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Merck
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重要文件

GF69207240

foil, 10m coil, thickness 0.075mm, half hard, 99.95+%

同義詞:

Copper, CV000540

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About This Item

經驗公式(希爾表示法):
Cu
CAS號碼:
分子量::
63.55
MDL號碼:
分類程式碼代碼:
12141711
PubChem物質ID:
NACRES:
NA.23

化驗

99.95%

形狀

foil

製造商/商標名

Goodfellow 692-072-40

電阻係數

1.673 μΩ-cm, 20°C

長度 × 厚度

10 m × 0.075 mm

bp

2567 °C (lit.)

mp

1083.4 °C (lit.)

密度

8.94 g/mL at 25 °C (lit.)

SMILES 字串

[Cu]

InChI

1S/Cu

InChI 密鑰

RYGMFSIKBFXOCR-UHFFFAOYSA-N

一般說明

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

法律資訊

Product of Goodfellow

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Donita C Brady et al.
Nature, 509(7501), 492-496 (2014-04-11)
The BRAF kinase is mutated, typically Val 600→Glu (V600E), to induce an active oncogenic state in a large fraction of melanomas, thyroid cancers, hairy cell leukaemias and, to a smaller extent, a wide spectrum of other cancers. BRAF(V600E) phosphorylates and
Jonas Duus Stevens Lekfeldt et al.
Environmental pollution (Barking, Essex : 1987), 194, 78-85 (2014-08-06)
Copper (Cu) is known to accumulate in agricultural soils receiving urban waste products as fertilizers. We here report the use of the leucine incorporation technique to determine pollution-induced community tolerance (Leu-PICT) to Cu in a long-term agricultural field trial. A
Julie E Gleason et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(16), 5866-5871 (2014-04-09)
The human fungal pathogens Candida albicans and Histoplasma capsulatum have been reported to protect against the oxidative burst of host innate immune cells using a family of extracellular proteins with similarity to Cu/Zn superoxide dismutase 1 (SOD1). We report here
L Marchand et al.
Environmental pollution (Barking, Essex : 1987), 193, 205-215 (2014-07-25)
Intra-specific variability of root biomass production (RP) of six rooted macrophytes, i.e. Juncus effusus, Phragmites australis, Schoenoplectus lacustris, Typha latifolia, Phalaris arundinacea, and Iris pseudacorus grown from clones, in response to Cu exposure was investigated. Root biomass production varied widely
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)

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