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Postion:Product Catalog >Cefuroxime Sulfoxide
Cefuroxime Sulfoxide
  • Cefuroxime Sulfoxide
  • Cefuroxime Sulfoxide
  • Cefuroxime Sulfoxide
  • Cefuroxime Sulfoxide
  • Cefuroxime Sulfoxide

Cefuroxime Sulfoxide NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Cefuroxime Sulfoxide Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/07/31

Cefuroxime Sulfoxide

Article illustration

Product Information

  • Product Code:C022021

  • English Name:Cefuroxime Sulfoxide

  • English Alias:(6R,7R)-3-((carbamoyloxy)methyl)-7-((Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid 5-oxide

  • CAS No.:[Not Available]

  • Molecular Formula:C??H??N?O?S

  • Molecular Weight:440.38

Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR (1H, 13C), HRMS, and circular dichroism for stereostructure, suitable for precise analysis of Cefuroxime sulfoxide impurities.

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.2% in acetonitrile-water solution within 6 months.

Applications

  • Quality Control Testing:Used for UPLC-MS/MS detection of sulfoxide impurities in Cefuroxime API and formulations, controlling impurity content to meet ICH Q3A standards (≤0.1%).

  • Process Optimization Research:Monitors Cefuroxime Sulfoxide formed by oxidation side reactions during Cefuroxime synthesis or storage, reducing generation by >60% by adjusting reaction temperature (e.g., 5-10℃) and antioxidant dosage.

  • Method Validation:Serves as a standard for developing sulfoxide impurity detection methods, verifying UPLC resolution (≥3.0) and LOD (0.01 ng/mL).

Background Description

Cefuroxime, a second-generation cephalosporin antibiotic, may generate Cefuroxime Sulfoxide as an oxidation impurity during production (sulfur atom oxidation) or under storage conditions (e.g., light, high temperature). The sulfoxide structure of this impurity may affect Cefuroxime's antibacterial activity, stability, and safety. With stricter international regulatory requirements for drug impurity control, studying such oxidative degradation impurities is crucial for ensuring Cefuroxime quality.

Research Status

  • Detection Technology:UPLC-MS/MS with C18 column (1.7μm) and 0.1% formic acid-acetonitrile gradient elution achieves separation within 3 minutes, with LOD of 0.005 ng/mL for trace analysis.

  • Formation Mechanism:Formed by oxidation of the sulfur atom in Cefuroxime molecules under the action of oxygen or peroxides; optimizing antioxidant conditions (e.g., nitrogen protection) and purification processes (e.g., cryogenic crystallization) inhibits its formation.



We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.


This product is intended for laboratory use only!

WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com


NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 







Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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