From Surf Wiki (app.surf) — the open knowledge base
Octane
Hydrocarbon compound with the formula C8H18
Hydrocarbon compound with the formula C8H18
- 0.509 mPa·s (25 °C)
- 0.542 mPa·s (20 °C)}} | NFPA-H = 1 | NFPA-F = 3 | NFPA-R = 0
Octane is a hydrocarbon and also an alkane with the chemical formula C8H18, and the condensed structural formula CH3(CH2)6CH3. Octane has many structural isomers that differ by the location of branching in the carbon chain. One of these isomers, 2,2,4-trimethylpentane (commonly called iso-octane), is used as one of the standard values in the octane rating scale.
Octane is a component of gasoline and petroleum. Under standard temperature and pressure, octane is an odorless, colorless liquid. Like other short-chained alkanes with a low molecular weight, it is volatile, flammable, and toxic. Octane is 1.2 to 2 times more toxic than heptane.
Isomers
N-octane has 23 constitutional isomers. 8 of these isomers have one stereocenter; 3 of them have two stereocenters.
Achiral isomers:
- 2-Methylheptane
- 4-Methylheptane
- 3-Ethylhexane
- 2,2-Dimethylhexane
- 2,5-Dimethylhexane
- (meso)-3,4-Dimethylhexane
- 3,3-Dimethylhexane
- 3-Ethyl-2-methylpentane
- 3-Ethyl-3-methylpentane
- 2,2,4-Trimethylpentane (i.e. iso-octane)
- 2,3,3-Trimethylpentane
- 2,3,4-Trimethylpentane
- 2,2,3,3-Tetramethylbutane
Chiral isomers:
Production and use
In petrochemistry, octanes are not typically differentiated or purified as specific compounds. Octanes are components of particular boiling fractions.
A common route to such fractions is the alkylation reaction between iso-butane and 1-butene, which forms iso-octane.
Octane is commonly used as a solvent in paints and adhesives.
| [[File:N-octane.jpg | none | thumb | 338x338px | N-octane is the octane isomer that has the longest carbon skeleton. Unlike its constitutional isomers, it has a very low knock resistance.]] | [[File:Iso-octane.jpg | none | thumb | 271x271px | The octane isomer, iso-octane, is used as one of the standards for octane ratings. It has a rating of 100 by definition.]] | [[File:2,3,3-Trimethylpentane_(view_2).jpg | none | thumb | 224x224px | The octane isomer 2,3,3-Trimethylpentane has an octane rating exceeding 100.]] |
|---|
References
References
- (16 September 2004). "octane - Compound Summary". National Center for Biotechnology Information.
- https://srdata.nist.gov/solubility/sol_detail.aspx?sysID=38_103
- (1994). "Viscosity of Selected Liquid ''n''-Alkanes". Journal of Physical and Chemical Reference Data.
- {{PGCH. 0470
- {{IDLH. 111659. Octane
- (2020-02-27). "1988 OSHA PEL Project - Octane {{!}} NIOSH {{!}} CDC".
- "Fractionation".
- Ross, Julian. (January 1986). "Ullmann's Encyclopedia of industrial chemistry". Applied Catalysis.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Octane — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report