2-Methylanthraquinone is a compound that plays a crucial role in the production of dyes and pigments used in various everyday products. These include textiles, plastics, and inks, among others. Its ability to impart vibrant and long-lasting color to these products makes it an essential ingredient in the manufacturing industry. Additionally, 2-Methylanthraquinone is also used in the production of pharmaceuticals and as a reagent in organic synthesis. Overall, this compound contributes significantly to enhancing the visual appeal and functionality of numerous products 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-Methylanthraquinone, a derivative of anthraquinone, has various commercial and industrial applications. This compound is commonly used as a dye intermediate in the textile industry for the production of various colored dyes. Additionally, it is utilized in the manufacturing of photochemicals for photography and photocopying processes.
In terms of drug and medication applications, 2-Methylanthraquinone has been explored for its potential therapeutic properties. Research has shown that this compound exhibits anti-inflammatory and antioxidant effects, making it a potential candidate for the development of pharmaceuticals targeting inflammatory conditions and oxidative stress-related diseases. However, further studies are required to fully understand its pharmacological effects and potential clinical applications.
⚗️ Chemical & Physical Properties
2-Methylanthraquinone is a yellow solid with a melting point of 113-115 degrees Celsius. It does not have a significant odor, making it relatively odorless compared to other chemicals.
The molar mass of 2-Methylanthraquinone is approximately 228.24 g/mol, with a density of 1.45 g/cm3. This places it in the range of common household items such as table salt, which has a molar mass of 58.44 g/mol and a density of 2.16 g/cm3.
The melting point of 2-Methylanthraquinone is higher than that of many common household items, such as sugar (melting point of 186 degrees Celsius) and butter (melting point of 32-35 degrees Celsius). It has a boiling point of 276 degrees Celsius, which is also higher than boiling points of many household items, such as water (boiling point of 100 degrees Celsius).
2-Methylanthraquinone is insoluble in water but soluble in organic solvents. It has a relatively low viscosity compared to common household items like honey or syrup. This makes it more easily pourable and less sticky when handling.
🏭 Production & Procurement
2-Methylanthraquinone, a key compound in the field of organic chemistry, is typically produced through a multistep synthesis process starting from anthraquinone. The synthesis involves the introduction of a methyl group to the anthraquinone molecule, resulting in the formation of 2-Methylanthraquinone. This process requires specialized equipment and expertise due to the sensitive nature of the compounds involved.
In order to procure 2-Methylanthraquinone, one must first identify reputable chemical suppliers who offer the compound for purchase. Once a supplier has been identified, the compound can be procured in varying quantities, depending on the needs of the researcher or manufacturer. Transporting 2-Methylanthraquinone typically involves compliance with strict regulations governing the transportation of hazardous chemicals, including proper labeling, packaging, and handling procedures.
It is important to note that the production and procurement of 2-Methylanthraquinone require adherence to stringent safety protocols to prevent accidents or exposure to harmful chemicals. Researchers and manufacturers should be well-versed in handling procedures and precautions to ensure the safe production and transportation of this essential compound. Additionally, proper documentation and record-keeping are imperative to track the sourcing, production, and distribution of 2-Methylanthraquinone for regulatory compliance and accountability.
⚠️ Safety Considerations
Safety considerations for 2-Methylanthraquinone include the need for proper handling procedures to minimize exposure. This compound should be stored in a cool, dry place away from heat and light sources. It is important to wear appropriate personal protective equipment, such as gloves and goggles, when working with 2-Methylanthraquinone to prevent skin and eye irritation.
In terms of pharmacology, 2-Methylanthraquinone has been shown to exhibit various biological activities, including anti-inflammatory and antioxidant properties. Studies have indicated that this compound may have potential therapeutic applications in the treatment of inflammatory diseases and oxidative stress-related conditions. Further research is needed to fully elucidate the pharmacological mechanisms of 2-Methylanthraquinone and its potential medical uses.
Hazard statements for 2-Methylanthraquinone include the potential for skin and eye irritation upon contact. Inhalation of this compound may cause respiratory irritation, while ingestion can lead to gastrointestinal discomfort. Prolonged or repeated exposure to 2-Methylanthraquinone may result in more serious health effects, such as dermatitis or respiratory sensitization. It is essential to follow proper safety protocols when handling this chemical to minimize the risk of adverse health consequences.
Precautionary statements for 2-Methylanthraquinone emphasize the importance of avoiding direct contact with the skin, eyes, and respiratory system. If exposure occurs, it is recommended to remove contaminated clothing and rinse affected areas with plenty of water. In cases of inhalation or ingestion, seek medical attention immediately. It is crucial to work with 2-Methylanthraquinone in a well-ventilated area and to use appropriate protective equipment to prevent exposure and potential health risks.
🔬 Potential Research Directions
Research on 2-Methylanthraquinone has shown potential applications in the field of organic electronics. Studies have indicated that this compound could be utilized as a redox shuttle in rechargeable batteries, leading to enhanced performance and stability. Further investigation into the electrochemical properties of 2-Methylanthraquinone may uncover new possibilities for energy storage devices.
In the realm of medicinal chemistry, 2-Methylanthraquinone has garnered interest for its potential antitumor properties. Preliminary studies have suggested that this compound exhibits cytotoxic effects against cancer cells, making it a promising candidate for further exploration in the development of novel anticancer agents. Future research endeavors could focus on elucidating the molecular mechanisms underlying the antitumor activity of 2-Methylanthraquinone.
Moreover, the environmental implications of 2-Methylanthraquinone are worth exploring in depth. Given its structural features and chemical reactivity, this compound may serve as an effective catalyst for eco-friendly organic transformations. Investigating the catalytic potential of 2-Methylanthraquinone in various reactions could pave the way for the development of sustainable methodologies in the field of green chemistry.
🧪 Related Compounds
One similar compound to 2-Methylanthraquinone is 1,4-Dimethylanthraquinone, which has two methyl groups attached to the first and fourth carbon atoms of the anthraquinone ring. This compound shares a similar molecular structure with 2-Methylanthraquinone but has different substitution patterns, resulting in altered chemical properties.
Another related compound is Anthraquinone, which is the parent compound of 2-Methylanthraquinone. Anthraquinone has a similar core structure, but lacks the methyl group attached to the anthraquinone ring in 2-Methylanthraquinone. This difference in substitution leads to distinct chemical reactivity and physical properties between the two compounds.
Additionally, 2-Ethylanthraquinone is a compound closely related to 2-Methylanthraquinone, differing only in the alkyl group attached to the anthraquinone ring. The presence of an ethyl group instead of a methyl group alters the steric hindrance and electronic effects of the compound, resulting in different chemical behavior and reactivity.
