Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
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Acetate de Cis-3-Hexenyle - 30 Gr | - |
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CIS-3-HEXENYL ACETATE | M_0050639 |
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Naturel | - | - | - | - | - |
Acetate de Cis-3-Hexenyle - 30 Gr
Certifications :
CIS-3-HEXENYL ACETATE
ID : M_0050639
Certifications :
General Presentation
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CAS N° : 3681-71-8
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EINECS number : 222-960-1
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FEMA number : 3171
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FLAVIS number : 09.197
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JECFA number : 134
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Appearance : Colorless liquid
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Density : 0,908
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Volatility : Head/Heart
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Price Range : €€
Physico-chemical properties
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Molecular formula : C8H14O2
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Molecular Weight : 142,2 g/mol
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Log P : 2,7
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Fusion Point : Donnée indisponible.
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Boiling Point : 75°C (à 26 hPa)
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Detection Threshold : 15,5193 ng/l air
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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 : 57°C
Uses
Uses in perfumery :
cis-3-Hexenyl acetate is used in fruity-pear, apple and banana accords and in floral notes for an aqueous and airy note. Brings a green, aqueous and fruity facet at the same time.
Year of discovery :
Data not available.
Natural availability :
Cis-3-Hexenyl acetate is present in the fragrant principle of several fruits such as apple or guava and is also present in hyacinth, Sambac Jasmine Absolute and Ylang-Ylang Extra EO (and other ylang fractions), from which it can be extracted in its natural state in small quantities.
Isomerism :
Cis-3-Hexenyl acetate diastereoisomer, trans-3-Hexenyl acetate, has almost identical facets as its smell is green, fruity-pear and banana. Another position isomer, called trans-2-Hexenyl acetate, is also useful in perfumery for a less green but more fruity note, reminiscent of apple and pear. Moreover, cis-3-Hexenyl acetate is a constitutional isomer of delta-Octalactone, although they do not share the same smell and their structure are very different.
Synthesis precursor :
Cis-3-Hexenyl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Cis-3-Hexenyl acetate results from an esterification of cis-3-Hexenol with acetic acid, in the presence of an acid catalysor as concentrated sulfuric acid. Using acetic anhydride or chloroacetic acid can also enhance the yield of this reaction.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
