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13533-05-6

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13533-05-6 Usage

General Description

2-(2-hydroxyethoxy)ethyl acrylate is a chemical compound that is commonly used in the production of various commercial products such as adhesives, coatings, and paints. It is a clear, colorless liquid with a slight odor, and is soluble in water. 2-(2-hydroxyethoxy)ethyl acrylate is known for its ability to enhance the flexibility, adhesion, and durability of coatings and adhesives. It is also used as a raw material in the synthesis of polymers and resins. However, it is important to handle and use this chemical with caution as it can cause skin and eye irritation, and may be harmful if ingested or inhaled in large quantities. Therefore, appropriate safety measures and protective equipment should be used when working with 2-(2-hydroxyethoxy)ethyl acrylate.

Check Digit Verification of cas no

The CAS Registry Mumber 13533-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13533-05:
(7*1)+(6*3)+(5*5)+(4*3)+(3*3)+(2*0)+(1*5)=76
76 % 10 = 6
So 13533-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O4/c1-6(7(9)10)2-4-11-5-3-8/h8H,1-5H2,(H,9,10)/p-1

13533-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxyethoxy)ethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,2-(2-hydroxyethoxy)ethyl ester

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:13533-05-6 SDS

13533-05-6Downstream Products

13533-05-6Relevant articles and documents

Phosphate cross-linking agent and preparation method thereof, phosphate-based cross-linked gel polymer electrolyte and preparation method and application thereof

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Paragraph 0047-0048; 0052, (2020/08/17)

According to the invention, the safety of the battery can be improved based on introduction of phosphate into the gel polymer electrolyte, , the adjustable flexibility is improved by introduction of aPEO chain segment, and the stability and the polymerization capability are improved by introduction of acrylate; thus, further research is carried out on the basis of the prior art, the polyfunctional phosphate cross-linking agent is obtained and is applied to the preparation of the phosphate-based cross-linked gel polymer electrolyte, so the cross linking agent can be copolymerized with other functional monomers to synthesize gel polymer electrolyte; the gel polymer electrolyte has the advantages of simple and convenient preparation method, high ionic conductivity, high thermal stability andgood electrochemical stability, the assembled sodium ion battery has good cycling stability and high-temperature performance, and the phosphate-based gel polymer electrolyte with high safety is provided for quasi-solid sodium/lithium ion batteries.

A process for the production of hydroxyalkyl (meth)acrylates

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Page/Page column 3-4, (2008/12/07)

The present invention relates to a process for producing high purity hydroxyalkyl (meth)acrylates. Specifically, the present invention relates to an improved process which can commercially and advantageously yield high purity hydroxyalkyl (meth)acrylates from (meth)acrylic acid and alkylene oxides.

PROCESSES FOR PRODUCING HYDROXYALKYL (METH)ACRYLATE

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Page/Page column 24--27; 34-37, (2008/06/13)

Processes for producing a hydroxyalkyl (meth)acrylate which comprise reacting (meth)acrylic acid with an alkylene oxide in the presence of a catalyst. A first process is characterized in that the amount of the acid ingredient is kept, on calculation, at 0.010 or more in terms of molar ratio to the catalyst present in the liquid reaction mixture and that the liquid reaction mixture from which the hydroxyalkyl (meth)acrylate has been distilled off is used in the subsequent reaction. A second process is characterized in that a dialkylene glycol mono(meth)acrylate is supplied to the reaction system to cause the dialkylene glycol mono(meth)acrylate to coexist in the liquid reaction mixture.

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