266620
Boron
crystalline, 1 cm, 99.7% trace metals basis
Synonym(s):
B
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About This Item
Empirical Formula (Hill Notation):
B
CAS Number:
Molecular Weight:
10.81
EC Number:
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99.7% trace metals basis
form
crystalline
reaction suitability
core: boron
reagent type: catalyst
resistivity
1.5E12 μΩ-cm, 20 °C
particle size
1 cm
density
2.34 g/mL at 25 °C (lit.)
SMILES string
[B]
InChI
1S/B
InChI key
ZOXJGFHDIHLPTG-UHFFFAOYSA-N
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Application
Boron can be used as a:
- Dopant on single-walled carbon nanotubes (SWCNT) used as a catalyst for acetylene hydrochlorination.
- Catalyst for enhancing the graphitization of various industrial carbons.
Storage Class Code
13 - Non Combustible Solids
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Apparent catalysis of graphitization. 3. Effect of boron
Murty HN, et al.
Fuel: The Science and Technology of Fuel and Energy, 56(3) (1977)
Single Au Anion Can Catalyze Acetylene Hydrochlorination: Tunable Catalytic Performance from Rational Doping
Ali S, et al.
The Journal of Physical Chemistry C (2019)
Tara A Devirian et al.
Critical reviews in food science and nutrition, 43(2), 219-231 (2003-04-23)
Boron may be an essential nutrient for animals and humans. Dietary boron influences the activity of many metabolic enzymes, as well as the metabolism of steroid hormones and several micronutrients, including calcium, magnesium, and vitamin D. Boron supplementation in rats
Yu Zhao et al.
Journal of the American Chemical Society, 135(4), 1201-1204 (2013-01-16)
Two kinds of boron and nitrogen co-doped carbon nanotubes (CNTs) dominated by bonded or separated B and N are intentionally prepared, which present distinct oxygen reduction reaction (ORR) performances. The experimental and theoretical results indicate that the bonded case cannot
Daniel L Silverio et al.
Nature, 494(7436), 216-221 (2013-02-15)
The discovery of catalysts that can be used to synthesize complex organic compounds by enantioselective transformations is central to advances in the life sciences; for this reason, many chemists aim to discover catalysts that allow for preparation of chiral molecules
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