Photo credits: ScenTree SAS
Syringa Aldehyde
Floral > White Flowers > Solar > Honeyed > Animalic
Syringua aldehyde ; Seringa aldehyde ; 4-methylbenzene acetaldehyde ; Lilac acetaldehyde ; Para-methylbenzene acetaldehyde ; Syringaldehyde ; Syringa aldehyde ; 2-(4-methylphenyl)acetaldehyde ; Para-tolyl acetaldehyde
Photo credits: ScenTree SAS
| Company | Ingredient Name | Learn more | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|
|
SYRINGA ALDEHYDE (50%)
ALS-1
|
Discover | - | 10 grs | - |
General Presentation
-
CAS N° :
104-09-6 -
EINECS number :
203-173-2 -
FEMA number :
3071 -
FLAVIS number :
5,042
-
JECFA number :
1023 -
Volatility :
Heart -
Price Range :
€€€€€
Physico-chemical properties
-
Appearance :
Colorless liquid -
Density :
1,032 -
Refractive Index @20°C :
Donnée indisponible. -
Optical rotation :
Donnée indisponible. -
Vapor pressure :
Donnée indisponible. -
Flash Point :
70°C (158°F)
-
Molecular formula :
C9H10O -
Molecular Weight :
134,18 g/mol -
Log P :
2,21 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
-
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
Uses in perfumery :
Syringa Aldehyde is used for mimosa accords, and for its honey and powdery facet in floral notes, also bringing an animalic facet.
Year of discovery :
Data not available.
Natural availability :
Syringa Aldehyde is found in corn oil in small quantity, not allowing to use dit in its natural state.
Isomerism :
Syringa Aldehyde has two positional isomers : ortho-methyl benzyl acetaldehyde and meta-methyl benzyl acetaldehyde. Both are not used in perfumery. Syringa Aldehyde also is a constitutional isomer of Cinnamic Alcohol, although it does not have the same smell.
Synthesis precursor :
Syringa Aldehyde is not used for the synthesis of another compound of olfactive interest.
Synthesis route :
Syringa Aldehyde can be synthesized from para-methylbenzaldehyde, by reacting with a random chloroacetate. This step has to be followed by an acidic hydrolysis of the obtained glycidate, with a subsequent decarboxylation.
Stability :
Aldehydes can form their diethylacetal in alcoholic stability, with not great impact on their smell. They can react with nitrogen-containing compounds as Methyl Anthranilate or Indol.
Aromatic compounds are chromophorous. They can cause coloring problems, especially in alkaline bases.
Very unstable in acidic bases (detergents and antiperspirants), very alkaline bases (liquid bleach), but stable in shampoos and soaps.
Other comments :
Data not available.
Labelling
Allergens :
This ingredient does not contain any allergen.
Signal word :
Warning
Hazard pictograms :
Precautionary statements :
| HAZARD | PRECAUTION |
|---|---|
| H317 May cause an allergic skin reaction.
H319 Causes serious eye irritation. |
P261 Avoid breathing dust/fume/gas/mist/vapours/spray. P280 Wear protective gloves/protective clothing/eye protection/face protection. P333 + P313 If skin irritation or rash occurs: Get medical advice/attention. P337 + P313 If eye irritation persists: Get medical advice/attention. P362 Take off contaminated clothing. P501 Dispose of contents/container to… |
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment