2C-x: Difference between revisions
>8Brainzap8 2c-x legality |
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| 2C-TFM || CF<sub>3</sub> || [[File:2C-TFM.svg|201px]] | | 2C-TFM || CF<sub>3</sub> || [[File:2C-TFM.svg|201px]] | ||
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| 2C-T<!-- general structure for a 2C-T-x compound --> || SCH<sub>3</sub> || [[File:2C-T.svg|200px]] | |||
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| [[2C-T-2]] || SCH<sub>2</sub>CH<sub>3</sub> || [[File:2C-T-2.svg|200px]] | | [[2C-T-2]] || SCH<sub>2</sub>CH<sub>3</sub> || [[File:2C-T-2.svg|200px]] | ||
Revision as of 12:59, 3 January 2019
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This article is a stub. As such, it may contain incomplete or wrong information. You can help by expanding it. |
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 | SCH3 | 
|
| 2C-T-2 | SCH2CH3 | 
|
| 2C-T-4 | SCH(CH3)2 | 
|
| 2C-T-7 | SCH2CH2CH3 | 
|
| 2C-T-21 | SCH2CH2 | 
|
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 status
- Austria: The 2C-x family is illegal to possess, produce and sell under the SMG (Suchtmittelgesetz Österreich) or the NPSG (Neue-Psychoaktive-Substanzen-Gesetz Österreich).[citation needed]
- 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]
- Canada: All 2C-x phenethylamines are schedule III in Canada. [4]
- United Kingdom - Most of the 2C-x chemical class are Class A drugs in the United Kingdom as a result of the phenethylamine catch-all clause.[5]
See also
External links
Literature
- Dean, B. V., Stellpflug, S. J., Burnett, A. M., & Engebretsen, K. M. (2013). 2C or not 2C: Phenethylamine Designer Drug Review. Journal of Medical Toxicology, 9(2), 172-178. https://doi.org/10.1007/s13181-013-0295-x
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
- ↑ http://laws-lois.justice.gc.ca/eng/acts/c-38.8/page-14.html#docCont
- ↑ United Kingdom. (1977). Misuse of Drugs Act 1971 (S.I. 1977/1243). London: The Stationery Office Limited. Retrieved July 5, 2017, from http://www.legislation.gov.uk/uksi/1977/1243/made