Anodyne

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DOAM
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
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Physical properties
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265.39 g/mol [1]
4.4 [1]
Structural Identifiers
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C16H27NO2 [1]
1-(2,5-dimethoxy-4-pentylphenyl)propan-2-amine [1]
CCCCCC1=CC(=C(C=C1OC)CC(C)N)OC [1]
InChI=1S/C16H27NO2/c1-5-6-7-8-13-10-16(19-4)14(9-12(2)17)11-15(13)18-3/h10-12H,5-9,17H2,1-4H3 [1]
InChIKeyVLJORLCVOAUUKM-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-amylamphetamine

2,5-Dimethoxy-4-amylamphetamine (also known as 2,5-Dimethoxy-4-pentylamphetamine, DOAM, α-Methyl-4-amyl-2,5-dimethoxyphenethylamine, 1-(2,5-Dimethoxy-4-pentylphenyl)propan-2-amine, US20240166618, Compound 23, US20240166618, Compound 29, CS-0083652, Q4596788, 2,5-Dimethoxy-I+/--methyl-4-pentylbenzeneethanamine or Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-pentyl-) is a substance of the 2,5-dimethoxyamphetamine class.

Chemistry

Salts []

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

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

Stereoisomers
(S)-2,5-Dimethoxy-4-amylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(R)-2,5-Dimethoxy-4-amylamphetamineGenerated 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 12262512, 2,5-Dimethoxy-4-amylamphetamine. Accessed July 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/12262512

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-amylamphetamine. UNII: N80EWL36CB. Global Substance Registration System. Accessed July 14, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/N80EWL36CB