105-87-3
105-87-3
Chemical Structure
Geranyl acetate
- CAS No.: 105-87-3
- Formula:C12H20O2
- Molecular Weight:196.29
IUPAC Name: (E)-3,7-dimethylocta-2,6-dien-1-yl acetate
InChIKey: HIGQPQRQIQDZMP-DHZHZOJOSA-N
SMILES: C/C(C)=C\CC/C(C)=C/COC(C)=O
Biological Activity: Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent[1]. Geranyl acetate can induces cell apoptosis[2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Geranyl acetate | 99.74% | Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent. Geranyl acetate can induces cell apoptosis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Geranyl acetate (Standard) | ≥98% | Geranyl acetate (Standard) is the analytical standard of Geranyl acetate. This product is intended for research and analytical applications. Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent. Geranyl acetate can induces cell apoptosis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(-)-Lavandulyl acetate | (-)-Lavandulyl acetate is a nature product that can be found in Lavandula angustifolia. (-)-Lavandulyl acetate shows toxicity for mosquito vectors. (-)-Lavandulyl acetate can be used as mosquito larvicide. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(±)-Lavandulyl acetate | 98.42% | (±)-Lavandulyl acetate is an isomer of (-)-Lavandulyl acetate (HY-117419). (-)-Lavandulyl acetate is a nature product that can be found in Lavandula angustifolia. (-)-Lavandulyl acetate shows toxicity for mosquito vectors. (-)-Lavandulyl acetate can be used as mosquito larvicide. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Geranylacetone | 99.42% | Geranylacetone is a natural compound isolated from the stems of Ferula akitschkensis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Geraniol (Standard) | 96.88% | Geraniol (Standard) is the analytical standard of Geraniol. This product is intended for research and analytical applications. Geraniol, an olefinic terpene, was found to inhibit growth of Candida albicans and Saccharomyces cerevisiae strains. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Citronellyl acetate (Standard) | ≥98% | Citronellyl acetate (Standard) is the analytical standard of Citronellyl acetate (HY-N7144A). This product is intended for research and analytical applications. Citronellyl acetate is a monoterpene product of the secondary metabolism of plants, with antinociceptive activity. Citronellyl acetate exhibits pro-apoptotic activity in human hepatoma cells. Citronellyl acetate shows fungicidal, larvicidal, bactericidal and repelling/insecticidal effects. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(E/Z)-Geranylacetone | 97.0% | (E/Z)-Geranylacetone is an organic compound commonly used as an ingredient in fragrances and fragrances. It can be used in some products such as perfumes, soaps and cosmetics, and can bring a fresh aromatic smell. In addition, the compound is used in some foods and pharmaceuticals, for example in candy, chewing gum and herbal remedies. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Prenyl acetate | Prenyl acetate is an insecticide. At low concentrations, prenyl acetate exhibits an attractant effect on worker ants of the red imported fire ant, and it elicits strong antennal electroantennogram (EAG) responses in all castes of the red imported fire ant. Prenyl acetate shows low toxicity to mammals. It can be used in research related to the control of the red imported fire ant (Solenopsis invicta) . | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Neryl acetate (Standard) | ≥98% | Neryl acetate (Standard) is the analytical standard of Neryl acetate. This product is intended for research and analytical applications. Neryl acetate is an essential oil component. Neryl acetate upregulates genes associated with epidermal differentiation, skin barrier formation and ceramide synthesis; it also increases filaggrin expression, total lipid and ceramide contents. Neryl acetate acts as the core driver mediating the skin barrier-forming and antibacterial effects of Helichrysum italicum essential oil. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Nerylformate | Nerylformate is a terpenoid derivative secreted by American house dust mites (Dermatophagoides farinae) and European house dust mites (Dermatophagoides pteronyssinus). Nerylformate has a significant attraction effect on both male and female individuals of the two species of house dust mites. Nerylformate guides the mites to gather together to reduce dehydration and enhance defense. Nerylformate can be used for the research of immunology and inflammation, such as allergic rhinitis. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Geranic acid | 90.0% | Geranic acid (Geranate) acts as a tyrosinase inhibitor and antifungal agent, with an IC50 value of 0.14-2.3 mM against mushroom tyrosinase. Geranic acid reduces the viability of human pancreatic cancer cells and B-lymphoma cells. Geranic acid inhibits mycelial growth of the maize pathogens Colletotrichum graminicola and Fusarium graminearum. Geranic acid is applicable to research related to fungal infections, pancreatic cancer and B-lymphoma. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Wu T, et al. Engineering Saccharomyces cerevisiae for the production of the valuable monoterpene ester geranyl acetate. Microb Cell Fact. 2018 Jun 5;17(1):85. [Content Brief]
- [2]. Qi F, et al. Geraniol and geranyl acetate induce potent anticancer effects in colon cancer Colo-205 cells by inducing apoptosis, DNA damage and cell cycle arrest. J BUON. 2018 Mar-Apr;23(2):346-352. [Content Brief]
