| Identification | More | [Name]
Diethylene glycol divinyl ether | [CAS]
764-99-8 | [Synonyms]
1,1'-[oxybis(ethyleneoxy)]diethylene
Bis(2-vinyloxyethyl)ether
DIETHYLENE GLYCOL DIVINYL ETHER
DIETHYLENGLYCOLDIVINYLETHER
DIVINYL DIETHYLENE GLYCOL DIETHER
1-(2-[2-(Vinyloxy)ethoxy]ethoxy)ethylene
1,1-[oxybis(2,1-ethanediyloxy)bis]ethene
1,1’-[oxybis(2,1-ethanediyloxy)]bis-ethen
3,6,9-Trioxaundeca-1,10-diene
Divinyl ether diethylenglykolu
Divinylcarbitol
divinyletherdiethylenglykolu
Dvedeg
Ether, bis[2-(vinyloxy)ethyl]
ether,bis(2-vinyloxyethyl)
1,5-Divinyloxy-3-oxapentane
DEGDiethyleneglycoldivinylether
Diethyleneglycoldivinylether,98%
Ethene, 1,1-oxybis(2,1-ethanediyloxy)bis-
Diethylene glycol divinyl ether, 95%, stab. with 0.1% potassium hydroxide | [EINECS(EC#)]
212-133-3 | [Molecular Formula]
C8H14O3 | [MDL Number]
MFCD00054610 | [Molecular Weight]
158.19 | [MOL File]
764-99-8.mol |
| Safety Data | Back Directory | [Risk Statements ]
R36/38:Irritating to eyes and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
2
| [RTECS ]
KN3850000
| [TSCA ]
Yes | [HS Code ]
29091990 | [Toxicity]
LD50 oral in rat: 3730mg/kg |
| Hazard Information | Back Directory | [Chemical Properties]
diethylene glycol divinyl ether is monomeric in character and is used as a chemical intermediate or as a crosslinking agent. Addition of isocyanic acid produces secondary diisocyanates. Divinyl ethers hydrolyze to the glycol and acetaldehyde. Chlorine or bromine add to the double bonds. Reaction with an alcohol in the presence of water produces a diacetal. Polymerization of divinyl ether of diethylene glycol with acidic catalysts produce crosslinked gels. Unsaturated polyesters, crosslinked with styrene, have been made noncorrosive to metals through use of divinyl ethers to reduce hydroxyl ond acid numbers. | [Uses]
Diethylene glycol divinyl ether is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. | [Application]
Diethylene glycol divinyl ether (DEGDVE) has attracted much attention due to the homopolymerization and structural diversity of copolymerization products, and it is often used as a cross-linking agent in various functional materials. Hydrogels are hydrophilic network polymers that absorb large amounts of water but are insoluble in water. The properties of high water content and insolubility in water make the materials widely used in biomedical fields such as drug delivery systems, biosensors, contact lenses, catheters, and wound dressings. Using DEGDVE as a cross-linking agent and 60Co as γ-radiation light source, hydrogels were prepared by radiation copolymerization of hydrophilic ethylene glycol monovinyl ether, hydrophobic BVE, and acidic acrylic acid. The resulting hydrogels were pH- and temperature-sensitive functional materials.
Using DEGDVE as a cross-linking agent, 2-acrylamido-2-methylpropanesulfonic acid and sodium styrene sulfonate as monomers, a plugging agent with high-temperature resistance and salt resistance was synthesized by emulsion polymerization, which has practical significance in solving the problem of water production in oil wells and plays a vital role in improving oil recovery ratio.
A three-dimensional substance with a special space structure can be synthesized by cross-linking copolymerization with DEGDVE and used as a modified substrate material. For example, cross-linking copolymerization of methyl vinyl sulfide with DEGDVE gave a solid polymer with a crown structure, which was modified and used as active matrices of solid superbases for ethynylation of acetone and vinylation of diethylene glycol or ethylene glycol. | [Flammability and Explosibility]
Nonflammable | [Synthesis]
Acetylene reacts with diethylene glycol in the presence of a catalyst such as potassium hydroxide or potassium diethylene glycol to yield DEGMVE and Diethylene glycol divinyl ether (DEGDVE):
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