Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Acetate de Géranyle - 30 Gr | - | - | - | - | - | - | more | - | |
|
Geranyl Acetate 98%+ | CT-202 | Natural | 98%+ | Cymbopogon winterianus jowitt | Citronella Oil | Indonesia | more | 25 Kgs | |
|
GERANYL ACETATE | M_0050634 | Naturel | - | - | - | - | more | - | |
|
Geranyl Acetate 60 | 30333479 | Molecule | - | - | - | - |
|
more | - |
|
|
Geranyl Acetate Extra | 30292732 | Molecule | - | - | - | - |
|
more | - |
|
|
Geranyl Acetate Extra BMBcert™ | 30786721 | Molecule | - | - | - | - |
|
more | - |
General Presentation
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CAS N° : : 105-87-3
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EINECS number : 203-341-5
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FEMA number : 2509
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Density : 0,907
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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 : Heart
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Price Range : €
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Appearance : Colorless liquid
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FLAVIS number : 09.011
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JECFA number : 58
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 138°C (à 33 hPa)
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Detection Threshold : Il peut aller de 9 ppb à 460 ppb (0,000046%), ce qui reste très faible
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Molecular formula : C12H20O2
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Log P : 3,7
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Molecular Weight : 196,29 g/mol
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Fusion Point : <-100°C
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Flash Point : 104°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
acetates may form acetic acid through time. Geranyl acetate is particularly unstable.
Uses in perfumery :
Geranyl acetate is used in fruity-pear, rose, lavender, lily of the valley, apple and verbena notes among others.
Year of discovery :
Data not available.
Isomerism :
Neryl acetate, a (Z) diastereoisomer of Geranyl acetate, has a lighter, more terpenic smell than Geranyl acetate. Linalyl acetate, Terpenyl acetate and Isobornyl acetate are constitutional isomers of Geranyl acetate. However, Linalyl acetate and Terpenyl acetate are reminiscent of Bergamot EO, and Isobornyl acetate is reminiscent of pine.
Synthesis precursor :
Geranyl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Geranyl acetate is present in Palmarosa EO, Rose EO and Lemongrass EO, from which it can be extracted.
Synthesis route :
Geranyl acetate can be synthesized from Geraniol by an esterification reaction using acetic acid or acetic anhydride, or from Myrcene, in two stages: an addition reaction with hydrochloric acid, catalysed by copper chloride II, then an acetolysis reaction using sodium ethanoate and a base such as triethylamine. This reaction allows to obtain both (E) Geranyl acetate and (Z) Neryl acetate, two diastereoisomers.
Regulations & IFRA
This ingredient is not restricted
