Neofolione® (CAS N° 111-79-5)​

Photo credits: ScenTree SAS

Aldehydes > Green > Green Fruits > Mushroom > Violet Flower

Neofolione®

Methyl non-2-enoate ; Beauvertate ; Lanfolene ; Melon nonenoate ; Methyl 2-nonenoate ; Methyl nonylenate ; Novafolene

Neofolione® (CAS N° 111-79-5)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : 111-79-5

  • EINECS number : 203-908-7

  • FEMA number : 2725

  • FLAVIS number : 09.234

  • JECFA number : 1813

  • Appearance : Colorless to yellow liquid

  • Density : 0,898

  • Volatility : Heart

  • Price Range : €€

Physico-chemical properties

  • Molecular formula : C10H18O2

  • Molecular Weight : 170,3 g/mol

  • Log P : 4,4

  • Fusion Point : Donnée indisponible.

  • Boiling Point : 115°C (à 28 hPa)

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 77°C

Utilisation

Uses

Uses in perfumery :

Neofolione® is most often used in home care, detergents, fabric care and shampoos. Used in small quantities because of its power. Interesting for fruity notes and aldehydic floral notes for a fresh touch. Provides freshness and diffusion. Often used as a replacor of Methyl Octine Carbonate.

Year of discovery :

Data not available.

Natural availability :

Neofolione® is one of the compounds of the fragrant principle of artichoke. However, it cannot be extracted.

Isomerism :

Neofolione® has a double bond that offers the possibility of obtaining two diastereoisomers for this molecule. In perfumery, Neofolione® is a racemic mixture of these two isomers. The two isomers are not separated as they have no olfactory interest. In addition, Gamma-Decalactone and Linalool Oxide are constitutional isomers of Neofolione®. However, they have a very different smell.

Synthesis precursor :

Neofolione® is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

The synthesis of Neofolione® is made from Heptanal (Aldehyde C-7), condensed with malonic acid. This reaction is carried out in an acid medium. Then, follows a decarboxylation of the compound to remove the second acid function of the malonic acid, and a final step of esterification of the obtained molecule with methanol. This step requires an acid catalysis (with sulfuric acid for example) to improve the reaction yield.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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