Cuminaldehyde (CAS N° 122-03-2)​

Photo credits: ScenTree SAS

Cuminaldehyde

Spicy > Warm Spices > Dry Woods > Anisic

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

Cuminaldehyde (CAS N° 122-03-2)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo CUMINIC ALDEHYDE
ALDCU-1
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Tilley Distribution logo Cuminaldehyde/Cuminic aldehyde Discover Synthetic Aroma Chemicals - -
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CUMINIC ALDEHYDE

ALDCU-1

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Cuminaldehyde/Cuminic aldehyde
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General Presentation

General Presentation

  • CAS N° :

    122-03-2
  • EINECS number :

    204-516-9
  • FEMA number :

    2341
  • FLAVIS number :

    5,022
  • JECFA number :

    868
  • Volatility :

    Head
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,985
  • Refractive Index @20°C :

    1,529 – 1,534
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,0697 mmHg @20°C 0,048 mHg @25°C
  • Flash Point :

    94°C (201,2°F)
  • Molecular formula :

    C10H12O
  • Molecular Weight :

    148,2 g/mol
  • Log P :

    2,98
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    235°C (455°F)
  • Detection Threshold :

    34,1731 ng/l air
Chemistry & Uses

Chemistry & Uses

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.

Natural availability :

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

New
Ingredient % min % max
Cumin seed oil 15 46

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.

Synthesis route :

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

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

Other comments :

Data not available.

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