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266892

Sigma-Aldrich

Molybdenum

powder, <150 μm, 99.9% trace metals basis

Sinónimos:

Molybdenum element

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About This Item

Fórmula empírica (notación de Hill):
Mo
Número de CAS:
7439-98-7
Peso molecular:
95.94
EC Number:
231-107-2
MDL number:
MFCD00003465
UNSPSC Code:
12161600
PubChem Substance ID:
24856166
NACRES:
NA.23

Quality Level

100

assay

99.9% trace metals basis

form

powder

reaction suitability

reagent type: catalyst
core: molybdenum

resistivity

5.0 μΩ-cm, 20°C

particle size

<150 μm

bp

4612 °C (lit.)

mp

2617 °C (lit.)

density

10.3 g/mL at 25 °C (lit.)

SMILES string

[Mo]

InChI

1S/Mo

InChI key

ZOKXTWBITQBERF-UHFFFAOYSA-N

Categorías relacionadas

Storage Class

13 - Non Combustible Solids

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Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Nuclear nonproliferation. Iranian 'medical' reactor stokes search for alternatives.
Richard Stone
Science (New York, N.Y.), 340(6139), 1392-1392 (2013-06-22)
Measurement of mobility in dual-gated MoS₂ transistors.
Michael S Fuhrer et al.
Nature nanotechnology, 8(3), 146-147 (2013-03-06)
Joyee Mitra et al.
Inorganic chemistry, 52(6), 3032-3042 (2013-03-07)
A series of [Mo(IV)O(mnt)(SR)(N-N)](-) (mnt = maleonitriledithiolate; R = Ph, nap, p-Cl-Ph, p-CO2H-Ph, and p-NO2-Ph; N-N = 2,2'-bipyridine (bipy) and 1,10-phenanthroline (phen)) complexes analogous to the reduced active site of enzymes of the sulfite oxidase family has been synthesized and
Phillip Ringel et al.
The Journal of biological chemistry, 288(20), 14657-14671 (2013-03-30)
Nitrate reductase (NR) is a complex molybdenum cofactor (Moco)-dependent homodimeric metalloenzyme that is vitally important for autotrophic organism as it catalyzes the first and rate-limiting step of nitrate assimilation. Beside Moco, eukaryotic NR also binds FAD and heme as additional
Alexander O Terent'ev et al.
Organic & biomolecular chemistry, 11(16), 2613-2623 (2013-03-01)
Phosphomolybdic acid (PMA) and phosphotungstic acid (PTA) efficiently catalyze the addition of H2O2 to β-diketones to form bridged 1,2,4,5-tetraoxanes. These reactions are not accompanied by the formation of monocyclic peroxides containing hydroxy and hydroperoxide groups or polymeric peroxides. The use
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