4,4′-Dithiodimorpholine 

4,4′-Dithiodimorpholine, a chemical compound commonly used as a vulcanizing agent in the production of rubber, holds significant relevance to everyday life. Specifically, it plays a crucial role in the manufacturing of various rubber products, such as tires, hoses, and conveyor belts. The vulcanization process facilitated by 4,4′-Dithiodimorpholine enhances the elasticity, durability, and overall performance of rubber goods, ultimately contributing to their widespread use in modern society. Consequently, this compound indirectly impacts the daily lives of individuals by ensuring the functionality and reliability of essential rubber-based products found in numerous industries and applications.

Table of Contents:

💡  Commercial Applications

4,4′-Dithiodimorpholine, a chemical compound with the formula C8H16N2S2, has various commercial and industrial applications. It is used as a vulcanizing agent in the rubber industry to improve the properties of rubber products. Additionally, it is employed as a crosslinking agent in the production of polymers, coatings, and adhesives, enhancing their strength and durability.

In terms of drug and medication applications, 4,4′-Dithiodimorpholine is not commonly utilized. Due to its chemical structure and potential toxicity, it is not suitable for use in pharmaceuticals or medical treatments. However, ongoing research may uncover potential applications in the future.

Overall, the primary commercial and industrial applications of 4,4′-Dithiodimorpholine lie in the rubber industry and the production of polymers, coatings, and adhesives. While it does not currently have significant drug or medication applications, its properties make it a valuable component in various manufacturing processes.

⚗️  Chemical & Physical Properties

4,4′-Dithiodimorpholine appears as a white crystalline powder with a faint odor.

The molar mass of 4,4′-Dithiodimorpholine is 236.38 g/mol, and its density is 1.55 g/cm3. This molar mass is higher than that of common food items such as sugar (180.16 g/mol) and salt (58.44 g/mol), while its density is similar to that of water (1 g/cm3).

The melting point of 4,4′-Dithiodimorpholine is around 110°C, and its boiling point is approximately 316°C. These values are significantly higher than those of common food items like butter (melting point around 32°C) and water (boiling point at 100°C).

🏭  Production & Procurement

4,4′-Dithiodimorpholine is produced through a multi-step synthesis process that involves the reaction of morpholine with carbon disulfide and sodium hydroxide. This reaction forms the intermediate sodium morpholinedithiocarbamate, which is further reacted with a strong acid to yield 4,4′-Dithiodimorpholine in high purity.

4,4′-Dithiodimorpholine can be procured from chemical suppliers that specialize in rubber chemicals and antioxidants. It is commonly available in either powdered or granular form, packaged in sealed containers to prevent moisture exposure. The compound can be transported in bulk in sealed containers or drums, following strict regulations for handling hazardous materials.

The transportation of 4,4′-Dithiodimorpholine must comply with international regulations for the transport of hazardous chemicals. Proper labeling, packaging, and documentation are required to ensure safe handling during shipping. Special precautions must be taken to prevent exposure to moisture or heat, which can degrade the compound and reduce its effectiveness in industrial applications.

⚠️  Safety Considerations

Safety considerations for 4,4′-Dithiodimorpholine (DTDM) should be carefully observed due to its potential hazards. This chemical is classified as harmful if swallowed, with potential effects including irritation of the respiratory system, skin, and eyes. Additionally, long-term exposure to DTDM may cause damage to organs through prolonged or repeated exposure.

Hazard statements for 4,4′-Dithiodimorpholine include the classification as harmful if swallowed, with potential effects including irritation of the respiratory system, skin, and eyes. Prolonged or repeated exposure to this chemical may result in damage to internal organs. It is important to handle DTDM with caution and adhere to proper safety protocols to minimize the risk of harm.

Precautionary statements for 4,4′-Dithiodimorpholine should be followed to ensure safe handling of this chemical. These include wearing protective gloves, clothing, and eye protection when working with DTDM to prevent skin and eye irritation. Adequate ventilation should be maintained to avoid inhalation of vapors, and measures should be taken to prevent ingestion or accidental exposure. It is important to store DTDM in a well-ventilated area away from incompatible materials and sources of ignition to minimize the risk of accidents.

🔬  Potential Research Directions

One potential research direction for 4,4′-Dithiodimorpholine is its investigation as a vulcanizing agent in rubber manufacturing processes. The compound has shown promising results in improving the mechanical properties of rubber products.

Another area of interest is its potential use as a crosslinking agent in polymer chemistry. The ability of 4,4′-Dithiodimorpholine to form stable crosslinks between polymer chains makes it suitable for enhancing the strength and durability of various polymeric materials.

Furthermore, the compound’s antimicrobial properties have sparked interest in exploring its potential as a biocidal agent in various applications. Research in this direction may involve investigating its effectiveness against a wide range of microorganisms and its potential impact on environmental and human health.

Additionally, given its unique chemical structure, further research could be focused on exploring the reactivity and potential applications of 4,4′-Dithiodimorpholine in other fields such as materials science, organic synthesis, and pharmaceutical chemistry. Its versatility and potential utility make it a promising candidate for further investigation and development.

One similar compound to 4,4′-Dithiodimorpholine based on molecular structure is 4,4′-Thiodimorpholine. This compound also contains two morpholine rings connected by a sulfur atom in the middle. The difference lies in the presence of only one sulfur atom in 4,4′-Thiodimorpholine, compared to two sulfur atoms in 4,4′-Dithiodimorpholine.

Another compound that bears resemblance to 4,4′-Dithiodimorpholine is Morpholine disulfide. This compound consists of two morpholine rings linked by a disulfide bond, similar to the structure of 4,4′-Dithiodimorpholine. The difference between the two compounds lies in the presence of oxygen atoms in the disulfide bond of Morpholine disulfide, while sulfur atoms are present in the dithioether linkage of 4,4′-Dithiodimorpholine.

A further compound similar to 4,4′-Dithiodimorpholine in terms of molecular structure is Morpholine disulfide diacetate. This compound contains two morpholine rings connected by a disulfide bond, similar to 4,4′-Dithiodimorpholine. The addition of acetyl groups on the oxygen atoms in the disulfide bond differentiates Morpholine disulfide diacetate from 4,4′-Dithiodimorpholine, which has sulfur atoms in the linkage.

Previous Post

(2S,6S)-2,6-diaminoheptanedioic acid

Next Post

Mephobarbital

You cannot copy content of this page