1559-36-0

Usage

Uses

Used in Paints and Coatings Industry:
2-[2-[(2-Ethylhexyl)Oxy]EthOxy]Ethanol is used as a dispersant in the paints and coatings industry to improve the flow and stability of the paint formulations, ensuring a smooth application and even distribution of pigments.
Used in Inks Industry:
In the inks industry, 2-[2-[(2-Ethylhexyl)Oxy]EthOxy]Ethanol is utilized as a solvent to facilitate the dispersion of ink components, enhancing print quality and performance.
Used in Cleaning Products:
2-[2-[(2-Ethylhexyl)Oxy]EthOxy]Ethanol is used as a solvent in cleaning products to dissolve and remove various types of dirt, grease, and stains, contributing to effective cleaning action.
Used in Agrochemicals:
In agrochemicals, 2-[2-[(2-Ethylhexyl)Oxy]EthOxy]Ethanol is employed as a component to improve the solubility and effectiveness of pesticides and herbicides, ensuring better crop protection.
Used in Personal Care Products:
Although not extensively detailed in the provided materials, EHE is also used in some personal care products, likely for its solvent properties to help dissolve other ingredients and improve product consistency.

InChI:InChI=1/C12H26O4/c1-3-5-6-12(16-4-2)11-15-10-9-14-8-7-13/h12-13H,3-11H2,1-2H3

Synthetic route

oxirane (75-21-8) + 2-Ethylhexyl alcohol (104-76-7) → diethylene glycol mono(2-ethylhexyl)ether (1559-36-0)

Conditions	Yield
With sodium

2-ethylhexyl bromide (18908-66-2) + diethylene glycol (111-46-6) → diethylene glycol mono(2-ethylhexyl)ether (1559-36-0)

Conditions	Yield
With sodium hydride

diethylene glycol mono(2-ethylhexyl)ether (1559-36-0) + oxiranyl-methanol (556-52-5) → di(ethylene glycol) 2-ethylhexyl polyglyceryl ether

Conditions	Yield
lanthanum(lll) triflate at 90℃; for 8h;

diethylene glycol mono(2-ethylhexyl)ether (1559-36-0) → C12H26O6S*C6H15NO

Conditions	Yield
Multi-step reaction with 2 steps 1: toluene / 3 h / 110 °C 2: toluene / 3 h / 120 °C View Scheme
Multi-step reaction with 2 steps 1: toluene / 3 h / 110 °C 2: hydrogenchloride / water / 1 h / 25 °C View Scheme

diethylene glycol mono(2-ethylhexyl)ether (1559-36-0) → C12H25O6S(1-)*C7H18NO(1+)

Conditions	Yield
Multi-step reaction with 2 steps 1: toluene / 3 h / 110 °C 2: water / 1 h / 25 °C View Scheme

diethylene glycol mono(2-ethylhexyl)ether (1559-36-0) + aminosulfonic acid (5329-14-6) → diethylene glycol mono(2-ethylhexyl)ether sulfate ammonium salt

Conditions	Yield
In toluene at 110℃; for 3h;

3-(trimethoxysilyl)propan-1-amine (13822-56-5) + diethylene glycol mono(2-ethylhexyl)ether (1559-36-0) → C12H26O6S*C6H17NO3Si

Conditions	Yield
Stage #1: diethylene glycol mono(2-ethylhexyl)ether With sulfuric acid In toluene at 110℃; for 3h; Stage #2: 3-(trimethoxysilyl)propan-1-amine In toluene at 120℃; for 3h;

4-butanolide (96-48-0) + diethylene glycol mono(2-ethylhexyl)ether (1559-36-0) → C16H32O5

Conditions	Yield
Stage #1: 4-butanolide; diethylene glycol mono(2-ethylhexyl)ether With toluene-4-sulfonic acid at 120℃; for 64h; Stage #2: With water; potassium hydroxide at 80℃; for 2h;	305 g

Upstream product

• 75-21-8 oxirane 
• 104-76-7 2-Ethylhexyl alcohol 
• 18908-66-2 3-bromomethylheptane 
• 111-46-6 diethylene glycol 

Relevant academic research and scientific papers

Topical mosquito repellents VII: Alkyl triethylene glycol monoethers

Normal and branched chain aliphatic monoethers of triethylene glycol are effective topical mosquito repellents. In terms of duration of protection, they are generally superior to the corresponding diethylene glycol analogs, and some are superior to diethyltoluamide. The n heptyl monoether of triethylene glycol affords double the protection time of diethyltoluamide under controlled laboratory conditions, and appears to be a useful new mosquito repellent.