Dynascone®
Synthétique
Green > Crisp Green > Tropical Fruits
Crédits photo: ScenTree SAS
Other names :
1-(5,5-dimethyl-1- cyclohexen-1-yl)-4-Penten-1-one
Same molecule as Alpha-neobutenone® and Galbascone® but obtained by a different synthesis road.
Same molecule as Alpha-neobutenone® and Galbascone® but obtained by a different synthesis road.
Volatility :
Base
Uses in perfumery :
Dynascone® is used in in all types of fragrances to give unique green, floral and fruity effects. It works very well for green notes such as cis-3-hexenol or galbanum but be careful, this raw material is very powerful and have an important volume. Very interesting for works around yellow fruits (bananas, pineapple) or for floral undertones in hyacinth, lilac ou lilly of the valley.
Natural availability :
Dynascone® is not available naturaly
Year of discovery :
Discovered in 1972 as a by-product during alpha-damascone® synthesis. Firmenich intern captive since 1974.
''Dynascone® '' tradename has been published and protected by Firmenich SA since 16/10/1991 (brand N°577667)
Other comments :
Very close to alpha-neobutenone® and Galbascone®
Price Range :
€€€€
Stability :
Very stable in all application
Crédits photo: ScenTree SAS
- Molecular formula :
- C13H20O
- Molecular Weight :
- 192,3 g/mol
- Density :
- 1,008 - 1,016 @20°C
- Flash Point :
- >100°C (>212°F)
- Fusion Point :
- Donnée indisponible.
- Appearance :
- Colorless to pale yellow liquid
- Log P :
- 3,89
- Boiling Point :
- Donnée indisponible.
- Detection Threshold :
- Donnée indisponible.
Synthesis route :
Data not available.
Synthesis precursor :
Data not available.
Isomerism :
Dynascone® may have two isomeric forms : Alpha-Dynascone® and Beta-Dynascone®. The alpha one is mainly used because of it is more green, powerful and linear.
- EINECS number :
- 260-486-7
- FEMA number :
- Donnée indisponible.
- JECFA number :
- Donnée indisponible.
- FLAVIS number :
- Donnée indisponible.
- Allergens :
- This ingredient does not contain any allergen.
- IFRA :
- This ingredient is restricted by IFRA
- Restriction type :
- RESTRICTION
- Cause of restriction :
- DERMAL SENSITIZATION AND SYSTEMIC TOXICITY
- Amendment :
- 49
- Quantitative limit on the use :
-
Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A Cat.5B Cat.5C Cat.5D Cat.6 0,19 % 0,057 % 0,18 % 1,1 % 0,27 % 0,27 % 0,27 % 0,091 % 0,54 % Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12 0,54 % 0,54 % 0,091 % 1,4 % 1,4 % 3,4 % 0,091 % 0,091 % No Restriction - Restriction type :
- RESTRICTION
- Cause of restriction :
- DERMAL SENSITIZATION AND SYSTEMIC TOXICITY
- Amendment :
- 49
- Comments :
- For Treemoss and Oakmoss extracts, the restrictions in the Standards are directly linked to the presence of Atranol and Chloroatranol in the finished products. To ensure that those remain below trace levels, the upper concentration levels have not been increased (compared its last publication in the Amendment 43 (2008)). In the presence of Oakmoss extracts, the level of Treemoss in the respective category has to be reduced accordingly, such that the total amount of both extracts does not exceed the maximum permitted level in each category as listed in the table above. If the same fragrance mixture is intended to be used in more than one IFRA Category, then the most restrictive limitation (based on foreseen use concentrations and maximum permitted level) will apply. Treemoss extracts shall not contain more than 0.8% of Dehydroabietic acid (DHA) as a marker of 2% of total resin acids. The concentration of DHA (about 40% of the total resin acids) in Treemoss can be measured with an High Performance Liquid Chromatography (HPLC) reverse phase - spectrofluorometry method. Further, levels of Atranol and Chloroatranol should each be below 100 ppm in Treemoss extracts.
- Quantitative usage limits :
-
Cat.1 Cat.2 Cat.3 Cat.4 Cat.5 Cat.6 Cat.7 Cat.8 Cat.9 Cat.10 Cat.11 0,19 % 0,057 % 0,18 % 1,1 % 0,27 % 0,54 % 0,54 % 0,091 % 1,4 % 1,4 % 0,091 %
To learn more about IFRA's standards : https://ifrafragrance.org/safe-use/library
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