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''Toxicodendron succedaneum'', the wax tree, Japanese Hazenoki tree (Sumac or wax tree), sơn in Vietnam or charão in Portuguese, is a flowering plant species in the genus ''Toxicodendron'' found in Asia, although it has been planted elsewhere, most notably Australia and New Zealand. It is a large shrub or tree, up to 8 m tall, somewhat similar to a sumac tree. Because of its beautiful autumn foliage, it has been planted outside Asia as an ornamental plant, often by gardeners who were apparently unaware of the dangers of allergic reactions. It is now officially classified as a noxious weed in Australia and New Zealand. It is one of the city tree symbols of Kurume, Fukuoka, Japan. The larvae of the moths '' Eteoryctis deversa'', ''Caloptilia aurifasciata'', '' Caloptilia protiella'', '' Caloptilia rhois'' and '' Callidrepana patrana'' feed on ''T. succedaneum''. Chemistry The plant produces hinokiflavone, a cytotoxic biflavonoid. Its stems are also a commercial source of fis ...
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Köhler's Medicinal Plants
''Köhler's Medicinal Plants'' (or, ''Köhler's Medizinal-Pflanzen'') is a German herbal written principally by Hermann Adolph Köhler (1834 - 1879, physician and chemist), and edited after his death by Gustav Pabst. The work was first published in the late 19th century by Franz Eugen Köhler of Gera. Its complete title is . Publication history Originally, Köhler published the herbal in two volumes: the first in 1887, the second in 1890. Volume one is illustrated with 84 full-page, multi-colour plates, and volume two with 110. A third volume was added in 1898, entitled ''Neueste Medizinalpflanzen und Verwechslungen'', which is a supplement containing additions and corrections. Among the additions are 80 more colour plates. A fourth volume was announced by the publisher, but never released. All the colour plates in the herbal were produced through a process called ''chromolithography''. The botanical illustrators were Walther Otto Müller, C. F. Schmidt, and K. Gunther. A repri ...
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Flavonoid
Flavonoids (or bioflavonoids; from the Latin word ''flavus'', meaning yellow, their color in nature) are a class of polyphenolic secondary metabolites found in plants, and thus commonly consumed in the diets of humans. Chemically, flavonoids have the general structure of a 15-carbon skeleton, which consists of two phenyl rings (A and B) and a heterocyclic ring (C, the ring containing the embedded oxygen). This carbon structure can be abbreviated C6-C3-C6. According to the IUPAC nomenclature, they can be classified into: *flavonoids or bioflavonoids *isoflavonoids, derived from 3-phenyl chromen-4-one (3-phenyl-1,4-benzopyrone) structure *neoflavonoids, derived from 4-phenylcoumarine (4-phenyl-1,2-benzopyrone) structure The three flavonoid classes above are all ketone-containing compounds and as such, anthoxanthins ( flavones and flavonols). This class was the first to be termed bioflavonoids. The terms flavonoid and bioflavonoid have also been more loosely used to describe non ...
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Solvent
A solvent (s) (from the Latin '' solvō'', "loosen, untie, solve") is a substance that dissolves a solute, resulting in a solution. A solvent is usually a liquid but can also be a solid, a gas, or a supercritical fluid. Water is a solvent for polar molecules and the most common solvent used by living things; all the ions and proteins in a cell are dissolved in water within the cell. The quantity of solute that can dissolve in a specific volume of solvent varies with temperature. Major uses of solvents are in paints, paint removers, inks, and dry cleaning. Specific uses for organic solvents are in dry cleaning (e.g. tetrachloroethylene); as paint thinners (toluene, turpentine); as nail polish removers and solvents of glue (acetone, methyl acetate, ethyl acetate); in spot removers (hexane, petrol ether); in detergents ( citrus terpenes); and in perfumes (ethanol). Solvents find various applications in chemical, pharmaceutical, oil, and gas industries, including in chemical syn ...
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Olein
Triolein is a symmetrical triglyceride derived from glycerol and three units of the unsaturated fatty acid oleic acid. Most triglycerides are unsymmetrical, being derived from mixtures of fatty acids. Triolein represents 4–30% of olive oil. Triolein is also known as glyceryl trioleate and is one of the two components of Lorenzo's oil. The oxidation of triolein is according to the formula: : + 80 → 57 + 52 This gives a respiratory quotient The respiratory quotient (RQ or respiratory coefficient) is a dimensionless number used in calculations of basal metabolic rate (BMR) when estimated from carbon dioxide production. It is calculated from the ratio of carbon dioxide produced by the b ... of 57/80 or 0.7125. The heat of combustion is per mole or per gram. Per mole of oxygen it is . References Triglycerides {{ester-stub ...
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Stearin
Stearin , or tristearin, or glyceryl tristearate is an odourless, white powder. It is a triglyceride derived from three units of stearic acid. Most triglycerides are derived from at least two and more commonly three different fatty acids. Like other triglycerides, stearin can crystallise in three polymorphs. For stearin, these melt at 54 (α-form), 65, and (β-form). Note that stearin is also used to mean the solid component of an oil or fat that can be separated into components that melt at higher (the stearin) and lower (the olein) temperatures. This is the usage meant in an example such as palm stearin. Occurrence Stearin is obtained from animal fats created as a byproduct of processing beef. It can also be found in tropical plants such as palm. It can be partially purified by dry fractionation by pressing tallow or other fatty mixtures, leading to separation of the higher melting stearin-rich material from the liquid, which is typically enriched in fats derived from ole ...
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Palmitin
Tripalmitin is a triglyceride derived from the fatty acid palmitic acid Palmitic acid (hexadecanoic acid in IUPAC nomenclature) is a fatty acid with a 16-carbon chain. It is the most common saturated fatty acid found in animals, plants and microorganisms.Gunstone, F. D., John L. Harwood, and Albert J. Dijkstra. The Li .... References Triglycerides Palmitate esters {{ester-stub ...
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Japan Wax
Japan wax (木蝋 ''Mokurō''), also known as sumac wax, sumach wax, vegetable wax, China green tallow, and Japan tallow, is a pale-yellow, waxy, water-insoluble solid with a gummy feel, obtained from the berries of certain sumacs native to Japan and China, such as ''Toxicodendron vernicifluum'' (lacquer tree) and ''Toxicodendron succedaneum'' (Japanese wax tree).Claude Leray "Waxes" in Kirk-othmer encyclopedia of chemical technology 2006, Wiley-VCH, Weinheim. Japan wax is a byproduct of lacquer manufacture. The fruits of the ''Toxicodendron'' trees are harvested, steamed, and pressed for the waxy substance which hardens when cool. It is not a true wax but a fat that contains 95% palmitin. Japan wax is sold in flat squares or disks and has a rancid odor. It is extracted by expression and heat, or by the action of solvents. Uses Japan wax is used in candles, furniture polishes, floor waxes, wax matches, soaps, food packaging, pharmaceuticals, cosmetics, pastels, crayons, buffin ...
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Lacquer Painting
Lacquer painting is a form of painting with lacquer which was practised in East Asia for decoration on lacquerware, and found its way to Europe and the Western World both via Persia and the Middle East and by direct contact with Continental Asia. The artistic form was revived and developed as a distinct genre of fine art painting by Vietnamese artists in the 1930s; the genre is known in Vietnamese as "sơn mài." Technique Making a lacquer painting may take several months depending on the technique used and the number of layers of lacquer. In Vietnam's ''sơn mài'' lacquer painting, a black board is prepared first. Then colour chalks are used on the prepared board for base sketch. Needles can also be used for carving the base sketch as an alternative. In lacquer painting, eggshells are used as white colour due to the lack of pure white colour in lacquer. Layers of clear varnish can be applied optionally depending on the purpose of the painting. Polishing is done in the end to reve ...
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Lacquer
Lacquer is a type of hard and usually shiny coating or finish applied to materials such as wood or metal. It is most often made from resin extracted from trees and waxes and has been in use since antiquity. Asian lacquerware, which may be called "true lacquer", are objects coated with the treated, dyed and dried sap of ''Toxicodendron vernicifluum'' or related trees, applied in several coats to a base that is usually wood. This dries to a very hard and smooth surface layer which is durable, waterproof, and attractive in feel and look. Asian lacquer is sometimes painted with pictures, inlaid with shell and other materials, or carved, as well as dusted with gold and given other further decorative treatments. In modern techniques, lacquer means a range of clear or pigmented coatings that dry by solvent evaporation to produce a hard, durable finish. The finish can be of any sheen level from ultra matte to high gloss, and it can be further polished as required. Lacquer finishes ...
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Nature (journal)
''Nature'' is a British weekly scientific journal founded and based in London, England. As a multidisciplinary publication, ''Nature'' features peer-reviewed research from a variety of academic disciplines, mainly in science and technology. It has core editorial offices across the United States, continental Europe, and Asia under the international scientific publishing company Springer Nature. ''Nature'' was one of the world's most cited scientific journals by the Science Edition of the 2019 ''Journal Citation Reports'' (with an ascribed impact factor of 42.778), making it one of the world's most-read and most prestigious academic journals. , it claimed an online readership of about three million unique readers per month. Founded in autumn 1869, ''Nature'' was first circulated by Norman Lockyer and Alexander Macmillan as a public forum for scientific innovations. The mid-20th century facilitated an editorial expansion for the journal; ''Nature'' redoubled its efforts in exp ...
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Fisetin
Fisetin (7,3′,4′- flavon-3-ol) is a plant flavonol from the flavonoid group of polyphenols. It can be found in many plants, where it serves as a yellow/ochre colouring agent. It is also found in many fruits and vegetables, such as strawberries, apples, persimmons, onions and cucumbers. Its chemical formula was first described by Austrian chemist Josef Herzig in 1891. The biological activity of fisetin has been studied in many laboratory assays; like other polyphenols it has many activities. Biological sources Fisetin can be found in a wide variety of plants. It is found in Eudicotyledons, such as trees and shrubs in the family Fabaceae, such as the acacias ''Acacia greggii'' and ''Acacia berlandieri'', the parrot tree ('' Butea frondosa''), the honey locust (''Gleditsia triacanthos''), members of the family Anacardiaceae such as the ''Quebracho colorado'' and species of the genus '' Rhus'', which contains the sumacs. Along with myricetin, fisetin provides the color of the tra ...
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