This impurity is related to Diflucortolone Valerate Impurity 8 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.
Diflucortolone Valerate Impurity 8 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:2-((6S,8S,9R,10S,11S,13S,16R,17S)-6,9-difluoro-11-hydroxy-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 pentanoate, De-6-fluoro valerateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Diflucortolone Valerate Molecular Formula: C27H36F2O5
Molecular Weight: 478.6
Storage: Store in a cool, dry place.