Ammelide

Ammelide, a chemical compound derived from the uric acid cycle, may not seem immediately relevant to everyday life. However, it plays a crucial role in the pharmaceutical industry as a potential therapeutic agent. Researchers are exploring the potential of Ammelide in the treatment of various medical conditions, such as inflammation and cancer. Its development could lead to new drugs that improve the quality of life for individuals suffering from these ailments. Therefore, despite its esoteric origins, Ammelide has the potential to have a tangible impact on everyday life through its potential medical applications.

Table of Contents:

💡  Commercial Applications

Ammelide, a white crystalline compound derived from uric acid, has several commercial and industrial applications. In the field of agriculture, it is used as a herbicide and pesticide due to its effectiveness in controlling weeds and pests. It is also utilized in the production of flame retardants for various materials to increase fire safety measures.

In addition to its commercial and industrial uses, Ammelide has also found application in the field of medicine. Due to its antifungal properties, it is used in the manufacturing of antifungal medications to treat fungal infections in humans and animals. Its ability to inhibit the growth of certain fungi makes it a valuable component in pharmaceutical formulations for skin, nail, and respiratory infections.

The versatility of Ammelide extends beyond its agricultural and medicinal applications. In the cosmetics industry, it is used as an ingredient in skincare products and hair care formulations. Its antimicrobial properties make it an effective preservative in beauty products, ensuring their longevity and safety for consumer use.

⚗️  Chemical & Physical Properties

Ammelide is a white crystalline solid that has no distinct odor. It is often described as odorless or having a faint chemical smell.

With a molar mass of 110.08 g/mol and a density of 1.58 g/cm³, Ammelide is heavier and more dense than common food items like sugar and salt.

Ammelide has a melting point of 275 °C and a boiling point of 460 °C. These values are significantly higher than those of common food items, such as butter and chocolate.

Ammelide is sparingly soluble in water and has low viscosity. In comparison to common food items like sugar and salt, Ammelide has lower solubility in water and higher viscosity.

🏭  Production & Procurement

Ammelide is a chemical compound that is produced through a series of reactions involving guanine, cyanuric chloride, and ammonia. These reactions result in the formation of Ammelide as a white crystalline substance.

Ammelide can be procured from chemical suppliers who specialize in providing rare and specialty compounds. The compound can be transported in sealed containers to prevent degradation and contamination during transit.

Due to its specialized nature, Ammelide may not be readily available from all chemical suppliers. It may require special ordering procedures and handling due to its potentially hazardous properties.

When procuring Ammelide, it is important to follow proper safety protocols for handling and storage to ensure the integrity of the compound and protect those handling it. It is advisable to consult with a chemical safety expert to determine the best practices for procurement and use of Ammelide.

⚠️  Safety Considerations

Safety considerations for Ammelide are paramount due to its potential health hazards. It is important to handle this compound with care to avoid exposure. Ammelide should only be used in well-ventilated areas and personal protective equipment, such as gloves and goggles, should be worn when working with this substance.

Hazard statements for Ammelide include its ability to cause skin irritation and serious eye damage. This compound can also be harmful if inhaled or swallowed. It is important to keep Ammelide away from heat, sparks, open flames, and hot surfaces as it may react dangerously.

Precautionary statements for Ammelide include avoiding ingestion, inhalation, and skin contact. It is essential to wash hands and any exposed skin thoroughly after handling this compound. In case of skin irritation or rash, seek medical attention immediately. Additionally, store Ammelide in a cool, dry place away from incompatible materials.

🔬  Potential Research Directions

Ammelide, a compound derived from uric acid degradation, has shown promise in various biomedical and pharmaceutical studies. Potential research directions for Ammelide could include investigating its therapeutic potential in treating conditions related to oxidative stress and inflammation, as well as its role in metabolic disorders such as gout.

Furthermore, research on Ammelide could explore its potential as a novel antioxidant agent, particularly in mitigating the effects of free radicals and oxidative damage in cells. Studying the mechanism of action of Ammelide in scavenging reactive oxygen species and protecting cellular components from damage could provide valuable insights for developing new therapeutic interventions.

Additionally, investigation into the pharmacokinetics and pharmacodynamics of Ammelide could shed light on its bioavailability, distribution, metabolism, and excretion in the body. Understanding the absorption and elimination patterns of Ammelide could help optimize its dosage and administration for potential clinical applications.

One similar compound to Ammelide based on molecular structure is ammeline. Ammeline is a chemical compound with the same molecular formula as Ammelide, C3H4N4O2, but with a different structural arrangement. The main difference between the two compounds lies in the positioning of the nitrogen atoms within the molecule.

Another compound that shares a similar molecular structure with Ammelide is amobarbital. Amobarbital is a barbiturate derivative with the molecular formula C11H18N2O3, which is similar to Ammelide in terms of the number and type of atoms present. However, the arrangement of atoms within the molecule and the functional groups attached to the core structure differ between the two compounds.

Previous Post

Betaine

Next Post

2,3-Dihydroxybenzoic acid

You cannot copy content of this page