Ethyl linalool (CAS N° 10339-55-6)​

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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

Ethyl linalool (CAS N° 10339-55-6)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
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Ethyllinalool 30255405 Visit website Je me procure cet ingrédient Molecule - - - - -

Ethyllinalool

ID : 30255405

Certifications :

Information Générales

General Presentation

  • CAS N° : 10339-55-6

  • EINECS number : 233-732-6

  • FEMA number : Donnée indisponible.

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 0,862

  • Volatility : Head/Heart

  • Price Range : €€€

Physico-chemical properties

  • 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

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 86°C

Utilisation

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.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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