Sigma Aldrich 217964 Tetrabutylammonium tetrafluoroborate 99% 25 gr
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Stok Kodu
LB.SA.217964-25G
Kısa Bilgi
Synonym(s): Ammonium tetra-n-butyl tetrafluoroborate Linear Formula: (CH3CH2CH2CH2)4N(BF4) CAS Number: 429-42-5 Molecular Weight: 329.27 Beilstein: 3577508 EC Number: 207-058-8 MDL number: MFCD00011634 UNSPSC Code: 12352116 PubChem Substance ID: 24853042 NACRES: NA.22
Bilgi
CAS Number: 429-42-5
Sigma Aldrich 217964 Tetrabutylammonium tetrafluoroborate 99% |
Synonym(s): Ammonium tetra-n-butyl tetrafluoroborate Linear Formula: (CH3CH2CH2CH2)4N(BF4) CAS Number: 429-42-5 Molecular Weight: 329.27 Beilstein: 3577508 EC Number: 207-058-8 MDL number: MFCD00011634 UNSPSC Code: 12352116 PubChem Substance ID: 24853042 NACRES: NA.22 |
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PROPERTIES
Quality Level 200
Assay 99% form powder mp 155-161 °C (lit.) solubility methanol: soluble 10%, clear, colorless SMILES string F[B-](F)(F)F.CCCC[N+](CCCC)(CCCC)CCCC InChI 1S/C16H36N.BF4/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;2-1(3,4)5/h5-16H2,1-4H3;/q+1;-1 InChI key NNZZSJSQYOFZAM-UHFFFAOYSA-N DESCRIPTION General description Tetrabutylammonium tetrafluoroborate is used as an electrolyte for the series of arylketone synthesis.[1] [2] Tetrabutylammonium tetrafluoroborate (TBATFB) is a phase transfer catalyst.[3] It can be synthesized by the reaction between 30% aqueous solution of tetrafluoroboric acid and 40% aqueous solution of tetrabutylamonium hydroxide.[4] Tetrabutylammonium tetrafluoroborate acts as an electrolyte and inhibits the self-assembly of alkylthiosulfate on gold.[5] Application Tetrabutylammonium tetrafluoroborate may be used in the following studies: - As supporting electrolyte in the voltammetric determination of Δ(9)-tetrahydrocannabinol (Δ(9)-THC).[6] - Synthesis of biologically relevant macrolactones, Sansalvamide A.[7] - As supporting electrolyte in the determination of the oxidation and reduction potentials of 5,10,15,20-tetra[3-(3-trifluoromethyl)phenoxy]porphyrin by cyclic voltammetry.[8] - Preparation of 1:1 adduct with 1,10-phenanthroline.[9] - Used to prepare other tetrabutylammonium salts in aqueous solutions.[10] - As electrolyte additive in the synthesis of conducting poly(thiophenes).[11] |
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