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409006

Sigma-Aldrich

Di(ethylene glycol) dimethacrylate

95%, cross-linking reagent polymerization reactions, methacrylate, 300 ppm monomethyl ether hydroquinone as inhibitor

Sinônimo(s):

2,2′-Oxybisethanol dimethacrylate, 2,2′-Oxydiethyl dimethacrylate, Diethylene glycol, dimethacrylate, Polyethylene glycol

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About This Item

Fórmula linear:
[H2C=C(CH3)CO2CH2CH2]2O
Número CAS:
2358-84-1
Peso molecular:
242.27
Número CE:
219-099-9
Número MDL:
MFCD00014931
Código UNSPSC:
12162002
ID de substância PubChem:
24865615
NACRES:
NA.23

product name

Di(ethylene glycol) dimethacrylate, 95%

Nível de qualidade

200

Ensaio

95%

forma

liquid

contém

300 ppm monomethyl ether hydroquinone as inhibitor

adequação da reação

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

índice de refração

n20/D 1.458 (lit.)

pb

134 °C/2 mmHg (lit.)

densidade

1.082 g/mL at 25 °C (lit.)

Ω-final

methacrylate

α-final

methacrylate

arquitetura do polímero

shape: linear
functionality: homobifunctional

cadeia de caracteres SMILES

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

chave InChI

XFCMNSHQOZQILR-UHFFFAOYSA-N

Aplicação

  • Urethane dimethacrylate-based photopolymerizable resins for stereolithography 3D printing: A physicochemical characterisation and biocompatibility evaluation.: This study explores the use of urethane dimethacrylate-based resins in stereolithography 3D printing. It includes an in-depth physicochemical characterization and assesses the biocompatibility of the materials, highlighting their potential for medical and dental applications (Pitzanti G et al., 2024).

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
MKCN9488
MKCK9887
MKCD7013
MKCD4044
STBB8019V

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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
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
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.
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
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