Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
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L-Isopulegol FG | 30695624 |
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Molecule | - | - | - | - | - | |
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ISOPULEGOL | 274 |
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Molecule | - | - | - | - | - |
General Presentation
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CAS N° : 89-79-2
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EINECS number : 201-940-6
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FEMA number : 2962
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FLAVIS number : Donnée indisponible.
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JECFA number : 755
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Appearance : Colorless liquid
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Density : 0,91
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Volatility : Base
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Price Range : Data not available.
Physico-chemical properties
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Molecular formula : C10H18O
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Molecular Weight : 154,25 g/mol
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Log P : 2,4
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Fusion Point : Donnée indisponible.
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Boiling Point : 211,66°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 : Donnée indisponible.
Uses
Uses in perfumery :
Year of discovery :
Data not available.
Natural availability :
Isopulegol is a molecule commonly found in nature. It is present in concentrations from 0.5% to 1.7% in citronella Java EO, as well as in several species of the Citrus genus as well as the majority of essential oils from the Mentha genus. It can also be found in Abies balsamea, Picea mariana, and various eucalyptus species.
Isomerism :
Data not available.
Synthesis precursor :
Koumalactone can be obtained from isopulegol through epoxidation. Dihydromintlactone can be obtained from isopulegol via ozonolysis. Menthol can also be derived from isopulegol. The process is as follows: Citral -> Distillation to separate Geranial/Neral -> Chiral catalysis to produce (R)-Citronellal -> Acid catalysis to create isopulegol -> Hydrogenation to produce (-)-Menthol.
Synthesis route :
Isopulegol can be obtained thanks to acidic catalysis of (R)-Citronellal
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment