Unfortunately, this product is not tested for purity.
227609
Decaborane(14)
white
Synonym(s):
Boron hydride, Decaborane, Decaboron tetradecahydride, NSC 39828, Tetradecahydrodecaborane, nido-Decaborane(14)
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All Photos(2)
About This Item
Linear Formula:
B10H14
CAS Number:
Molecular Weight:
122.22
EC Number:
MDL number:
UNSPSC Code:
12352000
form:
solid
Pricing and availability is not currently available.
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vapor pressure
0.15 mmHg ( 20 °C)
Quality Level
form
solid
reaction suitability
reagent type: reductant
color
white
bp
213 °C (lit.)
mp
98-100 °C (lit.)
density
0.94 g/mL at 25 °C (lit.)
SMILES string
[BH]4321[BH]765[BH]984[BH]%11%103[BH]%13%122[BH]%1471[BH]%156([BH]%1695[BH]%118([H]%10)[H]%16)[BH]%14%13([H]%12)[H]%15
InChI
1S/B10H14/c11-5-1-2-3(1,5)7(2,9(3,5,11)13-7)8(2)4(1,2)6(1,5)10(4,8,12-6)14-8/h1-10H
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Related Categories
Application
Reactant for:
- Chemical vapor deposition of boron nitride nanosheets on Ni or Cu foils in the presence of ammonia
- Stereoselective catalytic hydrogenation reactions
- Chemical hydrogen storage
- Preparation of carborane-conjugated quinoline carboxamide ligands of translocator protein for boron neutron capture therapy (BNCT)
- Synthesis of hydrogenated boron clusters B12Hn with controlled hydrogen content
- Preparation of alkenyldecaboranes by regioselective transition-metal-catalyzed decaborane-alkyne hydroboration reactions
Boron source for ion-implantation processes.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Ilias Sioutis et al.
The journal of physical chemistry. A, 110(45), 12528-12534 (2006-11-10)
The interaction of decaborane (B(10)H(14)) with the I(-) ion and the (isoelectronic) Xe atom is investigated using a number of theoretical methods: MP2, CCSD(T), CCSD, spin-orbit CISD, and DFT using the B3LYP, B3PW91, PW91PW91, and PBE0 methods. All non-DFT and
Kiminori Ohta et al.
Bioorganic & medicinal chemistry letters, 14(23), 5913-5918 (2004-10-27)
We designed and synthesized novel retinoid X receptor (RXR)-selective antagonists bearing a carborane moiety. Compounds 8a-d or 9a-d themselves have no differentiation-inducing activity toward HL-60 cells and no inhibitory activity towards a retinoic acid receptor (RAR) agonist. However, they inhibit
Yuqi Li et al.
Inorganic chemistry, 47(20), 9193-9202 (2008-09-20)
Unlike in conventional organic solvents, where Lewis base catalysts are required, decaborane dehydrogenative alkyne-insertion reactions proceed rapidly in biphasic ionic-liquid/toluene mixtures with a wide variety of terminal and internal alkynes, thus providing efficient, one-step routes to functional o-carborane 1-R-1,2-C2B10H11 and
Zhu Yinghuai et al.
Journal of the American Chemical Society, 129(20), 6507-6512 (2007-05-03)
Well dispersed ruthenium(0) nanoparticles, stabilized in the ionic liquid agent, trihexyltetradecylphosphonium dodecylbenzenesulfonate, have been successfully prepared via a reduction reaction of the precursor [CpRuCp*RuCp*]PF6 (Cp* = C5Me5). The ruthenium(0) nanoparticles were shown to catalyze the isotope exchange reaction between 10B
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