Methyleugenol (CAS N° 93-15-2)​

Photo credits: ScenTree SAS

Methyleugenol

Spicy > Cool Spices > Mossy > Earthy

1,2-dimethoxy-4-prop-2-enylbenzene ; 4-allyl veratrole ; 4-allyl-1,2-dimethoxybenzene ; 4-allyl-1,2-dimethoxybenzol ; 4-allylveratrole ; 1,2-dimethoxy-4-(2-propen-1-yl)benzene ; 1,2- dimethoxy-4-allyl benzene ; Eugenol methyl ether ; Veratrole methyl ether ; 1,2-dimethoxy-4-prop-2-enylbenzene

Methyleugenol (CAS N° 93-15-2)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
Van Aroma logo Methyl Eugenol
CL-801
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Indesso logo Methyl Eugenol Discover Molecule Certifications : Halal Certifications : Kasher - -
PCW logo METHYL EUGENOL
MEG-1
Discover - 10 grs 98
Quosentis logo Méthyl Eugenol - 30gr Discover - 30grs -
Van Aroma logo
Methyl Eugenol

CL-801

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Indesso logo
Methyl Eugenol
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PCW logo
METHYL EUGENOL

MEG-1

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Quosentis logo
Méthyl Eugenol - 30gr
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General Presentation

General Presentation

  • CAS N° :

    93-15-2
  • EINECS number :

    202-223-0
  • FEMA number :

    2475
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    1790
  • Volatility :

    Heart
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,035
  • Refractive Index @20°C :

    1,532 – 1,536
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    < 0,075 mmHg @20°C
  • Flash Point :

    117°C (242,6°F)
  • Molecular formula :

    C11H14O2
  • Molecular Weight :

    178,23 g/mol
  • Log P :

    2,4
  • Fusion Point :

    -4°C (24,8°F)
  • Boiling Point :

    248°C (478,4°F)
  • Detection Threshold :

    68 ppb à 8,5 ppm (0,00085%)
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Methyl Eugenol is used in rosy floral notes, carnation, lilac, jasmine, hyacinth and other heady flowers. Useful in a chocolate or coffee note.

Year of discovery :

Data not available.

Natural availability :

Methyl Eugenol is present in the Bay St-Thomas EO, Tuberose Absolute and Angelica Root EO among others, Methyl Eugenol can be extracted from these plants in its natural state.

Isomerism :

Methyl Isoeugenol is a position isomer of Methyl Eugenol. Their smell is different : Methyl Isoeugenol is more floral, reminiscent of Tuberose Absolute, while Methyl Eugenol is more spicy. Both are keeping an earthy and wet facet, more noticeable for Methyl Eugenol. Canthoxal® is an isomer of Methyl Eugenol. Its smell is however radically different, as it is marine and aldehydic.

Synthesis precursor :

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

Synthesis route :

Methyl Eugenol is obtained synthetically from Eugenol by a methylation reaction. This etherification reaction is made by a Williamson synthesis, which consists in forming a sodium alkoxide in the presence of pure sodium in the reaction medium, and then reacting the obtained eugenolate with methyl chloride.

Stability :

Becomes red under the effect of light. This raw material is not convenient in every functional base : can't be used in a candle or shower gel base.

Other comments :

Methyl Eugenol is one of the 26 allergens in perfumery.
It has a less floral smell than Methyl Isoeugenol.

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