9-Ethyladenine is a chemical compound that is commonly used in the production of various drugs, including anticancer and antiviral medications. Due to its therapeutic properties, this compound plays a significant role in the pharmaceutical industry, ultimately impacting the health and well-being of individuals in their everyday lives. Additionally, 9-Ethyladenine is also employed in scientific research as a precursor to other bioactive molecules, further underscoring its relevance to various academic disciplines.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
9-Ethyladenine, a purine derivative, is primarily used in commercial and industrial applications as a building block in the synthesis of pharmaceutical compounds, agrochemicals, and dyes. Its unique structure and chemical properties make it a valuable tool in organic chemistry for creating various products used in these industries.
In the realm of drug discovery and pharmaceuticals, 9-Ethyladenine has shown promise as a potential therapeutic agent for various medical conditions. It has demonstrated antimicrobial, antiviral, and antiproliferative activities, making it a target for developing new medications to treat bacterial and viral infections, as well as certain types of cancers.
9-Ethyladenine has also been studied for its potential role in the treatment of neurological disorders, such as Parkinson’s disease and Alzheimer’s disease. Research suggests that this compound may have neuroprotective properties and could be developed into drugs that target specific pathways involved in these conditions. The exploration of its pharmacological potential in these areas continues to be an active area of investigation in the scientific community.
⚗️ Chemical & Physical Properties
9-Ethyladenine is a white crystalline solid with no distinct odor. It is a water-soluble compound commonly used in biochemical research.
9-Ethyladenine has a molar mass of 153.18 g/mol and a density of 1.32 g/cm³. In comparison, common food items such as sugar and salt have lower molar masses and higher densities.
The melting point of 9-Ethyladenine is approximately 300°C, while its boiling point is around 500°C. These values are much higher than those of typical food items like butter or chocolate.
9-Ethyladenine is highly soluble in water and has a low viscosity. This stands in contrast to many food items which may have limited solubility and higher viscosity when dissolved in water.
🏭 Production & Procurement
9-Ethyladenine is typically produced through a multistep synthetic process in a laboratory setting. The starting material for this synthesis is usually adenine, a nitrogenous base found in DNA and RNA. Through the introduction of an ethyl group in a controlled reaction, 9-Ethyladenine is formed.
Once produced, 9-Ethyladenine can be procured from chemical suppliers or pharmaceutical companies. It is often sold in the form of a white powder or crystalline solid. The compound is stable under normal conditions and can be transported safely in airtight containers to prevent degradation.
In transportation, 9-Ethyladenine is handled with care to avoid contamination or exposure to moisture. Proper labeling and documentation are required to ensure compliance with regulatory standards. Typically, the compound is shipped in sealed containers with appropriate safety measures to prevent accidental release or mishandling.
⚠️ Safety Considerations
Safety considerations for 9-Ethyladenine should be taken seriously due to its potential hazards. This chemical substance should be handled with care to avoid skin contact, as it can cause irritation or allergic reactions. Additionally, 9-Ethyladenine should only be used in well-ventilated areas to prevent inhalation of its vapors, which can lead to respiratory issues. It is also important to store this compound in a secure location away from direct sunlight and heat sources to prevent decomposition or other hazardous reactions.
Hazard statements for 9-Ethyladenine include warnings about its potential toxicity and irritant properties. This chemical can cause skin irritation upon contact, as well as severe eye damage if not properly handled. Ingestion or inhalation of 9-Ethyladenine may lead to serious health effects, such as respiratory tract irritation or systemic toxicity. Therefore, it is crucial to follow safety guidelines and wear appropriate personal protective equipment when working with this compound to minimize the risk of exposure.
Precautionary statements for 9-Ethyladenine focus on the necessary measures to ensure safe handling and storage of this chemical. It is recommended to wear protective gloves, clothing, and eye protection when working with 9-Ethyladenine to prevent skin contact or eye exposure. Additionally, respiratory protection should be used in well-ventilated areas to avoid inhalation of vapors or dust particles. Proper labeling of containers and storage in a cool, dry place away from incompatible materials are also advised to prevent accidents or chemical reactions.
🔬 Potential Research Directions
One potential research direction for 9-Ethyladenine is exploring its pharmacological properties and potential applications in drug discovery and development.
Another research avenue could involve investigating the biochemical mechanisms of action of 9-Ethyladenine within biological systems, such as its effects on cellular metabolism or gene expression.
Furthermore, studies may be conducted to elucidate the physiological effects of 9-Ethyladenine on various organisms to understand its potential role in growth, development, or disease pathways.
🧪 Related Compounds
One similar compound to 9-Ethyladenine based on molecular structure is 2-Methyladenine. This compound differs from 9-Ethyladenine by having a methyl group (-CH3) attached to the 2-position of the adenine ring instead of an ethyl group.
Another related compound is 6-Methyladenine, which contains a methyl group at the 6-position of the adenine ring. This structural difference leads to varying biological activities and properties compared to 9-Ethyladenine.
Additionally, 2-Ethyladenine is a compound that shares structural similarity with 9-Ethyladenine. However, in this compound, the ethyl group is attached to the 2-position of the adenine ring instead of the 9-position, resulting in distinct chemical and biological characteristics.
