并加购,请在购物车里查看协议价、货期和发货地。
选择规格
变更视图
关于此项目
线性分子式:
CH2=C(CH3)COO(CH2CH2O)3COC(CH3)=CH2
化学文摘社编号:
分子量:
286.32
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
203-652-6
MDL number:
Beilstein/REAXYS Number:
1797351
产品名称
三甘醇二甲基丙烯酸酯, contains 200 ppm monomethyl ether hydroquinone as inhibitor, 99%
Quality Segment
assay
99%
form
liquid
contains
200 ppm monomethyl ether hydroquinone as inhibitor
reaction suitability
reagent type: cross-linking reagent
reaction type: Polymerization Reactions
refractive index
n
bp
170-172 °C/5 mmHg (lit.)
density
1.092 g/mL at 25 °C (lit.), 1.074 g/mL
polymer architecture
shape: linear
functionality: homobifunctional
storage temp.
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
General description
Triethylene glycol dimethacrylate is used as a cross-linking agent in the synthesis of poly (methacrylic acid-g-ethylene glycol ) hydrogels which shows large changes in swelling due to changes in pH, temperature and solvent composition. They are also used as a divinylic methacrylic monomer which are widely used to form copolymers with divinylbenzene (DVB) and glycidyl methacrylate (GMA) or hydroxyethyl methacrylate (HEMA) comonomers.
Application
- Used as a diluent comonomer in dimethacrylate based dental composites.
- Used as a branching agent in the atom transfer radical polymerization (ATRP) of styrene.
Features and Benefits
Lower viscosity compared to other dimethacrylate monomers enabling higher amounts of filler to be incorporated in dental composites. Non-toxic and can be rapidly polymerized in the presence of oxygen and water.
Still not finding the right product?
Explore all of our products under 三甘醇二甲基丙烯酸酯
signalword
Warning
hcodes
存储类别
10 - Combustible liquids
flash_point_f
332.6 °F - closed cup
flash_point_c
167 °C - closed cup
Hazard Classifications
Skin Sens. 1B
