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Vilanterol Impurity 1 is chemically (R)-5-(2-((6-(2-((2,6-Dichlorobenzyl)oxy)ethoxy)hexyl)amino)-1-hydroxyethyl)-2-hydroxybenzaldehyde 2,2,2-trifluoroacetate.
Vilanterol Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Vilanterol Impurity 1 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 Vilanterol.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.