Paclitaxel Impurity 40

Paclitaxel Impurity 40 is chemically (αR,βS)-β-(Benzoylamino)-α-[[(2,2,2-trichloroethoxy)carbonyl]oxy]-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-4-O-(triethylsilyl)-11-hydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl Ester;. It is also known as 2’-O-{[(2,2,2,-Trichloroethyl)oxy]carbonyl-7-O-(triethylsilyl) Paclitaxel. Paclitaxel Impurity 40 is supplied with detailed characterization data compliant with regulatory guideline. Paclitaxel Impurity 40 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Paclitaxel.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.