This impurity is related to Raltegravir EP Impurity F 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.
Raltegravir EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Ethyl (1E)-N-[[2-[4-[[(4-fluorophenyl)methyl]carbamoyl]-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl]propan-2-yl]oxamoyl]ethanehydrazonate ; Ethyl (E)-N-{2-[(2-{4-[(4-fluorobenzyl)carbamoyl]-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl}propan-2-yl)amino]-2-oxoacetyl}acetohydrazonate (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Raltegravir Molecular Formula: C22H27FN6O6
Molecular Weight: 490.5
Storage: Store in a cool, dry place.