167161-92-4

Usage

Uses

Used in Fragrance Industry:
2-(butylthio)-3,5,5-triMethyl-2-cyclohexen-1-one is used as a fragrance ingredient for its fruity and floral aroma, which provides a long-lasting scent in perfumes and other scented products. It is often combined with other ingredients to create unique and complex fragrances.
Used in Pharmaceutical Industry:
2-(butylthio)-3,5,5-triMethyl-2-cyclohexen-1-one has potential applications in the pharmaceutical industry due to its unique chemical properties and pleasant odor. It may be utilized in the development of medications or as a component in drug formulations.
Used in Cosmetic Industry:
In the cosmetic industry, 2-(butylthio)-3,5,5-triMethyl-2-cyclohexen-1-one is used for its pleasant odor and may be incorporated into various cosmetic products to enhance their scent and appeal to consumers.

Upstream product

• 10276-21-8 isophorone oxide 
• 109-79-5 n-butanethiol 

Relevant academic research and scientific papers

Synthesis and characterization of two novel second-order nonlinear optical chromophores based on julolidine donors with excellent electro-optic activity

Julolidine and its derivatives are excellent electron-rich structures thus two novel second order nonlinear optical (NLO) chromophores based on julolidine donors and tricyanofuran (TCF) acceptors linked via isophorone bridge (zh-1) and modified isophorone bridge (zh-2) have been synthesized. Density functional theory (DFT) was used to optimize the geometrical structures, calculate the HOMO-LUMO energy gaps and first-order hyperpolarizability (β) of these chromophores. Besides, to determine the redox properties of these chromophores, cyclic voltammetry (CV) experiments were performed. The optimized structures suggest that chromophore zh-1 possesses better planarity which increases the ability of electron delocalization. These chromophores showed good thermal stability with their decomposition temperatures all above 210 °C. The electro-optic coefficients (r33) of poled films containing 25 wt% of these chromophores doped in amorphous polycarbonate (APC) afforded values of 170 and 101 pm V-1 at 1310 nm for chromophores zh-1 and zh-2, respectively. These properties show the potential use of the new chromophores as advanced material devices.