This impurity is related to Halometasone Impurity 7 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 7 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(Z)-2-((6S,8S,9R,10S,11S,13S,14S,16R)-2-Chloro-6,9-difluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-3,6,7,8,9,10,11,12,13,14,15,16-dodecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-2-hydroxyacetaldehydeCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Halometasone Molecular Formula: C22H25ClF2O4
Molecular Weight: 426.9
Storage: Store in a cool, dry place.