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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 ).
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]
The density and boiling are the lowest of the isomers of heptane. The dielectric constant is 1.915, the lowest of the heptane isomers. The critical temperature is 247.7 °C and critical pressure 28.4 atmospheres. The refractive index at 20° is 1.38233, the same as for 2,4-dimethylpentane, equal lowest for the heptane isomers.
Norbornane (also known as bicyclo[2.2.1]heptane) is an organic compound and a saturated hydrocarbon with chemical formula C 7 H 12. It is a crystalline compound with a melting point of 88 °C . The carbon skeleton is derived from cyclohexane ring with a methylene bridge in the 1,4- position, and is a bridged bicyclic compound.
Microemulsions also have industrial applications, one of them being the synthesis of polymers. Microemulsion polymerization is a complex heterogeneous process where transport of monomers, free radicals and other species (such as chain transfer agent, co-surfactant and inhibitors) between the aqueous and organic phases, takes place. [ 4 ]
Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; Appearance. ... Properties Chemical formula. C 7 H 14 O: Molar mass: 114.188 g ...
2-Heptanone, also known as methyl n-amyl ketone, or Heptan-2-one, is a ketone with the molecular formula C 7 H 14 O. It is a colorless, water-like liquid with a banana-like, fruity odor. 2-Heptanone has a neutral formal charge, and is only slightly soluble in water. [4]
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