Thymol

Thymol is produced by the alkylation of m-cresol and propene.^[6][7] CH₃C₆H₄OH + CH₂CHCH₃ → ((CH₃)₂CH)CH₃C₆H₃OH

A predicted method of biosynthesis of thymol in thyme and oregano begins with the cyclization of geranyl diphosphate by TvTPS2 to γ-terpinene. Oxidation by a cytochrome P450 in the CYP71D subfamily creates a dienol intermediate, which is then converted into a ketone by short-chain dehydrogenase. Lastly, keto-enol tautomerization gives thymol. Its dissociation constant (pK_a) is 10.59±0.10.^[8] Thymol absorbs maximum UV radiation at 274 nm.^[9]

The bee balms Monarda fistulosa and Monarda didyma, North American wildflowers, are natural sources of thymol. The Blackfoot Native Americans recognized these plants' strong antiseptic action and used poultices of the plants for skin infections and minor wounds. A tisane made from them was also used to treat mouth and throat infections caused by dental caries and gingivitis.^[10]

Thymol was first isolated by German chemist Caspar Neumann in 1719.^[11] In 1853, French chemist Alexandre Lallemand^[12] (1816-1886) named thymol and determined its empirical formula.^[13] Possible antiseptic properties of thymol were discovered in 1875,^[14] and it was first synthesized by Swedish chemist Oskar Widman (1852-1930) in 1882.^[15]

The conventional method of extracting is hydro-distillation (HD), but can also be extracted with solvent-free microwave extraction (SFME). In 30 minutes, SFME yields similar amounts of thymol with more oxygenated compounds than 4.5 hours of hydro-distillation at atmospheric pressures without the need for solvent.^[16]

During the 1910s, thymol was used for hookworm infection in the United States.^[18][19] People of the Middle East continue to use za'atar, a delicacy made with large amounts of thyme, to reduce and eliminate internal parasites.^[20] It is also used as a preservative in halothane, an anaesthetic, and as an antiseptic in mouthwash. When used to reduce plaque and gingivitis, thymol has been found to be more effective when used in combination with chlorhexidine than when used purely by itself.^[21]

Thymol is a fragrance ingredient in some cosmetics.^[4] Thymol has been used to successfully control varroa mites and prevent fermentation and the growth of mold in bee colonies.^[22] Thymol is also used as a rapidly degrading, non-persisting pesticide,^[4][23] such as insecticides and fungicides which are leveraged in plant care products. Thymol can also be used as a medical disinfectant and general purpose disinfectant.^[24] Thymol is also used in the production of menthol through the hydrogenation of the aromatic ring.^[25]

Thymol (and its isomer carvacrol) is commonly used to synthesize thymoquinone, a quinone derivative, through catalytic oxidation.^[26][27]

In 2009, the U.S. Environmental Protection Agency (EPA) reviewed the research literature on the toxicology and environmental impact of thymol and concluded that "thymol has minimal potential toxicity and poses minimal risk".^[42]

• British Pharmacopoeia^[44]
• Japanese Pharmacopoeia^[45]

• Thymoquinone
• Nigella sativa
• Bromothymol