Anodyne

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2C-B
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)
Hydrobromide
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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260.13 g/mol [1]
2.1 [1]
Structural Identifiers
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C10H14BrNO2 [1]
2-(4-bromo-2,5-dimethoxyphenyl)ethanamine [1]
COC1=CC(=C(C=C1CCN)OC)Br [1]
InChI=1S/C10H14BrNO2/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12/h5-6H,3-4,12H2,1-2H3 [1]
InChIKeyYMHOBZXQZVXHBM-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-bromophenethylamine

2,5-Dimethoxy-4-bromophenethylamine (also known as 4-Bromo-2,5-dimethoxyphenethylamine, 2-(4-Bromo-2,5-dimethoxyphenyl)ethylamine, 2-(4-Bromo-2,5-dimethoxyphenyl)ethanamine, 4-Bromo-2,5-dimethoxyphenylethylamine, Benzeneethanamine, 4-bromo-2,5-dimethoxy-, 2C-B, Nexus, BDMPEA, 2-CB or 4-Bromo-2,5-dimethoxybenzeneethanamine) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

Salts []

2,5-Dimethoxy-4-bromophenethylamine is typically found in the form of its hydrochloride and hydrobromide salts.

 []

2,5-Dimethoxy-4-bromophenethylamine is a achiral mixture

Anodyne Usernotes
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0xea / 2,5-Dimethoxy-4-bromophenethylamine via Oral and Intravenous; ; ; ; ; ; Minor ; ; Intense 2.5 hour experience when intravenously injected;

See also []

  • 4-Substituted 2,5-dimethoxyphenethylamines (2C-x)
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 98527, 2,5-Dimethoxy-4-bromophenethylamine. Accessed August 6, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/98527

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-bromophenethylamine. UNII: V77772N32H. Global Substance Registration System. Accessed August 6, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/V77772N32H