BA

Molecular structure via molpic based on CDK

Conformer []

Conformer structure via 3Dmol.js

Physical properties []
Molecular mass	191.31 g/mol ^[1]
Predicted LogP	3.4 ^[1]

Structural Identifiers []
Molecular formula	C₁₃H₂₁N ^[1]
IUPAC name	N-(1-phenylpropan-2-yl)butan-1-amine ^[1]
SMILES	CCCCNC(C)CC1=CC=CC=C1 ^[1]
InChI	InChI=1S/C13H21N/c1-3-4-10-14-12(2)11-13-8-6-5-7-9-13/h5-9,12,14H,3-4,10-11H2,1-2H3 ^[1]
InChIKey	VIAVBPFRYASSKF-UHFFFAOYSA-N ^[1]

Butylamphetamine

Butylamphetamine (also known as N-n-butylamphetamine, 51799-33-8, N-Butylamphetamine, 1-Phenyl-2-butylaminopropane, 1-Phenyl-2-n-butylamino-propan, n-butylamphetamine, Phenethylamine, N-butyl-α-methyl-, Benzeneethanamine, N-butyl-α-methyl-, 4-12-00-02592 or Ncgc00247329-01) is a stimulant and prodrug substance of the amphetamine class.

Chemistry

Stereochemistry []

Butylamphetamine is a racemic mixture of the enantiomers

Stereoisomers
(R)-Butylamphetamine (S)-Butylamphetamine

Pharmacology

Butylamphetamine acts as a prodrug for:

Active metabolites []
Amphetamine

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 94547, Butylamphetamine. Accessed July 20, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/94547

Anodyne