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Key Documents

PHR1763

Supelco

Cefepime hydrochloride

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

Cefepime hydrochloride, Cefepime dihydrochloride monohydrate

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About This Item

Formule linéaire :
C19H25N6O5S2Cl · HCl · H2O
Numéro CAS:
Poids moléculaire :
571.50
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.24

Qualité

certified reference material
pharmaceutical secondary standard

Niveau de qualité

Agence

traceable to Ph. Eur. Y0000633
traceable to USP 1097636

Famille d'API

cefepime

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

pkg of 1 g

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

InChI

1S/C19H24N6O5S2.2ClH.H2O/c1-25(5-3-4-6-25)7-10-8-31-17-13(16(27)24(17)14(10)18(28)29)22-15(26)12(23-30-2)11-9-32-19(20)21-11;;;/h9,13,17H,3-8H2,1-2H3,(H3-,20,21,22,26,28,29);2*1H;1H2/b23-12-;;;/t13-,17-;;;/m1.../s1

Clé InChI

LRAJHPGSGBRUJN-OMIVUECESA-N

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Description générale

Cefepime hydrochloride is one of the fourth-generation, semisynthetic, broad-spectrum, cephalosporin β-lactam antibiotic drugs administered parenterally in patients with moderate-to-severe infections like pneumonia, uncomplicated urinary tract infections, skin and soft tissue infections, etc. Its mode of action involves the penetration of outer cell wall of gram negative bacteria.
Pharmaceutical secondary standard for application in quality control. Provides pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Application

Cefepime hydrochloride has been used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by spectrophotometry and chromatography techniques.
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 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 LRAB8503 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Code de la classe de stockage

11 - Combustible Solids

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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Les clients ont également consulté

Analysis of N-methylpyrrolidine in cefepime hydrochloride by ion chromatography using suppressed conductivity detection with solid-phase extraction pre-treatment
Page N, et al.
Analytical Methods for Therapeutic Drug Monitoring and Toxicology, 6(4), 1248-1253 (2014)
RP-HPLC method for simultaneous estimation of cefepime hydrochloride and tazobactam sodium in bulk and pharmaceuticals
Tamboli SR and Patil DD
Journal of Chemistry, 2013(4), 1248-1253 (2013)
Development and validation of a green analytical method of RP-HPLC for quantification of Cefepime hydrochloride in pharmaceutical dosage form: Simple, sensitive and economic
Rodrigues DF and Salgado HRN
Current Pharmaceutical Analysis, 12(4), 306-314 (2016)
Spectrophotometric determination of cefepime hydrochloride, cefoperazone sodium, ceftazidime pentahydrate. cefuroxime sodium and etamsylate using ammonium molybdate
Elazazy M, et al.
Scientia Pharmaceutica, 71(3), 211-228 (2003)

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