Tritech Catalyst & Intermediate Pvt. Ltd

Additional Information:

• Packaging Details: 25 - 50 KG Packings

Benzyltriethylammonium chloride is a lipophilic phase-transfer catalyst that can be used in phase-transfer catalysis (PTC) to catalyze polycondensation reactions to form high molecular weight polymers under bi-phasic conditions.

It can also be used:

To activate hydroxyapatite and natural phosphate for use as a solid support for Knoevenagel condensation and Claisen-Schmidt condensation, respectively at room temperature and in the absence of a solvent.

To increase the efficiency of mCPBA oxidation of sulfonimine generated from arenesulfonamide and diethyl acetal of an aromatic aldehyde to form 2-sulfonyloxaziridines.

In combination with antimony(V) chloride to form a catalytic system for the Friedel-Crafts acylation reactions of arenes with acyl and sulfonyl chlorides.

It finds its application as a protein purification reagent. Triethylamine is used as a competing base for the separation of acidic basic and neutral drugs by reverse-phased high-performance liquid chromatography (HPLC). Triethylamine induces visual disturbances (such as foggy vision) in humans, and is also used in industry as a quenching agent in the ozonolysis of alkenes (e.g. (E)-2-Pentene.

Benzyltributyl ammonium chloride (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

Benzyltributyl ammonium 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.

Trimethylamine hydrochloride is a precursor to prepare aluminium chloride- trimethylamine hydrochloride ionic liquid, which is commonly used in electrodeposition of aluminum wires. It is also used in the synthesis of trimethylamine gallane, trimethylamine-borane and azido-bridged perovskite-type metal-organic frameworks (MOFs).

• The synthesis of alkyl and aryl sulfonamides from thiols and disulfides in the presence of 1,3-dichloro-5,5-dimethylhydantoin (DCH).
• The selective oxidation of benzyl alcohol to benzaldehyde using hydrogen peroxide as oxidant.
• The esterification reaction of ethanol and lauric acid.