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
  • Volatility :

    Heart
  • Price Range :

Physico-chemical properties

Physico chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,955
  • Refractive Index @20°C :

    1,548 - 1,552
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    0,00068 hPa @25°C
  • Flash Point :

    151°C
  • 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.
Utilisation

Chemistry & Uses

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.

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell.
Jamsonal A colors through time.

Other comments :

Jasmonal A® is more powerful, rising and soapy, but less watery than Jasmonal H®.
Jasmonal H® is one of the 26 allergens in perfumery.

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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