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2-Aminoethyl methacrylate hydrochloride

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2-Aminoethyl methacrylate hydrochloride Basic information

Product Name:
2-Aminoethyl methacrylate hydrochloride
Synonyms:
  • 2-propenoicacid,2-methyl-,2-aminoethylester,hydrochloride
  • TIMTEC-BB SBB003905
  • 2-AMINOETHYL METHACRYLATE HYDROCHLORIDE
  • 2-AminoethylmethacrylateHCl
  • 2-Aminoethyl methacrylate hydrochloride, stabilized, 90%
  • AMINOETHYLMETHACRYLATE
  • Aminoethylmethacrylate hydrochloride
  • 2-AminoethyL
CAS:
2420-94-2
MF:
C6H11NO2.ClH
MW:
165.62
EINECS:
219-343-4
Product Categories:
  • Thiophenes
  • Acrylic Monomers
  • C6 to C7Monomers
  • Carbonyl Compounds
  • Esters
  • Methacrylate
Mol File:
2420-94-2.mol
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2-Aminoethyl methacrylate hydrochloride Chemical Properties

Melting point:
102-110 °C(lit.)
storage temp. 
2-8°C
form 
Crystalline Powder
color 
White to light green to light brown
Water Solubility 
Soluble
InChI
InChI=1S/C6H11NO2.ClH/c1-5(2)6(8)9-4-3-7;/h1,3-4,7H2,2H3;1H
InChIKey
XSHISXQEKIKSGC-UHFFFAOYSA-N
SMILES
C(=O)(OCCN)C(=C)C.Cl
CAS DataBase Reference
2420-94-2(CAS DataBase Reference)
EPA Substance Registry System
2-Propenoic acid, 2-methyl-, 2-aminoethyl ester, hydrochloride (2420-94-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
1
HS Code 
29221990

MSDS

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2-Aminoethyl methacrylate hydrochloride Usage And Synthesis

Chemical Properties

WHITE TO ALMOST WHITE CRYSTALLINE POWDER

Uses

suzuki reaction

Uses

2-Aminoethyl methacrylate hydrochloride has been used to create ampiphilic copolymers.

Synthesis

The synthesis of 2-Aminoethyl methacrylate hydrochloride:
In a 500 mL three-neck flask equipped with a thermometer and a reflux condenser were placed 300 g of toluene and 60.0 g (0.62 mol) of ethanolamine hydrochloride, followed by heating to 110° C. with stirring. After the inner temperature reached 110° C., 77.1 g (0.74 mol) of methacryloyl chloride was added dropwise thereto over a period of 30 minutes. After completion of the dropwise addition, the mixture was continued to stir for further 3 hours and then cooled to 0° C. with stirring. The precipitated solid was collected by filtration and then the resulting solid was washed with 300 g of diisopropyl ether. The solid was collected by filtration and then dried under reduced pressure to obtain 85.2 g of 2-Aminoethyl methacrylate hydrochloride.

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