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Merck
모든 사진(1)

문서

409456

Sigma-Aldrich

Tetrahydrofurfuryl methacrylate

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

동의어(들):

(Tetrahydrofuran-2-yl)methyl methacrylate

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C9H14O3
CAS Number:
2455-24-5
Molecular Weight:
170.21
EC Number:
219-529-5
MDL number:
MFCD00014515
UNSPSC 코드:
12162002
PubChem Substance ID:
24865647
NACRES:
NA.23

분석

97%

형태

liquid

포함

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

관련 카테고리

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point (°F)

195.8 °F - closed cup

Flash Point (°C)

91 °C - closed cup

개인 보호 장비

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

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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Tetrahydrofurfuryl alcohol 99%

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.
Biomaterials, 15(15), 1197-1200 (1994-12-01)
Newly designed composite resins for dental applications have been studied. The matrix phases were based on 2,2 bis-4(2-hydroxy-3-methacryloyloxypropoxy)phenyl propane and a urethane dimethacrylate. Tetrahydrofurfuryl methacrylate was added as a diluent to both dimethacrylates in a proportion of 30 wt%. Heat-cured
P Y Ghi et al.
Biomacromolecules, 2(2), 504-510 (2001-12-26)
The diffusion of water into a series of hydroxyethyl methacrylate, HEMA, copolymers with tetrahydrofurfuryl methacrylate, THFMA, has been studied over a range of copolymer compositions using NMR imaging analyses. For polyHEMA the diffusion was found to be consistent with a
G A Hutcheon et al.
Biomaterials, 22(7), 667-676 (2001-03-15)
The surface and bulk properties of novel methacrylate polymers prepared by gelling poly(ethyl methacrylate) (PEMA) powder with different ratios of tetrahydrofurfuryl methacrylate (THFMA) and hydroxyethyl methacrylate (HEMA) monomers were investigated. The water adsorption and desorption characteristics of these polymers were
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
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