AnodyneWiki

Triprolidine

Triprolidine
Triprolidine
Salts
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Triprolidine hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Rotamer
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Conformer structure via 3Dmol.js
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Physical properties
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278.4 g/mol [1]
AppearanceCrystals from light petroleum [1]
Melting point59-61 °C [1]
Solubility5.37e-02 g/L [1]
3.9 [1]
Structural Identifiers
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C19H22N2 [1]
2-[(E)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-enyl]pyridine [1]
CC1=CC=C(C=C1)/C(=C\CN2CCCC2)/C3=CC=CC=N3 [1]
InChI=1S/C19H22N2/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21/h2-3,6-12H,4-5,13-15H2,1H3/b18-11+ [1]
InChIKeyCBEQULMOCCWAQT-WOJGMQOQSA-N [1]

Triprolidine (also known as Triprolidin, Actidil, Tripolidina, Triprolidinum, Triprolidina, trans-1-(2-Pyridyl)-3-pyrrolidino-1-p-tolylprop-1-ene, NCI-C61450, trans-1-(4-Methylphenyl)-1-(2-pyridyl)-3-pyrrolidinoprop-1-ene, trans-2-(3-(1-Pyrrolidinyl)-1-p-tolylpropenyl)pyridine or Dtxsid3023718) is a substance of the phenethylamine class.

Chemistry

Salts []

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

 []

Triprolidine is a achiral mixture.

Pharmacology

In the () triprolidine acts

Experience reports []

There are currently 1 experience reports involving triprolidine on :

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 5282443, triprolidine. Accessed May 8, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/5282443

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Triprolidine. UNII: 2L8T9S52QM. Global Substance Registration System. Accessed May 8, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/2L8T9S52QM