Anodyne

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DMCPA
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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207.27 g/mol [1]
1.5 [1]
Structural Identifiers
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C12H17NO2 [1]
(1S,2R)-2-(2,5-dimethoxy-4-methylphenyl)cyclopropan-1-amine [1]
CC1=CC(=C(C=C1OC)[C@H]2C[C@@H]2N)OC [1]
InChI=1S/C12H17NO2/c1-7-4-12(15-3)9(6-11(7)14-2)8-5-10(8)13/h4,6,8,10H,5,13H2,1-3H3/t8-,10+/m1/s1 [1]
InChIKeyHYVPPECPQRBJEQ-SCZZXKLOSA-N [1]

2,5-Dimethoxy-4-methylphenylcyclopropylamine

2,5-Dimethoxy-4-methylphenylcyclopropylamine (also known as DMCPA, 2-(2,5-Dimethoxy-4-methylphenyl)cyclopropanamine, 2-(2,5-dimethoxy-4-methylphenyl)cyclopropan-1-amine, Dmcpa, (1S,2R)-, 49F6CJ4MFY, 2,5-Dimethoxy-4-methylphenylcyclopropylamine, (1S,2R)-, Cyclopropanamine, 2-(2,5-dimethoxy-4-methylphenyl)-, (1S-trans)- or 69980-36-5) is a psychedelic substance of the 2,5-dimethoxyamphetamine class.

Chemistry

Salts []

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

 []

2,5-Dimethoxy-4-methylphenylcyclopropylamine is a achiral mixture of the optical stereoisomers

See also []

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

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 92950747, 2,5-Dimethoxy-4-methylphenylcyclopropylamine. Accessed July 20, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/92950747

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-methylphenylcyclopropylamine. UNII: U2YC8RFK7B. Global Substance Registration System. Accessed July 20, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/U2YC8RFK7B