This impurity is related to Paclitaxel EP Impurity K 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 K is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(aR,?S)-?-(Benzoylamino)-a-7-O-(Triethylsilyl) Paclitaxel ;hydroxy-benzenepropanoic Acid (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-6,12b-Bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-11-hydroxy-4a,8,13,13-tetramethyl-5-oxo-4-[(triethylsilyl)oxy]-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl Ester; 7-O-(Triethylsilyl)paclitaxel; 7-O-(Triethylsilyl)taxol; (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-9-(((2R,3R)-3-benzamido-2-hydroxy-3-phenylpropanoyl)oxy)-12-(benzoyloxy)-11-hydroxy-4a,8,13,13-tetramethyl-5-oxo-4-((triethylsilyl)oxy)-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: C53H65NO14Si
Molecular Weight: 968.2
Storage: Store in a cool, dry place.