2095-01-4

Usage

Physical Appearance

Colorless to pale yellow liquid

Odor

Faint amine odor

Usage

Commonly used in the production of polymers, resins, and coatings

Typical Application

Curing agent in epoxy systems and polyurethane coatings, monomer in the production of polyurethane foams and rubbers, component in adhesives and sealants

Mechanical and Chemical Properties

Offers excellent mechanical and chemical resistance

Safety Measures

Toxic if ingested, inhaled, or comes into contact with skin. Proper safety measures, including the use of gloves and protective clothing, should be taken when handling this chemical.

InChI:InChI=1/C11H18N2/c1-4-8-6-9(5-2)11(13)7(3)10(8)12/h6H,4-5,12-13H2,1-3H3

Upstream product

• 74-85-1 ethene 
• 823-40-5 2,6-toluenediamine 
• 95-80-7 4-methylbenzene-1,3-diamine 
• 7429-90-5 aluminium 

Downstream Products

• 1373247-97-2 4-chloro-3,5-diethyltoluene-2,6-diamine 
• 1373248-01-1 4-bromo-3,5-diethyltoluene-2,6-diamine 
• 1373247-99-4 N,N'-diacetyl-4-bromo-3,5-diethyltoluene-2,6-diamine 
• 910915-19-4 N,N'-diisopropylidene-(4,6-diethyl-2-methyl-1,3-benzenediamine) 
• 910915-15-0 N,N'-diisopropylidene-(2,4-diethyl-6-methyl-1,3-benzenediamine) 
• 910915-26-3 N,N'-di-sec-butyl-(4,6-diethyl-2-methyl-1,3-benzenediamine) 
• 910915-06-9 N,N'-di-sec-butyl-(2,4-diethyl-6-methyl-1,3-benzenediamine) 
• 910915-20-7 N,N'-di-sec-butylidene-(4,6-diethyl-2-methyl-1,3-benzenediamine) 
• 910915-12-7 N,N'-di-sec-butylidene-(2,4-diethyl-6-methyl-1,3-benzenediamine) 

Relevant academic research and scientific papers

Process for the isolation of alkylated aromatic amines

Alkylated aromatic amines can be isolated from crude catalyst-containing mixtures of these with olefins by a procedure in which in general equivalent amounts of an inorganic base and water are added to the alkylation mixture, the catalyst is hydrolysed, the water present in the reaction mixture after the hydrolysis is removed by distillation and the solid catalyst residue is separated off. The catalyst-free alkylation mixture which remains is then fed to customary further working up.

Process for the ortho-alkylation of optionally alkyl-substituted m-phenylenediamines

m-Phenylenediamines are alkylated in the orthoposition by heating them with an Al/Zn alloy and aluminium chloride, and reacting them with lower alkenes at elevated pressures and temperatures when the evolution of hydrogen is complete.