Английская Википедия:Geraniol
Шаблон:Short description Шаблон:Dist Шаблон:Chembox
Geraniol is a monoterpenoid and an alcohol. It is the primary component of citronella oil and is a primary component of rose oil and palmarosa oil. It is a colorless oil, although commercial samples can appear yellow. It has low solubility in water, but it is soluble in common organic solvents. The functional group derived from geraniol (in essence, geraniol lacking the terminal −OH) is called geranyl.
Uses and occurrence
In addition to rose oil, palmarosa oil, and citronella oil, it also occurs in small quantities in geranium, lemon, and many other essential oils. With a rose-like scent, it is commonly used in perfumes and in scents such as peach, raspberry, grapefruit, red apple, plum, lime, orange, lemon, watermelon, pineapple, and blueberry.
Geraniol is produced by the scent glands of honeybees to mark nectar-bearing flowers and locate the entrances to their hives.[1] It is also commonly used as an insect repellent, especially for mosquitoes.[2]
The scent of geraniol is reminiscent of, but chemically unrelated to, 2-ethoxy-3,5-hexadiene, also known as geranium taint, a wine fault resulting from fermentation of sorbic acid by lactic acid bacteria.[3]
Geranyl pyrophosphate is important in biosynthesis of other terpenes such as myrcene and ocimene.[4] It is also used in the biosynthesis pathway of many cannabinoids in the form of CBGA.[5]
Reactions
In acidic solutions, geraniol is converted to the cyclic terpene α-terpineol. The alcohol group undergoes expected reactions. It can be converted to the tosylate, which is a precursor to the chloride. Geranyl chloride also arises by the Appel reaction by treating geraniol with triphenylphosphine and carbon tetrachloride.[6][7] It can be hydrogenated.[8] It can be oxidized to the aldehyde geranial.[9]
Health and safety
Geraniol is classified as D2B (Toxic materials causing other effects) using the Workplace Hazardous Materials Information System (WHMIS).[10]
History
Geraniol was first isolated in pure form in 1871 by the German chemist Oscar Jacobsen (1840–1889).[11][12] Using distillation, Jacobsen obtained geraniol from an essential oil which was obtained from geranium grass (Andropogon schoenanthus) and which was produced in India.[13] The chemical structure of geraniol was determined in 1919 by the French chemist Albert Verley (1867–1959).[14]
See also
- Citronellol
- Citral
- Nerol
- Rhodinol
- Geranyl pyrophosphate
- Geranylgeranyl pyrophosphate
- Linalool
- 8-Hydroxygeraniol
- Geraniol 8-hydroxylase
- Bergamottin
- Perfume allergy
References
External links
Шаблон:Transient receptor potential channel modulators Шаблон:Authority control
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Holcombe, Luke (9 January 2018) "Wine faults", p. 11.
- ↑ Шаблон:Ullmann
- ↑ Шаблон:Cite journal
- ↑ Шаблон:OrgSynth
- ↑ Шаблон:OrgSynth
- ↑ Шаблон:OrgSynth
- ↑ Шаблон:OrgSynth
- ↑ Шаблон:Cite web
- ↑ Шаблон:Cite journal Jacobsen named geraniol on p. 234: "Danach ist dieser Körper, das Geraniol, isomer mit dem Borneol … " (Accordingly this body [i.e., substance], geraniol, is isomeric with borneol … )
- ↑ Шаблон:Cite book From p. 292: "Von dem Geraniol ist zu erwähnen, daß … erst Jacobsen (A. 157, 232) brachte im Jahre 1870 über den Alkohol, den er Geraniol nannte, nähere Angaben, er stellte die Formel C10H18O auf, ohne weitere Konstitionsangaben zu machen." (It should be mentioned about geraniol that … Jacobsen (A. 157, 232) first gathered in 1870 more detailed data about the alcohol, which he named geraniol ; he established its [empirical] formula C10H18O, without providing further data about its chemical structure.) See also: § 49. Geraniol C10H18O, pp. 439-493. On p. 439, two hypothetical structures of geraniol are proposed.
- ↑ (Semmler, 1906), p. 491.
- ↑ Шаблон:Cite journal The chemical structure of geraniol appears on p. 70.
