Description

Cefonicid Disodium Salt is a second-generation cephalosporin antibiotic in its disodium salt form, offering enhanced stability and solubility for pharmaceutical manufacturing. This compound is critical for formulating sterile injectable antibiotic preparations, ensuring reliable therapeutic efficacy against a broad spectrum of bacterial infections. It is primarily required by pharmaceutical companies and research institutions engaged in the development and production of parenteral antibiotics, serving the global healthcare market.

Application

• Active Pharmaceutical Ingredient (API) in injectable antibiotic formulations.
• Reference standard for analytical method development and quality control in pharmaceutical laboratories.
• Intermediate in the synthesis of more complex cephalosporin derivatives for research purposes.
• Raw material for the preparation of clinical trial supplies and non-commercial medicinal products.

Basic Information

Product Name	Cefonicid Disodium Salt
CAS No.	190181-58-9
Molecular Formula	C18H16N6Na2O8S3
Molecular Weight	586.52 g/mol
Synonyms	Cefonicid Sodium; Cefonicid Disodium; (6R,7R)-7-[[(2R)-2-Hydroxy-2-phenylacetyl]amino]-8-oxo-3-[[(1-sulfomethyl-1H-tetrazol-5-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Disodium Salt; SKF 75073; Monocid; Cefonicidum; Cefonicid Acid Disodium Salt
EINECS	Contact for details

Quality Control

Our Cefonicid Disodium Salt is manufactured under strict quality systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with every shipment to support your regulatory and quality assurance requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 5.0%
pH (10% solution)	5.5 - 7.5
Related Substances (HPLC)	Individual impurity ≤ 1.0%; Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines

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