Green > Cut Grass > Mushroom

Isocyclocitral®

2,4,6-trimethylcyclohex-3-ene-1-carbaldehyde ; Isocyclo citral ; Isocyclovert ; Isoleaf ; 1-formyl-3,5,6-trimethyl-3-cyclohexene

Isocyclocitral® (CAS N° 1335-66-6 ; 1423-46-7)​

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Information Générales

General Presentation

  • CAS N° : : 1335-66-6 ; 1423-46-7

  • EINECS number : 215-638-7

  • FEMA number : Donnée indisponible.

  • Density : 0,922

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Head

  • Price Range : €€

  • Appearance : Colorless liquid

  • FLAVIS number : 05.157

  • JECFA number : Donnée indisponible.

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 203°C

  • Detection Threshold : 5,2547 ng/l air

  • Molecular formula : C10H16O

  • Log P : 3,1

  • Molecular Weight : 152,24 g/mol

  • Fusion Point : -20°C

  • Flash Point : 66°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Isocyclocitral® is much different from other cut grass smell as Triplal® because of its powerful mushroom identity.

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell.

Uses in perfumery :

Isocyclocitral® is used in chypre and fougere perfumes, in woody, carnation, geranium, honeysuckle and tomato leaf notes.

Year of discovery :

Data not available.

Isomerism :

Isocyclocitral® contains three asymmetric carbons that give various conformational possibilities. As the reagents used for its synthesis are mixtures of diastereoisomers, it is a mixture of isomers that is used in perfumery. Citral is a constitutional isomer of Isocyclocitral®. Nevertheless, its smell is much more hesperidated and less green.

Synthesis precursor :

Isocyclocitral® forms a Schiff base by reaction with Methyl Anthranilate. The resulting compound is quite woody and close to orange blossom.

Natural availability :

Isocyclocitral® is not available in its natural state.

Synthesis route :

The molecule of Isocyclocitral® can be synthesized by a Diels-Alder reaction between 2-butenal and 2-methylpenta-1,3-diene.

Utilisation

Regulations & IFRA

  • IFRA 51th : This ingredient is restricted by IFRA

  • Restriction type : RESTRICTION

  • Cause of restriction : DERMAL SENSITIZATION

  • Amendment : 49

Quantitative limit on the use :
Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A Cat.5B Cat.5C Cat.5D Cat.6
0,54 % 0,16 % 3,2 % 3 % 0,76 % 0,76 % 0,76 % 0,76 % 1,8 %
Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12
6,1 % 6,1 % 0,32 % 5,9 % 21 % 21 % 12 % 12 % No Restriction
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