アッセイ
99.95%
形状
foil
メーカー／製品名
Goodfellow 316-267-16
抵抗性
4.9 μΩ-cm, 20°C
L ×厚み×幅
0.2 m × 0.035 mm × 0.5 mm
bp
5660 °C (lit.)
mp
3410 °C (lit.)
密度
19.3 g/mL at 25 °C (lit.)
SMILES記法
[W]
InChI
1S/W
InChI Key
WFKWXMTUELFFGS-UHFFFAOYSA-N
関連するカテゴリー
詳細
For updated SDS information please visit www.goodfellow.com.
法的情報
Goodfellow製品
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Congshang Wan et al.
Ultramicroscopy, 119, 106-110 (2011-11-15)
Thermionic electron emission from 200 to 500 nm thick coatings of scandium oxide on tungsten foil have been examined in thermionic emission microscopy, spectroscopic photoelectron microcopy, synchrotron radiation and ultraviolet photoelectron spectroscopy (UPS). A clear dependence of the scandium oxide-W
J R Marbach et al.
Physics in medicine and biology, 26(3), 435-443 (1981-05-01)
Curves relating beam energy, scattering foil thickness, central-axis depth-dose, and beam flatness have been generated using data taken on a Siemens 200A betatron. The curve set allows a single combination of tungsten foil thickness and electron beam energy to be
Malcolm H Chisholm et al.
Chemical record (New York, N.Y.), 5(5), 308-320 (2005-10-08)
The reaction of M2(O2CBu(t))4 (M = Mo, W) with a dicarboxylic acid in toluene yields compounds of general formula [M2]-O2C-X-CO2-[M2] ([M2] = M2(O2CBu(t))3; X = conjugated spacer). The M2 units are electronically coupled via interactions between the M2 delta and
José L Domingo
Biological trace element research, 88(2), 97-112 (2002-09-26)
Tungstate is an oxyanion that has biological similarities to vanadate. In recent years, a number of studies have shown the antidiabetic effects of oral tungstate in animal models of diabetes. However, because of the tissue accumulation and potential toxicity derived
Matthias Boll et al.
Biological chemistry, 386(10), 999-1006 (2005-10-13)
The molybdenum enzymes 4-hydroxybenzoyl-CoA reductase and pyrogallol-phloroglucinol transhydroxylase and the tungsten enzyme acetylene hydratase catalyze reductive dehydroxylation reactions, i.e., transhydroxylation between phenolic residues and the addition of water to a triple bond. Such activities are unusual for this class of
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