This impurity is related to Atosiban Impurity G 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.
Atosiban Impurity G is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-1-((4R,7S,10S,13S,16R)-7-(2-amino-2-oxoethyl)-13-((S)-sec-butyl)-16-(4-ethoxybenzyl)-10-((R)-1-hydroxyethyl)-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosane-4-carbonyl)-N-((S)-2-oxopiperidin-3-yl)pyrrolidine-2-carboxamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Atosiban Molecular Formula: C41H61N9O11S2
Molecular Weight: 920.1
Storage: Store in a cool, dry place.