The latest report titled “B-Naphthylamine Production” by Procurement Resource, a global procurement research and consulting firm, provides an in-depth cost analysis of the production process of B-Naphthylamine.
Procurement Resource study is based on the latest prices and other economic data available. It also offers additional analysis of the report with detailed breakdown of all cost components (capital investment details, production cost details, economics for another plant location, dynamic cost model). In addition, the report incorporates the production process with detailed process and material flow, capital investment, operating costs along with financial expenses and depreciation charges.
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Procurement Resource’s detailed report describes the stepwise consumption of material and utilities along with a detailed process flow diagram. Furthermore, the study assesses the latest developments within the industry that might influence B-Naphthylamine production cost, looking into capacity expansions, plant turnarounds, mergers, acquisitions, and investments.
Procurement Resource Assessment of B-Naphthylamine Production Process:
- From Bucherer Reaction: This report presents the detailed production methodology and cost analysis of B-Naphthylamine industrial production across B-Naphthylamine manufacturing plants. The synthesis initiates when 2-naphthol (also known as B-naphthol) reacts with an ammonia solution saturated with sulfur dioxide. This reaction leads to the replacement of the hydroxyl group in 2-naphthol with an amino group, ultimately producing B-naphthylamine as the end product.
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Product Definition:
B-Naphthylamine, also known as 2-naphthylamine, is an organic compound with the formula C10H7NH2. It is a derivative of naphthalene where an amino group (-NH2) replaces a hydrogen atom on the second carbon of the naphthalene ring, making it a primary aromatic amine. This structural modification places the amino group at the beta position, hence the prefix “B-” in its name. Historically, B-naphthylamine was used in the manufacture of dyes, rubber chemicals, and in the synthesis of other industrial compounds. However, its use has significantly declined due to its carcinogenic properties; exposure to B-naphthylamine has been linked to an increased risk of bladder cancer. Its synthesis can be achieved through the Bucherer reaction, which involves the conversion of 2-naphthol with ammonia and sulfur dioxide under specific conditions. Despite its hazardous nature, B-naphthylamine remains of interest for its role in chemical research and its historical importance in industrial chemistry.
Market Drivers:
The market drivers for B-naphthylamine, or 2-naphthylamine, have evolved over time, primarily influenced by its applications and the regulatory environment surrounding its use. Historically, B-naphthylamine was widely used in the synthesis of dyes, rubber antioxidants, and other industrial chemicals, driving its demand within these sectors. The demand was further propelled by the growth of the textile and rubber industries, where its derivatives played a crucial role in manufacturing processes and product enhancements. However, the discovery of its carcinogenic properties led to stringent regulations and a significant decline in its use. Nowadays, market drivers include its limited application in research and development, particularly in the synthesis of compounds for academic and potentially pharmaceutical research, where its unique chemical properties may be of value. The market for B-naphthylamine is now more niche, with demand driven by specialized applications that manage its health risks appropriately.
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