Tritech Catalyst & Intermediate Pvt. Ltd

Tetrabutylammonium hydrogensulfate (TBAHS)

Tetrabutylammonium hydrogensulfate is an ammonium salt. It serves as solvent for the dissolution of ruthenium(II) complex. It participates as a cocatalyst in the reaction medium for the preparation of alternating polyketones and propionic acid
Application - 

• Tetrabutylammonium hydrogensulfate may be employed as a catalyst for the green synthesis of glycosyl 1,4-dihydropyridines.
• Tetrabutylammonium hydrogensulfate may be employed as a catalyst for the green synthesis of glycosyl 1,4-dihydropyridines.

Tetrabutylammonium hydrogensulfate can serve as ion-pairing agent in the determination of the following using gas chromatography(GC) method :

• linear alkylbenzenesulfonates(LASs)
• acidic herbicides

Butyl Tri-Ethyl Ammonium Bromide

It is a white crystalline powder. Butyl tri-ethyl ammonium bromide also known as (1-Butyl)triethylammonium bromide is an important organic intermediate. It can be used in agrochemical, pharmaceutical & dye stuff field.

It is typically supplied as solution.
The compound acts as a strong organic base in a variety of organic and polymer reactions.
It is widely used in quaternization, methylation, and base-catalyzed condensation reactions.
Due to its hydroxide counterion, it serves as a halide-free phase-transfer catalyst in sensitive syntheses.
It is also explored in resin and ion-exchange chemistry, especially where chloride contamination must be avoided.
Applications extend to materials science, ionic liquids, and electronic-grade chemical processes.

Tetra Methyl Ammonium Chloride (TMACL)

Tetramethylammonium chloride is one of the simplest quaternary ammonium salts, with four methyl groups tetrahedrally attached to the central N. It is a hygroscopic colourless solid that is soluble in water and polar organic solvents. Tetramethylammonium chloride is a major industrial chemical, being used widely as a chemical reagent and also as a low-residue bactericide in such processes as hydrofracking. In the laboratory, it has fewer synthetic chemical applications than quaternary ammonium salts containing longer N-alkyl substituents, which are used extensively as phase-transfer catalysts.