Acephenanthrylene is a chemical compound with various applications in everyday life. It is commonly used in the synthesis of pharmaceuticals, dyes, and other organic compounds. This compound plays a crucial role in the development of new medications and materials that improve our quality of life. Its versatile properties make it a valuable ingredient in numerous industries, highlighting its significance in modern society.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
Acephenanthrylene, a polycyclic aromatic hydrocarbon, has commercial and industrial applications primarily as a key intermediate in the synthesis of various organic compounds. Known for its high purity and stability, Acephenanthrylene is utilized in the production of dyes, pigments, and pharmaceuticals. Its strong chemical properties make it a valuable component in the manufacturing of specialty chemicals and fine chemicals used in numerous industries.
In the realm of drug and medication applications, Acephenanthrylene plays a crucial role as a building block in the synthesis of pharmaceutical compounds. Its unique chemical structure and properties make it ideal for creating specific drug molecules with therapeutic effects. Through various chemical processes, Acephenanthrylene is transformed into active pharmaceutical ingredients that are essential for the production of medications to treat a wide range of medical conditions.
Furthermore, Acephenanthrylene is utilized in the development of various drugs targeting specific diseases and health conditions. Its versatile nature allows for the synthesis of pharmaceutical compounds with distinct pharmacological activities, making it a valuable resource in the pharmaceutical industry. As a key component in drug synthesis, Acephenanthrylene contributes significantly to the advancement of medical treatments and therapies for improved healthcare outcomes.
⚗️ Chemical & Physical Properties
Acephenanthrylene is a white crystalline solid with a distinct odor similar to mothballs. It has a relatively low vapor pressure, contributing to its strong aroma even at room temperature.
With a molar mass of 202.26 g/mol and a density of 1.21 g/cm³, Acephenanthrylene is heavier than most common household items. For comparison, water has a molar mass of 18.015 g/mol and a density of 1.0 g/cm³.
Acephenanthrylene has a melting point of 120°C and a boiling point of 420°C. These values are significantly higher than those of many common household items, such as water (melting point of 0°C and boiling point of 100°C).
Acephenanthrylene is sparingly soluble in water and has a relatively low viscosity. This sets it apart from common household items like sugar, which is highly soluble in water, and honey, which has a high viscosity.
🏭 Production & Procurement
Acephenanthrylene is produced through a series of chemical reactions involving the condensation of naphthalene with benzene. This process typically takes place in a controlled laboratory setting utilizing specialized equipment and expertise in organic chemistry.
Acephenanthrylene can be procured from chemical suppliers or manufacturers who produce it in bulk quantities for commercial use. The compound is typically packaged and transported in sealed containers to ensure its stability and purity during transit. Special precautions may be necessary due to its flammability and potential health hazards.
In some cases, Acephenanthrylene may be obtained through custom synthesis services from chemical companies or research institutions. This process involves collaborating with chemists to tailor the production of the compound to specific requirements or quantities. Proper handling and storage protocols must be followed to ensure the safety and effectiveness of Acephenanthrylene in various applications.
⚠️ Safety Considerations
Safety considerations for Acephenanthrylene should include proper handling, storage, and disposal methods to prevent any potential harm. It is crucial to wear appropriate personal protective equipment such as gloves, goggles, and a lab coat when working with this chemical to minimize exposure. Adequate ventilation should be maintained to reduce the risk of inhalation of fumes or vapors. Additionally, it is important to be aware of the potential fire and explosion hazards associated with Acephenanthrylene and take necessary precautions to prevent accidents.
The pharmacology of Acephenanthrylene involves its role as a potent inhibitor of certain enzymes in the body, leading to its use in various biochemical studies and research applications. This compound has been shown to interfere with specific metabolic pathways, making it a valuable tool for investigating different cellular processes. Due to its unique pharmacological properties, Acephenanthrylene is often used in laboratory settings to study the effects of enzyme inhibition on biochemical reactions and pathways.
Hazard statements for Acephenanthrylene should include information about its potential health risks and environmental hazards. This chemical may cause skin irritation, eye irritation, and respiratory problems if proper precautions are not taken during handling. Ingestion or inhalation of Acephenanthrylene can result in serious health effects, including nausea, vomiting, and difficulty breathing. It is important to store this compound in a secure area away from incompatible materials and to follow proper disposal guidelines to prevent environmental contamination.
Precautionary statements for Acephenanthrylene should emphasize the importance of following safe handling practices and wearing appropriate protective equipment. In case of skin contact, it is recommended to wash the affected area thoroughly with soap and water. If Acephenanthrylene is accidentally ingested or inhaled, seek medical attention immediately. When working with this compound, it is essential to have access to emergency eye wash stations and safety showers in case of exposure. Proper training on the hazards associated with Acephenanthrylene should be provided to all individuals working with this chemical to ensure their safety and well-being.
🔬 Potential Research Directions
One potential research direction regarding Acephenanthrylene could involve exploring its potential applications in organic synthesis. Understanding its reactivity and unique properties could lead to the development of novel methods for the construction of complex organic molecules.
Another avenue for research could involve investigating the potential biological activities of Acephenanthrylene. Studying its interaction with biological systems could shed light on its potential as a drug candidate or as a probe for studying biological processes.
Furthermore, research on the environmental fate and toxicity of Acephenanthrylene could provide valuable information for risk assessment and environmental management. Understanding its behavior in the environment and its potential impact on ecosystems could guide regulatory decisions and risk mitigation strategies.
🧪 Related Compounds
One similar compound to Acephenanthrylene based on molecular structure is 9,10-Dimethylanthracene. This compound is a polycyclic aromatic hydrocarbon with a similar fused ring structure as Acephenanthrylene, but with methyl groups at the 9 and 10 positions. The presence of these methyl groups can affect the chemical properties of the compound compared to Acephenanthrylene.
Another analogous compound is 4,4′-Bis(dimethylamino)benzophenone. This compound also contains a similar fused ring structure, but with different substituents attached to the rings. In this case, dimethylamino groups are attached to the benzophenone backbone. This compound could exhibit different reactivity or properties compared to Acephenanthrylene due to the nature of the substituents.
A third compound with a comparable structure is Dibenzo[a,h]pyrene. This compound contains a similar polycyclic aromatic hydrocarbon framework, but with an extended structure compared to Acephenanthrylene. The presence of additional fused rings in Dibenzo[a,h]pyrene may lead to different chemical reactivity or physical properties compared to Acephenanthrylene.
