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Cuminaldehyde

4-propan-2-ylbenzaldehyde ; Cuminaldehyde ; 4-isopropyl benzaldehyde ; Cumaldehyde ; Cuminal ; Cuminic aldehyde

Cuminaldehyde (CAS N° 122-03-2)​

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Information Générales

General Presentation

  • CAS N° : : 122-03-2

  • EINECS number : 204-516-9

  • FEMA number : 2341

  • Density : 0,985

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Head

  • Price Range : €€€

  • Appearance : Colorless liquid

  • FLAVIS number : 05.022

  • JECFA number : 868

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 235°C

  • Detection Threshold : 34,1731 ng/l air

  • Molecular formula : C10H12O

  • Log P : 2,98

  • Molecular Weight : 148,2 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 94°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time

Uses in perfumery :

Cuminaldehyde is used in leather, spicy notes, in heavy and spicy flower accords (e. g. carnation), in oriental and woody accords and for sweaty notes. Used as a replacor for Cumin EO, in which it is found at about 30% of the composition.

Year of discovery :

Data not available.

Isomerism :

The ortho and meta isomers isolated from Cuminaldehyde are not used in fine perfumery. Cuminaldehyde is a constitutional isomer of Anethole, which has a very different smell reminiscent of Star Anise EO.

Synthesis precursor :

Cuminaldehyde is the precursor to several raw materials. Its oxidation gives Cuminic Acid, the hydrogenation of the aldehyde function leads to Cuminic Alcohol and its total hydrogenation synthesizes Mayol with a smell of lily of the valley. It can also form a Schiff base with Methyl Anthranilate, with a fruity and more artificial smell, or a dimethyl acetal which also has an olfactory interest.

Natural availability :

Cuminaldehyde can be extracted in its natural state from Cumin EO, as it represents 40% of its composition.

Synthesis route :

Cuminaldehyde synthesis is made by reduction of 4-Isopropylbenzoyl chloride or by formylation of cumene.

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
0,085 % 0,025 % 0,51 % 0,47 % 0,12 % 0,12 % 0,12 % 0,12 % 0,28 %
Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12
0,96 % 0,96 % 0,05 % 0,92 % 3,3 % 3,3 % 1,8 % 1,8 % No Restriction
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