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Usage

Uses

Used in Personal Care Products:
2-ethoxy-N,N,N-trimethylethanaminium is used as an emulsifier and surfactant for enhancing the spreadability and stability of personal care products, such as creams, lotions, and shampoos.
Used in Detergents:
2-ethoxy-N,N,N-trimethylethanaminium is used as a surfactant in detergent formulations to improve their cleaning efficiency and reduce surface tension.
Used in Agricultural Chemicals:
2-ethoxy-N,N,N-trimethylethanaminium is used as a surfactant and emulsifier in agricultural chemicals to enhance their effectiveness and stability.
Used in Fabric Softeners:
2-ethoxy-N,N,N-trimethylethanaminium is used as a softening agent in fabric softeners to provide a smooth and soft texture to fabrics.
Used in Corrosion Inhibition:
2-ethoxy-N,N,N-trimethylethanaminium is used as a corrosion inhibitor in various industrial applications to protect metal surfaces from corrosion.
Overall, 2-ethoxy-N,N,N-trimethylethanaminium is a versatile compound with a wide range of applications in different industries, including personal care products, detergents, agricultural chemicals, fabric softeners, and corrosion inhibition. Its strong hydrophobic and lipophilic properties, along with its relatively low toxicity and environmental impact, make it a valuable ingredient in various formulations.

Upstream product

• 628-34-2 2-chloroethyl ethyl ether 
• 75-50-3 trimethylamine 
• 64894-59-3 2-ethoxyethyltrimethylammonium bromide 

Relevant academic research and scientific papers

Shape-Selective Recognition of Quaternary Ammonium Chloride Ion Pairs

Synthetic receptors that recognize ion pairs are potentially useful for many technical applications, but to date there has been little work on selective recognition of quaternary ammonium (Q+) ion pairs. This study measured the affinity of a tetralactam macrocycle for 11 different Q+·Cl- salts in chloroform solution. In each case, NMR spectroscopy was used to determine the association constant (Ka) and the structure of the associated complex. Ka was found to depend strongly on the molecular shape of Q+ and was enhanced when Q+ could penetrate the macrocycle cavity and engage in attractive noncovalent interactions with the macrocycle's NH residues and aromatic sidewalls. The highest measured Ka of 7.9 × 103 M-1 was obtained when Q+ was a p-CN-substituted benzylic trimethylammonium. This high-affinity Q+·Cl- ion pair was used as a template to enhance the synthetic yield of macrocyclization reactions that produce the tetralactam receptor or structurally related derivatives. In addition, a permanently interlocked rotaxane was prepared by capping the end of a noncovalent complex composed of the tetralactam macrocycle threaded by a reactive benzylic cation. The synthetic method provides access to a new family of rotaxanated ion pairs that can likely act as anion sensors, molecular shuttles, or transport molecules.

The importance of molecular parameters of quaternary ammonium salts in their antigibberellin (retardant) activity

The importance of six theoretically calculated molecular parameters in the antigibberellin (retardant) activity of quaternary ammonium salts is studied using a regression analysis. A bioassay system based on cell culture of fungus Gibberella fujikuroi is used to determine the activity. In the case of N,N,N-trimethyl-N-(2-hydroxyethyl)ammonium chloride (choline) and N,N,N-triethyl-N-(2-hydroxyethyl)ammonium chloride (N,N,N-triethylcholine) derivatives with linear structure, the polarizability, proton acceptor activity, and lipophilicity of these compounds exert the largest effect on the antigibberellin activity. The antigibberellin activity of more sterically hindered N,N-dialkylpiperidinium salts was mainly defined by the steric parameter, while the polarizability, proton acceptor activity, and (through them) lipophilicity exert a lesser effect. Other parameters are of minor importance for the three groups of compounds studied.