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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
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
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
Phuong Y Ghi et al.
Biomacromolecules, 3(3), 554-559 (2002-05-15)
The self-diffusion coefficients for water in a series of copolymers of 2-hydroxyethyl methacrylate, HEMA, and tetrahydrofurfuryl methacrylate, THFMA, swollen with water to their equilibrium states have been studied at 310 K using PFG-NMR. The self-diffusion coefficients calculated from the Stejskal-Tanner
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