Photo credits: ScenTree SAS
| Company | Ingredient Name | Learn more | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|
|
MANDARINE ALDEHYDE (10%CE)
ALDM-1
|
Discover | - | 10 grs | - | |
|
TRANS 2 DODECENAL
T2DO-1
|
Discover | - | 10 grs | - | |
|
Aldéhyde Mandarine - 30gr | Discover | - | 30grs | - | |
|
MANDARIN ALDEHYDE 10 TEC
965765
|
Discover | Molecules | - | - | |
|
TRANS-2-DODECENAL
M_0062898
|
Discover | Naturel | - | - |
General Presentation
-
CAS N° :
20407-84-5 -
EINECS number :
243-797-2 -
FEMA number :
2402 -
FLAVIS number :
5,144
-
JECFA number :
1350 -
Volatility :
Head/Heart -
Price Range :
€€€
Physico-chemical properties
-
Appearance :
Pale yellow liquid -
Density :
0,841 - 0,849 @25°C -
Refractive Index @20°C :
1,455 – 1,459 @20°C -
Optical rotation :
Donnée indisponible. -
Vapor pressure :
0,01 mmHg @20°C 0,0105 mmHg @25°C -
Flash Point :
113°C (235,4°F)
-
Molecular formula :
C12H22O -
Molecular Weight :
182,31 g/mol -
Log P :
4,53 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
126°C (258,8°F) -
Detection Threshold :
Donnée indisponible.
Chemistry & 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.
Stability :
Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell
Other comments :
comparing it to other aldehydesas Aldehyde C-12 lauric, Mandarin Aldehyde has a more fuity smell of Mandarin Yellow EO.
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. | P261 Avoid breathing dust/fume/gas/mist/vapours/spray. P272 Contaminated work clothing should not be allowed out of the workplace. P280 Wear protective gloves/protective clothing/eye protection/face protection. P302 + P352 IF ON SKIN: Wash with plenty of water/… P333 + P313 If skin irritation or rash occurs: Get medical advice/attention. P362 Take off contaminated clothing. |
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment