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1-methyl-1,2-ethanediyl diacrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25151-33-1

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25151-33-1 Usage

Chemical category

Diacrylates

Use

Monomers in the production of polymers and plastics

Reactivity

High

Versatility

Versatile in polymerization reactions

Applications

Synthesis of coatings, adhesives, and various polymer materials

Chemical structure

Methyl group attached to 1,2-ethanediyl backbone

Unique properties

Provided by the chemical structure

Functionalities

Intended for specific applications

Safety precautions

Skin and eye irritant, potential health hazards if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 25151-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,5 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25151-33:
(7*2)+(6*5)+(5*1)+(4*5)+(3*1)+(2*3)+(1*3)=81
81 % 10 = 1
So 25151-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O4/c1-4-8(10)12-6-7(3)13-9(11)5-2/h4-5,7H,1-2,6H2,3H3

25151-33-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-prop-2-enoyloxypropyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names EINECS 246-664-7

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25151-33-1 SDS

25151-33-1Downstream Products

25151-33-1Relevant academic research and scientific papers

PREPARATION OF DIESTERS OF (METH)ACRYLIC ACID FROM EPOXIDES

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Page/Page column 23, (2020/03/05)

The application relates to a process for preparing a (meth)acrylic acid diester by reacting a (meth)acrylic acid anhydride with an epoxide in the presence of a catalyst system comprising a first and/or second catalyst in combination with a co-catalyst. The first catalyst is a halide of Mg or a trifluoromethanesulfonate of a rare earth element; the second catalyst is a Cr(lll) salt; and the co- catalyst is a tertiary amine, a quaternary ammonium salt, a tertiary phosphine or a quaternary phosphonium salt.

Hydroxy functional acrylate and methacrylate monomers prepared via lipase-catalyzed transacylation reactions

Popescu, Dragos,Hoogenboom, Richard,Keul, Helmut,Moeller, Martin

experimental part, p. 80 - 89 (2010/08/20)

Candida antarctica lipase B (CAL-B, Novozyme 435) catalyzes the transacylation of methyl acrylate and methyl methacrylate with diols and triols in 2-methyl-2-butanol at 50 °C. Under the experimental conditions, up to 70 mol% of the acyl donor methyl acrylate was converted. Methyl methacrylate is the less efficient acyl donor (up to 60 mol%) due to the higher sterical hindrance in the enzymatic transacylation. Under the reaction conditions high yields of the mono-acylated products are obtained, which contain minor amounts of bis(meth)acrylates. In addition it was observed that Novozyme 435 catalyzes regioselectively the acylation of the primary hydroxyl groups. In comparison with the chemical catalyzed route no selectivity was observed for unsubstituted diols. For substituted diols more mono-acylated product was formed in the lipase-catalyzed reaction than in the chemical catalyzed reaction.

Free radical and nitroxide mediated polymerization of hydroxy-functional acrylates prepared via lipase-catalyzed transacylation reactions

Popescu, Dragos,Hoogenboom, Richard,Keul, Helmut,Moeller, Martin

experimental part, p. 2610 - 2621 (2011/04/22)

3-Hydroxypropyl acrylate, 4-hydroxybutyl acrylate, 2-methyl-3-hydroxypropyl acrylate, 2-hydroxypropyl acrylate, neopentyl glycol acrylate, glyceryl acrylate, and dihydroxyhexyl acrylate were prepared via transacylation reaction of methyl acrylate with diols and triols catalyzed by Candida antarctica lipase B. After removal of the enzyme by filtration and the methyl acrylate by distillation, the monomers were polymerized via free radical polymerization (FRP) with azobisisobutyronitrile as initiator and nitroxide mediated polymerization (NMP) employing Blocbuilder alkoxyamine initiator and SG-1 free nitroxide resulting in hydroxy functional poly(acrylates). The NMP kinetics are discussed in detail. In addition, the polymers obtained by FRP and NMP are compared and the results are related to the amount of bisacrylates that are present in the initial monomer mixtures resulting from the transacylation reactions

COMPOSITION FOR POLYELECTROLYTES, POLYELECTROLYTES, ELECTRICAL DOUBLE LAYER CAPACITORS AND NONAQUEOUS ELECTROLYTE SECONDARY CELLS

-

, (2008/06/13)

A polymer electrolyte-forming composition containing (A) a quaternary ammonium salt of general formula (1) below and (B) an ionic liquid can be converted into a polymer without compromising the excellent properties of the ionic liquid, thus enabling an electrolyte having an excellent safety and electrical conductivity and also a broad potential window to be obtained. In formula (1), R1 to R3 are each independently an alkyl group of 1 to 5 carbons or a substituent having a reactive unsaturated bond and any two from among R1 to R3 may together form a ring, and R4 is methyl, ethyl or a substituent having a reactive unsaturated bond, with the proviso that at least one of R1 to R4 is a substituent having a reactive unsaturated bond. X is a monovalent anion, the letter m is an integer from 1 to 8, and the letter n is an integer from 1 to 4.

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