(5R)-2-Oxazolidinone, 3-[6-[2-[(2,6-dichlorophenyl)Methoxy]ethoxy]hexyl]-5-(2,2-diMethyl-4H-1, 3-benzodioxin-6-yl)
Vilanterol Impurity 19 is listed by Simson Pharma as a impurity standards for laboratory research, analytical development and quality-control workflows.
Suitability is method- and purpose-specific. Before use, verify the product name, catalogue number, chemical identifiers, storage requirements and the information reported in the current product or batch documentation. Your laboratory remains responsible for method qualification or validation.
Vilanterol Impurity 19 for method validation Vilanterol Impurity 19 reference standard Vilanterol Impurity 19 for ANDA filing Vilanterol Impurity 19 for forced degradation studies Vilanterol Impurity 19 identification standard Vilanterol Impurity 19 for DMF filing Vilanterol Impurity 19 HPLC standard Vilanterol Impurity 19 supplier Vilanterol Impurity 19 manufacturer Vilanterol Impurity 19 distributor
