2,5-Dimethoxy-4-propylamphetamine

Psychedelic drug
Identifiers
  • 1-(2,5-Dimethoxy-4-propylphenyl)propan-2-amine
CAS Number
  • 63779-88-4 ☒N
    53581-55-8 (hydrochloride)
PubChem CID
  • 542051
ChemSpider
  • 472021 checkY
UNII
  • L3P287BI9W
ChEMBL
  • ChEMBL8569 checkY
CompTox Dashboard (EPA)
  • DTXSID40337347 Edit this at Wikidata
Chemical and physical dataFormulaC14H23NO2Molar mass237.343 g·mol−13D model (JSmol)
  • Interactive image
  • O(c1cc(c(OC)cc1CC(N)C)CCC)C
InChI
  • InChI=1S/C15H25NO2/c1-5-6-11-8-14(17-4)12(7-10(2)15)9-13(11)16-3/h8-10H,5-7,15H2,1-4H3 ☒N
  • Key:UEEAUFJYLUJWQJ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

2,5-Dimethoxy-4-propylamphetamine (DOPR) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized by Alexander Shulgin, and was described in his book PiHKAL (Phenethylamines i Have Known And Loved). Shulgin described DOPR as a "heavy duty psychedelic", complete with alterations of the thought process and visual distortion.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of DOPR.

The alternative structural isomer DOIP, with a 4-isopropyl substitution, is also known but is around ten times weaker than DOPR, with an active dose of some 20–30 mg (as compared to 2–5 mg for DOPR).[1]

Structure of DOIP

See also

References

  1. ^ a b Shulgin A, Shulgin A (September 1991). PiHKAL: A Chemical Love Story. United States: Transform Press. p. 978. ISBN 0-9630096-0-5.
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