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Tetrafluoroboric acid

Catalog No. L14037 Name Alfa Aesar
CAS Number 16872-11-0 Website
M. F. BF4- Telephone
M. W. 86.8046128 Fax
Purity ca 50% w/w aq. soln. Email
Storage Chembase ID: 94278

SYNONYMS

Title
四氟硼酸
IUPAC name
hydrogen tetrafluoroboranuide
IUPAC Traditional name
hydrogen tetrafluoroborate
Synonyms
Fluoboric acid
Tetrafluoroboric acid

DATABASE IDS

MDL Number MFCD00011345
Merck Index 144149
EC Number 240-898-3
CAS Number 16872-11-0

PROPERTIES

Purity ca 50% w/w aq. soln.
Boiling Point 130°C dec.
Density 1.410
GHS Pictograms GHS05
GHS Hazard statements H314-H227
European Hazard Symbols Corrosive Corrosive (C)
GHS Precautionary statements P210-P260-P303+P361+P353-P305+P351+P338-P405-P501A
Risk Statements 34
RTECS ED2685000
Safety Statements 26-27-45
TSCA Listed
Hazard Class 8
UN Number UN1775
Packing Group II

DETAILS

REFERENCES

  • Precursor of tetrafluoroborate salts of various stabilized cations. See, e.g.: Org. Synth. Coll., 5, 1135 (pyrylium), 1138 (tropylium); 6, 364 (sulfonium), 991 (cyclopropenium).
  • Addition to aqueous solutions of aryldiazonium salts usually results in precipitation of the diazonium tetrafluoroborates, which are often stable enough to be isolated, and can undergo various reactions in non-aqueous solvents. For hydrodediazoniation in the presence of formamide, see: J. Chem. Soc., Perkin 1, 873 (1986). Probably their most important use is the Schiemann (or Balz-Schiemann) synthesis of aryl fluorides in which the tetrafluoroborate salt is heated neat or in an inert solvent. For examples, see: Org. Synth. Coll., 2, 188, 295, 299 (1943). Reviews: Org. React., 5, 193 (1949); Adv. Fluorine. Chem., 4, 1 (1965). See also Hexafluorophosphoric acid, L15728.