Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Polysantol® - 30gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 107898-54-4
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EINECS number : 411-580-3
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FEMA number : Donnée indisponible.
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Density : 0,902
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Base
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point :
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Detection Threshold : Donnée indisponible.
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Molecular formula : C15H26O
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Log P : 4,7
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Molecular Weight : 222,37 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : >100°C (>212°F)
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Several sandalwood compounds have similar structures. This is the case of Ebanol, Bacdanol®, Javanol® and Polysantol®. Their structure is composed of a branched cyclopentenic body, and a long carbon chain attached to this cycle. It is on this chain that the differences between the compounds are made.
Stability :
Stable in perfumes and diverse functional bases
Uses in perfumery :
Polysantol® is used in woody accords, linked with musky notes, in milk accords and in sandalwood notes in woody perfumes. Brings a cosmetic note.
Year of discovery :
1984 'Polysantol®' trademark has been published and protected by Firmenich SA since 22/10/1985 (brand N°497404)
Isomerism :
Polysantol® has a double bond and two asymmetric carbons that give rise to several isomers of this molecule. It is nevertheless its mixture of isomers that is used in perfumery. In addition, Polysantol® is a constitutional isomer of Javanol®. These two compounds have a similar structure, and are used for similar reasons in perfumery. Javanol® has a less milky note than Polysantol®, but is more powerful.
Synthesis precursor :
Polysantol® is not used to synthesize other compounds of organoleptic interest.
Natural availability :
Polysantol® is not available in its natural state.
Synthesis route :
Polysantol® is synthesized from campholenaldehyde, condensed with butan-2-one in an acid medium to give 3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-3-penten-2-one as an intermediate product. A methylation step under phase transfer conditions provides a new product, which can be reduced by sodium borohydride to get Polysantol®.
Regulations & IFRA
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IFRA 51th : This ingredient is restricted by IFRA
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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 Cat.5B Cat.5C Cat.5D Cat.6 0,031 % 0,057 % 0,25 % 1,1 % 0,27 % 0,27 % 0,27 % 0,091 % 0,031 % Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12 0,63 % 0,63 % 0,091 % 1,7 % 1,7 % 4 % 0,091 % 0,091 % No Restriction
