Hydrocortisone Cyclic Phosphate Impurity - Request Quote
Hydrocortisone Cyclic Phosphate Impurity
| SZ CAT No: | SZ-H008119 |
| CAS No | NA |
| Mol.F. | C21H28O7P : Na |
| Mol.Wt. | 423.4 : 23.0 |
| Inv. Status | Synthesis on demand |
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Hydrocortisone Cyclic Phosphate Impurity is chemically Sodium (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-10,13-dimethyl-3,5'-dioxo-1,2,3,6,7,8,9,10,11,12,13,14,15,16-tetradecahydrospiro[cyclopenta[a]phenanthrene-17,4'-[1,3,2]dioxaphosphinan]-2'-olate 2'-oxide. Hydrocortisone Cyclic Phosphate Impurity is supplied with detailed characterization data compliant with regulatory guideline. Hydrocortisone Cyclic Phosphate Impurity 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 Hydrocortisone.
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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Hydrocortisone Cyclic Phosphate Impurity for Method Validation
Hydrocortisone Reference Standard
Hydrocortisone Cyclic Phosphate Impurity for ANDA Filing
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