Malic acid
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 DL-Malic acid
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| Names | |
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| Preferred IUPAC name
2-Hydroxybutanedioic acid | |
Other names
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.027.293 
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| EC Number |
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| E number | E296 (preservatives) |
IUPHAR/BPS
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C4H6O5 | |
| Molar mass | 134.09 g/mol |
| Appearance | Colorless |
| Density | 1.609 g⋅cm−3 |
| Melting point | 130 °C (266 °F; 403 K) |
| 558 g/L (at 20 °C)[1] | |
| Acidity (pKa) | pKa1 = 3.40 pKa2 = 5.20[2] |
| Hazards | |
| GHS pictograms | 
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| Flash point | 203 °C[3] |
| Related compounds | |
Other anions
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Malate |
Related carboxylic acids
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Succinic acid Tartaric acid Fumaric acid |
Related compounds
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Butanol Butyraldehyde Crotonaldehyde Sodium malate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 (what is   ?)
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| Infobox references | |
Malic acid is an organic compound with the molecular formula C4H6O5. It is a dicarboxylic acid that is made by all living organisms, contributes to the sour taste of fruits, and is used as a food additive. Malic acid has two stereoisomeric forms (L- and D-enantiomers), though only the L-isomer exists naturally. The salts and esters of malic acid are known as malates. The malate anion is an intermediate in the citric acid cycle.
Etymology[]
The word 'malic' is derived from Latin 'mālum', meaning 'apple'. It is also the name of the genus Malus, which includes all apples and crabapples; and the origin of other taxonomic classifications such as Maloideae, Malinae, and Maleae. This derivation is also seen in the traditional German name for malic acid, 'Äpfels��ure' meaning 'apple acid' as well as in modern Greek, 'mēlicon oxy' (Μηλικόν οξύ), after the original European discovery of apples in modern-day Kazakhstan 2350 years ago by Alexander the Great's expeditionary foray into Asia.[citation needed]
Biochemistry[]
L-Malic acid is the naturally occurring form, whereas a mixture of L- and D-malic acid is produced synthetically.
L-Malic acid 
D-Malic acid
Malate plays an important role in biochemistry. In the C4 carbon fixation process, malate is a source of CO2 in the Calvin cycle. In the citric acid cycle, (S)-malate is an intermediate, formed by the addition of an -OH group on the si face of fumarate. It can also be formed from pyruvate via anaplerotic reactions.
Malate is also synthesized by the carboxylation of phosphoenolpyruvate in the guard cells of plant leaves. Malate, as a double anion, often accompanies potassium cations during the uptake of solutes into the guard cells in order to maintain electrical balance in the cell. The accumulation of these solutes within the guard cell decreases the solute potential, allowing water to enter the cell and promote aperture of the stomata.
In food[]
Malic acid was first isolated from apple juice by Carl Wilhelm Scheele in 1785.[4] Antoine Lavoisier in 1787 proposed the name acide malique, which is derived from the Latin word for apple, mālum—as is its genus name Malus.[5][6] In German it is named Äpfelsäure (or Apfelsäure) after plural or singular of the fruit apple, but the salt(s) Malat(e). Malic acid is the main acid in many fruits, including apricots, blackberries, blueberries, cherries, grapes, mirabelles, peaches, pears, plums, and quince[7] and is present in lower concentrations in other fruits, such as citrus.[8] It contributes to the sourness of unripe apples. Sour apples contain high proportions of the acid. It is present in grapes and in most wines with concentrations sometimes as high as 5 g/l.[9] It confers a tart taste to wine; the amount decreases with increasing fruit ripeness. The taste of malic acid is very clear and pure in rhubarb, a plant for which it is the primary flavor. It is also a component of some artificial vinegar flavors, such as "salt and vinegar" flavored potato chips.[10]
In citrus, fruits produced in organic farming contain higher levels of malic acid than fruits produced in conventional agriculture.[8]
The process of malolactic fermentation converts malic acid to much milder lactic acid. Malic acid occurs naturally in all fruits and many vegetables, and is generated in fruit metabolism.[11]
Malic acid, when added to food products, is denoted by E number E296. It is sometimes used with or in place of the less sour citric acid in sour sweets. These sweets are sometimes labeled with a warning stating that excessive consumption can cause irritation of the mouth. It is approved for use as a food additive in the EU,[12] US[13] and Australia and New Zealand[14] (where it is listed by its INS number 296).
Malic acid contains 10 kJ (2.39 kilocalories) of energy per gram.[15]
Production and main reactions[]
Racemic malic acid is produced industrially by the double hydration of maleic anhydride. In 2000, American production capacity was 5000 tons per year. Both enantiomers may be separated by chiral resolution of the racemic mixture, and the (S)- enantiomer may be specifically obtained by fermentation of fumaric acid.[16]
Self-condensation of malic acid with fuming sulfuric acid gives the pyrone coumalic acid:[17]
Malic acid was important in the discovery of the Walden inversion and the Walden cycle, in which (−)-malic acid first is converted into (+)-chlorosuccinic acid by action of phosphorus pentachloride. Wet silver oxide then converts the chlorine compound to (+)-malic acid, which then reacts with PCl5 to the (−)-chlorosuccinic acid. The cycle is completed when silver oxide takes this compound back to (−)-malic acid.
Uses[]
L-malic acid is used to resolve α-phenylethylamine, a versatile resolving agent in its own right.[18]
Interactive pathway map[]
Click on genes, proteins and metabolites below to link to respective articles.[§ 1]
- ^ The interactive pathway map can be edited at WikiPathways: "GlycolysisGluconeogenesis_WP534".
See also[]
- Acids in wine
- Crassulacean acid metabolism
- Malate-aspartate shuttle
- Maleic acid, resulting from malic acid dehydration
References[]
- ^ "chemBlink Database of Chemicals from Around the World". chemblink.com. Archived from the original on 2009-01-22.
- ^ Dawson, R. M. C. et al., Data for Biochemical Research, Oxford, Clarendon Press, 1959.
- ^ "DL-Malic acid - (DL-Malic acid) SDS". Merck Millipore.
- ^ Carl Wilhelm Scheele (1785) "Om Frukt- och Bår-syran" (On fruit and berry acid), Kongliga Vetenskaps Academiens Nya Handlingar (New Proceedings of the Royal Academy of Science), 6 : 17-27. From page 21: " ... vil jag hådanefter kalla den Åple-syran." ( ... I will henceforth call it apple acid.)
- ^ de Morveau, Lavoisier, Bertholet, and de Fourcroy, Méthode de Nomenclature Chimique (Paris, France: Cuchet, 1787), p. 108.
- ^ The Origin of the Names Malic, Maleic, and Malonic Acid Jensen, William B. J. Chem. Educ. 2007, 84, 924. Abstract
- ^ Tabelle I of "Fruchtsäuren". Wissenschaft Online Lexikon der Biologie. Archived from the original on May 15, 2016.
- ^ Jump up to: a b Duarte, A.M.; Caixeirinho, D.; Miguel, M.G.; Sustelo, V.; Nunes, C.; Fernandes, M.M.; Marreiros, A. (2012). "Organic Acids Concentration in Citrus Juice from Conventional Versus Organic Farming". Acta Horticulturae (933): 601–606. doi:10.17660/actahortic.2012.933.78. hdl:10400.1/2790. ISSN 0567-7572.
- ^ "Methods For Analysis of Musts and Wines", Ough and Amerine, John Wiley and Sons, 2nd Edition, 1988, page 67
- ^ "The Science Behind Salt and Vinegar Chips". seriouseats.com.
- ^ Malic Acid Archived 2018-06-25 at the Wayback Machine, (retrieved 2 February 2012)
- ^ UK Food Standards Agency: "Current EU approved additives and their E Numbers". Retrieved 2011-10-27.
- ^ US Food and Drug Administration: "Listing of Food Additives Status Part II". Retrieved 2011-10-27.
- ^ Australia New Zealand Food Standards Code"Standard 1.2.4 - Labelling of ingredients". Retrieved 2011-10-27.
- ^ Greenfield, Heather; Southgate, D.A.T. (2003). Food composition data: production, management and use (2 ed.). Rome: Food and Agriculture Organization of the United Nations. p. 146. ISBN 9789251049495. Retrieved 10 February 2014.
- ^ Karlheinz Miltenberge. "Hydroxycarboxylic Acids, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a13_507.
- ^ Richard H. Wiley, Newton R. Smith (1951). "Coumalic acid". Organic Syntheses. 31: 23. doi:10.15227/orgsyn.031.0023.
- ^ A. W. Ingersoll (1937). "D- and l-α-Phenylethylamine". Organic Syntheses. 17: 80. doi:10.15227/orgsyn.017.0080.
External links[]
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- Cellular respiration
- Citric acid cycle compounds
- Cosmetics chemicals
- Dicarboxylic acids
- Food acidity regulators
- Alpha hydroxy acids
- Acids in wine
- Chelating agents
- E-number additives