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Hexadecyl pyridinium chloride structure, CAS 123-03-5

Hexadecyl pyridinium chloride

CAS Number123-03-5

SynonymsPyrisept; 1-HEXADECYL-PYRIDINIUM,CHLORIDE; Pristacin; MFCD00011731; EINECS 204-593-9; Cetafilm; Medilave; Pyridinium, 1-hexadecyl-, chloride (1:1); cetylpyridinium chloride; Aktivex; cpc; Ceepryn chloride; Pionin B 651P; 1-hexadecylpyridinum chloride; Cetamium; Ceepryn; Biosept; N-hexadecylpyridinium chloride; Cetyl-pyridinium chloride; Merothol; Merocet; Dobendan; hexadecylpyridinium chloride; 1-Hexadecylpyridinium chloride; Cloruro di cetilpiridinio; tserigel; Ipanol; 1-hexadecylpyridin-1-ium,chloride; Newkalgen B 651P; N-cetyl-pyridinium chloride

Molecular FormulaC21H38ClN

Molecular Weight363.03

Purity98 (CP)%

Density

Boiling Point

Melting Point81 °C (lit.)

Flash Point

Appearancesolid

EINECS

MSDSChineseEnglish

Symbol6.1(b)

Signal WordWarning

Cat. No.: 2A-9007956 Purity: 98 (CP)%
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Quality Control of [ 123-03-5 ] Purity: 98 (CP)% SDS Specification MoL

COA NMR CNMR HPLC LC-MS
Chemical & Physical Properties
CAS Number123-03-5
Catalog No.2A-9007956
Chinese Name西吡氯铵
SynonymsPyrisept; 1-HEXADECYL-PYRIDINIUM,CHLORIDE; Pristacin; MFCD00011731; EINECS 204-593-9; Cetafilm; Medilave; Pyridinium, 1-hexadecyl-, chloride (1:1); cetylpyridinium chloride; Aktivex; cpc; Ceepryn chloride; Pionin B 651P; 1-hexadecylpyridinum chloride; Cetamium; Ceepryn; Biosept; N-hexadecylpyridinium chloride; Cetyl-pyridinium chloride; Merothol; Merocet; Dobendan; hexadecylpyridinium chloride; 1-Hexadecylpyridinium chloride; Cloruro di cetilpiridinio; tserigel; Ipanol; 1-hexadecylpyridin-1-ium,chloride; Newkalgen B 651P; N-cetyl-pyridinium chloride
Molecular FormulaC21H38ClN
Molecular Weight363.03
Purity98 (CP)
Melting Point81 °C (lit.)
Appearancesolid
Storage ConditionWarehouse low temperature ventilation and drying
PackagingIII
ApplicationCetylpyridinium chloride, a cationic quaternary ammonium compound, is an antimicrobial agent with broad-spectrum activity. Cetylpyridinium chloride is a potent anti-HBV capsid assembly inhibitor with
HTC2933399090
PubChem ID329758497
MDL NumberMFCD08702799
SMILESO.[Cl-].[2H]c1c([2H])c([2H])[n+](CCCCCCCCCCCCCCCC)c([2H])c1[2H]
InChI1S/C21H38N.ClH.H2O/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;1H2/q+1;;/p-1/i15D,17D,18D,20D,21D;;
InChI KeyNFCRBQADEGXVDL-UGIAOSMXSA-M
UNSPSC12352005
Hazard Symbols6.1(b)
MSDSmsds/7956_1_123_03_5.pdf
BioactivityCetylpyridinium chloride, a cationic quaternary ammonium compound, is an anti-bacterial agent with broad-spectrum activity. Cetylpyridinium chloride is an effective anti-HBV capsid assembly inhibitor with an IC50 of 2.5 μM. Cetylpyridinium chloride is used in pesticides and various types of mouthwashes, and other personal care products[1][2]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> HBV Research Areas >> Inflammation/Immunology Signaling Pathways >> Anti-infection >> Bacterial Target IC50: 2.5 μM (HBV capsid assembly)[1] In Vitro Cetylpyridinium chloride interacts with dimeric viral nucleocapsid protein (known as core protein or HBcAg) specifically. Compared with other HBV inhibitors, Cetylpyridinium chloride achieves significantly better reduction of HBV particle number in HepG2.2.15 cell line. Cetylpyridinium chloride inhibits capsid assembly and leads to reduced HBV biogenesis[1]. Cetylpyridinium chloride is a safe antimicrobial agent with broad-spectrum activity for preventing biofilm formation and gingivitis[2]. In Vivo Cetylpyridinium chloride (30 μg/kg; intramuscular injection; daily; for 3 days; male C57BL/6 mice) treatment inhibits HBV replication in mouse hydrodynamic model system[1]. Animal Model: Male C57BL/6 mice (6-week old) injected with the plasmid [1] Dosage: 272 μg/kg/day Administration: Intramuscular injection; daily; for 3 days Result: Suppressed serum HBV DNA levels, decreased by 60% in day2 and 45% in day3 compared to the control. References [1]. Hyun Wook Seo, et al. Cetylpyridinium chloride interaction with the hepatitis B virus core protein inhibits capsid assembly. Virus Res. 2019 Apr 2;263:102-111. [2]. Hiroto Imai, et al. Cetylpyridinium chloride at sublethal levels increases the susceptibility of rat thymic lymphocytes to oxidative stress. Chemosphere. 2017 Mar;170:118-123. Chemical & Physical Properties Melting Point 77°C Molecular Formula C21H38ClN Molecular Weight 339.986 Exact Mass 339.269287 PSA 3.88000 LogP 3.45940 Stability Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
Use ofCetylpyridinium chloride, a cationic quaternary ammonium compound, is an anti-bacterial agent with broad-spectrum activity. Cetylpyridinium chloride is an effective anti-HBV capsid assembly inhibitor with an IC50 of 2.5 μM. Cetylpyridinium chloride is used in pesticides and various types of mouthwashes, and other personal care products[1][2]. Properties Name cetylpyridinium chloride Synonym More Synonyms cetylpyridinium chloride Biological Activity Description Cetylpyridinium chloride, a cationic quaternary ammonium compound, is an anti-bacterial agent with broad-spectrum activity. Cetylpyridinium chloride is an effective anti-HBV capsid assembly inhibitor with an IC50 of 2.5 μM. Cetylpyridinium chloride is used in pesticides and various types of mouthwashes, and other personal care products[1][2]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> HBV Research Areas >> Inflammation/Immunology Signaling Pathways >> Anti-infection >> Bacterial IC50: 2.5 μM (HBV capsid assembly)[1] References [1]. Hyun Wook Seo, et al. Cetylpyridinium chloride interaction with the hepatitis B virus core protein inhibits capsid assembly. Virus Res. 2019 Apr 2;263:102-111. [2]. Hiroto Imai, et al. Cetylpyridinium chloride at sublethal levels increases the susceptibility of rat thymic lymphocytes to oxidative stress. Chemosphere. 2017 Mar;170:118-123. Chemical & Physical Properties Exact Mass 339.269287 PSA 3.88000 LogP 3.45940 Stability Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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