AnodyneWiki

Cotinine

Cotinine
Cotinine
Salts
[]
Cotinine hemifumarate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Cotinine tartrate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
176.21 g/mol [1]
AppearanceViscous oil [1]
Boiling point210-211 °C at 6 mm Hg [1]
-0.3 [1]
Structural Identifiers
[]
C10H12N2[1]
(5S)-1-methyl-5-pyridin-3-ylpyrrolidin-2-one [1]
CN1[C@@H](CCC1=O)C2=CN=CC=C2 [1]
InChI=1S/C10H12N2O/c1-12-9(4-5-10(12)13)8-3-2-6-11-7-8/h2-3,6-7,9H,4-5H2,1H3/t9-/m0/s1 [1]
InChIKeyUIKROCXWUNQSPJ-VIFPVBQESA-N [1]
Pharmacokinetics[]
Elimination half-life20 hours

Cotinine (also known as Cotinine, Cotinina, Cotininum, S-(-)-Cotinine, (5S)-1-methyl-5-(pyridin-3-yl)pyrrolidin-2-one, Dtxsid1047576, 1-Methyl-5-(3-pyridinyl)-2-pyrrolidinone, 2-Pyrrolidinone, 1-methyl-5-(3-pyridinyl)-, (5S)-, Chebi:68641 or n-methyl-2-(3-pyridyl)-5-pyrrolidone) is a substance of the racetam class.

Chemistry

Salts []

Cotinine is typically found in the form of its hemifumarate and tartrate salts.

 []

Cotinine is a absolute mixture.

Pharmacology

Metabolism

Subjective effects []

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 854019, Cotinine. Accessed April 20, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/854019

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Cotinine. UNII: K5161X06LL. Global Substance Registration System. Accessed April 20, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/K5161X06LL