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| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
ETHYL OCTANOATE (ETHYL CAPRYLATE) | 441E130000 |
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|
Synthetic Aroma Chemicals |
|
- | - | - | UK | - |
ETHYL OCTANOATE (ETHYL CAPRYLATE)
ID : 441E130000
UK
Certifications :
General Presentation
-
CAS N° :
106-32-1 -
EINECS number :
203-385-5 -
FEMA number :
2449 -
FLAVIS number :
09.111
-
JECFA number :
33 -
Volatility :
Head -
Price Range :
€€
Physico chemical properties
-
Appearance :
Colorless liquid -
Density :
0,86 -
Refractive Index @20°C :
1,418 -
Optical rotation :
Data not available. -
Vapor pressure :
Data not available. -
Flash Point :
79 °C
-
Molecular formula :
C10H20O2 -
Molecular Weight :
172,27 g/mol -
Log P :
3,84 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
208°C -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
Year of discovery :
Data not available.
Natural availability :
Ethyl Octanoate is present in nature in alcohols such as Rum, Whisky, Beer, Cognac
Isomerism :
Ethyl Octanoate is a constitutional isomer of Hydroxycitronellal and Florol®. However, its smell is quite different from the latter two compounds.
Synthesis precursor :
Ethyl Octanoate is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Ethyl Octanoate can be synthesized by an esterification reaction between octanoic acid and Ethanol. This reaction involves an acid catalyst such as concentrated sulphuric acid, which speeds up the reaction.
Stability :
Esters may form their corresponding acid through time
Other comments :
Data not available.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
