Fruity > Berries > Rosy > Earthy

(E)-Béta-damascenone

Fermentone® ; (E)-1-(2,6,6-trimethyl-1-cyclohexa-1,3-dienyl)but-2-en-1-one ; Floriffone ; Roastarome ; Rose ketone-4 ; Rosenone ; Trimethyl cyclohexadienyl butenone

(E)-Béta-damascenone (CAS N° 23726-93-4)​

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Information Générales

General Presentation

  • CAS N° : : 23726-93-4

  • EINECS number : 245-833-2

  • FEMA number : 3420

  • Density : 0,946

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Heart/Base

  • Price Range : €€€€

  • Appearance : Colorless to pale yellow liquid

  • FLAVIS number : 07.108

  • JECFA number : 387

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 199°C

  • Detection Threshold : 0,0007 to 0,009 ppb

  • Molecular formula : C13H18O

  • Log P : 3,4

  • Molecular Weight : 190,29 g/mol

  • Fusion Point : 2°C

  • Flash Point : >100°C (>212°F)

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Stability :

Stable in perfumes and diverse functional bases

Uses in perfumery :

Damascenone-Beta® brings a fruity nuance for rosy notes. Gives a ''baked apple '' effect.

Year of discovery :

First rose ketones were discovered in 1965, by chemists P. Ruzicka and Dr. Demole, by analyzing Damask Rose Absolute. This opened the way to synthesize a major molecule category of the perfume industry.

Isomerism :

There is an isomer of Damascenone-Beta® called Damascenone-Alpha®. Its smell is similar but the location of the double bonds in the ring is not the same (1,3 positions for beta and 2,4 positions for alpha). Cyclamen Aldehyde is a constitutional isomer of Damascenone-Beta, although its smell is completely different, as it is very marine, floral and aldehydic.

Synthesis precursor :

Damascenone-Beta® is not a precursor to the synthesis of another compound of olfactory interest.

Natural availability :

Damascenone-Beta® is present in small quantities in Damask Rose Absolute and Damask Rose EO (and other roses), from which it can be extracted. It is also present in Clary Sage Absolute and salvia officinale among others, always in very small proportions.

Synthesis route :

Damascenone-Beta® is part of the ''rose ketones '' family, present in a small amount in Damask Rose Absolute, while playing an important role in their smell. Rose ketones are synthesized from the appropriate derivative of cyclogeranic acid (ester, halide, ...). A reaction of this derivative with an allyl magnesium halide followed by a pyrolysis, allows to obtain the desired compound by rearranging the double bond of the branched chain.

Utilisation

Regulations & IFRA

  • IFRA 51th : This ingredient is restricted by IFRA

  • Restriction type : RESTRICTION

  • Cause of restriction : DERMAL SENSITIZATION

  • 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
0,0077 % 0,0023 % 0,046 % 0,043 % 0,011 % 0,011 % 0,011 % 0,011 % 0,025 %
Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12
0,088 % 0,088 % 0,0045 % 0,084 % 0,3 % 0,3 % 0,17 % 0,17 % No Restriction

Comments :

The above limits apply to Rose Ketones used individually or in combination. The sum of concentrations of Rose ketones isomers should not exceed the maximum concentration levels established by this Standard.

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