Description

Faropenem Sodium is a synthetic broad-spectrum carbapenem antibiotic, specifically formulated as the sodium salt for enhanced stability and solubility. This compound is a critical intermediate in the pharmaceutical synthesis of oral and injectable antibiotic formulations, offering potent activity against a wide range of Gram-positive and Gram-negative bacteria. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development and production of advanced antibacterial therapies.

Application

• Active Pharmaceutical Ingredient (API) Synthesis: Serves as the key intermediate for the production of finished faropenem antibiotic dosage forms.
• Pharmaceutical Research & Development: Used in preclinical and clinical studies to develop new antibacterial drugs and combination therapies.
• Generic Drug Manufacturing: Essential for companies producing generic versions of faropenem-based antibiotics.
• Veterinary Medicine: Applied in the development of antibacterial treatments for veterinary use.
• Reference Standard: Employed as a high-purity analytical standard for quality control and regulatory testing in laboratories.

Basic Information

Item	Details
Product Name	Faropenem Sodium
CAS No.	122547-49-3
Molecular Formula	C12H14NNaO5S
Molecular Weight	307.30 g/mol
Synonyms	Faropenem Sodium Salt; (5R,6S)-6-[(1R)-1-Hydroxyethyl]-7-oxo-3-[(2R)-tetrahydro-2-furanyl]-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic Acid Sodium Salt; Faropenem Na; SUN-5555; FRPM; Farom
EINECS	Contact for details

Quality Control

Our Faropenem Sodium is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing specifications for identity, purity, and impurities 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 place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 2.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Bacterial Endotoxins	< 0.10 EU/mg

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