Photo credits: ScenTree SAS
Iso E Super®
Amberonne® ; Orbitone® ; Arborone® ; 1-(2,3,8,8-tetramethyl-1,3,4,5,6,7-hexahydronaphthalen-2-yl)ethanone ; 1,2,3,4,5,6,7,8-octahydro-2,3,8,8-tetramethyl-2-acetonaphthone ; Amber fleur ; Isoamber super ; Amberfleur ; Ambergris ketone ; Amberix super ; Amberlan ; Ambroise super ; Anthamber ; Boisvelone ; Isocyclemone E ; Dimethyl myrcetone ; Hamber ; Iso gamma super ; Methyl cyclomyrcetone ; Patchouli ethanone ; Sylvamber ; Timbersilk ; Timbrone supra ; Iso velvetone
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Iso E Super - 30 Gr | - |
Visit website
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Iso E Super - 30 Gr
Certifications :
General Presentation
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CAS N° : 54464-57-2
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EINECS number : 259-174-3
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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 : 0,964
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Volatility : Base
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Price Range : €€
Physico-chemical properties
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Molecular formula : C16H26O
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Molecular Weight : 234,38 g/mol
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Log P : 5,65
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Fusion Point : Donnée indisponible.
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Boiling Point : 290°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 : 134°C
Uses
Uses in perfumery :
Iso E Super® is used in masculine, woody and ambery notes as a woody base. Allows to bring a light violet flower note to woody accords.
Year of discovery :
Discovered in 1956. Iso E Super® was first patented in 1973, by scientists John B. Hall and James M. Sanders.
Natural availability :
Iso E Super® is not available in its natural state.
Isomerism :
Iso E Super® is composed by more than 20 isomeric molecules. The molecule called Isocyclemone in its pure state, has almost no smell, but the Iso E Super® called '' Plus '', so-called Arborone, found at between 2 and 5% in the commercialised Iso E Super®, has a very strong smell (10 000 times more powerful than Iso E Super), and is responsible for the smell of Iso E Super®. Iso E Super® Plus alone is not marketed because its production is too expensive.
Synthesis precursor :
Iso E Super® is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Iso E Super® is synthesized by a Diels-Alder reaction between Myrcene and 3-methyl-3-penten-2-one in the presence of aluminum chloride. The cyclization of the intermediate product obtained is made thanks to the action of phosphoric acid. This cyclization gives birth to two isomers : Iso E Super® and Arborone, in 95/5 proportions.
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 : 49
- Quantitative limit on the use :
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Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A B C DCat.6 0,41 % 1,1 % 0,41 % 20 % 5,1 % 0,56 % 0,76 % 0,19 %0,0093 % Cat.5A B C DCat.6 5,1 % 0,56 % 0,76 % 0,19 %0,0093 % Cat.7A BCat.8 Cat.9 Cat.10A BCat.11A BCat.12 0,67 % 0,67 %0,19 % 2,4 % 2,4 % 6,6 %0,19 % 0,19 %No Restriction Cat.10A BCat.11A BCat.12 2,4 % 6,6 %0,19 % 0,19 %No Restriction
