Tetrafluoroboric acid, ca 50% w/w aq. soln., Thermo Scientific Chemicals
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Tetrafluoroboric acid, ca 50% w/w aq. soln., Thermo Scientific Chemicals
Tetrafluoroboric acid, ca 50% w/w aq. soln., Thermo Scientific Chemicals
Tetrafluoroboric acid, ca 50% w/w aq. soln., Thermo Scientific Chemicals
Thermo Scientific Chemicals

Tetrafluoroboric acid, ca 50% w/w aq. soln., Thermo Scientific Chemicals

CAS: 16872-11-0
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Catalog NumberQuantity
ALFL14037.36500 g
Catalog number ALFL14037.36
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Quantity:
500 g
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Chemical Identifiers
CAS7440-22-4
IUPAC Namesilver
Molecular FormulaAg
InChI KeyBQCADISMDOOEFD-UHFFFAOYSA-N
SMILES[Ag]
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SpecificationsSpecification SheetSpecification Sheet
Total Metal Impurities0.002% max.
Comment0.025mm (0.001in) thick
Tetrafluoroboric acid is used in conjunction with various methods of cleaning and to treat the surface of substrates. It is also used as a radiotracer.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Tetrafluoroboric acid is used in conjunction with various methods of cleaning and to treat the surface of substrates. It is also used as a radiotracer.

Solubility
Miscible with water.

Notes
Incompatible with strong bases, oxidizing agents and acids.
RUO – Research Use Only

General References:

  1. Precursor of tetrafluoroborate salts of various stabilized cations. See, e.g.: Org. Synth. Coll., 5, 1135 (pyrylium), 1138 (tropylium); 6, 364 (sulfonium), 991 (cyclopropenium).
  2. 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.
  3. Chen, L.; Cao, X.; Huang, D.; Pan, Q. Switchable dielectric phase transition in tris(1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane) tetra(tetrafluoroborate) dichloride. Inorg. Chem. Commun. 2015, 61, 93-96.
  4. Zhong, Z.; Brokmeiera, H.; Maawad, E.; Schell, N. In-situ investigation of the anisotropic mechanical behavior of rolled AA 7020-T6 alloy through lattice strain evolution during uniaxial tension. Mater. Sci. Eng., A 2015, 639, 519-525.