358673
Tetrabutylammonium fluoride on silica gel
~1.5 mmol/g (F-)
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About This Item
Fórmula lineal:
(CH3CH2CH2CH2)4N(F)
Peso molecular:
261.46
Beilstein/REAXYS Number:
3570522
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
capacity
~1.5 mmol/g (F-)
SMILES string
[F-].CCCC[N+](CCCC)(CCCC)CCCC
InChI
1S/C16H36N.FH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1
InChI key
FPGGTKZVZWFYPV-UHFFFAOYSA-M
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2
supp_hazards
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Mehrdad Balandeh et al.
Journal of the Electrochemical Society, 164(9), G99-G103 (2017-09-12)
Electrochemical fluorination of methyl(phenylthio)acetate was achieved using tetrabutylammonium fluoride (TBAF). Electrochemical fluorination was performed under potentiostatic anodic oxidation using an undivided cell in acetonitrile containing TBAF and triflic acid. The influence of several parameters including: oxidation potential, time, temperature, sonication
Santosh Kumar Behera et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 14(12), 2225-2237 (2015-10-31)
The mechanism for the dual emission of 2-(4'-N,N-dimethylaminophenyl)imidazo[4,5-c]pyridine (DMAPIP-c) in protic solvents was investigated by synthesizing and studying its analogues. Theoretical calculations were carried out to corroborate the experimental findings. The deprotonation studies suggest that the enhancement in the TICT
Delia López-Velázquez et al.
Carbohydrate polymers, 125, 224-231 (2015-04-11)
We have synthesized and characterized five members of a homologous series of side chain polymers of hydroxypropyl cellulose esters obtained by homogeneous esterification with 6-[4'-(ethoxycarbonyl)biphenyl-4-yloxy]hexanoic acid. Two acylation procedures were studied. One procedure involved the acid chloride derivative and the
Eric P Gillis et al.
Journal of medicinal chemistry, 58(21), 8315-8359 (2015-07-23)
The role of fluorine in drug design and development is expanding rapidly as we learn more about the unique properties associated with this unusual element and how to deploy it with greater sophistication. The judicious introduction of fluorine into a
Soumen Ghosh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 149, 869-874 (2015-05-24)
A series of Schiff bases synthesized by the condensation of benzohydrazide and -NO2 substituted benzaldehyde have been used as selective fluoride ion sensor. Test paper coated with these synthetic Schiff bases (test kits) can detect fluoride ion selectively with a
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