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Key Documents

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411760

Sigma-Aldrich

Furfuryl methacrylate

97%, contains 200 ppm monomethyl ether hydroquinone as inhibitor

Sinónimos:

Methacrylic Acid Furfuryl Ester

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About This Item

Fórmula empírica (notación de Hill):
C9H10O3
Número de CAS:
3454-28-2
Peso molecular:
166.17
EC Number:
222-383-5
MDL number:
MFCD00046113
UNSPSC Code:
12162002
PubChem Substance ID:
24865763
NACRES:
NA.23

assay

97%

form

liquid

contains

200 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.482 (lit.)

bp

80-82 °C/5 mmHg (lit.)

density

1.078 g/mL at 25 °C (lit.)

SMILES string

CC(=C)C(=O)OCc1ccco1

InChI

1S/C9H10O3/c1-7(2)9(10)12-6-8-4-3-5-11-8/h3-5H,1,6H2,2H3

InChI key

DWXAVNJYFLGAEF-UHFFFAOYSA-N

Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

195.8 °F - closed cup

flash_point_c

91 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

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2,2′-(Dithiodimethylene)difuran ≥95%, FG

Sigma-Aldrich

W314609

2,2′-(Dithiodimethylene)difuran

Isobornyl methacrylate technical grade

Sigma-Aldrich

392111

Isobornyl methacrylate

Sunanda Sain et al.
Polymers, 12(11) (2020-10-30)
The fabrication of smart biocomposites from sustainable resources that could replace today's petroleum-derived polymer materials is a growing field of research. Here, we report preparation of novel biocomposites using nanocellulose networks extracted from food residue (onion skin) and a vegetable
D Zaldívar et al.
Biomaterials, 14(14), 1073-1079 (1993-11-01)
Biocompatible copolymers of N-vinylpyrrolidone (P) and furfuryl methacrylate (F) were prepared by free radical polymerization in N,N-dimethylformamide solution at 50 degrees C, using 2,2'-azobisisobutyronitrile as initiator, at low and high conversion. The microstructure of copolymers prepared at low conversion was
Sunanda Sain et al.
Polymers, 12(2) (2020-01-26)
This work focuses on the development of cross-linked polymer from a highly unsaturated vegetable oil, tung oil (TO) and a bio-based acrylate, furfuryl methacrylate (FMA). The presence of a high degree of unsaturated carbon-carbon bonding in TO makes it a
A Amalin Kavitha et al.
ACS applied materials & interfaces, 1(7), 1427-1436 (2010-04-02)
This investigation reports the effective use of the Diels-Alder (DA) reaction, a "click reaction" in the preparation of thermally amendable and self-healing polymeric materials having reactive furfuryl functionality. In this case, the DA and retro-DA (rDA) reactions were carried out
Chuanwei Lu et al.
Carbohydrate polymers, 242, 116404-116404 (2020-06-23)
Well-defined sustainable and recyclable thermoset elastomers derived from cellulose, fatty acid and furfural were successfully prepared via photoinduced metal-free ATRP and Diels-Alder (DA) reaction. Firstly, metal free ATRP was applied to prepare a range of thermoplastic cellulose graft copolymers with
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