655422
QuadraPure® TU
macroporous, 400-600 μm particle size
Sinônimo(s):
QuadraPure® Thiourea
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About This Item
Produtos recomendados
adequação da reação
reagent type: catalyst
reagent type: chelator
tamanho de partícula
400-600 μm
Descrição geral
QuadraPure® TU is a thiourea-based metal scavenger resin that can be used to prevent metal contamination that occurs during pharmaceutical or fine chemical processing.
Aplicação
Metal Scavenger: Pd, Pt, Ru, Rh, Au, Ag, Cu, Hg, Pb, Cd, Ni, Co, Fe, V, Zn
QuadraPure® TU has been used to remove color from the solution due to leaching of copper species during the copper(I)-mediated 1,2,3-triazole formation via [3+2] cycloaddition of acetylenic compounds with azides. It has also been used as a modifier for carbon pastes to develop QuadraPure® TU residue functionalized resin-modified carbon paste electrode (“TUR-CPE”) for the determination of Pb(II) ions.
Other applications include the removal of metal ions like copper and palladium that leach out during continuous flow coupling reactions.
Other applications include the removal of metal ions like copper and palladium that leach out during continuous flow coupling reactions.
Informações legais
QuadraPure is a registered trademark of Johnson Matthey Finland Oy
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
Certificados de análise (COA)
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Continuous flow ligand-free Heck reactions using monolithic Pd [0] nanoparticles.
Nikbin N, et al.
Organic Process Research & Development, 11(3), 458-462 (2007)
Sebastian Wesselbaum et al.
Angewandte Chemie (International ed. in English), 51(34), 8585-8588 (2012-07-19)
Dual role for CO(2): Pure formic acid can be obtained continuously by hydrogenation of CO(2) in a single processing unit. An immobilized ruthenium organometallic catalyst and a nonvolatile base in an ionic liquid (IL) are combined with supercritical CO(2) as
Michael J. Girgis, et al.
Organic Process Research & Development, 12, 1209-1217 (2008)
Continuous flow coupling and decarboxylation reactions promoted by copper tubing.
Zhang Y, et al.
Organic Letters, 13(2), 280-283 (2010)
Paolo Tosatti et al.
The Journal of organic chemistry, 76(13), 5495-5501 (2011-05-14)
The sequential use of Cu-catalyzed asymmetric allylic alkylation, olefin cross-metathesis, and Ir-catalyzed asymmetric allylic amination allows the concise, stereodivergent synthesis of complex chiral amines with complete regiocontrol and good diastereoselectivity, exemplified by the synthesis of a pair of diastereoisomeric unnatural
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