α-Methylphenethylpyrrolidine

MPEP

Molecular structure via molpic based on CDK

Rotamer []

Conformer structure via 3Dmol.js

Physical properties []
Molecular mass	189.30 g/mol ^[1]
Predicted LogP	3.1 ^[1]

Structural Identifiers []
Molecular formula	C₁₃H₁₉N ^[1]
IUPAC name	1-(1-phenylpropan-2-yl)pyrrolidine ^[1]
SMILES	CC(CC1=CC=CC=C1)N2CCCC2 ^[1]
InChI	InChI=1S/C13H19N/c1-12(14-9-5-6-10-14)11-13-7-3-2-4-8-13/h2-4,7-8,12H,5-6,9-11H2,1H3 ^[1]
InChIKey	AWNZMWZMSDWFCV-UHFFFAOYSA-N ^[1]

α-Methylphenethylpyrrolidine (also known as 1-(1-Methyl-2-phenylethyl)pyrrolidine, Schembl12503880 or 1-(1-methyl-2-phenylethyl)pyrrolidine) is a stimulant substance of the phenylethylpyrrolidine class.

Chemistry

Stereochemistry []

α-Methylphenethylpyrrolidine is a racemic mixture of the enantiomers.

Stereoisomerism
(R)-α-Methylphenethylpyrrolidine (S)-α-Methylphenethylpyrrolidine
Stereoisomer enumberation with rdkit

Subjective effects []

class / Stimulant

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 53665923, α-Methylphenethylpyrrolidine. Accessed August 23, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/53665923

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