Anodyne

Metrotonin
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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163.26 g/mol [1]
2.7 [1]
Structural Identifiers
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C11H17[1]
N,N-dimethyl-1-phenylpropan-2-amine [1]
CC(CC1=CC=CC=C1)N(C)C [1]
InChI=1S/C11H17N/c1-10(12(2)3)9-11-7-5-4-6-8-11/h4-8,10H,9H2,1-3H3 [1]
InChIKeyOBDSVYOSYSKVMX-UHFFFAOYSA-N [1]

Dimethylamphetamine

Dimethylamphetamine (also known as N,N-dimethylamphetamine, N,N,α-Trimethylphenethylamine, N,N,α-Trimethylbenzeneethanamine, Phenethylamine, n,n,α-trimethyl-, dimethyl(1-phenylpropan-2-yl)amine, J14.522J, N-methyl-methamphetamine, 1-Phenyl-2-dimethylaminopropane, 2-Dimethylamino-1-phenylpropane or 1-Phenyl-2-dimethylamino-propan) is a prodrug and stimulant substance of the amphetamine class.

Chemistry

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Dimethylamphetamine is a racemic mixture of the

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

Pharmacology

Dimethylamphetamine acts as a for:

Active metabolites
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Amphetamine Generated by the Chemistry Development Kit (http://github.com/cdk)
Methamphetamine Generated 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 20006, Dimethylamphetamine. Accessed July 20, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/20006

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Dimethylamphetamine. UNII: IYE3F3MHCU. Global Substance Registration System. Accessed July 20, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/IYE3F3MHCU