Category:
Preclinical Research Services
Standard:
USP, EP,
Sodium Fusidate EP Impurity D is a specified degradation product in the synthesis of sodium fusidate, utilized for quality control per European Pharmacopoeia standards. It serves as a critical reference standard to ensure the purity and safety of the active pharmaceutical ingredient during manufacturing processes. Molecular Formula: C31H45NO8. CAS No.: 62789-76-0.
Store strictly under inert atmosphere at 2-8°C to prevent hydrolysis. Avoid direct skin contact; use appropriate PPE including nitrile gloves and safety goggles during handling. Not intended for clinical administration or therapeutic use.