This impurity is related to Lovastatin EP Impurity B 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.
Lovastatin EP Impurity B is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[[(2S)-2-methylbutanoyl]oxy]-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acidCountry of Origin: India Product Category: API NAME: Molecular Formula: C24H37NaO6
Molecular Weight: 221.6
Storage: Store in a cool, dry place.