Shenzhen Excellent Biomedical Technology Co.,Ltd.(SZEB) is a leading supplier of high quality pharmaceutical impurities,API related compounds,intermediates,labeled standards and impurity custom synthesis services.E-mail:sales@ex-biotech.com.
Discover all our products through our official website (https://www.ex-biotech.com/), and get in touch if you have any questions about how we can help support your work. Email:sale@ex-biotech.com.
*The following content is generated by AI and is for reference only.
Overview
Cefoxitin EP Impurity D is a critical reference standard for pharmaceutical quality control, specifically defined within the European Pharmacopoeia (EP) monograph for Cefoxitin. It serves as an identification and quantification tool for process-related impurities during synthesis. The compound acts as a degradation product or synthetic intermediate.
Molecular Formula: C
19H
23N
5O
6S
CAS No: 7428-04-2
Application
- Quality Control: Used in HPLC method validation to identify and quantify trace levels of related substances in bulk API batches.
- R&D: Employed in stability studies to monitor degradation pathways under various stress conditions.
- Regulatory Compliance: Essential for generating data required by FDA and EMA submissions to ensure purity specifications are met.
Precautions
- Storage: Maintain at -20°C in a dry, inert atmosphere to prevent hydrolysis.
- Handling: Use appropriate PPE; avoid inhalation of dust or skin contact.
- Usage: Strictly for laboratory research and analytical calibration only; not for human clinical administration.