Diisopropyl phosphonate

Diisopropyl phosphonate, a chemical compound commonly used in the synthesis of various phosphorus-containing compounds, plays a crucial role in industries such as agriculture, pharmaceuticals, and material science. Despite its niche application, diisopropyl phosphonate indirectly contributes to everyday life by enabling the production of a wide range of products that impact society’s overall well-being and technological advancement.

Table of Contents:

💡  Commercial Applications

Diisopropyl phosphonate, commonly known as DIPP, finds various commercial and industrial applications. It is primarily used as a chemical intermediate in the synthesis of organophosphorus compounds, such as pesticides and flame retardants. Additionally, DIPP is utilized in the production of plasticizers, which are additives that improve the flexibility and durability of plastics.

In the field of drug and medication applications, Diisopropyl phosphonate plays a crucial role as a precursor in the synthesis of nerve agent antidotes. These antidotes are essential in counteracting the toxic effects of nerve agents, which are chemical substances that disrupt the transmission of nerve impulses. Furthermore, DIPP is also used in the manufacture of pharmaceuticals like antiviral drugs and certain chemotherapy agents, contributing to advancements in medical treatment.

⚗️  Chemical & Physical Properties

Diisopropyl phosphonate is a clear, colorless liquid with a mild, chemical odor that is characteristic of organic phosphorus compounds.

With a molar mass of 170.16 g/mol and a density of 0.920 g/cm3, diisopropyl phosphonate is comparable to common food items such as sugar (molar mass around 342 g/mol, density of 1.59 g/cm3) in terms of molar mass and density.

The melting point of diisopropyl phosphonate is -78°C, while the boiling point is 152°C. In comparison, common food items like table salt have a melting point of 801°C and a boiling point of 1465°C.

Diisopropyl phosphonate is sparingly soluble in water and has a low viscosity. This contrasts with common food items like sugar, which are highly soluble in water and have higher viscosities.

🏭  Production & Procurement

Diisopropyl phosphonate is typically produced through the reaction between phosphorus trichloride and isopropyl alcohol. This process results in the formation of the desired compound along with the release of hydrogen chloride gas as a byproduct. The reaction is commonly carried out in a controlled laboratory setting to ensure safety and optimal yield.

Once Diisopropyl phosphonate is produced, it can be procured from chemical suppliers or manufacturers specializing in organophosphorus compounds. The compound is often transported in sealed containers to prevent contamination or leakage during transit. Proper labeling and handling procedures should be followed to ensure the safe transport of Diisopropyl phosphonate.

Diisopropyl phosphonate is a key intermediate in the synthesis of various organophosphorus compounds used in industries such as agriculture and pharmaceuticals. Due to its importance, efforts are made to ensure a reliable supply chain for the procurement of this compound. Quality control measures are implemented to maintain the purity and consistency of Diisopropyl phosphonate for different applications.

⚠️  Safety Considerations

Safety considerations for Diisopropyl phosphonate include its flammability and potential for causing skin irritation. The chemical should be stored in a cool, dry place away from sources of ignition. Proper personal protective equipment, such as gloves and goggles, should be worn when handling Diisopropyl phosphonate to prevent skin and eye contact.

Hazard statements for Diisopropyl phosphonate include “Highly flammable liquid and vapor” and “Causes skin irritation.” These statements indicate that the chemical poses a fire hazard and can irritate the skin upon contact. It is important to take proper precautions to prevent accidents and exposure when working with Diisopropyl phosphonate.

Precautionary statements for Diisopropyl phosphonate include “Keep away from heat/sparks/open flames/hot surfaces” and “Wear protective gloves/protective clothing/eye protection/face protection.” These statements emphasize the need to keep the chemical away from sources of ignition and to use appropriate personal protective equipment to prevent skin and eye contact. Following these precautions can help minimize the risk of accidents and ensure safe handling of Diisopropyl phosphonate.

🔬  Potential Research Directions

One potential research direction for Diisopropyl phosphonate is its use as a reagent in organic synthesis. Its ability to selectively phosphorylate nucleophiles makes it a valuable tool for the creation of new compounds. Researchers may explore different reaction conditions and substrates to optimize its utility in various synthetic pathways.

Another potential area of research is the study of the biological activity of Diisopropyl phosphonate and its derivatives. Understanding how these compounds interact with enzymes or signaling pathways could lead to the development of new pharmaceuticals or agrochemicals. By investigating their mechanism of action, researchers can uncover new potential targets for drug discovery.

Furthermore, there is potential for research into the environmental fate and toxicity of Diisopropyl phosphonate. Studying its behavior in soil, water, and air can provide valuable information on its persistence and potential impact on ecosystems. Toxicological studies can help assess the risks associated with exposure to this compound and guide regulatory decisions regarding its use.

One similar compound to Diisopropyl phosphonate is Diethyl phosphonate. This compound shares a similar structure to Diisopropyl phosphonate, but with ethyl groups instead of isopropyl groups. Diethyl phosphonate is commonly used in organic synthesis and as a reagent in the preparation of various phosphorus-containing compounds.

Another compound with a molecular structure similar to Diisopropyl phosphonate is Dimethyl methylphosphonate. This compound contains a methyl group attached to a phosphorus atom, similar to the isopropyl groups in Diisopropyl phosphonate. Dimethyl methylphosphonate is used in the production of flame retardants and as a precursor in the synthesis of organophosphorus compounds.

Trimethyl phosphite is also a compound that bears similarity to Diisopropyl phosphonate in terms of molecular structure. Trimethyl phosphite contains three methyl groups attached to a phosphorus atom, as opposed to the two isopropyl groups in Diisopropyl phosphonate. This compound is utilized as a reagent in organic synthesis and as a ligand in coordination chemistry.

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