12816
Copper
foil, ≥99.8% (complexometric)
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About This Item
Formula empirica (notazione di Hill):
Cu
Numero CAS:
Peso molecolare:
63.55
Numero CE:
Numero MDL:
Codice UNSPSC:
12141711
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
≥99.8% (complexometric)
Stato
foil
Impiego in reazioni chimiche
core: copper
reagent type: catalyst
Resistività
1.673 μΩ-cm, 20°C
P. ebollizione
2567 °C (lit.)
Punto di fusione
1083.4 °C (lit.)
Densità
8.94 g/mL at 25 °C (lit.)
Cationi in tracce
As: ≤2 mg/kg
Fe: ≤50 mg/kg
Mn: ≤50 mg/kg
Pb: ≤500 mg/kg
Sb: ≤50 mg/kg
Sn: ≤50 mg/kg
Stringa SMILE
[Cu]
InChI
1S/Cu
RYGMFSIKBFXOCR-UHFFFAOYSA-N
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I clienti hanno visto anche
Hiroshi Sato et al.
Science (New York, N.Y.), 343(6167), 167-170 (2013-12-18)
Carbon monoxide (CO) produced in many large-scale industrial oxidation processes is difficult to separate from nitrogen (N2), and afterward, CO is further oxidized to carbon dioxide. Here, we report a soft nanoporous crystalline material that selectively adsorbs CO with adaptable
Seonah Kim et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(1), 149-154 (2013-12-18)
Lytic polysaccharide monooxygenases (LPMOs) exhibit a mononuclear copper-containing active site and use dioxygen and a reducing agent to oxidatively cleave glycosidic linkages in polysaccharides. LPMOs represent a unique paradigm in carbohydrate turnover and exhibit synergy with hydrolytic enzymes in biomass
Stephen G Kaler et al.
The New England journal of medicine, 358(6), 605-614 (2008-02-08)
Menkes disease is a fatal neurodegenerative disorder of infancy caused by diverse mutations in a copper-transport gene, ATP7A. Early treatment with copper injections may prevent death and illness, but presymptomatic detection is hindered by the inadequate sensitivity and specificity of
Daniel L Priebbenow et al.
Organic letters, 15(24), 6155-6157 (2013-11-28)
A method has been developed for the preparation of N-alkynylated sulfoximines involving the copper-catalyzed decarboxylative coupling of sulfoximines with aryl propiolic acids. A range of substituents on both the sulfoximidoyl moiety and the aryl group of the propiolic acid were
Huawen Huang et al.
Organic letters, 15(24), 6254-6257 (2013-11-23)
A rapid and environmentally friendly conversion of pyridine to imidazo[1,2-a]pyridines has been developed via copper-catalyzed aerobic dehydrogenative cyclization with ketone oxime esters.
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