BMA, βMA

Salts []
%!s() hydrochloride

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	135.21 g/mol ^[1]
Predicted LogP	2.2 ^[1]

Structural Identifiers []
Molecular formula	C₉H₁₃N ^[1]
IUPAC name	2-phenylpropan-1-amine ^[1]
SMILES	CC(CN)C1=CC=CC=C1 ^[1]
InChI	InChI=1S/C9H13N/c1-8(7-10)9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3 ^[1]
InChIKey	AXORVIZLPOGIRG-UHFFFAOYSA-N ^[1]

Toxicity []
LD_Lo	Rat: - intraperitoneal: 150 mg/kg

β-Methylamphetamine

β-Methylamphetamine (also known as 2-Phenylpropylamine, β-Methylphenethylamine, 2-phenyl-1-propanamine, 2-phenyl-1-propylamine, Benzeneethanamine, β-methyl-, 2-Phenylpropanamine, 209-479-2, 1-Amino-2-phenylpropane, BMPEA or β-Methylphenylethylamine) is a stimulant substance of the β-alkylphenethylamine class.

Chemistry

Salts []

β-Methylamphetamine is typically found in the form of its hydrochloride salt.

Stereochemistry []

β-Methylamphetamine is a racemic mixture of the enantiomers

Stereoisomers
(S)-β-Methylamphetamine (R)-β-Methylamphetamine

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 11398, β-Methylamphetamine. Accessed August 12, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/11398
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. β-Methylamphetamine. UNII: 6XL7O3V13L. Global Substance Registration System. Accessed August 12, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/6XL7O3V13L

Anodyne