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Merck

411760

Sigma-Aldrich

甲基丙烯酸糠酯

97%, contains 200 ppm monomethyl ether hydroquinone as inhibitor

别名:

Methacrylic Acid Furfuryl Ester

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About This Item

经验公式(希尔记法):
C9H10O3
CAS号:
分子量:
166.17
EC號碼:
MDL號碼:
分類程式碼代碼:
12162002
PubChem物質ID:
NACRES:
NA.23

品質等級

化驗

97%

形狀

liquid

包含

200 ppm monomethyl ether hydroquinone as inhibitor

折射率

n20/D 1.482 (lit.)

bp

80-82 °C/5 mmHg (lit.)

密度

1.078 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

DWXAVNJYFLGAEF-UHFFFAOYSA-N

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

195.8 °F - closed cup

閃點(°C)

91 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

Lot/Batch Number

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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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