Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
ISOAMYL BUTYRATE | M_0050643 | Naturel | - | - | - | - | more | - |
General Presentation
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CAS N° : : 106-27-4
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EINECS number : 203-380-8
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FEMA number : 2060
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Density : 0,862
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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 : 09.055
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JECFA number : 45
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 179°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C9H16O2
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Log P : 3,3
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Molecular Weight : 158,27 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 :
May form butyric acid through time.
Uses in perfumery :
Isoamyl Butyrate is used in all types of perfumes, for fruity-red, yellow and exotic notes. Boosts head notes and provides power and diffusivity.
Year of discovery :
Data not available.
Isomerism :
Allyl Caproate and gamma-Nonalactone are constitutional isomers of Isoamyl Butyrate. Allyl Caproate also has a fruity and butyric note, but gamma-Nonalactone has a very different peach and coconut smell.
Synthesis precursor :
Isoamyl Butyrate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Isoamyl Butyrate is present in many fruits in particular, and can be extracted from mastic.
Synthesis route :
Isoamyl Butyrate is synthesized by an esterification reaction between butyric acid and isoamyl alcohol, or 3-Methylbutanol, using an acid catalyst.
Regulations & IFRA
This ingredient is not restricted
