午夜插插,噜噜噜影院,啪啪伊人网,欧美熟夫,景甜吻戏视频,男人强操性感蕾丝美女视频在线网站,日本美女跳舞视频

Welcome to chemicalbook!
+1 (818) 612-2111
RFQ
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

RFQ
skype
MY Account
Top
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 CAS No.: 69384-96-9
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31

Cefuroxime Sulfoxide

Article illustration

Product Information

  • Product Code:C022019

  • English Name:Cefuroxime Impurity 19

  • English Alias:(E)-2-(furan-2-yl)-2-(methoxyimino)acetic acid

  • CAS No.:69384-96-9

  • Molecular Formula:C?H?NO?

  • Molecular Weight:169.13

Advantages

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

  • Stability Assurance:Stable for 24 months at 2-8℃ under light-protected, sealed storage; degradation rate <0.3% in methanol solution within 1 month.

Applications

  • Quality Control Testing:Used for HPLC and LC-MS detection of Impurity 19 in Cefuroxime API and formulations, controlling impurity content to meet ICH Q3A standards (≤0.1%).

  • Process Optimization Research:Monitors impurity formation during Cefuroxime synthesis, reducing generation by >50% by adjusting methoxyimination temperature (e.g., 10-15℃) and reaction time.

  • Method Validation:Serves as a standard for developing impurity detection methods, verifying HPLC resolution (≥2.0) and LOD (0.01 ng/mL).

Background Description

Cefuroxime, a second-generation cephalosporin antibiotic, is used to treat various bacterial infections. Impurity 19 may originate from side reactions during the synthesis of Cefuroxime's side chain. The furan ring and methoxyimino group in its structure may affect drug stability and antibacterial activity. With stricter WHO requirements for antibiotic impurity control, studying such process impurities is key to ensuring drug quality.

Research Status

  • Detection Technology:UPLC-MS/MS with C18 column (1.7μm) and 0.1% formic acid-acetonitrile gradient elution achieves separation within 1.8 minutes, with LOD of 0.002 ng/mL for trace analysis.

  • Formation Mechanism:Formed by reaction of furanacetic acid with methoxyamine under alkaline conditions (e.g., sodium carbonate catalysis); optimizing reaction pH (8.0-9.0) and reagent ratio inhibits side reactions.

  • Safety Evaluation:In vitro antibacterial assays show MIC >64 μg/mL against Staphylococcus aureus (Cefuroxime MIC=0.5 μg/mL), with low toxicity but requiring ≤0.1% limit. Long-term stability testing is ongoing for degradation monitoring.

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.

You may like

Recommended supplier

Product name Price   Suppliers Update time
$/
VIP5Y
RongNa Biotechnology Co.,Ltd
2025-04-29
$0.00/1kg
VIP1Y
Shaanxi Xianhe Biotech Co., Ltd
2025-04-23
$0.00/1kg
VIP3Y
Henan Aochuang Chemical Co.,Ltd.
2022-09-27
INQUIRY