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Merck
CN

86600

Tetraethylammonium borohydride

technical, ≥95% (T)

Synonym(s):

NSC 164898, NSC 76086, TEAB, Tetraethylammonium tetrahydroborate

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About This Item

Linear Formula:
(C2H5)4N(BH4)
CAS Number:
17083-85-1
Molecular Weight:
145.09
UNSPSC Code:
12352000
NACRES:
NA.22
PubChem Substance ID:
57653168
EC Number:
241-140-4
Beilstein/REAXYS Number:
3693695
MDL number:
MFCD00031600

Key Documents

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Product Name

Tetraethylammonium borohydride, technical, ≥95% (T)

InChI key

JFXPWTFDWBWOAZ-UHFFFAOYSA-N

InChI

1S/C8H20N.BH4/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;1H4/q+1;-1

SMILES string

[BH4-].CC[N+](CC)(CC)CC

grade

technical

assay

≥95% (T)

form

crystals

reaction suitability

reagent type: reductant

mp

>230 °C

functional group

amine

Quality Level

200

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Related Categories

Application

  • Reducing agent for the preparation of hydroxybaccatin III carbonate derivatives
  • Reductant for the preparation of edge-bridged all-ferrous double cubane
  • Reducing agent for the reduction of heterometal cubane iron/molybdenum cluster trigonally symmetrized with hydrotris(pyrazolyl)borate capping ligand
  • Reactant for reactions with ruthenium phenanthroline carbonyl complexes yielding formyl complexes

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 - Water-react 2

target_organs

Respiratory system

Storage Class

4.3 - Hazardous materials which set free flammable gases upon contact with water

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000143253
0000135298
0000133314
0000133070
0000124513

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Intestinal ischemia and reperfusion injury are widely used models, which result into tissue injury and multiple organ failure also observed after trauma and surgery. Ischemic preconditioning (IPC) preceding ischemia and reperfusion (IR) was shown to attenuate this injury and has
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Nature communications, 9(1), 1870-1870 (2018-05-16)
Selective modification of native proteins in live cells is one of the central challenges in recent chemical biology. As a unique bioorthogonal approach, ligand-directed chemistry recently emerged, but the slow kinetics limits its scope. Here we successfully overcome this obstacle
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Journal of agricultural and food chemistry, 67(31), 8485-8492 (2019-07-16)
How short-chain fatty acids (FAs) affect cell membrane morphology and milk fat biosynthesis in mammary epithelial cells (MECs) is yet unclear. This study investigated the primary bovine MEC response to different FAs. We observed that the cell surface ultrastructures were
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