Category:
Preclinical Research Services
CAS NO:
24377-08-0
Standard:
USP, EP,
Progesterone EP Impurity A is a reference standard used for quality control of progesterone pharmaceuticals. It represents a specific degradation product or synthetic by-product defined in the European Pharmacopoeia. The compound features a distinct steroid backbone with modified functional groups.
This material is strictly for research and analytical use only, not for human consumption. Store in a cool, dry place protected from light at temperatures between 2°C and 8°C. Personnel must wear appropriate PPE including gloves and eye protection to prevent direct contact.