(8S,9S,10R,11S,13S,14S,16R,17S)-11,16,17-trihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one; 16?-Hydroxycortisol; U 34908; 16?,17-Dihydroxy-corticosterone;11?,16?,17,21-Tetrahydroxy-pregn-4-ene-3,20-dione; 11?,16?,17,21-Tetrahydroxypregn-4-ene-3,20-dione
Budesonide EP Impurity H is a fully characterized chemical compound used as a reference standard of API Budesonide. The standard offered is compliant with regulatory guidelines. Budesonide EP Impurity H 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 - 1171-81-9
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