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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250 ML
€91.20
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
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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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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
R M Wyre et al.
Biomaterials, 21(4), 335-343 (2000-02-03)
A polymer system consisting of poly(ethyl methacrylate)/tetrahydrofurfuryl methacrylate (PEMA/THFMA) was investigated as a biomaterial for cartilage repair using chondrocyte culture. The PEMA/THFMA system and Thermanox control were shown to support chondrocytes seeded directly onto the surface for up to 28
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
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
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