Cyclacet (CAS N° 54830-99-8)​

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

Cyclacet (CAS N° 54830-99-8)​

Photo credits: ScenTree SAS

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

Certifications :

Information Générales

General Presentation

  • CAS N° : 54830-99-8

  • EINECS number : 259-367-2

  • FEMA number : Donnée indisponible.

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 1,07

  • Volatility : Base

  • Price Range :

Physico-chemical properties

  • 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.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 111°C

Utilisation

Uses

Uses in perfumery :

Cyclacet can be used in soap, detergent and air freshner bases for its stability, and to bring a quite functional green and aromatic note.

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.

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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