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409456

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

Qualitätsniveau

100

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)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCV3585
MKCS4181
MKCN1563
MKCL2429
MKCH3084

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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

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
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 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
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