Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Eucalyptol - 30gr | - |
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- | - | - | - | - | - | |
|
EUCALYPTOL | M_0053330 |
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Naturel | - | - | - | - | - |
Eucalyptol - 30gr
Certifications :
EUCALYPTOL
ID : M_0053330
Certifications :
General Presentation
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CAS N° : 470-82-6
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EINECS number : 207-431-5
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FEMA number : 2465
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FLAVIS number : 03.001
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JECFA number : 1234
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Appearance : Colorless liquid
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Density : 0,925
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Volatility : Head
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Price Range : €€
Physico-chemical properties
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Molecular formula : C10H18O
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Molecular Weight : 154,25 g/mol
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Log P : Donnée indisponible.
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Fusion Point : 1°C
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Boiling Point : 176°C
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Detection Threshold : 1 et 64 ppb (0,0000064%)
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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 : 48°C
Uses
Uses in perfumery :
Eucalyptol is used in woody, aromatic and fougere perfumes, to boost a lavender and to ice flowers and fruits, bringing them a cold facet.
Year of discovery :
Data not available.
Natural availability :
Eucalyptus EO contains up to 85% Eucalyptol, therefore the molecule can be extracted with a purity of up to 99,8%. Bay Leaf EO also contains up to 70% Eucalyptol.
Isomerism :
Eucalyptol has several constitutional isomers, mainly with a floral note: Linalool, Geraniol and Nerol are part of it. Menthone® is also an isomer of Eucalyptol, and has a very minty note, but less coniferous.
Synthesis precursor :
Eucalyptol can be a precursor to the synthesis of other terpenes, by a Diels-Alder reaction for example.
Synthesis route :
Eucalyptol is a little synthesized raw material, as it can be extracted from Eucalyptus EO and other oils with a high yield and high purity.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
