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Ambermax 50®

Ambermax 10 ; 2-(2,2,7,7-tetramethyltricyclo[6.2.1.0](1,6)undec-4-en-5-yl)propan-1-ol ; 2-(2,2,7,7-tetramethyltricyclo[6.2.1.0](1,6)undec-5-en-5-yl)propan-1-ol

Ambermax 50® (CAS N° 929625-08-1- 1001252-30-7)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : : 929625-08-1- 1001252-30-7

  • EINECS number : 482-030-8

  • FEMA number : Donnée indisponible.

  • Density : 0,98

  • 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 :

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C18H30O

  • Log P : 6,3

  • Molecular Weight : 262,48 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : >93°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Ambermax® is the most efficient and powerful ambery note ever. Ambermax® can also be diluted in Triethyl Citrate, at 10%. This does not change its olfactive character, but its power is less important. Then, dilution in TEC helps controling the Ambermax® impact in a composition.
Good synergy with Kephalis® (in 30/70 proportions) to bring a cistus note, nuanced by confierous, earthy and fruity facets.

Stability :

Stable in perfumes and in various bases, except stong acidic (detergents) and very alkaline (detergents, liquid bleach) bases.

Uses in perfumery :

Ambermax® is used most of the time in perfumes for power and stability reasons. It brings an strong ambery identity in any kind of perfumes, especially in fabric care products, combined with other ambery molecules as Ambroxan®, Kephalis®and Amberketal®.

Year of discovery :

2005

Isomerism :

Ambermax® used in perfumery is a mixture of two positional isomers, depending on the position of the double bond found in this molecule. These two isomers are formed during the synthesis of Ambermax®. They are not separated for cost reasons. Anyway, the olfactive contribution of one isomer, compared to the other, would not be so valuable.

Synthesis precursor :

Ambermax® is not a precursor for the synthesis of another material used in perfumery.

Natural availability :

Ambermax® is not found in nature.

Synthesis route :

Data not available.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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