Английская Википедия:Gallic acid

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Шаблон:Short description Шаблон:Chembox

Gallic acid (also known as 3,4,5-trihydroxybenzoic acid) is a trihydroxybenzoic acid with the formula C6H2(OH)3CO2H. It is classified as a phenolic acid. It is found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants.[1] It is a white solid, although samples are typically brown owing to partial oxidation. Salts and esters of gallic acid are termed "gallates".

Its name is derived from oak galls, which were historically used to prepare tannic acid. Despite the name, gallic acid does not contain gallium.

Isolation and derivatives

Файл:Gallic acid ESP.png
Electrostatic potential map of surface of gallic acid molecule
Файл:Ellagic acid.svg
Ellagic acid molecule structure resembles that of two gallic acid molecules assembled in head to tail position and linked together by a C–C bond (as in biphenyl) and two cyclic ester links (lactones) forming two additional 6-piece cycles.

Gallic acid is easily freed from gallotannins by acidic or alkaline hydrolysis. When heated with concentrated sulfuric acid, gallic acid converts to rufigallol. Hydrolyzable tannins break down on hydrolysis to give gallic acid and glucose or ellagic acid and glucose, known as gallotannins and ellagitannins, respectively.[2]

Biosynthesis

Файл:3,5-didehydroshikimate.PNG
Chemical structure of 3,5-didehydroshikimate

Gallic acid is formed from 3-dehydroshikimate by the action of the enzyme shikimate dehydrogenase to produce 3,5-didehydroshikimate. This latter compound aromatizes.[3][4]

Reactions

Oxidation and oxidative coupling

Alkaline solutions of gallic acid are readily oxidized by air. The oxidation is catalyzed by the enzyme gallate dioxygenase, an enzyme found in Pseudomonas putida.

Oxidative coupling of gallic acid with arsenic acid, permanganate, persulfate, or iodine yields ellagic acid, as does reaction of methyl gallate with iron(III) chloride.[5] Gallic acid forms intermolecular esters (depsides) such as digallic and cyclic ether-esters (depsidones).[5]

Hydrogenation

Hydrogenation of gallic acid gives the cyclohexane derivative hexahydrogallic acid.[6]

Decarboxylation

Heating gallic acid gives pyrogallol (1,2,3-trihydroxybenzene). This conversion is catalyzed by gallate decarboxylase.

Esterification

Many esters of gallic acid are known, both synthetic and natural. Gallate 1-beta-glucosyltransferase catalyzes the glycosylation (attachment of glucose) of gallic acid.

Historical context and uses

Gallic acid is an important component of iron gall ink, the standard European writing and drawing ink from the 12th to 19th centuries, with a history extending to the Roman empire and the Dead Sea Scrolls. Pliny the Elder (23-79 AD) describes the use of gallic acid as a means of detecting an adulteration of verdigris[7] and writes that it was used to produce dyes. Galls (also known as oak apples) from oak trees were crushed and mixed with water, producing tannic acid. It could then be mixed with green vitriol (ferrous sulfate) — obtained by allowing sulfate-saturated water from a spring or mine drainage to evaporateШаблон:Citation needed — and gum arabic from acacia trees; this combination of ingredients produced the ink.[8]

Gallic acid was one of the substances used by Angelo Mai (1782–1854), among other early investigators of palimpsests, to clear the top layer of text off and reveal hidden manuscripts underneath. Mai was the first to employ it, but did so "with a heavy hand", often rendering manuscripts too damaged for subsequent study by other researchers.[9]

Gallic acid was first studied by the Swedish chemist Carl Wilhelm Scheele in 1786.[10] In 1818, French chemist and pharmacist Henri Braconnot (1780–1855) devised a simpler method of purifying gallic acid from galls;[11] gallic acid was also studied by the French chemist Théophile-Jules Pelouze (1807–1867),[12] among others.

When mixed with acetic acid, gallic acid had uses in early types of photography, like the calotype to make the silver more sensitive to light; it was also used in developing photographs.[13]

Occurrence

Gallic acid is found in a number of land plants, such as the parasitic plant Cynomorium coccineum,[14] the aquatic plant Myriophyllum spicatum, and the blue-green alga Microcystis aeruginosa.[15] Gallic acid is also found in various oak species,[16] Caesalpinia mimosoides,[17] and in the stem bark of Boswellia dalzielii,[18] among others. Many foodstuffs contain various amounts of gallic acid, especially fruits (including strawberries, grapes, bananas),[19][20] as well as teas,[19][21] cloves,[22] and vinegars.[23]Шаблон:Clarify Carob fruit is a rich source of gallic acid (24–165 mg per 100 g).[24]

Esters

Also known as galloylated esters:

Gallate esters are antioxidants useful in food preservation, with propyl gallate being the most commonly used. Their use in human health is scantly supported by evidence.

Spectral data

colspan="2" Шаблон:Chemical datatable header | UV-Vis
Lambda-max: 220, 271 nm (ethanol)
Файл:Gallic acid spectrum.PNG
Spectrum of gallic acid
Extinction coefficient (log ε)
colspan="2" Шаблон:Chemical datatable header | IR
Major absorption bands ν : 3491, 3377, 1703, 1617, 1539, 1453, 1254 cm−1 (KBr)
colspan="2" Шаблон:Chemical datatable header | NMR
Proton NMR


(acetone-d6):
d : doublet, dd : doublet of doublets,
m : multiplet, s : singlet

δ :

7.15 (2H, s, H-3 and H-7)

Carbon-13 NMR


(acetone-d6):

δ :

167.39 (C-1),
144.94 (C-4 and C-6),
137.77 (C-5),
120.81 (C-2),
109.14 (C-3 and C-7)

Other NMR data
colspan="2" Шаблон:Chemical datatable header | MS
Masses of
main fragments 		ESI-MS [M-H]- m/z : 169.0137 ms/ms (iontrap)@35 CE m/z product 125(100), 81(<1)

[17]

See also

References

Шаблон:Reflist

Шаблон:Gallotannin Шаблон:Phenolic acid

Шаблон:Authority control

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  1. ↑ Шаблон:Cite journal
  2. ↑ Шаблон:Citation
  3. ↑ Gallic acid pathway on metacyc.org
  4. ↑ Шаблон:Cite journal
  5. ↑ 5,0 5,1 Шаблон:Citation
  6. ↑ Шаблон:Cite journal
  7. ↑ Pliny the Elder with John Bostock and H.T. Riley, trans., The Natural History of Pliny (London, England: Henry G. Bohn, 1857), vol. 6, p. 196. In Book 34, Chapter 26 of his Natural History, Pliny states that verdigris (a form of copper acetate (Cu(CH3COO)2·2Cu(OH)2), which was used to process leather, was sometimes adulterated with copperas (a form of iron(II) sulfate (FeSO4·7H2O)). He presented a simple test for determining the purity of verdigris. From p. 196: "The adulteration [of verdigris], however, which is most difficult to detect, is made with copperas; … The fraud may also be detected by using a leaf of papyrus, which has been steeped in an infusion of nut-galls; for it becomes black immediately upon the genuine verdigris being applied."
  8. ↑ Шаблон:Cite web
  9. ↑ L.D. Reynolds and N.G. Wilson, "Scribes and Scholars" 3rd Ed. Oxford: 1991, pp 193–4.
  10. ↑ Carl Wilhelm Scheele (1786) "Om Sal essentiale Gallarum eller Gallåple-salt" (On the essential salt of galls or gall-salt), Kongliga Vetenskaps Academiens nya Handlingar (Proceedings of the Royal [Swedish] Academy of Science), 7: 30–34.
  11. ↑ Шаблон:Cite journal
  12. ↑ J. Pelouze (1833) "Mémoire sur le tannin et les acides gallique, pyrogallique, ellagique et métagallique," Annales de chimie et de physique, 54: 337–365 [presented February 17, 1834].
  13. ↑ Шаблон:Cite book
  14. ↑ Шаблон:Cite journal
  15. ↑ Шаблон:Cite journal
  16. ↑ Шаблон:Cite journal
  17. ↑ 17,0 17,1 Шаблон:Cite journal
  18. ↑ Шаблон:Cite journal
  19. ↑ 19,0 19,1 Шаблон:Cite journal
  20. ↑ Шаблон:Cite journal
  21. ↑ Шаблон:Cite journal
  22. ↑ Шаблон:Cite journal
  23. ↑ Шаблон:Cite journal
  24. ↑ Шаблон:Cite journal
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