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PHR1226

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Cetylpyridinum chloride

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

Cetylpyridinium chloride monohydrate, 1-Hexadecylpyridinium chloride, Hexadecylpyridinium chloride monohydrate

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About This Item

Formule empirique (notation de Hill):
C21H38ClN · H2O
Numéro CAS:
Poids moléculaire :
358.00
Numéro Beilstein :
3578606
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

certified reference material
pharmaceutical secondary standard

Niveau de qualité

Agence

traceable to Ph. Eur. C1000000
traceable to USP 1104006

Famille d'API

cetylpyridinium

CofA (certificat d'analyse)

current certificate can be downloaded

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

83-86 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

O.[Cl-].CCCCCCCCCCCCCCCC[n+]1ccccc1

InChI

1S/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

Clé InChI

NFCRBQADEGXVDL-UHFFFAOYSA-M

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Description générale

Cetylpyridinum chloride is a quaternary ammonium compound and an active ingredient of antiseptic oral mouth rinses with broad spectrum antimicrobial activity. Its mode of action involves a rapid bactericidal effect on Gram-positive pathogens and a fungicide effect on certain yeasts.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Application

Cetylpyridinum chloride may be used as a pharmaceutical reference standard for the quantification of the analyte in pharmaceutical preparations using reversed-phase high-performance liquid chromatography technique.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Remarque sur l'analyse

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Autres remarques

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Note de bas de page

To see an example of a Certificate of Analysis for this material enter LRAC0149 in the slot below. This is an example certificate only and may not be the lot that you receive.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

Skull and crossbonesCorrosionEnvironment

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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Journal of Pharmaceutical and Biomedical Analysis, 51(07), 588-595 (2001)
Pharmaceutical Emulsions and Suspensions: Second Edition, Revised and Expanded
Drugs and the Pharmaceutical Sciences (2000)
Determination of cetylpyridinium chloride and tetracaine hydrochloride in buccal tablets by RP-HPLC
Wang J, et al.
Journal of Pharmaceutical and Biomedical Analysis, 32(2), 381-386 (2003)
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