This impurity is related to Chlormadinone Acetate EP Impurity D is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Chlormadinone Acetate EP Impurity D is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:6-Chloro-3,20-dioxopregna-1,4,6-trien-17-yl acetate ; 17-(Acetyloxy)-6-chloropregna-1,4,6-triene-3,20-dione ; (8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-8,9,10,11,12,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-17-yl acetateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Chlormadinone Molecular Formula: C23H27ClO4
Molecular Weight: 402.9
Storage: Store in a cool, dry place.