(4aS,4bR,5aR,6aS,7R,8R,9aS,9bS)-7-hydroxy-7-(2-hydroxyacetyl)-4a,6a,8-trimethyl-5a,6,6a,7,8,9,9a,9b,10,11-decahydrocyclopenta[1,2]phenanthro[4,4a-b]oxiren-2(4aH)-one; (11?,16?)-9,11-Epoxy-17,21-dihydroxy-16-methylpregna-1,4-diene-3,20-dione; 9,11?-Epoxy-17,21-dihydroxy-16?-methylpregna-1,4-diene-3,20-dione; 9,11-Epoxy-9H-cyclopenta[a]phenanthrene pregna-1,4-diene-3,20-dion
Dexamethasone EP Impurity I is a fully characterized chemical compound used as a reference standard of API Dexamethasone. The standard offered is compliant with regulatory guidelines. Dexamethasone EP Impurity I 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 - 14622-47-0
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