This impurity is related to Prednisolone Impurity 14 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.
Prednisolone Impurity 14 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(8S,10R,13S,14S,17S)-11-hydroxy-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-17-carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Prednisolone Molecular Formula: C20H26O4
Molecular Weight: 330.4
Storage: Store in a cool, dry place.