Category:
Preclinical Research Services
CAS NO:
1393890-33-9
Standard:
USP, EP,
Tacrolimus EP Impurity F is a critical reference standard for quality control of the immunosuppressant Tacrolimus. It serves as an identified degradation product or synthetic by-product defined in the European Pharmacopoeia. The compound features the molecular formula C45H74N2O9 and CAS number 180639-23-2, utilized to validate assay methods and impurity profiles during manufacturing.
Store strictly below -20°C in a desiccated environment under inert gas to prevent hydrolysis. Handle only within a fume hood using appropriate PPE, as high-potency compounds require strict containment to avoid occupational exposure.