Labetalol EP Impurity F (HCl salt) | CAS 96441-14-4 - Request Quote
Labetalol EP Impurity F (HCl salt)
| SZ CAT No: | SZ-L007035 |
| CAS No | 96441-14-4 |
| Mol.F. | C19H22N2O3 |
| Mol.Wt. | 326.4 |
| Inv. Status | Under QC Approval |
| Rel. CAS No | 85665-85-6 (free base) |
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Usage Note:
Labetalol EP Impurity F (HCl salt) is chemically 2-Hydroxy-5-[2-[[(2RS)-4-phenylbutan-2-yl]amino]acetyl]benzamide hydrochloride (as per EP) ; 2-Hydroxy-5-[(4-phenylbutan-2-yl)glycyl]benzamide hydrochloride (as per USP). It is also known as Labetalol USP Related Compound F ; Labetalol Keto Impurity ; Labetalone. Labetalol EP Impurity F (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Labetalol EP Impurity F (HCl salt) 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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Labetalol EP Impurity F (HCl salt) for Method Validation
Labetalol Reference Standard
Labetalol EP Impurity F (HCl salt) for ANDA Filing
Labetalol EP Impurity F (HCl salt) for Forced Degradation Studies
Labetalol EP Impurity F (HCl salt) Identification Standards
Labetalol EP Impurity F (HCl salt) for DMF Filing
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