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Prednisolone Impurity 21

SZ CAT No SZ-P027072
Mol.F. C20H24O11P2 : 4(Na)
Mol.Wt. 502.4 : 4(23.0)
Inv. Status Custom Synthesis

Smiles: C[C@@]12[C@](C(OP([O-])([O-])=O)=O)(O)CC[C@@]1([H])[C@@](CCC3=CC4=O)([H])[C@@]([H])([C@]3(C=C4)C)[C@@H](OP([O-])([O-])=O)C2.[Na+].[Na+].[Na+].[Na+]

Inchi: InChI=1S/C28H46N4/c1-2-3-4-5-10-13-20-30-28-18-25-32(26-19-28)22-15-12-9-7-6-8-11-14-21-31-23-16-27(29)17-24-31/h16-19,23-26,29H,2-15,20-22H2,1H3

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