This impurity is related to Dolutegravir stage-I 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.
Dolutegravir stage-I is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:((4S,12aS)-7-Methoxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylic Acid)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Dolutegravir Molecular Formula: C14H16N2O6
Molecular Weight: 308.29
Storage: Store in a cool, dry place.