Photo credits: ScenTree SAS
Triplal®
Cyclal C® ; Vertocitral® ; Ligustral® ; 2,4-dimethylcyclohex-3-ene-1-carbaldehyde ; Acroval ; Citrulan ; Cyclogreenal ; 2,4-dimethyl-3-cyclohexene-1-carbaldehyde ; 4-formyl-1,3-dimethylcyclohex-1-ene ; Hivertal ; 2,4-ivy carbaldehyde ; Lantral ; Tricyclal ; Trigustral ; Trivertal ; Zestover
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
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Triplal - 30 Gr | - |
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SCHIFF LIGUSTRAL | 85530 |
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Molecule | - | - | - | - | - |
Triplal - 30 Gr
Certifications :
SCHIFF LIGUSTRAL
ID : 85530
Certifications :
General Presentation
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CAS N° : 68039-49-6
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EINECS number : 268-264-1
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FEMA number : 4505
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
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Appearance : Colorless liquid
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Density : 0,937
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Volatility : Head/Heart
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Price Range : €
Physico-chemical properties
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Molecular formula : C9H14O
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Molecular Weight : 138,21 g/mol
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Log P : 2,34
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Fusion Point : Donnée indisponible.
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Boiling Point :
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Detection Threshold : Donnée indisponible.
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Optical rotation : Donnée indisponible
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Vapor pressure : Donnée indisponible
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Refractive Index @20°C : Donnée indisponible
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Acid Value : Donnée indisponible.
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Flash Point : 70°C
Uses
Uses in perfumery :
Triplal® is used in jasmine, colognes and fougere notes, to bring a different green and fruity note and freshness. Brings a spring facet to floral notes.
Year of discovery :
1920
Natural availability :
Triplal® is not available in its natural state.
Isomerism :
Triplal® used in perfumery is a mixture of two enantiomers with very similar smells. This is why they are not separated by fractional distillation. Trans-2-cis-6-Nonadienal is a constitutional isomer of Triplal® but has a very different cucumber smell.
Synthesis precursor :
Triplal® forms a Schiff base with Methyl Anthranilate, with a still very green smell but fruity and more artificial.
Synthesis route :
Triplal® is synthesized by a Diels-Alder reaction between 2-methyl-1,3-pentadiene and acrolein. A mixture of two enantiomers is obtained.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is restricted by the 51th amendment
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Restriction type : RESTRICTION
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Cause of restriction : DERMAL SENSITIZATION
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Amendment : 49
- Quantitative limit on the use :
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Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A B C DCat.6 0,45 % 0,14 % 2,7 % 2,5 % 0,64 % 0,64 % 0,64 % 0,64 %1,5 % Cat.5A B C DCat.6 0,64 % 0,64 % 0,64 % 0,64 %1,5 % Cat.7A BCat.8 Cat.9 Cat.10A BCat.11A BCat.12 5,2 % 5,2 %0,27 % 4,9 % 18 % 18 %9,8 % 9,8 %No Restriction Cat.10A BCat.11A BCat.12 18 % 18 %9,8 % 9,8 %No Restriction
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Restricted ingredients: notes
The above limits apply to Dimethylcyclohexen-3-ene-1-carbaldehyde (mixed isomers) used individually or in combination. The sum of concentrations of Dimethylcyclohexen-3-ene-1-carbaldehyde isomers should not exceed the maximum concentration levels established by this Standard.
