This impurity is related to Atorvastatin EP Impurity P 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.
Atorvastatin EP Impurity P is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:[(4R,6R)-6-[2-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]ethyl]-2,2-dimethyl-1,3-dioxan-4-yl]acetic acid Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Atorvastatin Molecular Formula: C36H39FN2O5
Molecular Weight: 598.7
Storage: Store in a cool, dry place.