GF16499986
Tungsten
wire, straight, 100mm, diameter 0.20mm, 99.9+%
Synonym(s):
Tungsten, W 005320, W
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About This Item
Empirical Formula (Hill Notation):
W
CAS Number:
Molecular Weight:
183.84
MDL number:
UNSPSC Code:
12141747
PubChem Substance ID:
NACRES:
NA.23
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Assay
99.90%
form
wire
manufacturer/tradename
Goodfellow 164-999-86
resistivity
4.9 μΩ-cm, 20°C
L × diam.
100 mm × 0.20 mm
bp
5660 °C (lit.)
mp
3410 °C (lit.)
density
19.3 g/mL at 25 °C (lit.)
SMILES string
[W]
InChI
1S/W
InChI key
WFKWXMTUELFFGS-UHFFFAOYSA-N
General description
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Jan R Andreesen et al.
Annals of the New York Academy of Sciences, 1125, 215-229 (2007-12-22)
The history and changing function of tungsten as the heaviest element in biological systems is given. It starts from an inhibitory element/anion, especially for the iron molybdenum-cofactor (FeMoCo)-containing enzyme nitrogenase involved in dinitrogen fixation, as well as for the many
P Thongkumkoon et al.
Toxicology letters, 226(1), 90-97 (2014-02-08)
The toxicity of nanomaterials has been well known, but mechanisms involved have been little known. This study was aimed at looking at direct interaction between nanomaterials and naked DNA for some fundamental understanding. Two different types of nanomaterials, carbon nanotubes
Synthetic analogues and reaction systems relevant to the molybdenum and tungsten oxotransferases.
John H Enemark et al.
Chemical reviews, 104(2), 1175-1200 (2004-02-12)
Elias Papaconstantinou et al.
Frontiers in bioscience : a journal and virtual library, 8, s813-s825 (2003-09-06)
Polyoxometalates (POM) have a rich and promising photochemical behavior. Upon illumination at the O M CT band (i.e., in UV and near-visible area) become powerful oxidizing reagents able to oxidize various organic compounds. In the process POM undergo stepwise reduction
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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