
The study offers a detailed cost analysis of Linalool Production Via Total Chemical Synthesis. In addition, the report incorporates the manufacturing process with detailed process and material flow, operating costs along with financial expenses and depreciation charges.
Last Updated: January, 2025
This report comprises the extensive cost dynamics of linalool production process via chemical synthesis. In this process, acetylene and acetone yield 3-methyl-1-butyn-3-ol (upon reacting with each other), which is hydrogenated to 3-methyl-1-buten-3-ol. This compound can react with diketene or acetic acid ester to form the aceto-acetate, undergoing thermal reaction to produce 2-methyl-2-hepten-6-one. Finally, by subjecting 2-methyl-2-hepten-6-one to a reaction with acetylene, dehydrolinalool is produced. Subsequently, dehydrolinalool can undergo partial hydrogenation to yield linalool.
Alternatively, 3-methyl-1-buten-3-ol reacts with isopropenyl methyl ether or isoprene hydrochloride and acetone, generating 2-methyl-2-hepten-6-one. Dehydrolinalool is obtained by the subsequent reaction of 2-methyl-2-hepten-6-one with acetylene, which can be partially hydrogenated.to create linalool.
The project economic analysis provided in the report discusses a Germany-based plant:
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