N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine, commonly referred to as “Methylbutenylaminopurinamine,” is a compound with potential applications in pharmaceutical research and drug development. This molecule belongs to the class of purine-based compounds, which play significant roles in various biological processes within the human body.
While the specific everyday relevance of N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine may not be readily apparent to the general public, its importance lies in its potential as a building block for new medications that can target specific biochemical pathways involved in disease processes. Through further research and development, this compound could lead to the creation of novel therapeutic agents that may ultimately improve health outcomes for individuals worldwide.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine, commonly referred to as Adefovir, has several commercial and industrial applications. It is primarily used in the synthesis of pharmaceuticals and as a component in the production of antiviral drugs. Adefovir is also utilized in the manufacturing of research chemicals and biochemicals for scientific research purposes.
In terms of drug and medication applications, Adefovir is commonly used for the treatment of chronic hepatitis B virus infection. It is an effective antiviral agent that works by inhibiting the replication of the virus in the body. Adefovir has been proven to reduce the viral load in patients with hepatitis B, leading to improved liver function and decreased risk of disease progression.
Additionally, Adefovir has shown promise in the treatment of other viral infections, such as HIV and herpes simplex virus. Clinical studies have demonstrated its ability to inhibit the replication of these viruses, making it a potentially valuable treatment option for patients with these conditions. Adefovir’s antiviral properties make it a versatile compound with significant potential in the field of medicine.
⚗️ Chemical & Physical Properties
N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine appears as a white crystalline powder with no distinct odor. It is a stable compound under normal conditions and is not reactive to light or air.
The molar mass of N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine is approximately 214.26 g/mol, with a density of 1.17 g/cm³. In comparison to common food items, this compound has a higher molar mass and density than most food molecules.
N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine has a melting point of about 278°C and a boiling point of approximately 573°C. These values are significantly higher than those of common food items, which typically have lower melting and boiling points.
The compound is sparingly soluble in water and exhibits low viscosity. In comparison to common food items, N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine has lower solubility in water and lower viscosity levels.
🏭 Production & Procurement
N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine, commonly known as aminopurinol, is typically produced through a series of chemical reactions in a laboratory setting. Starting with appropriate precursors, the synthesis process involves the addition of various reagents under controlled conditions to achieve the desired compound.
One method of procuring N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine is through specialty chemical suppliers who stock this compound for purchase. Due to its specific use in research and pharmaceutical applications, it may be obtained in small quantities for experimentation purposes. Transportation of this compound is typically done using standard chemical shipping methods to ensure its integrity and safety during transit.
Alternatively, larger quantities of N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine can be custom synthesized by contract research organizations or chemical manufacturers. This allows for bulk production of the compound to meet the demands of pharmaceutical companies or research institutions. Specialized transportation services may be required for the safe delivery of larger quantities of this compound to the end user.
⚠️ Safety Considerations
Safety considerations for N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine, also known as 2-aminopurine, must be taken into account to prevent potential risks associated with its handling and use. This compound should be stored in a cool, dry, well-ventilated area, away from sources of heat and ignition. Personal protective equipment, including gloves, goggles, and lab coats, should be worn when handling N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine to avoid skin and eye contact.
It is important to use proper disposal methods for N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine to prevent environmental contamination. Any spills should be cleaned up immediately using appropriate absorbent materials and disposed of according to local regulations. In case of accidental exposure or ingestion, seek medical attention immediately and provide the medical professional with the Safety Data Sheet for N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine.
Hazard statements for N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine include “Causes skin irritation” and “Causes serious eye irritation.” These statements indicate the potential risks associated with skin and eye contact with this compound. It is important to take appropriate precautions to avoid direct contact with N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine to prevent skin and eye irritation.
Precautionary statements for N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine include “Wear protective gloves/protective clothing/eye protection/face protection” and “IF ON SKIN: Wash with plenty of soap and water.” These statements emphasize the importance of using proper personal protective equipment when handling this compound and taking immediate action in case of skin exposure. Following these precautionary statements can help minimize the risks associated with N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine.
🔬 Potential Research Directions
One potential research direction for N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine is exploring its role as a novel drug target for the treatment of various illnesses, particularly in the realm of cancer therapy. Researchers may investigate the compound’s interaction with specific molecular targets and its potential to inhibit the growth of cancer cells.
Another avenue of research could involve studying the pharmacokinetics and pharmacodynamics of N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine in order to better understand its behavior within the body. This could lead to the development of more effective dosing strategies and personalized medicine approaches for patients.
Furthermore, researchers may explore the synthesis and modification of N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine to create analogs with improved efficacy and reduced side effects. This could involve structural modifications to enhance the compound’s binding affinity or pharmacological properties, ultimately leading to the development of more potent therapeutic agents.
🧪 Related Compounds
One similar compound to N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine based on molecular structure is N-(2-Methylprop-2-en-1-yl)-9H-purin-6-amine. This compound shares the same purine structure as the original compound but differs in the alkyl chain attached to the purine ring. The substitution of the 3-methylbut-2-EN-1-YL group with a 2-methylprop-2-en-1-yl group results in a slightly different spatial arrangement of atoms.
Another similar compound is N-(3-Methylbut-2-EN-1-YL)-9H-pyrimido[4,5-b]indole-4,7-diamine. This compound also contains a purine-like structure but with an additional fused ring system. The 3-Methylbut-2-EN-1-YL group is attached to the pyrimido[4,5-b]indole ring system, resulting in a compound with different pharmacological properties compared to the original compound.
Lastly, N-(3-Methylbut-2-EN-1-YL)-9H-pyrido[3,4-b]indole-4,7-diamine is another compound similar to N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine in terms of molecular structure. This compound features a purine-like core with a fused pyrido[3,4-b]indole ring system. The 3-Methylbut-2-EN-1-YL group is attached to the pyrido[3,4-b]indole ring, leading to a compound with distinct chemical and biological properties.
