Description

Cefeprime Dihydrochloride is a high-purity pharmaceutical intermediate and reference standard, primarily used in the research and development of advanced cephalosporin antibiotics. Its significance lies in its role as a key building block for synthesizing potent, broad-spectrum antibacterial agents. This compound is essential for pharmaceutical manufacturers, R&D laboratories, and analytical facilities focused on developing new antibiotic formulations and conducting quality control testing.

Application

• Pharmaceutical Intermediate: A critical precursor in the chemical synthesis of advanced-generation cephalosporin antibiotics.
• Reference Standard: Used for analytical method development, validation, and quality control (QC) testing in pharmaceutical manufacturing.
• Research & Development: Serves as a key material in medicinal chemistry for studying structure-activity relationships and developing novel antibacterial compounds.
• Active Pharmaceutical Ingredient (API) Synthesis: Employed in the production of bulk active pharmaceutical ingredients under Good Manufacturing Practice (GMP) conditions.
• Microbiological Research: Used in studies to evaluate the efficacy and resistance mechanisms of β-lactam antibiotics.

Basic Information

Product Name	Cefeprime Dihydrochloride
CAS No.	107648-80-6
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Cefeprime HCl; Cefeprime Dihydrochloride Salt; (6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(1-methylpyrrolidinium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Dihydrochloride; Cefepime Dihydrochloride Impurity; Cefepime Related Compound
EINECS	Contact for details

Quality Control

Our Cefeprime Dihydrochloride is manufactured and tested to meet stringent quality standards suitable for pharmaceutical R&D and intermediate use. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation. A comprehensive Certificate of Analysis (COA) detailing purity, impurities, and other critical parameters is provided to ensure traceability and compliance with your quality requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	≥ 98.0%
Water Content	≤ 2.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents	Complies with ICH guidelines

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