Ubicación del inventario
- New Jersey, USA
- Czech Republic, EU
- Mumbai, India
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Documentation
Incluye: HPLC, MASS/LC-MS, RMN de 1H, FT-IR, potencia, informe de elucidación estructural (SER) y datos analíticos adicionales según el producto.
Prednisolone Phosphate Impurity E; Synthesis Attempts and Failure Report
● Report Available Immediately
| Número de catálogo: | VE0023115 |
|---|---|
| N.º CAS: | N/A |
Pedido en línea
Información adicional sobre el Prednisolone Phosphate Impurity E: Synthesis Attempts and Failure Report (NAP Test)
Report Format
Delivered in digital PDF format. Printed copies available on request (additional shipping and handling charges apply).Report Language
English by default. Certified translations available at extra cost via our third-party translation partner.Descripción
Prednisolone Phosphate Impurity E is a derivative of Prednisolone Phosphate, a corticosteroid, containing a structural modification that raises potential concerns about impurity formation under specific conditions.
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Our synthesis failure report provides a detailed account of the findings from our synthesis attempts and rigorous testing, demonstrating the non-formation of the nitroso impurity. It offers a comprehensive overview of the evaluated conditions and the resulting data.
Prednisolone Phosphate Impurity E Technical Information
- Molecular Weight: 534.56 g/mol
- Molecular Formula: C28H30N407
- IUPAC Name: 3-(1-benzylpiperidin-3-yl) 5-methly 2, 6-dimethly-4-(3-nitrophenly)-1-nitroso-1, 4-dihydropyridine-3, 5-dicarboxylate
- CAS Number: N/A
- Synonyms: N/A
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