This impurity is related to Methylprednisolone Dimer Impurity (RRT 2.28) 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.
Methylprednisolone Dimer Impurity (RRT 2.28) is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(6S,8S,9S,10R,11S,13S,14S,17R)-11-hydroxy-17-(((6S,8S,9S,10R,11S,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-6,10,13-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-11-yl)oxy)-17-(2-hydroxyacetyl)-6,10,13-trimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Methylprednisolone Molecular Formula: C44H58O9
Molecular Weight: 730.9
Storage: Store in a cool, dry place.