This impurity is related to Rosuvastatin EP Impurity C (Sodium Salt) 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 EP Impurity C (Sodium Salt) is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name: (3R,6E)-7-[4-(4-fluorophenyl)-2-(N-methylmethanesulfonamido)-6-(propan-2-yl)pyrimidin-5-yl]-3-hydroxy-5-oxohept-6-enoic acid Sodium salt (as per EP);(R,E)-7-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)-3-hydroxy-5-oxohept-6-enoic acid Sodium salt (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Rosuvastatin Molecular Formula: C22H25FN3NaO6S
Molecular Weight: 501.5
Storage: Store in a cool, dry place.