Category:
Preclinical Research Services
Standard:
USP, EP,
Dexamethasone Sodium Phosphate EP Impurity E is a critical reference standard used for the identification and quantification of degradation products in pharmaceutical formulations. Synthesized via controlled oxidation or hydrolysis pathways during API manufacturing, it serves as an essential tool for ensuring drug quality under ICH guidelines. Its molecular formula is C22H29FO8P and CAS number is 50724-16-8.
Store strictly below -20°C in airtight, light-resistant containers to prevent hydrolysis. Handle only with appropriate PPE in fume hoods due to potential sensitization risks. Not intended for direct clinical administration; use exclusively as a laboratory reference material.