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| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Aldéhyde C12 MNA - 30 Gr | - |
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Aldéhyde C12 MNA - 30 Gr
Certifications :
General Presentation
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CAS N° : 110-41-8
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EINECS number : 203-765-0
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FEMA number : 2749
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FLAVIS number : 05.077
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JECFA number : 275
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Appearance : Colorless liquid
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Density : 0,832
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Volatility : Heart
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Price Range : €€
Physico-chemical properties
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Molecular formula : C12H24O
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Molecular Weight : 184,32 g/mol
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Log P : 4,9
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Fusion Point : <-50°C
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Boiling Point : 231°C
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Detection Threshold : 0,0209 ng/l air
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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 : 68°C
Uses
Uses in perfumery :
Aldehyde C-12 MNA is used in citrus notes, in colognes and eaux fraiches in small quantities. Boosts the top note of the formula.
Year of discovery :
Discovered in 1903.
Natural availability :
Aldehyde C-12 MNA is not available in its natural state.
Isomerism :
Aldehyde C-12 MNA is less zesty than Aldehyde C-12 Lauric.
Synthesis precursor :
Aldehyde C-12 MNA forms a Schiff base by reaction with Methyl Anthranilate or Indole for example. It can also be used for condensation with another aldehyde or ketone to form the desired alcene.
Synthesis route :
Aldehyde C-12 MNA (for Methyl Nonyl Acetaldehyde) is synthesized in two different ways. 2-Undecanone reacts with a Chloroacetate to give a glycidate, which can be saponified and decarboxylated to obtain the final product. The second route of synthesis firstly reacts Aldehyde C-11 Undecylenic with formaldehyde in the catalytic presence of an amine, and then a hydrogenation of the intermediate product allows to obtain the Aldehyde C-12 MNA.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
