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2C-Se

From Wikipedia, the free encyclopedia

Pharmaceutical compound
2C-Se
Clinical data
Other names4-Methylseleno-2,5-dimethoxyphenethylamine;
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic;Hallucinogen[1]
ATC code
  • None
Pharmacokinetic data
Onset of action45 minutes[1]
Duration of action6–8 hours[1]
Identifiers
  • 2-[2,5-dimethoxy-4-(methylselanyl)phenyl]ethan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H17NO2Se
Molar mass274.233 g·mol−1
3D model (JSmol)
Melting point240 to 241 °C (464 to 466 °F)
  • NCCc1cc(OC)c(cc1OC)[Se]C

2C-Se, also known as4-methylseleno-2,5-dimethoxyphenethylamine, is apsychedelic drug of thephenethylamine and2C families.[1] It was originally named byAlexander Shulgin as described in his 1991 bookPiHKAL (Phenethylamines I Have Known and Loved).[1] Shulgin listed its dose as perhaps 100 mgorally and itsduration as 6 to 8 hours.[1] Itsonset was 45 minutes, peak effects occurred after 1.5 hours, and doses of 50 to 70 mg orally produced threshold effects.[1] Shulgin considered 2C-Se to be around three times thepotency ofmescaline, but was too concerned abouttoxicity to test it extensively, though he considered it noteworthy as the only psychedelic drug to contain aselenium atom.[1][2][3][4][5] 2C-Se was first described in the literature by Shulgin inPiHKAL in 1991.[1] It is acontrolled substance inCanada under phenethylamine blanket-ban language.[6]

See also

[edit]

References

[edit]
  1. ^abcdefghijShulgin A,Shulgin A (September 1991).PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.
  2. ^Shulgin A, Manning T, Daley PF (2011). The Shulgin Index. Volume 1. Psychedelic Phenethylamines and Related Compounds. Transform Press. p. 346.ISBN 978-0-9630096-3-0.
  3. ^Shulgin AT (2003)."Basic Pharmacology and Effects". In Laing RR (ed.).Hallucinogens: A Forensic Drug Handbook. Forensic Drug Handbook Series. Elsevier Science. pp. 67–137.ISBN 978-0-12-433951-4. Retrieved1 February 2025.
  4. ^Trachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: Von der Struktur zur Funktion. Nachtschatten Verlag AG. pp. 801–802.ISBN 978-3-03788-700-4.
  5. ^Jacob P, Shulgin AT (1994). "Structure-activity relationships of the classic hallucinogens and their analogs".NIDA Research Monograph.146:74–91.PMID 8742795. NIH Publication 94-3872.
  6. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.

External links

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