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Octadecyl alcohol

Hexadecyl and octadecyl alcohol have been extensively studied and shown to be highly effective in evaporation retardation. Scattering powdered samples of commercial-grade alcohols by boat on lake surfaces or the continuous addition of alcohol slurries from floating dispensers are two of the methods that have been employed to apply these monolayers. Wind conditions and the activity of aquatic birds have a considerable effect on the stability of the monolayer and therefore on the rate at which the monolayer chemicals must be reapplied. Rates of application rarely exceed 0.5 lb acre- day-1, however, so that the cost of the materials used is not excessive. [Pg.321]

R-Octadecyl alcohol [112-92-5] M 270.5, m 61°, b 153-154°/0.3mm. Crystd from MeOH, or dry ethyl ether and benzene, then fractionally distd under reduced pressure. Purified by column chromatography. Freed from cetyl alcohol by zone melting. [Pg.290]

DYTOL E-46 LOROL 28 OCTADECANOL n-OCTADECANOL OCTA DECYL ALCOHOL n-OCTADECYL ALCOHOL POLAAX SIPOLS SIPONOL S STEAROL STEARYL ALCOHOL STERAFFINE USP XIII STEARYL ALCOHOL... [Pg.1042]

A mixture of 7.8 g. (0.062 gram atom) of iodine and 1 g. of red phosphorus is put in a flask equipped with an air condenser on which is placed a calcium chloride tube to protect the system from atmospheric moisture. The flask is heated in an oil or metal bath to a temperature of 100°, and 15.6 g. (0.058 mole) of n-octadecyl alcohol is added. The bath temperature is then raised to 180° and held there for 1 hour. The cooled reaction mixture is extracted with petroleum ether (b.p. 70-80°), and the resulting solution is boiled with fuller s earth and filtered. The solvent is evaporated from the filtrate, giving 21.5 g. (97.5%) of n-octadecyl iodide melting at 34.5-35°. [Pg.247]

Fig. 19. Dependence of ethyl acryiate polyntetizntion rate lt moVdin Bee) on concentration (mol/dm of(l) SDDS (2)su1fated polyoxyethylated llt octadecyl alcohol and (3) oxyeihylated (30) cetyl alcohol. Fig. 19. Dependence of ethyl acryiate polyntetizntion rate lt moVdin Bee) on concentration (mol/dm of(l) SDDS (2)su1fated polyoxyethylated llt octadecyl alcohol and (3) oxyeihylated (30) cetyl alcohol.
Cachalot Crodacol S9S Hyfatol 18-95 Hyfatal 18-98 Lanette 18 Lipocol S Lipocol S-DEO -octadecanol octadecyl alcohol Rita SA Stearol Stenol Tego Alkanol 18. [Pg.740]

Nhrobutanol (2-) Nitrogen Tetraoxlde Nitfo methane Octadecyl Alcohol Ozone Pentachlorobenzamlde Up lo the bailing point up 10 boiling pi. up to Ihe boiling point u a a 8 8 8 DuPont TofJon FEP 44 tf a... [Pg.180]

NItrobutanol (2-) Nitrogen Tetraoxide Nltrom ethane Octadecyl Alcohol Ozone... [Pg.188]

Nitrogen Tetraoxlde NItromettiane Octadecyl Alcohol Ozone... [Pg.203]

The solubility datum at 362.8 K and 330 bar was corrected as it is one order of magnitude smaller in th source than the actual value in the Friedrich s thesis. Synonyms n-Octadecyl alcohol 1-Stearyl alcohol Source Friedrich, J. Schneider, G. M. J. Chem. Thermodyn. (1989), 21(3), 307-319. [Pg.576]

Synonyms n-Octadecyl alcohol 1-Stearyl alcohol Source Kramer, A. Thodos, G. J. Chem. [Pg.576]

Synonyms 1-Octadecanol n-Octadecyl alcohol Source Iwai, Y. Koga, Y. Maruyama, H. Aral, Y. J. Chem. Eng. Data (1993), 38(4), 506-508. [Pg.725]


See other pages where Octadecyl alcohol is mentioned: [Pg.103]    [Pg.441]    [Pg.316]    [Pg.57]    [Pg.259]    [Pg.170]    [Pg.737]    [Pg.141]    [Pg.290]    [Pg.290]    [Pg.326]    [Pg.45]    [Pg.290]    [Pg.21]    [Pg.137]    [Pg.144]    [Pg.188]    [Pg.210]    [Pg.101]    [Pg.23]    [Pg.1815]    [Pg.600]    [Pg.283]    [Pg.85]    [Pg.406]    [Pg.444]    [Pg.316]    [Pg.84]    [Pg.1078]    [Pg.917]    [Pg.1177]    [Pg.577]   
See also in sourсe #XX -- [ Pg.188 ]

See also in sourсe #XX -- [ Pg.740 ]




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Octadecyl

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