Anodyne

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DOM
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Conformer structure via JSmol
Physical properties
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209.28 g/mol [1]
Melting point60.5 to 60.1 °C [1]
DecompositionWhen heated to decomposition it emits toxic vapors of /Nitrogen oxides/. [1]
2.2 [1]
Structural Identifiers
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C12H19NO2 [1]
1-(2,5-dimethoxy-4-methylphenyl)propan-2-amine [1]
CC1=CC(=C(C=C1OC)CC(C)N)OC [1]
InChI=1S/C12H19NO2/c1-8-5-12(15-4)10(6-9(2)13)7-11(8)14-3/h5,7,9H,6,13H2,1-4H3 [1]
InChIKeyNTJQREUGJKIARY-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-methylamphetamine

2,5-Dimethoxy-4-methylamphetamine (also known as 2,5-Dimethoxy-4-methylamphetamine, STP, DOM, 4-Methyl-2,5-dimethoxyamphetamine, 2,5-Dimethoxymethylamphetamine, 2',5'-Dimethoxy-4'-methylamphetamine, 2,5-Dimethoxy-4-methylphenylisopropylamine, 2,5-Dimethoxy-4,α-dimethylphenethylamin, 1-(2,5-Dimethoxy-4-methylphenyl)-2-aminopropane or 2,5-Dimethoxy-α,4-dimethylphenylethylamine) is a psychedelic substance of the 2,5-dimethoxyamphetamine class.

Chemistry

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

Stereoisomers
(S)-2,5-Dimethoxy-4-methylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(R)-2,5-Dimethoxy-4-methylamphetamineGenerated 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 85875, 2,5-Dimethoxy-4-methylamphetamine. Accessed August 3, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/85875