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Merck
CN

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:
25777-71-3
NACRES:
NA.23
PubChem Substance ID:
24870029
UNSPSC Code:
12162002
MDL number:
MFCD00677749

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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

SMILES string

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

InChI key

XBDAKYZJVVYINU-UHFFFAOYSA-N

form

particles (spherical)

crosslinking

5 % cross-linked

particle size

50 μm

density

1.19 g/mL at 25 °C (lit.)

Quality Level

100

Related Categories

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ6867
MKBW2879V
MKBQ0475V
MKBN4969V
MKBH7218V

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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)
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
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
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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