This impurity is related to N-Nitroso Buserelin Impurity 1 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.
N-Nitroso Buserelin Impurity 1 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-N-((6S,9S,12R,15S,18S,21S,24S)-1-amino-12-(tert-butoxymethyl)-6-((S)-2-(ethylcarbamoyl)pyrrolidine-1-carbonyl)-15-(4-hydroxybenzyl)-18-(hydroxymethyl)-1-imino-9-isobutyl-25-(1-nitroso-1H-imidazol-4-yl)-21-((1-nitroso-1H-indol-3-yl)methyl)-8,11,14,17,20,23-hexaoxo-2,7,10,13,16,19,22-htaazapentacosan-24-yl)-5-oxopyrrolidine-2-carboxamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Buserelin Molecular Formula: C60H84N18O15
Molecular Weight: 1297.42
Storage: Store in a cool, dry place.