Anodyne

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DOBU
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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251.36 g/mol [1]
3.9 [1]
Structural Identifiers
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C15H25NO2 [1]
1-(4-butyl-2,5-dimethoxyphenyl)propan-2-amine [1]
CCCCC1=CC(=C(C=C1OC)CC(C)N)OC [1]
InChI=1S/C15H25NO2/c1-5-6-7-12-9-15(18-4)13(8-11(2)16)10-14(12)17-3/h9-11H,5-8,16H2,1-4H3 [1]
InChIKeyNGVDYAULSQKEGW-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-butylamphetamine

2,5-Dimethoxy-4-butylamphetamine (also known as Benzeneethanamine, 4-butyl-2,5-dimethoxy-α-methyl-, 4-Butyl-2,5-dimethoxy-α-methylbenzeneethanamine, 1-(2,5-Dimethoxy-4-n-butylphenyl)-2-aminopropane, α-Methyl-4-butyl-2,5-dimethoxyphenethylamine, DOBU, 1-(4-Butyl-2,5-dimethoxyphenyl)propan-2-amine, 1-(2,5-Dimethoxy-4-N-butylphenyl)-2-aminopropane, NCA77989, Pdsp1_001368 or Pdsp2_001352) is a psychedelic substance of the 2,5-dimethoxyamphetamine class.

Chemistry

Salts []

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

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

Stereoisomers
(S)-2,5-Dimethoxy-4-butylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(R)-2,5-Dimethoxy-4-butylamphetamineGenerated 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 10060720, 2,5-Dimethoxy-4-butylamphetamine. Accessed July 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/10060720

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-butylamphetamine. UNII: 6ARH6DPN4N. Global Substance Registration System. Accessed July 14, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/6ARH6DPN4N