Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
---|---|---|---|---|---|---|---|---|---|---|
![]() |
Isoraldéine 70 - 30 Gr | - |
Visit website
|
- | - | - | - | - | - |
General Presentation
-
CAS N° :
1335-46-2 -
EINECS number :
204-846-3 -
FEMA number :
2714 -
FLAVIS number :
07.036
-
JECFA number :
404 -
Volatility :
Heart/Base -
Price Range :
€€
Physico chemical properties
-
Appearance :
Colorless to pale yellow liquid -
Density :
0,93 -
Refractive Index @20°C :
Data not available. -
Optical rotation :
Data not available. -
Vapor pressure :
0,0067 hPa @20°C -
Flash Point :
124°C
-
Molecular formula :
C14H22O -
Molecular Weight :
206,3 g/mol -
Log P :
4,7 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
238°C -
Detection Threshold :
1,706 ng/l air
Chemistry & Uses
Year of discovery :
Data not available.
Natural availability :
Isoraldeine 70® is not available in its natural state.
Isomerism :
As for conventional Ionones, the synthesis of alpha-Isomethylionone gives rise to other isomers of this molecule. beta-Isomethylionone has a more ambergris, orris and less fruity smell. Alpha-Irone and Cashmaeran are constitutional isomers of Isoraldeine®. Nevertheless, Cashmeran® has a distant smell, while Irone is closer to its violet aspect.
Synthesis precursor :
Isoraldeine 70® is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Isoraldeine 70® is composed of a predominantly methylionone isomer, called alpha-Isomethyl Ionone. The synthesis of methylionones is made from Citral and methyl ethyl ketone (instead of acetone for ionones). This synthesis step gives rise to two molecules called n-methyl pseudoionone and Isomethyl pseudoionone, both having cis and trans diastereoisomers. The ratio of one molecule relative to the other is favoured by the choice of the reaction catalyst: the stronger the catalyst base, the more Isomethyl pseudoionone will be favoured. For the cyclization step of Pseudoionone, as for Alpha-Ionone, the use of concentrated phosphoric acid favours alpha-Isomethylionone rather than the beta or gamma isomer. In general, each isomethyl ionone synthesis results in the formation of isomers of the desired molecule. In the case of Isoraldine 70®, its purity can reach 75% maximum (comparision with Isoraleine 95®).
Stability :
Unstable in acid products, except fabric conditioners, and in very alkaline products.
Other comments :
Isoraldeine 70® has a woodier note than Iralia®, less sweet than alpha-Ionone and less dusty than beta-Ionone.
Originally, the synthesis of some ionones gave birth to several organic waste, stored in barrels (fûts in French). The perfumer, Edmond Roudnitska, chose to use one of them in the creation of one of his biggest hits: fût n°5, which was subsequently regulated.
Then, Isoraldeine® served as a substitute for the note of fût n°5.
Methyl ionones are one of the 26 allergens in perfumery.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is restricted by the 51th amendment
- Quantitative limit on the use :
-
Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A B C DCat.6 5,4 % 1,6 % 32 % 30 % 7,6 % 7,6 % 7,6 % 7,6 %18 % Cat.5A B C DCat.6 7,6 % 7,6 % 7,6 % 7,6 %18 % Cat.7A BCat.8 Cat.9 Cat.10A BCat.11A BCat.12 61 % 61 %3,2 % 59 % 100 % 100 %100 % 100 %No Restriction Cat.10A BCat.11A BCat.12 100 % 100 %100 % 100 %No Restriction
-
Restricted ingredients: notes
The above limits apply to Methyl ionone isomers used individually or in combination.
Specified ingredients: notes
Pseudo methyl ionones (CAS numbers 26651-96-7, 72968-25-3, 1117-41-5) should not be used as fragrance ingredient as such. A level of up to 2% of Pseudo methyl ionones as an impurity in Methyl ionones is accepted.