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Merck
CN

409006

Sigma-Aldrich

二乙二醇二甲基丙烯酸酯

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

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别名:
2,2′-氧双乙醇二甲基丙烯酸酯, 二甘醇、二甲基丙烯酸酯
线性分子式:
[H2C=C(CH3)CO2CH2CH2]2O
CAS号:
分子量:
242.27
EC 号:
MDL编号:
UNSPSC代码:
12162002
PubChem化学物质编号:
NACRES:
NA.23

质量水平

检测方案

95%

形式

liquid

包含

300 ppm monomethyl ether hydroquinone as inhibitor

反应适用性

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

折射率

n20/D 1.458 (lit.)

bp

134 °C/2 mmHg (lit.)

密度

1.082 g/mL at 25 °C (lit.)

Ω端

methacrylate

α端

methacrylate

聚合物结构设计

shape: linear
functionality: homobifunctional

SMILES字符串

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

应用

  • 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).

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

靶器官

Respiratory system

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves


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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
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.
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
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
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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