Skip to Content
Merck
All Photos(1)

Documents

86600

Sigma-Aldrich

Tetraethylammonium borohydride

technical, ≥95% (T)

Synonym(s):

NSC 164898, NSC 76086, TEAB, Tetraethylammonium tetrahydroborate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C2H5)4N(BH4)
CAS Number:
Molecular Weight:
145.09
Beilstein:
3693695
EC Number:
MDL number:
UNSPSC Code:
12352000
PubChem Substance ID:
NACRES:
NA.22

grade

technical

Assay

≥95% (T)

form

crystals

reaction suitability

reagent type: reductant

mp

>230 °C

SMILES string

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

InChI

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

InChI key

JFXPWTFDWBWOAZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Tomonori Tamura et al.
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
J Y Liu et al.
Veterinary parasitology, 231, 32-38 (2016-07-01)
Trichinella spiralis, an intracellular parasitic nematode, can cause severe foodborne zoonosis, trichinellosis. The life cycle of T. spiralis consists of adult (Ad), muscle larvae (ML) and newborn larvae (NBL). The protein profiles in different developmental stages of the parasite remain
Qiongxian Yan et al.
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
Charnpal S Grewal et al.
Methods (San Diego, Calif.), 125, 16-24 (2017-07-04)
Here we describe the synthesis and use of a directed hydroxyl radical probe, tethered to a pre-mRNA substrate, to map the structure of this substrate during the spliceosome assembly process. These studies indicate an early organization and proximation of conserved
Fernanda Negrão et al.
ACS infectious diseases, 5(8), 1295-1305 (2019-05-17)
Cutaneous leishmaniasisis is the most common clinical form of leishmaniasis and one of the most relevant neglected diseases. It is known that the progress of the disease is species specific and the host's immune response plays an important role in

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service