This impurity is related to Sitagliptin 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.
Sitagliptin EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-3-Amino-1-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl)butan-1-one phosphateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Sitagliptin Molecular Formula: C16H15F6N5O
Molecular Weight: 407.3
Storage: Store in a cool, dry place.