This impurity is related to Retapamulin Impurity 1 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.
Retapamulin Impurity 1 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-vinyldecahydro-4,9a-propanocyclopenta[8]annulen-5-yl 2-(((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-hydroxyacetoxy)-4,7,9,12-tetramethyl-3-oxo-7-vinyldecahydro-4,9a-propanocyclopenta[8]annulen-8-yl)oxy)acetateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Retapamulin Molecular Formula: C44H66O9
Molecular Weight: 739
Storage: Store in a cool, dry place.