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Merck

202215

Sodium tetrafluoroborate

98%

Synonym(s):

Sodium fluoroborate

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About This Item

Linear Formula:
NaBF4
CAS Number:
Molecular Weight:
109.79
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
237-340-6
MDL number:
Assay:
98%
Form:
powder or crystals
Solubility:
water: soluble(lit.)
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Quality Level

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

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.


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pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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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)