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409456

Sigma-Aldrich

Tetrahydrofurfuryl methacrylate

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

Sinónimos:

(Tetrahydrofuran-2-yl)methyl methacrylate

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About This Item

Fórmula empírica (notación de Hill):
C9H14O3
Número de CAS:
2455-24-5
Peso molecular:
170.21
EC Number:
219-529-5
MDL number:
MFCD00014515
UNSPSC Code:
12162002
PubChem Substance ID:
24865647
NACRES:
NA.23

Quality Level

100

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

Categorías relacionadas

Storage Class

10 - Combustible liquids

wgk_germany

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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Certificados de análisis (COA)

Lot/Batch Number
MKCV3585
MKCS4181
MKCN1563
MKCL2429
MKCH3084

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Sigma-Aldrich

185396

Tetrahydrofurfuryl alcohol

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

Sigma-Aldrich

234958

1,4-Butanediol dimethacrylate

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
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
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
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