Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Ethyllinalool | 30255405 | Molecule | - | - | - | - |
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more | - |
General Presentation
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CAS N° : : 10339-55-6
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EINECS number : 233-732-6
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FEMA number : Donnée indisponible.
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Density : 0,862
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head/Heart
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Price Range : €€€
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 215°C
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Detection Threshold : 4,2518 ng/l air
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Molecular formula : C11H20O
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Log P : 3,3
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Molecular Weight : 168,28 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 86°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Ethyl Linalool is less agrestic and rising but rounder, fruitier and fresher than Linalool.
Stability :
Exclusively stable in shampoo, hair conditioner and in soaps.
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.
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.
Natural availability :
Ethyl Linalool is not available in its natural state.
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.
Regulations & IFRA
This ingredient is not restricted
