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About This Item
Linear Formula:
(C2H5)3O(BF4)
CAS Number:
Molecular Weight:
189.99
Beilstein:
3598090
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
Quality Level
concentration
1.0 M in methylene chloride
density
1.328 g/mL at 25 °C
functional group
ether
storage temp.
2-8°C
SMILES string
F[B-](F)(F)F.CC[O+](CC)CC
InChI
1S/C6H15O.BF4/c1-4-7(5-2)6-3;2-1(3,4)5/h4-6H2,1-3H3;/q+1;-1
InChI key
IYDQMLLDOVRSJJ-UHFFFAOYSA-N
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Application
Used in the preparation of ω-aminoesters from lactams.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Central nervous system
Supplementary Hazards
Storage Class Code
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Synthetic Communications, 18, 1625-1625 (1988)
Some detoxification methods for N-nitrosamine-contaminated wastes.
M Castegnaro et al.
IARC scientific publications, (41)(41), 151-157 (1982-01-01)
J Aguado et al.
Biotechnology and applied biochemistry, 17 ( Pt 1), 49-55 (1993-02-01)
beta-Glucosidase from Penicillium funiculosum was immobilized on nylon powder previously activated with triethyloxonium tetrafluoroborate, 1,2-diaminoethane and glutaraldehyde. The activation of the nylon powder and the immobilization processes were studied and optimized for the enzyme and the matrix. A high activity
R Ben Avraham et al.
FEBS letters, 180(2), 239-242 (1985-01-28)
Treatment of trypsin with triethyloxonium tetrafluoroborate at pH 8, 25 degrees C, results in abolition of binding to the enzyme of specific cationic substrates and inhibitors. The binding constant of soybean trypsin inhibitor to ethylated trypsin is 10000-fold smaller than
Enea Pagliano et al.
Analytical chemistry, 84(5), 2592-2596 (2012-02-11)
The alkylation of nitrite and nitrate by triethyloxonium tetrafluoroborate allows determination of their ethyl esters by headspace gas chromatography/mass spectrometry (GC/MS). In the present study, significant improvement in analytical performance is achieved using negative chemical ionization providing detection limits of
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