Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
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Acetate de Vetiveryle - 30 Gr | - | - | - | - | - | - | more | - | |
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Vetiveryl Acetate | VT-005 | Natural | 100 | Chrysopogon zizanioides | Vetiver Oil | Indonesia | more | 50 Kgs | |
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Vetiveryl Acetate | 4410000159 | Naturel | - | - | - | - | more | - |
General Presentation
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CAS N° : : 84082-84-8
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EINECS number : 204-225-7
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FEMA number : 4218
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Density : 0,99
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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 : Base
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Price Range : €€€
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Appearance : Amber liquid
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FLAVIS number : 09.821
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JECFA number : 1867
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 286°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C17H26O2
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Log P : 6,16
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Molecular Weight : 262,39 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 90°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Derivating from Vetiver Haiti EO, Vetiveryl acetate keeps a grapefruit note, compared with Vetiver Java EO, much more smoky.
Stability :
acetates may form acetic acid through time
Uses in perfumery :
Vetiveryl acetate is used in woody, ambery and chypre perfumes for its long-lasting tenacity. Goes well with floral and spicy notes. More delicate and smoky than vetiver but less faceted and woody. Both are often associated in perfumes.
Year of discovery :
Data not available.
Isomerism :
Vetiverol is not a pure compound. It is a mixture of alcohols in which the major compound is Khusimol. Therefore, Vetiveryl acetate is a mixture of esters whose major compound is Khusimyl acetate. Vetyvenal® is a constitutional isomer of Vetiveryl acetate. However, all can be used to reconstitute Vetiver EO.
Synthesis precursor :
Vetiveryl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Vetiveryl acetate is an hemi-synthetic product, derivated from Vetiver Haiti EO, and particularly from the couple of molecules called Vetiverol.
Synthesis route :
Vetiveryl acetate is prepared from the mixture of sesquiterpene alcohols obtained from Vetiver Haiti EO, Vetiverol, by an esterification reaction using acetic acid or acetic anhydride, in the presence of a catalyst like sulfuric acid. Thus, its synthesis requires a first step to isolate Vetiverol from the vetiver root, which makes it an expensive raw material.
Regulations & IFRA
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IFRA 51th : This ingredient is restricted by IFRA
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Restriction type : RESTRICTION
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Cause of restriction : DERMAL SENSITIZATION AND SYSTEMIC TOXICITY
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Amendment : 49
- Quantitative limit on the use :
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Cat.1 Cat.2 Cat.3 Cat.4 Cat.5A Cat.5B Cat.5C Cat.5D Cat.6 0,05 % 0,05 % 0,05 % 0,9 % 0,1 % 0,1 % 0,1 % 0,033 % 0,098 % Cat.7A Cat.7B Cat.8 Cat.9 Cat.10A Cat.10B Cat.11A Cat.11B Cat.12 0,1 % 0,1 % 0,033 % 0,2 % 0,2 % 3,8 % 0,033 % 0,033 % No Restriction