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 |
|---|---|---|---|---|---|---|---|---|---|---|
|
(R) GAMMA DECALACTONE | M_0050448 |
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|
Naturel | - | - | - | - | - |
(R) GAMMA DECALACTONE
ID : M_0050448
Certifications :
General Presentation
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CAS N° : 706-14-9
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EINECS number : 211-892-8
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FEMA number : 2360
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FLAVIS number : 10.017
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JECFA number : 231
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Appearance : Colorless liquid
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Density : 0,967
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Volatility : Heart/Base
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Price Range : €€€
Physico-chemical properties
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Molecular formula : C10H18O2
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Molecular Weight : 170,25 g/mol
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Log P : 3
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Fusion Point : <-20°C
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Boiling Point : 281°C
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Detection Threshold : 11 ppb (0,0000011%)
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Optical rotation : Donnée indisponible
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Vapor pressure : Donnée indisponible
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Refractive Index @20°C : Donnée indisponible
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Acid Value : Donnée indisponible.
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Flash Point : 150°C
Uses
Uses in perfumery :
Gamma-Decalactone adds a fruity and velvety touch to floral accords. Used in peach reconstitutions, accompanied by Aldehyde C14.
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.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
