Woody > Vetiver > Grapefruit > Cedar

Vetiveryl acetate

Acetyver ; Vetyver acetate ; 4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1H-azulen-6-yl acetate ; Acetivenol ; Vetyverol acetate ; Vetiveryl ethanoate

Vetiveryl acetate (CAS N° 84082-84-8)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Naturality Purity Latin name Treated part Geographical origin Certifications Comments MOQ
Quosentis logo
Acetate de Vetiveryle - 30 Gr - - - - - - more -
Van Aroma logo
Vetiveryl Acetate VT-005 Natural 100 Chrysopogon zizanioides Vetiver Oil Indonesia more 50 Kgs
Synthite logo
Vetiveryl Acetate 4410000159 Naturel - - - - more -
Information Générales

General Presentation

  • CAS N° : : 84082-84-8

  • EINECS number : 204-225-7

  • FEMA number : 4218

  • Density : 0,99

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Base

  • Price Range : €€€

  • Appearance : Amber liquid

  • FLAVIS number : 09.821

  • JECFA number : 1867

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 286°C

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C17H26O2

  • Log P : 6,16

  • Molecular Weight : 262,39 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 90°C

  • Vapor pressure : Lorem Ipsum

Utilisation

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.

Utilisation

Regulations & IFRA

  • IFRA 51th : This ingredient is restricted by IFRA

  • Restriction type : RESTRICTION

  • Cause of restriction : DERMAL SENSITIZATION AND SYSTEMIC TOXICITY

  • Amendment : 49

Quantitative limit on the use :
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
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