n-octane

n-octane

[¦en ′äk‚tān]
(organic chemistry)
C8H18 Colorless liquid boiling at 126°C; soluble in alcohol, acetone, and ether, insoluble in water; used as a solvent and chemical intermediate.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
References in periodicals archive ?
The probes used were n-pentane, n-hexane, n-heptane, and n-octane, all reagents were obtained in the higher purity grade possibly and directly used as received without further purification.
The other reagents, Sn[(Oct).sub.2], tetrabutyl titanate (TBT), dimethyl sulfoxide-[d.sub.6] (DMSO-[d.sub.6]), monobutyltin oxide (MBTO), n-octane, methylbenzene, and diethylene glycol, purchasing from Aladdin Reagent Co., Ltd., were used without further purification.
[41] developed a detailed chemical kinetic model to describe the pyrolysis and oxidation of nine n-alkanes, from n-octane to n-hexadecane.
As can be seen from the analytical results, the concentration of M-hexane, M-heptane, n-octane, and n-nonane increased dramatically.
Solutes A [([[gamma].sup.d]).sup.0.5] a AN* DN (kJ [cm.sup.2] [(mJ/ ([nm.sup.2]) (kJ/ /mol) [cm.sup.2]).sup.0.5] mol) n-Pentane 1.84E-16 0.461 -- -- n-Hexane 2.21E-16 0.515 -- -- n-Heptane 2.57E-16 0.570 -- -- n-Octane 2.91E-16 0.630 -- -- AC 1.73E-16 0.425 10.5 71.4 DE 1.82E-16 0.470 6.30 80.60 DCM 1.65E-16 0.315 16.4 0 TCM 2.24E-16 0.440 22.7 0 THF 2.13E-16 0.450 2.1 84.4 [DELTA][G.sub.a]/T = [DELTA][H.sub.a]/T - [DELTA][S.sub.a].
On the second analytical path the heavier components are grouped into hexanes, heptanes and octanes, with the components larger than n-octane back-flushed to provide a C9+ grouped component value.
To the best of our knowledge, the properties of the binary mixtures of n-octane, n-decane, n-dodecane, and n-tetradecane with octan-2-ol have not been reported earlier.
Yi and Cai [8] used perfluoroalkylated pyridine as a catalyst; benzaldehyde was slowly added into a mixture of malononitrile, n-octane and the catalyst and was stirred for 1.5 hours at 80[degrees]C.
The measurement results of water contact angles and the solvent absorptions in water and n-octane for cured films showed that the water and the oil repellency for FSiPUA had been improved significantly with a suitable content of fluorine and siloxane.
The chromatographic grade molecular probes used in this study, including ethyl alcohol (C2), 1-propyl alcohol (C3), 1-butyl alcohol (C4), n-hexane (C6), n-heptane (C7), and n-octane (C8), were obtained from Merck Chemical Co.