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Sigma-Aldrich

Tetrahydrofurfurylmethacrylat

contains 75 ppm HQ as inhibitor, 900 ppm MEHQ as inhibitor, 97%

Synonym(e):

(Tetrahydrofuran-2-yl)methyl methacrylate

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About This Item

Empirische Formel (Hill-System):
C9H14O3
CAS-Nummer:
2455-24-5
Molekulargewicht:
170.21
EG-Nummer:
219-529-5
MDL-Nummer:
MFCD00014515
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24865647
NACRES:
NA.23

Assay

97%

Form

liquid

Enthält

75 ppm HQ as inhibitor
900 ppm MEHQ as inhibitor

Brechungsindex

n20/D 1.458 (lit.)

bp

52 °C/0.4 mmHg (lit.)

Dichte

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

InChIKey

LCXXNKZQVOXMEH-UHFFFAOYSA-N

Verwandte Kategorien

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

195.8 °F - closed cup

Flammpunkt (°C)

91 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Analysenzertifikate (COA)

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Tetrahydrofurfurylalkohol 99%

Sigma-Aldrich

185396

Tetrahydrofurfurylalkohol

1,4-Butandioldimethacrylat 95%, contains 200-300 ppm MEHQ as inhibitor

Sigma-Aldrich

234958

1,4-Butandioldimethacrylat

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.
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
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
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