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| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
CINNAMIC ALDEHYDE | M_0050621 | Naturel | - | - | - | - | more | - |
General Presentation
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CAS N° : : 104-55-2
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EINECS number : 203-213-9
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FEMA number : 2286
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Density : 1,05
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Heart/Base
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Price Range : €
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Appearance : Viscous yellow liquid
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FLAVIS number : 05.014
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JECFA number : 656
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 248°C
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Detection Threshold : 50 et 750 ppb (0,000075%)
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Molecular formula : C9H8O
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Log P : Donnée indisponible.
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Molecular Weight : 132,16 g/mol
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Fusion Point : -7,5°C
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Flash Point : 71°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Cinnamaldehyde is one of the 26 allergens in perfumery.
Stability :
Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Uses in perfumery :
Cinnamaldehyde gives a spicy note to fruity and oriental accords.
Year of discovery :
Discovered en 1856.
Isomerism :
Like Cinnamyl Alcohol, Cinnamaldehyde can be divided into two diastereoisomers: trans or cis. Trans is the most found in nature. Both have a cinnamon-like smell, but the trans is warmer and smells even more like cinnamon than cis. The raw material used in perfumery is usually a mixture of the two isomers.
Synthesis precursor :
Hydrogenation of Cinnamaldehyde provides DihydroCinnamaldehyde and DihydroCinnamyl Alcohol. Moreover, the oxidation of the aldehyde gives a Cinnamic Acid, another compound of olfactory interest. Finally, Cinnamaldehyde forms a Schiff base by reaction with Methyl Anthranilate or Indole for example.
Natural availability :
Cinnamaldehyde is present in a large quantity in Cassia EO (about 90%) and Ceylon Cinnamon EO (about 75%). It can therefore be extracted from these essential oils by fractional distillation.
Synthesis route :
The synthesis of Cinnamaldehyde is made by a condensation of Benzaldehyde with Acetaldehyde, using an excess of Benzaldehyde and gradually adding Acetaldehyde, in order to avoid self-condensation of the latter.
Regulations & IFRA
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IFRA 51th : This ingredient is restricted by IFRA
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Restriction type : RESTRICTION
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Cause of restriction : DERMAL SENSITIZATION AND SYSTEMIC TOXICITY
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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 Cat.5B Cat.5C Cat.5D Cat.6 0,045 % 0,014 % 0,021 % 0,25 % 0,064 % 0,042 % 0,064 % 0,014 % 0,15 % Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12 0,17 % 0,17 % 0,014 % 0,49 % 0,49 % 1,8 % 0,014 % 0,014 % No Restriction
Comments :
This ingredient is part of the Schiff base (Cinnamic aldehyde methyl anthranilate - N°CAS : 94386-48-8) and induces the application of IFRA regulations for 49,8% of the Schiff base usage. Please also refer to the IFRA Annex II for more information
