N-Acetylamphetamine

Molecular structure via molpic based on CDK

Conformer []

Conformer structure via 3Dmol.js

Physical properties []
Molecular mass	177.24 g/mol ^[1]
Predicted LogP	1.9 ^[1]

Structural Identifiers []
Molecular formula	C₁₁H₁₅NO ^[1]
IUPAC name	N-(1-phenylpropan-2-yl)acetamide ^[1]
SMILES	CC(CC1=CC=CC=C1)NC(=O)C ^[1]
InChI	InChI=1S/C11H15NO/c1-9(12-10(2)13)8-11-6-4-3-5-7-11/h3-7,9H,8H2,1-2H3,(H,12,13) ^[1]
InChIKey	YPKBVWZHVTZSPU-UHFFFAOYSA-N ^[1]

N-Acetylamphetamine

N-Acetylamphetamine (also known as acetylamphetamine, Acetamide, N-(1-methyl-2-phenylethyl)-, N-(1-Methyl-2-phenylethyl)acetamide, N-(α-Methylphenethyl)acetamide, Acetamide, N-(α-methylphenethyl)-, Acetamide, n-(α-methylphenethyl)-, Mls000532578, HMS2156K14, HMS3312M14 or N-(α-methylphenethyl) acetamide) is a stimulant substance of the amphetamine class.

Chemistry

Stereochemistry []

N-Acetylamphetamine is a racemic mixture of the enantiomers

Stereoisomers
(R)-N-Acetylamphetamine (S)-N-Acetylamphetamine

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 26660, N-Acetylamphetamine. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/26660

Anodyne