Photo credits: ScenTree SAS

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Cyclacet

acetate de verdyl ; Verdyl acetate ; Herbaflorat ; Jasmacyclene ; Greenenyl acetate ; 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-indenyl acetate ; acetate de 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-indenyl ; Tricyclo(5.2.1.02,6)dec-3-enyl acetate ; acetate de tricyclo(5.2.1.02,6)dec-3-enyl

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	Purity	Latin name	Treated part	Geographical origin	MOQ
	Cyclacet - 30gr	-	Visit website	-		-	-	-	-	-

Cyclacet - 30gr

Certifications :

General Presentation

CAS N° :
54830-99-8
EINECS number :
259-367-2
FEMA number :
Donnée indisponible.
FLAVIS number :
Donnée indisponible.

JECFA number :
Donnée indisponible.
Volatility :
Base
Price Range :
€

Physico chemical properties

Appearance :
Colorless liquid
Density :
1,07
Refractive Index @20°C :
Data not available.
Optical rotation :
Data not available.
Vapor pressure :
Data not available.
Flash Point :
111°C

Molecular formula :
C₁₂H₁₆O₂
Molecular Weight :
192,26 g/mol
Log P :
3,9
Fusion Point :
Donnée indisponible.
Boiling Point :
247°C
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

Year of discovery :

1959

Natural availability :

Cyclacet is not found in nature. Thus, it is not extracted from any plant.

Isomerism :

Cyclacet is made of two isomers, formed during its synthesis. Their smell being not so different (one of the isomers is more woody and coniferous anyway), a mixture of the two isomers is used in perfumery.

Synthesis precursor :

Cyclacet is not used for the synthesis of another compound used in perfumes.

Synthesis route :

Cyclacet can be obtained with an addition reaction involving Acetic Acid and dicyclopentadiene, also using an acidic catalysor as concentrated sulfuric acid. This reaction gives birth to a mixture of two positional isomers, that are not separated afterwards.

Stability :

Esters may form their corresponding acid under the effect of heat.

Other comments :

Both imbricated cycles of the molecule are often associated with a woody note. It is the case for example in Mysore acetate, whose ester function is on the other side of the two cycles. This woody facet is anyway less percievable in Cyclacet.

Cyclacet

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

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Cyclacet

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

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :