Photo credits: ScenTree SAS
Gamma-Decalactone
5-hexyloxolan-2-one ; 2-decalactone ; Decan-4-olide ; Decano-1,4-lactone ; Alpha-decanolactone ; 4-decanolide ; Decanolide-1,4 ; 4,5-dihydro-5-hexyl-2(3H)-furanone ; 4-hexyl butan-4-olide ; 4-hexyl-4-butanolide ; 4-hexyl-gamma-butyrolactone ; Gamma-hexyl-gamma-butyrolactone ; 4-hexylbutan-4-olide ; 5-hexyloxolan-2-one
Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
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(R) GAMMA DECALACTONE | M_0050448 |
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Naturel | - | - | - | - | - |
General Presentation
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CAS N° :
706-14-9 -
EINECS number :
211-892-8 -
FEMA number :
2360 -
FLAVIS number :
10.017
-
JECFA number :
231 -
Volatility :
Heart/Base -
Price Range :
€€€
Physico chemical properties
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Appearance :
Colorless liquid -
Density :
0,967 -
Refractive Index @20°C :
1,447 – 1,451 -
Optical rotation :
Data not available. -
Vapor pressure :
0,006 hPa @25°C -
Flash Point :
150°C
-
Molecular formula :
C10H18O2 -
Molecular Weight :
170,25 g/mol -
Log P :
3 -
Fusion Point :
<-20°C -
Boiling Point :
281°C -
Detection Threshold :
11 ppb (0,0000011%)
Chemistry & Uses
Year of discovery :
Data not available.
Natural availability :
Gamma-Decalactone is included in the fragrant principle of many fruits such as apricot or peach, and can be extracted from Osmanthus Absolute or from Carrot Leaf EO.
Isomerism :
Gamma-Decalactone has an asymmetric carbon. However, it is its racemic mixture that is used in perfumery. Delta-Decalactone is a constitutional isomer of Gamma-Decalactone, having one carbon atom less in its cycle, and one more in its ramified carbon chain. The resulting smell is very peachy for the isomer, and coconut-like for Delta-Decalactone.
Synthesis precursor :
Gamma-Decalactone is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Gamma-Decalactone is part of the family of gamma-lactones: cyclic esters whose cycle consists of five atoms. This molecule is synthesized biochemically. A beta-oxidation of ricinoleic acid (derived from castor oil) causes the formation of 4-Hydroxydecanoic acid, which can be cyclized at an acidic pH to obtain the final product: gamma-Decalactone.
Stability :
Lactones tend to polymerize through time, making them more viscous and leading to a phase shift in alcohol.
Other comments :
Gamma-Decalactone has a more sweet and syrupy peach side, while Aldehyde C-14 is renowned for its paper-like note.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment