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463183

Sigma-Aldrich

Poly(methyl methacrylate-co-ethylene glycol dimethacrylate)

50 μm particle size

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About This Item

Linear Formula:
[-CH2C(CH3)(CO2CH3)-]X[CH2(C-)(CH3)CO2CH2CH2O2C(C-)(CH3)CH2-]Y
CAS Number:
25777-71-3
MDL number:
MFCD00677749
UNSPSC Code:
12162002
PubChem Substance ID:
24870029
NACRES:
NA.23

form

particles (spherical)

crosslinking

5 % cross-linked

particle size

50 μm

density

1.19 g/mL at 25 °C (lit.)

SMILES string

COC(=O)C(C)=C.CC(=C)C(=O)OCCOC(=O)C(C)=C

InChI

1S/C10H14O4.C5H8O2/c1-7(2)9(11)13-5-6-14-10(12)8(3)4;1-4(2)5(6)7-3/h1,3,5-6H2,2,4H3;1H2,2-3H3

InChI key

XBDAKYZJVVYINU-UHFFFAOYSA-N

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General description

Particles of this polymer can be prepared by dispersion polymerization.

Application

Light diffusing agent in plastics, matting agent, anti-blocking agent and pore-forming agent in ceramics.
Poly(methyl methacrylate-co-ethylene glycol dimethacrylate) may be used as an extraction media coupled to gas chromatography with electron-capture detection (GC-ECD) to investigate remnants of six polychlorinated biphenyls (PCBs) in water samples.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Preparation and characterization of acrylic?based black particles of poly (methyl methacrylate?co?ethylene glycol dimethacrylate) by dispersion polymerization for electrophoretic displays.
Yu D G and An J H
Journal of Polymer Science Part A: Polymer Chemistry, 42(22), 5608-5616 (2004)
Novel polymer monolith microextraction using a poly-(methyl methacrylate-co-ethylene dimethacrylate) monolith and its application to the determination of polychlorinated biphenyls in water samples.
Liu L, et al.
Chemosphere, 83(10), 1307-1312 (2011)
Gregory L Polyzois et al.
The International journal of prosthodontics, 15(6), 535-538 (2002-12-12)
The aim of this study was to evaluate the interfacial bond strength between different types of silicone facial elastomers and denture resins. The facial materials studied were Cosmesil and Ideal, whereas SR 3/60, SR 3/60 Quick, and Triad were included
S Sadamori et al.
Australian dental journal, 40(5), 322-326 (1995-10-01)
The dimensional changes of relined denture bases were evaluated in a laboratory study. Heat-cured resin, two autopolymerizing resins, microwave-activated resin and a new visible light-cured resin were used as relining materials in this study. The gaps between the metal die
Alcibiades Zissis et al.
The European journal of prosthodontics and restorative dentistry, 16(2), 81-84 (2008-07-22)
The aim of this long term study was to investigate the release of residual monomer from different denture materials, throughout a 38 months time period after curing and storage in water Specimens made of four denture base resins (three heat
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