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About This Item
Empirical Formula (Hill Notation):
C9H14O3
CAS Number:
Molecular Weight:
170.21
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
219-529-5
MDL number:
InChI key
LCXXNKZQVOXMEH-UHFFFAOYSA-N
InChI
1S/C9H14O3/c1-7(2)9(10)12-6-8-4-3-5-11-8/h8H,1,3-6H2,2H3
SMILES string
CC(=C)C(=O)OCC1CCCO1
assay
97%
form
liquid
contains
75 ppm HQ as inhibitor, 900 ppm MEHQ as inhibitor
refractive index
n20/D 1.458 (lit.)
bp
52 °C/0.4 mmHg (lit.)
density
1.044 g/mL at 25 °C (lit.)
Quality Level
Related Categories
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
195.8 °F - closed cup
flash_point_c
91 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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P D Riggs et al.
Biomaterials, 21(4), 345-351 (2000-02-03)
A series of different methacrylate monomers (with either 1 or 2.5% dimethyl-p-toluidine, DMPT) was gelled with poly(ethyl methacrylate) powder (containing benzoyl peroxide) thus forming a room temperature curing system. When doped with 5.625% chlorhexidine diacetate the release from the tetrahydrofurfuryl
R Labella et al.
European journal of oral sciences, 106(3), 816-824 (1998-07-22)
Polymerisation shrinkage is widely recognised as a major drawback of resin based dental restoratives. Bis-GMA is often employed as the principal dimethacrylate monomer. Due to its high viscosity, Bis-GMA is normally mixed with large proportions of low viscosity glycol dimethacrylates.
R Labella et al.
Biomaterials, 17(4), 431-436 (1996-02-01)
This study investigates the physical properties of a range of dental resins containing up to 30% by weight of tetrahydrofurfuryl methacrylate (THFMA). The principal monomer was 2,2-bis-(4(2-hydroxy-3-methacryloyloxypropoxy)-phenyl)-propane (bis-GMA) or 1,6-bis-(methacryloxy-2-ethoxycarbony lamino)-2,4,4-trimethyl-hexane (UDMA). Heat-cured resins were tested for Young's modulus, flexural
M P Patel et al.
Biomaterials, 22(1), 81-86 (2000-11-21)
The room temperature polymerising system poly(ethyl methacrylate) (PEM)/tetrahydrofurfuryl methcrylate (THFM) has been modified by replacing some of the THFM by hydroxyethyl methacrylate (HEMA) and hydroxypropyl methacrylate (HPM), respectively. In both cases, the equilibrium uptake of the parent system is reduced
Phuong Y Ghi et al.
Biomacromolecules, 3(3), 554-559 (2002-05-15)
The self-diffusion coefficients for water in a series of copolymers of 2-hydroxyethyl methacrylate, HEMA, and tetrahydrofurfuryl methacrylate, THFMA, swollen with water to their equilibrium states have been studied at 310 K using PFG-NMR. The self-diffusion coefficients calculated from the Stejskal-Tanner
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