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Postion:Product Catalog >Chemical Reagents>Organic reagents>Amine salt (ammonium salt)>Tetrabutylammonium bromide
Tetrabutylammonium bromide
  • Tetrabutylammonium bromide
  • Tetrabutylammonium bromide
  • Tetrabutylammonium bromide
  • Tetrabutylammonium bromide
  • Tetrabutylammonium bromide

Tetrabutylammonium bromide

Price Get Latest Price
Package 1kg 25kg 50kg
Min. Order: 1kg
Supply Ability: 50tons
Update Time: 2023-09-20

Product Details

Product Name: Tetrabutylammonium bromide CAS No.: 1643-19-2
EC-No.: 216-699-2 Min. Order: 1kg
Purity: 99% Supply Ability: 50tons
Release date: 2023/09/20

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Product details:



NameTetrabutylammonium bromide
CAS1643-19-2
Molecular FormulaC16H36BrN
Molar Mass322.37
Boiling point102 °C
Density1.039 g/mL at 25 °C
AppearanceWhite to crystalline powder


Usage:


Tetrabutylammonium bromide (TBAB) is a quaternary ammonium compound. It is the most widely used phase transfer catalyst. Its interfacial properties have been studied in case of hydroxide initiated reactions. This may be applied in understanding the mechanism of phase transfer reactions. TBAB is reported to decrease retention time and remove peak tailing by acting as an ion pair reagent during the chromatographic analysis of quaternary ammonium compounds. In the molten state TBAB behaves like an ionic liquid which is a promising green alternative to organic solvents in organic synthesis. Its molar heat capacity, entropy and free energy function have been determined.
Recently, molten tetrabutylammonium bromide (TBAB) was used as a low toxic and cost-effective IL in a number of constructive synthetic transformations.
Tetrabutylammonium bromide (TBAB) may be used in the molten state in the following processes:
Synthesis of (2S)-5-(3-phenyl-2-phthalimidylpropanoylamino)isophthalic acid.
Synthesis of alkyl-substituted pyrroles in the absence of catalyst and organic solvent.
Synthesis of dithioacetals from acetals by transthioacetalisation in a solvent free environment.
Synthesis of polyamides (PAs) by the polymerization of terephthalic acid and diisocyanates.
Catalyze the addition of thiols to conjugated alkenes.
Dehydrochlorination of poly(vinyl chloride).


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Company Profile Introduction

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