1070-01-5

Basic information

• Product Name: TRI-N-DECYLAMINE
• Synonyms: N,N-DIDECYL-1-DECANAMINE;N,N-DI-N-DECYL-1-DECANAMINE;TRI-N-DECYLAMINE;TRI-N-DECYLAMINE (TERTIARY AMINE);1-Decanamine,N,N-didecyl-;n,n-didecyl-1-decanamin;n,n-didecyl-1-decanamine,isomericmixture;tridecanitrile(mixedisomers)
• CAS NO: 1070-01-5
• Molecular Formula: C₃₀H₆₃N
• Molecular Weight: 437.83
• EINECS: 213-966-5
• Mol File: 1070-01-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: -5--3 °C
• Boiling Point: 430 °C
• Flash Point: 121 °C
• Appearance: /
• Density: 0.8
• Vapor Pressure: 2.67E-10mmHg at 25°C
• Refractive Index: 1.454-1.456
• CAS DataBase Reference: TRI-N-DECYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: TRI-N-DECYLAMINE(1070-01-5)
• EPA Substance Registry System: TRI-N-DECYLAMINE(1070-01-5)

Safety Data

• Hazard Codes: Xn
• Statements: 21
• Safety Statements: 24/25
• RTECS: YD3675000
• Hazardous Substances Data: 1070-01-5(Hazardous Substances Data)

Usage

Chemical Properties

clear light yellow viscous liquid

Safety Profile

Moderately toxic by ingestion andskin contact. When heated to decomposition it emits toxicfumes of NOx and CNí.

InChI:InChI=1/C30H63N/c1-4-7-10-13-16-19-22-25-28-31(29-26-23-20-17-14-11-8-5-2)30-27-24-21-18-15-12-9-6-3/h4-30H2,1-3H3

Upstream product

• 1975-78-6 n-decanenitrile 
• 24424-99-5 di-tert-butyl dicarbonate 
• 1120-49-6 didecylamine 
• 2016-57-1 1-aminodecane 
• 1002-69-3 decyl chloride 
• 112-30-1 1-Decanol 
• 74-89-5 methylamine 

Related news

Extractive lactic acid fermentation with TRI-N-DECYLAMINE (cas 1070-01-5) as the extractant07/25/2019

In this study, the possibility of tri-n-decylamine (TDA) was investigated as the extractant in extractive lactic acid fermentation with a recombinant yeast being used. Extractive fermentation with TDA did not provide high l-lactic acid production relative to fermentation without extraction. Thro...detailed

Relevant articles and documents

Selective Synthesis of Primary Amines from Nitriles under Hydrogenation Conditions

The hydrogenation of aliphatic nitriles over Pd/C, Pd/Al2O3, and Pd?Au/Al2O3 catalysts were evaluated for the selective hydrogenation of aliphatic nitriles to the corresponding primary amines. The highest selectivity (>99%) toward primary amines was achieved when the reaction was carried out in acetic acid using 10 mol% of 25% Pd-5% Au/Al2O3 under relatively low hydrogen pressure (0.8 MPa). Characterization of the catalysts by XRD, CO adsorption experiments, and EXAFS revealed that the excellent selectivity of 25% Pd-5% Au/Al2O3 toward the synthesis of primary amines is determined by the electronic properties and/or the surface structure resulting from alloying Pd with Au. (Figure presented.).

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.).

Catalyst-Dependent Selective Hydrogenation of Nitriles: Selective Synthesis of Tertiary and Secondary Amines

In the presence of palladium on carbon (Pd/C) as a catalyst, hydrogenation of aliphatic nitriles in cyclohexane efficiently proceeded at 25-60 °C under ordinary hydrogen gas pressure to afford the corresponding tertiary amines. However, the use of rhodium on carbon (Rh/C) led to the highly selective generation of secondary amines. Hydrogenation of aromatic nitriles and cyclohexanecarbonitrile selectively produced secondary amines in the presence of either Pd/C or Rh/C.