2,4,6-Triphenyl-1,3,5-triazine is a compound that has various applications in everyday life. One of its most notable uses is as a UV absorber in sunscreens and other personal care products. This compound helps to protect the skin from the harmful effects of ultraviolet radiation, thus reducing the risk of skin damage and sunburn. Additionally, 2,4,6-Triphenyl-1,3,5-triazine is also used in the manufacturing of dyes, pigments, and other industrial products. Its properties make it a valuable ingredient in a wide range of consumer goods, contributing to its relevance in everyday life.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
2,4,6-Triphenyl-1,3,5-triazine, commonly known as TPT, is primarily used in the commercial and industrial sectors as a chemical intermediate for the production of dyes, pigments, and plastics. Its unique molecular structure allows for various color options in dye formulations and enhances the UV stability of plastics, making it a valuable ingredient in these industries.
In addition to its commercial and industrial applications, 2,4,6-Triphenyl-1,3,5-triazine has also found use in the pharmaceutical field. It has demonstrated potential as an anti-inflammatory agent and a photochemotherapy drug. Research is ongoing to explore its therapeutic properties further and potentially develop new medications for various conditions.
While 2,4,6-Triphenyl-1,3,5-triazine plays a crucial role in commercial and industrial applications, its versatility extends to potential drug and medication uses. Its unique properties make it a promising candidate for pharmaceutical research, demonstrating its relevance in both the chemical and healthcare industries. Continued exploration of its applications may lead to innovative treatments and therapies in the future.
⚗️ Chemical & Physical Properties
2,4,6-Triphenyl-1,3,5-triazine is a white, odorless crystalline compound. It has a characteristic appearance of fine granules which are insoluble in water and organic solvents.
With a molar mass of 312.36 g/mol and a density of 1.20 g/cm^3, 2,4,6-Triphenyl-1,3,5-triazine is significantly heavier than common food items such as sugar (molar mass of 342.30 g/mol and density of 1.59 g/cm^3).
2,4,6-Triphenyl-1,3,5-triazine has a melting point of approximately 210°C and a boiling point of around 440°C. These values are much higher compared to common food items such as butter (melting point of 32-35°C) and water (boiling point of 100°C).
The compound is practically insoluble in water and exhibits low viscosity. This contrasts with common food items like salt and sugar, which have high solubility in water and lower viscosity.
🏭 Production & Procurement
2,4,6-Triphenyl-1,3,5-triazine is produced through a series of chemical reactions involving the condensation of anilines and cyanogen chloride. This process typically takes place in a laboratory setting under controlled conditions to ensure the purity and yield of the final product.
In order to procure 2,4,6-Triphenyl-1,3,5-triazine, it can be purchased from chemical suppliers or synthesized in-house by chemists with expertise in organic chemistry. Once obtained, the compound can be transported in sealed containers to prevent contamination or degradation during transit.
When transporting 2,4,6-Triphenyl-1,3,5-triazine, it is important to follow regulations set by governing bodies regarding the handling and transportation of hazardous chemicals. Proper labeling, packaging, and storage protocols should be adhered to in order to ensure the safety of individuals and the environment during transportation.
⚠️ Safety Considerations
Safety considerations for 2,4,6-Triphenyl-1,3,5-triazine include the need to handle the substance with caution due to its potential hazards. It is recommended to wear appropriate personal protective equipment, such as gloves, goggles, and lab coat, when working with this compound to prevent skin contact, eye irritation, or inhalation of harmful vapors. Additionally, it is important to store 2,4,6-Triphenyl-1,3,5-triazine in a cool, dry place away from sources of ignition and incompatible materials to reduce the risk of fire or chemical reactions.
Hazard statements for 2,4,6-Triphenyl-1,3,5-triazine include “Causes skin irritation” and “May cause an allergic skin reaction.” These statements indicate that contact with the substance can result in irritation or allergic reactions, highlighting the importance of using proper personal protective equipment, such as gloves and lab coat, to minimize skin exposure. It is important to be aware of these hazards and take necessary precautions to prevent any adverse effects when handling 2,4,6-Triphenyl-1,3,5-triazine.
Precautionary statements for 2,4,6-Triphenyl-1,3,5-triazine include “Wear protective gloves/protective clothing/eye protection/face protection” and “Wash hands thoroughly after handling.” These statements emphasize the importance of wearing appropriate personal protective equipment and practicing good hygiene when working with the substance to prevent skin contact and minimize the risk of exposure. It is also recommended to work in a well-ventilated area and avoid releasing the compound into the environment to ensure safety when handling 2,4,6-Triphenyl-1,3,5-triazine.
🔬 Potential Research Directions
Potential research directions for 2,4,6-Triphenyl-1,3,5-triazine include studying its potential applications in the field of organic electronics, due to its unique electronic properties and conjugated structure.
Further research could explore the use of 2,4,6-Triphenyl-1,3,5-triazine as a building block for the synthesis of novel organic materials with enhanced properties for applications in optoelectronics and photovoltaics.
Investigations into the potential of 2,4,6-Triphenyl-1,3,5-triazine as a photocatalyst for organic transformations and environmental remediation could also yield valuable insights into its reactivity and potential practical applications.
🧪 Related Compounds
One similar compound to 2,4,6-Triphenyl-1,3,5-triazine in terms of molecular structure is 2,4,6-Triphenyl-1,3,5-oxadiazine. This compound also contains a six-membered heterocyclic ring with three phenyl groups attached at positions 2, 4, and 6. This similarity in structure allows for similar reactivity and potential applications in organic synthesis.
Another compound with a structure closely related to 2,4,6-Triphenyl-1,3,5-triazine is 2,4,6-Triphenyl-1,3,5-thiadiazine. This compound features a six-membered heterocyclic ring with three phenyl groups attached, analogous to the triazine structure. Like 2,4,6-Triphenyl-1,3,5-triazine, 2,4,6-Triphenyl-1,3,5-thiadiazine may exhibit comparable chemical properties and be utilized in similar synthetic pathways.
2,4,6-Tri(4-fluorophenyl)-1,3,5-triazine is a compound that shares structural similarities with 2,4,6-Triphenyl-1,3,5-triazine. The primary difference is in the substitution of the phenyl groups with 4-fluorophenyl groups. Despite this variation, both compounds retain a central triazine ring, enabling comparable reactivity and potential applications in organic chemistry.
