Hydrocortisone Impurity 35 | CAS 83196-56-9 - Request Quote
Hydrocortisone Impurity 35
| SZ CAT No: | SZ-H008123 |
| CAS No | 83196-56-9 |
| Mol.F. | C20H25NO2 |
| Mol.Wt. | 311.4 |
| Inv. Status | Synthesis on demand |
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Hydrocortisone Impurity 35 is chemically (8S,10S,13S,14S,17R)-17-hydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,10,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-17-carbonitrile. Hydrocortisone Impurity 35 is supplied with detailed characterization data compliant with regulatory guideline. Hydrocortisone Impurity 35 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 Impurity 35 for Method Validation
Hydrocortisone Reference Standard
Hydrocortisone Impurity 35 for ANDA Filing
Hydrocortisone Impurity 35 for Forced Degradation Studies
Hydrocortisone Impurity 35 Identification Standards
Hydrocortisone Impurity 35 for DMF Filing
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