Lactic acid

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Lactic acid
L-Lactic acid

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DL-Lactic acid
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This page is a soft redirect. Names

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IUPAC name
2-Hydroxypropanoic acid
Other names
Milk acid
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ATC code G01AD01
QP53AG02 50-21-5 7pxY
79-33-4 (L) 7pxY
10326-41-7 (D) 7pxY ChEBI CHEBI:422 7pxY ChEMBL ChEMBL330546 7pxY ChemSpider 96860 7pxY Jmol-3D images Image Template:Chembox UNII colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Properties

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C3H6O3 Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1 Melting point L: 53 °C
D: 53 °C
D/L: 16.8 °C Boiling point Script error: No such module "convert". @ 12 mmHg Acidity (pKa) 3.86[1] colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Thermochemistry

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1361.9 kJ/mol, 325.5 kcal/mol, 15.1 kJ/g, 3.61 kcal/g colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Related compounds

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Other anions
lactate acetic acid
glycolic acid
propionic acid
3-hydroxypropanoic acid
malonic acid
butyric acid
hydroxybutyric acid
Related compounds
sodium lactate colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Hazards

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GHS pictograms 60px[2] H315, H318[2] P280, P305+351+338[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 14pxN verify (what is10pxY/10pxN?) Infobox references

Lactic acid is a chemical compound that plays a role in various biochemical processes. It was first isolated in 1780 by the Swedish chemist Carl Wilhelm Scheele. Lactic acid is a carboxylic acid with the chemical formula C2H4OHCOOH. It has a hydroxyl group adjacent to the carboxyl group, making it an alpha hydroxy acid (AHA).

In solution, it can lose a proton from the carboxyl group, producing the lactate ion CH3CH(OH)COO. Compared to acetic acid, its pKa is 1 unit less, meaning lactic acid deprotonates ten times more easily than acetic acid does. This higher acidity is the consequence of the intramolecular hydrogen bridge between the α-hydroxyl and the carboxylate group, making the latter less capable of strongly attracting its proton.

Lactic acid is chiral and has two optical isomers. One is known as L-(+)-lactic acid or (S)-lactic acid and the other, its mirror image, is D-(−)-lactic acid or (R)-lactic acid. A mixture of the two in equal amounts is called DL-lactic acid.

Lactic acid is hygroscopic. DL-lactic acid is miscible with water and with ethanol above its melting point which is around 17 or 18 °C. D-lactic acid and L-lactic acid have a higher melting point.

In animals, L-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation during normal metabolism and exercise. It does not increase in concentration until the rate of lactate production exceeds the rate of lactate removal, which is governed by a number of factors, including monocarboxylate transporters, concentration and isoform of LDH, and oxidative capacity of tissues. The concentration of blood lactate is usually 1–2 mmol/L at rest, but can rise to over 20 mmol/L during intense exertion.[citation needed]

In industry, lactic acid fermentation is performed by lactic acid bacteria, which convert simple carbohydrates such as glucose, sucrose, or galactose to lactic acid. These bacteria can also grow in the mouth; the acid they produce is responsible for the tooth decay known as caries.[3][4][5][6]

In medicine, lactate is one of the main components of lactated Ringer's solution and Hartmann's solution. These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood. It is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burn injury.


Lactic acid was refined for the first time by the Swedish chemist Carl Wilhelm Scheele in 1780 from sour milk. In 1808, Jöns Jacob Berzelius discovered that lactic acid (actually L-lactate) also is produced in muscles during exertion.[7] Its structure was established by Johannes Wislicenus in 1873.

In 1856, Louis Pasteur discovered Lactobacillus and its role in the making of lactic acid. Lactic acid started to be produced commercially by the German pharmacy Boehringer Ingelheim in 1895.

In 2006, global production of lactic acid reached 275,000 tonnes with an average annual growth of 10%.[8]

Exercise and lactate

During power exercises such as sprinting, when the rate of demand for energy is high, glucose is broken down and oxidized to pyruvate, and lactate is then produced from the pyruvate faster than the body can process it, causing lactate concentrations to rise. The production of lactate is a beneficial process because it regenerates NAD+ (pyruvate is reduced to lactate while NADH is oxidized to NAD+), which is used up in oxidation of glyceraldehyde 3-phosphate during creation of pyruvate from glucose, and this ensures that energy production is maintained and exercise can continue. (During intense exercise, the respiratory chain cannot keep up with the amount of hydrogen atoms that join to form NADH, and cannot regenerate NAD+ quickly enough.)

The resulting lactate can be used in two ways:

However, lactate is continually formed even at rest and during moderate exercise. This occurs due to metabolism in red blood cells that lack mitochondria, and limitations resulting from the enzyme activity that occurs in muscle fibers having a high glycolytic capacity.[10]

Robergs et al. have discussed the creation of H+ during exercise,[11] and claim the idea that lactic acid causes acidosis is a "construct" or myth, pointing out that part of the H+ comes from ATP hydrolysis (ATP−4 + H2O → ADP−3 + HPO4−2 + H+), and that reducing pyruvate to lactate (pyruvate + NADH + H+ → lactate + NAD+) actually consumes H+. Lindinger et al.[12] claimed that Robergs et al. ignored the causative factors of the increase in [H+]. The production of lactate from a neutral molecule would increase [H+] to maintain electroneutrality. However, lactate is produced from pyruvate, which has the same charge: "Lactate− production is not associated with a stoichiometrically equivalent net production of protons (H+)".[12]
It is pyruvate production from neutral glucose that generates H+:

C6H12O6 + 2 NAD+ + 2 ADP−3 + 2 HPO4−2 → 2 CH3COCOO + 2 H+ + 2 NADH + 2 ATP−4 + 2 H2O

Subsequent lactate production absorbs these protons:

2 CH3COCOO + 2 H+ + 2 NADH → 2 CH3CHOHCOO + 2 NAD+


C6H12O6 + 2 NAD+ + 2 ADP−3 + 2 HPO4−2 → 2 CH3COCOO + 2 H+ + 2 NADH + 2 ATP−4 + 2 H2O → 2 CH3CHOHCOO + 2 NAD+ + 2 ATP−4 + 2 H2O

Although the reaction glucose → 2 lactate + 2 H+ releases two H+ when viewed on its own, the H+ are absorbed in the creation of ATP. The absorbed acidity is released during subsequent hydrolysis of ATP: ATP−4 + H2O → ADP−3 + HPO4−2 + H+. Overall, [H+] does increase.

The creation of CO2 during respiration also causes an increase in [H+].

Brain metabolism

Although glucose is usually assumed to be the main energy source for living tissues, there are some indications that it is lactate, and not glucose, that is preferentially metabolized by neurons in the brain of several mammalian species (the notable ones being mice, rats, and humans).[13][14] According to the lactate-shuttle hypothesis, glial cells are responsible for transforming glucose into lactate, and for providing lactate to the neurons.[15][16] Because of this local metabolic activity of glial cells, the extracellular fluid immediately surrounding neurons strongly differs in composition from the blood or cerebro-spinal fluid, being much richer with lactate, as was found in microdialysis studies.[13]

The role of lactate for brain metabolism seems to be even more important at early stages of development (prenatal and early postnatal), with lactate at these stages having higher concentrations in body liquids, and being utilized by the brain preferentially over glucose.[13] It was also hypothesized that lactate may exert a strong action over GABAergic networks in the developing brain, making them more inhibitory than it was previously assumed,[17] acting either through better support of metabolites,[13] or alterations in base intracellular pH levels,[18][19] or both.[20]

A more recent paper by Zilberter's group looked directly at the energy metabolism features in brain slices of mice and showed that beta-hydroxybutyrate, lactate, and pyruvate acted as oxidative energy substrates, causing an increase in the NAD(P)H oxidation phase, that glucose was insufficient as an energy carrier during intense synaptic activity and, finally, that lactate can be an efficient energy substrate capable of sustaining and enhancing brain aerobic energy metabolism in vitro.[21] The paper was positively commented by Kasischke: "The study by Ivanov et al. (2011) also provides novel data on biphasic NAD(P)H fluorescence transients, an important physiological response to neural activation that has been reproduced in many studies and that is believed to originate predominately from activity-induced concentration changes to the cellular NADH pools."[22]

Blood testing

File:Blood values sorted by mass and molar concentration.png
Reference ranges for blood tests, comparing lactate content (shown in violet at center-right) to other constituents in human blood.

Blood tests for lactate are performed to determine the status of the acid base homeostasis in the body. Blood sampling for this purpose is often by arterial blood sampling (even if it is more difficult than venipuncture), because lactate differs substantially between arterial and venous levels, and the arterial level is more representative for this purpose.[citation needed]

Reference ranges
Lower limit Upper limit Unit
Venous 4.5[23] 19.8[23] mg/dL
0.5[24] 2.2[24] mmol/L
Arterial 4.5[23] 14.4[23] mg/dL
0.5[24] 1.6[24] mmol/L

During childbirth, lactate levels in the fetus can be quantified by fetal scalp blood testing.

Polymer precursor

Main article: polylactic acid

Two molecules of lactic acid can be dehydrated to lactide, a cyclic lactone. A variety of catalysts can polymerize lactide to either heterotactic or syndiotactic polylactide, which as biodegradable polyesters with valuable (inter alia) medical properties are currently attracting much attention.

Lactic acid is used also as a monomer for producing polylactic acid (PLA), which later has developed application as biodegradable plastic. This kind of plastic is a good option for substituting conventional plastic produced from petroleum oil because of low emission of carbon dioxide. The commonly used process in producing lactic acid is via fermentation, and, later, to obtain the polylactic acid, the polymerization process follows.

Pharmaceutical and cosmetic applications

Lactic acid is also employed in pharmaceutical technology to produce water-soluble lactates from otherwise-insoluble active ingredients. It finds further use in topical preparations and cosmetics to adjust acidity and for its disinfectant and keratolytic properties.


Lactic acid is found primarily in sour milk products, such as koumiss, laban, yogurt, kefir, some cottage cheeses, and kombucha. The casein in fermented milk is coagulated (curdled) by lactic acid. Lactic acid is also responsible for the sour flavor of sourdough breads. This acid is used in beer brewing to lower the wort pH in order to reduce some undesirable substances such as tannins without giving off-flavors such as citric acid and increase the body of the beer.[citation needed] Some brewers and breweries will use food grade lactic acid to lower the pH in finished alcohols.[citation needed]

In winemaking, a bacterial process, natural or controlled, is often used to convert the naturally present malic acid to lactic acid, to reduce the sharpness and for other flavor-related reasons. This malolactic fermentation is undertaken by the family of lactic acid bacteria.

As a food additive it is approved for use in the EU,[25] USA[26] and Australia and New Zealand;[27] it is listed by its INS number 270 or as E number E270. Lactic acid is used as a food preservative, curing agent, and flavoring agent.[28] It is an ingredient in processed foods and is used as a decontaminant during meat processing.[29] Lactic acid is produced commercially by fermentation of carbohydrates such as glucose, sucrose, or lactose, or by chemical synthesis.[28] Carbohydrate sources include corn, beets, and cane sugar.[30]


Lactic acid has gained importance in the detergent industry the last decade. It is a good descaler, soap-scum remover, and a registered anti-bacterial agent. It is also economically beneficial as well as part of a trend toward environmentally safer and natural ingredients.[31]

Mosquito lure

Lactic acid, along with ammonium bicarbonate, is used in the Lurex brand mosquito attractant.[32]

See also


  1. ^ Dawson, R. M. C. et al., Data for Biochemical Research, Oxford, Clarendon Press, 1959.
  2. ^ a b c Sigma-Aldrich Co., DL-Lactic acid. Retrieved on 2013-07-20.
  3. ^ Badet, C; Thebaud, NB (2008). "Ecology of Lactobacilli in the Oral Cavity: A Review of Literature". The open microbiology journal 2: 38–48. PMC 2593047. PMID 19088910. doi:10.2174/1874285800802010038. 
  4. ^ Nascimento, MM; Gordan, VV; Garvan, CW; Browngardt, CM; Burne, RA (2009). "Correlations of oral bacterial arginine and urea catabolism with caries experience". Oral microbiology and immunology 24 (2): 89–95. PMC 2742966. PMID 19239634. doi:10.1111/j.1399-302X.2008.00477.x. 
  5. ^ Aas, JA; Griffen, AL; Dardis, SR; Lee, AM; Olsen, I; Dewhirst, FE; Leys, EJ; Paster, BJ (2008). "Bacteria of Dental Caries in Primary and Permanent Teeth in Children and Young Adults". Journal of clinical microbiology 46 (4): 1407–17. PMC 2292933. PMID 18216213. doi:10.1128/JCM.01410-07. 
  6. ^ Caufield, PW; Li, Y; Dasanayake, A; Saxena, D (2007). "Diversity of Lactobacilli in the Oral Cavities of Young Women with Dental Caries". Caries Res. 41 (1): 2–8. PMC 2646165. PMID 17167253. doi:10.1159/000096099. 
  7. ^ Roth, Stephen M. "Why does lactic acid build up in muscles? And why does it cause soreness?". Retrieved 23 January 2006. 
  8. ^ NNFCC Renewable Chemicals Factsheet: Lactic Acid
  9. ^ McArdle, W. D., Katch, F. I., & Katch, V. L. (2010). Exercise physiology: Energy, nutrition, and human performance. Wolters Kluwer/Lippincott Williams & Wilkins Health. ISBN 978-0-683-05731-7. ISBN 0-683-05731-6. 
  10. ^ McArdle, Katch & Katch (2010). Exercise Physiology: Energy, Nutrition, and Human Performance. Wolters Kluwer/Lippincott Williams & Wilkins Health. ISBN 978-0-683-05731-7. ISBN 0-683-05731-6. 
  11. ^ Robergs, RA; Ghiasvand, F; Parker, D (2004). "Biochemistry of exercise-induced metabolic acidosis" (PDF). Am J Physiol Regul Integr Comp Physiol 287 (3): R502–R516. PMID 15308499. doi:10.1152/ajpregu.00114.2004. 
  12. ^ a b Lindinger, M. I. (2004). "Applying physicochemical principles to skeletal muscle acid-base status". Am J Physiol Regul Integr Comp Physiol 289 (3): R890–94. doi:10.1152/ajpregu.00225.2005. 
  13. ^ a b c d Zilberter Y, Zilberter T, Bregestovski P (September 2010). "Neuronal activity in vitro and the in vivo reality: the role of energy homeostasis". Trends Pharmacol. Sci. 31 (9): 394–401. PMID 20633934. doi:10.1016/ 
  14. ^ Wyss MT, Jolivet R, Buck A, Magistretti PJ, Weber B (May 2011). "In vivo evidence for lactate as a neuronal energy source". J. Neurosci. 31 (20): 7477–85. PMID 21593331. doi:10.1523/JNEUROSCI.0415-11.2011. 
  15. ^ Gladden LB (July 2004). "Lactate metabolism: a new paradigm for the third millennium". J. Physiol. (Lond.) 558 (Pt 1): 5–30. PMC 1664920. PMID 15131240. doi:10.1113/jphysiol.2003.058701. 
  16. ^ Pellerin L; Bouzier-Sore AK; Aubert A et al. (September 2007). "Activity-dependent regulation of energy metabolism by astrocytes: an update". Glia 55 (12): 1251–62. PMID 17659524. doi:10.1002/glia.20528. 
  17. ^ Holmgren CD, Mukhtarov M, Malkov AE, Popova IY, Bregestovski P, Zilberter Y (February 2010). "Energy substrate availability as a determinant of neuronal resting potential, GABA signaling and spontaneous network activity in the neonatal cortex in vitro". J. Neurochem. 112 (4): 900–12. PMID 19943846. doi:10.1111/j.1471-4159.2009.06506.x. 
  18. ^ Tyzio R; Allene C; Nardou R et al. (January 2011). "Depolarizing actions of GABA in immature neurons depend neither on ketone bodies nor on pyruvate". J. Neurosci. 31 (1): 34–45. PMID 21209187. doi:10.1523/JNEUROSCI.3314-10.2011. 
  19. ^ Ruusuvuori E, Kirilkin I, Pandya N, Kaila K (November 2010). "Spontaneous network events driven by depolarizing GABA action in neonatal hippocampal slices are not attributable to deficient mitochondrial energy metabolism". J. Neurosci. 30 (46): 15638–42. PMID 21084619. doi:10.1523/JNEUROSCI.3355-10.2010. 
  20. ^ Khakhalin AS (May 2011). "Questioning the depolarizing effects of GABA during early brain development". J Neurophysiol 106 (3): 1065–7. PMID 21593390. doi:10.1152/jn.00293.2011. 
  21. ^ Zilberter, Yuri; Bregestovski, Piotr; Mukhtarov, Marat; Ivanov, Anton (2011). "Lactate Effectively Covers Energy Demands during Neuronal Network Activity in Neonatal Hippocampal Slices". Frontiers in Neuroenergetics 3: 2. PMC 3092068. PMID 21602909. doi:10.3389/fnene.2011.00002. 
  22. ^ Kasischke, Karl (2011). "Lactate Fuels the Neonatal Brain". Frontiers in Neuroenergetics 3. doi:10.3389/fnene.2011.00004. 
  23. ^ a b c d Blood Test Results - Normal Ranges Bloodbook.Com
  24. ^ a b c d Derived from mass values using molar mass of 90.08 g/mol
  25. ^ UK Food Standards Agency: "Current EU approved additives and their E Numbers". Retrieved 2011-10-27. 
  26. ^ US Food and Drug Administration: "Listing of Food Additives Status Part II". Retrieved 2011-10-27. 
  27. ^ Australia New Zealand Food Standards Code"Standard 1.2.4 - Labelling of ingredients". Retrieved 2011-10-27. 
  28. ^ a b "Listing of Specific Substances Affirmed as GRAS:Lactic Acid". US FDA. Retrieved 20 May 2013. 
  29. ^ "Purac Carcass Applications". Purac. Retrieved 20 May 2013. 
  30. ^ "Agency Response Letter GRAS Notice No. GRN 000240". FDA. US FDA. Retrieved 20 May 2013. 
  31. ^
  32. ^

[1]==External links==

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