This impurity is related to Pitavastatin Hydroxymethyl Impurity 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.
Pitavastatin Hydroxymethyl Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2-Cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl)methanolCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Pitavastatin Molecular Formula: C19H16FNO
Molecular Weight: 293.3
Storage: Store in a cool, dry place.