(2S,6aS,6bS,7aS,8aS,8bS,11aR,12aS,12bS)-2-fluoro-8b-(2-hydroxyacetyl)-6a,8a,10,10-tetramethyl-1,6a,7a,8,8a,8b,11a,12,12a,12b-decahydronaphtho[2',1':4,5]oxireno[2',3':5,6]indeno[1,2-d][1,3]dioxol-4(2H)-one;(6?,9?,11?,16?)-9,11-Epoxy-6-fluoro-21-hydroxy-16,17-[(1-methylethylidene)bis(oxy)]pregna-1,4-diene-3,20-dione
Fluocinolone Acetonide EP Impurity E is a fully characterized chemical compound used as a reference standard of API Fluocinolone Acetonide. The standard offered is compliant with regulatory guidelines. Fluocinolone Acetonide EP Impurity E 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 - 68352-03-4
