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2-(Trifluoromethylsulfonamido)ethyl methacrylate

CAS No.:314756-98-4
Product Grade: Industrial Grade
Purity / Assay: ≥98.0%
Molecular Formula:C₇H₁₀F₃NO₄S
Molecular Weight:261.22 g/mol
Synonym(s):2-(trifluoromethylsulfonamido)ethyl methacrylate, TFMSAEMA, trifluoromethylsulfonylaminoethyl methacrylate

2-(Trifluoromethylsulfonamido)ethyl methacrylate, identified by CAS 314756-98-4, is a specialized fluorinated monomer that integrates a reactive methacrylate group with a trifluoromethylsulfonamide moiety. This unique chemical structure imparts distinctive properties to the resulting polymers, notably high thermal stability and chemical resistance. The presence of the trifluoromethyl group significantly lowers the surface energy of materials, while the sulfonamide group provides a site for potential hydrogen bonding or ionic interactions.

In industrial and research settings, this compound serves as a critical building block for synthesizing advanced functional polymers. It is typically handled as a liquid or solid depending on purity and temperature, requiring standard laboratory precautions for reactive monomers. Its dual functionality—combining the polymerizable vinyl group with a highly electronegative fluorinated sulfonamide—makes it a versatile tool for tailoring the physical and chemical characteristics of macromolecular systems in high-performance applications.

• Advanced Polymer Synthesis: This monomer is primarily utilized in the development of specialized fluoropolymers and copolymers. The trifluoromethylsulfonamide side chain introduces unique acidity and hydrophobic character to the polymer backbone, which is essential for creating materials with specific wetting properties or chemical sensitivity. Researchers leverage this monomer to produce coatings that exhibit both water and oil repellency.

• Proton-Conducting Membranes: Due to the acidic nature of the sulfonamide proton, CAS 314756-98-4 is frequently explored in the fabrication of proton-exchange membranes (PEMs) for fuel cell technology. It serves as a stable alternative to traditional sulfonic acid monomers, offering improved mechanical integrity and oxidative stability under the demanding electrochemical conditions found in energy conversion devices.

• Surface Modification and Lithography: The compound finds significant application in the electronics industry, particularly in photoresist formulations and lithographic processes. Its ability to modify surface energy and provide high-resolution patterning capabilities makes it valuable for manufacturing microelectronic components. Additionally, it is used to treat surfaces to enhance adhesion or create protective barriers against environmental degradation.

• Specialty Chemical Intermediates: Beyond direct polymerization, this substance acts as a versatile intermediate in the synthesis of complex organic molecules. It is employed in the development of smart materials that respond to pH changes or specific chemical stimuli, benefiting from the electron-withdrawing effect of the trifluoromethyl group which modulates the reactivity of the adjacent nitrogen atom.

25 kg/drum, 180 kg/drum, 25 kg/bag
CAS No.: 314756-98-4

Product Name: 2-(Trifluoromethylsulfonamido)ethyl methacrylate

Purity / Assay:≥98.0%
Molecular Formula:C₇H₁₀F₃NO₄S
Molecular Weight:261.22 g/mol
Synonym(s):2-(trifluoromethylsulfonamido)ethyl methacrylate, TFMSAEMA, trifluoromethylsulfonylaminoethyl methacrylate

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