Ambroxan®
Ambremore® ; Ambermor® ; Ambrox® ; Synambrane® ; Cétalox® (Firmenich SA - 13/05/1993) ; Ambrofix® ; (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran ; Amber ether ; Amberxan ; Ambermox ; Amberol ; Ambronica ; Ambroxene ; 8-alpha-12-oxido-13,14,15,16-tetranorlabdane ; Dodecahydrotetramethyl naphtofuran ; Lanbroxyde ; Orcanox ; Superamber
Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
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Ambroxan - 30 Gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 6790-58-5
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EINECS number : 229-861-2
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FEMA number : 3471
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Density : 0,939
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Base
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Price Range : €€€€
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Appearance : White solid
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 318°C (604,4°F) at 1 013 hPa
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Detection Threshold : 0,3 ppb (0,00000003%)
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Molecular formula : C16H28O
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Log P : 5,9
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Molecular Weight : 236,4 g/mol
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Fusion Point : 75°C
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Flash Point : 161°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Ambroxan® is the major ambery note, since ambergris, a natural dejection of an ill spermwhale, is no longer used in fragrances.
In the perfume vocabulary, amber notes also refer to amber perfumes, which use cistus notes as Cistus EO and Cistus Labdanum Absolute Green.
Ambrofix is the most widely used and most biodegradable ambery molecule.
Stability :
Stable in perfumes and diverse functional bases, except some acid cleaners.
Uses in perfumery :
Ambroxan® brings an animalic and ambery facet with woody notes. Very good fixator. Replaces ambergris since its discovery, for ethical and price concerns.
Year of discovery :
Discovered in 1951
Isomerism :
The Ambroxan® most often used in perfumery is the laevorotatory isomer of this molecule. Ambrox DL (dextrorotatory and laevorotatory) refers to a racemic mixture of all the isomers of this molecule. The latter, however, is more unstable, as Ambrox tends to return to its laevorotatory form (L). Ambroxan® is a constitutional isomer of Cedramber®, Muscenone® and Sandela®. Cedramber® and Sandela® also have a woody, even ambery note for Cedramber®, but Muscenone® is a pretty different musk.
Synthesis precursor :
Ambroxan® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Initially, Ambroxan® is present in ambergris which is a whale excretion found dry on beaches. However, it is not extracted. Also, for ethical reasons, ambergris is no longer produced for perfumery. A natural quality of Ambroxan® is used in perfumes : it is called Ambrofix®.
Synthesis route :
Ambroxan® is a molecule synthesized from laevorotatory Sclareol, obtained from Clary Sage Absolute. The first step in this synthesis is to oxidize Sclareol into a lactone called Sclareolide, in its dextrorotatory form. The second is a hydrogenation of this compound into a diol. The last step is dehydration to obtain Ambroxan® (laevorotatory), the final product. Sclareolide in its racemic form can also be obtained by a purely synthetic route. Therefore, its laevorotatory isomer must be separated before the synthesis of Ambroxan®. Nowaday, there is a better process to obtain Ambrofix. This molecule can be obtained throught a unique multi-step bioconversion process starting from sugar cane. This new process is considered as the most sustainable process for Ambrofix in the market.All carbon atoms of the bio-based starting material are ending up in the product – no Carbon wasted leading to optimal carbon efficiency. Also, it needs 100x less land use to produce 1 kg of the Ambrofix compared to the traditional route based on Clary Sage This new bioconversion route maintains the classification as 100% Naturally Derived. ''
Regulations & IFRA
This ingredient is not restricted