86261-90-7

Basic information

• Product Name: 2-(2-OXO-1-IMIDAZOLIDINYL)ETHYL METHACRYLATE
• Synonyms: 2-(2-oxo-1-imidazolidinyl)ethylmethacryl-ate,25;2-methyl-2-propenoicaci2-(2-oxo-1-imidazolidinyl)ethylester;2-Propenoicacid,2-methyl-,2-(2-oxo-1-imidazolidinyl)ethylester;2-(2-OXO-1-IMIDAZOLIDINYL)ETHYL METHACRYLATE;N-(2-METHACRYLOYLOXYETHYL) ETHYLENE UREA;2-(2-Oxo-1-imidazolidinyl)ethyl methacrylate solution;Ethylene ureaethyl methacrylate;2-(2-oxoimidazolidin-1-yl)ethyl methacrylate
• CAS NO: 86261-90-7
• Molecular Formula: C9H14N2O3
• Molecular Weight: 198.22
• EINECS: 289-214-5
• Mol File: 86261-90-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: −30 °C
• Boiling Point: 100 °C
• Flash Point: 60 °F
• Appearance: /
• Density: 0.99 g/mL at 25 °C
• Vapor Pressure: 8.64E-07mmHg at 25°C
• Refractive Index: n20/D 1.437
• PKA: 14.27±0.20(Predicted)
• Water Solubility: 1000g/L at 20℃
• CAS DataBase Reference: 2-(2-OXO-1-IMIDAZOLIDINYL)ETHYL METHACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-OXO-1-IMIDAZOLIDINYL)ETHYL METHACRYLATE(86261-90-7)
• EPA Substance Registry System: 2-(2-OXO-1-IMIDAZOLIDINYL)ETHYL METHACRYLATE(86261-90-7)

Safety Data

• Hazard Codes: F,C,Xn
• Statements: 11-34-42/43-43-36/37/38-22
• Safety Statements: 16-26-33-36/37/39-45-46-36/37-24
• RIDADR: UN 2924 3/PG 2
• WGK Germany: 1
• Hazardous Substances Data: 86261-90-7(Hazardous Substances Data)

Usage

Flammability and Explosibility

Nonflammable

InChI:InChI=1/C9H14N2O3/c1-7(2)8(12)14-6-5-11-4-3-10-9(11)13/h1,3-6H2,2H3,(H,10,13)

Upstream product

• 3699-54-5 2-oxo-imidazolidine-1-ethanol 
• 80-62-6 methacrylic acid methyl ester 
• 161663-36-1 2-hydroxyethylethyleneurea 

Relevant articles and documents

PROCESS FOR THE PREPARATION OF (METH)ACRYLIC ESTERS AND DERIVATIVES

Transesterification processes for producing a compound of formula (I) wherein R1 is H or a methyl group, A and B are each, independently, a linear or branched C2-C5 alkylene group, comprising reacting: an acrylate or methacrylate of formula (II) wherein R1 is H or a methyl group and R2 is a C1-C4 alkyl group, with a compound of formula (III) wherein the reaction is performed: (i) in the presence of calcium oxide and calcium hydroxide, and (ii) wherein the molar ratio of the compounds of formula (II) to formula (III) is less than 4:1 or 3:1 respectively.

Transesterification process for production of (meth)acrylate ester monomers

This invention utilizes a mixed salt transesterification catalyst in a transesterification process for the production of esters of alkyl(meth)acrylate monomers.

Transesterification process for production of (meth)acrylate ester monomers

This invention utilizes multiple charges of a transesterification catalyst in a transesterification process for the production of esters of alkyl (meth)acrylate monomers. The multiple catalyst charge addition strategy and reaction conditions provide for higher productivity and enhanced consistency.