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Merck
모든 사진(1)

주요 문서

358673

Sigma-Aldrich

Tetrabutylammonium fluoride on silica gel

~1.5 mmol/g (F-)

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About This Item

Linear Formula:
(CH3CH2CH2CH2)4N(F)
Molecular Weight:
261.46
Beilstein:
3570522
EC Number:
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.22

Quality Level

용량

~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

픽토그램

Health hazardExclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2

보충제 위험성

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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시험 성적서(COA)

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문서 라이브러리 방문

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
Michelle L Ingalsbe et al.
Bioorganic & medicinal chemistry letters, 19(17), 4984-4987 (2009-08-08)
Due to the increasing number of strains of drug-resistant bacteria, the development of new antibiotics has become increasingly important. The antibacterial properties of quaternary amines and their derivatives on both Gram-positive and Gram-negative bacteria are well known. However, an encompassing

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