104-75-6 Usage
Description
2-Ethylhexylamine is a water-white liquid with a fish-like odor, less dense than water, and has a flash point of 140°F. It is a corrosive liquid that is extremely irritating to skin and eyes, with vapors heavier than air. 2-Ethylhexylamine is used as an intermediate in the synthesis of various chemicals and materials.
Uses
Used in Organic Syntheses:
2-Ethylhexylamine is used as an intermediate in organic syntheses for the production of a wide range of chemicals.
Used in Pharmaceutical and Chemical Production:
2-Ethylhexylamine is utilized in the manufacturing of pharmaceuticals and other chemicals, playing a crucial role in the development of various medical and industrial products.
Used as a Beam Material and Surface Active Agent:
2-Ethylhexylamine serves as a beam material and surface active agent, contributing to its versatility in different applications.
Used in Synthesis of Aliphatic Amines:
2-Ethylhexylamine is involved in the synthesis of aliphatic amines, which are essential building blocks for various chemical products.
Used in Detergent, Rubber Chemical, and Oil Additive Synthesis:
The compound is employed in the synthesis of detergents, rubber chemicals, oil additives, and insecticides, highlighting its importance in the chemical industry.
Used in Agricultural Chemicals:
2-Ethylhexylamine is used as an intermediate to manufacture agricultural chemicals, contributing to its role in the agricultural sector.
Used in Surfactants, Polymerization Auxiliaries, and Plastic Additives:
2-Ethylhexylamine is also used in the production of surfactants, polymerization auxiliaries, and plastic additives, further expanding its applications across various industries.
Used in Dyes, Insecticides, Flotation Agents, and Corrosion Inhibitors:
2-Ethylhexylamine finds use in the synthesis of dyes, insecticides, flotation agents, and corrosion inhibitors, showcasing its diverse applications.
Used in Paint Additives, Detergents, Fuel Additives, and Lubricant Additives:
The compound is also utilized in the production of paint additives, detergents, fuel additives, and lubricant additives, demonstrating its widespread use in the chemical industry.
Used in Novel 2-Ethylhexylamine Salt Anionic Monoazo Dyes:
Novel 2-Ethylhexylamine salt anionic monoazo dyes are very useful for dyeing solvents, printing inks, or polymeric film-forming materials, highlighting its importance in the dye and ink industries.
Reference
www.chemicalland21.com/industrialchem/organic/2-ETHYLHEXYLAMINE.htm?
Loeffler, Hermann, and R. Dyllick-Brenzinger. "2-ethylhexylamine salts of anionic monoazo dyes." US, US 4668774 A. 1987.
Air & Water Reactions
Flammable. Soluble in water. Sensitive to prolonged exposure to air.
Reactivity Profile
2-Ethylhexylamine reacts 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.
Hazard
Moderate fire risk. Toxic by ingestion and
inhalation.
Health Hazard
INHALATION: High concentration of vapor will produce irritation of the respiratory tract and the lungs. Prolonged exposure may cause systemic effects. EYES: Contact with liquid may result in severe eye irritation. Exposure to concentrated vapor may result in corneal edema. SKIN: Contact with liquid may result in severe skin irritation, burns and possible skin absorption. INGESTION: May cause systemic poisoning.
Flammability and Explosibility
Flammable
Safety Profile
Poison by
intraperitoneal route. Moderately toxic by
ingestion, inhalation, and skin contact.
Corrosive. A severe skin and eye irritant.Flammable liquid when exposed to heat or
flame; can react with oxidizing materials. To
fight fire, use alcohol foam, CO2, dry
chemical. When heated to decomposition it
emits toxic fumes of NOx. See also
AMINES.
Check Digit Verification of cas no
The CAS Registry Mumber 104-75-6 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 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104-75:
(5*1)+(4*0)+(3*4)+(2*7)+(1*5)=36
36 % 10 = 6
So 104-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H19N/c1-3-5-6-8(4-2)7-9/h8H,3-7,9H2,1-2H3/p+1/t8-/m0/s1
104-75-6Relevant 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.
Utilization of common ligands for the ruthenium-catalyzed amination of alcohols
Baumann, Wolfgang,Spannenberg, Anke,Pfeffer, Jan,Haas, Thomas,Koeckritz, Angela,Martin, Andreas,Deutsch, Jens
supporting information, p. 17702 - 17706 (2014/01/17)
Simultaneous presence of bidentate phosphines with surprisingly simple structure and of the ligand triphenylphosphine were revealed as structural characteristics of new Ru catalysts for the selective conversion of primary and secondary alcohols and diols into their corresponding primary amines and diamines (see scheme). Copyright
Combinations of sunscreens
-
, (2008/06/13)
Combinations of sunscreens comprising at least one specific anti uv-B filter with triazinoaniline structure and at least one specific anti UV-A filter selected from filters with benzoxazol substituted triazinoaniline structure and a long chain alkyl ester of a benzoxazolyl-aminophenyl-cyanoacrylic acid. Cosmetic and dermatological compositions containing them, optionally in combination with vitamins and/or other anti UV-A and anti UV-B filters.