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Merck
CN

193771

Benzyltributylammonium chloride

≥98%, solid

Sustainability features

Synonym(s):

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

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About This Item

Linear Formula:
C6H5CH2N(Cl)(CH2CH2CH2CH3)3
CAS Number:
Molecular Weight:
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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Product Name

Benzyltributylammonium chloride, ≥98%

Quality Segment

assay

≥98%

form

solid

reaction suitability

core: ammonium, reaction type: phase-transfer, reagent type: organic catalyst

sustainability

Sustainability features

mp

155-163 °C (lit.)

greener alternative category

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

We are committed to providing greener alternatives that adhere to the 12 Principles of Green Chemistry. This salt reagent serves as a weakly coordinating anion source for efficient catalyst activation, reducing toxic halide levels while maintaining high reactivity, thus aligns with Green Chemistry principle "Catalysis". Click here for more information.
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

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Signal Word

Warning

Hazard Codes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

PPE (personal protective equipment)

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

Storage Class

11 - Combustible Solids



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