Musky > Green Fruits > Fresh Flowers

Applelide®

1-(3,3-dimethylcyclohexyl)ethyl propanedioate d'ethyle ; Ethyl 1-(3,3-dimethylcyclohexyl)ethyl propanedioate ; Applelide stab ; Applelide stabilisé ; Edenolide

Applelide® (CAS N° 478695-70-4)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : : 478695-70-4

  • EINECS number : 455-260-1

  • FEMA number : Donnée indisponible.

  • Density : 1,006

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Base

  • Price Range : €€€

  • Appearance : Colorless liquid

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 289°C

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C15H26O4

  • Log P : 4,9

  • Molecular Weight : 270,37 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 94°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Frequently stabilized before usage in pefumes. Its two ester functions brings it a great instability. Applelide® is related to Helvetolide® for its fruity and green smell of apple, while Helvetolide® has a pear aspect.

Stability :

Unstable compound, frequently stabilized before being used.

Uses in perfumery :

Applelide® is a musk used for its smell, in addition to its fixative aspect. It brings a deep effect to fruity notes and in floral-fruity perfumes, bringing an apple note.

Year of discovery :

2002

Isomerism :

Applelide® has two asymetric carbons. A mixture of the cis and trans forms is used in perfumery.

Synthesis precursor :

Applelide® is not a precursor to the synthesis of another compound of olfactive interest.

Natural availability :

Applelide® is not found in nature.

Synthesis route :

Data not available.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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