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General Presentation
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CAS N° :
30168-23-1 -
EINECS number :
250-078-7 -
FEMA number :
Donnée indisponible. -
FLAVIS number :
Donnée indisponible.
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JECFA number :
Donnée indisponible. -
Volatility :
Base -
Price Range :
€€€€
Physico chemical properties
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Appearance :
Colorless liquid -
Density :
1,01 -
Refractive Index @20°C :
Data not available. -
Optical rotation :
Data not available. -
Vapor pressure :
Data not available. -
Flash Point :
>93°C
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Molecular formula :
C14H20O -
Molecular Weight :
204,31 g/mol -
Log P :
4,1 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
300°C -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
Year of discovery :
1969
Natural availability :
Dupical does not exist on a natural state. Thus, it can't be used as extracted from a plant.
Isomerism :
Dupical contains a few asymmetric carbons and a double bond, giving birth to many possible isomers. Nevertheless, a blend of these isomers is used in perfumery.
Synthesis precursor :
Dupical is not used for the synthesis of another molecule of olfactive interest.
Synthesis route :
Dupical can be synthesized starting from tricyclododecanone, by reacting it with a Grignard reagent called vinylmagnesium bromide, to form and alcoholic intermediate with a vinylic group. A Claisen rearrangement can then be carried out by heating the intermediary product, converting it into Dupical.
Stability :
Very unstable in stong acidic (detergents) and alkaline (liquid bleach) bases. Only stable in shampoo, candle and soap bases.
Other comments :
Synergy with Methyl Laitone, to give a lactonic effect to a floral or fruity note.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment