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About This Item
Empirical Formula (Hill Notation):
V
CAS Number:
Molecular Weight:
50.94
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12141749
MDL number:
InChI
1S/V
SMILES string
[V]
InChI key
LEONUFNNVUYDNQ-UHFFFAOYSA-N
vapor pressure
8 mmHg ( 20 °C)
assay
99.8%
form
wire
manufacturer/tradename
Goodfellow 397-232-39
resistivity
24.8-26.0 μΩ-cm, 20°C
L × diam.
0.5 m × 0.1 mm
bp
3380 °C (lit.)
mp
1890 °C (lit.)
density
6.11 g/mL at 25 °C (lit.)
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General description
For updated SDS information please visit www.goodfellow.com.
Legal Information
Product of Goodfellow
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Dieter Rehder
Journal of inorganic biochemistry, 102(5-6), 1152-1158 (2008-02-08)
In the present focused review, vanadate-dependent haloperoxidases and vanadate-inhibited enzymes which catalyze the hydrolysis of phosphoester bonds are addressed. In these systems, vanadate [HxVO4](3-x)(-) is covalently coordinated to the imidazolyl moiety of an active site histidine, with a geometrical arrangement
Mohamad Z Mehdi et al.
Cell biochemistry and biophysics, 44(1), 73-81 (2006-02-04)
Among several metals, vanadium has emerged as an extremely potent agent with insulin-like properties. These insulin-like properties have been demonstrated in isolated cells, tissues, different animal models of type I and type II diabetes as well as a limited number
Lise Coderre et al.
Canadian journal of physiology and pharmacology, 82(10), 833-839 (2004-12-02)
Inorganic and organic compounds of vanadium have been shown to exhibit a large range of insulinomimetic effects in the cardiovascular system, including stimulation of glucose transporter 4 (GLUT-4) translocation and glucose transport in adult cardiomyocytes. Furthermore, administration of vanadium compounds
D M Smith et al.
QJM : monthly journal of the Association of Physicians, 101(5), 351-358 (2008-03-06)
To assess the effectiveness of oral vanadium supplementation for glycaemic control in type 2 diabetes by conducting a systematic review of the literature. Eligible studies were identified by searching 14 databases using standardized terms. Experts, study authors and manufacturers were
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.
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