Description

Cephradine (200 Mg) is a first-generation cephalosporin antibiotic belonging to the β-lactam class. This high-purity active pharmaceutical ingredient (API) is critical for ensuring the efficacy and safety of finished pharmaceutical formulations. It is primarily required by pharmaceutical manufacturers for the production of oral solid dosage forms, such as capsules and tablets, targeting a range of bacterial infections.

Application

• Primary API for the manufacture of oral antibiotic formulations (capsules, tablets).
• Used in clinical research and development of antibacterial therapies.
• Essential raw material for generic pharmaceutical production.
• Reference standard in quality control laboratories for analytical testing.
• Potential use in veterinary pharmaceutical applications (subject to regional regulations).

Basic Information

Product Name	Cephradine (200 Mg)
CAS No.	58456-86-3
Molecular Formula	C16H19N3O4S
Molecular Weight	349.41 g/mol
Synonyms	Cephradine; Cefradine; (6R,7R)-7-[(R)-2-Amino-2-(1,4-cyclohexadien-1-yl)acetamido]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; SQ 11436; Velosef; Sefril; Anspor; Eskacef
EINECS	261-272-7

Quality Control

Our Cephradine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets or exceeds relevant pharmacopeial standards, including USP and EP monographs. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and conformance to specifications.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Conforms to standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 6.0%
Residue on Ignition	≤ 0.2%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Microbial Enumeration	Meets USP/EP criteria

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