Malic acid
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 DL-Malic acid | |
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| Preferred IUPAC name 2-Hydroxybutanedioic acid | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.027.293 |
| EC Number |
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| E number | E296 (preservatives) |
| 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] pKa3 = 14.5[3] |
| Hazards | |
| GHS labelling: | |
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| Flash point | 203 °C[4] |
| Related compounds | |
Other anions |
Malate |
Related carboxylic acids |
Succinic acid Tartaric acid Fumaric acid |
Related compounds |
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). | |
Malic acid is an organic compound with the molecular formula HO2CCH(OH)CH2CO2H. 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 a metabolic intermediate in the citric acid cycle.
Etymology
The word 'malic' is derived from Latin mālum, meaning 'apple'. The related Latin word mālus, meaning 'apple tree', is used as the name of the genus Malus, which includes all apples and crabapples;[5] and is the origin of other taxonomic classifications such as Maloideae, Malinae, and Maleae.
Biochemistry
L-Malic acid is the naturally occurring form, whereas a mixture of L- and D-malic acid is produced synthetically.
L-Malic acid (S)
D-Malic acid (R)
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.[6] 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.[7][8] In German it is named Äpfelsäure (or Apfelsäure) after plural or singular of a sour thing from the apple fruit, but the salt(s) are called Malat(e). Malic acid is the main acid in many fruits, including apricots, blackberries, blueberries, cherries, grapes, mirabelles, peaches, pears, plums, and quince,[9] and is present in lower concentrations in other fruits, such as citrus. 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.[10] 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 the compound responsible for the tart flavor of sumac spice. It is also a component of some artificial vinegar flavors, such as "salt and vinegar" flavored potato chips.[11]
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.[12]
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,[13] US[14] and Australia and New Zealand[15] (where it is listed by its INS number 296).
Malic acid contains 10 kJ (2.39 kilocalories) of energy per gram.[16]
Production and main reactions
Racemic malic acid is produced industrially by the double hydration of maleic anhydride. In 2000, American production capacity was 5,000 tons per year. The enantiomers may be separated by chiral resolution of the racemic mixture. S-Malic acid is obtained by fermentation of fumaric acid.[17]
Self-condensation of malic acid in the presence of fuming sulfuric acid gives the pyrone coumalic acid:[18]
- 2 HO2CCH(OH)CH2CO2H → HO2CC4H3O2 + 2 CO + 4 H2O
Carbon monoxide and water are liberated during this reaction.
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.
L-malic acid is used to resolve α-phenylethylamine, a versatile resolving agent in its own right.[19]
Plant defense
Soil supplementation with molasses increases microbial synthesis of malic acid. This is thought to occur naturally as part of soil microbe suppression of disease, so soil amendment with molasses can be used as a crop treatment in horticulture.[20]
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
- Citrate–malate shuttle
- 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.
- ^ Data for biochemical research (3rd ed.). Oxford: Clarendon Press. 1986. ISBN 0-19-855358-7. OCLC 11865673.
- ^ Silva, Andre M. N.; Kong, Xiaole; Hider, Robert C. (2009). "Determination of the pKa value of the hydroxyl group in the α-hydroxycarboxylates citrate, malate and lactate by 13C NMR: implications for metal coordination in biological systems". BioMetals. 22 (5): 771–778. doi:10.1007/s10534-009-9224-5. ISSN 0966-0844. PMID 19288211.
- ^ "DL-Malic acid - (DL-Malic acid) SDS". Merck Millipore.
- ^ Peffley, Ellen. "Peffley: Crabapples steal the show in autumn". Lubbock Avalanche-Journal. Retrieved 2022-08-08.
- ^ 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.
- ^ Jensen, William B. (June 2007). "The Origin of the Names Malic, Maleic, and Malonic Acid". Journal of Chemical Education. 84 (6): 924. Bibcode:2007JChEd..84..924J. doi:10.1021/ed084p924. ISSN 0021-9584.
- ^ Tabelle I of "Fruchtsäuren". Wissenschaft Online Lexikon der Biologie. Archived from the original on May 15, 2016.
- ^ Ough, C. S. (1988). Methods for analysis of musts and wines (2nd ed.). New York: J. Wiley. p. 67. ISBN 0-471-62757-7. OCLC 16866762.
- ^ "The Science Behind Salt and Vinegar Chips". seriouseats.com.
- ^ Malic Acid Archived 2018-06-25 at the Wayback Machine, Bartek Ingredients (retrieved 2 February 2012)
- ^ UK Food Standards Agency: "Current EU approved additives and their E Numbers". Retrieved 2011-10-27.
- ^ "Food Additive Status List". FDA. 26 August 2021. Retrieved 5 May 2022.
- ^ Australia New Zealand Food Standards Code"Standard 1.2.4 - Labelling of ingredients". 8 September 2011. 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 978-92-5-104949-5. Retrieved 10 February 2014.
- ^ Karlheinz Miltenberge. "Hydroxycarboxylic Acids, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a13_507. ISBN 978-3527306732.
- ^ 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.
- ^ Rosskopf, Erin; Di Gioia, Francesco; Hong, Jason C.; Pisani, Cristina; Kokalis-Burelle, Nancy (2020-08-25). "Organic Amendments for Pathogen and Nematode Control". Annual Review of Phytopathology. 58 (1). Annual Reviews: 277–311. doi:10.1146/annurev-phyto-080516-035608. ISSN 0066-4286. PMID 32853099. S2CID 221360634.
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