This impurity is related to Ulipristal Acetate N-Oxide 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.
Ulipristal Acetate N-Oxide Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:4-((8S,11R,13S,14S,17R)-17-acetoxy-17-acetyl-13-methyl-3-oxo-2,3,6,7,8,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-11-yl)-N,N-dimethylaniline oxideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ulipristal Molecular Formula: C30H37NO5
Molecular Weight: 491.6
Storage: Store in a cool, dry place.