Search Results for " Vilanterol "
Vilanterol Impurity 15
| N° de SZ CAT: | SZ-V031018 |
| Número CAS | NA |
| Mol.F. | C47H51Cl2NO6 |
| Peso Molecular | 796.8 |
| Status de Fatura | Custom Synthesis |
Nome Químico: (R)-2-((6-(2-((2,6-Dichlorobenzyl)oxy)ethoxy)hexyl)amino)-1-(2,2-dimethyl-4H-benzo[d][1,3]dioxin-6-yl)ethyl 2,2,2-triphenylacetate
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: CC1(C)OCC2=CC([C@@H](OC(C(C3=CC=CC=C3)(C4=CC=CC=C4)C5=CC=CC=C5)=O)CNCCCCCCOCCOCC6=C(Cl)C=CC=C6Cl)=CC=C2O1
Vilanterol Impurity 15 is chemically (R)-2-((6-(2-((2,6-Dichlorobenzyl)oxy)ethoxy)hexyl)amino)-1-(2,2-dimethyl-4H-benzo[d][1,3]dioxin-6-yl)ethyl 2,2,2-triphenylacetate. Vilanterol Impurity 15 is supplied with detailed characterization data compliant with regulatory guideline. Vilanterol Impurity 15 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. SynZeal products are for analytical purpose only and not for human use.
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