Home Page   
Home PageE
Today is
Java Applets
BIOLOGY
CHEMISTRY
HIGH SCHOOL CHEMISTRY
BIOCHEMISTRY
MATHEMATICS
JUST MOLECULES
PHYSICS

 

 

 

 

interactive Library

 

The Hexane Molecule

For the 3D Jmol image

Click here

Hexane is an alkane hydrocarbon with the chemical formula CH3(CH2)4CH3. The "hex" prefix refers to its six carbons, while the "ane" ending indicates that its carbons are connected by single bonds. Hexane isomers are largely unreactive, and are frequently used as an inert solvent in organic reactions because they are very non-polar. They are also common constituents of gasoline and glues used for shoes, leather products and roofing. Additionally, it is used in solvents to extract oils for cooking and as a cleansing agent for shoe, furniture and textile manufacturing.

Production

Hexane is produced by the refining of crude oil. The exact composition of the fraction depends largely on the source of the oil (crude or reformed) and the constraints of the refining. The industrial product (usually around 50% by weight of the straight-chain isomer) is the fraction boiling at 65-70 °C.

Toxicity

The acute toxicity of hexane is relatively low, although it is a mild anesthetic. Inhalation of high concentrations produces first a state of mild euphoria, followed by somnolence with headaches and nausea.

Chronic intoxication from hexane has been observed in recreational solvent abusers and in workers in the shoe manufacturing, furniture restoration and automobile construction industries. The initial symptoms are tingling and cramps in the arms and legs, followed by general muscular weakness. In severe cases, atrophy of the skeletal muscles is observed, along with a loss of coordination and problems of vision.

Similar symptoms are observed in animal models. They are associated with a degeneration of the peripheral nervous system (and eventually the central nervous system), starting with the distal portions of the longer and wider nerve axons. The toxicity is not due to hexane itself but to one of its metabolites, hexane-2,5-dione. It is believed that this reacts with the amino group of the side chain of lysine residues in proteins, causing cross-linking and a loss of protein function.

The effects of hexane poisoning in humans are uncertain. In 1994, n-hexane was included in the list of chemicals on the Toxic Release Inventory (TRI).[2] In the latter part of the 20th and early part of the 21st centuries, a number of explosions have been attributed to the combustion of hexane gas. In 2001, the U.S. Environmental Protection Agency issued regulations on the control of emissions of hexane gas due to its potential carcinogenic properties and environmental concerns.[3]

References

  1. C5 and C6 alkanes. A and B Scott Organic Chemistry. Retrieved on 2007-10-30.
  2. N-Hexane Chemical Backgrounder. National Safety Council. Retrieved on 25 May 2007.
  3. Anuradee Witthayapanyanon and Linh Do. Nanostructured Microemulsions as Alternative Solvents to VOCs in Cleaning Technologies and Vegetable Oil Extraction. National Center For Environmental Research. Retrieved on 25 May 2007.
  • Institut national de recherche (2005). "Hexane". Fiche toxicologique 113, 8pp. (in French)

External links

 

______

 

Some or all of this text has been obtained from Wikipedia, the free encyclopedia. All text is available under the terms of the GNU Free Documentation License (see Copyrights for details). Disclaimers. Wikipedia is powered by MediaWiki, an open source wiki engine.

3d Molecules
COMPLETE DATABASE OF 3D MOLECULES
WATER
ICE
METHANE
CARBON MONOXIDE
DIAMOND
FULLERENE
SALT
SOAP
DNA
---more 3D molecules

 

 


Questions or Comments?
Copyright © 1999 EdInformatics.com
All Rights Reserved.