Aldehyde C-11 Undecylenic (CAS N° 112-45-8)​

Photo credits: ScenTree SAS

Aldehydes > Orange > Zesty

Aldehyde C-11 Undecylenic

Intrelevenaldehyde ; Aldehyde C11 Iso ; 10-Undecenal ; Undecylenic aldehyde

Aldehyde C-11 Undecylenic (CAS N° 112-45-8)​

Photo credits: ScenTree SAS

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Aldéhyde C11 Undécylénique - 30gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 112-45-8

  • EINECS number : 203-973-1

  • FEMA number : 3095

  • FLAVIS number : 05.035

  • JECFA number : 330

  • Appearance : Colorless liquid

  • Density : 0,844

  • Volatility : Head

  • Price Range : €€

Physico-chemical properties

  • Molecular formula : C11H20O

  • Molecular Weight : 168,28 g/mol

  • Log P : 5,1

  • Fusion Point : 7°C

  • Boiling Point : 235°C

  • Detection Threshold : 2,8541 ng/l air

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 96°C

Utilisation

Uses

Uses in perfumery :

Aldehyde C-11 Undecylenic provides an aldehydic facet in green, chypre, rose, floral-violet, tuberose notes. Used in detergents for its stability.

Year of discovery :

Data not available.

Natural availability :

Aldehyde C-11 Undecylenic has been identified as present in trace amounts in Coriander Leaf EO, but is not extracted in its natural state.

Isomerism :

Ethyl Linalool is a constitutional isomer of Aldehyde C-11 Undecylenic. Its smell is however much more floral-fresh and less zesty.

Synthesis precursor :

Aldehyde C-11 undecylenic forms a Schiff base by reaction with Methyl Anthranilate or Indole, for example. It can also be used for condensation with another aldehyde or ketone to form the desired alcene.

Synthesis route :

Like the other aliphatic aldehydes, Aldehyde C-11 undecylenic, can be synthesized by a reaction of undecylenyl halides (chloride, for example) with dimethyl sulfoxide (DMSO), followed by an alkaline treatment with sodium bicarbonate. Other synthetic routes exist, such as a reduction of Rosenmund from undecylenic acid, using an acid chloride.

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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