Aliphatic compound
In organic chemistry, hydrocarbons (compounds composed of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (/ˌælᵻˈfætᵻk/; G. aleiphar, fat, oil) also known as non-aromatic compounds. Aliphatics can be cyclic, but only aromatic compounds contain an especially stable ring of atoms, such as benzene.[1] Aliphatic compounds can be saturated, like hexane, or unsaturated, like hexene. Open-chain compounds (whether straight or branched) contain no rings of any type, and are thus aliphatic.
Structure
Aliphatic compounds can be saturated, joined by single bonds (alkanes), or unsaturated, with double bonds (alkenes) or triple bonds (alkynes). Besides hydrogen, other elements can be bound to the carbon chain, the most common being oxygen, nitrogen, sulphur, and chlorine.
The simplest aliphatic compound is methane (CH4). Aliphatics include alkanes, alkenes, and alkynes.
Properties
Most aliphatic compounds are flammable, allowing the use of hydrocarbons as fuel, such as methane in Bunsen burners and as liquefied natural gas (LNG), and acetylene in welding.
Examples of aliphatic compounds / non-aromatic
The most important aliphatic compounds are:
- n-, iso- and cyclo-alkanes (saturated hydrocarbons)
- n-, iso- and cyclo-alkenes and -alkynes (unsaturated hydrocarbons).
Important examples of low-molecular aliphatic compounds can be found in the list below (sorted by the number of carbon-atoms):
| Formula | Name | CAS-Number | Structural Formula | Chemical Classification |
|---|---|---|---|---|
| CH4 | Methane | 74-82-8 |  | Alkane |
| C2H2 | Ethyne | 74-86-2 |  | Alkyne |
| C2H4 | Ethene | 74-85-1 |  | Alkene |
| C2H6 | Ethane | 74-84-0 |  | Alkane |
| C3H4 | Propyne | 74-99-7 |  | Alkyne |
| C3H6 | Propene | - |  | Alkene |
| C3H8 | Propane | - |  | Alkane |
| C4H6 | 1,2-Butadiene | 590-19-2 |  | Diene |
| C4H6 | 1-Butyne | - |  | Alkyne |
| C4H8 | Butene | - | e.g.  | Alkene |
| C4H10 | Butane | - | | Alkane |
| C6H10 | Cyclohexene | 110-83-8 |  | Cycloalkene |
| C5H12 | n-pentane | 109-66-0 |  | Alkane |
| C7H14 | Cycloheptane | 291-64-5 |  | Cycloalkane |
| C7H14 | Methylcyclohexane | 108-87-2 |  | Cyclohexane |
| C8H8 | Cubane | 277-10-1 |  | Cyclobutane |
| C9H20 | Nonane | 111-84-2 |  | Alkane |
| C10H12 | Dicyclopentadiene | 77-73-6 |  | Diene, Cycloalkene |
| C10H16 | Phellandrene | 99-83-2 |   | Terpene, Diene Cycloalkene |
| C10H16 | α-Terpinene | 99-86-5 |  | Terpene, Cycloalkene, Diene |
| C10H16 | Limonene | 5989-27-5 | -Limonen.svg.png) -Limonen.svg.png) | Terpene, Diene, Cycloalkene |
| C11H24 | Undecane | 1120-21-4 |  | Alkane |
| C30H50 | Squalene | 111-02-4 |  | Terpene, Polyene |
| C2nH4n | Polyethylene | 9002-88-4 |  | Alkane |
A few structures can be shown as example:
But-1-ene can be shown as
CH2=CH-CH2-CH3
Aliphatic acids
Aliphatic acids are the acids of nonaromatic hydrocarbons, such as acetic, propionic, and butyric acids.
See also
References
- ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (1995) "Aliphatic compounds".
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