254177
Copper
beads, 2-8 mm, 99.9995% trace metals basis
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About This Item
Empirical Formula (Hill Notation):
Cu
CAS Number:
Molecular Weight:
63.55
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12141711
EC Number:
231-159-6
MDL number:
Quality Level
assay
99.9995% trace metals basis
form
beads
reaction suitability
core: copper
resistivity
1.673 μΩ-cm, 20°C
particle size
2-8 mm
bp
2567 °C (lit.)
mp
1083.4 °C (lit.)
density
8.94 g/mL at 25 °C (lit.)
SMILES string
[Cu]
InChI
1S/Cu
InChI key
RYGMFSIKBFXOCR-UHFFFAOYSA-N
General description
Copperbeads are versatile catalysts in organic synthesis and material science because of their recyclability, sustainability, and superior catalytic performance. They are employed as heterogeneous catalysts in a range of organic reactions, including Click chemistry and cross-coupling reactions.
Application
- Spray-dried ternary bioactive glass microspheres: This study examines the structural effects of copper doping in bioactive glass microspheres, highlighting their potential in biomedical applications for controlled drug delivery (Vecchio et al., 2024).
- Design, Synthesis, and Characterization of Stable Copper Nanofluid: Reports on the synthesis of copper nanofluids for enhanced thermal conductivity, relevant in industrial production and various thermal applications (Bhat et al., 2024).
Storage Class
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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
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