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Tetrabutylammonium Bromide (TBAB)

Tetrabutylammonium Bromide (TBAB)
Tetrabutylammonium Bromide (TBAB)
Product Code : CAS 1643-19-2
Product Description

Tetrabutylammonium Bromide (TBAB)

With the inclusion of advanced technology, we are engaged in manufacturing, exporting and supplying an excellent grade Tetrabutylammonium Bromide (TBAB). The chemical offered by us is accurately processed under the vigilance of our diligent team by making use of premium quality chemical compounds and modern technology in tandem with set international standards. Widely known as a flame retardant property and is used in the production of photographic emulsions and chemicals, we provide this chemical to the patrons in different packaging options. Furthermore, clients can purchase this Tetrabutylammonium Bromide (TBAB) from us at market leading prices.

Key Features:

  • Accurate composition
  • Non toxic
  • Precise pH value
  • Long shelf life

Our company is focused on bringing Greener Optional Products, which cling to at least one of The 12 standards of Greener Chemistry. Further, our Tetrabutylammonium Bromide (TBAB)

has been improved for power productivity. It is a quaternate ammonium ion binate. This is the most generally utilized stage transfer catalyst. Its interfacial qualities have been contemplated if there should arise an occurrence of hydroxide initiated responses. This might be used in knowing the process of stage transfer reactions. Our Tetrabutylammonium Bromide (TBAB)is accounted for to decline maintenance time and expel crest following by going about as a particle match reagent amid the chromatographic examination of quaternary ammonium binate. In the liquid state TBAB carries on like an ionic fluid, which is a likely green option to natural solvents in natural synthesis. Furthermore, its molar heatlimit, free energy and entropy work have been determined.

Uses:

Tetrabutylammonium bromide (TBAB) might be utilized as a part of the liquid condition in the below procedures:

  • Synthesis of isophthalic acid
  • Synthesis of alkyl-secondary pyrroles without impetus and natural solvent
  • Synthesis of dithioacetals against acetals through transthioacetalisation in a dissolvable free condition
  • Synthesis of polyamides through the polymerization of diisocyanates as well as terephthalic corrosive
  • Enzyme the expansion of thiols to bound alkenes
  • Poly(vinyl chloride) Dehydrochlorination
  • Utilized with phosphorus pentoxide for greener deoxybromination
  • Prepare for making Halogenated Heteroaryl Compounds

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