This impurity is related to Calcifediol EP Impurity A 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.
Calcifediol EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:9?,10a-cholesta-5,7-diene-3?,25-diolCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Calcifediol Molecular Formula: C27H44O2 : H2O
Molecular Weight: C27H44O2
Storage: Store in a cool, dry place.