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Merck

GF09290426

Copper - O.F.H.C.

foil, 300x300mm, thickness, 0.5mm, half hard, flattened, 99.95+%

Sinónimos:

Copper, CV000744

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MXP 10,022.00

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About This Item

Fórmula empírica (notación de Hill):
Cu
Número de CAS:
Peso molecular:
63.55
Número MDL:
Código UNSPSC:
12141711
ID de la sustancia en PubChem:
NACRES:
NA.23

MXP 10,022.00


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Ensayo

≥99.95%

Formulario

foil

fabricante / nombre comercial

Goodfellow 092-904-26

resistividad

1.673 μΩ-cm, 20°C

bp

2567 °C (lit.)

mp

1083.4 °C (lit.)

densidad

8.94 g/mL at 25 °C (lit.)

cadena SMILES

[Cu]

InChI

1S/Cu

Clave InChI

RYGMFSIKBFXOCR-UHFFFAOYSA-N

Descripción general

For updated SDS information please visit www.goodfellow.com.

Información legal

Product of Goodfellow

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Alina Fedoseienko et al.
Annals of the New York Academy of Sciences, 1314, 6-14 (2014-04-05)
Copper is an important cofactor in numerous biological processes in all living organisms. However, excessive copper can be extremely toxic, so it is vital that the copper level within a cell is tightly regulated. The damaging effect of copper is
Giulia Cheloni et al.
Aquatic toxicology (Amsterdam, Netherlands), 155, 275-282 (2014-07-30)
The present study showed the important role of light intensity and spectral composition on Cu uptake and effects on green alga Chlamydomonas reinhardtii. High-intenisty light (HL) increased cellular Cu concentrations, but mitigated the Cu-induced decrease in chlorophyll fluorescence, oxidative stress
Adam Southon et al.
Metallomics : integrated biometal science, 5(10), 1346-1356 (2013-08-02)
Copper (Cu) is an essential redox active metal that is potentially toxic in excess. Multicellular organisms acquire Cu from the diet and must regulate uptake, storage, distribution and export of Cu at both the cellular and organismal levels. Systemic Cu
Lelita T Braiterman et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(14), E1364-E1373 (2014-04-08)
Wilson disease (WD) is a monogenic autosomal-recessive disorder of copper accumulation that leads to liver failure and/or neurological deficits. WD is caused by mutations in ATP7B, a transporter that loads Cu(I) onto newly synthesized cupro-enzymes in the trans-Golgi network (TGN)
Marta Ugarte et al.
Survey of ophthalmology, 58(6), 585-609 (2013-10-29)
The essential trace metals iron, zinc, and copper play important roles both in retinal physiology and disease. They are involved in various retinal functions such as phototransduction, the visual cycle, and the process of neurotransmission, being tightly bound to proteins

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