Description

Cefepime Sulfate is a fourth-generation, broad-spectrum cephalosporin antibiotic in its sulfate salt form. This advanced pharmaceutical intermediate is critical for the formulation of potent injectable antibacterial medications. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of sterile injectable drugs targeting serious infections.

Application

• Active Pharmaceutical Ingredient (API) for the manufacture of injectable antibiotic formulations.
• Pharmaceutical Research & Development as a key intermediate in synthesizing new drug delivery systems or combination therapies.
• Reference Standard for quality control and analytical testing in pharmaceutical laboratories.
• Hospital & Clinical Use as the core component in finished drugs for treating pneumonia, bacteremia, and febrile neutropenia.
• Veterinary Medicine for developing antibacterial treatments for severe infections in animals.

Basic Information

Product Name	Cefepime Sulfate
CAS No.	107648-78-2
Molecular Formula	C19H24N6O5S2 • H2SO4
Molecular Weight	612.66 g/mol (for Cefepime Sulfate)
Synonyms	Cefepime Sulphate; (6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(1-methylpyrrolidin-1-ium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate sulfate; Cefepime Hydrochloride Sulfate; BMY-28117 sulfate; Axepim Sulfate
EINECS	Contact for details

Quality Control

Our Cefepime Sulfate is manufactured under strict quality systems. It undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A detailed Certificate of Analysis (COA) is provided with each batch, confirming compliance with specified parameters for identity, purity, and impurities.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms
Identification (HPLC)	Conforms to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 2.0%
pH (1% Solution)	3.5 - 5.5
Related Substances (HPLC)	Total impurities ≤ 2.0% Any individual impurity ≤ 1.0%
Residual Solvents (GC)	Meets ICH Q3C guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.