BMMPEA

Salts []
Hydrochloride

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	149.23 g/mol ^[1]
Predicted LogP	2.1 ^[1]

Structural Identifiers []
Molecular formula	C₁₀H₁₅N ^[1]
IUPAC name	N-methyl-2-phenylpropan-1-amine ^[1]
SMILES	CC(CNC)C1=CC=CC=C1 ^[1]
InChI	InChI=1S/C10H15N/c1-9(8-11-2)10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3 ^[1]
InChIKey	AUFSOOYCQYDGES-UHFFFAOYSA-N ^[1]

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, amphetamine and phenethylamine class.

Chemistry

Salts []

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

Stereochemistry []

Phenpromethamine is a racemic mixture of the enantiomers

Stereoisomers
(S)-Phenpromethamine (R)-Phenpromethamine

Subjective effects []

Physical effects
Abnormal heartbeat Appetite suppression Dehydration Dry mouth Increased blood pressure Increased heart rate Increased libido Restless legs Shakiness Stamina enhancement Stimulation Teeth grinding Vasoconstriction

Cognitive effects
Analysis enhancement Cognitive euphoria Compulsive redosing Disinhibition Ego inflation Focus enhancement Increased music appreciation Mania Motivation enhancement Suggestibility suppression Thought acceleration Wakefulness

External links []

References []

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

Anodyne