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2223-82-7

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2223-82-7 Usage

General Description

Neopentyl glycol diacrylate is a chemical compound commonly used in the production of various polymers and coatings. It is a reactive diluent and crosslinking agent that helps to improve the flexibility, adhesion, and overall performance of the final product. Neopentyl glycol diacrylate is particularly popular in the manufacture of UV-curable inks, adhesives, and coatings due to its fast curing properties and excellent chemical resistance. Its low volatility and low odor make it a preferred choice for applications where odor and emissions control are important factors. Overall, neopentyl glycol diacrylate is a versatile chemical that plays a crucial role in enhancing the properties of various polymer and coating formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 2223-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2223-82:
(6*2)+(5*2)+(4*2)+(3*3)+(2*8)+(1*2)=57
57 % 10 = 7
So 2223-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O4/c1-6-8(12)14-10(11(3,4)5)15-9(13)7-2/h6-7,10H,1-2H2,3-5H3

2223-82-7 Well-known Company Product Price

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  • Aldrich

  • (408255)  Neopentylglycoldiacrylate  

  • 2223-82-7

  • 408255-100ML

  • 796.77CNY

  • Detail

2223-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Neopentyl glycol diacrylate

1.2 Other means of identification

Product number -
Other names Neopentyl Glycol Diacrylate

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:2223-82-7 SDS

2223-82-7Downstream Products

2223-82-7Relevant articles and documents

CURABLE COMPOSITION FOR IMPRINT, PATTERNING METHOD AND PATTERN

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, (2011/04/18)

A curable composition for imprints, which is excellent in patternability and in line edge roughness, is provided. The curable composition for imprints comprises at least one kind of polymerizable monomer (A) and at least one kind of photopolymerization initiator (B). The polymerizable monomer (A) comprises at least two fluorine-containing groups selected from a fluoroalkyl group and a fluoroalkylether group and each of two of the fluorine-containing groups is connected with each other through a linking group having at least two carbon atoms.

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

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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