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19812-60-3

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  • SAGECHEM/2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl acrylate /Manufacturer in China/SAGECHEM

    Cas No: 19812-60-3

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19812-60-3 Usage

General Description

2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl acrylate, also known as PGMEA, is a chemical compound used in various industrial applications. It is a clear, colorless liquid with a mild, sweet odor. PGMEA is commonly used as a solvent in the manufacturing of polymers, resins, and adhesives, and as a coalescing agent in latex paints. It is also utilized as a processing aid in the production of electronic materials, such as photoresists and circuit boards. Additionally, PGMEA is used as a component in the development of specialty coatings and inks. Despite its widespread use, PGMEA does pose potential health risks and must be handled with appropriate safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 19812-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19812-60:
(7*1)+(6*9)+(5*8)+(4*1)+(3*2)+(2*6)+(1*0)=123
123 % 10 = 3
So 19812-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O6/c1-2-11(13)17-10-9-16-8-7-15-6-5-14-4-3-12/h2,12H,1,3-10H2

19812-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names tetraethylene glycol monoacrylate

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:19812-60-3 SDS

19812-60-3Relevant articles and documents

Effects of novel boric acid esters on ion transport properties of lithium salts in nonaqueous electrolyte solutions and polymer electrolytes

Tabata, Sei-Ichiro,Hirakimoto, Takuro,Tokuda, Hiroyuki,Susan, Md Abu Bin Hasan,Watanabe, Masayoshi

, p. 19518 - 19526 (2004)

Three novel polymerizable anion receptors based on boric acid esters have been synthesized. The addition of these monomers appreciably enhanced the ionic conductivity of certain electrolyte solutions comprised of an aprotic organic solvent of low polarity and a lithium salt of low dissociation ability. Analysis of the viscosity and pulse-field-gradient spin-echo (PGSE) NMR results in association with the ionic conductivity data revealed that the conductivity enhancement originated from the increase in the degree of dissociation, resulting from the addition of these anion receptors. The 11B NMR spectra of dimethoxyethane electrolyte solutions with added boric acid ester monomers substantiated the finding that the ionic dissociation was facilitated by strong interaction between the Lewis-acidic anion receptor and Lewis-basic anions. The polymerizable anion receptor of the catechol borate derivative was cross-linked with a polyether macromonomer containing different lithium salts. The ionic conductivity could be correlated with glass transition temperatures of the polymer electrolytes by the WLF equation. The ionic conduction behavior of the boron polymer electrolytes was compared with that of the reference polymer electrolytes, and the lithium cation transference number was clarified to be higher for the former. The polymer electrolytes showed similar conduction behavior to that of the electrolyte solutions containing the anion receptor monomers.

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

-

Paragraph 0047-0048; 0056, (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.

Stabilized vesicles consisting of small amphiphiles for stepwise photorelease via UV light

Dong, Jianming,Zeng, Yi,Xun, Zhiqing,Han, Yongbin,Chen, Jinping,Lee, Ying-Ying,Li, Yi

experimental part, p. 1733 - 1737 (2012/06/15)

A small amphiphile consisting of hydrophilic tetraethylene glycol monoacrylate and hydrophobic alkyl chain which were connected by an o-nitrobenzyl unit, a photolabile group, was designed and synthesized. The critical aggregate concentration of the synthesized amphiphile was determined to be about 3 × 10-5 M by the fluorescence probe technique. Nanosized vesicles were prepared and stabilized by in-situ radical polymerization without altering the morphology. The polymeric vesicle was highly stable which retained vesicular shape under dilution or UV irradiation. Hydrophobic guests can be encapsulated within the vesicle membrane and released out of the vesicle by UV stimulus through splitting the amphiphilic structure of the amphiphile. Distinguished dose-controlled photorelease of the polymeric vesicle is achieved due to the maintenance of the vesicular shape integrity which makes the guest release depend on the cleavage amount of amphiphilic structure during UV irradiation. This study provides a promising strategy to develop stable drug delivery systems for sustained and phototriggered release.

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