This impurity is related to Auristatin E 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.
Auristatin E is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(S)-2-((S)-2-(dimethylamino)-3-methylbutanamido)-N-((3R,4S,5S)-1-((S)-2-((1R,2R)-3-(((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)amino)-1-methoxy-2-methyl-3-oxopropyl)pyrrolidin-1-yl)-3-methoxy-5-methyl-1-oxoheptan-4-yl)-N,3-dimethylbutanamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Auristatin Molecular Formula: C40H69N5O7
Molecular Weight: 732
Storage: Store in a cool, dry place.