(8R,9S,10R,13S,14S,17R)-2-(((8R,9S,10R,13S,14S,17R)-17-acetoxy-17-acetyl-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl)methyl)-17-acetyl-6,10,13-trimethyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-ylacetate
Megestrol Acetate EP Impurity L is a fully characterized chemical compound used as a reference standard of API Megestrol. The standard offered is compliant with regulatory guidelines. Megestrol Acetate EP Impurity L 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 - NA
Related products
Megestrol Acetate (Medroxyprogesterone Acetate EP Impurity G)
M.F.
M.W. 384.52
CAT# AR-M01274
CAS# 595-33-5
