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Mannitol structure.png
D-Mannitol 3d space fill.png
Trade namesOsmitrol, other
Other namesd-Mannitol, mannite, manna sugar
  • (2R,3R,4R,5R)-Hexane-1,2,3,4,5,6-hexol
Clinical data
Drug classOsmotic diuretic[1]
Main usesSweetener, glaucoma, increased intracranial pressure[2][3][4]
Side effectsElectrolyte problems, dehydration[1]
  • US: C (Risk not ruled out)
Routes of
by mouth
Defined daily dose0.8 g[5]
External links
License data
MetabolismLiver, negligible
Elimination half-life100 minutes
ExcretionKidney: 90%
Chemical and physical data
Molar mass182.172 g·mol−1
3D model (JSmol)
  • O[C@H]([C@H](O)CO)[C@H](O)[C@H](O)CO
  • InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4-,5-,6-/m1/s1 checkY

Mannitol is a type of sugar alcohol used as a sweetener and medication.[2][4] As a sweetener it is used in diabetic food as it is poorly absorbed by the intestines.[2] As a medication, it is used to decrease pressure in the eyes, as in glaucoma, and to lower increased intracranial pressure.[3][4] Medically, it is given by injection.[1] Effects typically begin within 15 minutes and last up to 8 hours.[1]

Common side effects from medical use include electrolyte problems and dehydration.[1] Other serious side effects may include worsening heart failure and kidney problems.[1][4] It is unclear if use is safe in pregnancy.[1] Mannitol is in the osmotic diuretic family of medications and works by pulling fluid from the brain and eyes.[1]

The discovery of mannitol is attributed to Joseph Louis Proust in 1806.[6] It is on the World Health Organization's List of Essential Medicines.[7] The wholesale cost in the developing world is about 1.12 to US$5.80 per dose.[8] In the United States, a course of treatment costs $25 to $50.[9] It was originally made from the flowering ash and called manna due to its supposed resemblance to the Biblical food.[10][11] Mannitol is on the World Anti-Doping Agency's banned drug list due to concerns that it may mask other drugs.[12]


Medical uses

Mannitol is used to reduce acutely raised intracranial pressure until more definitive treatment can be applied, e.g., after head trauma.

It may also be used for certain cases of kidney failure with low urine output, decreasing pressure in the eye, to increase the elimination of certain toxins, and to treat fluid build up.[1]

Intraoperative mannitol prior to vessel clamp release during renal transplant has been shown to reduce post-transplant kidney injury, but has not been shown to reduce graft rejection.[medical citation needed]

Mannitol acts as an osmotic laxative[13] in oral doses larger than 20 g,[14] and is sometimes sold as a laxative for children.[citation needed]

The use of mannitol, when inhaled, as a bronchial irritant as an alternative method of diagnosis of exercise-induced asthma has been proposed. A 2013 systematic review concluded evidence to support its use for this purpose at this time is insufficient.[15]

Mannitol is commonly used in the circuit prime of a heart lung machine during cardiopulmonary bypass. The presence of mannitol preserves renal function during the times of low blood flow and pressure, while the patient is on bypass. The solution prevents the swelling of endothelial cells in the kidney, which may have otherwise reduced blood flow to this area and resulted in cell damage.

Mannitol can also be used to temporarily encapsulate a sharp object (such as a helix on a lead for an artificial pacemaker) while it passes through the venous system. Because the mannitol dissolves readily in blood, the sharp point becomes exposed at its destination.

Mannitol is also the first drug of choice to treat acute glaucoma in veterinary medicine. It is administered as a 20% solution intravenously. It dehydrates the vitreous humor and, therefore, lowers the intraocular pressure. However, it requires an intact blood-ocular barrier to work.[16]


Mannitol increases blood glucose to a lesser extent than sucrose (thus having a relatively low glycemic index[17]) so is used as a sweetener for people with diabetes, and in chewing gums. Although mannitol has a higher heat of solution than most sugar alcohols, its comparatively low solubility reduces the cooling effect usually found in mint candies and gums. However, when mannitol is completely dissolved in a product, it induces a strong cooling effect.[18] Also, it has a very low hygroscopicity – it does not pick up water from the air until the humidity level is 98%. This makes mannitol very useful as a coating for hard candies, dried fruits, and chewing gums, and it is often included as an ingredient in candies and chewing gum.[19] The pleasant taste and mouthfeel of mannitol also makes it a popular excipient for chewable tablets.[20]

Analytical chemistry

Mannitol can be used to form a complex with boric acid. This increases the acid strength of the boric acid, permitting better precision in volumetric analysis of this acid.[21]


Mannitol is the primary ingredient of mannitol salt agar, a bacterial growth medium, and is used in others.

Mannitol is used as a cutting agent[22] in various drugs that are used intranasally (snorted), such as cocaine. A mixture of mannitol and fentanyl (or fentanyl analogs) in ratio 1:10 is labeled and sold as "China white", a popular heroin substitute.[citation needed]


The defined daily dose is 0.8 gram (inhalation)[5]


Mannitol is contraindicated in people with anuria, congestive heart failure.[citation needed]

Adverse effects include hyponatremia and volume depletion leading to metabolic acidosis.[6]


Mannitol is an isomer of sorbitol, another sugar alcohol; the two differ only in the orientation of the hydroxyl group on carbon 2.[23] While similar, the two sugar alcohols have very different sources in nature, melting points, and uses.


Mannitol is classified as a sugar alcohol; that is, it can be derived from a sugar (mannose) by reduction. Other sugar alcohols include xylitol and sorbitol. Mannitol and sorbitol are isomers, the only difference being the orientation of the hydroxyl group on carbon 2.[18]

Industrial synthesis

Mannitol is commonly produced via the hydrogenation of fructose, which is formed from either starch or sucrose (common table sugar). Although starch is a cheaper source than sucrose, the transformation of starch is much more complicated. Eventually, it yields a syrup containing about 42% fructose, 52% glucose, and 6% maltose. Sucrose is simply hydrolyzed into an invert sugar syrup, which contains about 50% fructose. In both cases, the syrups are chromatographically purified to contain 90–95% fructose. The fructose is then hydrogenated over a nickel catalyst into a mixture of isomers sorbitol and mannitol. Yield is typically 50%:50%, although slightly alkaline reaction conditions can slightly increase mannitol yields.[18]


Mannitol is one of the most abundant energy and carbon storage molecules in nature, produced by a plethora of organisms, including bacteria, yeasts, fungi, algae, lichens, and many plants.[24] Fermentation by microorganisms is an alternative to the traditional industrial synthesis. A fructose to mannitol metabolic pathway, known as the mannitol cycle in fungi, has been discovered in a type of red algae (Caloglossa leprieurii), and it is highly possible that other microorganisms employ similar such pathways.[25] A class of lactic acid bacteria, labeled heterofermentive because of their multiple fermentation pathways, convert either three fructose molecules or two fructose and one glucose molecule into two mannitol molecules, and one molecule each of lactic acid, acetic acid, and carbon dioxide. Feedstock syrups containing medium to large concentrations of fructose (for example, cashew apple juice, containing 55% fructose: 45% glucose) can produce yields 200 g (7.1 oz) mannitol per liter of feedstock. Further research is being conducted, studying ways to engineer even more efficient mannitol pathways in lactic acid bacteria, as well as the use of other microorganisms such as yeast[24] and E. coli in mannitol production. When food-grade strains of any of the aforementioned microorganisms are used, the mannitol and the organism itself are directly applicable to food products, avoiding the need for careful separation of microorganism and mannitol crystals. Although this is a promising method, steps are needed to scale it up to industrially needed quantities.[25]

Natural extraction

Since mannitol is found in a wide variety of natural products, including almost all plants, it can be directly extracted from natural products, rather than chemical or biological syntheses. In fact, in China, isolation from seaweed is the most common form of mannitol production.[19] Mannitol concentrations of plant exudates can range from 20% in seaweeds to 90% in the plane tree. It is a constituent of saw palmetto (Serenoa).[26]

Traditionally, mannitol is extracted by the Soxhlet extraction, using ethanol, water, and methanol to steam and then hydrolysis of the crude material. The mannitol is then recrystallized from the extract, generally resulting in yields of about 18% of the original natural product. Another method of extraction is using supercritical and subcritical fluids. These fluids are at such a stage that no difference exists between the liquid and gas stages, so are more diffusive than normal fluids. This is considered to make them much more effective mass transfer agents than normal liquids. The super- or subcritical fluid is pumped through the natural product, and the mostly mannitol product is easily separated from the solvent and minute amount of byproduct.

Supercritical carbon dioxide extraction of olive leaves has been shown to require less solvent per measure of leaf than a traditional extraction — 141.7 g (5.00 oz) CO2 versus 194.4 g (6.86 oz) ethanol per 1 g (0.035 oz) olive leaf. Heated, pressurized, subcritical water is even cheaper, and is shown to have dramatically greater results than traditional extraction. It requires only 4.01 g (0.141 oz) water per 1 g (0.035 oz) of olive leaf, and gives a yield of 76.75% mannitol. Both super- and subcritical extractions are cheaper, faster, purer, and more environmentally friendly than the traditional extraction. However, the required high operating temperatures and pressures are causes for hesitancy in the industrial use of this technique.[25]


Julije Domac elucidated the structure of hexene and mannitol obtained from Caspian manna. He determined the place of the double bond in hexene obtained from mannitol and proved that it is a derivative of a normal hexene. This also solved the structure of mannitol, which was unknown until then.[27][28][29][30]


The three studies[31][32][33] that initially found that high-dose mannitol was effective in cases of severe head injury were the subject of an investigation published in 2007.[34] Although several authors are listed with Dr. Julio Cruz, it is unclear whether the authors had knowledge of how the patients were recruited. Further, the Federal University of São Paulo, which Dr. Cruz gave as his affiliation, has never employed him. As a result of doubt surrounding Cruz's work, an updated version of the Cochrane review excludes all studies by Julio Cruz, leaving only 4 studies.[3] Due to differences in selection of control groups, a conclusion about the clinical use of mannitol could not be reached.

Compendial status

See also


  1. 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 "Mannitol". The American Society of Health-System Pharmacists. Archived from the original on 26 May 2015. Retrieved 8 January 2015.
  2. 2.0 2.1 2.2 Varzakas, Theodoros; Labropoulos, Athanasios; Anestis, Stylianos (2012). Sweeteners: Nutritional Aspects, Applications, and Production Technology. CRC Press. pp. 59–60. ISBN 9781439876732. Archived from the original on 10 September 2017.
  3. 3.0 3.1 3.2 Wakai A, McCabe A, Roberts I, Schierhout G (August 2013). "Mannitol for acute traumatic brain injury". The Cochrane Database of Systematic Reviews. 8 (8): CD001049. doi:10.1002/14651858.CD001049.pub5. PMC 7050611. PMID 23918314.
  4. 4.0 4.1 4.2 4.3 World Health Organization (2009). Stuart MC, Kouimtzi M, Hill SR (eds.). WHO Model Formulary 2008. World Health Organization. p. 332. hdl:10665/44053. ISBN 9789241547659.
  5. 5.0 5.1 "WHOCC - ATC/DDD Index". Archived from the original on 16 May 2021. Retrieved 19 September 2020.
  6. 6.0 6.1 Kremers, Edward; Sonnedecker, Glenn (1986). Kremers and Urdang's History of Pharmacy. Amer. Inst. History of Pharmacy. p. 360. ISBN 9780931292170. Archived from the original on 10 September 2017.
  7. World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  8. "Mannitol". International Drug Price Indicator Guide. Archived from the original on 7 July 2018. Retrieved 8 December 2016.
  9. Hamilton, Richart (2015). Tarascon Pocket Pharmacopoeia 2015 Deluxe Lab-Coat Edition. Jones & Bartlett Learning. p. 344. ISBN 9781284057560.
  10. Cottrell, James E.; Patel, Piyush (2016). Cottrell and Patel's Neuroanesthesia. Elsevier Health Sciences. p. 160. ISBN 9780323461122. Archived from the original on 10 September 2017. Retrieved 4 September 2017.
  11. Bardal, Stan; Waechter, Jason; Martin, Doug (2010). Applied Pharmacology. Elsevier Health Sciences. p. 411. ISBN 978-1437735789. Archived from the original on 10 September 2017. Retrieved 4 September 2017.
  12. "THE 2017 PROHIBITED LIST INTERNATIONAL STANDARD" (PDF). January 2017. p. 5. Archived (PDF) from the original on 22 April 2018. Retrieved 7 July 2018.
  13. "Select Committee on GRAS Substances (SCOGS) Opinion: Mannitol". April 2013. Archived from the original on 22 October 2014.
  14. Ellis FW, Krantz JC (1941). "Sugar alcohols: XXII. Metabolism and toxicity studies with mannitol and sorbitol in man and animals". J. Biol. Chem. 141: 147–154. Archived from the original on 10 September 2017.
  15. Stickland MK, Rowe BH, Spooner CH, Vandermeer B, Dryden DM (September 2011). "Accuracy of eucapnic hyperpnea or mannitol to diagnose exercise-induced bronchoconstriction: a systematic review". Annals of Allergy, Asthma & Immunology. 107 (3): 229–34.e8. doi:10.1016/j.anai.2011.06.013. PMID 21875541.
  16. Veterinary Class Notes, Ophthalmology, The Ohio State University, provided by David Wilkie, DVM, DACVO
  17. Grenby TH (2011). Advances in Sweeteners. Springer. p. 66. ISBN 978-1461285229.
  18. 18.0 18.1 18.2 Kearsley MW, Deis RC (2006). "Sorbitol and Mannitol". Sweeteners and Sugar Alternatives in Food Technology. Wiley-Blackwell. pp. 249–261. ISBN 0470659688.
  19. 19.0 19.1 Lawson P (2007). Mannitol. Blackwell Publishing Ltd. pp. 219–225.
  20. Weiner, Myra L.; Kotkoskie, Lois A. (1999). Excipient Toxicity and Safety. pp. 370. ISBN 9780824782108.
  21. Belcher R, Nutten AJ (1960). Quantitative Inorganic Analysis (2nd ed.). London, UK: Butterworths. p. 194.
  22. "Cut the Shit". December 2005. Archived from the original on 27 September 2016. Retrieved 4 September 2017.
  23. Kearsley MW, Deis RC (2006). "Sorbitol and Mannitol". Sweeteners and Sugar Alternatives in Food Technology. Ames: Oxford. pp. 249–261.
  24. 24.0 24.1 Song SH, Vieille C (August 2009). "Recent advances in the biological production of mannitol". Applied Microbiology and Biotechnology. 84 (1): 55–62. doi:10.1007/s00253-009-2086-5. PMID 19578847.
  25. 25.0 25.1 25.2 Ghoreishi SM, Shahrestani RG (2009). "Innovative strategies for engineering mannitol production". Trends in Food Science & Technology. 20 (6–7): 263–270. doi:10.1016/j.tifs.2009.03.006.
  26. Wagner H, Flachsbarth H, Vogel G (March 1981). "[A New Antiphlogistic Principle from Sabal serrulata, II]". Planta Medica. 41 (3): 252–8. doi:10.1055/s-2007-971711. PMID 17401849.
  27. Inić S, Kujundžić N (2011). "The first independent pharmacognosy institute in the world and its founder Julije Domac (1853–1928)". Die Pharmazie. 66 (6): 720–726.
  28. Domac J (1881). "Über das Hexylen aus Mannit". Sitzungsberichte der Kaiserlichen Akademie der Wissenschaften, Mathematisch-Naturwissenschaftliche Classe. 23: 1038–1051.
  29. Domac J (1881). "Über das Hexylen aus Mannit". Monatshefte für Chemie. 2: 309–322. doi:10.1007/BF01516516.
  30. Domac J (1882). "II. Ueber die Einwirkung der Unterchlorsäure auf Hexylen". Justus Liebig's Annalen der Chemie. 213: 124–132. doi:10.1002/jlac.18822130107. Archived from the original on 21 September 2020. Retrieved 16 January 2020.
  31. Cruz J, Minoja G, Okuchi K (October 2001). "Improving clinical outcomes from acute subdural hematomas with the emergency preoperative administration of high doses of mannitol: a randomized trial". Neurosurgery. 49 (4): 864–71. doi:10.1097/00006123-200110000-00016. PMID 11564247.
  32. Cruz J, Minoja G, Okuchi K (September 2002). "Major clinical and physiological benefits of early high doses of mannitol for intraparenchymal temporal lobe hemorrhages with abnormal pupillary widening: a randomized trial". Neurosurgery. 51 (3): 628–37, discussion 637–8. doi:10.1097/00006123-200209000-00006. PMID 12188940.
  33. Cruz J, Minoja G, Okuchi K, Facco E (March 2004). "Successful use of the new high-dose mannitol treatment in patients with Glasgow Coma Scale scores of 3 and bilateral abnormal pupillary widening: a randomized trial". Journal of Neurosurgery. 100 (3): 376–83. doi:10.3171/jns.2004.100.3.0376. PMID 15035271.
  34. Roberts I, Smith R, Evans S (February 2007). "Doubts over head injury studies". BMJ. 334 (7590): 392–4. doi:10.1136/bmj.39118.480023.BE. PMC 1804156. PMID 17322250.
  35. British Pharmacopoeia Commission Secretariat (2009). "Index, BP 2009" (PDF). Archived from the original (PDF) on 11 April 2009. Retrieved 31 January 2010.
  36. "Japanese Pharmacopoeia, Fifteenth Edition" (PDF). 2006. Archived from the original (PDF) on 22 July 2011. Retrieved 31 January 2010.
  37. USP 32 (2008). "Mannitol Injection" (PDF). Archived from the original (PDF) on 6 July 2010. Retrieved 31 January 2010.

External links

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