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Merocet

HexadecylPyridinium chloride

CAS: 123-03-5

Molecular Formula: C21H38ClN

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Merocet - Names and Identifiers

Name HexadecylPyridinium chloride
Synonyms biosept
Cepacol
ceepryn
Merocet
Ceepryn
aktivex
Medilave
Cetamium
Pyrisept
Dobendan
Pristacin
ammonyxcpc
acetoquatcpc
ceeprinchloride
ceeprynchloride
Cetylpyridinium Chloride
Cetyl pyridinium chloride
Chondroitin hydrochloride
1-CETYLPYRIDINIUM CHLORIDE
1-palmitylpyridiniumchloride
HexadecylPyridinium chloride
C16-alkylpyridinium chloride
Hexadecyl pyridinium chloride
1-Hexadecylpyridinium chloride
pyridinium, 1-hexadecyl-, dichloride
CAS 123-03-5
EINECS 204-593-9
InChI InChI=1/C21H38N.2ClH/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;2*1H/q+1;;/p-2

Merocet - Physico-chemical Properties

Molecular FormulaC21H38ClN
Molar Mass339.99
Density0.9362 (rough estimate)
Melting Point77°C
Boling Point496.25°C (rough estimate)
Water Solubility111g/L at 20℃
Solubility DMSO,Water,Ethanol
Vapor Presure0Pa at 25℃
AppearanceWhite powder or crystal
Storage ConditionInert atmosphere,Room Temperature
StabilityStable. Combustible. Incompatible with strong oxidizing agents, strong bases.
Refractive Index1.6000 (estimate)
MDLMFCD00011731
UseDisinfection antiseptics
In vitro studyCetylpyridinium chloride (CPC), as the active ingredient of antibacterial mouthwash, has broad-spectrum antibacterial activity and rapid bactericidal effect on Gram-positive bacteria, especially on yeast. A 0.05% concentration of PCP as a mouthwash resulted in an immediate reduction in bacterial numbers from 2.0 log steps to 2.5 log steps(> amp; Gt; 99%). After 1 hour of use, the number of bacteria will return to 1 log step (= 90%). CPC is able to inhibit plaque, thereby reducing gingivitis. Compared with chlorhexidine, CPC has a lower residual effect, so it has a weaker effect on plaque and gingivitis. CPC has definite curative effect on oropharyngeal candidiasis. In dental clinics, CPC mouthwash can significantly reduce infectious aerosols, thereby protecting staff and patients. Even in the case of prolonged use of CPC (up to 6 weeks), the balance of the flora in the oral cavity is not disturbed.
In vivo studyCetylpyridinium chloride increases the risk of severe allergic reactions such as swelling of the mouth, face, lips or tongue, difficulty breathing, rash and hives. Ingestion of high concentrations of Cetylpyridinium chloride can cause lung injury. Cetylpyridinium chloride is toxic if swallowed or inhaled.

Merocet - Risk and Safety

UN IDs2811
Hazard Class6.1(b)
Packing GroupIII

Merocet - Reference

Reference
Show more
1. Peng, Wei, et al. "Docking study and antiosteoporosis effects of a dibenzylbutane lignan isolated from Litsea cubeba targeting Cathepsin K and MEK1." Medicinal Chemistry Research 27.9 (2018): 2062-2070.https://doi.org/10.1007/s00044-018-2215-8

Merocet - Reference Information

LogP1.71 at 20℃
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
introduction decadecane pyridine chloride is a cationic quaternary ammonium compound, and it is also a very important surface activity and fungicide in life. Under the same conditions of use, the killing rate of heterotrophic bacteria, iron bacteria and sulfate unwilling bacteria is better than that of dodecyl dimethyl benzyl ammonium chloride, dodecyl dimethyl benzyl ammonium bromide and other commonly used quaternary ammonium salt fungicides.
biological activity Cetylpyridinium chloride is a cationic quaternary ammonium compound as an oropharyngeal disinfectant.
use antiseptic.
Production method In a mixture of 48mlSOCl 2 and 0.3gHCON(CH 3) 2, the temperature is controlled at 30-35°C under stirring, and 81g of decanol is dropped. After dropping, the mixture is boiled for 30min, cooled, and distilled to obtain a fraction of 138-140 ℃ (pressure 270Pa), which is chlorodecane with 92.2% yield. 80g of chloropetane and 32g of dry pyridine were heated to 150-160 ℃ in an oil bath, reacted for 12-15h, after the reaction, 80ml of dry acetone was added, and the mixture was heated and dissolved in a water bath before cooling to obtain a product with 994% yield. The melting point is 87-88 ℃.
category pesticide
toxicity classification highly toxic
acute toxicity oral-rat LD50: 200 mg/kg; Oral-mouse LD50: 108 mg/kg
stimulation data skin-rabbit 50 mg/24 hours moderate; Eye-rabbit 100 mg moderate
flammability hazard characteristics thermal decomposition discharges toxic nitrogen oxides and chloride smoke
storage and transportation characteristics warehouse low temperature ventilation and drying
fire extinguishing agent water, carbon dioxide, foam, dry powder
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 20:49:11
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