102-88-5

Basic information

• Product Name: N,N-dioctadecyloctadecan-1-amine
• Synonyms: Tri-octadecylAmine
• CAS NO: 102-88-5
• Molecular Formula: C₅₄H₁₁₁N
• Molecular Weight: 774.46584
• Mol File: 102-88-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 54°C
• Boiling Point: 619.36°C (rough estimate)
• Flash Point: 333°C
• Appearance: /
• Density: 0.9303 (estimate)
• Vapor Pressure: 8.21E-23mmHg at 25°C
• Refractive Index: 1.4927 (estimate)
• CAS DataBase Reference: N,N-dioctadecyloctadecan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dioctadecyloctadecan-1-amine(102-88-5)
• EPA Substance Registry System: N,N-dioctadecyloctadecan-1-amine(102-88-5)

Safety Data

• Hazardous Substances Data: 102-88-5(Hazardous Substances Data)

Usage

General Description

N,N-dioctadecyloctadecan-1-amine, often referred to as Dioctadecylamine, is a chemical compound with a complex molecular structure. It consists of an octadecyl (C18H37) alkyl chain attached to an octadecan-1-amine (C18H39N) functional group. N,N-dioctadecyloctadecan-1-amine falls into the category of long-chain amines and is frequently used as a surfactant and emulsifying agent in various industrial applications, including the production of detergents, cosmetics, and coatings.

InChI:InChI=1/C54H111N/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-52-55(53-50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2)54-51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3/h4-54H2,1-3H3

Upstream product

• 3386-33-2 1-chlorooctadecane 
• 112-99-2 Dioctadecylamine 
• 7664-41-7 ammonia 
• 638-65-3 stearonitrile 
• 112-92-5 1-octadecanol 
• 112-89-0 1-Bromooctadecane 
• 112-76-5 Stearoyl chloride 
• 124-30-1 1-aminooctadecane 
• 13276-08-9 N-(octadecanoyl)octadecylamide 
• 103568-30-5 Octadecanoic acid dioctadecylamide 
• 629-93-6 n-iodooctadecane 

Relevant articles and documents

New lyotropic phases (thermally-reversible organogels) of simple tertiary amines and related tertiary and quaternary ammonium halide salts

Small concentrations of some structurally simple tertiary amines and related tertiary and quaternary ammonium halide salts form viscoelastic, thermally reversible gels with a wide variety of organic liquids.

Conversion of Primary Amines to Symmetrical Secondary and Tertiary Amines using a Co-Rh Heterobimetallic Nanocatalyst

Symmetrical tertiary amines have been efficiently realized from amine and secondary amines via deaminated homocoupling with heterogeneous bimetallic Co2Rh2/C as catalyst (molar ratio Co:Rh=2:2). Unsymmetric secondary anilines were produced from the reaction of anilines with symmetric tertiary amines. The Co2Rh2/C catalyst exhibited very high catalytic activity towards a wide range of amines and could be conveniently recycled ten times without considerable leaching. (Figure presented.).