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Heptane or n-heptane is the straight-chain alkane with the chemical formula H 3 C(CH 2) 5 CH 3 or C 7 H 16. When used as a test fuel component in anti-knock test engines, a 100% heptane fuel is the zero point of the octane rating scale (the 100 point is 100% iso-octane ).
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(Benzine is a mixture of alkanes, such as pentane, hexane, and heptane; whereas benzene is a cyclic, aromatic hydrocarbon.) A hydrocarbon is any chemical compound that consists only of the elements carbon (C) and hydrogen (H). They all contain a carbon frame, and have hydrogen atoms attached to the frame.
Cycloheptane, synonym suberane, is a cycloalkane [citation needed] with the molecular formula C 7 H 14. [1] It is a poorly water soluble organic liquid (melting point –12 deg C, solubility in water <30 mg /liter at 25 deg C), [1] and is used as a nonpolar solvent for the chemical industry and as an intermediate in the manufacture of chemicals and pharmaceutical drugs.
Norcarane, or bicyclo[4.1.0]heptane, is a colorless liquid. It is an organic compound prepared using the Simmons–Smith reaction , by the action of diiodomethane and a zinc-copper couple on cyclohexene in diethyl ether .
Carl Schaschke, 2014, A Dictionary of Chemical Engineering, Oxford University Press. G. I. Nikishin, Yu. N. Ogibin & L. Kh. Rakhmatullina, 1975, ‘Peroxydisulfate-initiated reactions of 1-heptene with acetic and propionic acids’, Bulletin of the Academy of Sciences of the USSR, Division of chemical science, volume 23, pages1479–1483
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
The formation of heptanal in the fractional distillation of castor oil [3] was already described in 1878. The large-scale production is based on the pyrolytic cleavage of ricinoleic acid [4] (Arkema method) and on the hydroformylation of 1-hexene with rhodium 2-ethylhexanoate as a catalyst upon addition of some 2-ethylhexanoic acid (Oxea method): [2] [5]
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