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Sigma-Aldrich

Di(ethylene glycol) dimethacrylate

95%

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Synonym(s):
2,2′-Oxybisethanol dimethacrylate, 2,2′-Oxydiethyl dimethacrylate, Diethylene glycol, dimethacrylate
Linear Formula:
[H2C=C(CH3)CO2CH2CH2]2O
CAS Number:
Molecular Weight:
242.27
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.23

Quality Level

Assay

95%

form

liquid

contains

300 ppm monomethyl ether hydroquinone as inhibitor

reaction suitability

reagent type: cross-linking reagent
reaction type: Polymerization Reactions

refractive index

n20/D 1.458 (lit.)

bp

134 °C/2 mmHg (lit.)

density

1.082 g/mL at 25 °C (lit.)

Ω-end

methacrylate

α-end

methacrylate

polymer architecture

shape: linear
functionality: homobifunctional

SMILES string

CC(=C)C(=O)OCCOCCOC(=O)C(C)=C

InChI

1S/C12H18O5/c1-9(2)11(13)16-7-5-15-6-8-17-12(14)10(3)4/h1,3,5-8H2,2,4H3

InChI key

XFCMNSHQOZQILR-UHFFFAOYSA-N

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This Item
335681437468409510
form

liquid

form

liquid

form

liquid

form

liquid

reaction suitability

reagent type: cross-linking reagent
reaction type: Polymerization Reactions

reaction suitability

reagent type: cross-linking reagent
reaction type: Polymerization Reactions

reaction suitability

reagent type: cross-linking reagent
reaction type: Polymerization Reactions

reaction suitability

reagent type: cross-linking reagent
reaction type: Polymerization Reactions

density

1.082 g/mL at 25 °C (lit.)

density

1.051 g/mL at 25 °C (lit.)

density

1.11 g/mL at 25 °C

density

1.099 g/mL at 25 °C

Ω-end

methacrylate

Ω-end

methacrylate

Ω-end

methacrylate

Ω-end

methacrylate

α-end

methacrylate

α-end

methacrylate

α-end

methacrylate

α-end

methacrylate

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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K S Anseth et al.
Journal of dental research, 75(8), 1607-1612 (1996-08-01)
During the polymerization of multifunctional monomers for dental restorations, typical final double-bond conversions range from 55 to 75%. The low conversion results in a large amount of extractable monomer, reduced adhesion to the filler, and the potential for increased swelling.
Y Takahashi et al.
Journal of dental research, 83(4), 302-306 (2004-03-27)
Ethyleneglycol dimethacrylate monomers have been previously reported to stimulate the growth of certain caries-associated bacteria on the basis of turbidity measurements. To elucidate the detail of this effect, we examined the influence of resin monomers on the growth of Streptococcus
Ahmad Joumaa et al.
Polymers, 12(5) (2020-05-16)
A latex of amphiphilic star polymer particles, functionalized in the hydrophobic core with nixantphos and containing P(MAA-co-PEOMA) linear chains in the hydrophilic shell (nixantphos-functionalized core-crosslinked micelles, or nixantphos@CCM), has been prepared in a one-pot three-step convergent synthesis using reversible addition-fragmentation
Liang-Qia Guo et al.
Guang pu xue yu guang pu fen xi = Guang pu, 26(8), 1483-1486 (2006-10-25)
A pH sensitive polymer was prepared by copolymerization of methacrylic acid as monomer, diethylene glycol dimethacrylate as cross-linking reagent, heptane as porogen, and fluorescent dye eosin as indicator. The factors of influence on the preparation, and the character of the
M Yoshida et al.
Journal of biomedical materials research, 19(6), 615-629 (1985-07-01)
A radiation polymerized drug-vinyl copolymer delivery composite (0.8 mm in diameter, 3 mm long) was inserted into the right-lobe ventral prostate (I), into the right testis (II), and subcutaneously (III) into the back of male Wistar rats. The implantation was

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