| Identification | Back Directory | [Name]
4-Hydroxybutyl acrylate glycidyl ether | [CAS]
119692-59-0 | [Synonyms]
4-(2,3-EPOXYPROPOXY)BUTYLACRYLATE
4-(Oxiran-2-ylmethoxy)butyl Acrylate
4-Hydroxybutyl acrylate glycidyl ether
4-(oxiran-2-ylmethoxy)butyl prop-2-enoate
2-Propenoic acid, 4-(2-oxiranylmethoxy)butyl ester
4-Hydroxybutyl acrylate glycidyl ether ISO 9001：2015 REACH | [Molecular Formula]
C10H16O4 | [MDL Number]
MFCD30474906 | [MOL File]
119692-59-0.mol | [Molecular Weight]
200.23 |
| Hazard Information | Back Directory | [Description]
4-Hydroxybutyl Acryrate Glycidyl Ether with a glycidylether group at the end of a longer alkyl chain, gives excellent scratch resistance due to its high crosslinking ratio and unique flexibility.This copolymer has good acid rain resistance.It is used in Paint and coating materials,UV/EB curable composition. | [Chemical Properties]
4HBAGE has a glycidylether functional group and a double bond group in the molecule.Various vinyl monomers can be copolymerized with 4HBAGE.The co-polymerized polymer with 4HBAGE achieves a higher crosslinking ratio with curing agents.This is because the glycidylether is further away from the copolymer backbone chain.This copolymer has good acid rain resistance. | [Application]
Paint and coating materials (excellent scratch resistance, mechanical properties, and chemical properties)
Powder coatings
UV/EB curable composition.
Epoxy acrylate
Adhesives | [Synthesis]
The flask was charged with 144 g of 4-hydroxybutyl acrylate and 0.7 g of boron trifluoride ether complex as a catalyst, heated to 55 ° C., and then 92.5 g of epichlorohydrin was added dropwise over 2 hours with stirring. After completion of the dropwise addition, analysis by gas chromatography revealed that the conversion rate of 4-hydroxybutyl acrylate was about 70%, and most of it was converted to a chloroether form. |
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