| Weight | 189.989 g/mol |
|---|---|
| Formula | C6H15BF4O |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Triethyloxonium tetrafluoroborate (368-39-8)
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- Cationic polymerization of cyclic sulphides. I. Kinetic study of the polymerization of 3.3-dimethylthietane initiated by triethyloxonium tetrafluoroborate (Macromolecular Chemistry and Physics, 1970)
- Negative chemical ionization GC/MS determination of nitrite and nitrate in seawater using exact matching double spike isotope dilution and derivatization with triethyloxonium tetrafluoroborate. (Analytical Chemistry, 2012)
- High-precision quadruple isotope dilution method for simultaneous determination of nitrite and nitrate in seawater by GCMS after derivatization with triethyloxonium tetrafluoroborate. (Analytica Chimica Acta, 2014)
- Reactions of methyl fluorosulphonate and triethyloxonium tetrafluoroborate with metal complexes (Journal of Organometallic Chemistry, 1973)
- Quantification of nitrite and nitrate in seawater by triethyloxonium tetrafluoroborate derivatizationHeadspace SPME GCMS (Talanta, 2011)
- NMR studies on the growing species in the cationic polymerization of cyclic formals: An oxycarbenium ion formed in the reaction of 1,3-dioxane with triethyloxonium tetrafluoroborate (Macromolecular Chemistry and Physics, 1975)
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SMILES[B-](F)(F)(F)F.CC[O+](CC)CC
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InChIKeyIYDQMLLDOVRSJJ-UHFFFAOYSA-N
- Pubchem - Triethyloxonium tetrafluoroborate
- Wikipedia - triethyloxonium tetrafluoroborate
Triethyloxonium tetrafluoroborate is the organic oxonium compound with the formula [(CH3CH2)3O]BF4. It is often called Meerwein's Reagent or Meerwein's Salt after its discoverer Hans Meerwein. Also well known and commercially available is the related trimethyloxonium tetrafluoroborate.
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(111-44-4)
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3 suppliers
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(6921-27-3)
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(1693-74-9)
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(27274-31-3, 111-45-5)
1 alternate name
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3973-18-0
(3973-18-0)
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(929-06-6)
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(6163-66-2)
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(109-92-2)
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(13755-29-8)
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(927-80-0)
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Triethyloxonium tetrafluoroborate
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