Decanal
Appearance
Names | |
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Preferred IUPAC name
Decanal | |
Other names
Decyl aldehyde, caprinaldehyde
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.598 |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C10H20O | |
Molar mass | 156.269 g·mol−1 |
Appearance | Colorless liquid |
Density | 0.83 g/mL |
Melting point | 7 °C (45 °F; 280 K) |
Boiling point | 207 to 209 °C (405 to 408 °F; 480 to 482 K) |
Hazards | |
GHS labelling: | |
Warning | |
H315, H319, H412 | |
P264, P273, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362, P501 | |
NFPA 704 (fire diamond) | |
Flash point | 85 °C (185 °F; 358 K) |
200 °C (392 °F; 473 K) | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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3730 mg/kg (rat, oral) 5040 mg/kg (rabbit, dermal) |
Safety data sheet (SDS) | Fisher Scientific |
Related compounds | |
Related compounds
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2-Decanone |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Decanal is an organic compound classified as an aldehyde with the chemical formula C10H20O.
Occurrence
[edit]Decanal occurs naturally in citrus, along with octanal, citral, and sinensal, in buckwheat,[1] and in coriander essential oil.[2] It is used in fragrances and flavoring.[3]
Preparation
[edit]Decanal can be prepared by oxidation of the related alcohol decanol.[4]
Safety
[edit]For safety information see the MSDS.[5]
References
[edit]- ^ Janes D, Kantar D, Kreft S, Prosen H (2008). "Identification of buckwheat (Fagopyrum esculentum Moench) aroma compounds with GC-MS". Food Chemistry. 112: 120–124. doi:10.1016/j.foodchem.2008.05.048.
- ^ Nurzyńska-Wierdak, Renata (2013). "Essential oil composition of the coriander (Coriandrum sativum L.) herb depending on the development stage". Acta Agrobotanica. 66: 53–60. doi:10.5586/aa.2013.006.
- ^ Rychlik, Schieberle & Grosch (1998). Compilation of Odor Thresholds, Odor Qualities and Retention Indices of Key Food Odorants. Lichtenbergstraße, Germany.
{{cite book}}
: CS1 maint: location missing publisher (link) - ^ R. W. Ratcliffe (1988). "Oxidation with the Chromium Trioxide-Pridine Complex Prepared in situ: 1- Decanal". Organic Syntheses; Collected Volumes, vol. 6, p. 373.
- ^ "Safety (MSDS) data for n-decanal". Archived from the original on 2004-05-20. Retrieved 2007-12-01.