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774065

Sigma-Aldrich

Vanadium

powder, -100 mesh, 99.9% trace metals basis

Synonym(s):

Vanadium element

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About This Item

Empirical Formula (Hill Notation):
V
CAS Number:
Molecular Weight:
50.94
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.23

vapor pressure

8 mmHg ( 20 °C)

Quality Level

assay

99.9% trace metals basis

form

powder

resistivity

24.8-26.0 μΩ-cm, 20°C

particle size

-100 mesh

bp

3380 °C (lit.)

mp

1890 °C (lit.)

density

6.11 g/mL at 25 °C (lit.)

SMILES string

[V]

InChI

1S/V

InChI key

LEONUFNNVUYDNQ-UHFFFAOYSA-N

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Application

Vanadium metal is commonly used industrially as a key component in alloys. Vanadium has also been shown to increase the efficiency of photocatalysis in TiO2 and hydrogen uptake in MgH2.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Anpo; M.;
Catalysis Surveys from Japan, 1(2), 169-179 (1997)
Ramzan; M.;
International Journal of Hydrogen Energy, 35(19), 10373-10376 (2010)
Gonzalez; J.E.G.;
Journal of Electroanalytical Chemistry (Lausanne Switzerland), 471(2), 109-115 (1999)
Jaclyn M Winter et al.
The Journal of biological chemistry, 284(28), 18577-18581 (2009-04-14)
Nature has developed an exquisite array of methods to introduce halogen atoms into organic compounds. Most of these enzymes are oxidative and require either hydrogen peroxide or molecular oxygen as a cosubstrate to generate a reactive halogen atom for catalysis.
Shinobu Takizawa
Chemical & pharmaceutical bulletin, 57(11), 1179-1188 (2009-11-03)
This review describes our recent efforts in the development of chiral dinuclear vanadium complexes which work as dual activation catalysts for oxidative coupling of 2-naphthols. A chiral dinuclear vanadium(IV) complex (R(a),S,S)-1a possessing (S)-tert-leucine moieties at the 3,3'-positions of the (R)-binaphthyl

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