Jasmonal H® (CAS N° 101-86-0)​

Photo credits: ScenTree SAS

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Jasmonal H®

Hexyl Cinnamaldehyde ; Hexyl Cinnamaldehyde ; 2-(phenylmethylidene)octanal ; 2-benzylidene octanal ; Hexyl cinnamal ; Hexyl cinnamic aldehyde ; 2-hexyl-3-phenyl-2-propenal ; Alpha-N-hexyl-beta-phenyl acrolein ; 2-(phenylmethylidene)octanal

Jasmonal H® (CAS N° 101-86-0)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
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Jasmonal H - 30 Gr - Visit website Je me procure cet ingrédient - - - - - -

Jasmonal H - 30 Gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 101-86-0

  • EINECS number : 202-983-3

  • FEMA number : 2569

  • FLAVIS number : 05.041

  • JECFA number : 686

  • Appearance : Colorless liquid

  • Density : 0,955

  • Volatility : Heart

  • Price Range :

Physico-chemical properties

  • Molecular formula : C15H20O

  • Molecular Weight : 216,32 g/mol

  • Log P : 5,3

  • Fusion Point : 18°C

  • Boiling Point : 311°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 : 151°C

Utilisation

Uses

Uses in perfumery :

Jasmonal H® is used in notes of jasmine and lily of the valley, for a waxy facet, close to narcissus, and for trail. Formerly used to replace Hedione®.

Year of discovery :

1930

Natural availability :

Jasmonal H® is found in trace amounts in Roman Chamomile EO and rice. However, it is the synthetic Jasmonal H® that is most often used in perfumery.

Isomerism :

Jasmonal H® has two possible diastereoisomers. However, it is the mixture of the two isomers that is used in perfumery.

Synthesis precursor :

Jasmonal H® is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

As for Jasmonal A®, the synthesis of Jasmonal H® is made by condensation of benzaldehyde with Octanal (Aldehyde C-8), using an excess of benzaldehyde and gradually adding the Aldehyde C-8 in the reaction medium in order to avoid its self-condensation.

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
1,8 % 0,53 % 11 % 9,9 %
2,5 % 2,5 % 2,5 % 2,5 %
5,8 %
Cat.5
A B C D
Cat.6
2,5 % 2,5 % 2,5 % 2,5 %
5,8 %
Cat.7
A B
Cat.8 Cat.9
Cat.10
A B
Cat.11
A B
Cat.12
20 % 20 %
1 % 19 %
69 % 69 %
38 % 38 %
No Restriction
Cat.10
A B
Cat.11
A B
Cat.12
69 % 69 %
38 % 38 %
No Restriction
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