Description

Latamoxef Sodium is a semi-synthetic, broad-spectrum oxacephem antibiotic belonging to the β-lactam class. This compound is valued for its potent activity against a wide range of Gram-positive and Gram-negative bacteria, including many strains resistant to other antibiotics. It is primarily utilized in the pharmaceutical industry for the research, development, and formulation of injectable antibacterial medications. Latamoxef Sodium CAS NO 64953-12-4 represents a critical intermediate and active pharmaceutical ingredient (API) for addressing serious systemic infections.

Application

• Pharmaceutical API Synthesis: Serves as the active pharmaceutical ingredient in the manufacture of injectable antibiotic formulations.
• Antimicrobial Research: Used in laboratory settings for studying bacterial resistance mechanisms and developing new therapeutic strategies.
• Veterinary Medicine: Employed in the development of treatments for bacterial infections in animals.
• Reference Standard: Functions as a high-purity analytical standard for quality control and regulatory testing in pharmaceutical labs.
• Hospital & Clinical Formulations: A key component in preparing sterile injectables for treating severe infections like sepsis, meningitis, and pneumonia.
• Biochemical Studies: Utilized in research to investigate the structure-activity relationship (SAR) of β-lactam antibiotics.

Basic Information

Product Name	Latamoxef Sodium
CAS No.	64953-12-4
Molecular Formula	C20H20N6O9S2
Molecular Weight	564.53 g/mol
Synonyms	Latamoxef Sodium; Moxalactam Sodium; LY127935; 6059-S; (6R,7R)-7-[(R)-2-Carboxy-2-(4-hydroxyphenyl)acetamido]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Sodium Salt; Moxam; Shiomarin
EINECS	Contact for details

Quality Control

Our Latamoxef Sodium is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. Specifications align with common pharmacopeial requirements for antibiotic APIs. A Certificate of Analysis (COA) detailing purity, potency, and impurity profiles 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, and well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under conditions that minimize exposure to atmospheric humidity to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
pH (Solution)	4.5 - 7.0
Water Content (KF)	≤ 2.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH limits
Bacterial Endotoxins	< 0.10 EU/mg
Sterility (where applicable)	Sterile

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