16083-20-8

Usage

Uses

Used in Organic Synthesis:
N,N,N-Tributyl-1-butanaminium·propenoic acidanion is used as a phase transfer catalyst in organic synthesis reactions. It facilitates the transfer of reactants between two immiscible phases, enhancing the efficiency and selectivity of the reactions.
Used in Metal Ion Extraction:
In the field of metal ion extraction, N,N,N-Tributyl-1-butanaminium·propenoic acidanion plays a crucial role in the selective extraction of metal ions. Its unique structure allows it to selectively bind and separate specific metal ions from complex mixtures, making it a valuable tool in various industries.
Used in Material Surface Modification:
N,N,N-Tributyl-1-butanaminium·propenoic acidanion is also employed in the modification of surface properties of materials. Its reactive nature enables it to alter the surface characteristics of various materials, improving their performance in different applications.

InChI:InChI=1/C16H36N.C3H4O2/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-2-3(4)5/h5-16H2,1-4H3;2H,1H2,(H,4,5)/q+1;/p-1

Upstream product

• 2052-49-5 tetra(n-butyl)ammonium hydroxide 
• 79-10-7 acrylic acid 

Relevant academic research and scientific papers

Isobutylene-rich macromonomers: Dynamics and yields of peroxide-initiated crosslinking

New isobutylene-rich elastomers bearing multiple pendant styrenic, acrylic, maleimidic, vinylic, and allylic functional groups have been prepared and examined in the context of peroxide-initiated crosslinking. Halide displacement from brominated poly(isobutylene-co-isoprene) (BIIR) by the requisite carboxylate nucleophiles in homogeneous toluene solutions provide the desired esters in quantitative yield without complications from dehydrohalogenation or premature crosslinking. Heating the resulting macromonomers with dicumyl peroxide to 160 °C under solvent-free conditions gives thermoset derivatives, with reaction rates and yields depending markedly on functional group structure. In general, high cure extents can only be achieved using highly reactive pendant functional groups, owing to the competitive balance between crosslinking through C=C oligomerization, and degradation through β-scission of backbone macroradical intermediates. Independent control of crosslinking rates and cure extents is gained through the use of nitroxyl radical traps bearing acrylate functionality.

Conductive polymers and method of preparation thereof

The present invention relates to a compound that can be reacted with a polymer resin to form the conductive polymer. More particularly, the present invention relates to a tetraalkylammonium acrylate that can be reacted with a conventional acrylic resin to