(S)-N-((R)-1-amino-1-oxopropan-2-yl)-1-((2S,5S,8R,11S,14S,17R,20R)-2,8-bis(4-((bis(ethylamino)methylene)amino)butyl)-20-(4-chlorobenzyl)-11-(4-hydroxybenzyl)-14-(hydroxymethyl)-5-isobutyl-4,7,10,13,16,19,22-heptaoxo-17-(pyridin-3-ylmethyl)-3,6,9,12,15,18,21-heptaazatricosan-1-oyl)pyrrolidine-2-carboxamide
Ganirelix Impurity A is a fully characterized chemical compound used as a reference standard of API Ganirelix. The standard offered is compliant with regulatory guidelines. Ganirelix Impurity A 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 -
