Styrene is an organic compound with the chemical formula C₆H₅CH=CH₂. Its structure consists of a vinyl group as substituent on benzene. Styrene is a colorless, oily liquid, although aged samples can appear yellowish. The compound evaporates easily and has a sweet smell, although high concentrations have a less pleasant odor.^[vague] Styrene is the precursor to polystyrene and several copolymers, and is typically made from benzene for this purpose. Approximately 25 million tonnes of styrene were produced in 2010, increasing to around 35 million tonnes by 2018.

Styrene is named after storax balsam (often commercially sold as styrax), the resin of Liquidambar trees of the Altingiaceae plant family. Styrene occurs naturally in small quantities in some plants and foods (cinnamon, coffee beans, balsam trees and peanuts) and is also found in coal tar.

In 1839, the German apothecary Eduard Simon isolated a fragrant volatile liquid from the resin (called storax or styrax (Latin)) of the American sweetgum tree (Liquidambar styraciflua). He called the liquid "styrol" (now called styrene). He also noticed that when styrol was exposed to air, light, or heat, it gradually transformed into a hard, rubber-like substance, which he called "styrol oxide".

By 1845, the German chemist August Wilhelm von Hofmann and his student John Buddle Blyth had determined styrene's empirical formula: C₈H₈. They had also determined that Simon's "styrol oxide"—which they renamed "metastyrol"—had the same empirical formula as styrene. Furthermore, they could obtain styrene by dry-distilling "metastyrol".

In 1865, the German chemist Emil Erlenmeyer found that styrene could form a dimer, and in 1866 the French chemist Marcelin Berthelot stated that "metastyrol" was a polymer of styrene (i.e. polystyrene). Meanwhile, other chemists had been investigating another component of storax, namely, cinnamic acid. They had found that cinnamic acid could be decarboxylated to form "cinnamene" (or "cinnamol"), which appeared to be styrene.

In 1845, French chemist Emil Kopp suggested that the two compounds were identical, and in 1866, Erlenmeyer suggested that both "cinnamol" and styrene might be vinylbenzene. However, the styrene that was obtained from cinnamic acid seemed different from the styrene that was obtained by distilling storax resin: the latter was optically active. Eventually, in 1876, the Dutch chemist van 't Hoff resolved the ambiguity: the optical activity of the styrene that was obtained by distilling storax resin was due to a contaminant.

The vast majority of styrene is produced from ethylbenzene, and almost all ethylbenzene produced worldwide is intended for styrene production. As such, the two production processes are often highly integrated. Ethylbenzene is produced via a Friedel–Crafts reaction between benzene and ethene; originally this used aluminum chloride as a catalyst, but in modern production this has been replaced by zeolites.

Around 80% of styrene is produced by the dehydrogenation of ethylbenzene. This is achieved using superheated steam (up to 600 °C) over an iron(III) oxide catalyst. The reaction is highly endothermic and reversible, with a typical yield of 88–94%.