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Merck

193771

Benzyltributylammonium chloride

≥98%, solid

別名:

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

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この商品について

化学式:
C6H5CH2N(Cl)(CH2CH2CH2CH3)3
CAS番号:
分子量:
311.93
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
245-787-3
MDL number:
Beilstein/REAXYS Number:
3776210
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製品名

Benzyltributylammonium chloride, ≥98%

Quality Level

assay

≥98%

form

solid

reaction suitability

core: ammonium

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

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

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

保管分類

8A - Combustible corrosive hazardous materials

wgk

WGK 3

ppe

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



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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