GF94868117
Tungsten
wire reel, 100m, diameter 0.3mm, clean, 99.95%
Synonym(s):
Tungsten, W 005153, 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
Recommended Products
Assay
≥99.95%
form
wire
manufacturer/tradename
Goodfellow 948-681-17
resistivity
4.9 μΩ-cm, 20°C
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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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
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
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)
Vernon G Thomas et al.
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
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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