Adoxal® (CAS N° 141-13-9)​

Photo credits: ScenTree SAS

Aldehydes > Marine > Oceanic

Adoxal®

Farenal® ; 2,6,10-trimethylundec-9-enal ; Waxy aldehyde ; Doxal

Adoxal® (CAS N° 141-13-9)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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ALDAROM 2311160710 Visit website Je me procure cet ingrédient Synthetic Aroma Chemicals Certifications : Kasher - -

ALDAROM

ID : 2311160710

China

Certifications : Certifications : Kasher

Information Générales

General Presentation

  • CAS N° :

    141-13-9
  • EINECS number :

    205-460-8
  • FEMA number :

    4768
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Head
  • Price Range :

    €€€
Physico-chemical properties

Physico chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,852
  • Refractive Index @20°C :

    1,450 - 1,455
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    0,004 hPa @20°C 0,004 hPa @25°C
  • Flash Point :

    126°C
  • Molecular formula :

    C14H26O
  • Molecular Weight :

    210,36 g/mol
  • Log P :

    >6,00
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    5,38 ng/l air
Utilisation

Chemistry & Uses

Uses in perfumery :

Adoxal® is used to work on aqueous, ozonic and juicy fruits notes for a very similar appearance to Calone®.

Year of discovery :

Data not available.

Natural availability :

Adoxal® is not available in its natural state.

Isomerism :

Adoxal® has several asymmetric carbons. A mixture of its isomers is used in perfumery. Sandalore® is a constitutional isomer of Adoxal®. Nevertheless, this isomer has a very different smell as it is woodier and more sandalwood.

Synthesis precursor :

Adoxal® forms a Schiff base by reaction with Methyl Anthranilate or Indole for example.

Synthesis route :

Adoxal® is synthesized from tetrahydroionone and alkyl chloroacetate by glycidyl ester condensation. This step is followed by a hydrolysis and a decarboxylation.

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell.
Olfactively stable in any kind of products, except bleaches and other alkaline or stongly acidic detergents.

Other comments :

Data not available.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
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