655422
QuadraPure® TU
macroporous, 400-600 μm particle size
Synonyma:
QuadraPure® Thiourea
Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
About This Item
Doporučené produkty
reaction suitability
reagent type: catalyst
reagent type: chelator
particle size
400-600 μm
General description
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.
Application
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.
Legal Information
QuadraPure is a registered trademark of Johnson Matthey Finland Oy
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Osvědčení o analýze (COA)
Vyhledejte osvědčení Osvědčení o analýze (COA) zadáním čísla šarže/dávky těchto produktů. Čísla šarže a dávky lze nalézt na štítku produktu za slovy „Lot“ nebo „Batch“.
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Dokumenty související s produkty, které jste v minulosti zakoupili, byly za účelem usnadnění shromážděny ve vaší Knihovně dokumentů.
[3+ 2] Cycloaddition of acetylenes with azides to give 1, 4-disubstituted 1, 2, 3-triazoles in a modular flow reactor.
Smith CD, et al.
Organic & Biomolecular Chemistry, 5(10), 1559-1561 (2007)
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
Continuous flow ligand-free Heck reactions using monolithic Pd [0] nanoparticles.
Nikbin N, et al.
Organic Process Research & Development, 11(3), 458-462 (2007)
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)
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