16839-48-8

Usage

Uses

Used in Adhesives Industry:
2-Allyloxyethyl methacrylate is used as an adhesive component for its strong adhesive properties, enhancing the bonding capabilities of various materials.
Used in Coatings Industry:
2-Allyloxyethyl methacrylate is used as a component in coatings to improve the flexibility and durability of the final product, providing a longer-lasting and more resilient finish.
Used in Textiles Industry:
2-Allyloxyethyl methacrylate is used in the textile industry to improve the flexibility and durability of fabrics, making them more resistant to wear and tear.
Used in Medical Devices:
2-Allyloxyethyl methacrylate is used in the manufacturing of medical devices due to its biocompatibility and low toxicity, making it suitable for use in products that come into contact with the human body.
Used in Dental Materials:
2-Allyloxyethyl methacrylate is used in dental materials for its strong adhesive properties and ability to improve the durability of dental restorations.
Used in Contact Lenses:
2-Allyloxyethyl methacrylate is used in the production of contact lenses due to its biocompatibility and low toxicity, ensuring the safety and comfort of the wearer.

InChI:InChI=1/C9H14O3/c1-4-5-11-6-7-12-9(10)8(2)3/h4H,1-2,5-7H2,3H3

Upstream product

• 111-45-5 ethylene glycol monoallyl ether 
• 920-46-7 Methacryloyl chloride 
• 79-41-4 poly(methacrylic acid) 

Relevant academic research and scientific papers

Dental adhesive composition

PROBLEM TO BE SOLVED: To provide a dental adhesive composition which does not have lower affinity to a tooth or the like and has high adhesive strength. SOLUTION: The present invention relates to the composition comprising a polymerizable monomer represented by general formula (1), and an acid group-containing polymerizable monomer. [X is a divalent group; Ar1 and Ar2 are each independently a divalent to tetravalent aromatic group; L1 and L2 are each independently a divalent to tetravalent hydrocarbon group having 2 to 60 atoms in the main chain; R1 and R2 are each independently H or methyl; or, m1, m2, n1 and n2 are each independently an integer of 1 to 3] SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

DENTAL CURABLE COMPOSITION

PROBLEM TO BE SOLVED: To provide a dental curable composition that promptly completes polymerization upon light irradiation. SOLUTION: A dental curable composition comprises: (A) a polymerizable monomer represented by general formula (1); and (B) a photoinitiator containing B1) an α-diketone compound, B2) a photoacid generator and B3) an aromatic amine compound. [X is -O-; Ar1 and Ar2 are divalent to tetravalent aromatic groups; L1 and L2 are divalent to tetravalent C2-60 hydrocarbon groups; R1 and R2 are hydrogen or methyl groups; and m1, m2, n1 and n2 are integers from 1 to 3.] SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Synthesis and characterization of network type single ion conductors

New single ion conductors were synthesized by grafting the allyl group-containing lithium salt, lithium bis(allylmalonato)borate (LiBAMB), onto allyl group-containing comb-branch polyacrylate or polymethacrylate ethers by means of hydrosilylation. The highest ambient temperature conductivity of 3.5 × 10-7 S cm-1 was obtained for a polyacrylate ether-based single ion conductor containing eight EO units in the side chain and five EO units in the cross-linking side chain, to which the anion was fixed with a salt concentration of EO/Li = 20. For polyacrylate ether-based single ion conductors, an increase of chain length in both side chains and cross-linking anion chains favors an increase of ionic conductivity. The addition of 50 wt % EC/DMC (1/1, wt/wt) increased the ionic conductivity by more than 2 orders of magnitude due to both the increase in ionic mobility from the liquid phase and the increase in the concentration of free ions from the high dielectric constant of the solvent. The preliminary Li/Li cycling profiles of dry polyacrylate- and polymethacrylate ether-based single ion conductors are encouraging as almost no concentration polarization or relaxation was observed. The observed increase in cell potential with cycling is apparently due to an increase in the interfacial impedance associated with the SEI layer, and the cell failure is accompanied by the decomposition of the ester bond of the polyacrylate backbone.