Andrane®
Andrane extra ; Cedr-8-ene epoxide ; 8,9-cedrane epoxide ; 8,9-epoxycedrane ; Cedrene epoxide ; Alpha-cedrene epoxide ; 2H-2a,7-(1aS,2aR,3R,5aS,7R,7aR)-octahydro-3,6,6,7a-tetramethyl-methanoazuleno(5,6-b)oxirene ; (1aS-(1aa,2ab,3aa,5aa,7b,7aa))-octahydro-3,6,6,7a-tetramethyl-2H-2a,7-methanoazuleno(5,6-b)oxirane
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 13567-39-0
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EINECS number : 236-971-4
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FEMA number : Donnée indisponible.
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Density : 1,001
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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 : Heart/Base
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Price Range : €€€€
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Appearance : Colorless to pale yellow liquid
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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 :
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Detection Threshold : Donnée indisponible.
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Molecular formula : C15H24O
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Log P : 4,7
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Molecular Weight : 220,36 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 94°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Compared to Cashmeran®, Andrane® has a less musky note, but an ambergris facet. Usage of Cashmeran® is more frequent than Andrane® in perfumes.
Stability :
Stable compound in most bases, except in shampoo base for example.
Uses in perfumery :
Andrane® is used to bring an earthy note of patchouli in a built up woody structure. It brings a fresh, ambergris and dry side, close to Cashmeran®, with strength to a woody, oriental and fresh perfumes.
Year of discovery :
Data not available.
Isomerism :
Andrane® has 4 asymetric carbons. A mixture of its isomers is used in perfumes.
Synthesis precursor :
Andrane® is not a precursor to the synthesis of another compound of olfactive interest.
Natural availability :
Andrane® is not found in nature.
Synthesis route :
Data not available.
Regulations & IFRA
This ingredient is not restricted
