Skip to Content
MilliporeSigma
All Photos(3)

Documents

202215

Sigma-Aldrich

Sodium tetrafluoroborate

98%

Synonym(s):

Sodium fluoroborate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
NaBF4
CAS Number:
Molecular Weight:
109.79
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

assay

98%

form

powder or crystals

solubility

water: soluble(lit.)

density

2.47 g/mL at 25 °C (lit.)

SMILES string

[Na+].F[B-](F)(F)F

InChI

1S/BF4.Na/c2-1(3,4)5;/q-1;+1

InChI key

KGJZTOFHXCFQIV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Sodium tetrafluoroborate (NaBF4) is colorless sodium salt and its crystals belong to the rhombic crystal system. It can be synthesized by reacting tetrafluoroboric acid with sodium carbonate or hydroxide.

Application

Sodium tetrafluoroborate may be used as a catalyst for the synthesis of bis(indolyl)methanes via electrophilic substitution reaction of indoles with aldehydes and ketones. It may also be used as a source of tetrafluoroborate anoins during the synthesis of ionic liquids like 1-butyl-3-methylimidazolium tetrafluoroborate and trihexyl(tetradecyl)phosphonium tetrafluoroborate.
Sodium tetrafluoroborate may be used for the laboratory synthesis of boron fluoride. It may be used for the synthesis of fluoro-nucleic acids and fluoroheterocyclic compounds.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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

Physical and electrochemical properties of 1-butyl-3-methylimidazolium bromide, 1-butyl-3-methylimidazolium iodide, and 1-butyl-3-methylimidazolium tetrafluoroborate.
Kim KS, et al.
Korean Journal of Chemical Engineering, 21(5), 1010-1014 (2004)
Highly efficient synthesis of bis (indolyl) methanes catalyzed by sodium tetrafluoroborate.
Kamble VT, et al.
Chin. J. Chem., 25(1), 13-15 (2007)
Industrial preparation of phosphonium ionic liquids.
Bradaric CJ, et al.
Green Chemistry, 5(2), 143-152 (2003)
Facile direct conversion of amino-heterocycles to fluoro-heterocycles using t-butylthionitrite or t-butylthionitrate with sodium tetrafluoroborate.
Yong HK, et al.
Tetrahedron Letters, 31(21), 3019-3022 (1990)
Eagleson M.
Concise Encyclopedia Chemistry, 1001-1001 (1994)

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