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| | 4-Hydroxybutyl acrylate glycidyl ether Basic information |
| Product Name: | 4-Hydroxybutyl acrylate glycidyl ether | | Synonyms: | 4-Hydroxybutyl acrylate glycidyl ether;4-(2,3-EPOXYPROPOXY)BUTYLACRYLATE;4-(oxiran-2-ylmethoxy)butyl prop-2-enoate;4-(Oxiran-2-ylmethoxy)butyl Acrylate;2-Propenoic acid, 4-(2-oxiranylmethoxy)butyl ester;4-Hydroxybutyl acrylate glycidyl ether ISO 9001：2015 REACH;4-(oxiran-2-ylmethoxy)butyl prop-2-enoate / in stock 119692-59-0 / 98% | | CAS: | 119692-59-0 | | MF: | C10H16O4 | | MW: | 200.23 | | EINECS: | | | Product Categories: | Crosslinking monomer | | Mol File: | 119692-59-0.mol |  |
| | 4-Hydroxybutyl acrylate glycidyl ether Chemical Properties |
| | 4-Hydroxybutyl acrylate glycidyl ether Usage And Synthesis |
| 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. |
| | 4-Hydroxybutyl acrylate glycidyl ether Preparation Products And Raw materials |
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