Geranyl acetate
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- Category :
Organic chemicals and Derivatives/Aroma compounds
- CAS NO : 105-87-3
- EC NO : 203-341-5
- Molecular Formula : C12H20O2
- Main Specifications : 99% min
- Synonyms : Trans-3,7-dimethyl-2,6-octadien-1-yl ethanoate; Geranyl ethanonte;3,7-dimethylocta-2,6-dien-1-yl acetate;(2E)-3,7-dimethylocta-2,6-dien-1-yl acetate;
Package: 25kg,50kg 200kg
Uses : used in essence and fragrance,Edible flavor, as fragrances in cosmetics, soaps, etc.
Molecular Structure:

Product description:
What is the chemical of Geranyl acetate ?
Appearance: Colorless to light yellow liquid ;
Assay:99%min by GC ;
IR Identity: conform to standard ;
HNMR: conform to standard ;
carbon spectrum: conform to standard ;
Water by K. F.:0.5% max or as per the customer’s request ;
Loss on drying:0.5% max. or as per the customer’s request ;
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Geranyl acetate is a multifunctional compound primarily used in the following fields:
Essence and fragrance: Used to formulate floral essences such as rose, orange blossom, and osmanthus, and as a modifier to enhance sweetness; also an important ingredient in raw materials such as artificial bay leaf oil and bergamot oil.
Edible flavor: According to the GB 2760-96 standard, it is allowed to be used in food, mainly for apple, pear, berry and other fruit-flavored essences, and can also be applied to wine, spicy and other edible essences.
Daily chemical products: often added as fragrances in cosmetics, soaps, etc.
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The production methods of (geranyl acetate) mainly include natural extraction and chemical synthesis.
Natural extraction method: Geranyl acetate occurs naturally in aromatic oils such as camphor oil, ylang-ylang oil, neroli oil, orange leaf oil, coriander seed oil, and lemongrass oil. It can be directly extracted from these natural sources through methods such as distillation.
Chemical synthesis method: It is primarily prepared through the esterification reaction of geraniol. Common routes include: Acetic anhydride method: Geraniol reacts with acetic anhydride catalyzed by sodium acetate at room temperature, with a yield of nearly 90%. It is then purified through washing and vacuum distillation.
Acetic anhydride method: In the presence of mineral acid (such as sulfuric acid), geraniol reacts with sodium acetate under the action of acetic anhydride.
In addition, the literature also mentions a method involving esterification through azeotropic distillation of acetic acid and isopropanol in a benzene solution in the presence of trace sulfuric acid, but this route may not be mainstream.