Category:
Preclinical Research Services
CAS NO:
16088-19-0
Standard:
USP, EP,
Neostigmine EP Impurity C is a critical reference standard for pharmaceutical quality control, specifically designed to identify and quantify degradation products in neostigmine preparations. Synthesized via controlled oxidation or hydrolysis pathways during active pharmaceutical ingredient manufacturing, its molecular formula is C8H11NO2 with CAS No. 60-54-4.
Store at -20°C in a desiccated environment to prevent hydrolysis. Handle only within certified fume hoods using appropriate PPE due to potential cholinergic toxicity risks associated with structural analogs.