3C-P

Psychedelic drug From Wikipedia, the free encyclopedia

3C-P, also known as 4-propoxy-3,5-dimethoxyamphetamine or as α-methylproscaline (3C-proscaline), is a psychedelic drug of the phenethylamine, amphetamine, and 3C families related to 3,4,5-trimethoxyamphetamine (TMA).[2][4] It is the amphetamine (3C) analogue of proscaline.[2][4]

Other names4-Propoxy-3,5-dimethoxyamphetamine; 3,5-Dimethoxy-4-propoxyamphetamine; α-Methylproscaline; 3C-Proscaline
Legal status
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class A
Quick facts Clinical data, Other names ...
3C-P
Clinical data
Other names4-Propoxy-3,5-dimethoxyamphetamine; 3,5-Dimethoxy-4-propoxyamphetamine; α-Methylproscaline; 3C-Proscaline
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic; Hallucinogen
Legal status
Legal status
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class A
Pharmacokinetic data
Duration of actionUnknown[2][3]
Identifiers
  • 1-(3,5-dimethoxy-4-propoxyphenyl)propan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H23NO3
Molar mass253.342 g·mol−1
3D model (JSmol)
  • CC(N)Cc1cc(OC)c(OCCC)c(c1)OC
  • InChI=1S/C14H23NO3/c1-5-6-18-14-12(16-3)8-11(7-10(2)15)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3 checkY
  • Key:KKMCHCCXGKYEKJ-UHFFFAOYSA-N checkY
  (verify)
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Use and effects

3C-P has been reported to have a dose range of 20 to 40 mg orally, with a typical dose estimate of 30 mg, based on informal anecdotal reports.[1] Although 3C-P produces hallucinogenic effects, very little is known about its effects.[5]

Interactions

Pharmacology

Pharmacodynamics

3C-P acts as a serotonin 5-HT2 receptor agonist, including of the serotonin 5-HT2A receptor.[4][6] It produces the head-twitch response, a behavioral proxy of psychedelic effects, in rodents.[5][1][6]

Chemistry

Synthesis

The chemical synthesis of 3C-P has been described.[7]

Analogues

Analogues of 3C-P include TMA, MEM, 3C-E, 3C-AL, 3C-MAL, and 3C-FP, among others.[2][3][4]

History

3C-P was first described in the scientific literature by Otakar Leminger by 1972.[8][9] Alexander Shulgin mentioned it in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved)[2] and Daniel Trachsel synthesized it in 2002, but neither of them reported its properties or effects in humans.[7][3][10] The drug has been sold online as a designer drug and was first detected in September 2013 in Finland.[11][12]

Society and culture

Canada

3C-P is a controlled substance in Canada under amphetamine blanket-ban language.[13]

United States

3C-P is not an explicitly controlled substance in the United States, although it would most likely be considered a controlled substance under the Federal Analogue Act as an analogue of 2C-P.[14]

See also

References

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