Photo credits: ScenTree SAS
Gamma-nonalactone
Aldehyde C18 ; Coconut Aldehyde ; 5-pentyloxolan-2-one ; Prunolide ; Abricolin ; Gamma-amyl butyrolactone ; 4-amyl-4-hydroxybutyric acid lactone ; Amylbutyrolactone ; Apricolin ; Coconut aldehyde ; Dihydro-5-pentyl-2(3H)-furanone ; 4-nonalactone ; 1,4-nonalolide ; 1,4-nonanolide ; Gamma-nonanolide ; Gamma-nonyl lactone ; Gamma- pelargolactone ; 4-pentyl butanolide ; 5-pentyl-dihydro-furan-2-one ; 5- pentyloxolan-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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Aldéhyde C18 Gamma Nonalactone - 30 Gr | - |
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|
(S) GAMMA NONALACTONE | M_0054342 |
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Naturel | - | - | - | - | - |
Aldéhyde C18 Gamma Nonalactone - 30 Gr
Certifications :
(S) GAMMA NONALACTONE
ID : M_0054342
Certifications :
General Presentation
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CAS N° : 104-61-0
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EINECS number : 203-219-1
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FEMA number : 2781
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FLAVIS number : 10.001
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JECFA number : 229
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Appearance : Colorless liquid
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Density : 0,964
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Volatility : Heart
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Price Range : €€
Physico-chemical properties
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Molecular formula : C9H16O2
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Molecular Weight : 156,22 g/mol
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Log P : 2,5
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Fusion Point : Donnée indisponible.
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Boiling Point : 243°C
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Detection Threshold : 7 ppb (0,0000007%)
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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 : 126°C
Uses
Uses in perfumery :
Gamma-Nonalactone contributes to an exotic, fruity-peach, milky and gourmet facet, in adequation with fruity notes in particular.
Year of discovery :
Data not available.
Natural availability :
Gamma-Nonalactone is present in several foods and in the Eschweilera coriacea flower, from Central America. However, it is synthetic gamma-Nonalactone which is most often used in perfumery.
Isomerism :
Gamma-Nonalactone, like other lactones, has an asymmetric carbon. The smell of the two enantiomers of this molecule is similar. The racemic mixture is most often used in perfumery. Isoamyl Butyrate and Allyl Caproate are constitutional isomers of gamma-Nonalactone, but they have a very different butyric and cheesy smell.
Synthesis precursor :
Gamma-Nonalactone is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Gamma-Nonalactone is a cyclic lactone synthesized in the same way as other lactones. The reaction between acrylic acid and hexanol, in the presence of a sulfate or an alkaline phosphate, allows to synthesize this molecule. An intramolecular esterification of 4-hydroxynonanoic acid, catalysed by a strong acid such as concentrated sulfuric acid, also allows to obtain this compound. Finally, biochemical synthesis pathways are being studied by producing companies.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
