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Malic acid

DL-Malic acid
Names
Preferred IUPAC name 2-Hydroxybutanedioic acid
Other names Hydroxybutanedioic acid 2-Hydroxysuccinic acid L-Malic acid D-Malic acid (–)-Malic acid (+)-Malic acid (S)-Hydroxybutanedioic acid (R)-Hydroxybutanedioic acid
Identifiers
CAS Number	617-48-1 N 6915-15-7 N
3D model (JSmol)	Interactive image
ChEBI	CHEBI:6650 Y
ChEMBL	ChEMBL1455497 N
ChemSpider	510 Y 83793 D-(+)-malic acid Y 193317 L-(–)-malic acid Y
ECHA InfoCard	100.027.293
EC Number	230-022-8
E number	E296 (preservatives)
IUPHAR/BPS	2480
KEGG	C00149 N
PubChem CID	525
UNII	817L1N4CKP Y
CompTox Dashboard (EPA)	DTXSID0027640
InChI InChI=1S/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9) Y Key: BJEPYKJPYRNKOW-UHFFFAOYSA-N Y InChI=1/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9) Key: BJEPYKJPYRNKOW-UHFFFAOYAM
SMILES O=C(O)CC(O)C(=O)O
Properties
Chemical formula	C4H6O5
Molar mass	7002134086999999999♠134.087 g·mol−1
Density	1.609 g cm−3
Melting point	130 °C (266 °F; 403 K)
Solubility in water	558 g/L (at 20 °C)[1]
Acidity (pKa)	pKa1 = 3.40, pKa2 = 5.20[2]
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).
N verify (what is YN ?)
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 'malus', 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, 'Äpfelsäure' meaning 'apple acid'.

Biochemistry

L-Malic acid is the naturally occurring form, whereas a mixture of L- and D-malic acid is produced synthetically.

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  L-Malic acid
  

  
  


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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.^[3]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.^[4][5]
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^[6] and is present in lower concentrations in other fruits, such as citrus.^[7] 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.^[8] 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.^[9]

In citrus, fruits produced in organic farming contain higher levels of malic acid than fruits produced in conventional agriculture^[7].

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.^[10]

Malic acid, when added to food products, is denoted by E number E296. Malic acid is the source of extreme tartness in United States-produced confectionery, the so-called extreme candy. It is also 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,^[11] US^[12] and Australia and New Zealand^[13] (where it is listed by its INS number 296).

Malic acid provides 10 kJ (2.39 Calories) of energy per gram during digestion.^[14]

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.^[15]

Self-condensation of malic acid with fuming sulfuric acid gives the pyrone coumalic acid:^[16]

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.

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles. ^{[§ 1]}

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|{{{bSize}}}px|alt=Glycolysis and Gluconeogenesis edit]]

Glycolysis and Gluconeogenesis edit

1. 
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See also

• Acids in wine


• Crassulacean acid metabolism


• Malate-aspartate shuttle

References

External links

• Malic acid MS Spectrum


• Calculator: Water and solute activities in aqueous malic acid

v t e Citric acid cycle metabolic pathway
Acetyl-CoA + H 2O	Oxaloacetate NADH +H+ NAD+ Malate   H2O Fumarate FADH2 FAD Succinate CoA + ATP (GTP) Pi + ADP (GDP) Succinyl-CoA
			NADH + H+ + CO 2
CoA			NAD+
	Citrate   H 2O cis-Aconitate H 2O   Isocitrate NAD(P)+ NAD(P)H +  H+ Oxalosuccinate   CO 2 2-oxoglutarate