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Merck

373761

Sigma-Aldrich

2,2,2-Trifluoroethyl methacrylate

contains 50-200 ppm MEHQ as inhibitor, 99%

Sinónimos:

2,2,2-Trifluoroethyl 2-methylprop-2-enoate

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About This Item

Fórmula lineal:
H2C=C(CH3)CO2CH2CF3
Número de CAS:
Peso molecular:
168.11
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de la sustancia en PubChem:
NACRES:
NA.23

Nivel de calidad

Ensayo

99%

Formulario

liquid

contiene

50-200 ppm MEHQ as inhibitor

índice de refracción

n20/D 1.361 (lit.)

bp

59 °C/100 mmHg (lit.)

densidad

1.181 g/mL at 25 °C (lit.)

temp. de almacenamiento

2-8°C

cadena SMILES

CC(=C)C(=O)OCC(F)(F)F

InChI

1S/C6H7F3O2/c1-4(2)5(10)11-3-6(7,8)9/h1,3H2,2H3

Clave InChI

QTKPMCIBUROOGY-UHFFFAOYSA-N

Descripción general

2,2,2-Trifluoroethyl methacrylate (TFEMA) is a semifluorinated monomer that can be synthesized from methacryloyl chloride and 2,2,2-trifluoroethanol in presence of triethylamine. Its properties include chemical inertness, good wear resistance and low dielectric constant.

Aplicación

TFEMA can be used in the preparation of poly(TFEMA), which can be used in the development of acrylic protective coatings.

Pictogramas

FlameSkull and crossbones

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Flam. Liq. 2

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

62.6 °F - closed cup

Punto de inflamabilidad (°C)

17 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Los clientes también vieron

Radical copolymerization of 2, 2, 2-trifluoroethyl methacrylate with cyano compounds for dielectric materials: Synthesis and characterization
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Journal of Fluorine Chemistry, 127(3), 391-399 (2006)
Antonios M Douvas et al.
Analytical and bioanalytical chemistry, 381(5), 1027-1032 (2005-02-03)
A new methodology for protein microarray fabrication is proposed based on the ablation of polymer film using laser at 157 nm (F2). The polymer has been selected among others with the criterion of negligible protein adsorption. Improved results have been
Photochemical stability of partially fluorinated acrylic protective coatings I. Poly (2, 2, 2-trifluoroethyl methacrylate) and poly (1H, 1H, 2H, 2H-perfluorodecyl methacrylate-co-2-ethylhexyl methacrylate) s
Chiantore O, et al.
Polymer Degradation and Stability, 67(3), 461-467 (2000)
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Electrophoresis, 30(4), 589-598 (2009-01-22)
A new, fluorinated monolithic stationary phase for CEC was first synthesized by a single-stage, thermally initiated copolymerization of a fluorinated monomer, 2,2,2-trifluoroethyl methacrylate (TFEM) and ethylene dimethacrylate (EDMA) in the presence of a porogen mixture. In this preparation, 2-acrylamido-2-methyl-1-propanesulfonic acid
Grafting modification of ramie fibers with poly (2, 2, 2-trifluoroethyl methacrylate) via reversible addition-fragmentation chain transfer (RAFT) polymerization in supercritical carbon dioxide
Liu X, et al.
Reactive and Functional Polymers, 70(12), 972-979 (2010)

Artículos

Polymeric materials, with unique refractive index properties, find applications in photonics and optical coatings for various devices.

Polymeric materials, with unique refractive index properties, find applications in photonics and optical coatings for various devices.

Polymeric materials, with unique refractive index properties, find applications in photonics and optical coatings for various devices.

Polymeric materials, with unique refractive index properties, find applications in photonics and optical coatings for various devices.

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