(8S,9R,10S,11S,13S,14S,16S,17R)-9,11-dichloro-10,13,16-trimethyl-3-oxo-17-(2-(propionyloxy)acetyl)-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl propionate; 9,11?-Dichloro-17,21-dihydroxy-16?-methyl-pregna-1,4-diene-3,20-dione Dipropionate; (8S,9R,10S,11S,13S,14S,16S,17R)-9,11-Dichloro-10,13,16-trimethyl-3-oxo-17-(2-(propionyloxy)acetyl)-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl Propionate; 11-Chlorobeclomethasone 17,21-Dipropionate; Beclometasone Dipropionate EP Impurity Q
Beclomethasone Dipropionate EP Impurity O is a fully characterized chemical compound used as a reference standard of API Beclomethasone. The standard offered is compliant with regulatory guidelines. Beclomethasone Dipropionate 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 - 14527-61-8
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