Your Location：Home > Products > Catalysts and additives > Tri-n-octylamine

Tri-n-octylamine

  • Product Name
  • CasNo
  • MF
  • MW
  • Content
  • Appearance
  • Packing
  • Apply
  • Tri-n-octylamine
  • 1116-76-3
  • C24H51N
  • 353.676
  • clear liquid
Inquiry

Factory supply good quality Tri-n-octylamine 1116-76-3 with stock

  • Molecular Formula:C24H51N
  • Molecular Weight:353.676
  • Appearance/Colour:clear liquid 
  • Vapor Pressure:1.79E-05mmHg at 25°C 
  • Melting Point:34 °C 
  • Refractive Index:1.448 - 1.450 
  • Boiling Point:363.535 °C at 760 mmHg 
  • PKA:10.08±0.50(Predicted) 
  • Flash Point:147.357 °C 
  • PSA：3.24000 
  • Density:0.809 g/cm3 
  • LogP:8.36990 

Tri-n-octylamine(Cas 1116-76-3) Usage

Purification Methods

It is converted to the amine hydrochloride etherate which is recrystallised four times from diethyl ether at -30o (see below). Neutralisation of this salt regenerates the free amine which distil under high vacuum. [Wilson & Wogman J Phys Chem 66 1552 1962.] Distil the amine at 1-2mm pressure. [Beilstein 4 H 196, 4 III 382, 4 IV 754.]

InChI:InChI=1/C24H51N/c1-4-7-10-13-16-19-22-25(23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3

1116-76-3 Relevant articles

A multifaceted role of a mobile bismuth promoter in alcohol amination over cobalt catalysts

Bahri, Mounib,Ersen, Ovidiu,Khodakov, Andrei Y.,Kusema, Bright T.,Niu, Feng,Ordomsky, Vitaly V.,Yan, Zhen

, p. 4270 - 4278 (2020)

Promotion with small amounts of differen...

Ru(II)-triphos catalyzed amination of alcohols with ammonia via ionic species

Derrah, Eric J.,Hanauer, Matthias,Plessow, Philipp N.,Schelwies, Mathias,Da Silva, Marion K.,Schaub, Thomas

, p. 1872 - 1881 (2015)

An active and selective system for the a...

Catalytic amination of octanol for synthesis of trioctylamine and catalyst characterization

Li, Yunling,Li, Qiuxiao,Zhi, Lifei,Zhang, Minghui

, p. 1635 - 1642 (2011)

Synthesis of trioctylamine by the aminat...

Rapid Multialkylation of Aqueous Ammonia with Alcohols by Heterogeneous Iridium Catalyst under Simple Conditions

Yu, Han,Ma, Lin,Wada, Kenji,Kurihara, Ryohsuke,Feng, Qi,Uemura, Shinobu,Isoda, Kyosuke

, p. 3588 - 3593 (2021)

This paper reports the synthesis of tert...

Highly Selective Hydrogenative Conversion of Nitriles into Tertiary, Secondary, and Primary Amines under Flow Reaction Conditions

Furugen, Chikara,Ito, Naoya,Jiang, Jing,Park, Kwihwan,Sajiki, Hironao,Shimizu, Eisho,Yamada, Tsuyoshi

, (2021/12/13)

Flow reaction methods have been develope...

Nanoceria-promoted low Pd-Ni catalyst for the synthesis of secondary amines from aliphatic alcohols and ammonia

Fang,Yan,Vits,Southward,Pera-Titus

, p. 1215 - 1230 (2019/03/12)

This paper describes the preparation of ...

1116-76-3 Process route

trioctyl-amine; compound with 2,4,6-trichloro-phenol

trioctyl-amine; compound with 2,4,6-trichloro-phenol

Tri-n-octylamine
1116-76-3

Tri-n-octylamine

2,4,6-Trichlorophenol
88-06-2,67471-29-8

2,4,6-Trichlorophenol

Conditions
Conditions Yield
In tetrachloromethane; at 25 ℃; Equilibrium constant;
trioctyl-amine; compound with 2,4,6-trichloro-phenol

trioctyl-amine; compound with 2,4,6-trichloro-phenol

Tri-n-octylamine
1116-76-3

Tri-n-octylamine

2,4,6-Trichlorophenol
88-06-2,67471-29-8

2,4,6-Trichlorophenol

Conditions
Conditions Yield
In tetrachloromethane; at 25 ℃; Equilibrium constant;

1116-76-3 Upstream products

  • 111-85-3
    111-85-3

    n-chlorooctane

  • 629-27-6
    629-27-6

    1-Iodooctane

  • 1120-48-5
    1120-48-5

    n-dioctylamine

  • 111-86-4
    111-86-4

    n-Octylamine

1116-76-3 Downstream products

  • 16829-91-7
    16829-91-7

    tetraoctylammonium iodide

  • 24298-17-7
    24298-17-7

    trioctylpropylammonium bromide

  • 13103-04-3
    13103-04-3

    trioctylamine oxide

  • 74386-44-0
    74386-44-0

    (4-Benzoyl-benzyl)-trioctyl-ammonium; bromide

*Product Name:
*Email:
*Description:
*Code:
Contact Now