(Hydroxyethyl)methacrylate

From Wikipedia, the free encyclopedia
(Redirected from Hydroxyethylmethacrylate)
Jump to navigation Jump to search
(Hydroxyethyl)methacrylate
Error creating thumbnail:
Ball-and-stick model of the hydroxyethyl methacrylate molecule
Names
Preferred IUPAC name
2-Hydroxyethyl 2-methylprop-2-enoate
Other names
HEMA; hydroxyethylmethacrylate; glycol methacrylate; glycol monomethacrylate; hydroxyethyl methacrylate; ethylene glycol methacrylate; 2-(methacryloyloxy)ethanol
Identifiers
3D model (JSmol)
1071583
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
EC Number
  • 212-782-2
E number Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).
936557
KEGG
RTECS number
  • OZ4725000
UNII
  • {{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
  • InChI=1S/C6H10O3/c1-5(2)6(8)9-4-3-7/h7H,1,3-4H2,2H3 checkY
    Key: WOBHKFSMXKNTIM-UHFFFAOYSA-N checkY
  • InChI=1/C6H10O3/c1-5(2)6(8)9-4-3-7/h7H,1,3-4H2,2H3
    Key: WOBHKFSMXKNTIM-UHFFFAOYAH
  • O=C(OCCO)\C(=C)C
  • CC(=C)C(=O)OCCO
Properties
C6H10O3
Molar mass 130.143 g·mol−1
Appearance Colourless liquid
Density 1.07 g/cm3
Melting point −99 °C (−146 °F; 174 K)[2]
Boiling point 213 °C (415 °F; 486 K)[2]
miscible
log P 0.50[1]
Vapor pressure 0.08 hPa
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Eye irritation
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H317, H319
P261, P264, P272, P280, P302+P352, P305+P351+P338, P321, P332+P313, P333+P313, P337+P313, P362, P363, P501
Flash point 97 °C (207 °F; 370 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hydroxyethylmethacrylate (also known as glycol methacrylate)[3][4] is the organic compound with the chemical formula H2C=C(CH3)CO2CH2CH2OH. It is a colorless viscous liquid that readily polymerizes, i.e. it is a monomer that is used to make various polymers.

Synthesis

[edit | edit source]

Hydroxyethylmethacrylate was first synthesized around 1925. Common methods of synthesis are:[5]

H2C=C(CH3)CO2H + CH2CH2O → H2C=C(CH3)CO2CH2CH2OH
H2C=C(CH3)CO2H + HOCH2CH2OH → H2C=C(CH3)CO2CH2CH2OH + H2O

Both these methods give also some amount of ethylene glycol dimethacrylate. During polymerization of hydroxyethylmethacrylate, it works as crosslinking agent.[5]

Properties

[edit | edit source]

Hydroxyethylmethacrylate is completely miscible with water and ethanol, but its polymer is practically insoluble in common solvents. Its viscosity is 0.0701 Pa⋅s at 20°C[6] and 0.005 Pa⋅s at 30°C.[3] During polymerization, it shrinks by approximately 6%.[6]

Applications

[edit | edit source]

Contact lenses

[edit | edit source]

In 1960, O. Wichterle and D. Lím[7] described its use in synthesis of hydrophilic crosslinked networks, and these results had great importance for manufacture of soft contact lenses.[5] Polyhydroxyethylmethacrylate is hydrophilic: it is capable of absorbing from 10 to 600% water relative to the dry weight. Because of this property, it was one of the first materials to be used in the manufacture of soft contact lenses.[8]

Use in 3D printing

[edit | edit source]

Hydroxyethylmethacrylate lends itself well to applications in 3D printing as it cures quickly at room temperature when exposed to UV light in the presence of photoinitiators. It may be used as a monomeric matrix in which 40nm silica particles are suspended for 3D glass printing.[9] When combined with a suitable blowing agent such as BOC anhydride it forms a foaming resin which expands when heated.[10]

Other

[edit | edit source]

In electron microscopy, later in light microscopy, hydroxyethylmethacrylate serves as an embedding medium.[4][3]

When treated with polyisocyanates, polyhydroxyethylmethacrylate makes a crosslinked polymer, an acrylic resin, that is a useful component in some paints.[11]

Hazards

[edit | edit source]

Hydroxyethylmethacrylate is a mild skin irritant and can cause allergic skin reactions.[3]

References

[edit | edit source]
  1. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  2. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  3. ^ a b c d Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  4. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  5. ^ a b c Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  6. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  7. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  8. ^ Blasco, Joe; Kehoe, Vincent J-R; The professional make-up artist : motion pictures, television, print, theatre; Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).; LCC# PN2068.B53 2005
  9. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  10. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  11. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).