Clarithromycin EP Impurity F
| VS CAT No | VS-C040007 |
| CAS No | 128940-83-0 |
| Mol.F. | C39H71NO13 |
| Mol.Wt. | 762.0 |
| Inv. Status | Custom Synthesis |
Chemical Name: 6,12-di-O-methylerythromycin A (as per EP); 6,12-Di-O-methylerythromycin A (as per USP)
Synonym: Clarithromycin Impurity F (USP) ; 12-O-Methyl Clarithromycin
Shipping Temperature: Ambient
Country of Origin: India
Smiles: C[C@@H]([C@@H]([C@H](C(O[C@@H]1CC)=O)C)O[C@@](O[C@@H](C)[C@@H]2O)([H])C[C@@]2(C)OC)[C@H]([C@@](C)(C[C@H](C([C@@H]([C@@H](O)[C@]1(C)OC)C)=O)C)OC)O[C@@](O[C@H](C)C[C@@H]3N(C)C)([H])[C@@H]3O
larithromycin EP Impurity F is chemically 6,12-di-O-methylerythromycin A (as per EP) ; 6,12-Di-O-methylerythromycin A (as per USP). It is also known as Clarithromycin Impurity F (USP) ; 12-O-Methyl Clarithromycin. Clarithromycin EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Clarithromycin EP 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 Clarithromycin.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. Vsquare products are for analytical purpose only and not for human use.