This impurity is related to Halometasone Impurity 10 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.
Halometasone Impurity 10 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:2-((6S,8S,9R,10S,11S,13S,14S,16S,17R)-2-Chloro-6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Halometasone Molecular Formula: C24H29ClF2O6
Molecular Weight: 486.9
Storage: Store in a cool, dry place.