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Methylprednisolone EP Impurity L

N° de SZ CAT:SZ-M037012
Número CAS6870-94-6
Mol.F.C22H30O4
Peso Molecular358.5
Status de FaturaIn Stock

Nome Químico: 11β,17-dihydroxy-6α-methylpregna-1,4-diene-3,20-dione; 11,17-Dihydroxy-6-methyl-(6α,11β)-pregna-1,4-diene-3,20-dione; 11β,17-Dihydroxy-6α-methyl-pregna-1,4-diene-3,20-dione; 11β,17α-Dihydroxy-6α-methylpregna-1,4-diene-3,20-dione

Sinônimo: Methylprednisolone Acetate EP impurity I ; Deltamedrane; methylprednisolone acetate; methylprednisolone hydrogen succinate EP impurity G

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: CC([C@@]1(O)CC[C@@]2([H])[C@]3([H])C[C@H](C)C4=CC(C=C[C@]4(C)[C@@]3([H])[C@@H](O)C[C@]12C)=O)=O

Methylprednisolone EP Impurity L is chemically 11β,17-dihydroxy-6α-methylpregna-1,4-diene-3,20-dione; 11,17-Dihydroxy-6-methyl-(6α,11β)-pregna-1,4-diene-3,20-dione; 11β,17-Dihydroxy-6α-methyl-pregna-1,4-diene-3,20-dione; 11β,17α-Dihydroxy-6α-methylpregna-1,4-diene-3,20-dione. It is also known as Methylprednisolone Acetate EP impurity I ; Deltamedrane; methylprednisolone acetate; methylprednisolone hydrogen succinate EP impurity G. Methylprednisolone EP Impurity L is supplied with detailed characterization data compliant with regulatory guideline. Methylprednisolone EP Impurity L 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 Methylprednisolone.

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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