Anodyne

Thiopropamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Conformer structure via JSmol
Physical properties
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141.24 g/mol [1]
1.8 [1]
Structural Identifiers
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C7H11NS [1]
1-thiophen-2-ylpropan-2-amine [1]
CC(CC1=CC=CS1)N [1]
InChI=1S/C7H11NS/c1-6(8)5-7-3-2-4-9-7/h2-4,6H,5,8H2,1H3 [1]
InChIKeyNYVQQTOGYLBBDQ-UHFFFAOYSA-N [1]

Thiopropamine

Thiopropamine (also known as 2-(2-Aminopropyl)thiophene, 2-Thiopheneethanamine, α-methyl-, 1-(2-Thienyl)-2-propanamine, 1-(Thien-2-yl)propan-2-amine, 1-Methyl-2-(thien-2-yl)ethylamine, (1-Methyl-2-(thiophen-2-yl)ethyl)amine, α-Methyl-2-thiopheneethanamine, α-Methyl-2-thiopheneethylamine, 1-(3,3-diphenylpropyl)amino-3-phenylthiopropane or 1-(thiophen-2-yl)propan-2-amine) is a stimulant substance of the thiopropamine class.

Chemistry

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Thiopropamine is a racemic mixture of the optical stereoisomers

Subjective effects []

Legal status []

  • Canada: Thiopropamine is a
  • Germany: Thiopropamine is a Anlage I substance.

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 6484133, Thiopropamine. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/6484133

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Thiopropamine. UNII: N60H4ZDD14. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/N60H4ZDD14