Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 7392-19-0
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EINECS number : 230-983-3
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FEMA number : 3735
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Density : 0,87
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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 : Head
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : 13.094
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JECFA number : 1236
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 171°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C10H18O
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Log P : 3,1
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Molecular Weight : 154,25 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 58°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Stable in perfumes and diverse functional bases, except bleach.
Uses in perfumery :
Limetol® gives a minty effect to the top note. Brings freshness, head and power to the beginning of minty notes. May be useful to give a fresh effect to lime notes, and for woody and lemon notes.
Year of discovery :
Data not available.
Isomerism :
Limetol® has an asymmetric carbon. It is the enantiomeric mixture of this molecule that is used in perfumery. Moreover, Limetol® is a constitutional isomer of Isomenthone or Borneol for example. All have a minty smell, although they are used for different purposes. In the case of Limetol®, it is used to bring a zesty top note in perfumes.
Synthesis precursor :
Limetol® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Limetol® is particularly present in Lime EO. To increase its presence, it is possible to acidify the essential oil to promote its formation. Then, it is possible to extract it from the obtained product.
Synthesis route :
Limetol® can be synthesized by a cyclization and a dehydration of Citral and Linalool. These reactions are catalysed by the presence of a strong acid such as sulfuric acid.
Regulations & IFRA
This ingredient is not restricted