106-20-7 Usage
Description
1-Hexanamine,2-ethyl-N-(2-ethylhexyl)-, also known as Bis(2-ethylhexyl)amine (BEA), is a clear colorless liquid with a slight ammonia-like odor. It is a chemical compound that possesses unique properties, making it suitable for various applications across different industries.
Uses
Used in Chemical Synthesis:
1-Hexanamine,2-ethyl-N-(2-ethylhexyl)is used as a chemical intermediate for the synthesis of stable nanosized CdS particles. These particles are coated by an oriented monolayer of chemically bonded BEA molecules, which enhances their stability and performance in various applications.
Used in Nanotechnology Industry:
In the nanotechnology industry, 1-Hexanamine,2-ethyl-N-(2-ethylhexyl)is used as a stabilizing agent for the production of nanosized particles. The application reason is to improve the stability and performance of these particles, making them more suitable for various applications such as electronics, solar cells, and other advanced technologies.
Used in Pharmaceutical Industry:
1-Hexanamine,2-ethyl-N-(2-ethylhexyl)may also find applications in the pharmaceutical industry, potentially serving as a building block for the development of new drugs or drug delivery systems. The application reason is its unique chemical properties, which could be harnessed to create innovative and effective treatments for various medical conditions.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Bis(2-ethylhexyl)amine can react with oxidizing materials . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
Fire Hazard
Bis(2-ethylhexyl)amine is combustible.
Flammability and Explosibility
Nonflammable
Check Digit Verification of cas no
The CAS Registry Mumber 106-20-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106-20:
(5*1)+(4*0)+(3*6)+(2*2)+(1*0)=27
27 % 10 = 7
So 106-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H23N/c1-4-7-8-9-10-11(5-2)6-3/h4-10H2,1-3H3
106-20-7Relevant articles and documents
Amination of aliphatic alcohols with urea catalyzed by ruthenium complexes: effect of supporting ligands
Dindar, Sara,Nemati Kharat, Ali
, (2020/09/02)
In the present study, ruthenium-catalyzed amination of alcohols by urea as a convenient ammonia carrier in the presence of free diphosphine ligands has been described. A number of ruthenium-phosphine complexes have been studied among which, [(Cp)RuCl(dppe)] was found as an efficient catalyst for alcohol amination reaction. The crystal structures of two new half-sandwich ruthenium complexes, [(Cp)RuCl(dppe)] and [(C6H6)RuCl2(PHEt2)], were determined by X-ray crystallographic analysis. Also the effect of using different supporting phosphines, ratio of raw materials and reaction temperature on conversion and selectivity was investigated. Under optimum reaction conditions high conversion (98percent) and chemo-selectivity toward secondary amines were obtained.
Ruthenium-catalyzed deaminative redistribution of primary and secondary amines
Kostera,Wyrzykiewicz,Pawlu?,Marciniec
supporting information, p. 11552 - 11555 (2017/09/18)
A ruthenium-hydride complex, [Ru(H)(Cl)(CO)(PCy3)2], was found to be active in the highly selective redistribution of primary and secondary amines bearing an α-hydrogen atom. This new deaminative coupling of amines enables the highly selective synthesis of secondary amines from primary amines and of tertiary amines from secondary amines with the evolution of ammonia. A preliminary mechanistic view of this novel reaction based on catalytic experiments using NMR methods confirms the synthetic observations.
Process for the preparation of nonadecanediols
-
, (2008/06/13)
The present invention relates to a process for the preparation of nonadecanediols by the hydroformylation of oleyl alcohol. Rhodium and salts of sulfonated or carboxylated triarylphosphines, which are soluble in organic media and insoluble in water, are used as hydroformylation catalysts. The hydroformylation product is then treated with a diluted solution of a base dissolved in water, the aqueous phase separated and the hydroformylation product treated with hydrogen at elevated temperature in the presence of a hydrogenation catalyst.