Gallic acid

Gallic acid
Names
Preferred IUPAC name
3,4,5-Trihydroxybenzoic acid
Other names
Gallic acid
Identifiers
149-91-7 YesY
5995-86-8 (monohydrate) N
3D model (Jmol) Interactive image
ChEBI CHEBI:30778 YesY
ChEMBL ChEMBL288114 YesY
ChemSpider 361 YesY
ECHA InfoCard 100.005.228
EC Number 205-749-9
5549
KEGG C01424 YesY
PubChem 370
RTECS number LW7525000
UNII 632XD903SP YesY
Properties
C7H6O5
Molar mass 170.12 g/mol
Appearance White, yellowish-white, or
pale fawn-colored crystals.
Density 1.694 g/cm3 (anhydrous)
Melting point 260 °C (500 °F; 533 K)
1.19 g/100 mL, 20°C (anhydrous)
1.5 g/100 mL, 20 °C (monohydrate)
Solubility soluble in alcohol, ether, glycerol, acetone
negligible in benzene, chloroform, petroleum ether
log P 0.70
Acidity (pKa) COOH: 4.5, OH: 10.
Hazards
Main hazards Irritant
Safety data sheet External MSDS
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity (yellow): no hazard code Special hazards (white): no codeNFPA 704 four-colored diamond
0
1
Lethal dose or concentration (LD, LC):
5000 mg/kg (rabbit, oral)
Related compounds
Related
phenols,
carboxylic acids
Related compounds
 Benzoic acid, Phenol, Pyrogallol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Gallic acid (also known as 3,4,5-trihydroxybenzoic acid) is a trihydroxybenzoic acid, a type of phenolic acid, found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants.[1] The chemical formula of gallic acid is C6H2(OH)3COOH. Gallic acid is found both free and as part of hydrolyzable tannins. The gallic acid groups are usually bonded to form dimers such as ellagic acid. Hydrolyzable tannins break down on hydrolysis to give gallic acid and glucose or ellagic acid and glucose, known as gallotannins and ellagitannins respectively.[2]

Gallic acid forms intermolecular esters (depsides) such as digallic and trigallic acids, and cyclic ether-esters (depsidones).[3]

Gallic acid is commonly used in the pharmaceutical industry.[4] It is used as a standard for determining the phenol content of various analytes by the Folin-Ciocalteau assay; results are reported in gallic acid equivalents.[5] Gallic acid can also be used as a starting material in the synthesis of the psychedelic alkaloid mescaline.[6]

The name is derived from oak galls, which were historically used to prepare tannic acid. Despite the name, gallic acid does not contain gallium. Salts and esters of gallic acid are termed "gallates".

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 century with a history extending to the Roman empire and the Dead Sea Scrolls. Pliny the Elder (23-79 AD) describes his experiments with it 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 evaporate — and gum arabic from acacia trees; this combination of ingredients produced the ink.[7]

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.

Gallic acid was first studied by the Swedish chemist Carl Wilhelm Scheele in 1786.[8] In 1818 the French chemist and pharmacist Henri Braconnot (1780–1855) devised a simpler method of purifying gallic acid from galls;[9] gallic acid was also studied by the French chemist Théophile-Jules Pelouze (1807–1867),[10] among others.

Gallic acid is a component of some pyrotechnic whistle mixtures.

Metabolism

Biosynthesis

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 tautomerizes to form the redox equivalent gallic acid, where the equilibrium lies essentially entirely toward gallic acid because of the coincidentally occurring aromatization.[11][12]

Degradation

Gallate dioxygenase is an enzyme found in Pseudomonas putida that catalyses the reaction

gallate + O2 → (1E)-4-oxobut-1-ene-1,2,4-tricarboxylate.

Gallate decarboxylase is another enzyme in the degradation of gallic acid.

Conjugation

Gallate 1-beta-glucosyltransferase is an enzyme that uses UDP-glucose and gallate, whereas its two products are UDP and 1-galloyl-beta-D-glucose.

Health effects

It is a weak carbonic anhydrase inhibitor.[13] In basic research, gallic acid extracted from grape seeds has been shown to inhibit the formation of amyloid fibrils, one of the potential causes of Alzheimer's disease and Parkinson's disease.[14][15][16] One study indicated that gallic acid has this effect on amyloid protein formation by modifying the properties of alpha-synuclein, a protein associated with the onset of neurodegenerative diseases.[16]

Gallic acid is classified as a mutagen and a teratogen.[3]

Natural occurrence

Gallic acid is found in a number of land plants, such as the parasitic plant Cynomorium coccineum,[17] the aquatic plant Myriophyllum spicatum, and the blue-green alga Microcystis aeruginosa.[18] Gallic acid is also found in various oak species,[19] Caesalpinia mimosoides,[20] and in the stem bark of Boswellia dalzielii,[21] among others. Many foodstuffs contain various amounts of gallic acid, especially fruits (including strawberries, grapes, bananas),[22][23] as well as teas,[22][24] cloves,[25] and vinegars.[26]

Production

Gallic acid is easily freed from gallotannins by acidic or alkaline hydrolysis. When gallic acid is heated with concentrated sulfuric acid, rufigallol is produced by condensation. Oxidation with arsenic acid, permanganate, persulfate, or iodine yields ellagic acid, as does reaction of methyl gallate with iron(III) chloride.[3]

Spectral data

UV-Vis
Lambda-max: 220, 271 nm (ethanol)
Spectrum of gallic acid
Extinction coefficient (log ε)
IR
Major absorption bands ν : 3491, 3377, 1703, 1617, 1539, 1453, 1254 cm−1 (KBr)
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
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)

Reference[20]

Esters

Also known as galloylated esters:

See also

References

  1. ↑ LD Reynolds and NG Wilson, "Scribes and Scholars" 3rd Ed. Oxford: 1991. pp193–4.
  2. ↑ Andrew Pengelly (2004), The Constituents of Medicinal Plants (2nd ed.), Allen & Unwin, pp. 29–30
  3. 1 2 3 Edwin Ritzer; Rudolf Sundermann (2007), "Hydroxycarboxylic Acids, Aromatic", Ullmann's Encyclopedia of Industrial Chemistry (7th ed.), Wiley, p. 6
  4. ↑ Fiuza, S. M.; Gomes, C.; Teixeira, L. J.; Girão da Cruz, M. T.; Cordeiro, M. N. D. S.; Milhazes, N.; Borges, F.; Marques, M. P. M. "Phenolic acid derivatives with potential anticancer properties—a structure-activity relationship study. Part 1: Methyl, propyl, and octyl esters of caffeic and gallic acids". Bioorganic & Medicinal Chemistry. Elsevier. 12 (13): 3581–3589. doi:10.1016/j.bmc.2004.04.026.
  5. ↑ Andrew Waterhouse. "Folin-Ciocalteau Micro Method for Total Phenol in Wine". UC Davis.
  6. ↑ Tsao, Makepeasce (July 1951). "A New Synthesis Of Mescaline". Journal of the American Chemical Society. 73 (11): 5495–5496. doi:10.1021/ja01155a562. ISSN 0002-7863.
  7. ↑ Fruen, Lois. "Iron Gall Ink".
  8. ↑ 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), vol 7, pages 30-34.
  9. ↑ Braconnot Henri (1818). "Observations sur la préparation et la purification de l'acide gallique, et sur l'existence d'un acide nouveau dans la noix de galle" [Observations on the preparation and purification of gallic acid, and on the existence of a new acid in galls]. Annales de chimie et de physique. 9: 181–184.
  10. ↑ J. Pelouze (1833) "Mémoire sur le tannin et les acides gallique, pyrogallique, ellagique et métagallique," Annales de chimie et de physique, vol. 54, pages 337-365 [presented February 17, 1834].
  11. ↑ Gallic acid pathway on metacyc.org
  12. ↑ Dewick, PM; Haslam, E (1969). "Phenol biosynthesis in higher plants. Gallic acid". Biochemical Journal. 113 (3): 537–542. doi:10.1042/bj1130537. PMC 1184696Freely accessible. PMID 5807212.
  13. ↑ Satomi, H; Umemura, K; Ueno, A; Hatano, T; Okuda, T; Noro, T (1993). "Carbonic anhydrase inhibitors from the pericarps of Punica granatum L". Biological & Pharmaceutical Bulletin. 16 (8): 787–90. doi:10.1248/bpb.16.787. PMID 8220326.
  14. ↑ Liu, Y; Pukala, T. L.; Musgrave, I. F.; Williams, D. M.; Dehle, F. C.; Carver, J. A. (2013). "Gallic acid is the major component of grape seed extract that inhibits amyloid fibril formation". Bioorganic & Medicinal Chemistry Letters. 23 (23): 6336–40. doi:10.1016/j.bmcl.2013.09.071. PMID 24157371.
  15. ↑ Wang, Y. J.; Thomas, P; Zhong, J. H.; Bi, F. F.; Kosaraju, S; Pollard, A; Fenech, M; Zhou, X. F. (2009). "Consumption of grape seed extract prevents amyloid-beta deposition and attenuates inflammation in brain of an Alzheimer's disease mouse". Neurotoxicity Research. 15 (1): 3–14. doi:10.1007/s12640-009-9000-x. PMID 19384583.
  16. 1 2 Liu, Y; Carver, J. A.; Calabrese, A. N.; Pukala, T. L. (2014). "Gallic acid interacts with α-synuclein to prevent the structural collapse necessary for its aggregation". Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1844 (9): 1481–1485. doi:10.1016/j.bbapap.2014.04.013. PMID 24769497.
  17. ↑ Zucca, Paolo; Rosa, Antonella; Tuberoso, Carlo; Piras, Alessandra; Rinaldi, Andrea; Sanjust, Enrico; Dessì, Maria; Rescigno, Antonio (11 January 2013). "Evaluation of Antioxidant Potential of "Maltese Mushroom" (Cynomorium coccineum) by Means of Multiple Chemical and Biological Assays". Nutrients. 5 (1): 149–161. doi:10.3390/nu5010149. PMC 3571642Freely accessible. PMID 23344249.
  18. ↑ Nakai, S (2000). "Myriophyllum spicatum-released allelopathic polyphenols inhibiting growth of blue-green algae Microcystis aeruginosa". Water Research. 34 (11): 3026–3032. doi:10.1016/S0043-1354(00)00039-7.
  19. ↑ Mämmelä, Pirjo; Savolainen, Heikki; Lindroos, Lasse; Kangas, Juhani; Vartiainen, Terttu (2000). "Analysis of oak tannins by liquid chromatography-electrospray ionisation mass spectrometry". Journal of Chromatography A. 891 (1): 75–83. doi:10.1016/S0021-9673(00)00624-5. PMID 10999626.
  20. 1 2 Chanwitheesuk, Anchana; Teerawutgulrag, Aphiwat; Kilburn, Jeremy D.; Rakariyatham, Nuansri (2007). "Antimicrobial gallic acid from Caesalpinia mimosoides Lamk". Food Chemistry. 100 (3): 1044–1048. doi:10.1016/j.foodchem.2005.11.008.
  21. ↑ Alemika, Taiwo E.; Onawunmi, Grace O.; Olugbade, Tiwalade A. (2007). "Antibacterial phenolics from Boswellia dalzielii". Nigerian Journal of Natural Products and Medicine. 10 (1): 108–10.
  22. 1 2 Pandurangan AK, Mohebali N, Norhaizan ME, Looi CY (2015). "Gallic acid attenuates dextran sulfate sodium-induced experimental colitis in BALB/c mice". Drug Design, Development and Therapy. 9: 3923–34. doi:10.2147/DDDT.S86345. PMC 4524530Freely accessible. PMID 26251571.
  23. ↑ Koyama, K; Goto-Yamamoto, N; Hashizume, K (2007). "Influence of maceration temperature in red wine vinification on extraction of phenolics from berry skins and seeds of grape (Vitis vinifera)". Bioscience, Biotechnology, and Biochemistry. 71 (4): 958–65. doi:10.1271/bbb.60628. PMID 17420579.
  24. ↑ Hodgson JM, Morton LW, Puddey IB, Beilin LJ, Croft KD (2000). "Gallic acid metabolites are markers of black tea intake in humans". Journal of Agricultural and Food Chemistry. 48 (6): 2276–80. doi:10.1021/jf000089s. PMID 10888536.
  25. ↑ Pathak, S. B.; Niranjan, K.; Padh, H.; Rajani, M.; et al. (2004). "TLC Densitometric Method for the Quantification of Eugenol and Gallic Acid in Clove". Chromatographia. 60 (3–4): 241–244. doi:10.1365/s10337-004-0373-y.
  26. ↑ Gálvez, Miguel Carrero; Barroso, Carmelo García; Pérez-Bustamante, Juan Antonio (1994). "Analysis of polyphenolic compounds of different vinegar samples". Zeitschrift für Lebensmittel-Untersuchung und -Forschung. 199: 29–31. doi:10.1007/BF01192948.

External links

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