This MedLibrary.org supplementary page on Putrescine is provided directly from the open source Wikipedia as a service to our readers. Please see the note below on authorship of this content, as well as the Wikipedia usage guidelines. To search for other content from our encyclopedia supplement, please use the form below:
Related Sponsors
| Putrescine | |
|---|---|
| IUPAC name | butane-1,4-diamine |
| Identifiers | |
| CAS number | [110-60-1] |
| PubChem | |
| MeSH | |
| SMILES |
|
| Properties | |
| Molecular formula | C4H12N2 |
| Molar mass | 88.1516 |
| Melting point |
27 °C |
| Boiling point |
158-160 °C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
|
Putrescine (sometimes spelled putrescin or putrescene) is an organic chemical compound NH2(CH2)4NH2 (1,4-diaminobutane or butanediamine). It is related to cadaverine; both are produced by the breakdown of amino acids in living and dead organisms and both are toxic in large doses.[1][2] The two compounds are largely responsible for the foul odor of putrefying flesh, but also contribute to the odor of such processes as bad breath and bacterial vaginosis. They are also found in semen and some microalgae, together with related molecules like spermine and spermidine.
Contents |
History
Putrescine and cadaverine were first described by the Berlinese physician Ludwig Brieger in 1885.
Production and use
Putrescine is produced on industrial scale by hydrogenation of succinonitrile, which is produced by addition of hydrogen cyanide to acrylonitrile. Putrescine is reacted with adipic acid to yield the polyamide Nylon-4,6, which is marketed by DSM under the trade name Stanyl.
Biochemistry
Putrescine attacks s-adenosyl methionine and converts it to spermidine. Spermidine in turn attacks another s-adenosyl methionine and converts it to spermine.
Putrescine is synthesized in small quantities by healthy living cells by the action of ornithine decarboxylase. The polyamines, of which putrescine is one of the simplest, appear to be growth factors necessary for cell division.
Toxicity
Putrescine is toxic in large doses. In rats it had a fairly low acute oral toxicity of 2000 mg/kg body weight[1].
Cultural references
Putrescine is featured as a non-lethal weapon in the science fiction novel Zodiac, by Neal Stephenson. Its use is also suggested as a practical joke in an episode of Dinosaur Comics.
Notes
- ^ Lewis, Robert Alan (1998). Lewis' Dictionary of Toxicology. CRC Press, 212. ISBN 1566702232.
- ^ Kamhi, Ellen, Ph.D., RN, HNC (2007). Alternative Medicine Magazine's Definitive Guide to Weight Loss. Celestial Arts, 14. ISBN 1587612593. "Ornithine is converted by bowel bacteria into a toxic substance called putrescine, which in turn degrades into polyamines, such as spermadine, spermine, and cadaverine (literally meaning "the essence of dead cadavers")."
References
- "Nitriles". Ullmann's Encyclopedia of Industrial Chemistry (7th Ed.). Retrieved on 2007-09-10.
- "DSM Engineering Plastics". Retrieved on 2007-09-10.
External links
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Wikipedia content modification information:
- This page was last modified on 18 September 2008, at 06:29.
Wikipedia Authorship and Review
Wikipedia content provided here is not reviewed directly by MedLibrary.org. Wikipedia content is authored by an open community of volunteers and is not produced by or in any way affiliated with MedLibrary.org.
Wikipedia Usage Guidelines
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article on "Putrescine".
The URL for this specific entry is:
All Wikipedia text is available under the terms of the GNU Free Documentation License. (See Copyrights for details). Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc.
