Photo credits: ScenTree SAS
Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.
General Presentation
-
CAS N° : : 3391-86-4
-
EINECS number : 222-226-0
-
FEMA number : 2805
-
Density : 0,835
-
Optical rotation : Lorem Ipsum
-
Allergens : This ingredient does not contain any allergen.
-
Refractive Index @20°C : Lorem Ipsum
-
Volatility : Heart
-
Price Range : €€€
-
Appearance : Colorless liquid
-
FLAVIS number : 02.023
-
JECFA number : 1152
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point : 180°C
-
Detection Threshold : Seuil de détection : 14 ppb (0,0000014%)
Seuil de reconnaissance : 25 ppb (0,0000025%) -
Molecular formula : C8H16O
-
Log P : 2,7
-
Molecular Weight : 128,22 g/mol
-
Fusion Point : -49°C
-
Flash Point : 63°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Stable in acidic products, but not so much in alkaline bleaches or detergents.
Uses in perfumery :
1,3-Octenol is used mainly in mushroom, lavender, woody and foody notes.
Year of discovery :
Data not available.
Isomerism :
The (R) enantiomer of 1,3-Octenol is more powerful than the (S) enantiomer, which has a vegetable smell. In perfumery, the mixture both isomers is the most used.
Synthesis precursor :
1,3-Octenol is a precursor for the synthesis of esters obtained by reaction between this alcohol and a carboxylic acid.
Natural availability :
The (R) enantiomer of 1,3-Octenol is present at 97% in the aromatic principle of mushrooms and 89% in the chanterelles aromatic principle. Nevertheless, 1,3-Octenol is not extracted in its natural state.
Synthesis route :
1,3-Octenol can be obtained by a Grignard reaction reacting vinylmagnesium bromide with hexanal.
Regulations & IFRA
This ingredient is not restricted
