Anodyne

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2,5-DMA
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
195.26 g/mol [1]
1.7 [1]
Structural Identifiers
[]
C11H17NO2 [1]
1-(2,5-dimethoxyphenyl)propan-2-amine [1]
CC(CC1=C(C=CC(=C1)OC)OC)N [1]
InChI=1S/C11H17NO2/c1-8(12)6-9-7-10(13-2)4-5-11(9)14-3/h4-5,7-8H,6,12H2,1-3H3 [1]
InChIKeyLATVFYDIBMDBSY-UHFFFAOYSA-N [1]

2,5-Dimethoxyamphetamine

2,5-Dimethoxyamphetamine (also known as 1-(2,5-Dimethoxyphenyl)-2-aminopropane, Benzeneethanamine, 2,5-dimethoxy-α-methyl-, 1-(2,5-Dimethoxyphenyl)isopropylamine, 2,5-Dimethoxy-α-methylphenethylamine, 2,5-DMA, 2,5-Dimethoxy-α-methylbenzeneethanamine, 2-(2-Aminopropyl)hydroquinone dimethyl ether, 2,5-dimethoxy-amphetamine, U-10,648 or J46.485F) is a sympathomimetic substance of the 2,5-dimethoxyamphetamine class.

Chemistry

Salts []

2,5-Dimethoxyamphetamine is typically found in the form of its hydrochloride salt.

 []

2,5-Dimethoxyamphetamine is a racemic mixture of the

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

Subjective effects []

See also []

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

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 62787, 2,5-Dimethoxyamphetamine. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/62787

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxyamphetamine. UNII: OIM1536TQQ. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/OIM1536TQQ