Anodyne

IA
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Isopropylamphetamine hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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177.29 g/mol [1]
2.9 [1]
Structural Identifiers
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C12H19[1]
1-phenyl-N-propan-2-ylpropan-2-amine [1]
CC(C)NC(C)CC1=CC=CC=C1 [1]
InChI=1S/C12H19N/c1-10(2)13-11(3)9-12-7-5-4-6-8-12/h4-8,10-11,13H,9H2,1-3H3 [1]
InChIKeyPJXXJRMRHFYMEY-UHFFFAOYSA-N [1]

Isopropylamphetamine

Isopropylamphetamine (also known as N-Isopropylamphetamine, Benzeneethanamine, α-methyl-N-(1-methylethyl)-, N-Isopropyl-1-phenyl-2-propanamine, RefChem:149850, (1-Phenylpropan-2-yl)(propan-2-yl)amine, N-isopropyl-2-amino-1-phenylpropane, Phenethylamine, N-isopropyl-α-methyl-, α-Methyl-N-(1-methylethyl)benzeneethanamine, 1-phenyl-N-(propan-2-yl)propan-2-amine or Nci60_003717) is a stimulant substance of the amphetamine class.

Chemistry

Salts []

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

 []

Isopropylamphetamine is a racemic mixture of the

Stereoisomers
(R)-IsopropylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-IsopropylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 213536, Isopropylamphetamine. Accessed October 9, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/213536

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Isopropylamphetamine. UNII: 8XR4H66ACF. Global Substance Registration System. Accessed October 9, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/8XR4H66ACF