Nonanal
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| Names | |
|---|---|
| Preferred IUPAC name
Nonanal | |
| Other names
Nonanaldehyde
Nonaldehyde Pelargonaldehyde Aldehyde C-9 | |
| Identifiers | |
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3D model (JSmol)
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| Properties | |
| C9H18O | |
| Molar mass | 142.242 g·mol−1 |
| Appearance | Colourless liquid |
| Density | 0.827 g/cm3 |
| Melting point | −18 °C (0 °F; 255 K) |
| Boiling point | 191 °C (376 °F; 464 K) |
| Insoluble | |
| Related compounds | |
Related aldehydes
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Octanal |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Template:Chembox Footer/trackingTemplate:Short description
Nonanal is an organic compound with the chemical formula Page Module:Chem2/styles.css has no content.CH3(CH2)7CHO. It is one of several isomers, all are colorless oil. The nonanals are classified as aldehydes. The linear nonanal is produced commercially by the hydroformylation of 1-octene. It is used as a fragrance.[2]
Mosquitoes
Nonanal has been identified as a compound that attracts Culex mosquitoes.[3][4] Nonanal acts synergistically with carbon dioxide in that regard.[5]
References
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- ^ Page Module:Citation/CS1/styles.css has no content."n-NONALDEHYDE (PELARGONALDEHYDE)". chemicalland21.com. Retrieved 2023-01-10.
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- ^ UC Davis News & Information :: UC Davis Researchers Identify Dominant Chemical That Attracts Mosquitoes to Humans. News.ucdavis.edu (2009-10-26). Retrieved on 2011-01-03.
- ^ Page Module:Citation/CS1/styles.css has no content.Syed, Z.; Leal, W. S. (2009). "Acute olfactory response of Culex mosquitoes to a human- and bird-derived attractant". Proceedings of the National Academy of Sciences. 106 (44): 18803–8. Bibcode:2009PNAS..10618803S. doi:10.1073/pnas.0906932106. PMC 2767364. PMID 19858490.
- ^ Page Module:Citation/CS1/styles.css has no content."Scientists Identify Key Smell that Attracts Mosquitoes to Humans". US News and World Report. October 28, 2009. Retrieved 2011-01-03.
