Online Database of Chemicals from Around the World

Dibutylamine monohydrochloride
[CAS# 6287-40-7]

List of Suppliers
Leap Chem Co., Ltd. China Inquire  
+86 (852) 3060-6658
market19@leapchem.com
QQ chat
Chemical manufacturer since 2006
chemBlink standard supplier since 2015
Matrix Scientific Inc. USA Inquire  
+1 (803) 788-9494
sales@matrixscientific.com
Chemical manufacturer
Complete supplier list of Dibutylamine monohydrochloride
Identification
Classification Chemical reagent >> Organic reagent >> Amine salt (ammonium salt)
Name Dibutylamine monohydrochloride
Synonyms Dibutylammonium chloride; N-Butyl-1-butanamine hydrochloride
Molecular Structure CAS # 6287-40-7, Dibutylamine monohydrochloride, Dibutylammonium chloride, N-Butyl-1-butanamine hydrochloride
Molecular Formula C8H19N.HCl
Molecular Weight 165.70
CAS Registry Number 6287-40-7
EC Number 228-521-0
SMILES CCCCNCCCC.Cl
Properties
Melting point 284-286 ºC*
* Kundiger, Donald G.; Journal of the American Chemical Society 1958, V80, P5988-90.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302+H312+H332-H302-H312-H315-H319-H332    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H332
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H302
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2AH319
Acute toxicityAcute Tox.3H301
SDS Available
up Discovory and Applicatios
Dibutylamine monohydrochloride is a chemical compound with the molecular formula C8H18ClN. It is the hydrochloride salt of dibutylamine, a tertiary amine characterized by the presence of two butyl groups attached to a nitrogen atom. This compound is typically encountered as a colorless to pale yellow liquid or crystalline solid and is soluble in water and alcohol.

The discovery of dibutylamine monohydrochloride can be traced back to the late 19th century when chemists began exploring the synthesis and properties of various amines. Dibutylamine itself was first synthesized in the early 20th century through the reaction of butylamine with butyl halides. The formation of dibutylamine monohydrochloride involves the protonation of dibutylamine with hydrochloric acid, resulting in the formation of the stable salt. This process highlights the significance of amine chemistry in producing a variety of functional compounds used across multiple applications.

Dibutylamine monohydrochloride is primarily used in organic synthesis as a reagent and catalyst. Its structure allows it to participate in various chemical reactions, including nucleophilic substitutions and acylations. In particular, dibutylamine derivatives are often employed in the synthesis of active pharmaceutical ingredients (APIs), where they serve as intermediates or building blocks for more complex molecules. The ability of dibutylamine monohydrochloride to function as a nucleophile and a base makes it a valuable component in medicinal chemistry.

In addition to its pharmaceutical applications, dibutylamine monohydrochloride has been utilized in the production of surfactants and other industrial chemicals. Its surfactant properties enable it to act as an emulsifying agent, which is essential in formulations for personal care products, detergents, and coatings. By improving the stability and solubility of these formulations, dibutylamine monohydrochloride plays a crucial role in enhancing product performance.

Research into the biological activities of dibutylamine derivatives has also revealed potential applications in the field of agrochemicals. Some studies suggest that certain dibutylamine derivatives exhibit herbicidal and pesticidal properties, making them of interest for developing environmentally friendly agricultural solutions. While specific research on dibutylamine monohydrochloride's biological effects is limited, its structural characteristics indicate that it may possess similar bioactive properties, warranting further investigation.

Despite its utility, safety precautions are essential when handling dibutylamine monohydrochloride. As with many amines, it can pose health risks, including skin irritation and respiratory issues. Therefore, proper laboratory practices, including the use of personal protective equipment and adherence to safety protocols, are crucial to minimize exposure and ensure safe handling.

In summary, dibutylamine monohydrochloride is an important chemical compound with a notable history of discovery and diverse applications in organic synthesis, pharmaceuticals, and industrial formulations. Its versatility as a reagent and its role in various chemical processes continue to make it a subject of interest in contemporary chemistry, highlighting its relevance across multiple fields.
Market Analysis Reports
List of Reports Available for Dibutylamine monohydrochloride
Related Products
N,N-Dibutyl-2-octyn-1-amine  Dibutyl oxalate  Dibutyl peroxydicarbonate  2,9-Dibutyl-1,10-phenanthroline  Dibutyl phosphate  Dibutoxytitanium bis(ethyl acetoacetate)  1,1-Dibutoxytrimethylamine  N,N-Dibutylacetamide  Dibutyl adipate  Dibutylamine  4-(Dibutylamino)-N-[4-(dibutylamino)phenyl]-N-[4-(dibutyliminio)-2,5-cyclohexadien-1-ylidene]benzenaminium hexafluoroantimonate(1-)  4-[2-(Dibutylamino)ethyl]-1,2-benzenediol hydrobromide  2-[4-(Dibutylamino)-2-hydroxybenzoyl]benzoic acid  3-Dibutylamino-6-methyl-7-bromofluoran  3-(Dibutylamino)phenol  (1R,2S)-2-Dibutylamino-1-phenyl-1-propanol  (1S,2R)-(N,N-Dibutylamino)-1-phenyl-1-propanol  4-[3-(Dibutylamino)propoxy]benzoic acid hydrochloride  4-(N,N-Dibutylamino)pyridine  2-[[5-(Dibutylamino)-2-thienyl]methylene]-1H-indene-1,3(2H)-dione