The latest report titled “Cyclopropene Production” by Procurement Resource, a global procurement research and consulting firm, provides an in-depth cost analysis of the production process of Cyclopropene.
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 Cyclopropene production cost, looking into capacity expansions, plant turnarounds, mergers, acquisitions, and investments.
Procurement Resource Assessment of Cyclopropene Production Process:
1. From Dehydrohalogenation of Allyl Chloride: This report presents the detailed production methodology and cost analysis of Cyclopropene industrial production across Cyclopropene manufacturing plants. Cyclopropene is commonly produced through the dehydrohalogenation of allyl chloride. In this process, the base chemical, allyl chloride, can eliminate a halogen atom when subjected to a strong base, such as sodium amide, at approximately 80 °C. This reaction yields cyclopropene as the end product, with a typical yield of about 10%.
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2. From Chemical Reaction of Allyl Chloride with sodium bis(trimethylsilyl)amide: This report provides the thorough economics of Cyclopropene industrial production across Cyclopropene manufacturing plants. The manufacturing process commences by combining allyl chloride with sodium bis(trimethylsilyl)amide in boiling toluene. This mixture is allowed to react for approximately 40-60 minutes. The outcome of the reaction is the formation of cyclopropene, typically obtained in a yield of about 40%. Additionally, the reaction generates sodium chloride and N-tert-Butyl-1,1-dimethyl-1-silacyclohexanamine as the final products.
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Product Definition:
Cyclopropene is a highly reactive and strained three-membered carbon ring compound with the molecular formula C3H4. Its unique structure imparts exceptional reactivity and instability, making it challenging to handle. Cyclopropene is not commonly encountered in nature but is synthesized for chemical research purposes. Its remarkable chemistry includes rapid isomerization and participation in cycloaddition reactions. Despite its inherent instability, cyclopropene has been employed as a valuable synthetic building block in organic chemistry, allowing for the creation of complex molecules with specific stereochemical arrangements.
Market Drivers:
Cyclopropene is primarily driven by its significance in chemical research and as a synthetic building block. Its demand arises from its unique reactivity and use in creating complex organic compounds. Researchers and the pharmaceutical industry value its role in designing novel molecules. Additionally, its application in the development of agrochemicals, such as herbicides and plant growth regulators, contributes to its market growth. The growth of the pharmaceutical and agricultural sectors, coupled with ongoing advancements in synthetic chemistry, fuel the demand for cyclopropene as a key component in innovative chemical processes.
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