Description

Cefcapene Pivoxil Hydrochloride is a third-generation, orally active cephalosporin antibiotic prodrug. This compound is valued for its broad-spectrum antibacterial activity against both gram-positive and gram-negative pathogens, offering enhanced stability and bioavailability. It is a critical active pharmaceutical ingredient (API) primarily required by pharmaceutical manufacturers for the formulation of oral antibiotic medications.

Application

• Pharmaceutical API: Primary use as the active ingredient in the manufacture of oral antibiotic capsules and tablets.
• Respiratory Tract Infections: Formulation of medications targeting bronchitis, pneumonia, and other bacterial respiratory diseases.
• Skin and Soft Tissue Infections: Used in antibiotic treatments for bacterial infections of the skin and underlying tissues.
• Otolaryngological Infections: Key component in drugs for treating bacterial sinusitis, tonsillitis, and otitis media.
• Urinary Tract Infections (UTIs): Formulation of effective treatments for uncomplicated bacterial UTIs.
• Research & Development: Serves as a reference standard and building block in antimicrobial research and new drug development.
• Veterinary Pharmaceuticals: Potential application in developing antibacterial treatments for veterinary use.

Basic Information

Product Name	Cefcapene Pivoxil Hydrochloride
CAS No.	147816-23-7
Molecular Formula	C23H31N5O8S2 • HCl
Molecular Weight	606.11 g/mol
Synonyms	Cefcapene Pivoxil HCl; Cefcapene Pivoxil Hydrochloride; (6R,7R)-7-[(Z)-2-(2-Amino-4-thiazolyl)-2-methoxyiminoacetamido]-3-(cyclopent-1-enylmethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid pivaloyloxymethyl ester hydrochloride; Flomox; Cefcapene pivoxil monohydrochloride; Cefcapene Pivoxil (Hydrochloride); Cefcapene Pivoxil HCl Salt
EINECS	Contact for details

Quality Control

Our Cefcapene Pivoxil Hydrochloride 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 guarantee traceability and compliance with your specifications.

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 (moisture-sensitive) nature, the container must be kept tightly sealed in a low-humidity environment to prevent degradation.

Specification

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

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