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
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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
  • Volatility :

    Base
  • Price Range :

    €€€€
Physico-chemical properties

Physico chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,01
  • Refractive Index @20°C :

    1,475 - 1,480
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    0,003 hPa @20°C
  • Flash Point :

    >110°C (>230°F)
  • 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.
Utilisation

Chemistry & Uses

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.

Stability :

Lactones tend to polymerize through time, making them more viscous and leading to a phase shift in alcohol.

Other comments :

Jasmolactone has a jasmine undernote that makes the difference with other lactones as Delta-Decalactone.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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