Musky > Berries > White Flowers

Helvetolide®

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

Helvetolide® (CAS N° 141773-73-1)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Naturality Purity Latin name Treated part Geographical origin Certifications Comments MOQ
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Helvetolide® - 30gr - - - - - - more -
Information Générales

General Presentation

  • CAS N° : : 141773-73-1

  • EINECS number : 415-490-5

  • FEMA number : Donnée indisponible.

  • Density : 0,94

  • 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 : 347°C

  • Detection Threshold : 1,7 ng/l air

  • Molecular formula : C17H32O3

  • Log P : 5,46

  • Molecular Weight : 284,44 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 139°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

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.

Stability :

Stable in perfumes and in various functional bases.

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)

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.

Natural availability :

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

Synthesis route :

Data not available.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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