This impurity is related to Paclitaxel 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.
Paclitaxel Impurity 1 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Benzenepropanoic acid, a-?hydroxy-??-?[(2-?methyl-?1-?oxopropyl)?amino]?-?, (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-?4,?11-?dihydroxy-?4a,?8,?13,?13-?tetramethyl-?5-?oxo-?7,?11-?methano-?1H-?cyclodeca[3,?4]?benz[1,?2-?b]?oxet-?9-?yl ester, (aR,??S)?-; Benzenepropanoic acid, a-hydroxy-?-[(2-methyl-1-oxopropyl)amino]-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, [2aR-[2aa,4?,4a?,6?,9a(aR*,?S*),11a,12a,12aa,12ba]]-; CanadensolCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Paclitaxel Molecular Formula: C44H53NO14
Molecular Weight: 819.9
Storage: Store in a cool, dry place.