Docetaxel EP Impurity A | CAS 1887057-05-7 - Solicitar cotización

Docetaxel EP Impurity A is chemically 5β,20-epoxy-1,7β,10β-trihydroxy-9-oxotax-11-ene-2α,4,13α-triyl 4-acetate 13-[(2R,3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxy-3-phenylpropanoate] 2-[(2E)-2-methylbut-2-enoate] (as per EP) ; (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-Dodecahydro-4,6,9,11,12,12b-hexahydroxy-4a,8,13,13-tetramethyl-7,11-methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one 12b-acetate, 12-[(E)-2-methylbut-2-enoate], 9-ester with (2R,3S)-N-tert-butoxycarbonyl-3-phenylisoserine (as per USP). It is also known as 2-O-desbenzoyl-2-O-tiglyldocetaxel (EP) ; 2-Debenzoxyl 2-pentenoyl docetaxel (USP). Docetaxel EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Docetaxel EP Impurity A 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 Docetaxel.

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.