429-06-1

  • Product Name:Tetraethylammonium tetrafluoroborate
  • Molecular Formula:C8H20N.BF4
  • Purity:99%
  • Molecular Weight:217.058
InquiryAdd to cart

Product Details;

CasNo: 429-06-1

Molecular Formula: C8H20N.BF4

Appearance: white crystals or crystalline powder

factory and manufacture 429-06-1 Tetraethylammonium tetrafluoroborate lonic liquid

  • Molecular Formula:C8H20N.BF4
  • Molecular Weight:217.058
  • Appearance/Colour:white crystals or crystalline powder 
  • Vapor Pressure:0-0Pa at 20-25℃ 
  • Melting Point:≥300 °C(lit.) 
  • PSA:0.00000 
  • Density:1.23 at 20℃ 
  • LogP:3.18280 

Tetraethylammonium tetrafluoroborate(Cas 429-06-1) Usage

General Description

Visit our Sensor Applications portal to learn more.

Purification Methods

Dissolve the salt in hot MeOH, filter and add Et2O. It is soluble in ethylene chloride [Thompson & Kraus J Am Chem Soc 69 1016 1947, Wheeler & Sandstadt 77 2025 1955]. It has also been recrystallised three times from a mixture of ethyl acetate/hexane (5:1) or MeOH/pet ether, then stored at 95o for 48hours under vacuum [Henry & Faulkner J Am Chem Soc 107 3436 1985, Huang et al. Anal Chem 58 2889 1986]. It is used as a supporting electrolyte. [Beilstein 4 IV 333.]

InChI:InChI=1/C8H20N.BF4/c1-5-9(6-2,7-3)8-4;2-1(3,4)5/h5-8H2,1-4H3;/q+1;-1

429-06-1 Relevant articles

Electrochemistry as an attractive and effective tool for the synthesis and immobilization of porphyrins on an electrode surface

Hebié, Seydou,Dimé, Abdou K. D.,Devillers, Charles H.,Lucas, Dominique

, p. 8281 - 8289 (2015)

Magnesium(II) 10-phenyl-5,15-p-ditolylpo...

Synthesis and characterization of {Ni(NO)}10 and {Co(NO) 2}10 complexes supported by thiolate ligands

Tennyson, Andrew G.,Dhar, Shanta,Lippard, Stephen J.

, p. 15087 - 15098 (2008)

Nitric oxide is an important molecule in...

Towards sustainable synthesis of pyren-1-yl azoliums via electrochemical oxidative C-N coupling

De Robillard, Guillaume,Makni, Oumayma,Cattey, Hélène,Andrieu, Jacques,Devillers, Charles H.

, p. 4669 - 4679 (2015)

Electrosynthesis of 1-methyl-3-(pyren-1-...

Electrochemical phosphorylation of coumarins catalyzed by transition metal complexes (Ni—Mn, Co—Mn)

Strekalova,Khrizanforov,Gryaznova,Khrizanforova,Budnikova, Yu. H.

, p. 1295 - 1298 (2016)

A possibility of electrochemical phospho...

The influence of temperature and concentration on viscous flow of solutions of Et4NBF4 in propylene carbonate

Afanas'ev,Tyunina, E. Yu.,Chekunova

, p. 2069 - 2073 (2009)

Solutions of tetraethylammonium tetraflu...

Mechanism of the Platinum(II)-Catalyzed Hydroamination of 4-Pentenylamines

Bender, Christopher F.,Brown, Timothy J.,Widenhoefer, Ross A.

, p. 113 - 125 (2016)

The mechanism of the platinum(II)-cataly...

Electrophilic additions of metal fragments containing 11- and 12-group elements to the anion carbide cluster [Fe5MoC(CO)17]2-. X-ray crystal structures of (NEt4)[Fe5MoAuC(CO)17(PMe3)] and [Fe5MoAu2C(CO)17(dppm)]

Reina, Roser,Rodríguez, Laura,Rossell, Oriol,Seco, Miquel,Font-Bardia, Mercè,Solans, Xavier

, p. 1575 - 1579 (2001)

The reaction of (NEt4)2[Fe5MoC(CO)17] wi...

Fe and Ni-catalyzed electrochemical perfluoroalkylation of C—H bonds of coumarins

Khrizanforov,Strekalova,Grinenko,Khrizanforova,Gryaznova,Budnikova, Yu. H.

, p. 1446 - 1449 (2017)

A new method for the preparation of perf...

A four-ethyl four simple method for preparing ammonium borofluoride (by machine translation)

-

Paragraph 0021-0042; 0045-0052, (2018/10/11)

The invention discloses an electronic po...

A general diastereoselective synthesis of highly functionalized ferrocenyl ambiphiles enabled on a large scale by electrochemical purification

Lerayer, Emmanuel,Renaut, Patrice,Roger, Julien,Pirio, Nadine,Cattey, Hélène,Devillers, Charles H.,Lucas, Dominique,Hierso, Jean-Cyrille

supporting information, p. 6017 - 6020 (2017/07/11)

A general synthesis of highly functional...

429-06-1 Process route

tetraethylammonium chloride
56-34-8

tetraethylammonium chloride

N,N,N,N-tetraethylammonium tetrafluoroborate
429-06-1

N,N,N,N-tetraethylammonium tetrafluoroborate

Conditions
Conditions Yield
With potassium tetrafluoroborate; In acetonitrile; at 20 ℃; for 0.25h;
tetraethylammonium bromide
71-91-0

tetraethylammonium bromide

N,N,N,N-tetraethylammonium tetrafluoroborate
429-06-1

N,N,N,N-tetraethylammonium tetrafluoroborate

Conditions
Conditions Yield
With tetrafluoroboric acid; In methanol; for 0.5h;
With tetrafluoroboric acid;

429-06-1 Upstream products

  • 64-67-5
    64-67-5

    diethyl sulfate

  • 121-44-8
    121-44-8

    triethylamine

  • 74-96-4
    74-96-4

    ethyl bromide

  • 68-05-3
    68-05-3

    tetraethylammonium iodide

429-06-1 Downstream products

  • 7242-58-2
    7242-58-2

    phosphoric acid dibutyl ester ethyl ester

  • 121-44-8
    121-44-8

    triethylamine

  • 114526-94-2
    114526-94-2

    tetraethylammonium salt of dibenzoylimide

  • 114526-96-4
    114526-96-4

    tetraethylammonium salt of p-cyanoformanilide

Shopping Cart

Clear Inquiry