2-Isopropyl-5-methylanisole, also known as para-cresyl isopropyl ether, is a chemical compound commonly used in the production of various consumer products such as perfumes, detergents, and soaps. Its pleasant odor and ability to mask unpleasant smells make it a popular ingredient in fragrance formulations. Additionally, it is used in the manufacturing of flavorings for food products and pharmaceuticals. As such, 2-Isopropyl-5-methylanisole plays a significant role in enhancing the olfactory experience and overall quality of everyday items that we encounter in our daily lives.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
2-Isopropyl-5-methylanisole, also known as ‘Sandela,’ is primarily used as a fragrance ingredient in various commercial and industrial applications. Its pleasing odor profile makes it a popular choice in perfumes, cosmetics, and personal care products. In addition to its use in fragrances, it is also utilized in household products such as air fresheners, laundry detergents, and cleaning agents.
This compound also finds application in the pharmaceutical industry for its potential therapeutic properties. Studies have shown that 2-Isopropyl-5-methylanisole exhibits anti-inflammatory and antioxidant effects, making it a candidate for drug development. It is being investigated for its potential use in medications for conditions such as arthritis, dermatitis, and other inflammatory disorders.
In conclusion, 2-Isopropyl-5-methylanisole plays a significant role in both commercial and industrial sectors as a fragrance ingredient and in the pharmaceutical industry for its potential therapeutic properties. Its versatility and favorable characteristics make it a valuable component in various products and research endeavors.
⚗️ Chemical & Physical Properties
2-Isopropyl-5-methylanisole is a colorless liquid with a characteristic sweet, fruity odor. Its appearance is that of a clear, volatile substance with a distinctive aroma that is commonly used in the fragrance industry.
This compound has a molar mass of approximately 150.23 g/mol and a density of about 0.94 g/cm³. In comparison to common food items, 2-Isopropyl-5-methylanisole has a higher molar mass and lower density than most edible substances.
The melting point of 2-Isopropyl-5-methylanisole is around -55°C, while the boiling point is approximately 218°C. These values are notably higher than those of many common food items, which typically have lower melting and boiling points.
2-Isopropyl-5-methylanisole is practically insoluble in water and exhibits low viscosity. In contrast, many common food items are more water-soluble and may have varying viscosities.
🏭 Production & Procurement
2-Isopropyl-5-methylanisole, commonly known as mesitylene or trimethyl benzene, is produced through the alkylation of mesityl oxide with propylene in the presence of acid catalysts such as aluminum chloride or sulfuric acid. This reaction yields 2-Isopropyl-5-methylanisole as the main product, which can then be purified and isolated through distillation.
2-Isopropyl-5-methylanisole can be procured from chemical suppliers or manufacturers who specialize in aromatic compounds and fine chemicals. It is typically available in various purities and quantities, ranging from laboratory-scale to industrial-grade volumes. The compound can be transported in sealed containers or drums to prevent contamination or loss during shipment.
The procurement of 2-Isopropyl-5-methylanisole may involve compliance with regulations and guidelines governing the handling, storage, and transportation of hazardous chemicals. Proper labeling, documentation, and packaging are essential to ensure safety and regulatory compliance throughout the supply chain. It is important to work with reputable suppliers who adhere to industry standards and best practices to guarantee the quality and integrity of the compound.
⚠️ Safety Considerations
Safety considerations for handling 2-Isopropyl-5-methylanisole, also known as p-menthane, include the need for proper ventilation to avoid inhalation of vapors which may cause irritation to the respiratory tract. Care should be taken to prevent skin contact as it may result in dermatitis or sensitization. Additionally, eye protection should be worn to prevent irritation or damage in case of accidental splashes.
The hazard statements for 2-Isopropyl-5-methylanisole include: may cause skin irritation, causes serious eye irritation, may cause respiratory irritation. It is also harmful if swallowed or inhaled. The substance is classified as a Category 2 skin sensitizer, meaning it may cause an allergic skin reaction.
Precautionary statements for handling 2-Isopropyl-5-methylanisole include: avoid breathing vapors, wear protective gloves and eye protection, wash hands thoroughly after handling, and seek medical advice if irritation or allergic skin reaction occurs. It is important to keep the substance away from heat, sparks, open flames, and hot surfaces to prevent fire hazards. Proper storage in a cool, dry, and well-ventilated area is also recommended to ensure safe handling.
🔬 Potential Research Directions
One potential research direction for 2-Isopropyl-5-methylanisole is the investigation of its chemical properties and potential applications in various industries. Researchers could explore the compound’s reactivity, stability, and solubility in different solvents to better understand its behavior in various environments.
Another avenue of research could involve the toxicological properties of 2-Isopropyl-5-methylanisole. Studies could focus on determining its effects on human health and the environment, including its potential carcinogenicity, mutagenicity, and ecotoxicity. This research could provide valuable information for regulatory agencies and industries that handle or use this compound.
🧪 Related Compounds
One similar compound to 2-Isopropyl-5-methylanisole based on its molecular structure is 1-Isopropyl-4-methylanisole. This compound has the same isopropyl group attached to the phenyl ring as in 2-Isopropyl-5-methylanisole, but in a different position. The methyl group is also attached to the phenyl ring in a similar manner.
Another related compound is 2-Isopropyl-4-methylanisole, which has the isopropyl group and the methyl group attached to the phenyl ring, similar to 2-Isopropyl-5-methylanisole. The only difference is the position of the methyl group on the phenyl ring, which gives this compound a unique molecular structure compared to 2-Isopropyl-5-methylanisole.
Additionally, 2-Isopropyl-3-methylanisole is another compound with a molecular structure similar to 2-Isopropyl-5-methylanisole. In this compound, the positioning of the isopropyl and methyl groups on the phenyl ring is maintained, but their specific positioning differs. This variation in positioning leads to distinct chemical properties and potential applications for 2-Isopropyl-3-methylanisole compared to its analog, 2-Isopropyl-5-methylanisole.
