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Merck
CN

193771

Benzyltributylammonium chloride

≥98%, solid

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
NACRES:
NA.22
PubChem Substance ID:
24851613
UNSPSC Code:
12352116
EC Number:
245-787-3
MDL number:
MFCD00011849
Beilstein/REAXYS Number:
3776210

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Product Name

Benzyltributylammonium chloride, ≥98%

InChI key

VJGNLOIQCWLBJR-UHFFFAOYSA-M

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

SMILES string

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

assay

≥98%

form

solid

mp

155-163 °C (lit.)

Quality Level

200

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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.

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).

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

WGK 3

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF6233V
WXBF5464V
WXBF4413V
WXBF3436V
WXBD8296V

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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)
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)
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)
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)
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