63302-43-2

Basic information

• Product Name: 1,4-BenzenediaMine, N-(1,4-diMethylpentyl)-
• Synonyms: 1,4-BenzenediaMine, N-(1,4-diMethylpentyl)-;N-(1,4-dimethylpentyl)benzene-1,4-diamine
• CAS NO: 63302-43-2
• Molecular Formula: C₁₃H₂₂N₂
• Molecular Weight: 206.32718
• EINECS: 1312995-182-4
• Mol File: 63302-43-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 334.3°C at 760 mmHg
• Flash Point: 182.8°C
• Appearance: /
• Density: 0.978g/cm³
• Vapor Pressure: 0.000129mmHg at 25°C
• Refractive Index: 1.556
• CAS DataBase Reference: 1,4-BenzenediaMine, N-(1,4-diMethylpentyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-BenzenediaMine, N-(1,4-diMethylpentyl)-(63302-43-2)
• EPA Substance Registry System: 1,4-BenzenediaMine, N-(1,4-diMethylpentyl)-(63302-43-2)

Safety Data

• Hazardous Substances Data: 63302-43-2(Hazardous Substances Data)

Usage

Uses

N1-(1,4-Dimethylpentyl)-1,4-benzenediamine is used as a reactant in the one-pot reductive alkylation of diamines.

InChI:InChI=1/C13H22N2/c1-10(2)4-5-11(3)15-13-8-6-12(14)7-9-13/h6-11,15H,4-5,14H2,1-3H3

Upstream product

• 110-12-3 5-Methyl-2-hexanone 
• 106-50-3 1,4-phenylenediamine 

Downstream Products

• 121246-28-4 2,4,6-tris-(N-(1,4-dimethylpentyl)-p-phenylenediamine)-1,3,5-triazine 
• 731026-33-8 2,6-di-tert-butyl-4-{[4-(1,4-dimethyl-pentylamino)-phenylamino]-methyl}-phenol 

Relevant articles and documents

Preparation method of 2, 4, 6-tri(N-1, 4-dimethylamyl-p-phenylenediamine)-1, 3, 5-triazine

The invention discloses a preparation method of 2, 4, 6-tri(N-1, 4-dimethylamyl-p-phenylenediamine)-1, 3, 5-triazine. The preparation method comprises the following steps: carrying out catalytic hydrogenation reaction on p-aminoacetanilide and methyl isoamyl ketone to obtain N-1, 4-dimethylamyl-p-acetanilide; removing acetyl from N-1, 4-dimethylamyl-p-acetanilide in an alkali solution, so as to obtain N-1, 4-dimethylamyl-p-aniline; and carrying out substitution reaction on cyanuric chloride and N-1, 4-dimethylamyl-p-phenylenediamine, and carrying out after-treatment to obtain the 2, 4, 6-tri(N-1, 4-dimethylamyl-p-phenylenediamine)-1, 3, 5-triazine. The method has the advantages of high reaction selectivity and yield, few byproducts, low cost and good quality.