(6S,8S,9R,10S,11S,13S,14S,16S,17R)-6,9-dichloro-11-hydroxy-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; 6?-Chlorobeclomethasone Dipropionate; (6?,11?,16?)-6,9-Dichloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)-pregna-1,4-diene-3,20-dione; (6S,8S,9R,10S,11S,13S,14S,16S,17R)-6,9-dichloro-11-Hydroxy-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; Beclomethasone Dipropionate EP Impurity E
Beclomethasone Dipropionate EP Impurity E 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 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 - 887130-68-9
Related products
Beclometasone Dipropionate EP Impurity S (Beclometasone Tripropionate)
M.F.
M.W. 577.11
CAT# AR-B01077
CAS# 1709825-83-1
