409456
Tetrahydrofurfuryl methacrylate
contains 75 ppm HQ as inhibitor, 900 ppm MEHQ as inhibitor, 97%
Synonym(s):
(Tetrahydrofuran-2-yl)methyl methacrylate
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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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J J A Barry et al.
Biomaterials, 25(17), 3559-3568 (2004-03-17)
This paper describes a method of foaming a polymer system comprising poly(ethyl methacrylate)/tetrahydrofurfuryl methacrylate (PEMA/THFMA), characterisation of the resulting porosity and use of the foam for chondrocyte culture. The potential for this polymer system to support cartilage repair has been
M P Patel et al.
Biomaterials, 19(21), 1911-1917 (1998-12-24)
The release of fluoride ions from two room-temperature polymerising systems containing sodium and potassium fluoride, respectively, has been studied. The polymer systems comprised poly(ethyl methacrylate) powder (PEM), with tetrahydrofurfuryl methacrylate (THFM), and n-butyl methacrylate (nBM), respectively. The water uptake of
M P Patel et al.
Biomaterials, 22(17), 2319-2324 (2001-08-21)
Oral candidal infections are often persistent and intractable and thus the aim of this study was to develop a polymeric sustained release device to improve the topical treatment of these infections. A self curing system based on poly(ethyl methacrylate) and
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.
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
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