Photo credits: ScenTree SAS

Canthoxal®

Herbal > Anisic > Ozonic > Almondy

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

Ingredient Name	ID	Comments	Naturality	MOQ	Purity
Canthoxal® - 30gr	-	Visit website	-	-	-
SCHIFF CANTHOXAL	85709	Visit website	Molecule	-	-
CANTONAL	CAN-1	Visit website	-	10 grs	98.0 - 100.0

Canthoxal® - 30gr

Certifications :

SCHIFF CANTHOXAL

ID : 85709

Certifications :

CANTONAL

ID : CAN-1

Roumanie

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

Appearance :
Colorless liquid
Density :
1,043
Refractive Index @20°C :
1,517 - 1,522
Optical rotation :
Donnée indisponible.
Vapor pressure :
0,0023 mmHg @23°C 0,0097 mmHg @25°C
Flash Point :
94°C (201,2°F)

Molecular formula :
C₁₁H₁₄O₂
Molecular Weight :
178,23 g/mol
Log P :
2,5
Fusion Point :
Donnée indisponible.
Boiling Point :
108°C (226,4°F)
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.

Labelling

Allergens :

This ingredient does not contain any allergen.

IFRA

IFRA 51^th :

This ingredient is restricted by the 51th amendment

Restriction type :

RESTRICTION

Cause of restriction :

DERMAL SENSITIZATION AND SYSTEMIC TOXICITY

Amendment :

Quantitative limit on the use :

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5 A B C D		Cat.6
0,11 %	0,14 %	0,75 %	2,5 %	0,64 % 0,64 % 0,64 % 0,21 %		0,11 %
Cat.5 A B C D			Cat.6
0,64 % 0,64 % 0,64 % 0,21 %			0,11 %
Cat.7 A B		Cat.8	Cat.9	Cat.10 A B	Cat.11 A B	Cat.12
0,86 % 0,86 %		0,21 %	2,7 %	0,75 % 4,1 %	0,21 % 0,21 %	No restriction
Cat.10 A B	Cat.11 A B	Cat.12
0,75 % 4,1 %	0,21 % 0,21 %	No restriction

Canthoxal®

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General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico-chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Labelling

Allergens :

IFRA

IFRA 51th :

Restriction type :

Cause of restriction :

Amendment :

IFRA 51^th :