This impurity is related to Fulvestrant 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.
Fulvestrant EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:7?[9-[(RS)-(4,4,5,5,5-pentafluoropentyl)sulfinyl]nonyl]estra-1,3,5(10)-triene-3,17?diol ; 7?{9-[(4,4,5,5,5,-Pentafluoropentyl)sulfinyl]nonyl}estra-1,3,5(10)-triene-3,17?diol (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: fulvestrant Molecular Formula: C32H47F5O3S
Molecular Weight: 606.8
Storage: Store in a cool, dry place.