GF22463995
Wolfram
rod, 200mm, diameter 2.0mm, centerless ground, 99.95%
Synonym(e):
Wolfram
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About This Item
Assay
99.95%
Form
rod
Hersteller/Markenname
Goodfellow 224-639-95
Widerstandsfähigkeit
4.9 μΩ-cm, 20°C
L × Durchm.
200 mm × 2.0 mm
bp
5660 °C (lit.)
mp (Schmelzpunkt)
3410 °C (lit.)
Dichte
19.3 g/mL at 25 °C (lit.)
SMILES String
[W]
InChI
1S/W
InChIKey
WFKWXMTUELFFGS-UHFFFAOYSA-N
Allgemeine Beschreibung
For updated SDS information please visit www.goodfellow.com.
Rechtliche Hinweise
Product of Goodfellow
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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
Journal of hazardous materials, 136(1), 1-19 (2005-12-14)
Since its discovery, tungsten, a transition element of Group VIb of the Periodic Table of Elements, and its compounds have been considered environmentally benign. Its presence in biological and drinking water samples in Fallon, Nevada, an acute lymphocytic leukemia cluster
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
Ecotoxicology and environmental safety, 72(4), 1031-1037 (2009-02-24)
The toxicity of elemental tungsten released from discharged shot was assessed against previous studies that established a 1% toxic threshold for soil organisms. Extremely heavy theoretical shot loadings of 69,000shot/ha were used to generate estimated environmental concentrations (EEC) for two
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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