Anodyne

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Hydroxybupropion
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
255.74 g/mol [1]
2.2 [1]
Structural Identifiers
[]
C13H18ClNO2 [1]
1-(3-chlorophenyl)-2-[(1-hydroxy-2-methylpropan-2-yl)amino]propan-1-one [1]
CC(C(=O)C1=CC(=CC=C1)Cl)NC(C)(C)CO [1]
InChI=1S/C13H18ClNO2/c1-9(15-13(2,3)8-16)12(17)10-5-4-6-11(14)7-10/h4-7,9,15-16H,8H2,1-3H3 [1]
InChIKeyAKOAEVOSDHIVFX-UHFFFAOYSA-N [1]

Hydroxybupropion

Hydroxybupropion (also known as RefChem:423616, 4-Hydroxy bupropion, Hydroxybupropione, 6-Hydroxybupropion, BW-306U, 82793-84-8, 1-Propanone, 1-(3-chlorophenyl)-2-((2-hydroxy-1,1-dimethylethyl)amino)-, Hydroxybupropion?, Bupropion Impurity 7 or orb2893740) is a substance of the amphetamine class.

Chemistry

 []

Hydroxybupropion is a racemic mixture of the

Stereoisomers
(R)-HydroxybupropionGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-HydroxybupropionGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • Substituted amphetamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 446, Hydroxybupropion. Accessed August 31, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/446

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Hydroxybupropion. UNII: V94F513635. Global Substance Registration System. Accessed August 31, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/V94F513635