Description

Cefteram Pivoxil CAS NO 82547-58-8 is a third-generation, orally active prodrug cephalosporin antibiotic. It is valued for its broad-spectrum antibacterial activity against a wide range of Gram-positive and Gram-negative pathogens. This compound is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of advanced antibiotic formulations.

Application

• Pharmaceutical Active Ingredient (API): Core component in the manufacture of oral antibiotic medications.
• Clinical Research: Used in preclinical and clinical studies for evaluating new antibacterial therapies.
• Generic Drug Production: Serves as a key intermediate for formulating generic versions of cefteram pivoxil-based drugs.
• Veterinary Pharmaceuticals: Potential application in developing antibacterial treatments for veterinary use.
• Reference Standard: Employed as a high-purity standard in quality control (QC) and analytical laboratories.
• Academic & Institutional Research: Used in microbiological and pharmacological research within universities and institutes.

Basic Information

Item	Details
Product Name	Cefteram Pivoxil
CAS No.	82547-58-8
Molecular Formula	C₂₀H₂₅N₉O₇S₂
Molecular Weight	567.60 g/mol
Synonyms	Cefteram Pivoxil; Cefteram Pivoxil Hydrate; Cefteram Pivoxil Monohydrate; Cefteram Pivoxil (USP); Cefditoren Pivoxil (Note: Cefditoren is a distinct, related compound); (6R,7R)-7-[(Z)-2-(2-Amino-4-thiazolyl)-2-methoxyiminoacetamido]-3-[(Z)-2-(4-methyl-5-thiazolyl)vinyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid pivaloyloxymethyl ester; Ro 19-5248; T-2588; Tomiron (Brand Name)
EINECS	Contact for details

Quality Control

Our Cefteram Pivoxil is manufactured under strict quality management systems. It undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) is provided with each batch, detailing purity, identity, and impurity profiles. We can supply material compliant with various pharmacopeial standards, including USP, upon request.

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 maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0% (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
Heavy Metals	≤ 20 ppm

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