Photo credits: ScenTree SAS
Sandalore®
3-methyl-5-(2,2,3-trimethyl-1-cyclopent-3-enyl)pentan-2-ol ; Dersantol ; Landasweet ; Pentamethyl cyclopent-3-ene butanol ; Alpha,beta,2,2,3-pentamethyl cyclopent-3-ene-1-butanol ; Sandal pentanol ; Sandal touch ; Sandalorex ; Sandasweet
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Sandalore - 30 Gr | - |
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Sandalore - 30 Gr
Certifications :
General Presentation
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CAS N° : 65113-99-7
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EINECS number : 265-453-0
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FEMA number : Donnée indisponible.
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
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Appearance : Colorless viscous liquid
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Density : 0,898
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Volatility : Base
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Price Range : €€
Physico-chemical properties
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Molecular formula : C14H26O
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Molecular Weight : 210,36 g/mol
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Log P : 4,7
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Fusion Point : <-50°C
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Boiling Point : 275°C
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Detection Threshold : Donnée indisponible.
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Optical rotation : Donnée indisponible
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Vapor pressure : Donnée indisponible
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Refractive Index @20°C : Donnée indisponible
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Acid Value : Donnée indisponible.
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Flash Point : 95°C
Uses
Uses in perfumery :
Sandalore® is used in sandalwood reproductions, woody notes for bringing volume and trail. Used for a milky and creamy effect in sandalwood notes. To be combined with other sandalwood notes such as Sandela®, Bacdanol® or Polysantol®. Not to be put in candle base. Tends to flatten accords.
Year of discovery :
1976
Natural availability :
Sandalore® is not available in its natural state.
Isomerism :
The isomer of Sandalore® formed during the synthesis has a ramified alcohol function, while Sandalore® has it on its main carbon chain. Sandalore® has two asymmetric carbons. It is therefore a mixture of isomers that is used even when Sandalore® is isolated. Adoxal® is a constitutional isomer of Sandalore®. Its smell is however radically different, as it is marine and aldehydic.
Synthesis precursor :
Sandalore® is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Sandalore® is synthesized by a condensation of Campholenal with Methyl Ethyl Ketone. Then, two compounds are obtained and catalytically hydrogenated to ensure a selectivity of this hydrogenation (the alcene function of the ring must not be hydrogenated). A mixture of two hydrogenated molecules is obtained. These two isomers can be separated by a fractional distillation, or used together, as their smell is similar. The term Sandalore® refers to only one of these two molecules.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is restricted by the 51th amendment
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Restriction type : RESTRICTION
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Cause of restriction : DERMAL SENSITIZATION
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Amendment : 49
- Quantitative limit on the use :
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Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A B C DCat.6 0,21 % 0,062 % 1,2 % 1,2 % 0,29 % 0,29 % 0,29 % 0,29 %0,68 % Cat.5A B C DCat.6 0,29 % 0,29 % 0,29 % 0,29 %0,68 % Cat.7A BCat.8 Cat.9 Cat.10A BCat.11A BCat.12 2,4 % 2,4 %0,12 % 2,3 % 8,1 % 8,1 %4,5 % 4,5 %No Restriction Cat.10A BCat.11A BCat.12 8,1 % 8,1 %4,5 % 4,5 %No Restriction
