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409456

Sigma-Aldrich

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:
2455-24-5
Molecular Weight:
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

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCV3585
MKCS4181
MKCN1563
MKCL2429
MKCH3084

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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.
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
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
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
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
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