Meta Phenylenediamine Production Cost Reports

The report provides a detailed analysis essential for establishing a Meta Phenylenediamine production plant. It encompasses all critical aspects necessary for Meta Phenylenediamine production, including the cost of Meta Phenylenediamine production, Meta Phenylenediamine plant cost, Meta Phenylenediamine production costs, and the overall Meta Phenylenediamine production plant cost. Additionally, the study covers specific expenditures associated with setting up and operating a Meta Phenylenediamine production plant. These encompass production processes, raw material requirements, utility requirements, infrastructure needs, machinery and technology requirements, manpower requirements, packaging requirements, transportation requirements, and more.

Meta Phenylenediamine is an organic chemical compound with numerous applications across various industrial sectors. It is widely used as an intermediate in the production of dyestuffs and pigments. It also finds its application as a raw material in the production of fine chemicals and various polymers, such as polyurea elastomers, aramid fibers, and epoxy resins. It is also used as an accelerator for production adhesive resins. It is also utilized as a coupling agent in the preparation of blue color hair dye.

The demand for Meta Phenylenediamine is primarily driven by its application as a chemical intermediate in the synthesis of various fine chemicals. Its utilization as an intermediate for production pigments and dyes for fabrics and leather further enhances its demand in the textiles and leather industries. Its application as a precursor in the production of aramid fibers, adhesive resins, wire enamel coatings, and epoxy resins also contributes to its demand in the polymer and adhesives industries. Its usage as a coupling agent in the production of blue colors in hair dye also fuels its demand in the personal care and consumer goods industries.

The raw materials required for producing m-PDA include 1,3-dinitrobenzene, which is synthesized from benzene through dinitration processes.  Thus, the industrial Meta Phenylenediamine procurement is directly affected by the availability and cost of these precursor chemicals, which also impact its supply stability and production costs. The cost of production methods of Meta Phenylenediamine, such as chemical reduction and catalytic hydrogenation, also plays a crucial role in shaping its procurement strategies. Variations in consumer preferences towards natural or organic products can also affect the demand for synthetic dyes that contain m-phenylenediamine, which further impacts its market growth and procurement decisions.

Raw Material for Meta Phenylenediamine Production

According to the Meta Phenylenediamine production plant project report, the major raw materials for Meta Phenylenediamine production includes m-Dinitrobenzene.

Production Process of Meta Phenylenediamine

The extensive Meta Phenylenediamine production cost report consists of the following industrial production process:

• Production via Catalytic Hydrogenation: This method of production involves the synthesis of Meta Phenylenediamine by using m-dinitrobenzene as the starting material. The process starts with the catalytic hydrogenation of m-dinitrobenzene over a Ni/SiO2 catalyst in solution to form m-phenylenediamine. Further, the obtained product undergoes solvent crystallization for the process of separation and purification of m-phenylenediamine to obtain pure m-phenylenediamine as the final product.

Meta Phenylenediamine is also known as 1,3-phenylenediamine. It appears as colorless or white-colored needles, which turn purple or red in the presence of air. The density of the compound is 1.14 g/cm³. The molecular formula of the compound is C6H8N2, and its molar mass is around 108.14 g/mol. The IUPAC name of the compound is benzene-1,3-diamine. The boiling point of the compound ranges between 284-287 °C, and its melting point is around 62-63 °C. The flash point of the compound is 187 °C, and its solubility in water is less than 1 mg/mL at 66 °F. The compound is unstable in the air. The auto-ignition temperature of the compound is 560 °C. The compound, upon heating, decomposes to emit toxic fumes of nitrogen oxides.