(2R,3R,4R,5R,6R)-5-chloro-2-(((1R,3R,4S,7R)-3-(chloromethyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4-diol; 3,5-Anhydro-1-chloro-1-deoxy-?-D-fructofuranosyl 4-Chloro-4-deoxy-?-D-galactopyranoside; 2,5-Dioxabicyclo[2.2.1]heptane ?-D-galactopyranoside
Sucralose EP Impurity G is a fully characterized chemical compound used as a reference standard of API Sucralose. The standard offered is compliant with regulatory guidelines. Sucralose 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 - 105066-20-4
