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
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Quality Level
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.)
SMILES string
CC(=C)C(=O)OCC1CCCO1
InChI
1S/C9H14O3/c1-7(2)9(10)12-6-8-4-3-5-11-8/h8H,1,3-6H2,2H3
InChI key
LCXXNKZQVOXMEH-UHFFFAOYSA-N
Related Categories
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
195.8 °F - closed cup
Flash Point(C)
91 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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, 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
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
R Labella et al.
Biomaterials, 15(15), 1197-1200 (1994-12-01)
Newly designed composite resins for dental applications have been studied. The matrix phases were based on 2,2 bis-4(2-hydroxy-3-methacryloyloxypropoxy)phenyl propane and a urethane dimethacrylate. Tetrahydrofurfuryl methacrylate was added as a diluent to both dimethacrylates in a proportion of 30 wt%. Heat-cured
S N Nazhat et al.
Biomaterials, 22(17), 2411-2416 (2001-08-21)
Novel elastomer/methacrylate systems have been developed for potential soft prosthetic applications. Mixtures of varying compositions of an isoprene-styrene copolymer elastomer and tetrahydrofurfuryl methacrylate (SIS/THFMA) formed one-gel systems and were heat cured with a peroxide initiator. The blends were characterised in
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