Anodyne

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Methylephedrine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
179.26 g/mol [1]
Melting point87.5 °C [1]
1.7 [1]
Structural Identifiers
[]
C11H17NO [1]
2-(dimethylamino)-1-phenylpropan-1-ol [1]
CC(C(C1=CC=CC=C1)O)N(C)C [1]
InChI=1S/C11H17NO/c1-9(12(2)3)11(13)10-7-5-4-6-8-10/h4-9,11,13H,1-3H3 [1]
InChIKeyFMCGSUUBYTWNDP-UHFFFAOYSA-N [1]

Methylephedrine

Methylephedrine (also known as N-Methylephedrine, Methylephedrin, 1-Phenyl-2-dimethylaminopropanol, 2-(Dimethylamino)-1-phenyl-1-propanol, (1R,2S)-(-)-N-Methylephedrine, Benzyl alcohol, α-(1-(dimethylamino)ethyl)-, N-methylephedrine hydrochloride, 99, 1201-56-5, Methylephedrine hydrochloride or n-methyl-ephedrine) is a sympathomimetic substance of the phenylethanolamine class.

Chemistry

 []

Methylephedrine is a racemic mixture of the

Stereoisomers
(1R,2S)-MethylephedrineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(1S,2S)-MethylephedrineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(1R,2R)-MethylephedrineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(1S,2R)-MethylephedrineGenerated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

See also []

  • Substituted phenylethanolamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 4374, Methylephedrine. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/4374