Merck
CN

261548

Sigma-Aldrich

三甘醇二甲基丙烯酸酯

contains 80-120 ppm MEHQ as inhibitor, 95%

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别名:
TEGDMA
线性分子式:
CH2=C(CH3)COO(CH2CH2O)3COC(CH3)=CH2
CAS号:
分子量:
286.32
Beilstein:
1797351
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.23

质量水平

检测方案

95%

形式

liquid

包含

80-120 ppm MEHQ as inhibitor

reaction suitability

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

折射率

n20/D 1.461 (lit.)

bp

170-172 °C/5 mmHg (lit.)

密度

1.092 g/mL at 25 °C (lit.)

Ω端

methacrylate

α端

methacrylate

聚合物结构设计

shape: linear
functionality: homobifunctional

储存温度

2-8°C

SMILES string

CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C

InChI

1S/C14H22O6/c1-11(2)13(15)19-9-7-17-5-6-18-8-10-20-14(16)12(3)4/h1,3,5-10H2,2,4H3

InChI key

HWSSEYVMGDIFMH-UHFFFAOYSA-N

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此商品
335681409006409510
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

1.092 g/mL at 25 °C (lit.)

density

1.051 g/mL at 25 °C (lit.)

density

1.082 g/mL at 25 °C (lit.)

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

一般描述

三乙二醇二甲基丙烯酸酯(TEGDMA)是一种用作交联剂的亲水性低粘度双官能甲基丙烯酸单体。

应用

TEGDMA是一种通常用于牙科树脂材料的单体,可在真核细胞中引起特定的应激反应。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Sens. 1

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

332.6 °F - closed cup

闪点(°C)

167 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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其他客户在看

Helmut Schweikl et al.
Biomaterials, 29(10), 1377-1387 (2008-01-01)
Triethylene glycol dimethacrylate (TEGDMA) is a comonomer that is released from dental resin-based materials into hydrophilic solvents. The compound reduces cell vitality, and causes genotoxicity in mammalian cells in vitro. Here, we used gene expression profiling, combined with pathway analysis
Eleftherios G Andriotis et al.
Nanomaterials (Basel, Switzerland), 11(1) (2021-01-17)
Mini-emulsion polymerization was applied for the synthesis of cross-linked polymeric nanoparticles comprised of methyl methacrylate (MMA) and Triethylene Glycol Dimethacrylate (TEGDMA) copolymers, used as matrix-carriers for hosting D-limonene. D-limonene was selected as a model essential oil, well known for its
Geum-Jun Han et al.
The journal of adhesive dentistry, 14(5), 461-469 (2012-06-23)
To evaluate the effect of applied power on dental ceramic bonding of composite resin using nonthermal atmospheric pressure plasma (APP). A pencil-type APP torch was used to modify the surface chemical composition and hydrophilicity of dental ceramic and to improve
Vidhi Malik et al.
International journal of molecular sciences, 21(15) (2020-08-06)
The anti-metastatic and anti-angiogenic activities of triethylene glycol derivatives have been reported. In this study, we investigated their molecular mechanism(s) using bioinformatics and experimental tools. By molecular dynamics analysis, we found that (i) triethylene glycol dimethacrylate (TD-10) and tetraethylene glycol
Andrzej Dworak et al.
ACS applied materials & interfaces, 5(6), 2197-2207 (2013-03-02)
Well-defined thermosensitive poly[tri(ethylene glycol) monoethyl ether methacrylate] (P(TEGMA-EE)) brushes were synthesized on a solid substrate by the surface-initiated atom transfer radical polymerization of TEGMA-EE. The polymerization reaction was initiated by 2-bromo-2-methylpropionate groups immobilized on the surface of the wafers. The

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