Compound Profile

4,6-Dihydroxypyrimidine 

While 4,6-Dihydroxypyrimidine may seem like a niche chemical compound, it actually has significant relevance to everyday life. This compound serves as a building block for various pharmaceuticals, agricultural chemicals, and materials used in manufacturing processes. Its properties make it a crucial component in the development of new drugs, pesticides, and materials that are essential for numerous industries. As such, the study and utilization of 4,6-Dihydroxypyrimidine have a direct impact on the advancement of healthcare, agriculture, and industrial production, ultimately affecting the quality of life for individuals around the world.

Table of Contents:

💡  Commercial Applications

4,6-Dihydroxypyrimidine, also known as Dihydropyrimidine, is a compound commonly used in commercial and industrial applications. It is frequently employed as a precursor for the synthesis of various pharmaceuticals and agrochemicals due to its versatility and reactivity.

In the commercial sector, 4,6-Dihydroxypyrimidine is utilized as a key ingredient in the production of herbicides and pesticides. Its ability to inhibit the growth of unwanted plants and pests makes it a valuable component in agriculture and horticulture.

In the industrial realm, 4,6-Dihydroxypyrimidine is employed in the manufacturing of dyes, pigments, and other chemical compounds. Its properties as a nucleophilic reagent make it suitable for a wide range of chemical reactions, allowing for the creation of diverse products.

In the field of drug development and medication, 4,6-Dihydroxypyrimidine serves as a crucial building block for the synthesis of various pharmaceuticals. It is commonly used in the preparation of anticancer drugs, antiviral agents, and other therapeutic substances due to its ability to interact with biological systems effectively.

⚗️  Chemical & Physical Properties

4,6-Dihydroxypyrimidine is a white crystalline solid with no distinct odor. It appears as fine powder or crystals when observed under laboratory conditions.

The molar mass of 4,6-Dihydroxypyrimidine is 112.08 g/mol, with a density of 1.4 g/cm3. In comparison, common food items like sugar have a molar mass of 342.3 g/mol and a density of 1.59 g/cm3, while salt has a molar mass of 58.44 g/mol and a density of 2.16 g/cm3.

The melting point of 4,6-Dihydroxypyrimidine is approximately 295°C, with a boiling point around 318°C. In contrast, common food items like butter have a melting point of 32-35°C and a boiling point of 150-180°C, while water has a melting point of 0°C and a boiling point of 100°C.

4,6-Dihydroxypyrimidine is sparingly soluble in water, forming a clear solution. It has a low viscosity, similar to that of water. In comparison, common food items like sugar and salt are highly soluble in water, forming concentrated solutions, and have varying viscosity levels.

🏭  Production & Procurement

4,6-Dihydroxypyrimidine, a chemical compound with potential biological significance, is produced through a multi-step synthetic process in the laboratory. The starting materials for the synthesis are typically commercially available compounds that undergo specific chemical reactions to yield the desired product.

To procure 4,6-Dihydroxypyrimidine for research or industrial purposes, one can either synthesize it in-house following established protocols or purchase it from chemical suppliers. The compound is typically available in both bulk quantities and smaller quantities suitable for research purposes. Transportation of 4,6-Dihydroxypyrimidine is typically done in sealed containers to prevent contamination and ensure safety during transit.

When procuring 4,6-Dihydroxypyrimidine from chemical suppliers, one must ensure that the compound meets the required purity and quality standards for the intended application. It is essential to store 4,6-Dihydroxypyrimidine in a cool, dry place away from direct sunlight and incompatible chemicals to maintain its stability and integrity. Proper documentation and labeling of the compound are also necessary to ensure traceability and safe handling.

⚠️  Safety Considerations

Safety considerations for 4,6-Dihydroxypyrimidine should be taken into account when handling this chemical compound. It is important to wear appropriate personal protective equipment, such as gloves, goggles, and a lab coat, to prevent skin contact and inhalation of the substance. Additionally, proper ventilation should be ensured in the area where 4,6-Dihydroxypyrimidine is being used to minimize exposure to potentially harmful fumes.

Hazard statements for 4,6-Dihydroxypyrimidine include “Causes skin irritation” and “May cause respiratory irritation.” These statements indicate that direct contact with the compound can lead to irritation on the skin and respiratory tract. It is important to handle 4,6-Dihydroxypyrimidine with care and take necessary precautions to avoid any adverse effects on health.

Precautionary statements for 4,6-Dihydroxypyrimidine include “Wear protective gloves/eye protection/face protection” and “Avoid breathing dust/fume/gas/mist/vapors/spray.” These statements emphasize the importance of wearing appropriate protective gear when handling the compound and ensuring proper ventilation to minimize exposure to fumes. It is crucial to follow established safety protocols and guidelines when working with 4,6-Dihydroxypyrimidine to prevent any potential risks to health and safety.

🔬  Potential Research Directions

One potential research direction for 4,6-Dihydroxypyrimidine lies in its potential therapeutic applications. Studies could focus on its interaction with biological targets to elucidate its potential role in disease treatment.

Exploration of the synthesis and structural modification of 4,6-Dihydroxypyrimidine could also be a fruitful area of research. Investigating different synthetic routes and the effects of structural changes on its properties could provide valuable insights for designing new derivatives with enhanced properties.

Another avenue for research could center on the environmental impact of 4,6-Dihydroxypyrimidine. Understanding its behavior in the environment, its degradation pathways, and potential toxicity could provide crucial information for evaluating its environmental implications.

Furthermore, research could delve into the bioavailability and pharmacokinetics of 4,6-Dihydroxypyrimidine to assess its potential as a drug candidate. Studies could investigate its absorption, distribution, metabolism, and excretion to determine its suitability for therapeutic use.

One similar compound to 4,6-Dihydroxypyrimidine is 2,4-Dihydroxypyrimidine. This compound has hydroxyl groups attached at the 2 and 4 positions on the pyrimidine ring. This similarity in structure suggests that 2,4-Dihydroxypyrimidine may have similar chemical properties and biological activities to 4,6-Dihydroxypyrimidine.

Another compound with a similar structure to 4,6-Dihydroxypyrimidine is 2,6-Dihydroxypyrimidine. In this compound, the hydroxyl groups are located at the 2 and 6 positions on the pyrimidine ring. This structural similarity may indicate that 2,6-Dihydroxypyrimidine could exhibit comparable chemical reactivity and biological effects to 4,6-Dihydroxypyrimidine.

Additionally, 2,4,6-Trihydroxypyrimidine is a compound closely related to 4,6-Dihydroxypyrimidine. In this compound, hydroxyl groups are present at all three positions on the pyrimidine ring. The presence of an additional hydroxyl group in 2,4,6-Trihydroxypyrimidine compared to 4,6-Dihydroxypyrimidine may result in unique chemical properties and potential biological activities associated with this compound.

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