This impurity is related to Paclitaxel EP Impurity O 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.
Paclitaxel EP Impurity O is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12-(benzoyloxy)-9-(((2R,3S)-3-cinnamamido-2-hydroxy-3-phenylpropanoyl)oxy)-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-3,4,4a,5,6,9,10,11,12,12a-decahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxete-6,12b(2aH)-diyl diacetateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Paclitaxel Molecular Formula: C49H53NO14
Molecular Weight: 880
Storage: Store in a cool, dry place.