Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Isobutyl Quinoleine - 30 Gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 68198-80-1
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EINECS number : 269-204-7
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FEMA number : Donnée indisponible.
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Density : 1,011
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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 : Base
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Price Range : €€€
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Appearance : Colorless 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 : C13H15N
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Log P : 4,09
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Molecular Weight : 185,27 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 137°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
IsoButyl Quinoline was used for the first time in 1922 in Nuit de Noël by Caron. Also used in bases such as Cuir de Russie or Mousse de Saxe®.
Stability :
Stable in perfumes and diverse functional bases
Uses in perfumery :
IsoButyl Quinoline is used for chypre and leather notes, for a contribution of character and power. Gives character to floral accords when used in small quantity.
Year of discovery :
1908
Isomerism :
Butyl Quinoline is a positional isomer of Isobutyl Quinoline, but is very little used in perfumery.
Synthesis precursor :
IsoButyl Quinoline is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
IsoButyl Quinoline is not available in its natural state.
Synthesis route :
IsoButyl Quinoline is synthesized by a sequence of reactions called Skraup synthesis, reacting para-Isobutylaniline with glycerol in the presence of a concentrated sulfuric acid and nitrobenzene afterwards. This synthetic route is used for the synthesis of all quinolines.
Regulations & IFRA
This ingredient is not restricted
