Molecular Formula | C10H16O |
Molar Mass | 152.236 |
Density | 0.96 g/mL at 25 °C(lit.) |
Melting Point | 271-272 °C |
Boling Point | 119-121 °C11 mm Hg(lit.) |
Flash Point | >230 °F |
Solubility | DMSO : 250 mg/mL (1642.25 mM; Need ultrasonic) |
Appearance | oily liquid |
Storage Condition | 2-8℃ |
Refractive Index | n20/D 1.501(lit.) |
MDL | MFCD00001567 |
Physical and Chemical Properties | Physical and chemical properties viscous oily liquid. It smells like linalool and terpineol. Boiling point 118-121 ℃ (11 × 133.322Pa). Relative density 0.9690. Refractive index 1.4996 ,[α]D-7. Stable properties, heat and acid resistance, not easy to volatilize. |
Use | Overview perillyl alcohol scientific name 4-isopropenyl-1-cyclohexene methanol, with linalool and terpineol-like flavor of thick viscous oil, exists in ginger grass oil, green lemon oil, lavendin oil and spearmint oil. Because of its aromatic taste, it is often used as a formulation of food flavors and additives. Perillyl alcohol, as a monoterpene drug for the treatment and prevention of cancer, has a unique therapeutic effect in the treatment of tumors such as ovarian tumors, esophageal cancer, breast cancer and so on. This information was compiled by Zhang Qian of the chemical book. |
Hazard Symbols | Xi - Irritant |
Risk Codes | R37/38 - Irritating to respiratory system and skin. R41 - Risk of serious damage to eyes R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S39 - Wear eye / face protection. S36 - Wear suitable protective clothing. |
Reference Show more | 1. Yichen Song, Ruoxi Sun, Zhouye Ji, Xiaoxi Li, Qiang Fu, Shiping Ma, Perilla aldehyde attenuates CUMS-induced depressive-like behaviors via regulating TXNIP/TRX/NLRP3 pathway in rats, Life Sciences, Volume 206, 2018, Pages 117-124, ISSN 0024-3205, https://d 2. [IF=4.411] Li Chen et al."Screening a Strain of Klebsiella sp. O852 and the Optimization of Fermentation Conditions for Trans-Dihydrocarvone Production."Molecules. 2021 Jan;26(9):2432 |
application fields | 1. perilla alcohol, as a monomer spice, is a compound that gives dry tea aroma and ambergris aroma. it can be used to imitate citrus, vanilla and fruit-shaped edible essence, food flavoring agent and soy sauce preservative. 2, organic synthesis of important intermediates, perilla alcohol is the synthesis of perilla aldehyde, perilla key intermediates. 3. Synthetic plant production regulators, agricultural pesticides and insect antifeedants. 4. Perilla alcohol has a unique medicinal effect. It can be used for organ transplantation and can reduce the rejection of allografts. 5. As a monoterpene drug for the treatment and prevention of cancer, perilla alcohol has the characteristics of broad-spectrum, high-efficiency, and low-toxicity anti-cancer effects. It has unique treatment in the treatment of tumors, such as ovarian tumors, esophageal cancer, breast cancer, etc. Therapeutic effect. |
|
biological activity | Perillyl alcohol is a monoterpene, isolated from lavender, mint, cherry and other plant essential oils. Perillyl alcohol can induce tumor cell apoptosis (apoptosis) without affecting normal cells. | |
Target |
|
melting point | 271-272 °C |
boiling point | 119-121 °C11mm Hg(lit.) |
density | 0.96 g/mL at 25 °C(lit.) |
FEMA | 2664 | P-MENTHA-1,8-DIEN-7-OL |
refractive index | n20/D 1.501(lit.) |
flash point | >230 °F |
storage conditions | Inert atmosphere,2-8°C |
acidity coefficient (pKa) | 14.85±0.10(Predicted) |
JECFA Number | 974 |
Perilla alcohol, also known as perilla alcohol ether or perilla alcohol ketone, is an organic compound with a chemical structure consisting of isoprene rings and enol groups. The following are two synthesis methods for perilla alcohol:
1. Photochemical synthesis method: This is a common synthesis method, in which the photoreaction is used for the various steps of synthesizing perilla alcohol. During the synthesis process, cis-jasmonate is first exposed to ultraviolet light, and then transformed into the corresponding cyclopentadienyl ring compound by changing the temperature and acidic conditions. Next, enol groups are introduced through alkaline promoted alkylation reactions to ultimately obtain perilla alcohol.
2. Chemical synthesis method: This method is usually carried out in the laboratory. A common synthesis method is to start from salbutamol and synthesize perilla alcohol through several steps of reaction. Asamadinone reacts with sodium cyanide under alkaline conditions to obtain the corresponding cyclopentadienone. Then, through acidic hydrolysis and appropriate reducing agents, cyclopentadienone is converted into perilla alcohol.
Different methods are suitable for different experimental conditions and requirements, but ultimately, synthesized perilla alcohol compounds can be obtained.