This impurity is related to Beclometasone Dipropionate EP Impurity Mixture (F & N) 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.
Beclometasone Dipropionate EP Impurity Mixture (F & N) is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(6S,8S,9R,10S,11S,13S,14S,16S,17R)-6-Bromo-9-chloro-11-hydroxy-10,13,16-trimethyl-3-oxo-17-(2-(propionyloxy)acetyl)-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl propionate compound with (8S,9R,10S,11S,13S,14S,16S,17R)-2-bromo-9-chloro-11-hydroxy-10,13,16-trimethyl-3-oxo-17-(2-(propionyloxy)acetyl)-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl propionateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Beclomethasone Molecular Formula: C28H36BrClO7
Molecular Weight: 599.9
Storage: Store in a cool, dry place.