Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 2550-11-0
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EINECS number : 219-845-3
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FEMA number : Donnée indisponible.
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Density : 0,845
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Heart/Base
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 209°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C10H18O
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Log P : Donnée indisponible.
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Molecular Weight : 154,25 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 68°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Dimethyl Octenone is part of the terpenes family. These are molecules frequently synthesized by a Diels-Alder reaction, making the number of carbons in the empirical formula a multiple of five.
Stability :
Unstable in very acidic and very alkaline products.
Uses in perfumery :
Dimethyl Octenone is used in grapefruit notes and in fruity notes to bring a minthy nuance and depth. Also used in buchu or mint notes to bring a slightly zesty note.
Year of discovery :
Data not available.
Isomerism :
Dimethyl Octenone has an asymmetric carbon, giving rise to two possible enantiomers for this molecule. Nevertheless, the ingredient used in perfumery is a mix of the enantiomers of the molecule. Dimethyl Octenone is also a constitutional isomer of Linalool and Geraniol, among others, meanwhile it doesn't have the same smell as its isomers used in perfumery.
Synthesis precursor :
Dimethyl Octenone is not used for the synthesis of another molecule used in perfumery.
Natural availability :
Dimethyl Octenone is not found in nature.
Synthesis route :
Dimethyl Octenone can be synthesized by an alkylation reaction engaging diethyl ketone and prenyl chloride.
Regulations & IFRA
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IFRA 51th : This ingredient is restricted by IFRA
This ingredient is not restricted for the 49th amendment
