Photo credits: ScenTree SAS
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
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : 101-48-4
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EINECS number : 202-945-6
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FEMA number : 2876
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FLAVIS number : 06.006
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JECFA number : 1003
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Appearance : Colorless liquid
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Density : 1,004
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Volatility : Head/Heart
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Price Range : €
Physico-chemical properties
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Molecular formula : C10H14O2
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Molecular Weight : 166,22 g/mol
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Log P : 1,9
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Fusion Point : Donnée indisponible.
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Boiling Point : 220°C
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Detection Threshold : Donnée indisponible.
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Optical rotation : Donnée indisponible
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Vapor pressure : Donnée indisponible
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Refractive Index @20°C : Donnée indisponible
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Acid Value : Donnée indisponible.
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Flash Point : 88°C
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.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
