997-46-6

Usage

Uses

Used in Polymer and Coating Production:
4-Hydroxybutyl methacrylate is used as a monomer in the production of polymers and coatings due to its ability to undergo radical polymerization, which imparts desirable properties to these materials.
Used in Adhesive and Sealant Formulation:
4-HBMA is used as an ingredient in the formulation of adhesives and sealants, where its high reactivity and ability to form strong bonds contribute to the performance of these products.
Used in Surface Coating Development:
4-Hydroxybutyl methacrylate is used as a component in the development of surface coatings, enhancing their durability, adhesion, and other functional properties.
Used in Hydrogel Synthesis:
4-HBMA is used as a building block in the synthesis of hydrogels, taking advantage of its water-absorbent properties to create materials with potential applications in various industries.
Used in Dental Material Production:
4-Hydroxybutyl methacrylate is used in the production of dental materials, where its biocompatibility and ability to form strong bonds make it suitable for use in dental restorations and other applications.
Used in Medical Device Manufacturing:
4-HBMA is used in the manufacturing of medical devices, leveraging its biocompatible nature and reactivity to create materials that can be safely used in medical applications.

InChI:InChI=1/C8H14O3/c1-7(2)8(10)11-6-4-3-5-9/h9H,1,3-6H2,2H3

Upstream product

• 110-63-4 Butane-1,4-diol 
• 80-62-6 methacrylic acid methyl ester 
• 97-88-1 2-methyl-butyl acrylate 
• 116767-79-4 Ac-HBMA 
• 920-46-7 Methacryloyl chloride 
• 79-41-4 poly(methacrylic acid) 
• 82386-37-6 4-(Vinyloxy)butyl methacrylate 

Relevant academic research and scientific papers

Exploring the use of APTS as a fluorescent reporter dye for continuous glucose sensing

The anionic fluorescent dye, aminopyrene trisulfonic acid (APTS), was synthesized and used in a solution-based two-component glucose-sensing system comprising the dye and a boronic acid-appended viologen. The fluorescence of the dye was quenched in the pr

Sequential copper catalyzed alkyne-azide and thiol-ene click reactions for the multiple functionalization of fullerene hexaadducts

A fullerene hexakis-adduct incorporating complementary reactive centres with very different and selective reactivity has been prepared and functionalized with three different peripheral groups by successive alkyne-azide and thiol-ene click reactions.

Runge-Kutta analysis for optimizing the Zn-catalyzed transesterification conditions of MA and MMA with diols to maximize monoesterified products

Terminal hydroxylated acrylates and methacrylates were prepared by catalytic transesterification of acrylates and methacrylates with diols catalyzed by a system of a tetranuclear zinc alkoxide, [Zn(tmhd)(OMe)(MeOH)]4 (1a), with 4 equiv. of 2,2′-bipyridine (L1). The reaction time to reach the equilibrium state was analyzed by kinetic studies and a curve-fitting analysis based on the Runge-Kutta method for optimizing the best reaction conditions for mono-esterification. In addition to these kinetic analyses, DFT calculations estimated a proposed mechanism of the catalytic transesterification. This journal is

METHOD FOR PRODUCING HYDROXYALKYL(METH)ACRYLIC ACID ESTER

PROBLEM TO BE SOLVED: To provide a production method that permits efficient production of a hydroxyalkyl (meth)acrylate of high purity without necessitating a troublesome purification step.SOLUTION: The production method for a hydroxyalkyl (meth)acrylate comprises (meth)acrylating a vinyl ether-containing alcohol by a transesterification method to obtain a vinyl ether-containing (meth)acrylate, carrying out a devinylation reaction in the presence of an acid catalyst and water, and subsequently carrying out a deacetalization reaction by further adding water.

DENTAL CURABLE COMPOSITION

PROBLEM TO BE SOLVED: To provide a dental curable composition that comprises a polymerizable monomer, a cured product of which has excellent mechanical strength, and which has low viscosity and excellent handleability even in room temperature environment, and further has excellent operability. SOLUTION: A dental curable composition comprises (A) polymerizable monomer represented by formula (1), (B) polymerization initiator, and (C) organic-inorganic composite filler, where X is a divalent group; Ar1 and Ar2 each are an aromatic; L1 and L2 each are a hydrocarbon with the main chain consisting of 2-60 atoms; R1 and R2 independently represent H or methyl; m1, m2, n1 and n2 independently an integer of 1-3]. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPO&INPIT

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

(Meth) acrylic acid hydroxyalkyl ester method of manufacturing (by machine translation)

PROBLEM TO BE SOLVED: To provide a production method in which a hydroxyalkyl (meth)acrylic acid ester of high purity can be produced efficiently without requiring a complicated purification process.SOLUTION: Thr method of producing a hydroxyalkyl (meth)acrylic acid ester is characterized as follows. A vinyl ether containing alcohol is (meth)acrylated by a transesterification method to be a vinyl ether containing (meth)acrylic acid ester, the devinylation reaction is performed under the presence of an acid catalyst and glycol, and then the deacetalization reaction is performed adding glycol further.

COLORED COMPOSITION

The present invention is to provide a colored composition having higher heat resistance compared with conventional colored compositions. The present invention further relates to: “a polymer having a monomer unit derived from a monomer which has (i) a cationic rhodamine derivative having, as an counter anion, an anion including an aryl group having an electron-withdrawing substituent and an anion group and (ii) an ethylenically unsaturated bond”, “a monomer which has (i) a cationic rhodamine derivative having, as an counter anion, an anion including an aryl group having an electron-withdrawing substituent and an anion group and (ii) an ethylenically unsaturated bond”, “a colored composition comprising the above-described polymer or the monomer”, and “a colored composition for a color filter comprising the above-described polymer or the monomer”.

PROCESS FOR PREPARING 4-HYDROXYBUTYL ACRYLATE

A process for preparing 4-hydroxybutyl acrylate by transesterifying an alkyl acrylate with 1,4-butanediol in the presence of a dialkyltin oxide such that each of the alkyl groups has 4 to 8 carbon atoms, characterized in that the amount of the dialkyltin oxide is adjusted to 0.00001 to 0.01 moles per one mole of the alkyl acrylate.

COLORED COMPOSITION

The present invention is to provide a colored composition having higher heat resistance compared with conventional colored compositions. The present invention further relates to: "a polymer having a monomer unit derived from a monomer which has (i) a cationic rhodamine derivative having, as an counter anion, an anion including an aryl group having an electron-withdrawing substituent and an anion group and (ii) an ethylenically unsaturated bond", "a monomer which has (i) a cationic rhodamine derivative having, as an counter anion, an anion including an aryl group having an electron-withdrawing substituent and an anion group and (ii) an ethylenically unsaturated bond", "a colored composition comprising the above-described polymer or the monomer", and "a colored composition for a color filter comprising the above-described polymer or the monomer".