(5R)-2-Oxazolidinone, 3-[6-[2-[(2,6-dichlorophenyl)Methoxy]ethoxy]hexyl]-5-(2,2-diMethyl-4H-1, 3-benzodioxin-6-yl)
Vilanterol Impurity 15 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.
Buy 1199-30-0 Purchase 1199-30-0 Order 1199-30-0 Enquire 1199-30-0 1199-30-0 price 1199-30-0 supplier 1199-30-0 manufacturer 1199-30-0 exporter Vilanterol Impurity 15 for method validation Vilanterol Impurity 15 reference standard Vilanterol Impurity 15 for ANDA filing Vilanterol Impurity 15 for forced degradation studies Vilanterol Impurity 15 identification standard Vilanterol Impurity 15 for DMF filing Vilanterol Impurity 15 HPLC standard Vilanterol Impurity 15 supplier Vilanterol Impurity 15 manufacturer Vilanterol Impurity 15 distributor
