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1559-36-0

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1559-36-0 Usage

General Description

2-[2-[(2-ethylhexyl)oxy]ethoxy]ethanol, also known as EHE, is a chemical compound used as a solvent and in some personal care products. It is a clear, colorless liquid with a faint odor, and is insoluble in water. EHE is commonly used in various industrial applications, including as a dispersant in paints, inks, and coatings, as well as a component in cleaning products and agrochemicals. It is also used as a solvent in the formulation of pesticides and herbicides. EHE has low volatility and low acute toxicity, making it a relatively safe compound to handle. However, long-term exposure to high concentrations of EHE may cause irritation to the skin and eyes, and it is recommended to use protective equipment when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1559-36-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1559-36:
(6*1)+(5*5)+(4*5)+(3*9)+(2*3)+(1*6)=90
90 % 10 = 0
So 1559-36-0 is a valid CAS Registry Number.
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

1559-36-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name diethylene glycol mono2-ethylhexyl ether

1.2 Other means of identification

Product number -
Other names 2-{2-[(2-ETHYLHEXYL)OXY]ETHOXY}ETHANOL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1559-36-0 SDS

1559-36-0Synthetic route

oxirane
75-21-8

oxirane

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

diethylene glycol mono(2-ethylhexyl)ether
1559-36-0

diethylene glycol mono(2-ethylhexyl)ether

Conditions
ConditionsYield
With sodium
2-ethylhexyl bromide
18908-66-2

2-ethylhexyl bromide

diethylene glycol
111-46-6

diethylene glycol

diethylene glycol mono(2-ethylhexyl)ether
1559-36-0

diethylene glycol mono(2-ethylhexyl)ether

Conditions
ConditionsYield
With sodium hydride
diethylene glycol mono(2-ethylhexyl)ether
1559-36-0

diethylene glycol mono(2-ethylhexyl)ether

oxiranyl-methanol
556-52-5

oxiranyl-methanol

di(ethylene glycol) 2-ethylhexyl polyglyceryl ether

di(ethylene glycol) 2-ethylhexyl polyglyceryl ether

Conditions
ConditionsYield
lanthanum(lll) triflate at 90℃; for 8h;
diethylene glycol mono(2-ethylhexyl)ether
1559-36-0

diethylene glycol mono(2-ethylhexyl)ether

C12H26O6S*C6H15NO

C12H26O6S*C6H15NO

Conditions
ConditionsYield
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

diethylene glycol mono(2-ethylhexyl)ether

C12H25O6S(1-)*C7H18NO(1+)

C12H25O6S(1-)*C7H18NO(1+)

Conditions
ConditionsYield
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

diethylene glycol mono(2-ethylhexyl)ether

aminosulfonic acid
5329-14-6

aminosulfonic acid

diethylene glycol mono(2-ethylhexyl)ether sulfate ammonium salt

diethylene glycol mono(2-ethylhexyl)ether sulfate ammonium salt

Conditions
ConditionsYield
In toluene at 110℃; for 3h;
3-(trimethoxysilyl)propan-1-amine
13822-56-5

3-(trimethoxysilyl)propan-1-amine

diethylene glycol mono(2-ethylhexyl)ether
1559-36-0

diethylene glycol mono(2-ethylhexyl)ether

C12H26O6S*C6H17NO3Si

C12H26O6S*C6H17NO3Si

Conditions
ConditionsYield
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

4-butanolide

diethylene glycol mono(2-ethylhexyl)ether
1559-36-0

diethylene glycol mono(2-ethylhexyl)ether

C16H32O5

C16H32O5

Conditions
ConditionsYield
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

1559-36-0Downstream Products

1559-36-0Relevant articles and documents

Topical mosquito repellents VII: Alkyl triethylene glycol monoethers

Johnson,DeGraw,Engstrom,Skinner,Brown,Skidmore,Maibach

, p. 693 - 695 (2007/10/05)

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.

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