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2C-x: Difference between revisions

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>PsychoticCorpse
m Added a description of what phenethylamine is to the chemistry section, which formerly stated only where the substitutions occurred assuming the reader already knows what the structure of phenethylamine.
>Iiiluap
m added 2c_ef
 
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[[File:2C-x.svg|250px|thumbnail|The general structure for a 2C-x compound]]
[[File:2C-x.svg|250px|thumbnail|The general structure for a 2C-x compound]]
'''Substituted dimethoxyphenethylamines''' (also known as '''2C-''x''''') is the general name for the family of psychedelic [[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]]. Some of the most popular members of this group include [[2C-B]], [[2C-E]], and [[2C-I]].  
'''Substituted dimethoxyphenethylamines''' (also known as '''2C-''x''''') is the general name for the family of psychedelic [[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]]. He also coined the term 2C, being an acronym for the 2 carbon atoms between the benzene ring and the amino group. The 2C-''x'' chemicals vary in effect from being totally inactive to fully [[psychedelic]]. Some of the most popular members of this group include [[2C-B]], [[2C-E]], and [[2C-I]].  


==Chemistry==
==Chemistry==
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==List of 2C-x compounds==
==List of 2C-x compounds==
Note: This list does not include [[2C-T-x]], [[25x-NBOH]], [[25x-NBOMe]], [[DOx]].
===Classic 2C-x compounds===
===Classic 2C-x compounds===
{| class="wikitable"
{| class="wikitable"
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! scope="col" style="width: 50px;" |'''R<sub>4</sub>'''
! scope="col" style="width: 50px;" |'''R<sub>4</sub>'''
! scope="col" |'''Structure'''
! scope="col" |'''Structure'''
|-
|[[2C-H]]||H||[[File:2C-H.svg|200px]]
|-
|-
|[[2C-B]]||Br||[[File:2C-B.svg|200px]]
|[[2C-B]]||Br||[[File:2C-B.svg|200px]]
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|[[2C-E]]||CH<sub>2</sub>CH<sub>3</sub>||[[File:2C-E.svg|200px]]
|[[2C-E]]||CH<sub>2</sub>CH<sub>3</sub>||[[File:2C-E.svg|200px]]
|-
|-
|[[2C-H]]||H||[[File:2C-H.svg|200px]]
|[[2C-EF]]||CH<sub>2</sub>CFH<sub>2</sub>||[[File:2C-EF.svg|200px]]
|-
|-
|[[2C-I]]||I||[[File:2C-I.svg|200px]]
|[[2C-I]]||I||[[File:2C-I.svg|200px]]
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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]]
|-
|2C-T<!-- general structure for a 2C-T-x compound -->||SCH<sub>3</sub>||[[File:2C-T.svg|200px]]
|-
|[[2C-T-2]]||SCH<sub>2</sub>CH<sub>3</sub>||[[File:2C-T-2.svg|200px]]
|-
|2C-T-4||SCH(CH<sub>3</sub>)<sub>2</sub>||[[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.svg|200px]]
|-
|[[2C-T-21]]||SCH<sub>2</sub>CH<sub>2</sub>F||[[File:2C-T-21.svg|200px]]
|-
|-
|}
|}
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! scope="col" style="width: 50px;" |'''R<sub>β</sub>'''
! scope="col" style="width: 50px;" |'''R<sub>β</sub>'''
! scope="col" |'''Structure'''
! scope="col" |'''Structure'''
|-
|[[BOD]]||H||CH<sub>3</sub>||H||OCH<sub>3</sub>||[[File:BOD.svg|200px]]
|-
|-
|[[βk-2C-B]]||H||Br||H||=O||[[File:Βk-2C-B.svg|200px]]
|[[βk-2C-B]]||H||Br||H||=O||[[File:Βk-2C-B.svg|200px]]
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*'''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.<ref>http://www.justice.gov/ola/views-letters/112/093011-ltr-re-hr1254-synthetic-drug-control-act-2011.pdf</ref>
*'''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.<ref>http://www.justice.gov/ola/views-letters/112/093011-ltr-re-hr1254-synthetic-drug-control-act-2011.pdf</ref>
*'''Australia:''' Australia has a blanket ban over all substituted phenethylamines including the entire 2C-X family.<ref>New Psychoactive Substances (National Drug and Alcohol Research Centre 2014) | https://comorbidity.edu.au/sites/default/files/cre/page/New%20Psychoactive%20Substances.pdf</ref>
*'''Australia:''' Australia has a blanket ban over all substituted phenethylamines including the entire 2C-X family.<ref>New Psychoactive Substances (National Drug and Alcohol Research Centre 2014) | https://comorbidity.edu.au/sites/default/files/cre/page/New%20Psychoactive%20Substances.pdf</ref>
*'''Switzerland:''' Most 2C-x drugs are illegal to possess, produce and sell.<ref>http://web.archive.org/web/20170329020935/https://www.admin.ch/opc/de/classified-compilation/20101220/index.html</ref>
*'''Switzerland:''' Most 2C-x drugs are illegal to possess, produce and sell.<ref>{{Citation | year=2017 | title=SR 812.121.11 Verordnung des EDI vom 30. Mai 2011 über die Verzeichnisse der Betäubungsmittel, psychotropen Stoffe, Vorläuferstoffe und Hilfschemikalien (Betäubungsmittelverzeichnisverordnung, BetmVV-EDI) | url=http://web.archive.org/web/20170329020935/https://www.admin.ch/opc/de/classified-compilation/20101220/index.html}}</ref>
*'''Canada:''' All 2C-x phenethylamines are schedule III in Canada. <ref>http://laws-lois.justice.gc.ca/eng/acts/c-38.8/page-14.html#docCont</ref>
*'''Canada:''' All 2C-x phenethylamines are schedule III in Canada. <ref>{{Citation | title=Consolidated federal laws of Canada, Controlled Drugs and Substances Act | url=https://laws-lois.justice.gc.ca/eng/acts/c-38.8/page-14.html}}</ref>
*'''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.<ref>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</ref>
*'''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.<ref>{{Citation | title=The Misuse of Drugs Act 1971 (Modification) Order 1977 | url=https://www.legislation.gov.uk/uksi/1977/1243/made}}</ref>
*'''Germany:''' Most 2C-x compounds are controlled under BtMG Anlage I, making them illegal to manufacture, import, possess, sell, or transfer them without a license.<ref>https://www.gesetze-im-internet.de/btmg_1981/anlage_i.html</ref> Other 2C-x compounds are controlled by the NpSG, as they are derivatives of 2-Phenethylamine. Production, and sale is illegal. Possession and import, although illegal, is not penalized if intended for self-consumption.<ref>https://www.gesetze-im-internet.de/npsg/anlage.html</ref>
*'''Germany:''' Most 2C-x compounds are controlled under BtMG Anlage I, making them illegal to manufacture, import, possess, sell, or transfer them without a license.<ref>{{Citation | title=Anlage I BtMG - Einzelnorm | url=https://www.gesetze-im-internet.de/btmg_1981/anlage_i.html}}</ref> Other 2C-x compounds are controlled by the NpSG, as they are derivatives of 2-Phenethylamine. Production, and sale is illegal. Possession and import, although illegal, is not penalized if intended for self-consumption.<ref>{{Citation | title=Anlage NpSG - Einzelnorm | url=https://www.gesetze-im-internet.de/npsg/anlage.html}}</ref>


==See also==
==See also==
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[[Category:Chemical class]]
[[Category:Chemical class]]
[[Category:Hallucinogen]]
[[Category:2C-x| ]]
[[Category:Psychedelic]]
[[Category:Phenethylamine]]
[[Category:2C-x|*]]
Retrieved from "http://psy.st/wiki/2C-x"