193771
Benzyltributylammonium chloride
≥98%
Synonym(s):
N,N,N-Tributyl- N-benzylammonium chloride
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
Linear Formula:
C6H5CH2N(Cl)(CH2CH2CH2CH3)3
CAS Number:
Molecular Weight:
311.93
Beilstein:
3776210
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
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
Looking for similar products? Visit Product Comparison Guide
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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)
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
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)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service