Anodyne

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βOH-2C-B
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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β-Hydroxy-4-bromo-2,5-dimethoxyphenylamine hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic
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Physical properties
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Molecular mass276.13 g/mol [1]
Predicted LogP1 [1]
Structural Identifiers
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Molecular formulaC10H14BrNO3 [1]
IUPAC name2-amino-1-(4-bromo-2,5-dimethoxyphenyl)ethanol [1]
SMILESCOC1=CC(=C(C=C1C(CN)O)OC)Br [1]
InChIInChI=1S/C10H14BrNO3/c1-14-9-4-7(11)10(15-2)3-6(9)8(13)5-12/h3-4,8,13H,5,12H2,1-2H3 [1]
InChIKeyPCSKDXWCLQXURQ-UHFFFAOYSA-N [1]
Dosing

β-Hydroxy-4-bromo-2,5-dimethoxyphenylamine

β-Hydroxy-4-bromo-2,5-dimethoxyphenylamine (also known as β-Hydroxy-2c-b, BOH-2C-b, 2-Amino-1-(4-bromo-2,5-dimethoxyphenyl)ethan-1-ol, α-(Aminomethyl)-4-bromo-2,5-dimethoxybenzenemethanol, Benzenemethanol, α-(aminomethyl)-4-bromo-2,5-dimethoxy-, Bohb, FA182978, 2-Amino-1-(4-bromo-2,5-dimethoxy-phenyl)-ethanol or ?-(Aminomethyl)-4-bromo-2,5-dimethoxybenzenemethanol) is a psychedelic substance of the phenylethanolamine class.

Chemistry

Salts []

β-Hydroxy-4-bromo-2,5-dimethoxyphenylamine is typically found in the form of its hydrochloride salt.

Stereochemistry []

β-Hydroxy-4-bromo-2,5-dimethoxyphenylamine is a racemic mixture of the optical stereoisomers

See also []

  • Substituted phenylethanolamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 11370394, β-Hydroxy-4-bromo-2,5-dimethoxyphenylamine. Accessed July 12, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/11370394

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. β-Hydroxy-4-bromo-2,5-dimethoxyphenylamine. UNII: C4PW6RF2KZ. Global Substance Registration System. Accessed July 12, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/C4PW6RF2KZ