Category:
Preclinical Research Services
CAS NO:
7636-26-2
Standard:
USP, EP,
Levodopa EP Impurity C is a critical reference standard used in pharmaceutical quality control. It serves as an identification and quantification tool for process-related impurities during the synthesis of Levodopa, primarily formed via oxidative pathways. The molecular formula is C9H11NO4, with CAS No. 527-08-6.
Store strictly under inert atmosphere at controlled temperatures to prevent oxidation. Handle only within certified fume hoods using appropriate PPE due to potential sensitization risks. This substance is exclusively for laboratory use and not intended for direct human administration.