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2-Heptanone


Butyl acetone Methyl n-amyl ketone Methyl pentyl ketone 750 mg/kg (mouse, oral) 2000 ppm (guinea pig, 14.8 hr)

2-Heptanone, also known as methyl n-amyl ketone, or Heptan-2-one, is a ketone with the molecular formula C7H14O. It is a colorless, water-like liquid with a banana-like, fruity odor. 2-Heptanone has a neutral formal charge, and is only slightly soluble in water. It is one of several compounds that contributes to the odor of sweaty clothing.

2-Heptanone is listed by the FDA as a "food additive permitted for direct addition to food for human consumption" (21 CFR 172.515), and it occurs naturally in certain foods (e.g., beer, white bread, butter, various cheeses and potato chips).

The mechanism of action of 2-heptanone as a pheromone at odorant receptors in rodents has been investigated. 2-Heptanone is present in the urine of stressed rats and believe that it is used as a means to alert other rats. Certain species of worms are attracted to 2-heptanone and bacteria can use this as a means of pathogenesis. 2-Heptanone has also been found to be excreted by honey bees when they bite small pests within the colony such as wax moth larvae and Varroa mites. Though it was historically believed to be an alarm pheromone, 2-heptanone has been shown to act as an anaesthetic on the pests, enabling the honey bee to stun the pest and eject it from the hive. The work could lead to the use of 2-heptanone as an alternative local anaesthetic to lidocaine, which although well established for clinical use, has the disadvantage of provoking allergic reactions in some people.

2-Heptanone was one of the metabolites of n-heptane found in the urine of employees exposed to heptane in shoe and tire factories. This commonly occurs from exposure to plasticisers. 2-Heptanone can be absorbed through the skin, inhaled and consumed. Exposure to 2-Heptanone can cause irritation of skin/eyes, respiratory system, headaches, vomiting, and nausea.

In mice 2-H is a urinary component and pheromone. It has a high affinity for the main olfactory epithelium. Gaillard et al 2002 found that it agonizes one specific olfactory receptor, and that that OR only binds 2-H.

References

References

  1. [http://www.inchem.org/documents/icsc/icsc/eics0920.htm Methyl n-amyl ketone], International Occupational Safety and Health Information Centre (CIS)
  2. {{PGCH. 0399
  3. {{IDLH. 110430. Methyl (n-amyl) ketone
  4. "2-Heptanone". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. (2016). "Source, impact and removal of malodour from soiled clothing". Journal of Chromatography A.
  6. [https://www.osha.gov/chemicaldata/chemResult.html?RecNo=110 Methyl (n-amyl) ketone], Chemical Sampling Information, Occupational Safety & Health Administration
  7. (July 2006). "Pheromone detection in male mice depends on signaling through the type 3 adenylyl cyclase in the main olfactory epithelium". The Journal of Neuroscience.
  8. (February 2008). "A preliminary study for identifying olfactory markers of fear in the rat". Lab Animal.
  9. (May 2007). "Urine from stressed rats increases immobility in receptor rats forced to swim: role of 2-heptanone". Physiology & Behavior.
  10. (June 2018). "An alarm pheromone reduces ventral tegmental area-nucleus accumbens shell responsivity". Neuroscience Letters.
  11. (November 2016). "The Signaling Pathway of Caenorhabditis elegans Mediates Chemotaxis Response to the Attractant 2-Heptanone in a Trojan Horse-like Pathogenesis". The Journal of Biological Chemistry.
  12. (26 October 2012). "Honey-bees found to have bite that stuns". BBC News.
  13. (April 1986). "Identification of the n-heptane metabolites in rat and human urine". Archives of Toxicology.
  14. (April 2001). "Urine 4-heptanone: a beta-oxidation product of 2-ethylhexanoic acid from plasticisers". Clinica Chimica Acta; International Journal of Clinical Chemistry.
  15. "2-HEPTANONE". National Library of Medicine HSDB Database.
  16. Liberles, Stephen D.. (2014-02-10). "Mammalian Pheromones". [[Annual Reviews (publisher).
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