This impurity is related to Dapagliflozin Impurity 11 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 11 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(3R,4S,5S,6R)-6-((((2S,3R,4S,5S,6R)-2-(4-Chloro-3-(4-ethoxybenzyl)phenyl)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)-3,4,5-trihydroxytetrahydro-2H-pyran-2-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Dapagliflozin Molecular Formula: C27H33ClO12
Molecular Weight: 585
Storage: Store in a cool, dry place.