Cyclohexane
Title: Cyclohexane
CAS Registry Number: 110-82-7
Additional Names: Hexahydrobenzene; hexamethylene; hexanaphthene
Molecular Formula: C6H12
Molecular Weight: 84.16
Percent Composition: C 85.63%, H 14.37%
Literature References: Occurs in petr (0.5-1.0%). Obtained in the distillation of petr or by hydrogenation of benzene. In the distillation of petr the C4-400°F boiling range naphthas are fractionated to obtain a C5-200°F naphtha contg 10-14% cyclohexane which on superfractionation yields an 85% concentrate (which is sold as such); further purification necessitates isomerization of pentanes to cyclohexane, heat cracking for removing open chain hydrocarbons and sulfuric acid treatment to remove aromatic compds. The hydrogenation of benzene is done in the liq phase at 150° using Raney nickel catalyst and at least 10 atm H2 pressure: Sabatier, Ind. Eng. Chem. 18, 1005 (1926). Review and bibliography: Sachanen, Chemical Constituents of Petroleum (New York, 1945). Prepn of high purity cyclohexane: Seyer et al., Ind. Eng. Chem. 31, 759 (1939). Cyclohexane can exist in two interconvertible conformations, the boat and the chair. In the chair form its 12 extracyclic bonds fall into two classes: six lie parallel to the main axis of symmetry and are designated "axial", while six extend radially outward at ±109.5° angles to the axis and are designated as "equatorial", Barton et al., Nature 172, 1096 (1954); Science 119, 49 (1954). Solubility: F. P. Schwarz, Anal. Chem. 52, 10 (1980). Toxicity: Lazarew, Arch. Exp. Pathol. Pharmakol. 143, 223 (1929). Physical properties and methods of purification: L. Scheflan, M. B. Jacobs, The Handbook of Organic Solvents (Van Nostrand, 1953) p 233; Techniques of Chemistry vol. II, entitled "Organic Solvents", J. D. Riddick, W. B. Bunger, Eds. (Wiley-Interscience, New York, 3rd ed., 1970) p 592. Review: M. L. Campbell in Kirk-Othmer Encyclopedia of Chemical Technology vol. 12 (Wiley-Interscience, New York, 3rd ed., 1980) pp 931-937.
Properties: Flammable liq. Solvent odor. Pungent when impure. d420 0.7781; d480 0.7206. mp 6.47°. bp760 80.7°; bp400 60.8°; bp200 42.0°; bp100 25.5°; bp60 14.7°; bp40 6.7°. nD20 1.4264. Flash pt, closed cup: 1°F (-18°C). Flammability limits in air 1.3-8.4% v/v. Soly in water at 23.5°C (w/w): 0.0052%. 100 ml of methanol dissolves 57 grams at 20°C; miscible with ethanol, ethyl ether, acetone, benzene, carbon tetrachloride. LC in mice: ~60-70 mg/l air (Lazarew).
Melting point: mp 6.47°
Boiling point: bp760 80.7°; bp400 60.8°; bp200 42.0°; bp100 25.5°; bp60 14.7°; bp40 6.7°
Flash point: Flash pt, closed cup: 1°F (-18°C)
Index of refraction: nD20 1.4264
Density: d420 0.7781; d480 0.7206
Toxicity data: LC in mice: ~60-70 mg/l air (Lazarew)
CAUTION: Potential symptoms of overexposure are irritation of eyes, skin and respiratory system; drowsiness; dermatitis; narcosis, coma. See NIOSH Pocket Guide to Chemical Hazards (DHHS/NIOSH 97-140, 1997) p 82.
Use: Solvent for lacquers and resins. Paint and varnish remover. In the extraction of essential oils. In analytical chemistry for mol wt determinations (cryoscopic constant 20.3). In the manuf of adipic acid, benzene, cyclohexyl chloride, nitrocyclohexane, cyclohexanol and cyclohexanone. In the manuf of solid fuel for camp stoves. In fungicidal formulations (possesses slight fungicidal action). In the industrial recrystn of steroids.

Others monographs:
AmpicillinCaffeineEfonidipineDextran Sulfate Sodium
UrapidilIron PentacarbonylThrombinPlasmin
NicotineNeamineCarbon SuboxideCalcium Dichromate(VI)
SaporinsMercuryPituitary, PosteriorDicamba
©2016 DrugLead US FDA&EMEA