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Sku CI31583_1_KG
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Product Information

Product Name
Tetrabutylammonium chloride hydrate
Brand Name
Chem Impex
Product Number
31583
CAS
37451-68-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
16212273
IUPAC Name
tetrabutylazanium;chloride;hydrate
InChI Key
FODWRUPJCKASBN-UHFFFAOYSA-M
SMILES
CCCCN+(CCCC)(CCCC)CCCC.O.Cl-

Application

Tetrabutylammonium chloride hydrate is widely utilized in research focused on:

Phase Transfer Catalysis: This compound acts as an effective phase transfer catalyst, facilitating reactions between organic and aqueous phases, which is particularly useful in the synthesis of pharmaceuticals and agrochemicals.

Electrochemistry: It is employed in electrochemical applications, enhancing the conductivity of electrolytes in batteries and fuel cells, leading to improved energy efficiency and performance.

Organic Synthesis: Researchers use it in various organic synthesis processes, including the preparation of quaternary ammonium salts, which are essential in the production of surfactants and emulsifiers.

Analytical Chemistry: This chemical serves as a reagent in analytical methods, aiding in the extraction and separation of compounds, which is crucial for quality control in food and pharmaceuticals.

Biotechnology: In biotechnological applications, it is used to enhance the solubility of hydrophobic compounds, improving the efficacy of drug formulations and delivery systems.

References

Decarboxylative Arylation of Pyrrole -Carboxylates

Publication Name: Science of Synthesis
Publication Date: 2013

Tetrabutylammonium Salts of Ruthenium(II) Nitroso Complexes

Publication Name: Journal of Structural Chemistry
Publication Date: 2003-01
DOI: 10.1023/a:1024928913498

Formation of DNA adducts from oil-derived products analyzed by 32 P-HPLC

Publication Name: Archives of Toxicology
Publication Date: 2001-01-22
DOI: 10.1007/s002040000172

A stability-indicating HPLC method for the determination of 17β-estradiol-3-phosphate in an ophthalmic solution

Publication Name: Chromatographia
Publication Date: 1995-02
DOI: 10.1007/bf02272172

C16H30 - C16H56 (16-30-3 - 16-56-2)

Publication Name: Landolt-Börnstein - Group III Condensed Matter
Publication Date: 1971
DOI: 10.1007/10201446_70