Anther®
Antherex® ; Pommerol® ; 2-(3-methylbutoxy)ethylbenzene ; Isoamyl phenethyl ether ; Isoamyl phenyl ethyl ether ; Florether ; Green ether ; 3-methyl butyl oxyethyl benzene ; 3-methylbutyl 2-phenylethyl ether ; Isopentyl phenethyl ether ; Phenethyl isoamyl ether ; Phenylethyl isoamyl ether ; Treflon
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° : : 56011-02-0
-
EINECS number : 259-943-3
-
FEMA number : 4635
-
Density : 0,903
-
Optical rotation : Lorem Ipsum
-
Allergens : This ingredient does not contain any allergen.
-
Refractive Index @20°C : Lorem Ipsum
-
Volatility : Head
-
Price Range : €€
-
Appearance : Colorless liquid
-
FLAVIS number : Donnée indisponible.
-
JECFA number : 2136
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point : 110°C
-
Detection Threshold : Donnée indisponible.
-
Molecular formula : C13H20O
-
Log P : Donnée indisponible.
-
Molecular Weight : 192,3 g/mol
-
Fusion Point : Donnée indisponible.
-
Flash Point : >93°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Stable in perfumes and in diverse functional bases.
Uses in perfumery :
Anther® is usually used in fruity notes to bring out a floral and aromatic effect, close to lavander.
Year of discovery :
Data not available.
Isomerism :
Anther® is a constitutional isomer of alpha-Damascone® and beta-Damascone® and alpha-Ionone and beta-Ionone. Nevertheless, it doesn't have the same smell as these molecules.
Synthesis precursor :
Anther® is not a precursor to the synthesis of any other molecule used in perfumery.
Natural availability :
Anther® is not found in nature.
Synthesis route :
Anther® can be synthesized from Phenyl Ethyl Alcohol, using a Williamson synthesis. This reaction consists in ionizing the alcohol by subjecting it to the action of a reducing metal as pure sodium or potassium. Following this first step, adding a haloalkane to the reaction mixture, here halo-3-methylbutane, transforms the alcoholate and the alcane into an ether.
Regulations & IFRA
This ingredient is not restricted
