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Aliphatic compound

Hydrocarbon compounds without aromatic rings

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Aliphatic compounds (/ˌælɪˈfætɪk/; G. aleiphar, fat, oil) are chemical compounds containing the element carbon that are not aromatic compounds. Aliphatic compounds can be saturated, where all C-C bonds are single bonds (e.g., hexane), or unsaturated, where double or triple bonds are present between carbon atoms (e.g., hexene, hexyne).

01Other definitions

The definition given above is that promulgated by the International Union of Pure and Applied Chemistry (IUPAC), which sets accepted definitions for chemical terms and nomenclature. Other sources have previously applied additional restrictions, such as stating that only hydrocarbons (compounds made of only carbon and hydrogen) can be aliphatic or excluding cyclic compounds from being aliphatic. These criteria are not present in the current IUPAC definition.

02Structure

Aliphatic compounds can be saturated, i.e. alkanes (single carbon-carbon bonds), or unsaturated, with carbon-carbon double (alkenes) or triple bonds (alkynes). It may also be cyclic (as long as it is not aromatic).

Under definitions which require that aliphatic compounds are strictly hydrocarbons, the addition of other elements beyond carbon and hydrogen (heteroatoms) makes the compound no longer aliphatic. Nevertheless, such compounds are sometimes still referred to as aliphatic if the hydrocarbon portion of the molecule is aliphatic, e.g. aliphatic amines, to differentiate them from aromatic amines.

The least complex aliphatic compound is methane (CH4).

03Properties

Most aliphatic compounds are flammable, allowing the use of hydrocarbons as fuel, such as methane in natural gas for stoves or heating; butane in torches and lighters; various aliphatic (as well as aromatic) hydrocarbons in liquid transportation fuels like petrol/gasoline, diesel, and jet fuel; and other uses such as ethyne (acetylene) in welding.

04Examples

A few examples of aliphatic compounds is listed below (sorted by the number of carbon-atoms).

FormulaNameStructural formulaChemical classification
CH4MethaneAlkane
C2H2AcetyleneAlkyne
C2H4EthyleneAlkene
C2H6EthaneAlkane
C3H4PropadieneDiene
C3H4PropyneAlkyne
C3H6PropyleneAlkene
C3H8PropaneAlkane
C4H61,2-ButadieneDiene
C4H61-ButyneAlkyne
C4H81-ButeneAlkene
C4H10ButaneAlkane
C5H12PentaneAlkane
C6H10CyclohexeneCycloalkene
C6H12CyclohexaneCycloalkane
C6H14HexaneAlkane
C7H14MethylcyclohexaneCycloalkane
C8H8CubanePrismane, Platonic hydrocarbon
C8H18OctaneAlkane
C10H12DicyclopentadieneDiene, Cycloalkene
C10H16TerpineneTerpene, Diene, Cycloalkene
C10H16PhellandreneTerpene, Diene, Cycloalkene
C10H16LimoneneTerpene, Diene, Cycloalkene
C10H22DecaneAlkane
C30H50SqualeneTerpene, Polyene
C2nH4nPolyethyleneAlkane
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Sources and credits

This article is adapted from the Wikipedia article Aliphatic compound, written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.

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