citric acid


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citric acid

or

2-hydroxy-1,2,3-propanetricarboxylic acid,

HO2CCH2C(OH)(CO2H)CH2CO2H, an organic carboxylic acid containing three carboxyl groupscarboxyl group
, in chemistry, functional group that consists of a carbon atom joined to an oxygen atom by a double bond and to a hydroxyl group, OH, by a single bond. Carboxylic acids are compounds whose molecules contain a carboxyl group that is joined to a hydrogen atom, an
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; it is a solid at room temperature, melts at 153°C;, and decomposes at higher temperatures. It is responsible for the tart taste of various fruits in which it occurs, e.g., lemons, limes, oranges, pineapples, and gooseberries. It can be extracted from the juice of citrus fruits by adding calcium oxide (lime) to form calcium citrate, an insoluble precipitate that can be collected by filtration; the citric acid can be recovered from its calcium salt by adding sulfuric acid. It is obtained also by fermentation of glucose with the aid of the mold Aspergillus niger and can be obtained synthetically from acetone or glycerol. Citric acid is used in soft drinks and in laxatives and cathartics. Its salts, the citrates, have many uses, e.g., ferric ammonium citrate is used in making blueprintblueprint,
white-on-blue photographic print, commonly of a working drawing used during building or manufacturing. The plan is first drawn to scale on a special paper or tracing cloth through which light can penetrate.
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 paper. Sour salt, used in cooking, is citric acid.
The Columbia Electronic Encyclopedia™ Copyright © 2013, Columbia University Press. Licensed from Columbia University Press. All rights reserved. www.cc.columbia.edu/cu/cup/
The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.

Citric Acid

 

a tribasic organic hydroxy acid widely distributed in living nature. Citric acid is readily soluble in water and alcohol and poorly soluble in most organic solvents. Its melting point is 153°C; its structural formula is

At 175°C one molecule of water is split off, converting citric acid into aconitic acid. Citric acid forms monosubstituted, disub-stituted, and trisubstituted salts known as citrates. Sodium salts of citric acid are readily soluble in water, while tribasic calcium salts are poorly soluble in water, a fact used in extracting citric acid from solutions.

Citric acid is an essential link in the system of biochemical reactions of cell respiration. Along with other components of the tricarboxylic acid cycle, small quantities of citric acid are found in the mitochondria of all cells. Another function of citric acid involves maintenance of the acid-base balance and the ion composition in an organism. Unlike animals, a number of plants and microorganisms are capable of accumulating large quantities of citric acid (5–6 percent in lemon juice, 3–14 percent in makhorka [Nicotiana rustica] leaves, up to 10 percent in the culture fluid of the fungus Aspergillus niger).

Citric acid is used in the food-processing industry, in medicine (for blood preservation), and in photography; it is also used in various dyeing processes. In industry it is prepared from makhorka (after nicotine extraction) or, more often, by the fermentation of sugar or molasses with the aid of Aspergillus niger or other fungi.

E. P. SEREBRIAKOV

The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.

citric acid

[′si‚trik ′as·əd]
(biochemistry)
C6H8O7·H2O A colorless crystalline or white powdery organic, tricarboxylic acid occurring in plants, especially citrus fruits, and used as a flavoring agent, as an antioxidant in foods, and as a sequestering agent; the commercially produced form melts at 153°C.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.

citric acid

a water-soluble weak tribasic acid found in many fruits, esp citrus fruits, and used in pharmaceuticals and as a flavouring (E330). It is extracted from citrus fruits or made by fermenting molasses and is an intermediate in carbohydrate metabolism. Formula: CH2(COOH)C(OH)(COOH)CH2COOH FORMULA
Collins Discovery Encyclopedia, 1st edition © HarperCollins Publishers 2005
References in periodicals archive ?
1a), there was no significant difference in K release among Ca[Cl.sub.2], HCl and oxalic acid solutions in the short-term experiment but citric acid extracted more K.
Interactions of dietary microbial phytase, citric acid and crude protein level on mineral utilization by rohu (Labeo rohita) juveniles.
Effect of citric acid on other nutrients: Phytic acid (anti-nutritional factor) has found to form complexes with protein (Gifford and Clydesdale, 1990) and it also inhibit the activities of trypsin and pepsin (Caldwell, 1992).
The team wants to analyze these precursors to the citric acid cycle.
To optimize the reaction conditions for [BsPVPP]HS[O.sub.4]-catalyzed esterification reaction of n-butanol with citric acid, a three-level and four-factorial Box-Behnken design was designed to investigate the influences of the reaction conditions on the TBC yield.
The film solution was taken in a glass beaker which contained EAEP residue (4 g/100 ml), 62.5% glycerol (w/w, on EAEP residue basis), different concentrations of citric acid (0%, 10%, 15%, 20%, 25%, or 30% w/w, on a EAEP residue basis), sodium hypophosphite (50% w/w on a citric acid basis), and 100 ml deionized water.
Immediately after treatment of puree with preservatives, the highest pH values of 5.19 and 5.18 were obtained in the control sample at ambient and refrigeration temperatures, respectively, while least values of 4.60 and 4.61 were recorded in the sample with 1 % citric acid at ambient and refrigeration temperatures, respectively.
In the announcement, dated December 12, the EC says a significant change has been identified in the trade patterns of citric acid and related salts between China, Cambodia and the EU.
The same improvement in growth and nutrients absorption by citric acid was correspondingly testified in tilapia (Oreochromis niloticus x O.
Calibration curves were obtained by using authentic standards (glutamic acid, citric acid, isocitric acid, malic acid, succinic acid, fumaric acid, and lactic acid) spiked in a matrix containing deuterated D4-citric acid as internal standard.