GF79938039
Tungsten
lump, 50g, max. size 5mm
Sinonimo/i:
Tungsten, W 006100, W
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About This Item
Prodotti consigliati
Forma fisica
foil
Produttore/marchio commerciale
Goodfellow 799-380-39
Resistività
4.9 μΩ-cm, 20°C
Dimensione particelle
5 mm
P. eboll.
5660 °C (lit.)
Punto di fusione
3410 °C (lit.)
Densità
19.3 g/mL at 25 °C (lit.)
Stringa SMILE
[W]
InChI
1S/W
WFKWXMTUELFFGS-UHFFFAOYSA-N
Descrizione generale
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Current opinion in chemical biology, 10(2), 109-114 (2006-02-17)
Mononuclear molybdenum and tungsten are found in the active site of a diverse group of enzymes that, in general, catalyze oxygen atom transfer reactions. Enzymes of the xanthine oxidase family are the best-characterized mononuclear Mo-containing enzymes. Several 3D structures of
International journal of radiation oncology, biology, physics, 89(3), 666-673 (2014-04-23)
To demonstrate that utilization of the direction-modulated brachytherapy (DMBT) concept can significantly improve treatment plan quality in the setting of high-dose-rate (HDR) brachytherapy for cervical cancer. The new, MRI-compatible, tandem design has 6 peripheral holes of 1.3-mm diameter, grooved along
Military medicine, 172(9), 1002-1005 (2007-10-17)
Tungsten and tungsten compounds are considered toxicologically relatively safe. Concern regarding the potential health and environmental effects of depleted uranium and lead in military applications has lead many countries to explore the possibility of applying toxicologically safer metals. Heavy metal
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
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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