This impurity is related to Methylprednisolone Impurity 16 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.
Methylprednisolone Impurity 16 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:4-(2-((6S,8S,9S,10R,11S,13S,14S,17R)-11-((3-carboxypropanoyl)oxy)-17-hydroxy-6,10,13-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethoxy)-4-oxobutanoic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Methylprednisolone Molecular Formula: C30H38O11
Molecular Weight: 574.6
Storage: Store in a cool, dry place.