Photo credits: ScenTree SAS
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 | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
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Canthoxal® - 30gr | - |
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SCHIFF CANTHOXAL | 85709 |
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Molecule | - | - | - | - | - |
Canthoxal® - 30gr
Certifications :
SCHIFF CANTHOXAL
ID : 85709
Certifications :
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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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
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Appearance : Colorless liquid
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Density : 1,043
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Volatility : Heart
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Price Range : €€
Physico-chemical properties
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Molecular formula : C11H14O2
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Molecular Weight : 178,23 g/mol
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Log P : 2,5
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Fusion Point : Donnée indisponible.
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Boiling Point : 108°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 : 94°C
Uses
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
Natural availability :
Canthoxal® is not available in its natural state.
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.
Synthesis route :
Canthoxal® is synthesized by a condensation reaction of Anisic Aldehyde with propanal, followed by a hydrogenation of the intermediate product.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is restricted by the 51th amendment
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Restriction type : RESTRICTION
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Cause of restriction : DERMAL SENSITIZATION AND SYSTEMIC TOXICITY
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Amendment : 51
- Quantitative limit on the use :
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Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A B C DCat.6 0,11 % 0,14 % 0,75 % 2,5 % 0,64 % 0,64 % 0,64 % 0,21 %0,11 % Cat.5A B C DCat.6 0,64 % 0,64 % 0,64 % 0,21 %0,11 % Cat.7A BCat.8 Cat.9 Cat.10A BCat.11A BCat.12 0,86 % 0,86 %0,21 % 2,7 % 0,75 % 4,1 %0,21 % 0,21 %No restriction Cat.10A BCat.11A BCat.12 0,75 % 4,1 %0,21 % 0,21 %No restriction
