This impurity is related to Desmopressin Antiparallel Impurity 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.
Desmopressin Antiparallel Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S,2'S)-1,1'-((4R,7S,10S,13S,16S,24R,27S,30S,33S,36S)-7,27-bis(2-amino-2-oxoethyl)-10,30-bis(3-amino-3-oxopropyl)-13,33-dibenzyl-16,36-bis(4-hydroxybenzyl)-6,9,12,15,18,26,29,32,35,38-decaoxo-1,2,21,22-tetrathia-5,8,11,14,17,25,28,31,34,37-decaazacyclotetracontane-4,24-dicarbonyl)bis(N-((R)-1-((2-amino-2-oxoethyl)amino)-5-guanidino-1-oxopentan-2-yl)pyrrolidine-2-carboxamide)Country of Origin: India Product Category: PeptidesAPI NAME: Desmopressin Molecular Formula: C92H128N28O24S4
Molecular Weight: 2138.4
Storage: Store in a cool, dry place.