Prednisolone EP Impurity E is a steroid compound used as a reference standard for the analysis of prednisolone, a synthetic corticosteroid. It is primarily employed in quality control and research settings to identify and quantify this specific impurity during pharmaceutical manufacturing.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 95815-58-0
Rac Naproxen-d3
pharmaceutical raw material
Defluoroofloxacin
pharmaceutical raw material
Sotalol hydrochloride
pharmaceutical raw material
(3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-14-ethyl-7,12,13-trihydroxy-4-(5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl)oxy-6-[3-hydroxy-6-methyl-4-[methyl(trideuterio(113C)methyl)amino]oxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
pharmaceutical raw material
(8R,9S,10R,11S,13S,14R,17R)-11,14,17-trihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-3-one
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