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Cefoselis CAS NO 12284-10-5


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CAS No.:12284-10-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Cefoselis CAS NO 12284-10-5 is a fourth-generation cephalosporin antibiotic belonging to the β-lactam class. This compound is valued for its broad-spectrum activity against both Gram-positive and Gram-negative bacteria, including strains resistant to earlier-generation cephalosporins. It is primarily utilized in the pharmaceutical industry for the research, development, and synthesis of advanced injectable antibiotic formulations.

Application

  • Pharmaceutical Active Ingredient (API): Primary use in the formulation of injectable antibiotic drugs for clinical use.
  • Antibacterial Research: A key reference standard and intermediate in microbiological and pharmacological research studies.
  • Veterinary Medicine: Development of antibacterial treatments for veterinary applications.
  • Hospital-Acquired Infection Treatment: Research into formulations targeting multi-drug resistant infections prevalent in hospital settings.
  • Chemical Synthesis Intermediate: Serves as a crucial building block in the synthesis of more complex cephalosporin derivatives.
  • Quality Control Standard: Used as a certified reference material (CRM) in analytical laboratories for assay and impurity testing.

Basic Information

Product Name Cefoselis
CAS No. 12284-10-5
Molecular Formula C20H22N8O7S2
Molecular Weight 550.57 g/mol
Synonyms Cefoselis Sulfate; FK-037; FR-21818; Cefoselis Sulphate; (6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, (6R,7R)-
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Quality Control

Our Cefoselis is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and related substances, to ensure it meets high-grade pharmaceutical standards. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are available 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). 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%
Water Content (KF) ≤ 2.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC) Complies with ICH guidelines

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

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