Category:
Preclinical Research Services
CAS NO:
213997-73-0
Standard:
USP, EP,
Vancomycin EP Impurity A is a critical reference standard for the pharmaceutical industry, defined as a specific degradation product of vancomycin monitored during quality control. It serves as an essential tool for validating HPLC methods and ensuring compliance with European Pharmacopoeia (EP) limits. The compound is characterized by its distinct molecular structure used in purity assessment.
Store strictly at -20°C in a desiccated environment to prevent hydrolysis. Handle only within certified fume hoods using appropriate PPE due to potential sensitization risks. Do not use for clinical administration; intended solely for analytical purposes.