Jasmolactone extra (CAS N° 32764-98-0)​

Photo credits: ScenTree SAS

Fruity > Lactonic > Yellow Fruits > Jasmine

Jasmolactone extra

Jasmalactone ; 6-(pent-3-en-1-yl)tetrahydro-2H-pyran-2-one ; Dec-8-eno-1,5-lactone ; 8-decen-5-olide ; Petal pyranone ; Tetrahydro-6-(3-pentenyl)-2H-pyran-2-one ; Tetrahydro-6-pent-3-enyl pyran-2-one

Jasmolactone extra (CAS N° 32764-98-0)​

Photo credits: ScenTree SAS

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

Jasmolactone® - 30gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 32764-98-0

  • EINECS number : 251-201-7

  • FEMA number : 4441

  • FLAVIS number : 10.040

  • JECFA number : 1994

  • Appearance : Colorless liquid

  • Density : 1,01

  • Volatility : Base

  • Price Range : €€€€

Physico-chemical properties

  • Molecular formula : C10H16O2

  • Molecular Weight : 168,24 g/mol

  • Log P : Donnée indisponible.

  • Fusion Point : Donnée indisponible.

  • Boiling Point : 150°C (à 23 hPa)

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : >110°C (>230°F)

Utilisation

Uses

Uses in perfumery :

Jasmolactone is used in luxury perfumery for reconstitutions of white flowers, for ambery notes and to give facets to a tea note.

Year of discovery :

1961

Natural availability :

Jasmolactone is only present in trace amounts in Osmanthus Absolute, not allowing to obtain it in its natural state.

Isomerism :

Another molecule is also called δ-Jasmolactone, but is synthesized from 4-hydroxydec-7-enoic acid, which places the double bond of the final product on another carbon aside. The smell of this isomer is similar to the Jasmolactone described here. Gamma-Jasmolactone has a more fatty smell, close to peanut. Methyl Laitone® is a constitutional isomer of Jasmolactone, but has a coconut-like smell and a lactonic body.

Synthesis precursor :

Jasmolactone is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Like the other lactones, Jasmolactone, is synthesized by an intramolecular esterification reaction that involves 4-hydroxydec-8-enoic acid, in the presence of an acid catalyst. Then, the cyclization of this molecule gives rise to a δ-lactone.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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.