Acyclic aliphatic/non-aromatic compound (butane)
Cyclic aliphatic/non-aromatic compound (cyclobutane)

Aliphatic compounds (/ˌælɪˈfætɪk/; G. aleiphar, fat, oil) are chemical compounds containing the element carbon that are not aromatic compounds.[1] 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).

Other 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.[1] 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.[2][3] These criteria are not present in the current IUPAC definition.

Structure

Aliphatic compounds can be saturated, i.e. alkanes (single carbon-carbon bonds), or unsaturated, with carbon-carbon double (alkenes) or triple bonds (alkynes).[4] 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).

Properties

Most aliphatic compounds are flammable,[4] 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.

Examples

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

Formula Name Structural formula Chemical classification
CH4 Methane Alkane
C2H2 Acetylene Alkyne
C2H4 Ethylene Alkene
C2H6 Ethane Alkane
C3H4 Propadiene Diene
C3H4 Propyne Alkyne
C3H6 Propylene Alkene
C3H8 Propane Alkane
C4H6 1,2-Butadiene Diene
C4H6 1-Butyne Alkyne
C4H8 1-Butene Alkene
C4H10 Butane Alkane
C5H12 Pentane Alkane
C6H10 Cyclohexene Cycloalkene
C6H12 Cyclohexane Cycloalkane
C6H14 Hexane Alkane
C7H14 Methylcyclohexane Cycloalkane
C8H8 Cubane Prismane, Platonic hydrocarbon
C8H18 Octane Alkane
C10H12 Dicyclopentadiene Diene, Cycloalkene
C10H16 Terpinene Terpene, Diene, Cycloalkene
C10H16 Phellandrene Terpene, Diene, Cycloalkene
C10H16 Limonene Terpene, Diene, Cycloalkene
C10H22 Decane Alkane
C30H50 Squalene Terpene, Polyene
C2nH4n Polyethylene Alkane

References

  1. ^ a b IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025). Online version: (1995) "aliphatic compounds". doi:10.1351/goldbook.A00217
  2. ^ Hampel (1992). Glossary of Chemical Terms (2nd ed.). p. 11.
  3. ^ Hackh's Chemical Dictionary (5th ed.). 1987. p. 22.
  4. ^ a b "9.1: Aliphatic Hydrocarbons". Chemistry LibreTexts. 2019-05-26. Retrieved 2026-07-16.