This impurity is related to Dapagliflozin Impurity 12 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.
Dapagliflozin Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name: (2S,3R,4R,5S,6R)-2-(4-Chloro-3-((4-ethoxyphenyl)(hydroxy)methyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triolCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Dapagliflozin Molecular Formula: C21H25ClO7
Molecular Weight: 424.9
Storage: Store in a cool, dry place.