1-octyl-2,3-dimethylimidazolium chloride

Base Information

• Chemical Name: 1-octyl-2,3-dimethylimidazolium chloride
• CAS No.: 1007398-58-4
• Molecular Formula: C13H25N2.Cl
• Molecular Weight: 244.808
• Mol file: 1007398-58-4.mol

Synonyms:1,2-Dimethyl-3-octyl-1H-imidazolium chloride;

Chemical Property of 1-octyl-2,3-dimethylimidazolium chloride

Chemical Property:

• PSA: 8.81000
• LogP: -0.01450

Purity/Quality:

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

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• General Description: 1-Octyl-2,3-dimethylimidazolium chloride, also known as 1,2-dimethyl-3-octyl-1H-imidazolium chloride, is a hydrophilic trisubstituted imidazolium-based ionic liquid (IL) that influences micellization behavior and thermodynamic properties of cationic surfactants like tetradecyltrimethylammonium bromide (TTAB) and dodecyltrimethylammonium bromide (DTAB) in aqueous solutions. It reduces the critical micelle concentration (CMC) of surfactants, indicating enhanced micelle formation due to electrostatic and hydrophobic interactions. Thermodynamic studies reveal that the IL affects standard free energy (ΔG°_m), enthalpy (ΔH°_m), and entropy (ΔS°_m) of micellization, with its impact varying at different concentrations. Spectroscopic and scattering techniques confirm its role in modifying micelle size, aggregation number, and interfacial properties. The IL's hydrophilic nature and structural features contribute to its solvation effects and interactions with surfactants.

Technology Process of 1-octyl-2,3-dimethylimidazolium chloride

There total 1 articles about 1-octyl-2,3-dimethylimidazolium 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: 98.0%

1,2-dimethyl-1H-imidazole (1739-84-0) + n-chlorooctane (111-85-3) → 1-octyl-2,3-dimethylimidazolium chloride (1007398-58-4)

Guidance literature:

at 90 ℃; for 84h;

DOI:10.1016/j.tet.2007.12.009

Reference yield:

n-octyl methanesulfonate (16156-52-8) + 1-octyl-2,3-dimethylimidazolium chloride (1007398-58-4) → 1-octyl-2,3-dimethylimidazolium methanesulfonate + n-chlorooctane (111-85-3)

Guidance literature:

In water; chlorobenzene; at 60 ℃; Kinetics;

DOI:10.1016/j.tet.2007.12.009

Reference yield:

1-octyl-2,3-dimethylimidazolium chloride (1007398-58-4) + bis(trifluoromethane)sulfonimide lithium (90076-65-6) → 1,2-dimethyl-3-octylimidazolium bis(trifluoromethylsulfonyl)imide (350493-09-3)

Guidance literature:

In water; for 0.5h;

DOI:10.1134/S0036024418120245

upstream raw materials:

1,2-dimethyl-1H-imidazole

n-chlorooctane

Downstream raw materials:

n-chlorooctane

1,2-dimethyl-3-octylimidazolium bis(trifluoromethylsulfonyl)imide