Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | MOQ | Purity | 
|---|---|---|---|---|---|---|---|
|   | Aldéhyde C11 Undécylénique - 30gr | - | Visit website | - | - | - | 
General Presentation
- 
								CAS N° :112-45-8
- 
								EINECS number :203-973-1
- 
								FEMA number :3095
- 
									FLAVIS number :05.035
- 
									JECFA number :330
- 
								Volatility :Head
- 
								Price Range :€€
Physico chemical properties
- 
								Appearance :Colorless liquid
- 
								Density :0,844
- 
								Refractive Index @20°C :1,441 – 1,447
- 
								Optical rotation :Data not available.
- 
								Vapor pressure :0,04 hPa @20°C 0,051 hPa @25°C
- 
								Flash Point :96°C
- 
								Molecular formula :C11H20O
- 
								Molecular Weight :168,28 g/mol
- 
								Log P :5,1
- 
								Fusion Point :7°C
- 
								Boiling Point :235°C
- 
								Detection Threshold :2,8541 ng/l air
Chemistry & Uses
Uses in perfumery :
Aldehyde C-11 Undecylenic provides an aldehydic facet in green, chypre, rose, floral-violet, tuberose notes. Used in detergents for its stability.
Year of discovery :
Data not available.
Natural availability :
Aldehyde C-11 Undecylenic has been identified as present in trace amounts in Coriander Leaf EO, but is not extracted in its natural state.
Isomerism :
Ethyl Linalool is a constitutional isomer of Aldehyde C-11 Undecylenic. Its smell is however much more floral-fresh and less zesty.
Synthesis precursor :
Aldehyde C-11 undecylenic 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 :
Like the other aliphatic aldehydes, Aldehyde C-11 undecylenic, can be synthesized by a reaction of undecylenyl halides (chloride, for example) with dimethyl sulfoxide (DMSO), followed by an alkaline treatment with sodium bicarbonate. Other synthetic routes exist, such as a reduction of Rosenmund from undecylenic acid, using an acid chloride.
Stability :
Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell
Other comments :
Aldehyde C-11 Undecylenic is greener and less zesty-lemon than Aldehyde C-11 Undecylic. Aldehydes C-12 are more orange and less butyric. C-8 is less green.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
 
      
      
       
 
 
 
 
 
 
 
 
 
 
 
