(1R)-2-[[6-[2-[(2,6-Dichlorobenzyl)oxy]ethoxy]hexyl]amino]-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanol; (αR)-α-[[[6-[2-[(2,6-Dichlorophenyl)methoxy]ethoxy]hexyl]amino]methyl]-2,2-dimethyl-4H-1,3-benzodioxin-6-methanol
Vilanterol Impurity 1 is a fully characterized chemical compound used as a reference standard of API Vilanterol. The standard offered is compliant with regulatory guidelines. Vilanterol Impurity 1 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 - 503068-37-9
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