(E,E)-2,4-Decadienal
Names | |
---|---|
Systematic IUPAC name
(2E,4E)-Deca-2,4-dienal[1] | |
Identifiers | |
25152-84-5 | |
3D model (Jmol) | Interactive image |
ChEMBL | ChEMBL443949 |
ChemSpider | 4446470 |
ECHA InfoCard | 100.042.411 |
EC Number | 246-668-9 |
MeSH | 2-trans-4-trans-Decadienal |
PubChem | 5283349 |
UNII | 3G88X2RK09 |
| |
| |
Properties | |
C10H16O | |
Molar mass | 152.24 g·mol−1 |
Boiling point | 115 °C; 239 °F; 388 K at 1.3 kPa |
log P | 3.419 |
Refractive index (nD) |
1.515 |
Related compounds | |
Related alkenals |
Acrolein |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
(E,E)-2,4-Decadienal is an aromatic substance found in butter, cooked beef, fish, potato chips, roasted peanut,[2] buckwheat[3] and wheat bread crumb.[4] In an isolated state, it smells of deep fat flavor, characteristic of chicken aroma (at 10ppm). At lower concentration, it has the odor of citrus, orange or grapefruit. It might be carcinogenic.[5]
References
- ↑ "2,4-decadienal - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 27 March 2005. Identification and Related Records. Retrieved 7 October 2011.
- ↑ "2,4 Decadienal". USA.
- ↑ 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.
- ↑ Nicoline Vermeulena; Michael Czernyb; Michael G. Gänzlea; Peter Schieberleb & Rudi F. Vogel (2007). "Reduction of (E)-2-nonenal and (E,E)-2,4-decadienal during sourdough fermentation". Journal of Cereal Science. 45 (1): 78–87. doi:10.1016/j.jcs.2006.07.002.
- ↑ Louis W. Chang; Wai-Sze Lo & Pinpin Lin (2005). "Trans, Trans-2,4-Decadienal, a Product Found in Cooking Oil Fumes, Induces Cell Proliferation and Cytokine Production Due to Reactive Oxygen Species in Human Bronchial Epithelial Cells". Toxicological Sciences. 87 (2): 337–343. doi:10.1093/toxsci/kfi258. PMID 16014734.
This article is issued from Wikipedia - version of the 5/19/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.