Decanal
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Names | |
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IUPAC name
Decanal | |
Other names
Decyl aldehyde, caprinaldehyde | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.003.598 |
KEGG | |
PubChem CID |
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UNII | |
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Properties | |
C10H20O | |
Molar mass | 156.2 |
Appearance | colourless liquid |
Density | 0.83 g/mL |
Boiling point | 207 to 209 °C (405 to 408 °F; 480 to 482 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Decanal is an organic compound with the chemical formula C9H19CHO. It is the simplest ten-carbon aldehyde.
Occurrence
Decanal occurs naturally and is used in fragrances and flavoring.[1]
Decanal is an important component in citrus, along with octanal, citral, and sinensal.
Decanal is also an important component of buckwheat odour.[2]
Decanal is also the main component (17%) of coriander herb (Coriandrum sativum) essential oil.[3]
Preparation
Decanal can be prepared by oxidation of the related alcohol decanol.[4]
Safety
For safety information see the MSDS.[5]
References
- ↑ Rychlik, Schieberle & Grosch Compilation of Odor Thresholds, Odor Qualities and Retention Indices of Key Food Odorants, Lichtenbergstraße, Germany, 1998.
- ↑ Janes D, Kantar D, Kreft S, Prosen H (2008). "Identification of buckwheat (Fagopyrum esculentum Moench) aroma compounds with GC-MS". Food Chemistry. 112: 120. doi:10.1016/j.foodchem.2008.05.048.
- ↑ ESSENTIAL OIL COMPOSITION OF THE CORIANDER (Coriandrum sativum L.) HERB DEPENDING ON THE DEVELOPMENT STAGE, Renata Nurzyńska-Wierdak. ACTA AGROBOTANICA Vol. 66 (1), 2013: 53–60. https://pbsociety.org.pl/journals/index.php/aa/article/view/aa.2013.006
- ↑ R. W. Ratcliffe (1988). "Oxidation with the Chromium Trioxide-Pridine Complex Prepared in situ: 1- Decanal". Organic Syntheses. ; Collective Volume, 6, p. 373
- ↑ Safety (MSDS) data for n-decanal
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