Cis-jasmone (CAS N° 488-10-8)​

Photo credits: ScenTree SAS

Cis-jasmone

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3-methyl-2-[(Z)-pent-2-enyl]cyclopent-2-en-1-one ; (Z)-3-methyl-2-(2-pentenyl)-2-cyclopenten-1-one

Cis-jasmone (CAS N° 488-10-8)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo CIS JASMONE
CISJ-1
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Quosentis logo Cis-Jasmone - 30gr Discover - 30grs -
Synarome logo JASMONE CIS
85035
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PCW logo
CIS JASMONE

CISJ-1

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Quosentis logo
Cis-Jasmone - 30gr
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Synarome logo
JASMONE CIS

85035

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General Presentation

General Presentation

  • CAS N° :

    488-10-8
  • EINECS number :

    207-668-4
  • FEMA number :

    3196
  • FLAVIS number :

    7,094
  • JECFA number :

    1114
  • Volatility :

    Heart/Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,941
  • Refractive Index @20°C :

    1,495 – 1,501
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,0097 mmHg @20°C 0,0105 mmHg @25°C
  • Flash Point :

    121°C (249,8°F)
  • Molecular formula :

    C11H16O
  • Molecular Weight :

    164,25 g/mol
  • Log P :

    2,8
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    86°C (186,8°F)
  • Detection Threshold :

    2,9302 ng/l air
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Cis-jasmone is used in floral notes (tuberose, jasmine, gardenia) and ambery notes. Supports Hedione® and brings depth and power to jasmine notes.

Year of discovery :

Data not available.

Natural availability :

Cis-jasmone is found in Grandiflorum Jasmine Absolute (and other origins), Daffodil Absolute and Champaca Absolute. It can be extracted in its natural state from Grandiflorum Jasmine Absolute.

Isomerism :

The double bond guiding this cis-Jasmone conformation could also give rise to a trans conformation, depending on the synthesis conditions. The resulting smell would be much more earthy and close to mushroom.

Synthesis precursor :

Cis-jasmone is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

A synthetic route of cis-Jasmone consists of a nucleophilic substitution reaction between 3-methyl-2-cyclopenten-1-one and cis-2-pentenyl chloride, in the presence of sodium hydroxide.

Stability :

Unstable in acidic products, except fabric conditioners, and in very alkaline detergents.

Other comments :

Dihydrojasmone has a slightlymore almond and less green smell than cis-Jasmone.

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