Methional (CAS N° 3268-49-3)​

Photo credits: ScenTree SAS

Methional

Burnt Leather > Burnt > Sulfuric > Animalic

3-Methylthiopropionaldehyde ; 3-methylsulfanylpropanal ; Methyl mercaptopropionaldehyde ; Methyl mercaptopropionic aldehyde ; 3-methyl thiopropionaldehyde ; 3-(methylmercapto)propionaldehyde ; 3-methylthio propionaldehyde ; 3-(methylthio)propanal ; 3-methylthiopropanal ; 4-thiapentanal

Methional (CAS N° 3268-49-3)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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Methional

Certifications :

Information Générales

General Presentation

  • CAS N° :

    3268-49-3
  • EINECS number :

    221-882-5
  • FEMA number :

    2747
  • FLAVIS number :

    12.001
  • JECFA number :

    466
  • Volatility :

    Heart/Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,043
  • Refractive Index @20°C :

    1,484 – 1,493
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,397 mmhg @20°C
  • Flash Point :

    74°C (165,2°F)
  • Molecular formula :

    C4H8OS
  • Molecular Weight :

    104,17 g/mol
  • Log P :

    Donnée indisponible.
  • Fusion Point :

    -75°C (-103°F)
  • Boiling Point :

    166°C (330,8°F)
  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Methional is used in mushroom, wet undergrowth, food notes and heady flowery accords. Can bring naturalness to fruity notes in reasonable doses.

Year of discovery :

Data not available.

Natural availability :

Methional is present in many foods of our daily life, starting with some cheeses like gorgonzola. It is however synthetic Methional which is most often used in perfumery.

Isomerism :

Methional does not have any isomer used in perfumery.

Synthesis precursor :

Methional is an aldehyde capable of forming Schiff bases with Methyl Anthranilate or Indole for example.

Synthesis route :

Methional is a sulfur compound, synthesized by a sulfurylation of 3-thiopropanal.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Data not available.

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