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

Photo credits: ScenTree SAS

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)​

Photo credits: ScenTree SAS

Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.

Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.

Information Générales

General Presentation

  • CAS N° : 1335-66-6 ; 1423-46-7

  • EINECS number : 215-638-7

  • FEMA number : Donnée indisponible.

  • FLAVIS number : 05.157

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 0,922

  • Volatility : Head

  • Price Range : €€

Physico-chemical properties

  • Molecular formula : C10H16O

  • Molecular Weight : 152,24 g/mol

  • Log P : 3,1

  • Fusion Point : -20°C

  • Boiling Point : 203°C

  • Detection Threshold : 5,2547 ng/l air

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 66°C

Utilisation

Uses

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.

Natural availability :

Isocyclocitral® is not available in its natural state.

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.

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

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is restricted by the 51th amendment

    IFRA's logo
  • Restriction type : RESTRICTION

  • Cause of restriction : DERMAL SENSITIZATION

  • Amendment : 49

Quantitative limit on the use :
Cat.1 Cat.2 Cat.3 Cat.4
Cat.5
A B C D
Cat.6
0,54 % 0,16 % 3,2 % 3 %
0,76 % 0,76 % 0,76 % 0,76 %
1,8 %
Cat.5
A B C D
Cat.6
0,76 % 0,76 % 0,76 % 0,76 %
1,8 %
Cat.7
A B
Cat.8 Cat.9
Cat.10
A B
Cat.11
A B
Cat.12
6,1 % 6,1 %
0,32 % 5,9 %
21 % 21 %
12 % 12 %
No Restriction
Cat.10
A B
Cat.11
A B
Cat.12
21 % 21 %
12 % 12 %
No Restriction
I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.