Search Results for " Methylprednisolone "
Methylprednisolone EP Impurity L
| SZ CAT No: | SZ-M037012 |
| CAS No | 6870-94-6 |
| Mol.F. | C22H30O4 |
| Mol.Wt. | 358.5 |
| Inv. Status | In Stock |
| Rel. CAT No | SZ-F038007 |
Chemical Name: 11β,17-Dihydroxy-6α-methylpregna-1,4-diene-3,20-dione (as per EP) ; 11β,17,21,21-Tetrahydroxy-6α-methylpregna-1,4-diene-3,20-dione (as per USP)
Synonym: Methylprednisolone Acetate EP impurity I ; Deltamedrane; methylprednisolone acetate; methylprednisolone hydrogen succinate EP impurity G ; Methylprednisolone USP related compound B
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: 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 (as per EP) ; 11β,17,21,21-Tetrahydroxy-6α-methylpregna-1,4-diene-3,20-dione (as per USP). It is also known as Methylprednisolone Acetate EP impurity I ; Deltamedrane; methylprednisolone acetate; methylprednisolone hydrogen succinate EP impurity G ; Methylprednisolone USP related compound B. 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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