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2C-YN

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
2C-YN
Legal status
Legal status
Identifiers
  • 2-(4-ethynyl-2,5-dimethoxyphenyl)ethanamine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H15NO2
Molar mass205.257 g·mol−1
3D model (JSmol)
  • COc1cc(CCN)c(OC)cc1C#C
  • InChI=1S/C12H15NO2/c1-4-9-7-12(15-3)10(5-6-13)8-11(9)14-2/h1,7-8H,5-6,13H2,2-3H3 checkY
  • Key:MLJHHYIJBZVUEA-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

2C-YN is ananalog ofphenethylamine that can be synthesized from2C-I.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of 2C-YN, althoughDaniel Trachsel lists it as having a dosage of around 50mg and a duration of around 2 hours, with relatively mild psychedelic effects.[2]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Society and culture

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Legal status

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Canada

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As of October 31st, 2016; 2C-YN is a controlled substance (Schedule III) in Canada.[3]

United States

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2C-YN is not an explicitlycontrolled substance in theUnited States.[4] However, it could be considered a controlled substance under theFederal Analogue Act if intended for human consumption.

See also

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References

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  1. ^Trachsel D (August 2003). "Synthesis of Novel (Phenylalkyl) amines for the Investigation of Structure–Activity Relationships, Part 3: 4-Ethynyl-2,5-dimethoxyphenethylamine (= 4-Ethynyl-2, 5-dimethoxybenzeneethanamine; 2C-YN)".Helvetica Chimica Acta.86 (8):2754–2759.doi:10.1002/hlca.200390224.
  2. ^Trachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine Von der Struktur zur Funktion. Nachtschatten Verlag AG. p. 768.ISBN 978-3-03788-700-4.
  3. ^"Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)".Canada Gazette. 4 May 2016.
  4. ^Orange Book: List of Controlled Substances and Regulated Chemicals (January 2026)(PDF),United States: U.S.Department of Justice:Drug Enforcement Administration (DEA): Diversion Control Division, January 2026
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