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193771

Sigma-Aldrich

Benzyltributylammonium chloride

≥98%

Sinónimos:

N,N,N-Tributyl- N-benzylammonium chloride

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About This Item

Fórmula lineal:
C6H5CH2N(Cl)(CH2CH2CH2CH3)3
Número de CAS:
23616-79-7
Peso molecular:
311.93
Beilstein/REAXYS Number:
3776210
EC Number:
245-787-3
MDL number:
MFCD00011849
UNSPSC Code:
12352116
PubChem Substance ID:
24851613
NACRES:
NA.22

Quality Level

200

assay

≥98%

form

solid

mp

155-163 °C (lit.)

SMILES string

[Cl-].CCCC[N+](CCCC)(CCCC)Cc1ccccc1

InChI

1S/C19H34N.ClH/c1-4-7-15-20(16-8-5-2,17-9-6-3)18-19-13-11-10-12-14-19;/h10-14H,4-9,15-18H2,1-3H3;1H/q+1;/p-1

Inchi Key

VJGNLOIQCWLBJR-UHFFFAOYSA-M

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General description

Benzyltributylammoniumchloride (BTBAC, BTBA) is a chemical compound to produce a series of quaternary amino acids in moderate to good yields. BTBAC is most efficient phase transfer catalysts (PTC).

Application

Benzyltributylammonium chloride is used:
  • As a hydrogen bond acceptor (HBAs) in the synthesis of new series of deep eutectic solvents (DESs) with common hydrogen bond donors.
  • As a cationic surfactant to study the interactions with anionic dyes such as indigo carmine (IC) and amaranth (Amr)by conductometric method.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
WXBF4413V
WXBF3436V
WXBD8296V
MKCR9834
MKCR9835

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Effect of ethylene, diethylene, and triethylene glycols and glycerol on the physicochemical properties and phase behavior of benzyltrimethyl and benzyltributylammonium chloride based deep eutectic solvents at 283.15-343.15 K
Basaiahgari A, et al.
Journal of Chemical and Engineering Data, 63(7), 2613-2627 (2018)
Investigation of interactions between some anionic dyes and cationic surfactants by conductometric method
Sibel T and Duman O
Fluid Phase Equilibria, 251(1), 1-7 (2007)
Asymmetric chemoenzymatic synthesis of N-acetyl-?-amino esters based on lipase-catalyzed kinetic resolutions through interesterification reactions
da Silva MR, et al.
Tetrahedron, 70(30), 2264-2271 (2014)
Phase Transfer Catalyst Assisted One-Pot Synthesis of 5-(Chloromethyl) furfural from Biomass-Derived Carbohydrates in a Biphasic Batch Reactor
Onkarappa SB and Dutta S
ChemistrySelect, 4(25), 7502-7506 (2019)
Harish Babu Balaraman et al.
International journal of biological macromolecules, 146, 253-262 (2020-01-10)
The present research investigates on task-specific deep eutectic solvents (TDES) based aqueous two-phase extraction and purification of immunoglobulins by chromatography from quail egg. The synthesis of TDES was accomplished with quaternary ammonium salt as hydrogen bond acceptor (HBA) and glycerol
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