1-Hexadecyl vinyl ether

Methyl acrylate Ethyl acrylate Butyl acrylate Dodecyl acrylate Methyl methacrylate Butyl methacrylate Octyl methacrylate Dodecyl methacrylate Acrylonitrile Vinyl acetate Vinyl stearate Vinyl pelargonate Methyl vinyl ether Ethyl vinyl ether Octyl vinyl ether Dodecyl vinyl ether Vinyl chloride Vinyl bromide Vinyl iodide Methyl acrylate Butyl acrylate Octyl acrylate Dodecyl acrylate Octadodecyl acrylate Maleic anhydride Tetrachloroethylene Methyl methacrylate Butyl methacrylate Octyl methacrylate Vinyl chloride Vinyl chloride Ethyl vinyl ether Butyl vinyl ether Heptyl vinyl ether Hexadecyl vinyl ether Methyl methacrylate Butyl methacrylate Heptyl methacrylate Hexadecyl methacrylate Maleic anhydride Vinyl acetate Methyl acrylate Methyl methacrylate Diethyl maleate... [Pg.302]

The 1-1 copolymer of maleic anhydride and methylvinyl ether were commercial products and were used without fractionnation. The copolymers of maleic anhydride and decyl (or) hexadecyl vinyl ether were obtained by radical polymerization. For hydrolysis of the polymers with a long alkyl side chain, heat treatment was necessary (60 C for several days in pure water). This resulted however in a reduction of average DP and probably in an enlargement of the initial distribution. Therefore, after hydrolysis, the polymer sample was fractionated with 2 1 acetonerbenzene as solvent and methanol as precipitant. [Pg.226]

Poly(hexadecyl vinyl ether-alt-maleic acid), solution studies, 440... [Pg.860]

Partial specific volume of poly(hexadecyl vinyl ether)... [Pg.477]

Vinyl Ethers. The principal commercial vinyl ethers are methyl vinyl ether (methoxyethene, C H O) [107-25-5], ethyl vinyl ether (ethoxyethene, C HgO) [104-92-2], and butyl vinyl ether (1-ethenyloxybutane, C H 20) [111-34-2]. (See Table 8 for physical properties.) Others such as the isopropyl, isobutyl, hydroxybutyl, decyl, hexadecyl, and octadecyl ethers, as well as the divinyl ethers of butanediol and of triethylene glycol, have been offered as development chemicals (see Ethers). [Pg.114]

This method has been used to produce telechelics from ethyl vinyl ether (EVE), methyl vinyl ether (MVE), and hexadecyl (cetyl) vinyl ether (CVE) (201, 202). [Pg.8211]

Because initiation of vinyl ethers with HI/I2 yields polymers with extremely narrow poly-dispersities," " bifunctional vinyl ethers can be used in combination with HI/I2 to polymerize vinyl ethers and produce a,co-diiodo telechelics (Scheme 39). This method has been used to produce telechelics from ethyl vinyl ether, methyl vinyl ether and hexadecyl (cetyl) vinyl ether. Treatment of the living poly(ethyl vinyl ether) with mono- and di-amines yields telechelics with amino end groups (Scheme 39, equation 41). More jecently, telechelic poly(vinyl ether)s with terminal malonate or carboxy groups were synthesized using both a functional initiator and a functional terminator according to Scheme 40." ... [Pg.1099]