This impurity is related to Levofolite EP Impurity B 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.
Levofolite EP Impurity B is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S)-2-[4-[[[(6R)-2-amino-5-formyl-4-oxo-1,4,5,6,7,8-hexahydropteridin-6-yl]methyl](formyl)amino]benzamido]pentanedioic acid? (as per EP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Levofolite Molecular Formula: C21H23N7O8
Molecular Weight: 501.5
Storage: Store in a cool, dry place.