Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Acetate d'Isoamyle - 30 Gr | - |
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- | - | - | - | - | - | |
|
ISOAMYL ACETATE | M_0050642 |
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|
Naturel | - | - | - | - | - |
Acetate d'Isoamyle - 30 Gr
Certifications :
ISOAMYL ACETATE
ID : M_0050642
Certifications :
General Presentation
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CAS N° : 123-92-2
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EINECS number : 204-662-3
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FEMA number : 2055
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FLAVIS number : 09.024
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JECFA number : 43
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Appearance : Colorless liquid
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Density : 0,876
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Volatility : Head
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Price Range : €
Physico-chemical properties
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Molecular formula : C7H14O2
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Molecular Weight : 130,19 g/mol
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Log P : 2,7
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Fusion Point : -78°C
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Boiling Point : 142°C
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Detection Threshold : 2 à 43 ppb (0,0000043%)
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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 : 25°C
Uses
Uses in perfumery :
Isoamyl acetate is used in banana notes. Enhances the head of a perfume, and gives a fruity-banana or pear nuance, especially in jasmine notes. However, it can make an accord become very artificial in the case of an overdose.
Year of discovery :
Data not available.
Natural availability :
Isoamyl acetate can be extracted from Roman Chamomile EO, although it is present in very small quantities.
Isomerism :
Isoamyl acetate does not have any isomer used in perfumery.
Synthesis precursor :
Isoamyl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Isoamyl acetate is synthesized by an esterification reaction between acetic acid or acetic anhydride and Isoamyl alcohol, in the presence of an acid catalyst.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
