Anodyne

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DOPR
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
[]
Conformer structure via JSmol
Physical properties
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237.34 g/mol [1]
3.4 [1]
Structural Identifiers
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C14H23NO2 [1]
1-(2,5-dimethoxy-4-propylphenyl)propan-2-amine [1]
CCCC1=CC(=C(C=C1OC)CC(C)N)OC [1]
InChI=1S/C14H23NO2/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 [1]
InChIKeyUEEAUFJYLUJWQJ-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-propylamphetamine

2,5-Dimethoxy-4-propylamphetamine (also known as J273.474E, Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-propyl-, 1-(2,5-Dimethoxy-4-n-propylphenyl)-2-aminopropane, DOPR, 1-(2,5-Dimethoxy-4-N-propylphenyl)-2-aminopropane, Dopr, Pdsp1_000459, Pdsp2_000457, 1-(2,5-Dimethoxy-4-propylphenyl)-2-propanamine # or Q4596792) is a psychedelic substance of the 2,5-dimethoxyamphetamine class.

Chemistry

Salts []

2,5-Dimethoxy-4-propylamphetamine is typically found in the form of its hydrochloride salt.

 []

2,5-Dimethoxy-4-propylamphetamine is a racemic mixture of the

Stereoisomers
(S)-2,5-Dimethoxy-4-propylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(R)-2,5-Dimethoxy-4-propylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • 4-Substituted 2,5-dimethoxyamphetamines (DOx)
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 542051, 2,5-Dimethoxy-4-propylamphetamine. Accessed July 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/542051

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-propylamphetamine. UNII: L3P287BI9W. Global Substance Registration System. Accessed July 14, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/L3P287BI9W