Polysantol® (CAS N° 107898-54-4)​

Photo credits: ScenTree SAS

Woody > Sandalwood > Milky > Buttery

Polysantol®

Mysantol® ; (E)-3,3-dimethyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol ; Aquisantol ; Lansantol ; Megasantol ; Nirvanol ; Santol pentenol ; Supersantol ; Trimethyl cyclopentenyl dimethyl isopentenol

Polysantol® (CAS N° 107898-54-4)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
Quosentis logo
Polysantol® - 30gr - Visit website Je me procure cet ingrédient - - - - - -

Polysantol® - 30gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 107898-54-4

  • EINECS number : 411-580-3

  • FEMA number : Donnée indisponible.

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 0,902

  • Volatility : Base

  • Price Range : €€

Physico-chemical properties

  • Molecular formula : C15H26O

  • Molecular Weight : 222,37 g/mol

  • Log P : 4,7

  • Fusion Point : Donnée indisponible.

  • Boiling Point :

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : >100°C (>212°F)

Utilisation

Uses

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)

Natural availability :

Polysantol® is not available in its natural state.

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.

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®.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is restricted by the 51th amendment

    IFRA's logo
  • Restriction type : RESTRICTION

  • Cause of restriction : DERMAL SENSITIZATION AND SYSTEMIC TOXICITY

  • Amendment : 49

Quantitative limit on the use :
Cat.1 Cat.2 Cat.3 Cat.4
Cat.5
A B C D
Cat.6
0,031 % 0,057 % 0,25 % 1,1 %
0,27 % 0,27 % 0,27 % 0,091 %
0,031 %
Cat.5
A B C D
Cat.6
0,27 % 0,27 % 0,27 % 0,091 %
0,031 %
Cat.7
A B
Cat.8 Cat.9
Cat.10
A B
Cat.11
A B
Cat.12
0,63 % 0,63 %
0,091 % 1,7 %
1,7 % 4 %
0,091 % 0,091 %
No Restriction
Cat.10
A B
Cat.11
A B
Cat.12
1,7 % 4 %
0,091 % 0,091 %
No Restriction
I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.