This impurity is related to Fluocinolone Acetonide EP Impurity L 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.
Fluocinolone Acetonide EP Impurity L is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S,6aS,6bR,7S,8aS,8bS,11aR,12aS,12bS)-2-Chloro-6b-fluoro-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a,10,10-tetramethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Fluocinolone Molecular Formula: C24H30ClFO6
Molecular Weight: 469
Storage: Store in a cool, dry place.