(5R)-2-Oxazolidinone, 3-[6-[2-[(2,6-dichlorophenyl)Methoxy]ethoxy]hexyl]-5-(2,2-diMethyl-4H-1, 3-benzodioxin-6-yl)
Vilanterol Impurity 14 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 14 for method validation Vilanterol Impurity 14 reference standard Vilanterol Impurity 14 for ANDA filing Vilanterol Impurity 14 for forced degradation studies Vilanterol Impurity 14 identification standard Vilanterol Impurity 14 for DMF filing Vilanterol Impurity 14 HPLC standard Vilanterol Impurity 14 supplier Vilanterol Impurity 14 manufacturer Vilanterol Impurity 14 distributor
