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Cetylpyridinium chloride

Cetylpyridinium chloride
Cetylpyridinium chloride
Molecular structure via molpic based on CDK
Physical properties
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340.0 g/mol [1]
AppearanceWhite powder [1]
Melting point80 °C [1]
DecompositionWhen heated to decomposition it emits very toxic fumes of /nitrogen oxides and hydrogen chloride/. [1]
SolubilityVery soluble in water, chloroform [1]
Structural Identifiers
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C21H38ClN [1]
1-hexadecylpyridin-1-ium chloride [1]
CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1.[Cl-] [1]
InChI=1S/C21H38N.ClH/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-22-20-17-15-18-21-22;/h15,17-18,20-21H,2-14,16,19H2,1H3;1H/q+1;/p-1 [1]
InChIKeyYMKDRGPMQRFJGP-UHFFFAOYSA-M [1]

(Redirected from Cetylpyridinium chloride)

Cetylpyridinium chloride (also known as hexadecylpyridinium chloride, Pristacin, Cepacol, Ceprim, Cetamium, Dobendan, Pyrisept, Aktivex, Biosept or 1-Cetylpyridinium chloride)

Chemistry

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Cetylpyridinium chloride is a achiral mixture.

Subjective effects []

Pilz / Cetylpyridinium chloride []
Routes:
  • Oral (1.4mg)
  • Sublingual (1.4mg)
Indication:Notes:
  • Consumed as Dolo-Dobendan Lozenges with Benzocaine

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 31239, cetylpyridinium chloride. Accessed May 11, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/31239

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Cetylpyridinium chloride. UNII: 6BR7T22E2S. Global Substance Registration System. Accessed May 11, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/6BR7T22E2S