Tannin

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Representative chemical structure of a tannic acid, a type of tannin Tannic acid.svg
Representative chemical structure of a tannic acid, a type of tannin
Tannin powder (mixture of compounds) Tannin heap.jpeg
Tannin powder (mixture of compounds)
A bottle of tannic acid solution in water Bottle of tannic acid.jpg
A bottle of tannic acid solution in water

Tannins (or tannoids) are a class of astringent, polyphenolic biomolecules that bind to and precipitate proteins and various other organic compounds including amino acids and alkaloids.

Contents

The term tannin (from Anglo-Norman tanner, from Medieval Latin tannare, from tannum, "oak bark") refers to the use of oak and other bark in tanning animal hides into leather. By extension, the term tannin is widely applied to any large polyphenolic compound containing sufficient hydroxyls and other suitable groups (such as carboxyls) to form strong complexes with various macromolecules.

The tannin compounds are widely distributed in many species of plants, where they play a role in protection from predation (acting as pesticides) and might help in regulating plant growth. [1] The astringency from the tannins is what causes the dry and puckery feeling in the mouth following the consumption of unripened fruit, red wine or tea. [2] Likewise, the destruction or modification of tannins with time plays an important role when determining harvesting times.

Tannins have molecular weights ranging from 500 to over 3,000 [3] (gallic acid esters) and up to 20,000 daltons (proanthocyanidins).

Structure and classes of tannins

There are three major classes of tannins: Shown below are the base unit or monomer of the tannin. Particularly in the flavone-derived tannins, the base shown must be (additionally) heavily hydroxylated and polymerized in order to give the high molecular weight polyphenol motif that characterizes tannins. Typically, tannin molecules require at least 12 hydroxyl groups and at least five phenyl groups to function as protein binders. [4]

Base unit / scaffold Gallic acid.svg
Gallic acid 		Phloroglucinol structure.png
Phloroglucinol 		Flavan-3-ol.svg
Flavan-3-ol
Polymer class Hydrolyzable tannins Phlorotannins Condensed tannins [5] Phlobatannins (C-ring isomerized condensed tannins) [5]
SourcesPlants Brown algae PlantsTree heartwood

Oligostilbenoids (oligo- or polystilbenes) are oligomeric forms of stilbenoids and constitute a minor class of tannins. [6]

Pseudo-tannins

Pseudo-tannins are low molecular weight compounds associated with other compounds. They do not change color during the Goldbeater's skin test, unlike hydrolysable and condensed tannins, and cannot be used as tanning compounds. [4] Some examples of pseudo tannins and their sources are: [7]

Pseudo tanninSource(s)
Gallic acid Rhubarb
Flavan-3-ols (Catechins) Tea, acacia, catechu, cocoa, guarana
Chlorogenic acid Nux-vomica, coffee, mate
Ipecacuanhic acid Carapichea ipecacuanha

History

Ellagic acid, gallic acid, and pyrogallic acid were first discovered by chemist Henri Braconnot in 1831. [8] : 20  Julius Löwe was the first person to synthesize ellagic acid by heating gallic acid with arsenic acid or silver oxide. [8] : 20  [9]

Maximilian Nierenstein studied natural phenols and tannins [10] found in different plant species. Working with Arthur George Perkin, he prepared ellagic acid from algarobilla and certain other fruits in 1905. [11] He suggested its formation from galloyl-glycine by Penicillium in 1915. [12] Tannase is an enzyme that Nierenstein used to produce m-digallic acid from gallotannins. [13] He proved the presence of catechin in cocoa beans in 1931. [14] He showed in 1945 that luteic acid, a molecule present in the myrobalanitannin, a tannin found in the fruit of Terminalia chebula , is an intermediary compound in the synthesis of ellagic acid. [15]

At these times, molecule formulas were determined through combustion analysis. The discovery in 1943 by Martin and Synge of paper chromatography provided for the first time the means of surveying the phenolic constituents of plants and for their separation and identification. There was an explosion of activity in this field after 1945, including prominent work by Edgar Charles Bate-Smith and Tony Swain at Cambridge University. [16]

In 1966, Edwin Haslam proposed a first comprehensive definition of plant polyphenols based on the earlier proposals of Bate-Smith, Swain and Theodore White, which includes specific structural characteristics common to all phenolics having a tanning property. It is referred to as the White–Bate-Smith–Swain–Haslam (WBSSH) definition. [17] [ self-published source? ]

Occurrence

Tannins are distributed in species throughout the plant kingdom. They are commonly found in both gymnosperms and angiosperms. Mole (1993) studied the distribution of tannin in 180 families of dicotyledons and 44 families of monocotyledons (Cronquist). Most families of dicot contain tannin-free species (tested by their ability to precipitate proteins). The best known families of which all species tested contain tannin are: Aceraceae, Actinidiaceae, Anacardiaceae, Bixaceae, Burseraceae, Combretaceae, Dipterocarpaceae, Ericaceae, Grossulariaceae, Myricaceae for dicot and Najadaceae and Typhaceae in Monocot. To the family of the oak, Fagaceae, 73% of the species tested contain tannin. For those of acacias, Mimosaceae, only 39% of the species tested contain tannin, among Solanaceae rate drops to 6% and 4% for the Asteraceae. Some families like the Boraginaceae, Cucurbitaceae, Papaveraceae contain no tannin-rich species. [18]

The most abundant polyphenols are the condensed tannins, found in virtually all families of plants, and comprising up to 50% of the dry weight of leaves. [19] [20]

Cellular localization

In all vascular plants studied, tannins are manufactured by a chloroplast-derived organelle, the tannosome. [21] Tannins are mainly physically located in the vacuoles or surface wax of plants. These storage sites keep tannins active against plant predators, but also keep some tannins from affecting plant metabolism while the plant tissue is alive.

Tannins are classified as ergastic substances, i.e., non-protoplasm materials found in cells. Tannins, by definition, precipitate proteins. In this condition, they must be stored in organelles able to withstand the protein precipitation process. Idioblasts are isolated plant cells which differ from neighboring tissues and contain non-living substances. They have various functions such as storage of reserves, excretory materials, pigments, and minerals. They could contain oil, latex, gum, resin or pigments etc. They also can contain tannins. In Japanese persimmon ( Diospyros kaki ) fruits, tannin is accumulated in the vacuole of tannin cells, which are idioblasts of parenchyma cells in the flesh. [22]

Presence in soils

The convergent evolution of tannin-rich plant communities has occurred on nutrient-poor acidic soils throughout the world. Tannins were once believed to function as anti-herbivore defenses, but more and more ecologists now recognize them as important controllers of decomposition and nitrogen cycling processes. As concern grows about global warming, there is great interest to better understand the role of polyphenols as regulators of carbon cycling, in particular in northern boreal forests. [23]

Leaf litter and other decaying parts of kauri ( Agathis australis ), a tree species found in New Zealand, decompose much more slowly than those of most other species. Besides its acidity, the plant also bears substances such as waxes and phenols, most notably tannins, that are harmful to microorganisms. [24]

Presence in water and wood

The leaching of highly water soluble tannins from decaying vegetation and leaves along a stream may produce what is known as a blackwater river. Water flowing out of bogs has a characteristic brown color from dissolved peat tannins. The presence of tannins (or humic acid) in well water can make it smell bad or taste bitter, but this does not make it unsafe to drink. [25]

Tannins leaching from an unprepared driftwood decoration in an aquarium can cause pH lowering and coloring of the water to a tea-like tinge. A way to avoid this is to boil the wood in water several times, discarding the water each time. Using peat as an aquarium substrate can have the same effect. Many hours of boiling the driftwood may need to be followed by many weeks or months of constant soaking and many water changes before the water will stay clear. Raising the water's pH level, e.g. by adding baking soda, will accelerate the process of leaching. [26]

Softwoods, while in general much lower in tannins than hardwoods, [27] are usually not recommended for use in an aquarium [28] so using a hardwood with a very light color, indicating a low tannin content, can be an easy way to avoid tannins. Tannic acid is brown in color, so in general white woods have a low tannin content. Woods with a lot of yellow, red, or brown coloration to them (like cedar, redwood, red oak, etc.) tend to contain a lot of tannin. [29]

Extraction

There is no single protocol for extracting tannins from all plant material. The procedures used for tannins are widely variable. [30] It may be that acetone in the extraction solvent increases the total yield by inhibiting interactions between tannins and proteins during extraction [30] or even by breaking hydrogen bonds between tannin-protein complexes. [31]

Tests for tannins

There are three groups of methods for the analysis of tannins: precipitation of proteins or alkaloids, reaction with phenolic rings, and depolymerization. [32]

Alkaloid precipitation

Alkaloids such as caffeine, cinchonine, quinine or strychnine, precipitates polyphenols and tannins. This property can be used in a quantitation method. [33]

Goldbeater's skin test

When goldbeater's skin or ox skin is dipped in HCl, rinsed in water, soaked in the tannin solution for 5 minutes, washed in water, and then treated with 1% FeSO4 solution, it gives a blue black color if tannin was present. [34]

Ferric chloride test

The following describes the use of ferric chloride (FeCl3) tests for phenolics in general: Powdered plant leaves of the test plant (1.0 g) are weighed into a beaker and 10 ml of distilled water are added. The mixture is boiled for five minutes. Two drops of 5% FeCl3 are then added. Production of a greenish precipitate is an indication of the presence of tannins. [35] Alternatively, a portion of the water extract is diluted with distilled water in a ratio of 1:4 and few drops of 10% ferric chloride solution is added. A blue or green color indicates the presence of tannins (Evans, 1989). [36]

Other methods

The hide-powder method is used in tannin analysis for leather tannin and the Stiasny method for wood adhesives. [37] [38] Statistical analysis reveals that there is no significant relationship between the results from the hide-powder and the Stiasny methods. [39] [40]

Hide-powder method

400 mg of sample tannins are dissolved in 100 ml of distilled water. 3 g of slightly chromated hide-powder previously dried in vacuum for 24h over CaCl2 are added and the mixture stirred for 1 h at ambient temperature. The suspension is filtered without vacuum through a sintered glass filter. The weight gain of the hide-powder expressed as a percentage of the weight of the starting material is equated to the percentage of tannin in the sample.

Stiasny's method

100 mg of sample tannins are dissolved in 10 ml distilled water. 1 ml of 10M HCl and 2 ml of 37% formaldehyde are added and the mixture heated under reflux for 30 min. The reaction mixture is filtered while hot through a sintered glass filter. The precipitate is washed with hot water (5× 10 ml) and dried over CaCl2. The yield of tannin is expressed as a percentage of the weight of the starting material.

Reaction with phenolic rings

The bark tannins of Commiphora angolensis have been revealed by the usual color and precipitation reactions and by quantitative determination by the methods of Löwenthal-Procter and of Deijs [41] (formalin-hydrochloric acid method). [42]

Colorimetric methods have existed such as the Neubauer-Löwenthal method which uses potassium permanganate as an oxidizing agent and indigo sulfate as an indicator, originally proposed by Löwenthal in 1877. [43] The difficulty is that the establishing of a titer for tannin is not always convenient since it is extremely difficult to obtain the pure tannin. Neubauer proposed to remove this difficulty by establishing the titer not with regard to the tannin but with regard to crystallised oxalic acid, whereby he found that 83 g oxalic acid correspond to 41.20 g tannin. Löwenthal's method has been criticized. For instance, the amount of indigo used is not sufficient to retard noticeably the oxidation of the non-tannins substances. The results obtained by this method are therefore only comparative. [44] [45] A modified method, proposed in 1903 for the quantification of tannins in wine, Feldmann's method, is making use of calcium hypochlorite, instead of potassium permanganate, and indigo sulfate. [46]

Food items with tannins

Pomegranates

Accessory fruits

Strawberries contain both hydrolyzable and condensed tannins. [47]

Berries

Strawberries in a bowl Strawberries in white bowl.jpg
Strawberries in a bowl

Most berries, such as cranberries, [48] and blueberries, [49] contain both hydrolyzable and condensed tannins.

Nuts

Nuts vary in the amount of tannins they contain. Some species of acorns of oak contain large amounts. For example, acorns of Quercus robur and Quercus petraea in Poland were found to contain 2.4–5.2% and 2.6–4.8% tannins as a proportion of dry matter, [50] but the tannins can be removed by leaching in water so that the acorns become edible. [51] Other nuts – such as hazelnuts, walnuts, pecans, and almonds – contain lower amounts. Tannin concentration in the crude extract of these nuts did not directly translate to the same relationships for the condensed fraction. [52]

Herbs and spices

Cloves, tarragon, cumin, thyme, vanilla, and cinnamon all contain tannins.[ citation needed ]

Legumes

Most legumes contain tannins. Red-colored beans contain the most tannins, and white-colored beans have the least. Peanuts without shells have a very low tannin content. Chickpeas (garbanzo beans) have a smaller amount of tannins. [53]

Chocolate

Chocolate liquor contains about 6% tannins. [54]

Drinks with tannins

Principal human dietary sources of tannins are tea and coffee. [55] Most wines aged in charred oak barrels possess tannins absorbed from the wood. [56] Soils high in clay also contribute to tannins in wine grapes. [57] This concentration gives wine its signature astringency. [58]

Coffee pulp has been found to contain low to trace amounts of tannins. [59]

Fruit juices

Although citrus fruits do not contain tannins, orange-colored juices often contain tannins from food colouring. Apple, grape and berry juices all contain high amounts of tannins. Sometimes tannins are even added to juices and ciders to create a more astringent feel to the taste. [60]

Beer

In addition to the alpha acids extracted from hops to provide bitterness in beer, condensed tannins are also present. These originate both from malt and hops. Trained brewmasters, particularly those in Germany, consider the presence of tannins to be a flaw[ citation needed ]. However, in some styles, the presence of this astringency is acceptable or even desired, as, for example, in a Flanders red ale. [61]

In lager type beers, the tannins can form a precipitate with specific haze-forming proteins in the beer resulting in turbidity at low temperature. This chill haze can be prevented by removing part of the tannins or part of the haze-forming proteins. Tannins are removed using PVPP, haze-forming proteins by using silica or tannic acid. [62]

Properties for animal nutrition

Tannins have traditionally been considered antinutritional, depending upon their chemical structure and dosage. [63]

Many studies suggest that chestnut tannins have positive effects on silage quality in the round bale silages, in particular reducing NPNs (non-protein nitrogen) in the lowest wilting level. [64]

Improved fermentability of soya meal nitrogen in the rumen may occur. [65] Condensed tannins inhibit herbivore digestion by binding to consumed plant proteins and making them more difficult for animals to digest, and by interfering with protein absorption and digestive enzymes (for more on that topic, see plant defense against herbivory). Histatins, another type of salivary proteins, also precipitate tannins from solution, thus preventing alimentary adsorption. [66]

Legume fodders containing condensed tannins are a possible option for integrated sustainable control of gastrointestinal nematodes in ruminants, which may help address the worldwide development of resistance to synthetic anthelmintics. These include nuts, temperate and tropical barks, carob, coffee and cocoa. [67]

Tannin uses and market

Tannin in a plastic container Tannin in Plastic container.jpeg
Tannin in a plastic container

Tannins have been used since antiquity in the processes of tanning hides for leather, and in helping preserve iron artifacts (as with Japanese iron teapots).

Industrial tannin production began at the beginning of the 19th century with the industrial revolution, to produce tanning material for the need for more leather. Before that time, processes used plant material and were long (up to six months). [68]

There was a collapse in the vegetable tannin market in the 1950s–1960s, due to the appearance of synthetic tannins, which were invented in response to a scarcity of vegetable tannins during World War II. At that time, many small tannin industry sites closed. [69] Vegetable tannins are estimated to be used for the production of 10–20% of the global leather production.[ citation needed ]

The cost of the final product depends on the method used to extract the tannins, in particular the use of solvents, alkali and other chemicals used (for instance glycerin). For large quantities, the most cost-effective method is hot water extraction.

Tannic acid is used worldwide as clarifying agent in alcoholic drinks and as aroma ingredient in both alcoholic and soft drinks or juices. Tannins from different botanical origins also find extensive uses in the wine industry.[ citation needed ]

Uses

Tannins are an important ingredient in the process of tanning leather. Tanbark from oak, mimosa, chestnut and quebracho tree has traditionally been the primary source of tannery tannin, though inorganic tanning agents are also in use today and account for 90% of the world's leather production. [70]

Tannins produce different colors with ferric chloride (either blue, blue black, or green to greenish-black) according to the type of tannin. Iron gall ink is produced by treating a solution of tannins with iron(II) sulfate. [71]

Tannins can also be used as a mordant, and is especially useful in natural dyeing of cellulose fibers such as cotton. [72] The type of tannin used may or may not have an impact on the final color of the fiber.

Tannin is a component in a type of industrial particleboard adhesive developed jointly by the Tanzania Industrial Research and Development Organization and Forintek Labs Canada. [73] Pinus radiata tannins has been investigated for the production of wood adhesives. [74]

Condensed tannins, e.g., quebracho tannin, and Hydrolyzable tannins, e.g., chestnut tannin, appear to be able to substitute a high proportion of synthetic phenol in phenol-formaldehyde resins for wood particleboard.[ citation needed ]

Tannins can be used for production of anti-corrosive primers for treating rusted steel surfaces prior to painting, converting rust to iron tannate and consolidating and sealing the surface.

The use of resins made of tannins has been investigated to remove mercury and methylmercury from solution. [75] Immobilized tannins have been tested to recover uranium from seawater. [76]

Related Research Articles

<span class="mw-page-title-main">Tanning (leather)</span> Process of treating animal skin to produce leather

Tanning, or hide tanning, is the process of treating skins and hides of animals to produce leather. A tannery is the place where the skins are processed.

<span class="mw-page-title-main">Gallic acid</span> 3,4,5-Trihydroxybenzoic acid

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. It is a white solid, although samples are typically brown owing to partial oxidation. Salts and esters of gallic acid are termed "gallates".

<span class="mw-page-title-main">Polyphenol</span> Class of chemical compounds

Polyphenols are a large family of naturally occurring phenols. They are abundant in plants and structurally diverse. Polyphenols include phenolic acids, flavonoids, tannic acid, and ellagitannin, some of which have been used historically as dyes and for tanning garments.

<span class="mw-page-title-main">Astringent</span> Chemical compound that tends to shrink or constrict body tissues

An astringent is a chemical that shrinks or constricts body tissues. The word derives from the Latin adstringere, which means "to bind fast". Astringency, the dry, puckering or numbing mouthfeel caused by the tannins in unripe fruits, lets the fruit mature by deterring eating. Tannins, being a kind of polyphenol, bind salivary proteins and make them precipitate and aggregate, producing a rough, "sandpapery", or dry sensation in the mouth.

<span class="mw-page-title-main">Ellagic acid</span> Natural phenol antioxidant

Ellagic acid is a polyphenol found in numerous fruits and vegetables. It is the dilactone of hexahydroxydiphenic acid.

Proanthocyanidins are a class of polyphenols found in many plants, such as cranberry, blueberry, and grape seeds. Chemically, they are oligomeric flavonoids. Many are oligomers of catechin and epicatechin and their gallic acid esters. More complex polyphenols, having the same polymeric building block, form the group of condensed tannins.

<span class="mw-page-title-main">Procyanidin</span>

Procyanidins are members of the proanthocyanidin class of flavonoids. They are oligomeric compounds, formed from catechin and epicatechin molecules. They yield cyanidin when depolymerized under oxidative conditions.

<i>Terminalia chebula</i> Species of flowering plant

Terminalia chebula, commonly known as black- or chebulic myrobalan, is a species of Terminalia, native to South Asia from Pakistan, India and Nepal east to southwest China (Yunnan), and south to Sri Lanka, Malaysia, and Vietnam.

<span class="mw-page-title-main">Phenolic content in wine</span> Wine chemistry

Phenolic compounds—natural phenol and polyphenols—occur naturally in wine. These include a large group of several hundred chemical compounds that affect the taste, color and mouthfeel of wine. These compounds include phenolic acids, stilbenoids, flavonols, dihydroflavonols, anthocyanins, flavanol monomers (catechins) and flavanol polymers (proanthocyanidins). This large group of natural phenols can be broadly separated into two categories, flavonoids and non-flavonoids. Flavonoids include the anthocyanins and tannins which contribute to the color and mouthfeel of the wine. The non-flavonoids include the stilbenoids such as resveratrol and phenolic acids such as benzoic, caffeic and cinnamic acids.

<span class="mw-page-title-main">Phlobaphene</span>

Phlobaphenes are reddish, alcohol-soluble and water-insoluble phenolic substances. They can be extracted from plants, or be the result from treatment of tannin extracts with mineral acids. The name phlobaphen come from the Greek roots φλoιὀς (phloios) meaning bark and βαφή (baphe) meaning dye.

A hydrolysable tannin or pyrogallol-type tannin is a type of tannin that, on heating with hydrochloric or sulfuric acids, yields gallic or ellagic acids.

<span class="mw-page-title-main">Ellagitannin</span> Diverse class of hydrolyzable tannins, a type of polyphenol

The ellagitannins are a diverse class of hydrolyzable tannins, a type of polyphenol formed primarily from the oxidative linkage of galloyl groups in 1,2,3,4,6-pentagalloyl glucose. Ellagitannins differ from gallotannins, in that their galloyl groups are linked through C-C bonds, whereas the galloyl groups in gallotannins are linked by depside bonds.

<span class="mw-page-title-main">Grandinin</span> Chemical compound

Grandinin is an ellagitannin. It can be found in Melaleuca quinquenervia leaves and in oaks species like the North American white oak and European red oak. It shows antioxydant activity. It is an astringent compound. It is also found in wine, red or white, aged in oak barrels.

<span class="mw-page-title-main">Condensed tannin</span> Polymers formed by the condensation of flavans.

Condensed tannins are polymers formed by the condensation of flavans. They do not contain sugar residues.

<i>Quercus infectoria</i> Species of oak tree

Quercus infectoria or the Aleppo oak is a species of oak well known for producing galls that have been traditionally used for centuries in Asia medicinally while also used in softening leather and in making black dye and ink.

<span class="mw-page-title-main">Phenolic content in tea</span> Natural plant compounds

The phenolic content in tea refers to the phenols and polyphenols, natural plant compounds which are found in tea. These chemical compounds affect the flavor and mouthfeel of tea. Polyphenols in tea include catechins, theaflavins, tannins, and flavonoids.

<span class="mw-page-title-main">Naturally occurring phenols</span> Group of chemical compounds

In biochemistry, naturally occurring phenols are natural products containing at least one phenol functional group. Phenolic compounds are produced by plants and microorganisms. Organisms sometimes synthesize phenolic compounds in response to ecological pressures such as pathogen and insect attack, UV radiation and wounding. As they are present in food consumed in human diets and in plants used in traditional medicine of several cultures, their role in human health and disease is a subject of research. Some phenols are germicidal and are used in formulating disinfectants.

Maximilian Nierenstein was a professor of biochemistry at the University of Bristol.

<span class="mw-page-title-main">Luteic acid</span> Chemical compound

Luteic acid is a natural phenol found in numerous fruits. It is a monolactonized tergalloyl group. Maximilian Nierenstein showed in 1945 that luteic acid was a molecule present in the myrobalanitannin, a tannin found in the fruit of Terminalia chebula and is an intermediary compound in the synthesis of ellagic acid. It can form from hexahydroxydiphenic acid. It is also present in the structure of the tannins alnusiin and bicornin.

References

  1. ↑ Ferrell, Katie E.; Thorington, Richard W. (2006). Squirrels: the animal answer guide . Baltimore: Johns Hopkins University Press. p.  91. ISBN   978-0-8018-8402-3.
  2. ↑ McGee, Harold (2004). On food and cooking: the science and lore of the kitchen. New York: Scribner. p. 714. ISBN   978-0-684-80001-1.
  3. ↑ Bate-Smith and Swain (1962). "Flavonoid compounds". In Florkin M.; Mason H. S (eds.). Comparative biochemistry. Vol. III. New York: Academic Press. pp. 75–809.
  4. 1 2 "Notes on Tannins from PharmaXChange.info". Archived from the original on 4 January 2015.
  5. 1 2 page 113 "Chemistry and Significance of Condensed Tannins" By Richard W. Hemingway, Joseph J. Karchesy, ISBN   978-1-4684-7511-1
  6. ↑ Boralle, N.; Gottlieb, H. E.; Gottlieb, O. R.; Kubitzki, K.; Lopes, L. M. X.; Yoshida, M.; Young, M. C. M. (1993). "Oligostilbenoids from Gnetum venosum". Phytochemistry. 34 (5): 1403–1407. Bibcode:1993PChem..34.1403B. doi:10.1016/0031-9422(91)80038-3.
  7. ↑ Ashutosh Kar (2003). Pharmacognosy And Pharmacobiotechnology. New Age International. pp. 44–. ISBN   978-81-224-1501-8. Archived from the original on 2 June 2013. Retrieved 31 January 2011.
  8. 1 2 Grasser, Georg (1922). Synthetic Tannins. F. G. A. Enna. (trans.). Read Books. ISBN   978-1-4067-7301-9.
  9. ↑ Löwe, Zeitschrift für Chemie, 1868, 4, 603
  10. ↑ Drabble, E.; Nierenstein, M. (1907). "On the Rôle of Phenols, Tannic Acids, and Oxybenzoic Acids in Cork Formation". Biochemical Journal. 2 (3): 96–102.1. doi:10.1042/bj0020096. PMC   1276196 . PMID   16742048.
  11. ↑ Perkin, A. G.; Nierenstein, M. (1905). "CXLI – Some oxidation products of the hydroxybenzoic acids and the constitution of ellagic acid. Part I". Journal of the Chemical Society, Transactions. 87: 1412–1430. doi:10.1039/CT9058701412.
  12. ↑ Nierenstein, M. (1915). "The Formation of Ellagic Acid from Galloyl-Glycine by Penicillium". The Biochemical Journal. 9 (2): 240–244. doi:10.1042/bj0090240. PMC   1258574 . PMID   16742368.
  13. ↑ Nierenstein, M. (1932). "A biological synthesis of m-digallic acid". The Biochemical Journal. 26 (4): 1093–1094. doi:10.1042/bj0261093. PMC   1261008 . PMID   16744910.
  14. ↑ Adam, W. B.; Hardy, F.; Nierenstein, M. (1931). "The Catechin of the Cacao Bean". Journal of the American Chemical Society. 53 (2): 727–728. doi:10.1021/ja01353a041.
  15. ↑ Nierenstein, M.; Potter, J. (1945). "The distribution of myrobalanitannin". The Biochemical Journal. 39 (5): 390–392. doi:10.1042/bj0390390. PMC   1258254 . PMID   16747927.
  16. ↑ Haslam, Edwin (2007). "Vegetable tannins – Lessons of a phytochemical lifetime". Phytochemistry. 68 (22–24): 2713–2721. Bibcode:2007PChem..68.2713H. doi:10.1016/j.phytochem.2007.09.009. PMID   18037145.
  17. ↑ Quideau, Stéphane (22 September 2009). "Why bother with Polyphenols". Groupe Polyphenols. Archived from the original on 10 March 2012. Retrieved 21 August 2012.[ self-published source ]
  18. ↑ Simon Mole (1993). "The Systematic Distribution of Tannins in the Leaves of Angiosperms: A Tool for Ecological Studies". Biochemical Systematics and Ecology. 21 (8): 833–846. Bibcode:1993BioSE..21..833M. doi:10.1016/0305-1978(93)90096-A.
  19. ↑ "Tannin in Tropical Woods". Doat J, Bois. For Tmp., 1978, volume 182, pp. 34–37
  20. ↑ Kadam, S. S.; Salunkhe, D. K.; Chavan, J. K. (1990). Dietary tannins: consequences and remedies. Boca Raton: CRC Press. p. 177. ISBN   978-0-8493-6811-0.
  21. ↑ Brillouet, J.-M. (2013). "The tannosome is an organelle forming condensed tannins in the chlorophyllous organs of Tracheophyta". Annals of Botany. 112 (6): 1003–1014. doi:10.1093/aob/mct168. PMC   3783233 . PMID   24026439.
  22. ↑ "Identification of Molecular Markers Linked to the Trait of Natural Astringency Loss of Japanese Persimmon (Diospyros kaki) Fruit". Shinya Kanzaki, Keizo Yonemori and Akira Sugiura, J. Am. Soc. Hort. Sci., 2001, 126(1), pp. 51–55 (article Archived 4 September 2015 at the Wayback Machine )
  23. ↑ Hättenschwiler, S.; Vitousek, PM (2000). "The role of polyphenols in terrestrial ecosystem nutrient cycling". Trends in Ecology & Evolution. 15 (6): 238–243. doi:10.1016/S0169-5347(00)01861-9. PMID   10802549.
  24. ↑ Verkaik, Eric; Jongkindet, Anne G.; Berendse, Frank (2006). "Short-term and long-term effects of tannins on nitrogen mineralisation and litter decomposition in kauri (Agathis australis (D. Don) Lindl.) forests". Plant and Soil. 287 (1–2): 337–345. Bibcode:2006PlSoi.287..337V. doi:10.1007/s11104-006-9081-8. S2CID   23420808.
  25. ↑ "Tannins, lignins and humic acids in well water on www.gov.ns.ca" (PDF). Archived from the original (PDF) on 17 May 2013.
  26. ↑ Preparing Driftwood for Your Freshwater Aquarium Archived 7 July 2011 at the Wayback Machine
  27. ↑ Pizzi, A.; Conradie, W. E.; Jansen, A. (28 October 1986). "Polyflavonoid tannins ? a main cause of soft-rot failure in CCA-treated timber". Wood Science and Technology. 20 (1): 71–81. doi:10.1007/BF00350695. S2CID   21250123.
  28. ↑ "Driftwood Do's & Don'ts – Pet Fish". Archived from the original on 24 July 2011.
  29. ↑ "Tannin and hardwood flooring". Archived from the original on 17 April 2011.
  30. 1 2 The Tannin Handbook, Ann E. Hagerman, 1998 (book Archived 28 January 2014 at the Wayback Machine )
  31. ↑ "Condensed tannins". Porter L. J., 1989, in Natural Products of Woody Plants I, Rowe J. W. (ed), Springer-Verlag: Berlin, Germany, pages 651–690
  32. ↑ Scalbert, Augustin (1992). "Quantitative Methods for the Estimation of Tannins in Plant Tissues". Plant Polyphenols. pp. 259–280. doi:10.1007/978-1-4615-3476-1_15. ISBN   978-1-4613-6540-2.
  33. ↑ Plant Polyphenols: Synthesis, Properties, Significance. Richard W. Hemingway, Peter E. Laks, Susan J. Branham (page 263)
  34. ↑ Prakashan, Nirali (2009). Pharmacognosy. Nirali Prakashan. ISBN   978-81-963961-5-2.
  35. ↑ "Antibacterial activity of leave extracts of Nymphaea lotus (Nymphaeaceae) on Methicillin resistant Staphylococcus aureus (MRSA) and Vancomycin resistant Staphylococcus aureus (VRSA) isolated from clinical samples". Akinjogunla O. J., Yah C. S., Eghafona N. O. and Ogbemudia F. O., Annals of Biological Research, 2010, 1 (2), pages 174–184
  36. ↑ "Phytochemical Analysis and Antimicrobial Activity Of Scoparia dulcis and Nymphaea lotus". Jonathan Yisa, Australian Journal of Basic and Applied Sciences, 2009, 3(4): pp. 3975–3979
  37. ↑ "Tannin analysis of Acacia mearnsii bark – a comparison of the hide-powder and Stiasny methods". Zheng G.C., Lin Y.L. and Yazaki Y., ACIAR Proceedings Series, 1991, No. 35, pp. 128–131 (abstract Archived 9 July 2014 at the Wayback Machine )
  38. ↑ Study on Fast Determination Content of Condensed Tannin Using Stiasny Method. Chen Xiangming, Chen Heru and Li Weibin, Guangdong Chemical Industry, 2006-07 (abstract Archived 2 April 2015 at the Wayback Machine )
  39. ↑ Guangcheng, Zheng; Yunlu, Lin; Yazaki, Y. (1991). "Bark tannin contents of Acacia mearnsii provenances and the relationship between the hide-powder and the Stiasny methods of estimation". Australian Forestry. 54 (4): 209–211. Bibcode:1991AuFor..54..209G. doi:10.1080/00049158.1991.10674579.
  40. ↑ Leather Chemists' Pocket-Book: A Short Compendium of Analytical Methods. Henry Richardson Procter, Edmund Stiasny and Harold Brumwel, E. & F.N. Spon, Limited, 1912–223 pages (book at Internet Archive Archived 16 December 2016 at the Wayback Machine )
  41. ↑ Chemical study of bark from Commiphora angolensis Engl. Cardoso Do Vale, J., Bol Escola Farm Univ Coimbra Edicao Cient, 1962, volume 3, page 128 (abstract Archived 7 June 2014 at the Wayback Machine )
  42. ↑ Deijs, W. B. (1939). "Catechins isolated from tea leaves". Recueil des Travaux Chimiques des Pays-Bas. 58 (9): 805–830. doi:10.1002/recl.19390580907.
  43. ↑ Löwenthal, J. (December 1877). "Ueber die Bestimmung des Gerbstoffs". Zeitschrift für Analytische Chemie (in German). 16 (1): 33–48. doi:10.1007/BF01355993. S2CID   95511307.
  44. ↑ Spiers, C. W. (January 1914). "The Estimation of Tannin in Cider". The Journal of Agricultural Science. 6 (1): 77–83. doi:10.1017/S0021859600002173. S2CID   85362459.
  45. ↑ Snyder, Harry (October 1893). "Notes on Löwenthal's method for the determination of tanin". Journal of the American Chemical Society. 15 (10): 560–563. doi:10.1021/ja02120a004.
  46. ↑ "Nouvelle methode de dosage du tannin" (PDF). Schweizerische Wochenschrift für Chemie und Pharmacie (in French). Archived from the original (PDF) on 8 August 2014.
  47. ↑ Puupponen-Pimiä, R.; Nohynek, L; Meier, C; Kähkönen, M; Heinonen, M; Hopia, A; Oksman-Caldentey, KM (2001). "Antimicrobial properties of phenolic compounds from berries". Journal of Applied Microbiology. 90 (4): 494–507. doi:10.1046/j.1365-2672.2001.01271.x. PMID   11309059. S2CID   6548208.
  48. ↑ Vattem D. A.; Ghaedian R.; Shetty K. (2005). "Enhancing health benefits of berries through phenolic antioxidant enrichment: focus on cranberry" (PDF). Asia Pac J Clin Nutr. 14 (2): 120–130. PMID   15927928. Archived from the original (PDF) on 28 December 2010.
  49. ↑ Puupponen-Pimiä R.; Nohynek L.; Meier C.; et al. (April 2001). "Antimicrobial properties of phenolic compounds from berries". J. Appl. Microbiol. 90 (4): 494–507. doi:10.1046/j.1365-2672.2001.01271.x. PMID   11309059. S2CID   6548208.
  50. ↑ Łuczaj, Łukasz; Adamczak, Artur; Duda, Magdalena (2014). "Tannin content in acorns (Quercus spp.) from Poland". Dendrology. 72: 103–111. doi: 10.12657/denbio.072.009 . Retrieved 15 September 2020.
  51. ↑ Howes, F. N. (1948). Nuts: Their production and everyday uses. Faber.
  52. ↑ Amarowicz, R.; Pegg, R.B. (2008). Assessment of the antioxidant and pro-oxidant activities of tree nut extracts with a pork model system (PDF). International Congress of Meat Science and Technology. Archived from the original (PDF) on 27 April 2021. Retrieved 9 September 2019.
  53. ↑ Reed, Jess D. (1 May 1995). "Nutritional toxicology of tannins and related polyphenols in forage legumes". Journal of Animal Science. 73 (5): 1516–1528. doi:10.2527/1995.7351516x. PMID   7665384.
  54. ↑ Robert L. Wolke; Marlene Parrish (29 March 2005). What Einstein told his cook 2: the sequel: further adventures in kitchen science. W. W. Norton & Company. p. 433. ISBN   978-0-393-05869-7. Archived from the original on 16 December 2016.
  55. ↑ Clifford MN (2004). "Diet-derived phenols in plasma and tissues and their implications for health". Planta Med. 70 (12): 1103–1114. doi: 10.1055/s-2004-835835 . PMID   15643541.
  56. ↑ Tao Y, García JF, Sun DW (2014). "Advances in wine aging technologies for enhancing wine quality and accelerating wine aging process". Crit Rev Food Sci Nutr. 54 (6): 817–835. doi:10.1080/10408398.2011.609949. PMID   24345051. S2CID   42400092.
  57. ↑ Oz Clarke Encyclopedia of Grapes pp. 155–162 Harcourt Books 2001 ISBN   978-0-15-100714-1
  58. ↑ McRae JM, Kennedy JA (2011). "Wine and grape tannin interactions with salivary proteins and their impact on astringency: a review of current research". Molecules. 16 (3): 2348–2364. doi: 10.3390/molecules16032348 . PMC   6259628 . PMID   21399572.
  59. ↑ Clifford M. N.; Ramirez-Martinez J. R. (1991). "Tannins in wet-processed coffee beans and coffee pulp". Food Chemistry. 40 (2): 191–200. doi:10.1016/0308-8146(91)90102-T.
  60. ↑ "tannin2". www.cider.org.uk. Retrieved 21 March 2019.
  61. ↑ Deshpande, Sudhir S.; Cheryan, Munir; Salunkhe, D. K.; Luh, Bor S. (1 January 1986). "Tannin analysis of food products". C R C Critical Reviews in Food Science and Nutrition. 24 (4): 401–449. doi:10.1080/10408398609527441. ISSN   0099-0248. PMID   3536314.
  62. ↑ "Brewtan range – Natural solutions for beer stabilisation – Application fact-sheet" (PDF). natural-specialities.com. Ajinomoto OmniChem. Archived from the original (PDF) on 14 July 2011. Retrieved 10 March 2010.
  63. ↑ Muller-Harvey I.; McAllan A. B. (1992). "Tannins: Their biochemistry and nutritional properties". Adv. Plant Cell Biochem. Biotechnol. 1: 151–217.
  64. ↑ Tabacco E.; Borreani G.; Crovetto G. M.; Galassi G.; Colombo D.; Cavallarin L. (1 December 2006). "Effect of chestnut tannin on fermentation quality, proteolysis, and protein rumen degradability of alfalfa silage". Journal of Dairy Science. 89 (12): 4736–4746. doi: 10.3168/jds.S0022-0302(06)72523-1 . PMID   17106105.
  65. ↑ Mathieu F.; Jouany J. P. (1993). "Effect of chestnut tannin on the fermentability of soyabean meal nitrogen in the rumen". Ann Zootech. 42 (2): 127. doi: 10.1051/animres:19930210 .
  66. ↑ Shimada, Takuya (23 May 2006). "Salivary Proteins as a Defense Against Dietary Tannins". Journal of Chemical Ecology . 32 (6): 1149–1163. Bibcode:2006JCEco..32.1149S. doi:10.1007/s10886-006-9077-0. PMID   16770710. S2CID   21617545.
  67. ↑ Hoste, Hervé; Meza-OCampos, Griselda; Marchand, Sarah; Sotiraki, Smaragda; Sarasti, Katerina; Blomstrand, Berit M.; Williams, Andrew R.; Thamsborg, Stig M.; Athanasiadou, Spiridoula; Enemark, Heidi L.; Torres Acosta, Juan Felipe; Mancilla-Montelongo, Gabriella; Castro, Carlos Sandoval; Costa-Junior, Livio M.; Louvandini, Helder; Sousa, Dauana Mesquita; Salminen, Juha-Pekka; Karonen, Maarit; Engstrom, Marika; Charlier, Johannes; Niderkorn, Vincent; Morgan, Eric R. (2022). "Use of agro-industrial by-products containing tannins for the integrated control of gastrointestinal nematodes in ruminants". Parasite. 29: 10. doi:10.1051/parasite/2022010. PMC   8884022 . PMID   35225785. Open Access logo PLoS transparent.svg
  68. ↑ "1854 - 1906: The foundation". Silvateam. 15 May 2015. Retrieved 9 August 2022.
  69. ↑ ""The Status of Mangrove Ecosystems: Trends in the Utilisation and Management of Mangrove Resources". D. Macintosh and S. Zisman".
  70. ↑ Marion Kite; Roy Thomson (2006). Conservation of leather and related materials. Butterworth-Heinemann. p. 23. ISBN   978-0-7506-4881-3. Archived from the original on 16 December 2016.
  71. ↑ Lemay, Marie-France (21 March 2013). "Iron Gall Ink". Traveling Scriptorium: A Teaching Kit. Yale University. Archived from the original on 15 February 2017. Retrieved 18 January 2017.
  72. ↑ Prabhu, K. H.; Teli, M. D. (1 December 2014). "Eco-dyeing using Tamarindus indica L. seed coat tannin as a natural mordant for textiles with antibacterial activity". Journal of Saudi Chemical Society. 18 (6): 864–872. doi: 10.1016/j.jscs.2011.10.014 . ISSN   1319-6103.
  73. ↑ Bisanda E. T. N.; Ogola W. O.; Tesha J. V. (August 2003). "Characterisation of tannin resin blends for particle board applications". Cement and Concrete Composites. 25 (6): 593–598. doi:10.1016/S0958-9465(02)00072-0.
  74. ↑ Li, Jingge; Maplesden, Frances (1998). "Commercial production of tannins from radiata pine bark for wood adhesives" (PDF). IPENZ Transactions. 25 (1/EMCh). Archived from the original (PDF) on 22 January 2003.
  75. ↑ Torres J.; Olivares S.; De La Rosa D.; Lima L.; Martínez F.; Munita C. S.; Favaro D. I. T. (1999). "Removal of mercury(II) and methylmercury from solution by tannin adsorbents". Journal of Radioanalytical and Nuclear Chemistry. 240 (1): 361–365. Bibcode:1999JRNC..240..361T. doi:10.1007/BF02349180. S2CID   24811963.
  76. ↑ Takashi Sakaguchia; Akira Nakajimaa (June 1987). "Recovery of Uranium from Seawater by Immobilized Tannin". Separation Science and Technology. 22 (6): 1609–1623. doi:10.1080/01496398708058421.
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