Methyl Pamplemousse® (CAS N° 67674-46-8)​

Photo credits: ScenTree SAS

Methyl Pamplemousse®

Citrus > Zesty > Grapefruit > Sandalwood > Green

Grapefruit Acetal ; Amarocite® ; 6,6-dimethoxy-2,5,5-trimethylhex-2-ene ; 1,1-dimethox-2,2,5-trimethy-4-hexene ; 1,1-dimethoxy-2,2,5-trimethyl hex-4-ene ; 6,6-dimethoxy-2,5,5-trimethyl-2-hexene ; Methyl pomello ; Pamplerom ; Pomelocit

Methyl Pamplemousse® (CAS N° 67674-46-8)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
Quosentis logo
Méthyl Pamplemousse® - 30gr - Visit website Je me procure cet ingrédient - - -
PCW logo
METHYL PAMPLEMOUSSE AMAR-2 Visit website Je me procure cet ingrédient - 10 grs -

Méthyl Pamplemousse® - 30gr

Certifications :

METHYL PAMPLEMOUSSE

ID : AMAR-2

Certifications :

Information Générales

General Presentation

  • CAS N° :

    67674-46-8
  • EINECS number :

    266-885-2
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Head
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,877
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    75°C (167°F)
  • Molecular formula :

    C11H22O2
  • Molecular Weight :

    186,29 g/mol
  • Log P :

    4,3
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    215°C (419°F)
  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Methyl Pamplemousse® is used in all types of perfumes, in eau fraiche and soaps especially (for its stability), for notes of grapefruit. Gives naturalness to a grapefruit accord. Used in fougere, chypre and fruity notes to boost the head. Brings modernity to citrus fruits.

Year of discovery :

1983

Natural availability :

Methyl Pamplemousse® is not available in its natural state.

Isomerism :

Isononyl acetate is a constitutional isomer of Methyl Pamplemousse®. These two compounds do not have any olfactive similarities.

Synthesis precursor :

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

Synthesis route :

Methyl Pamplemousse® is synthesized by an acetalization reaction between 2,2,5-trimethyl-4-hexenal (obtained from isobutyraldehyde and prenyl chloride) and methanol, in the presence of calcium chloride.

Stability :

Stable in perfumes and diverse functional bases, except acidic cleaners, antiperspirants and in very alkaline detergents.

Other comments :

Comparing it to other sandalwood notes as Bacdanol® and Sandalore®, Methyl Pamplemousse® has a fruity note before all, followed by a woody undernote.

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