Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Acetate de Benzyle - 30 Gr | - |
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Acetate de Benzyle - 30 Gr
Certifications :
General Presentation
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CAS N° : 140-11-4
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EINECS number : 205-399-7
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FEMA number : 2135
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FLAVIS number : 09.014
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JECFA number : 23
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Appearance : Colorless liquid
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Density : 1,1
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Volatility : Head
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Price Range : €
Physico-chemical properties
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Molecular formula : C9H10O2
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Molecular Weight : 150,18 g/mol
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Log P : 1,96
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Fusion Point : -51°C
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Boiling Point : 206°C
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Detection Threshold : 2 et 270 ppb (0,000027%)
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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 : 91°C
Uses
Uses in perfumery :
Benzyl acetate is used in floral reconstructions, especially in jasmine, ylang-ylang and monoï notes.
Year of discovery :
Discovered in 1853. Benzyl acetate was first isolated from jasmine absolute during the 10's by german scientists Albert Hesse and Friedrich Müller, because this extract contains 20 to 35% of this molecule.
Natural availability :
Today, natural Benzyl acetate can be extracted from Grandiflorum Jasmine Absolute (and other origins), Ylang-Ylang Extra EO or Narcissus Absolute.
Isomerism :
Para-Cresyl acetate is a constitutional isomer of Benzyl acetate. Both have the same formula, but para-Cresyl acetate is much more animalic and less floral-jasmine than Benzyl acetate.
Synthesis precursor :
Benzyl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Nowadays, Benzyl acetate is synthesized by an esterification reaction from acetic acid and Benzyl Alcohol, in the presence of an acid catalyst such as concentrated sulfuric acid.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
