Anodyne

Methiopropamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Methiopropamine hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic
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Physical properties
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Molecular mass155.26 g/mol [1]
Predicted LogP1.9 [1]
Structural Identifiers
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Molecular formulaC8H13NS [1]
IUPAC nameN-methyl-1-thiophen-2-ylpropan-2-amine [1]
SMILESCC(CC1=CC=CS1)NC [1]
InChIInChI=1S/C8H13NS/c1-7(9-2)6-8-4-3-5-10-8/h3-5,7,9H,6H2,1-2H3 [1]
InChIKeyHPHUWHKFQXTZPS-UHFFFAOYSA-N [1]
Dosing

Methiopropamine

Methiopropamine (also known as 1-(Thiophen-2-yl)-2-methylaminopropane, 2-Thiopheneethylamine, N,α-dimethyl-, Synthacaine component methiopropamine, 2-Methiopropamine, 2-Thiopheneethylamine, n,α-dimethyl-, N -Methyl-1-(thiophen-2-yl)propan-2-amine, N-methyl-1-(thiophen-2-yl)propane-2-amine or C22795) is a stimulant substance of the thiopropamine class.

Chemistry

Salts []

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

Stereochemistry []

Methiopropamine is a racemic mixture of the optical stereoisomers:

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

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 436156, Methiopropamine. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/436156

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Methiopropamine. UNII: 64ON2ETH7I. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/64ON2ETH7I

  3. Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. July 24, 2023. Accessed July 13, 2025. https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451