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Prednisolone Impurity 19

SZ CAT No SZ-P027069
Mol.F. C24H32O5
Mol.Wt. 400.5
Inv. Status Custom Synthesis

Chemical Name: 2-hydroxy-1-(17-hydroxy-4',10,13-trimethyl-6,7,8,10,12,13,14,15,16,17-decahydrospiro[cyclopenta[a]phenanthrene-3,2'-[1,3]dioxolan]-17-yl)ethan-1-one

Smiles: CC12C3=CCC4(C)C(CCC4(C(CO)=O)O)C3CCC1=CC5(OCC(C)O5)C=C2

Inchi: InChI=1/C24H32O6/c1-21-9-10-23(29-14-16(12-25)30-23)11-15(21)3-4-17-18(21)5-7-22(2)19(17)6-8-24(22,28)20(27)13-26/h5,9-11,16-17,19,25-26,28H,3-4,6-8,12-14H2,1-2H3

Validated stability indicating RP-​LC assay for determination of gatifloxacin and prednisolone acetatein ophthalmic preparations and biological samples
By Qadir, Muhammad A.; Shahzad, Shabnam; Ahmed, Mahmood; Razzaq, Syed S.; Shafiq, Muhmmad I.
From Latin American Journal of Pharmacy (2016), 35(5), 912-920
Novel stability indicating RP-​HPLC method for the simultaneous estimation of moxifloxacin and prednisolone in bulk and their combined dosage form
By Potnuri, Naga Raju; Rao, G. Devala; Prasad, Y. Rajendra
From International Journal of Pharmaceutical Sciences and Research (2015), 6(5), 1965-1973
Development and validation of a new stability indicating reversed phase liquid chromatographic method for the determination of prednisolone acetate and impurities in an ophthalmic suspension
By Marley, Adrian; Stalcup, Apryll M.; Connolly, Damian
From Journal of Pharmaceutical and Biomedical Analysis (2015), 102, 261-266