2-hydroxy-5-(2-((4-phenylbutan-2-yl)amino)acetyl)benzamidehydrochloride;Labetalone; 2-?Hydroxy-?5-?[2-?[(1-?methyl-?3-?phenylpropyl)?amino]?acetyl]benzamide Hydrochloride; 2-Hydroxy-5-[[(1-methyl-3-phenylpropyl)amino]acetyl]benzamide Monohydrochloride; Labetalone Hydrochloride;
Labetalol EP Impurity F HCl is a fully characterized chemical compound used as a reference standard of API Labetalol. The standard offered is compliant with regulatory guidelines. Labetalol EP Impurity F HCl is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 96441-14-4
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