(1aR,10S,12S,12aS)-methyl 10-((3aR,3a1R,4R,5S,5aR,10bR)-4-acetoxy-3a-ethyl-5-hydroxy-8-methoxy-5-(methoxycarbonyl)-6-methyl-3a,3a1,4,5,5a,6,11,12-octahydro-1H-indolizino[8,1-cd]carbazol-9-yl)-1a-ethyl-1a,2,4,9,10,11,12,12a-octahydro-3,12-methanooxireno[2',3':8,9]azecino[4,3-b]indole-10-carboxylate
Vinorelbine EP Impurity G is a fully characterized chemical compound used as a reference standard of API Vinorelbine. The standard offered is compliant with regulatory guidelines. Vinorelbine EP Impurity G is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS -
