Zolpidem EP Impurity E | CAS 83192-85-2 - Request Quote
Zolpidem EP Impurity E
| SZ CAT No: | SZ-Z016006 |
| CAS No | 83192-85-2 |
| Mol.F. | C13H15NO2 |
| Mol.Wt. | 217.3 |
| Inv. Status | In Stock |
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Usage Note:
Zolpidem EP Impurity E is chemically (2E)-N,N-dimethyl-4-(4-methylphenyl)-4-oxobut-2-enamide (as per EP) ; N,N-Dimethyl-4-oxo-4-(p-tolyl)but-2-enamide (as per USP). It is also known as Tolyloyl Acrylamide (USP). Zolpidem EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Zolpidem EP Impurity E 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 Zolpidem.
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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Zolpidem EP Impurity E for Method Validation
Zolpidem Reference Standard
Zolpidem EP Impurity E for ANDA Filing
Zolpidem EP Impurity E for Forced Degradation Studies
Zolpidem EP Impurity E Identification Standards
Zolpidem EP Impurity E for DMF Filing
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SynZeal will update these details as per new developments or findings in product specifications without further notice.


