Helvetolide® (CAS N° 141773-73-1)​

Photo credits: ScenTree SAS

Helvetolide®

Musky > Berries > White Flowers

2-[1-(3,3-dimethylcyclohexyl)ethoxy]-2-methylpropyl propionate ; Herbactolide

Helvetolide® (CAS N° 141773-73-1)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
dsm-firmenich logo HELVETOLIDE®
947650
Discover Molecules Certifications : Biodegradable (Partially) Certifications : Upcycled - -
Quosentis logo Helvetolide® - 30gr Discover - 30grs -
Tilley Distribution logo Helvetolide/Padolide Discover Synthetic Aroma Chemicals - -
dsm-firmenich logo
HELVETOLIDE®

947650

Discover
Quosentis logo
Helvetolide® - 30gr
Discover
Tilley Distribution logo
Helvetolide/Padolide
Discover
General Presentation

General Presentation

  • CAS N° :

    141773-73-1
  • EINECS number :

    415-490-5
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,94
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    139°C (282,2°F)
  • Molecular formula :

    C17H32O3
  • Molecular Weight :

    284,44 g/mol
  • Log P :

    5,46
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    347°C (656,6°F)
  • Detection Threshold :

    1,7 ng/l air
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Helvetolide is used in all kinds of perfumes (but espacially in fine fragrance because of its price) to bring a heady pear note and an Ambrette Seeds Absolute base note. It can be used as a fixative, with no cheap sub-effect. It is basically used as Musk T®, but brings more volume and tenacity to the fragrance.

Year of discovery :

Discovered in 1990 by chemists Giersch and Schulte-Este. 'Helvetolide®' trademark has been published and protected by Firmenich SA since 30/04/1995 (brand N°636238). 'Helvetolide®' trademark has been published and protected by Firmenich SA since 12/12/2001 (brand N°772121)

Natural availability :

Helvetolide® does not exist on a natural state. It can't be extracted from a plant.

Isomerism :

Helvetolide® used in perfumery is a mix of two isomers, due to the presence of two asymmetric carbons inside the molecule. The first one is dextrorotatory Helvetolide® (+), less floral but more musky than the other isomer. This is why it is often preferred as the other isomers, and sometimes used alone, isolated from levorotatory Helvetolide® (-).

Synthesis precursor :

Helvetolide® can be used to synthesize Romandolide®, which is more powerful. This synthesis consists in replacing the dimethyl groupement of the ether function of Helvetolide®, by a carbonyle function, forming an ester.

Synthesis route :

Data not available.

Stability :

Stable in perfumes and in various functional bases.

Other comments :

Helvetolide® is the first acyclic musk ever used in perfumery. It participated to the opening of a new molecules category. After it, Romandolide®, Nebulone®, Edenolide® and Sylkolide® were synthesized.

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.