1-((8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethyl acetate;20?-Acetoxypregn-4-en-3-one; 20-Acetoxy-3-oxopregn-4-ene; 20?-Hydroxypregn-4-en-3-one Acetate; Progesterone EP Impurity E;
Progesterone EP Impurity E is a fully characterized chemical compound used as a reference standard of API Progesterone. The standard offered is compliant with regulatory guidelines. Progesterone EP Impurity E is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 5062-62-4
Related products
Mixture of Progesterone EP Impurity F and Progesterone EP Impurity G
M.F.
M.W. 394.59
CAT# AR-P02925
CAS# NA
Progesterone EP Impurity I (Mixture of Diastereomers)
M.F.
M.W. 328.49
CAT# AR-P29760
CAS# 24254-01-1
