Basic information Safety Supplier Related

2-Ethylhexyl glycidyl ether

Basic information Safety Supplier Related

2-Ethylhexyl glycidyl ether Basic information

Product Name:
2-Ethylhexyl glycidyl ether
Synonyms:
  • glycidyl2-ethylhexylether
  • Oxirane,[[(2-ethylhexyl)oxy]methyl]-
  • Propane, 1,2-epoxy-3-[(2-ethylhexyl)oxy]-
  • EHGE
  • (2-ETHYLHEXYLOXY)-2,3-EPOXYPROPANE
  • 2-ETHYLHEXYL GLYCIDYL ETHER
  • 1,2-epoxy-3-((2-ethylhexyl)oxy)propane
  • 1-(2-Ethylhexyloxy)-2,3-epoxypropane
CAS:
2461-15-6
MF:
C11H22O2
MW:
186.29
EINECS:
219-553-6
Product Categories:
  • Oxiranes
  • Simple 3-Membered Ring Compounds
  • Epoxide Monomers
  • Monomers
  • Polymer Science
  • KT00001
Mol File:
2461-15-6.mol
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2-Ethylhexyl glycidyl ether Chemical Properties

Boiling point:
60-62 °C/0.3 mmHg (lit.)
Density 
0.891 g/mL at 25 °C (lit.)
vapor pressure 
29Pa at 25℃
refractive index 
1.434
Flash point:
206°F
form 
clear liquid
Specific Gravity
0.910.891
color 
Colorless to Almost colorless
Water Solubility 
<0.1 g/100 mL at 19 ºC
Stability:
Stable. Combustible. Incompatible with strong oxidising agents, acids, bases.
LogP
3.83
CAS DataBase Reference
2461-15-6(CAS DataBase Reference)
NIST Chemistry Reference
Oxirane, [[(2-ethylhexyl)oxy]methyl]-(2461-15-6)
EPA Substance Registry System
2-Ethylhexyl glycidyl ether (2461-15-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
2
RTECS 
TZ3300000
HS Code 
29109000
Toxicity
rat,LD50,oral,7800mg/kg (7800mg/kg),"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2A, Pg. 2210, 1981.

MSDS

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2-Ethylhexyl glycidyl ether Usage And Synthesis

Chemical Properties

colourless liquid

Uses

It constitutes a reactive diluent and may be used as a relatively nonvolatile chloride-scavenging agent and stabilizer for vinyl resins and rubber.

Uses

2-Ethylhexyl glycidyl ether is a used as a commercial reactive diluent. 2-Ethylhexyl glycidyl ether is also known to induce sister-chromatid exchanges in Chinese hamster cells.

Production Methods

2-Ethylhexyl glycidyl ether is made by condensation of 2-ethylhexanol with epichlorohydrin followed by dehydrochlorination with caustic to form the epoxy ring.

General Description

Clear colorless liquid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

2-Ethylhexyl glycidyl ether is incompatible with acids, bases and oxidizing agents.

Fire Hazard

2-Ethylhexyl glycidyl ether is combustible.

Flammability and Explosibility

Non flammable

2-Ethylhexyl glycidyl etherSupplier

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