Grisalva® (CAS N° 68611-23-4)​

Photo credits: ScenTree SAS

Grisalva®

Balsamic Ambery > Ambergris > Dry Woods > Rosy

Amber furan ; 3a-ethyl dodecahydro-6,6,9a-trimethyl naphto(2,1-b)furan ; Ethyl dodecahydrotrimethyl naphtofuran ; Trimethyl-2-cyclohexenyl-3-pentanone-2-propynol

Grisalva® (CAS N° 68611-23-4)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
Quosentis logo
Grisalva® - 30gr - Visit website Je me procure cet ingrédient - - -
PCW logo
GRISALVA GRIS-1 Visit website Je me procure cet ingrédient - 10 grs -

Grisalva® - 30gr

Certifications :

GRISALVA

ID : GRIS-1

Certifications :

Information Générales

General Presentation

  • CAS N° :

    68611-23-4
  • EINECS number :

    271-889-2
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Base
  • Price Range :

    €€€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Yellow liquid
  • Density :

    0,962 - 0,970 @20°C
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,00049 mmHg @23°C
  • Flash Point :

    94°C (201,2°F)
  • Molecular formula :

    C17H30O
  • Molecular Weight :

    264,41 g/mol
  • Log P :

    6,58
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Used in low quantity (for cost reasons) in woody and ambery notes, in order to reproduce ambergris smell with great quality.

Year of discovery :

2007

Natural availability :

Grisalva® is exclusively resulting from a synthesis, an does not exist on its natural state.

Isomerism :

Both isomers of Grisalva® are enantiomers. They are not used separately in perfumery. The two other molecules that make up Grisalva® are very close in structure: one has a double bond on its 6-carbon cycle, while the other has none.

Synthesis precursor :

Grisalva® is not a precursor for the synthesis of another compound of olfactory interest.

Synthesis route :

Grisalva® is a mixture of four molecules, two of which are isomers. These molecules result from the reaction between prop-2-yn-1-ol and 1-(2,6,6-trimethyl-1-cyclohex-2-enyl)pentan-3-one, which is structurally very close to DihydroBeta-Ionone.

Stability :

Stable in perfumes and in diverse functional bases

Other comments :

Grisalva® takes its name from ambergris, a spermwhale rejection formerly used for perfumery.

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