463183
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:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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form
particles (spherical)
Quality Level
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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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)
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
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
A G Andreopoulos et al.
The Journal of prosthetic dentistry, 72(5), 462-468 (1994-11-01)
Specimens of denture base resins were repaired with autopolymerizing and visible light-cured (VLC) repair materials. Flexural properties were measured and revealed that the highest strength and toughness of joint are obtained by the autopolymerizing repair material and are independent on
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