Viridine® (CAS N° 101-48-4)​

Photo credits: ScenTree SAS

Viridine®

Floral > Rosy > Mushroom > Metallic

PADMA (PhenylAcetaldehyde Dimethylacetal) ; 2,2-dimethoxyethylbenzene ; 2,2-dimethoxy-1-phenyl ethane ; 1,1-dimethoxy-2-phenylethane ; Hyscylene p ; Phenacetaldehyde dimethyl acetal ; Rosal ; Vert de lilas ; Alpha-tolyl aldehyde dimethyl acetal

Viridine® (CAS N° 101-48-4)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
Natara logo
Phenylacetaldehyde DMA 2311172010 Visit website Je me procure cet ingrédient Synthetic Aroma Chemicals Certifications : Kasher - -
PCW logo
PHENYLACETALDEHYDE DIMETHYL ACETAL PADA-1 Visit website Je me procure cet ingrédient - 10 grs -

Phenylacetaldehyde DMA

ID : 2311172010

China

Certifications : Certifications : Kasher

PHENYLACETALDEHYDE DIMETHYL ACETAL

ID : PADA-1

Certifications :

Information Générales

General Presentation

  • CAS N° :

    101-48-4
  • EINECS number :

    202-945-6
  • FEMA number :

    2876
  • FLAVIS number :

    06.006
  • JECFA number :

    1003
  • Volatility :

    Head/Heart
  • Price Range :

Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,004
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    88°C (190,4°F)
  • Molecular formula :

    C10H14O2
  • Molecular Weight :

    166,22 g/mol
  • Log P :

    1,9
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    220°C (428°F)
  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Viridine® is used in rose, hyacinth, honeysuckle, lily of the valley, lilac, carnation, gardenia, lily and geranium notes. Useful in woody-patchouli and vetiver notes. Brings a ripe fruit effect to fruit accords. Also used in eaux fraiches and in fougere perfumes.

Year of discovery :

Data not available.

Natural availability :

Viridine® is not available in its natural state.

Isomerism :

Viridine® is a constitutional isomer of DihydroEugenol, even if both molecules do not have the same smell.

Synthesis precursor :

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

Synthesis route :

Viridine® is synthesized by an acetalization reaction between Phenylacetic Aldehyde (synthesized from styrene oxide for example) and methanol. This reaction is catalysed by a strong concentrated acid.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Viridine® has a distinctive mushroom and metallic note from other rosy materials.

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