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193771

Sigma-Aldrich

Benzyltributylammonium chloride

≥98%

Synonym(s):

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

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About This Item

Linear Formula:
C6H5CH2N(Cl)(CH2CH2CH2CH3)3
CAS Number:
23616-79-7
Molecular Weight:
311.93
Beilstein:
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

Signal Word

Warning

Hazard Statements

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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
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)
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