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Prednisolone Sodium Phosphate USP Impurity F

N° de SZ CAT:SZ-P027025
Número CASNA
Mol.F.C21H27O7P
Peso Molecular422.4
Status de FaturaUnder Synthesis

Nome Químico: 21-oxo-20-phosphoryloxy-11β-hydroxypregna-1,4-17-triene-3-one (as per USP) ; 21-Oxygroup-20-Phosphoryl-11beta-Hydroxylpregna-1,4, 17-triene-3-Ketone

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C1C=C[C@@]2(C)C(CC[C@]3([H])[C@]2([H])[C@@H](O)C[C@@]4(C)[C@]3(CC/C4=C(C=O)/OP(O)(O)=O)[H])=C1

Prednisolone Sodium Phosphate USP Impurity F is chemically 21-oxo-20-phosphoryloxy-11β-hydroxypregna-1,4-17-triene-3-one (as per USP) ; 21-Oxygroup-20-Phosphoryl-11beta-Hydroxylpregna-1,4, 17-triene-3-Ketone. Prednisolone Sodium Phosphate USP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Prednisolone Sodium Phosphate USP Impurity F can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Prednisolone.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

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