Evernyl® (CAS N° 4707-47-5)​

Photo credits: ScenTree SAS

Evernyl®

Atralone® ; Veramoss® ; Methyl 2,4-dihydroxy-3,6-dimethylbenzoate ; Ataric acid ; Atraric acid ; Crystal moss ; 2,4- dihydroxy-3,6-dimethylbenzoic acid methyl ester ; 3,6-dimethyl-beta-resorcylic acid methyl ester ; Evernilox ; Methyl 2,4-dihydroxy-3,6-dimethyl benzoate ; Methyl atrarate ; Methyl atratate ; Mousse cristal ; Musgolide ; Oakmoss #1 ; Phenomoss ; Rionyl ; Verymoss

Evernyl® (CAS N° 4707-47-5)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
Quosentis logo
Evernyl - 30 Gr - Learn more Je me procure cet ingrédient - - -
PCW logo
METHYL ATRARATE - Learn more Je me procure cet ingrédient - 10 grs -

Evernyl - 30 Gr

Certifications :

METHYL ATRARATE

Certifications :

Information Générales

General Presentation

  • CAS N° :

    4707-47-5
  • EINECS number :

    225-193-0
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    09.623
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    White solid
  • Density :

    1,02
  • Refractive Index @20°C :

    Data not available.
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    0.00097 mmHg @20°C
  • Flash Point :

    183°C (361,4°F)
  • Molecular formula :

    C10H12O4
  • Molecular Weight :

    196,2 g/mol
  • Log P :

    2,1
  • Fusion Point :

    144°C (291,2°F)
  • Boiling Point :

  • Detection Threshold :

    0,2473 ng/l air
Utilisation

Chemistry & Uses

Uses in perfumery :

Evernyl® replaces oak moss in chypre and fougere compositions, for example, as it is not restricted. Used at a quite low dosage, because it is a very effective molecule. Useful to give more facets to a floral note.

Year of discovery :

1968

Natural availability :

Extraction of natural Evernyl® can be made from Oak Moss Absolute, containing Atranol and Chloratranol. These two last molecules can cause an allergenic reaction when entering in contact with the skin.

Isomerism :

Evernyl® does not have any isomer used in perfumery.

Synthesis precursor :

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

Synthesis route :

The synthesis of Evernyl® can be made from atraric acid in particular, which can be extracted from African plum leaf oil or Oak Moss Absolute with a good yield. The reaction is an esterification reaction with methanol.

Stability :

Very stable in perfumes and diverse functional bases

Other comments :

Data not available.

Utilisation

IFRA

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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