207934
Tetrafluoroboric acid solution
48 wt. % in H2O
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About This Item
Linear Formula:
HBF4
CAS Number:
Molecular Weight:
87.81
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
Product Name
Tetrafluoroboric acid solution, 48 wt. % in H2O
InChI
1S/BF3.FH/c2-1(3)4;/h;1H
SMILES string
F.FB(F)F
InChI key
LEMQFBIYMVUIIG-UHFFFAOYSA-N
vapor density
3 (vs air)
vapor pressure
5 mmHg ( 20 °C)
form
liquid
concentration
46.0-52.0% in NaOH (titration)
48 wt. % in H2O
density
1.4 g/mL at 25 °C
Quality Level
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Application
Tetrafluoroboric acid solution may be used as a catalyst for the hydration of aromatic haloalkynes to α-halomethyl ketones in the absence of metal catalysts. It may also be used the epoxidized soybean oil (ESBO) ring opening step of fatty acids preparation.
General description
Tetrafluoroboric acid is used as a catalyst for the protection and deprotection reactions of various carbohydrates. It participates in the synthesis of 4-sulfonic acid phenyl diazonium tetrafluoroborate, which was required for the preparation of sulfonated graphene (SG).
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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Self-assembling sulfonated graphene/polyaniline nanocomposite paper for high performance supercapacitor.
Fan T, et al.
Synthetic Metals, 199, 79-86 (2015)
Polyols and polyurethanes prepared from epoxidized soybean oil ring-opened by polyhydroxy fatty acids with varying OH numbers.
Chen R, et al.
Journal of Applied Polymer Science, 132(1) (2015)
Tetrafluoroboric acid, an efficient catalyst in carbohydrate protection and deprotection reactions.
Albert R, et al.
Carbohydrate Research, 137, 282-290 (1985)
Metal-free hydration of aromatic haloalkynes to a-halomethyl ketones.
Ye M, et al.
Tetrahedron Letters, 57(45), 4983-4986 (2016)
Richard Ting et al.
Journal of the American Chemical Society, 130(36), 12045-12055 (2008-08-15)
The use of a boronic ester as a captor of aqueous [(18)F]-fluoride has been previously suggested as a means of labeling biomolecules in one step for positron emission tomography (PET) imaging. For this approach to be seriously considered, the [(18)F]-labeled
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