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Ethyl linalool

(6E)-3,7-dimethylnona-1,6-dien-3-ol ; Homolinalool ; Ethyllinalool ; 3,7-dimethyl-1,6-nonadien-3-ol

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	MOQ	Purity
	Ethyllinalool	30255405	Visit website	Molecule		-	-

Ethyllinalool

ID : 30255405

Certifications :

General Presentation

CAS N° :
10339-55-6
EINECS number :
233-732-6
FEMA number :
Donnée indisponible.
FLAVIS number :
Donnée indisponible.

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

Physico chemical properties

Appearance :
Colorless liquid
Density :
0,862
Refractive Index @20°C :
1,462 - 1,466
Optical rotation :
Data not available.
Vapor pressure :
0,0267 hPa @20°C 0,007 hPa @25°C
Flash Point :
86°C

Molecular formula :
C₁₁H₂₀O
Molecular Weight :
168,28 g/mol
Log P :
3,3
Fusion Point :
Donnée indisponible.
Boiling Point :
215°C
Detection Threshold :
4,2518 ng/l air

Chemistry & Uses

Uses in perfumery :

Ethyl Linalool is used in floral-fresh notes of bergamot, rose and lavender. This compound has a similar use to Linalool.

Year of discovery :

Data not available.

Natural availability :

Ethyl Linalool is not available in its natural state.

Isomerism :

Ethyl Linalool has an asymmetric carbon and a double bond capable of forming enantiomers and diastereoisomers. It is however a mixture of isomers that is used in perfumery. Aldehyde C-11 Undecylenic is a constitutional isomer of Ethyl Linalool. However, it has a much more aldehydic and less floral smell.

Synthesis precursor :

Ethyl Linalool is a precursor to the synthesis of Dihydro Ethyl Linalool, and several esters, little used in perfumery.

Synthesis route :

Like Linalool, Ethyl Linalool can be synthesized in many ways. One of them is made from 6-methyl-5-octen-2-one, which reacts with acetylene to form Dehydro Ethyl Linalool. Then, a Lindlar hydrogenation of catalysed palladium can be made in order to obtain Ethyl Linalool.

Stability :

Exclusively stable in shampoo, hair conditioner and in soaps.

Other comments :

Ethyl Linalool is less agrestic and rising but rounder, fruitier and fresher than Linalool.

Ethyl linalool

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

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Ethyl linalool

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

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :