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2C-x: Difference between revisions
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! scope="col" | '''Structure''' | ! scope="col" | '''Structure''' | ||
|- | |- | ||
| [[2C-B]] || Br || [[File:2C-B. | | [[2C-B]] || Br || [[File:2C-B.svg|200px]] | ||
|- | |- | ||
| [[2C-C]] || Cl || [[File:2C-C. | | [[2C-C]] || Cl || [[File:2C-C.svg|200px]] | ||
|- | |- | ||
| [[2C-D]] || CH<sub>3</sub> || [[File:2C-D. | | [[2C-D]] || CH<sub>3</sub> || [[File:2C-D.svg|200px]] | ||
|- | |- | ||
| [[2C-E]] || CH<sub>2</sub>CH<sub>3</sub> || [[File:2C-E. | | [[2C-E]] || CH<sub>2</sub>CH<sub>3</sub> || [[File:2C-E.svg|200px]] | ||
|- | |- | ||
| [[2C-H]] || H || [[File:2C-H. | | [[2C-H]] || H || [[File:2C-H.svg|200px]] | ||
|- | |- | ||
| [[2C-I]] || I || [[File:2C-I. | | [[2C-I]] || I || [[File:2C-I.svg|200px]] | ||
|- | |- | ||
| 2C-iP || CH<sub></sub>(CH<sub>3</sub>)<sub>2</sub> || [[File:2C-iP | | 2C-iP || CH<sub></sub>(CH<sub>3</sub>)<sub>2</sub> || [[File:2C-iP.svg|200px]] | ||
|- | |- | ||
| [[2C-P]] || CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || [[File:2C-P. | | [[2C-P]] || CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || [[File:2C-P.svg|200px]] | ||
|- | |- | ||
| 2C-TFM || CF<sub>3</sub> || [[File:2C-TFM. | | 2C-TFM || CF<sub>3</sub> || [[File:2C-TFM.svg|201px]] | ||
|- | |- | ||
| [[2C-T-2]] || SCH<sub>2</sub>CH<sub>3</sub> || [[File:2C-T-2. | | [[2C-T-2]] || SCH<sub>2</sub>CH<sub>3</sub> || [[File:2C-T-2.svg|200px]] | ||
|- | |- | ||
| 2C-T-4 || || [[File:2C-T-4. | | 2C-T-4 || || [[File:2C-T-4.svg|200px]] | ||
|- | |- | ||
| [[2C-T-7]] || SCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || [[File:2C-T-7. | | [[2C-T-7]] || SCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || [[File:2C-T-7.svg|200px]] | ||
|- | |- | ||
|} | |} | ||
Revision as of 05:30, 30 August 2017
2C-x is the general name for the family of synthetic phenethylamines originally studied by Alexander Shulgin. Shulgin first synthesized most of the 2C-x chemicals in the 1970s and later published his findings in his book PiHKAL. The 2C-x chemicals vary in effect from being totally inactive to fully psychedelic.
List of 2C-x compunds
| Compound | R4 | Structure |
|---|---|---|
| 2C-B | Br | 
|
| 2C-C | Cl | 
|
| 2C-D | CH3 | 
|
| 2C-E | CH2CH3 | 
|
| 2C-H | H | 
|
| 2C-I | I | 
|
| 2C-iP | CH(CH3)2 | 
|
| 2C-P | CH2CH2CH3 | 
|
| 2C-TFM | CF3 | 
|
| 2C-T-2 | SCH2CH3 | 
|
| 2C-T-4 | 
| |
| 2C-T-7 | SCH2CH2CH3 | 
|
Health effects, potential addiction and tolerance
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 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.
Legal issues
- USA: In the US, most of the 2C-x chemicals are Schedule I under the American Food and Drug Administration Safety and Innovation Act of 2012 and the Federal Analogue Act.[1]
- Australia: Australia has a blanket ban over all substituted phenethylamines including the entire 2C-X family.[2]
- Switzerland: Most 2C-x drugs are illegal to possess, produce and sell.[3]
See also
References
- ↑ http://www.justice.gov/ola/views-letters/112/093011-ltr-re-hr1254-synthetic-drug-control-act-2011.pdf
- ↑ New Psychoactive Substances (National Drug and Alcohol Research Centre 2014) | https://comorbidity.edu.au/sites/default/files/cre/page/New%20Psychoactive%20Substances.pdf
- ↑ http://web.archive.org/web/20170329020935/https://www.admin.ch/opc/de/classified-compilation/20101220/index.html