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About This Item
Fórmula empírica (notación de Hill):
B
Número CAS:
Peso molecular:
10.81
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12141907
MDL number:
Nombre del producto
Boron, monofilament, 5m, diameter 0.2mm
InChI
1S/B
SMILES string
[B]
InChI key
ZOXJGFHDIHLPTG-UHFFFAOYSA-N
form
foil
manufacturer/tradename
Goodfellow 403-381-32
resistivity
1.5E12 μΩ-cm, 20 °C
L × diam.
5 m × 0.2 mm
density
2.34 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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Clase de almacenamiento
13 - Non Combustible Solids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
Jan Fietzke et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(10), 2960-2965 (2015-02-26)
No records exist to evaluate long-term pH dynamics in high-latitude oceans, which have the greatest probability of rapid acidification from anthropogenic CO2 emissions. We reconstructed both seasonal variability and anthropogenic change in seawater pH and temperature by using laser ablation
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)
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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