Labetalol EP Impurity E - Request Quote
Labetalol EP Impurity E
| SZ CAT No: | SZ-L007006 |
| CAS No | NA |
| Mol.F. | C18H20N4O4 |
| Mol.Wt. | 356.4 |
| Inv. Status | Synthesis on demand |
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Usage Note:
Labetalol EP Impurity E is chemically Mixture of 3 stereoisomers of 5,5′-[(2Ξ,5Ξ)-piperazine-2,5-diyl]bis(2-hydroxybenzamide) (as per EP). Labetalol EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Labetalol 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 Labetalol.
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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