Trioctyl ammonium chloride

Base Information

• Chemical Name: Trioctyl ammonium chloride
• CAS No.: 1188-95-0
• Molecular Formula: C24H51 N . Cl H
• Molecular Weight: 390.1294
• Mol file: 1188-95-0.mol

Synonyms:trioctylammonium chloride;Trioctyl ammonium chloride;1-Octanamine, N,N-dioctyl-, hydrochloride;1-Octanamine, N,N-dioctyl-, hydrochloride (1:1);trioctylazanium chloride;C24H51N.ClH

Chemical Property of Trioctyl ammonium chloride

Chemical Property:

• Vapor Pressure: 1.79E-05mmHg at 25°C
• Boiling Point: 363.5°Cat760mmHg
• Flash Point: 147.4°C
• PSA: 3.24000
• Density: g/cm³
• LogP: 9.17190
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 21
• Exact Mass: 389.3788284
• Heavy Atom Count: 26
• Complexity: 188

Purity/Quality:

98%,99%, ^*data from raw suppliers

Trioctylamine hydrochloride 95%+ ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCC[NH+](CCCCCCCC)CCCCCCCC.[Cl-]

Technology Process of Trioctyl ammonium chloride

There total 1 articles about Trioctyl ammonium chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

Tri-n-octylamine (1116-76-3) → tri-n-octylamine hydrochloride (1188-95-0)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; for 0.0833333h; Cooling with ice;

DOI:10.3389/fmicb.2020.551189

Reference yield:

tri-n-octylamine hydrochloride (1188-95-0) + Ethyl 2-phenylethanoate (101-97-3) → ethyl 2-vinyl-1-phenylcyclopropane-1-carboxylate

Guidance literature:

With potassium hydroxide; In dichloromethane;

Reference yield:

ethyl bromide (74-96-4) + aqueous sodium chloride + 2,2,6-trimethyl-cyclohexanecarboxylic acid (4351-02-4) + tri-n-octylamine hydrochloride (1188-95-0) → ethyl 2,2,6-trimethoxycyclohexanecarboxylate + 2,2,6-trimethylcyclohexanecarboxylic acid ethyl ester (22471-55-2,153725-47-4)

Guidance literature:

With hydrogenchloride; potassium hydroxide; In water; toluene;

upstream raw materials:

Tri-n-octylamine

Downstream raw materials:

2,2,6-trimethylcyclohexanecarboxylic acid ethyl ester

Refernces

• 1、 Stoyanov, Evgenii S.,Stoyanova, Irina V.,Reed, Christopher A.. "The basicity of unsaturated hydrocarbons as probed by hydrogen-bond- acceptor ability: Bifurcated N-H+...μ hydrogen bonding". . p. 7880 - 7891. Retrieved 2008.