Anodyne

Benzphetamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
239.35 g/mol [1]
4.1 [1]
Structural Identifiers
[]
C17H21[1]
N-benzyl-N-methyl-1-phenylpropan-2-amine [1]
CC(CC1=CC=CC=C1)N(C)CC2=CC=CC=C2 [1]
InChI=1S/C17H21N/c1-15(13-16-9-5-3-6-10-16)18(2)14-17-11-7-4-8-12-17/h3-12,15H,13-14H2,1-2H3 [1]
InChIKeyYXKTVDFXDRQTKV-UHFFFAOYSA-N [1]

Benzphetamine

Benzphetamine (also known as Benzphetamine, benzphetamine, Benzfetamine, Benzphetaminw, N,α-Dimethyl-N-(phenylmethyl)benzeneethanamine, Benzeneethanamine, N,α-dimethyl-N-(phenylmethyl)-, N-Benzyl-N-methyl-1-phenyl-2-propanamine #, C07538, D07514 or N-benzyl-n,α-dimethylphenethylamine) is a prodrug and stimulant substance of the amphetamine class.

Chemistry

Salts []

Benzphetamine is typically found in the form of its hydrochloride salt.

 []

Benzphetamine is a racemic mixture of the

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

Pharmacology

Benzphetamine acts as a for:

Active metabolites
 []
Dextromethamphetamine Generated by the Chemistry Development Kit (http://github.com/cdk)
Dextroamphetamine Generated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 2341, Benzphetamine. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/2341

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Benzphetamine. UNII: QZH832I91B. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/QZH832I91B