This impurity is related to Vilanterol Impurity 28 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.
Vilanterol Impurity 28 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2R,3R,4S,5R,6R)-2-(((1S,2R,3R)-1-((2R,6R)-4-(6-(2-((2,6-dichlorobenzyl)oxy)ethoxy)hexyl)-2-hydroxy-6-(4-hydroxy-3-(hydroxymethyl)phenyl)morpholin-2-yl)-1,3,4-trihydroxybutan-2-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triolCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Vilanterol Molecular Formula: C36H53Cl2NO15
Molecular Weight: 810.7
Storage: Store in a cool, dry place.