Floral > Rosy > Mushroom > Metallic

Viridine®

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

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Information Générales

General Presentation

  • CAS N° : : 101-48-4

  • EINECS number : 202-945-6

  • FEMA number : 2876

  • Density : 1,004

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Head/Heart

  • Price Range :

  • Appearance : Colorless liquid

  • FLAVIS number : 06.006

  • JECFA number : 1003

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 220°C

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C10H14O2

  • Log P : 1,9

  • Molecular Weight : 166,22 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 88°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

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

Stability :

Stable in perfumes and diverse functional bases

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.

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.

Natural availability :

Viridine® is not available in its natural state.

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.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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