349178
Copper
foil, thickness 0.25 mm, 99.98% trace metals basis
Synonyme(s) :
Copper sheet
Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
About This Item
Formule empirique (notation de Hill):
Cu
Numéro CAS:
Poids moléculaire :
63.55
Numéro CE :
Numéro MDL:
Code UNSPSC :
11101604
ID de substance PubChem :
Nomenclature NACRES :
NA.23
Produits recommandés
Niveau de qualité
Pureté
99.98% trace metals basis
Forme
foil
Résistivité
1.673 μΩ-cm, 20°C
Épaisseur
0.25 mm
Point d'ébullition
2567 °C (lit.)
Pf
1083.4 °C (lit.)
Densité
8.94 g/mL at 25 °C (lit.)
Application(s)
battery manufacturing
Chaîne SMILES
[Cu]
InChI
1S/Cu
Clé InChI
RYGMFSIKBFXOCR-UHFFFAOYSA-N
Description générale
Copper foil with a thickness of 0.25 mm and a 99.98% trace metals basis is a top-quality product that has numerous industrial and commercial applications. It is produced using cutting-edge manufacturing processes that ensure superior quality and consistency. The foil is carefully inspected to meet the specified purity level and is free from any imperfections like scratches, dents, and tears. Copper foil is a highly versatile material that offers outstanding electrical conductivity, thermal conductivity, and corrosion resistance.
Application
Copper foil is commonly used in a variety of applications such as printed circuit boards (PCBs), electromagnetic shielding, and as a substrate in chemical vapor deposition. The 0.25 mm thickness of this foil makes it suitable for many applications, providing sufficient strength and durability while remaining easy to handle and manipulate. The 99.98% trace metals basis ensures that the copper foil is of the highest quality, with only minimal levels of impurities like lead, arsenic, and bismuth. This level of purity is critical for many industrial applications, particularly those in the electronics industry, where even small amounts of impurities can significantly impact the performance and reliability of the end product.
Quantité
50×50 mm (approximately 5.5 g)
150×150 mm (approximately 49.5 g)
150×150 mm (approximately 49.5 g)
Code de la classe de stockage
13 - Non Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
Faites votre choix parmi les versions les plus récentes :
Déjà en possession de ce produit ?
Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
Les clients ont également consulté
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
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
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
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.
Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..
Contacter notre Service technique