Maltol (CAS N° 118-71-8)​

Photo credits: ScenTree SAS

Maltol

Balsamic Ambery > Gourmand > Burnt

3-hydroxy-2-methylpyran-4-one ; Corps praline ; 3-hydroxy-2-methyl-4-pyranone ; 3-hydroxy-2-methylpyrone ; Larixic acid ; Larixinic acid ; 2-methyl pyromeconic acid ; 2-methyl-3-hydroxy-4-pyrone ; 2-methyl-3-hydroxypyrone ; 2-methyl-3-oxidanyl-pyran-4-one ; Palatone ; Talmon ; Veltol ; Vetol

Maltol (CAS N° 118-71-8)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo MALTOL
MAL-1
Discover - 10 grs 99 - 100
Quosentis logo Maltol - 30gr Discover - 30grs -
Tilley Distribution logo Maltol Discover Synthetic Aroma Chemicals - -
Tilley Distribution logo Maltol Natural Discover Natural Aroma Chemicals - -
PCW logo
MALTOL

MAL-1

Discover
Quosentis logo
Maltol - 30gr
Discover
Tilley Distribution logo
Maltol
Discover
Tilley Distribution logo
Maltol Natural
Discover
General Presentation

General Presentation

  • CAS N° :

    118-71-8
  • EINECS number :

    204-271-8
  • FEMA number :

    2656
  • FLAVIS number :

    7,014
  • JECFA number :

    1480
  • Volatility :

    Base
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    White solid
  • Density :

    1,35 g/cm³ (masse volumique)
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    Donnée indisponible.
  • Molecular formula :

    C6H6O3
  • Molecular Weight :

    126,11 g/mol
  • Log P :

    1,16
  • Fusion Point :

    162°C (323,6°F)
  • Boiling Point :

    285°C (545°F)
  • Detection Threshold :

    35 ppm
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Maltol is used in gourmet notes. Allows to bring a gourmet effect in woody, floral and fruity notes in particular, then bringing strength, character and sensuality. Often put aside in perfumery for the benefit of Ethyl maltol. Both molecules can also be associated, but with a lower amount of Ethyl maltol, compared to Maltol.

Year of discovery :

Data not available.

Natural availability :

Maltol is present in pine needles (Abies balsamea especially), beech wood and young larval wood (a conifer), from which it can be extracted in its natural state. It is produced by burning the wood and extracting the tar.

Isomerism :

Methyl Furoate is a constitutional isomer of Maltol. They both belong to families of molecules having olfactive similarities : furans and pyrans. Both families have foody and roasted notes.

Synthesis precursor :

Maltol is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Maltol is a molecule of the pyran family, synthesized from kojic acid, produced naturally by certain species of fungi.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Maltol is less powerful than Ethyl maltol. Both are often associated in perfumes with a smaller proportion of Ethyl maltol.

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