Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
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Anethol Naturel - 30 Gr | - |
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ANETHOL | M_0050614 |
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Naturel | - | - | - | - | - |
Anethol Naturel - 30 Gr
Certifications :
ANETHOL
ID : M_0050614
Certifications :
General Presentation
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CAS N° : 104-46-1 / 4180-23-8
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EINECS number : 224-052-0
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FEMA number : 2086
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FLAVIS number : 04.010
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JECFA number : 217
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Appearance : Colorless liquid
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Density : 0,983
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Volatility : Head/Heart
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Price Range : €€
Physico-chemical properties
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Molecular formula : C10H12O
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Molecular Weight : 148,2 g/mol
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Log P : Donnée indisponible.
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Fusion Point : 23°C
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Boiling Point : 236°C
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Detection Threshold : Donnée indisponible.
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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 : 91°C
Uses
Uses in perfumery :
Anethole enhances fruity and floral notes by bringing a greener and more anisic facet.
Year of discovery :
Data not available.
Natural availability :
Anethole can be obtained by crystallization of Anise EO or Star Anise EO, Sweet Fennel EO or from Turpentine EO, among others. In the case of turpentine, a mixture of Anethole and beta-Caryophyllene is obtained. Then, Anethole is separated from the mixture by crystallization. Another fraction of this extraction contains both Anethole and Estragol. Therefore, a potash treatment is necessary to obtain a mixture of Anethole and alpha-Terpineol. These two molecules are separable by fractional distillation.
Isomerism :
The trans-diastereoisomer of Anethole is always the most present in its natural state. In perfumery, it is usually a mixture of the two isomers that is used. Estragole is a positional isomer of Anethole. Both molecules have an anisic note, but Estragole is more aromatic and green.
Synthesis precursor :
Anethole is a precursor to the synthesis of Anisaldehyde by oxidation.
Synthesis route :
The synthesis of Anethole is made by a Friedel-Crafts reaction using methoxybenzene and propionyl chloride. A hydrogenation followed by an acid treatment allows to obtain Anethole.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
