) 2C (Wikipedia)] | ||
==References== | ==References== | ||
<references /> | <references /> | ||
[[Category:Chemical class]] | |||
[[Category:2C-T-x|*]] |
Latest revision as of 10:16, 3 March 2024
This article is a stub. As such, it may contain incomplete or wrong information. You can help by expanding it. |
2C-T-x is a subset of the 2C-x series. Alexander Shulgin has discovered over 25 2C-T-x compounds and more are currently being made by individual scientists such as Daniel Trachsel[1].[2]
The 2C-T-x series contains a very broad spectrum of compounds from barely active to fully psychedelic phenethylamines. It is theorized that all of the members are MAOIs, as it is seen within the ALEPH series[citation needed]. Many have not been synthesized yet.
Among the members, the most popular ones are 2C-T-2 and 2C-T-7, which are part of the so-called "magical half-dozen" which refers to Shulgin's self-rated most important phenethylamine compounds, all of which -- with the exception of mescaline -- he designed, synthesized and tested on himself. They can be found within the first book of PiHKAL, and are as follows: Mescaline, DOM, 2C-B, 2C-E, 2C-T-2 and 2C-T-7.[3]
List of 2C-T-x compunds
|
|
Toxicity and harm potential
The 2C-T-x chemicals, as with many other serotonergic psychedelics, should not be taken in combination with SSRIs (selective serotonin reuptake Inhibitor) or tricyclic antidepressants in general to avoid serotonin syndrome, a potentially life-threatening condition in which an abundance of serotonin is built up the body, causing many physical and cognitive health problems.
See also
External links
References
- ↑ Trachsel, D. (July 2003). "Synthese von neuen (Phenylalkyl)aminen zur Untersuchung von Struktur–Aktivitätsbeziehungen. Mitteilung 2: 4-Thio-substituierte[2-(2,5-Dimethoxyphenyl)ethyl]amine (=2,5-Dimethoxybenzolethanamine)". Helvetica Chimica Acta. 86 (7): 2610–2619. doi:10.1002/hlca.200390210. ISSN 0018-019X.
- ↑ http://countyourculture.com/2011/01/15/shulgins-sulfur-symphony-part-i/
- ↑ Erowid Online Books : “PIHKAL” - The Chemical Story