All Photos(2)
Synonym(s):
Boron, B 005915
Empirical Formula (Hill Notation):
B
CAS Number:
Molecular Weight:
10.81
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
form
foil
manufacturer/tradename
Goodfellow 746-870-80
resistivity
1.5E12 μΩ-cm, 20 °C
L × diam.
10 m × 0.2 mm
density
2.34 g/mL at 25 °C (lit.)
SMILES string
[B]
InChI
1S/B
InChI key
ZOXJGFHDIHLPTG-UHFFFAOYSA-N
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General description
For updated SDS information please visit www.goodfellow.com.
Legal Information
Product of Goodfellow
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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Kyoko Miwa et al.
Annals of botany, 105(7), 1103-1108 (2010-03-17)
The essentiality of boron (B) for plant growth was established > 85 years ago. In the last decade, it has been revealed that one of the physiological roles of B is cross-linking the pectic polysaccharide rhamnogalacturonan II in primary cell
Anne-Marie Alexander et al.
Chemical Society reviews, 39(11), 4388-4401 (2010-06-08)
Catalysts generated by the addition of carbon, nitrogen or phosphorus to transition metals have interesting properties and potential applications. The addition of carbon, nitrogen or phosphorus can lead to substantial modification of the catalytic efficacy of the parent metal and
Boron containing compounds as protease inhibitors.
Reem Smoum et al.
Chemical reviews, 112(7), 4156-4220 (2012-04-24)
Kyoko Miwa et al.
Advances in experimental medicine and biology, 679, 83-96 (2010-07-30)
Understanding of the molecular mechanisms of boron (B) transport has been greatly advanced in the last decade. BOR1, the first B transporter in living systems, was identified by forward genetics using Arabidopsis mutants. Genes similar to BOR1 have been reported
Ting Jiang et al.
Organic letters, 16(7), 1952-1955 (2014-03-29)
A novel stepwise and regioselective nucleophilic aromatic substitution (SNAr) reaction of halogenated boron dipyrrins (BODIPYs) with pyrroles has been developed under mild conditions with no catalyst needed and shown to be diversity oriented. The resultant pyrrole-substituted BODIPYs are interesting red
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