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.
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CAS 95815-58-0
Rac Naproxen-d3
Deuterated active pharmaceutical ingredient
Defluoroofloxacin
fluoroquinolone antibiotic impurity standard
Sotalol hydrochloride
beta-adrenergic antagonist antiarrhythmic agent
(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
antibiotic active pharmaceutical ingredient
(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
USJJKJYVBSEDNP-CNPAUTQISA-N
C[C@]12C[C@@H]([C@H]3[C@H]([C@@]1(CC[C@@]2(C(=O)CO)O)O)CCC4=CC(=O)C=C[C@]34C)O