Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 40379-24-6
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EINECS number : 254-898-6
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FEMA number : Donnée indisponible.
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Density : 0,866
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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 : Head/Heart
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Price Range : Data not available.
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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 :
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Detection Threshold : Donnée indisponible.
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Molecular formula : C11H22O2
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Log P : 4,1
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Molecular Weight : 186,29 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 71°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Olfactively, Isononyl acetate is close to Cetone V®, or Allyl Alpha-Ionone. Both molecules have fruity-pineapple facets, with a powdery violet flower note. Isononyl acetate stands out thanks to a bergamot and dry woody note, close to Iso E Super®.
Stability :
Esters tend to form their corresponding acid in stability.
Uses in perfumery :
Isononyl acetate is used in lavender and bergamot reconstitutions, to bring a very functionnal effect, with tea, powdery and orris root notes.
Year of discovery :
Data not available.
Isomerism :
Isononyl acetate is a constitutional isomer of Methyl Pamplemousse®. These two compounds do not have any olfactive similarities.
Synthesis precursor :
Isononyl acetate is not a precursor for the synthesis of another compound of olfactive interest.
Natural availability :
Isononyl acetate can be found in big quantity in some varieties of Lavandin EO and Bitter Orange EO.
Synthesis route :
Isononyl acetate is prepared by an esterification reaction involving Isononanol (or 8-methyl nonan-1-ol) and acetic acid. This acid can be replaced by acetic anhydride and chloroacetic acid, to raise the reaction yield.
Regulations & IFRA
This ingredient is not restricted
