This impurity is related to Clobetasone Butyrate EP Impurity A 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.
Clobetasone Butyrate EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:21-Chloro-9-fluoro-17-hydroxy-16?-methylpregna-1,4-diene-3,11,20-trione Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Clobetasone Butyrate Molecular Formula: C22H26ClFO4
Molecular Weight: 408.9
Storage: Store in a cool, dry place.