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Sigma-Aldrich

Tetrapropylammonium tetrafluoroborate

≥98.0%

Synonym(s):

Tetrapropylammonium tetrafluoroborate(1-), Tetrapropylammoniumtetrafluoroborate

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About This Item

Linear Formula:
(CH3CH2CH2)4N(BF4)
CAS Number:
338-38-5
Molecular Weight:
273.16
Beilstein:
3637590
EC Number:
206-416-0
MDL number:
MFCD00031619
UNSPSC Code:
12352116
PubChem Substance ID:
57653294
NACRES:
NA.22

Quality Level

100

Assay

≥98.0%

form

crystals

mp

245-247 °C

SMILES string

F[B-](F)(F)F.CCC[N+](CCC)(CCC)CCC

InChI

1S/C12H28N.BF4/c1-5-9-13(10-6-2,11-7-3)12-8-4;2-1(3,4)5/h5-12H2,1-4H3;/q+1;-1

InChI key

ADADJCUTHQJPCB-UHFFFAOYSA-N

Application

Tetrapropylammonium tetrafluoroborate (Pr4NBF4 or TPABF4) can be used as:
  • An electrolyte in the determination of phenolic compounds from grape seed extracts by capillary electrophoretic method.
  • A supporting electrolyte in the electrochemical hydrogenation of dimethylformamide (DMF) to trimethylamine (TMA).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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’.

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Electrochemical synthesis of trimethylamine by cathodic reduction of dimethylformamide using Cu and Pd cathodes
Jia R, et al.
Journal of Electroanalytical Chemistry, 741(11), 32-35 (2015)
Ludmila Šimková et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 323, 106895-106895 (2021-01-12)
The molecule of 2,2-dinitroethene-1,1-diamine (FOX-7) is one of the most interesting molecules with multiple redox centres stabilized by push-pull effect. To reveal the detailed mechanism of its electrochemical process radical intermediates formed in the course of its electrochemical reduction in

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