Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Aldéhyde Mandarine - 30gr | - |
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- | - | - | - | - | - | |
|
TRANS-2-DODECENAL | M_0062898 |
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|
Naturel | - | - | - | - | - |
Aldéhyde Mandarine - 30gr
Certifications :
TRANS-2-DODECENAL
ID : M_0062898
Certifications :
General Presentation
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CAS N° : 20407-84-5
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EINECS number : 243-797-2
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FEMA number : 2402
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FLAVIS number : 05.144
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JECFA number : 1350
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Appearance : Pale yellow liquid
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Density : 0,841 - 0,849 @25°C
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Volatility : Head/Heart
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Price Range : €€€
Physico-chemical properties
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Molecular formula : C12H22O
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Molecular Weight : 182,31 g/mol
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Log P : 4,53
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Fusion Point : Donnée indisponible.
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Boiling Point : 126°C
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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 : 113°C
Uses
Uses in perfumery :
Mandarin Aldehyde is used for all types of perfumes, for fresh notes. Used in floral-aldehydic, coniferous, ambery notes, for a contribution of a characteristic aldehydic note. Brings freshness, boosts the head and gives tenacity to citrus notes.
Year of discovery :
Data not available.
Natural availability :
Mandarin Aldehyde can be extracted from Coriander Leaf EO in its natural state, where it is present at about 20%.
Isomerism :
Mandarin Aldehyde has two diastereoisomers (Z) and (E). The isomer (E) in most often used in perfumery, to the detriment of the isomer (Z). Concentration of trans isomer is minimum 93%
Synthesis precursor :
Mandarin Aldehyde forms a Schiff base by reaction with Methyl Anthranilate or Indole for example.
Synthesis route :
Mandarin Aldehyde is an aliphatic aldehyde. As other aldehydes, it can be synthesized by reacting dodecenyl halides (chloride for example) with dimethyl sulfoxide (DMSO), followed by an alkaline treatment with sodium bicarbonate. Other synthesis routes exist using a Rosenmund reaction from dodecenic acid and an acid chloride.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
