Canthoxal®
Anisyl Propanal ; 3-(4-methoxyphenyl)-2-methylpropanal ; Foliaver® ; Fennaldehyde ; Cantonal ; Canthorg ; Floral anise ; 2-methoxy-3-(para-methoxyphenyl) propanal ; 4-methoxy-alpha-methyl benzene propanal ; Para-methoxy-alpha-methyl hydrocinnamaldehyde ; Methoxyhydratropaldehyde ; Methoxyphenal ; 3-(para- methoxyphenyl)-2-methyl propionaldehyde ; 3-(4- methoxyphenyl)-2-methylpropanal ; Alpha- methyl-4-methoxybenzene propanal
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Canthoxal® - 30gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 5462-06-6
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EINECS number : 226-749-5
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FEMA number : Donnée indisponible.
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Density : 1,043
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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 : Heart
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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 : 108°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C11H14O2
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Log P : 2,5
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Molecular Weight : 178,23 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 94°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Canthoxal® is one of the only molecules mixing an anisic and ozonic note.
Stability :
Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell.
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Uses in perfumery :
Canthoxal® is used to create juicy fruits accords (melon, pear...) and floral notes (mimosa, brooms, lilies...). Can be used both as a booster for a cologne head or as a fresh note for oriental perfumes.
Year of discovery :
1951
Isomerism :
Canthoxal® has an asymmetrical carbon that gives rise to two enantiomers. However, it is the racemic mixture of these two isomers that is used in perfumery. Methyl Eugenol is a constitutional isomer of Canthoxal®. Its smell is however much more spicy and earthy.
Synthesis precursor :
Canthoxal® forms a Schiff base by reaction with Methyl Anthranilate or Indole for example.
Natural availability :
Canthoxal® is not available in its natural state.
Synthesis route :
Canthoxal® is synthesized by a condensation reaction of Anisic Aldehyde with propanal, followed by a hydrogenation of the intermediate product.
Regulations & IFRA
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IFRA 51th : This ingredient is restricted by IFRA
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Restriction type : RESTRICTION
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Cause of restriction : DERMAL SENSITIZATION AND SYSTEMIC TOXICITY
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Amendment : 49
- Quantitative limit on the use :
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Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A Cat.5B Cat.5C Cat.5D Cat.6 0,034 % 0,11 % 0,011 % 0,82 % 0,12 % 0,017 % 0,02 % 0,0056 % 0,0028 % Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12 0,023 % 0,023 % 0,0056 % 0,054 % 0,054 % 0,12 % 0,0056 % 0,0056 % 4,5 %
Comments :
This ingredient is part of the Schiff base (Canthoxal-methyl anthranilate (or Canthalide, Anthranolene) - N°CAS :111753-62-9) and induces the application of IFRA regulations for 57,3% of the Schiff base usage. Please also refer to the IFRA Annex II for more information
