Photo credits: ScenTree SAS
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General Presentation
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CAS N° : 35044-59-8
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EINECS number : 252-335-9
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FEMA number : Donnée indisponible.
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
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Appearance : Colorless liquid
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Density : 0,967
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Volatility : Head/Heart
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Price Range : €€€
Physico-chemical properties
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Molecular formula : C12H18O2
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Molecular Weight : 194,27 g/mol
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Log P : Donnée indisponible.
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Fusion Point : Donnée indisponible.
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Boiling Point : 239°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 : 85°C
Uses
Uses in perfumery :
Ethyl Safranate is used in saffron notes, fruity notes of yellow fruits such as plum and other stone fruits, for notes of cooked apple, in woody perfumes to bring a fruity note and in floral notes. It can be used in various alkaline bases for its stability.
Year of discovery :
1955
Natural availability :
Ethyl Safranate is not available in its natural state.
Isomerism :
The Ethyl Safranate most commonly used in perfumery is a mixture of alpha, beta and gamma isomers of the molecule. These isomers are not isolated for their use in perfumery. In addition, Ethyl Safranate is a constitutional isomer of Scentenal® and Hyacinth Body®. Their smell is however very different.
Synthesis precursor :
Ethyl Safranate does not interfere with the synthesis of another compound of olfactory interest.
Synthesis route :
Ethyl Safranate can be synthesized by a reaction between Mesityl Oxide and Ethyl Acetoacetate. Both will cyclize when put in an acid medium. The obtained intermediate molecule can be reduced and dehydrated to obtain Ethyl Safranate.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
