Photo credits: ScenTree SAS

Aldehydes > Zesty > Orange > Agrestic

Aldehyde C-11 MOA

Aldehyde C11 MOA ; Aldehyde MOA ; MOA ; 2-methyl decanal ; 2-methyl-1-decanal ; Methyl octyl acetaldehyde ; 2-methyl decanal ; 2-methyldecanal ; Methyloctylacetaldehyde ; Methyl octyl acetic aldehyde

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	Purity	Latin name	Treated part	Geographical origin	MOQ
	Aldéhyde C11 MOA - 30gr	-	Visit website	-		-	-	-	-	-

Aldéhyde C11 MOA - 30gr

Certifications :

General Presentation

CAS N° :
19009-56-4
EINECS number :
242-745-6
FEMA number :
Donnée indisponible.
FLAVIS number :
05.160

JECFA number :
Donnée indisponible.
Volatility :
Head
Price Range :
€€

Physico chemical properties

Appearance :
Colorless liquid
Density :
0,823
Refractive Index @20°C :
Data not available.
Optical rotation :
Data not available.
Vapor pressure :
Data not available.
Flash Point :
81°C

Molecular formula :
C₁₁H₂₂O
Molecular Weight :
170,3 g/mol
Log P :
Donnée indisponible.
Fusion Point :
Donnée indisponible.
Boiling Point :
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

Year of discovery :

Data not available.

Natural availability :

Aldehyde C-11 MOA is a purely synthetic aldehyde, not found in nature.

Isomerism :

Aldehyde C11 MOA is a constitutional isomer of Aldehyde C11 Undecylic. It only has one ramification, while Aldehyde C11 Undecylic has a longer carbon chain. Its smell is much more fresh and zesty.

Synthesis precursor :

Aldehyde C-11 MOA 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-11 MOA (for Methyl Octyl Acetaldehyde) is synthesized in two different ways. 2-Decanone reacts with a Chloroacetate to give a glycidate, which can be saponified and decarboxylated to obtain the final product. The second synthesis route firstly reacts Aldehyde C-10 Decylenic with formaldehyde in the catalytic presence of an amine, and then a hydrogenation of the intermediate product allows to obtain the Aldehyde C-11 MOA.

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell

Other comments :

In comparision with Aldehyde C-12 MNA, Aldehyde C-11 MOA has one additional carbon atom. This changes it into a more fruity, a deeper and more agrestic smell.

Aldehyde C-11 MOA

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Aldehyde C-11 MOA

I buy this ingredient

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :