Anodyne

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BMMPEA
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Phenpromethamine 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 mass149.23 g/mol [1]
Predicted LogP2.1 [1]
Structural Identifiers
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Molecular formulaC10H15N [1]
IUPAC nameN-methyl-2-phenylpropan-1-amine [1]
SMILESCC(CNC)C1=CC=CC=C1 [1]
InChIInChI=1S/C10H15N/c1-9(8-11-2)10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3 [1]
InChIKeyAUFSOOYCQYDGES-UHFFFAOYSA-N [1]
Dosing

Phenpromethamine

Phenpromethamine (also known as Phenpromethaminum, Vonedrine, Fenprometamina, methyl(2-phenylpropyl)amine, N-Methyl-2-phenylpropylamine, Phenpromethadrinum, 1-Methylamino-2-phenylpropane, Phenpromethadrine, N,β-Dimethylphenethylamine or 1-Methylamino-2-methyl-2-phenylethane) is a stimulant substance of the β-alkylphenethylamine class.

Chemistry

Salts []

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

Stereochemistry []

Phenpromethamine is a racemic mixture of the :

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

Subjective effects
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See also []

  • Substituted β-alkylphenethylamines
  • Substituted amphetamines
  • Substituted phenethylamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 22276, Phenpromethamine. Accessed July 15, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/22276

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Phenpromethamine. UNII: 7D4542I59V. Global Substance Registration System. Accessed July 15, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/7D4542I59V