An alkylbenzene is a chemical compound that contains a monocyclic aromatic ring attaching to one or more saturated hydrocarbon chains.^[1] Alkylbenzenes are derivatives of benzene, in which one or more hydrogen atoms are replaced by alkyl groups. The simplest member, toluene (or methylbenzene), has the hydrogen atom of the benzene ring replaced by a methyl group. The chemical formula of alkylbenzenes is C_nH_2n-6.^[2]

Alkylbenzenes are a very important class of hydrocarbons, especially in the synthetic production industry. It is the raw material in the production of synthetic sulfonate detergents, which are found in a variety of household products such as soap, shampoo, toothpaste, laundry detergent, etc. Linear alkylbenzenes (LAB) and branched alkylbenzenes (BAB) are families of alkylbenzene used to prepare synthetic sulfonates. However, LABs are more industrially favoured since the discovery of its extensive biodegradable yield over BAB-based sulfonates in the 1960s.^[3]

• Friedel-Crafts alkylation: alkylbenzenes can be synthesized from olefins or alkyl halides with aromatic compounds in the presence of a catalyst such as AlCl₃, HF, or H₂SO₄.^[4]

• Gattermann-Koch reaction: named after German chemists Ludwig Gattermann and Julius Arnold Koch, the Gattermann-Koch reaction is a catalyzed formylation of alkylbenzenes with carbon monoxide and hydrochloric acid.^[5]
• Alkylbenzene sulfonation reaction: electrophilic addition of a sulfonic acid group onto the aromatic ring.^[4]

Alkylbenzene isomers can be differentiated by observing the position of alkyl substituents on the benzene ring using chemical ionization-proton exchange mass spectrometry. Conventional GC-MS yields limited results because the isomers have identical molecular weight and substituents.^[6]

Some alkylbenzenes such as toluene, trimethylbenzenes, and tetramethylbenzenes occur naturally in coal tar oil and as byproducts of the crude oil refinery process. Others can be prepared by Friedel-Crafts alkylation.^[3]

Alkylbenzenes used to be synthesized from tetrapropylene, however, the reaction is now rarely used because of the low biodegradable alkylbenzene sulfonates it yields.^[3]

Alkylbenzenes are flammable. Most of them are eye and skin irritants and pose an acute health hazard when ingested. Alkylbenzenes are toxic to aquatic life with long-lasting effects.

• Allinger, Cava, de Jongh, Johnson, Lebel, Stevens: Organische Chemie, 1. Auflage, Walter de Gruyter, Berlin 1980, ISBN 3-11-004594-X, pp. 367–368, 560–562.
• Streitwieser / Heathcock: Organische Chemie, 1. Auflage, Verlag Chemie, Weinheim 1980, ISBN 3-527-25810-8, pp. 1051, 1073–1080.
• Beyer / Walter: Lehrbuch der Organischen Chemie, 19. Auflage, S. Hirzel Verlag, Stuttgart 1981, ISBN 3-7776-0356-2, pp. 442–444.
• Morrison / Boyd: Lehrbuch der Organischen Chemie, 3. Auflage, Verlag Chemie, Weinheim 1986, ISBN 3-527-26067-6, pp. 707–728.