Droperidol EP Impurity E | CAS 1346604-17-8 - Request Quote
Droperidol EP Impurity E
| SZ CAT No: | SZ-D091006 |
| CAS No | 1346604-17-8 |
| Mol.F. | C34H34N6O3 |
| Mol.Wt. | 574.7 |
| Inv. Status | In Stock |
| Shipping Condition | Room Temperature |
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Usage Note:
Droperidol EP Impurity E is chemically 1-[1-[4-[4-[4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)-3,6-dihydropyridin-1(2H)-yl]-1-oxobutyl]phenyl]-1,2,3,6-tetrahydropyridin-4-yl]-1,3-dihydro-2H-benzimidazol-2-one (as per EP). Droperidol EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Droperidol 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 Droperidol.
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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Droperidol EP Impurity E for Method Validation
Droperidol Reference Standard
Droperidol EP Impurity E for ANDA Filing
Droperidol EP Impurity E for Forced Degradation Studies
Droperidol EP Impurity E Identification Standards
Droperidol EP Impurity E for DMF Filing
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