(8S,9S,10S,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10-(hydroxymethyl)-13-methyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one;(11?)-11,17,19,21-Tetrahydroxypregn-4-ene-3,20-dione; Hydrocortisone EP Impurity O;19-Hydroxycortisol
Hydrocortisone EP Impurity O is a fully characterized chemical compound used as a reference standard of API Cortisol. The standard offered is compliant with regulatory guidelines. Hydrocortisone EP Impurity O 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 - 154032-37-8
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