Description

Cefovecin Sodium is a third-generation cephalosporin antibiotic formulated as a sodium salt for enhanced stability and solubility. This compound is valued for its potent, broad-spectrum antibacterial activity and extended duration of action, making it a critical active pharmaceutical ingredient (API). It is primarily utilized in the veterinary pharmaceutical industry for the development of long-acting injectable treatments for companion animals. Cefovecin Sodium CAS NO 141195-77-9 represents a high-value, specialized antibiotic for targeted therapeutic applications.

Application

• Veterinary Pharmaceutical API: Primary use as the active ingredient in long-acting injectable antibiotic formulations for dogs and cats.
• Treatment of Skin and Soft Tissue Infections: Used in formulations targeting bacterial infections such as wounds, abscesses, and pyoderma.
• Management of Urinary Tract Infections (UTIs): Incorporated into therapies for bacterial cystitis and other urogenital infections in companion animals.
• Research & Development: Serves as a reference standard and key intermediate in pharmaceutical R&D for novel antibiotic delivery systems.
• Generic Drug Manufacturing: Essential for producers of generic veterinary medicines requiring a reliable, high-purity API source.

Basic Information

Product Name	Cefovecin Sodium
CAS No.	141195-77-9
Molecular Formula	C19H16N5NaO6S2
Molecular Weight	505.48 g/mol
Synonyms	Cefovecin Sodium; Sodium (6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(5-carboxy-1-methyl-1H-pyrrol-2-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; Convenia (Brand Name); Cefovecin; Cefovecinum; UNII-6QZ5Y2D5QH
EINECS	Contact for details

Quality Control

Our Cefovecin Sodium is manufactured under strict quality management systems. Each batch is tested to ensure it meets high-purity standards suitable for pharmaceutical use, with typical purity levels exceeding 98.5%. We provide comprehensive Certificates of Analysis (COA) that detail results for identity, assay, impurities, and residual solvents. Our quality commitment aligns with cGMP principles to ensure supply reliability and batch-to-batch consistency for our global B2B partners.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere packaging.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.5% - 101.0% (on anhydrous basis)
Water Content (KF)	≤ 2.0%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Meets ICH Q3C guidelines
pH (1% Solution)	6.0 - 8.0
Specific Optical Rotation	Contact for details
Bacterial Endotoxins	< 0.10 EU/mg

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