Alkylbenzene Explained

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 CnH2n-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.

Reactions

Spectroscopy

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.[5]

Production

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.

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

Safety hazards

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.

Application

Alkylbenzenes are the primary raw material in making synthetic alkylbenzene sulfonates. Synthetic sulfonates are the most widely used detergents, as industrial oil, emulsifiers, demulsifiers, rust inhibitors, dispersants, surfactants for enhanced oil recovery, ore-floatation agents, and wetting agents, among others. LABs such as alkylbenzene, dialkylbenzene, and alkyltoluene are most commonly used to prepare sulfonate detergents.

Solvent use

Some less substituted alkylbenzenes such as toluene and xylene are commonly used as solvents industrially.

Literature

References

References

Notes and References

  1. Francis . Alfred W. . 1948-02-01 . Properties of Alkylbenzenes. . Chemical Reviews . en . 42 . 1 . 107–162 . 10.1021/cr60131a003 . 18904921 . 0009-2665.
  2. Book: Sazhin, S. S. . Droplets and sprays : simple models of complex processes . 2022 . Springer . 978-3-030-99746-5 . Cham, Switzerland . 1333919856.
  3. Book: Lubricant additives : chemistry and applications . 2017 . Leslie R. Rudnick . 978-1-351-64696-3 . [Place of publication not identified] . 1003859957.
  4. Book: De, Surya K. . Applied Organic Chemistry: Reaction Mechanisms and Experimental Procedures in Medicinal Chemistry . 2021-01-26 . Wiley . 978-3-527-34785-8 . 1 . en . 10.1002/9783527828166.ch5. 242435919 .
  5. Hawthorne . Steven B. . Miller . David J. . 1985-03-01 . Identifying alkylbenzene isomers with chemical ionization-proton exchange mass spectrometry . Analytical Chemistry . en . 57 . 3 . 694–698 . 10.1021/ac00280a027 . 0003-2700.