774103
Copper
nanopowder, 60-80 nm particle size (APS), ≥99.5% trace metals basis
Synonym(s):
Copper nanoparticles
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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:
41141805
EC Number:
231-159-6
MDL number:
InChI key
RYGMFSIKBFXOCR-UHFFFAOYSA-N
InChI
1S/Cu
SMILES string
[Cu]
assay
≥99.5% trace metals basis
form
nanopowder
resistivity
1.673 μΩ-cm, 20°C
bp
2567 °C (lit.)
mp
1083.4 °C (lit.)
density
8.94 g/mL at 25 °C (lit.)
application(s)
battery manufacturing
Quality Level
particle size
60-80 nm (APS)
Related Categories
Application
Copper nanopowders have seen use in biomedical applications as an antimicrobial ; as plasmonic materials and as a component of reforming catalysts.
Preparation Note
Partially Passivated: < 5% oxygen added by weight
signalword
Danger
Storage Class
4.2 - Pyrophoric and self-heating hazardous materials
flash_point_f
Not applicable
flash_point_c
Not applicable
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Self-heat. 1
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Chan; G.H.; et al.
Nano Letters, 7, 1947-1952 (2007)
Vizcaino; A.J.; et al.
International Journal of Hydrogen Energy, 32, 1450-1461 (2007)
Jayesh P Ruparelia et al.
Acta biomaterialia, 4(3), 707-716 (2008-02-06)
The antimicrobial properties of silver and copper nanoparticles were investigated using Escherichia coli (four strains), Bacillus subtilis and Staphylococcus aureus (three strains). The average sizes of the silver and copper nanoparticles were 3 nm and 9 nm, respectively, as determined
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
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