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Merck
CN

178977

Borane triethylamine complex

97%

Synonym(s):

(N,N-Diethylethanamine)trihydroboron, NSC 59740, Triethylamine borane

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About This Item

Linear Formula:
(C2H5)3N · BH3
CAS Number:
1722-26-5
Molecular Weight:
115.02
NACRES:
NA.22
PubChem Substance ID:
24850785
UNSPSC Code:
12352116
EC Number:
217-022-3
MDL number:
MFCD00012423
Assay:
97%
Form:
liquid

Key Documents

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InChI key

ONRDAGWFOUZNLV-UHFFFAOYSA-N

InChI

1S/C6H18BN/c1-4-8(7,5-2)6-3/h4-6H2,1-3,7H3

SMILES string

[BH3-][N+](CC)(CC)CC

assay

97%

form

liquid

reaction suitability

reagent type: reductant

refractive index

n20/D 1.442 (lit.)

bp

97 °C/12 mmHg (lit.)

mp

−4 °C (lit.)

density

0.777 g/mL at 25 °C (lit.)

functional group

amine

Quality Level

100

Related Categories

Application

Borane triethylamine complex is a general reagent which can be used in the synthesis of silylhydroboranes and meso-triarylsubporphyrins. It can also be used in the preparation of liquid-phase hydrogen storage material.
Used for:
  • Ethanolysis of amine-borane adducts producing a reducing system
  • Photochemical hydroboration and oxidation of single-walled carbon nanotubes

Reactant for the synthesis of:
  • Silylboranate
  • N-heterocyclic carbene borane complexes via Lewis base exchange with amine-boranes
  • Boron carbide nitride films via low-pressure CVD
  • (Pyridine)tripyrrolylboron

Reactant for modification of the radionuclide 211 At for astatination of biomolecules

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

19.4 °F - closed cup

flash_point_c

-7 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SHBQ7268
SHBB2301V
SHBB0805V
52596PM
67296MMV

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ABC?Type meso?Triaryl?Substituted Subporphyrins.
Yoshida K, et al.
European Journal of Organic Chemistry, 2014(19), 3997-4004 (2014)
A single-component liquid-phase hydrogen storage material.
Luo W, et al.
Journal of the American Chemical Society, 133(48), 19326-19329 (2011)
The quest for silylhydroboranes:(Me3Si)3SiBH2.
Arp H, et al.
Dalton Transactions, 39(39), 9270-9274 (2010)
Rational Synthesis of A2B-type meso-Triarylsubporphyrins.
Tanaka T, et al.
Organic Letters, 14(11), 2694-2697 (2012)
Zizwe A Chase et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(46), 16541-16546 (2015-09-26)
The state of Ni supported on HZSM-5 zeolite, silica, and sulfonated carbon was studied during aqueous-phase catalysis of phenol hydrodeoxygenation using in situ extended X-ray absorption fine structure spectroscopy. On sulfonated carbon and HZSM-5 supports, NiO and Ni(OH)2 were readily

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