Photo credits: ScenTree SAS

Spicy > Cool Spices > Anisic > White Flowers > Green

Cis-jasmone

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

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	MOQ	Purity
	Cis-Jasmone - 30gr	-	Visit website	-		-	-
	JASMONE CIS	85035	Visit website	Molecule		-	-

Cis-Jasmone - 30gr

Certifications :

JASMONE CIS

ID : 85035

Certifications :

General Presentation

CAS N° :
488-10-8
EINECS number :
207-668-4
FEMA number :
3196
FLAVIS number :
07.094

JECFA number :
1114
Volatility :
Heart/Base
Price Range :
€€€

Physico chemical properties

Appearance :
Colorless liquid
Density :
0,941
Refractive Index @20°C :
1,495 – 1,501
Optical rotation :
Data not available.
Vapor pressure :
0,013 hPa @20°C 0,014 hPa @25°C
Flash Point :
121°C

Molecular formula :
C₁₁H₁₆O
Molecular Weight :
164,25 g/mol
Log P :
2,8
Fusion Point :
Donnée indisponible.
Boiling Point :
86°C
Detection Threshold :
2,9302 ng/l air

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.

Cis-jasmone

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Cis-jasmone

I buy this ingredient

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :