Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 141-13-9
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EINECS number : 205-460-8
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FEMA number : 4768
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Density : 0,852
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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
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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 :
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Detection Threshold : 5,38 ng/l air
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Molecular formula : C14H26O
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Log P : >6,00
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Molecular Weight : 210,36 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 126°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell.
Olfactively stable in any kind of products, except bleaches and other alkaline or stongly acidic detergents.
Uses in perfumery :
Adoxal® is used to work on aqueous, ozonic and juicy fruits notes for a very similar appearance to Calone®.
Year of discovery :
Data not available.
Isomerism :
Adoxal® has several asymmetric carbons. A mixture of its isomers is used in perfumery. Sandalore® is a constitutional isomer of Adoxal®. Nevertheless, this isomer has a very different smell as it is woodier and more sandalwood.
Synthesis precursor :
Adoxal® forms a Schiff base by reaction with Methyl Anthranilate or Indole for example.
Natural availability :
Adoxal® is not available in its natural state.
Synthesis route :
Adoxal® is synthesized from tetrahydroionone and alkyl chloroacetate by glycidyl ester condensation. This step is followed by a hydrolysis and a decarboxylation.
Regulations & IFRA
This ingredient is not restricted
