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 | MOQ | Purity |
|---|---|---|---|---|---|---|---|
|
Canthoxal® - 30gr | - |
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SCHIFF CANTHOXAL | 85709 |
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|
Molecule | - | - |
Canthoxal® - 30gr
Certifications :
SCHIFF CANTHOXAL
ID : 85709
Certifications :
General Presentation
-
CAS N° :
5462-06-6 -
EINECS number :
226-749-5 -
FEMA number :
Donnée indisponible. -
FLAVIS number :
Donnée indisponible.
-
JECFA number :
Donnée indisponible. -
Volatility :
Heart -
Price Range :
€€
Physico chemical properties
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Appearance :
Colorless liquid -
Density :
1,043 -
Refractive Index @20°C :
1,517 - 1,522 -
Optical rotation :
Data not available. -
Vapor pressure :
0,002269 mmHg @23°C 0,013 hPa @25°C -
Flash Point :
94°C
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Molecular formula :
C11H14O2 -
Molecular Weight :
178,23 g/mol -
Log P :
2,5 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
108°C -
Detection Threshold :
Donnée indisponible.
Chemistry & 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.
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
Other comments :
Canthoxal® is one of the only molecules mixing an anisic and ozonic note.
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 -
Cause of restriction :
DERMAL SENSITIZATION AND SYSTEMIC TOXICITY -
Amendment :
51
- Quantitative limit on the use :
-
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
