Description

Cefmepidium Chloride is a synthetic cephalosporin antibiotic intermediate. This compound is critical for the research and development of advanced antibacterial agents targeting resistant pathogens. It is primarily utilized by pharmaceutical R&D laboratories, API manufacturers, and academic institutions focused on novel antibiotic synthesis. Its specific structure makes it a valuable building block in medicinal chemistry.

Application

• Pharmaceutical Intermediate: Key starting material or advanced intermediate in the synthesis of cephalosporin-class antibiotics.
• Antibacterial Research: Used in R&D for developing new antibacterial agents with improved efficacy against drug-resistant bacteria.
• Active Pharmaceutical Ingredient (API) Manufacturing: Incorporated into the production process of bulk antibiotic substances.
• Medicinal Chemistry Studies: Serves as a reference standard or a precursor in structure-activity relationship (SAR) studies.
• Process Development: Employed in scaling up and optimizing synthetic routes for cephalosporin production.
• Academic Research: Used in university and institutional labs for pharmacological and microbiological research projects.

Basic Information

Item	Detail
Product Name	Cefmepidium Chloride
CAS No.	107452-79-9
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Cefmepidium Chloride; 7β-[2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido]-3-[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid chloride; (6R,7R)-7-[(Z)-2-(2-Aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid chloride; Cefepime Impurity; Cephalosporin Cefmepidium Chloride
EINECS	Contact for details

Quality Control

Our Cefmepidium Chloride is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets high-grade standards suitable for pharmaceutical research and development. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

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 structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 95.0%
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Total impurities ≤ 3.0%
Single Maximum Impurity	≤ 1.0%

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