This impurity is related to Rosuvastatin FP 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.
Rosuvastatin FP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Ethyl (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-(N-methylmethanesulfonamido)-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Rosuvastatin Molecular Formula: C24H32FN3O6S
Molecular Weight: 509.6
Storage: Store in a cool, dry place.