Search Results for " Dexamethasone sodium phosphate "
Dexamethasone Sodium Phosphate EP Impurity H
| N° de SZ CAT: | SZ-D060036 |
| Número CAS | 162968-22-1 |
| Mol.F. | C22H32FO8P |
| Peso Molecular | 474.5 |
| Status de Fatura | Custom Synthesis |
Nome Químico: 2-((8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl dihydrogen phosphate
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: O=P(O)(OCC([C@@]1(O)[C@H](C)C[C@@]2([H])[C@]3([H])CCC4=CC(CC[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)=O)=O)O
Dexamethasone Sodium Phosphate EP Impurity H is chemically 2-((8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl dihydrogen phosphate. Dexamethasone Sodium Phosphate EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Dexamethasone Sodium Phosphate EP Impurity H 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 Dexamethasone sodium phosphate.
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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