This impurity is related to Larotrectinib Impurity 7 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.
Larotrectinib Impurity 7 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-1-((5-((R)-2-(2,5-Difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)carbamoyl)pyrrolidin-3-yl hydrogen sulfateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Larotrectinib Molecular Formula: C21H22F2N6O5S
Molecular Weight: 508.5
Storage: Store in a cool, dry place.