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411760

Sigma-Aldrich

Furfuryl methacrylate

97%, contains 200 ppm monomethyl ether hydroquinone as inhibitor

Sinônimo(s):

Methacrylic Acid Furfuryl Ester

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About This Item

Fórmula empírica (Notação de Hill):
C9H10O3
Número CAS:
3454-28-2
Peso molecular:
166.17
Número CE:
222-383-5
Número MDL:
MFCD00046113
Código UNSPSC:
12162002
ID de substância PubChem:
24865763
NACRES:
NA.23

Ensaio

97%

forma

liquid

contém

200 ppm monomethyl ether hydroquinone as inhibitor

índice de refração

n20/D 1.482 (lit.)

pb

80-82 °C/5 mmHg (lit.)

densidade

1.078 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

DWXAVNJYFLGAEF-UHFFFAOYSA-N

Categorias relacionadas

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

195.8 °F - closed cup

Ponto de fulgor (°C)

91 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

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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
Sovan Lal Banerjee et al.
Soft matter, 13(47), 9024-9035 (2017-11-28)
Amphiphilic diblock copolymers of poly(furfuryl methacrylate) (PFMA) with cationic poly(2-(methacryloyloxy)ethyltrimethyl ammonium chloride) (PFMA-b-PMTAC) and anionic poly(sodium 4-vinylbenzenesulfonate) (PFMA-b-PSS) were prepared via reversible addition fragmentation chain-transfer (RAFT) polymerization by using PFMA as a macro-RAFT agent. The formation of the block copolymer

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