Aldehyde C-12 Lauric (CAS N° 112-54-9)​

Photo credits: ScenTree SAS

Aldehydes > Zesty > Orange

Aldehyde C-12 Lauric

Dodecanal ; Lauric aldehyde ; Dodecyl aldehyde ; Lauraldehyde ; Lauryl aldehyde ; Laurinaldehyde

Aldehyde C-12 Lauric (CAS N° 112-54-9)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
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Aldéhyde C12 Laurique - 30 Gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 112-54-9

  • EINECS number : 203-983-6

  • FEMA number : 2615

  • FLAVIS number : 05.011

  • JECFA number : 110

  • Appearance : Colorless liquid

  • Density : 0,831

  • Volatility : Heart

  • Price Range :

Physico-chemical properties

  • Molecular formula : C12H24O

  • Molecular Weight : 184,32 g/mol

  • Log P : 4,75

  • Fusion Point : 12°C

  • Boiling Point : 185°C (à 133hPa)

  • Detection Threshold : 0,5 à 1,5 ppb

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 101°C

Utilisation

Uses

Uses in perfumery :

Aldehyde C-12 Lauric is used in eaux fraiches, colognes, floral-aldehydic and zesty notes for its characteristic smell, strength and volume.

Year of discovery :

Data not available.

Natural availability :

Aldehyde C-12 Lauric can be found in its natural state in several essential oils as Coriander Leaf EO, citrus and pine from which it can be extracted.

Isomerism :

Aldehyde C-12 Lauric is more zesty than Aldehyde C-12 MNA.

Synthesis precursor :

Aldehyde C-12 Lauric 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-12 Lauric, can be synthesized by reaction of dodecyl 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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