Photo credits: ScenTree SAS
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 -
EINECS number :
236-971-4 -
FEMA number :
Donnée indisponible. -
FLAVIS number :
Donnée indisponible.
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JECFA number :
Donnée indisponible. -
Volatility :
Heart/Base -
Price Range :
€€€€
Physico chemical properties
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Appearance :
Colorless to pale yellow liquid -
Density :
1,001 -
Refractive Index @20°C :
Data not available. -
Optical rotation :
Data not available. -
Vapor pressure :
0,000268 mmHg @23°C -
Flash Point :
94°C
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Molecular formula :
C15H24O -
Molecular Weight :
220,36 g/mol -
Log P :
4,7 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
-
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
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.
Natural availability :
Andrane® is not found in nature.
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.
Synthesis route :
Data not available.
Stability :
Stable compound in most bases, except in shampoo base for example.
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.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment