Category:
Preclinical Research Services
CAS NO:
1020157-01-0
Standard:
USP, EP,
Olmesartan EP Impurity D is a critical reference standard for pharmaceutical quality control, specifically designed to support the identification and quantification of degradation products in Olmesartan medoxomil formulations. Synthesized via precise organic coupling reactions, it serves as an essential tool for HPLC method validation under ICH guidelines. The compound features the molecular formula C25H28N6O4 and carries CAS number 197013-99-9.
Storage requires sealed containers at 2°C–8°C away from light and moisture. Handling must occur within fume hoods using appropriate PPE due to potential sensitization risks; strictly prohibited for direct clinical administration.