Anodyne

Thiothinone
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
[]
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Physical properties
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169.25 g/mol [1]
1.6 [1]
Structural Identifiers
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C8H11NOS [1]
2-(methylamino)-1-thiophen-2-ylpropan-1-one [1]
CC(C(=O)C1=CC=CS1)NC [1]
InChI=1S/C8H11NOS/c1-6(9-2)8(10)7-4-3-5-11-7/h3-6,9H,1-2H3 [1]
InChIKeyDOZQPYDMJMLVKX-UHFFFAOYSA-N [1]

Thiothinone

Thiothinone (also known as 2-Thiothinone, 2-(Methylamino)-1-(2-thienyl)-1-propanone or 1-Propanone, 2-(methylamino)-1-(2-thienyl)-) is a stimulant substance of the thiopropamine class.

Chemistry

Salts []

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

 []

Thiothinone is a racemic mixture of the optical stereoisomers

Stereoisomers
(+)-ThiothinoneGenerated by the Chemistry Development Kit (http://github.com/cdk)
(-)-ThiothinoneGenerated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

Legal status []

  • Germany: Thiothinone is a Neuer-Psychoaktiver-Stoff under the "Neue-psychoaktive-Stoffe-Gesetz (NpSG)".
  • United Kingdom: Thiothinone is a Class B substance.

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 12198617, Thiothinone. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/12198617

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Thiothinone. UNII: 8C758Z7L72. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/8C758Z7L72