This impurity is related to Pitavastatin Impurity 15 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 Impurity 15 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name: 3-((3S,5R,E)-6-Carboxy-3,5-dihydroxyhex-1-en-1-yl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline 1-oxideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Pitavastatin Molecular Formula: C25H24FNO5
Molecular Weight: 437.5
Storage: Store in a cool, dry place.