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2-(Methacryloyloxy)ethyl acetoacetate is a special methacrylic ester monomer with a reactive methylene group. It is a methylene active compound that can be used in the synthesis of various compounds and as a polymerizable chelating agent for metal alkoxides to form polymerizable oxide precursors.

21282-97-3

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21282-97-3 Usage

Uses

Used in Adhesives and Coatings Industry:
2-(Methacryloyloxy)ethyl acetoacetate is used as a comonomer for adhesives and coatings to enhance their properties and performance. Its reactive methylene group allows for copolymerization with other monomers, resulting in improved adhesion, durability, and flexibility of the final product.
Used in Emulsion Polymerization:
2-(Methacryloyloxy)ethyl acetoacetate is used as a copolymer for emulsion polymerization. Its incorporation into the polymer chain improves the stability and performance of the emulsion, making it suitable for various applications such as paints, coatings, and adhesives.
Used in Synthesis of Complex Compounds:
2-(Methacryloyloxy)ethyl acetoacetate is used as a methylene active compound in the synthesis of 2-(methacryloyloxy)ethyl 6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate. This complex compound can have potential applications in various fields, such as pharmaceuticals or materials science.
Used as a Polymerizable Chelating Agent:
2-(Methacryloyloxy)ethyl acetoacetate is used as a polymerizable chelating agent for metal alkoxides to form polymerizable oxide precursors. This application allows for the development of new materials with unique properties, such as improved thermal stability, mechanical strength, or chemical resistance.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 21282-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,8 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21282-97:
(7*2)+(6*1)+(5*2)+(4*8)+(3*2)+(2*9)+(1*7)=93
93 % 10 = 3
So 21282-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3.C4H6O3/c1-3-5(7)4(2)6(8)9;1-3(5)2-4(6)7/h7H,3H2,1-2H3,(H,8,9);2H2,1H3,(H,6,7)/p-2/b5-4+;

21282-97-3 Well-known Company Product Price

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  • TCI America

  • (E0489)  Ethylene Glycol Monoacetoacetate Monomethacrylate (stabilized with BHT)  >95.0%(HPLC)

  • 21282-97-3

  • 25g

  • 165.00CNY

  • Detail
  • TCI America

  • (E0489)  Ethylene Glycol Monoacetoacetate Monomethacrylate (stabilized with BHT)  >95.0%(HPLC)

  • 21282-97-3

  • 500g

  • 720.00CNY

  • Detail

21282-97-3Downstream Products

21282-97-3Relevant academic research and scientific papers

Preparation method of acetoacetoxy ethyl methacrylate

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Paragraph 0016; 0017; 0018; 0019; 0020, (2017/08/28)

The invention discloses a preparation method of acetoacetoxy ethyl methacrylate, and the method is as follows: under the conditions of light and temperature of 20-100 DEG C, taking a reaction system comprising hydroxyethyl methylacrylate, a polymerization inhibitor, a catalyst and a diketene adduct for full reaction, after the reaction is complete, cooling the system to temperature of below 60 DEG C, then adding pure water, mixing evenly, standing for layering, and taking subnatant to obtain the acetoacetoxy ethyl methacrylate. The method has the advantages of simple process, simple post-treatment, high product yield, high product purity and stable product quality.

Method for preparing aceto acetoxy ethyl methacrylate

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Paragraph 0018, (2016/11/21)

The invention discloses a method for preparing aceto acetoxy ethyl methacrylate. The method comprises the following steps of mixing hydroxyethyl methylacrylate with ethyl acetoacetate; then adding a supported inorganic solid base serving as a catalyst and methylhydroquinone serving as a polymerization inhibitor, and enabling a mixture to fully react at the temperature of 118-125DEG C; in the reaction process, distilling out ethanol serving as a reaction side product by adopting a mode of reacting while distilling; after the reaction is ended, separating the catalyst, thus obtaining a liquid product, namely the aceto acetoxy ethyl methacrylate. The method has the advantages of high reaction speed, few side reaction products and high yield.

POLYMER PARTICLES

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, (2012/06/01)

The present invention relates to a method of forming polymer on the surface of polymer particles, the method comprising: (i) providing a dispersion comprising a continuous aqueous phase, a dispersed organic phase comprising one or more ethylenically unsaturated monomers, and a RAFT agent as a stabiliser for said organic phase; (ii) polymerising the one or more ethylenically unsaturated monomers under the control of the RAFT agent to form an aqueous dispersion of seed polymer particles; (iii) crosslinking the seed polymer particles; (iv) swelling the crosslinked seed particles with one or more ethylenically unsaturated monomers to form an aqueous dispersion of monomer swollen crosslinked seed polymer particles; (v) increasing the temperature of the monomer swollen crosslinked seed polymer particles to expel at least some of the monomer therein onto the surface of the particles; and polymerising at least the expelled monomer to form polymer on the surface of the particles.

Liquid oligomers containing acrylate unsaturation

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, (2008/06/13)

The liquid oligomeric compositions of this invention are made by the Michael addition reaction of acetoacetate functional donor compounds with multifunctional acrylate receptor compounds where the equivalent ratios of multifunctional acrylate to acetoacetate vary from >/=1:1 to >/=13.2:1 depending on the functionality of both multifunctional acrylate and acetoacetate. Unuseable gelled or solid oligomer products occur below the claimed ranges. The liquid oligomers of this invention are further crosslinked to make coatings, laminates and adhesives.

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