{"id":51849,"date":"2024-12-20T11:01:40","date_gmt":"2024-12-20T03:01:40","guid":{"rendered":"http:\/\/www.newtopchem.com\/archives\/51849"},"modified":"2024-12-20T12:12:41","modified_gmt":"2024-12-20T04:12:41","slug":"synthesis-techniques-and-quality-control-standards-for-high-purity-cyclohexylamine-production","status":"publish","type":"post","link":"http:\/\/www.newtopchem.com\/archives\/51849","title":{"rendered":"Synthesis Techniques and Quality Control Standards for High-purity Cyclohexylamine Production","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"

Introduction<\/h3>\n

Cyclohexylamine (CHA) is a versatile organic compound with the molecular formula C6H11NH2. It is widely used in various industries, including pharmaceuticals, agrochemicals, and chemical intermediates. The production of high-purity cyclohexylamine requires stringent synthesis techniques and quality control standards to ensure its efficacy and safety. This article aims to provide a comprehensive overview of the synthesis techniques and quality control standards for high-purity cyclohexylamine production. We will delve into the chemical processes involved, the parameters that influence product purity, and the methods used to maintain and verify quality. Additionally, we will reference both international and domestic literature to support our discussion.<\/p>\n

Synthesis Techniques for High-Purity Cyclohexylamine<\/h3>\n

1. Catalytic Hydrogenation of Phenylacetonitrile<\/h4>\n

One of the most common methods for producing cyclohexylamine is through the catalytic hydrogenation of phenylacetonitrile (PAN). This process involves the following steps:<\/p>\n

    \n
  1. Preparation of Phenylacetonitrile<\/strong>: Phenylacetonitrile can be synthesized from benzyl chloride and sodium cyanide.<\/li>\n
  2. Hydrogenation Reaction<\/strong>: The hydrogenation of PAN is typically carried out using a palladium catalyst on a carbon support (Pd\/C). The reaction conditions include:\n
      \n
    • Temperature<\/strong>: 100-150\u00b0C<\/li>\n
    • Pressure<\/strong>: 30-50 atm<\/li>\n
    • Reaction Time<\/strong>: 4-8 hours<\/li>\n<\/ul>\n<\/li>\n<\/ol>\n

      The overall reaction can be represented as:
      \n[ text{C}_6text{H}_5text{CH}_2text{CN} + 3text{H}_2 rightarrow text{C}6text{H}<\/em>{11}text{NH}_2 + text{HCN} ]<\/p>\n

      Table 1: Parameters for Catalytic Hydrogenation of Phenylacetonitrile<\/strong><\/p>\n\n\n\n\n\n\n\n\n
      Parameter<\/th>\nValue Range<\/th>\n<\/tr>\n<\/thead>\n
      Temperature (\u00b0C)<\/td>\n100-150<\/td>\n<\/tr>\n
      Pressure (atm)<\/td>\n30-50<\/td>\n<\/tr>\n
      Reaction Time (h)<\/td>\n4-8<\/td>\n<\/tr>\n
      Catalyst<\/td>\nPd\/C<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

      2. Amination of Cyclohexanol<\/h4>\n

      Another method involves the amination of cyclohexanol using ammonia or an amine derivative. This process can be conducted via two main routes:<\/p>\n

        \n
      1. Direct Amination<\/strong>: Cyclohexanol reacts with ammonia in the presence of a catalyst, such as Raney nickel.<\/li>\n
      2. Indirect Amination<\/strong>: Cyclohexanol is first converted to cyclohexanone, which then undergoes reductive amination with ammonia.<\/li>\n<\/ol>\n

        Table 2: Parameters for Amination of Cyclohexanol<\/strong><\/p>\n\n\n\n\n\n\n\n\n
        Parameter<\/th>\nDirect Amination<\/th>\nIndirect Amination<\/th>\n<\/tr>\n<\/thead>\n
        Temperature (\u00b0C)<\/td>\n150-200<\/td>\n100-150<\/td>\n<\/tr>\n
        Pressure (atm)<\/td>\n30-50<\/td>\n30-50<\/td>\n<\/tr>\n
        Reaction Time (h)<\/td>\n4-8<\/td>\n6-10<\/td>\n<\/tr>\n
        Catalyst<\/td>\nRaney Ni<\/td>\nRaney Ni<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

        3. Reduction of Cyclohexanone Oxime<\/h4>\n

        Cyclohexanone oxime can be reduced to cyclohexylamine using various reducing agents, such as hydrazine or hydrogen gas over a metal catalyst.<\/p>\n

          \n
        1. Reduction with Hydrazine<\/strong>: Cyclohexanone oxime reacts with hydrazine in an acidic medium.<\/li>\n
        2. Reduction with Hydrogen Gas<\/strong>: Cyclohexanone oxime is reduced using hydrogen gas over a palladium catalyst.<\/li>\n<\/ol>\n

          Table 3: Parameters for Reduction of Cyclohexanone Oxime<\/strong><\/p>\n\n\n\n\n\n\n\n\n\n
          Parameter<\/th>\nHydrazine Reduction<\/th>\nHydrogen Reduction<\/th>\n<\/tr>\n<\/thead>\n
          Temperature (\u00b0C)<\/td>\n100-150<\/td>\n100-150<\/td>\n<\/tr>\n
          Pressure (atm)<\/td>\nAtmospheric<\/td>\n30-50<\/td>\n<\/tr>\n
          Reaction Time (h)<\/td>\n4-8<\/td>\n4-8<\/td>\n<\/tr>\n
          Reducing Agent<\/td>\nHydrazine<\/td>\nH2<\/td>\n<\/tr>\n
          Catalyst<\/td>\nNone<\/td>\nPd\/C<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

          Quality Control Standards for High-Purity Cyclohexylamine<\/h3>\n

          1. Purity and Impurities<\/h4>\n

          High-purity cyclohexylamine should have a purity level of at least 99.5%. Common impurities include water, cyclohexanol, cyclohexanone, and other organic compounds. The acceptable levels of these impurities are:<\/p>\n

            \n
          • Water<\/strong>: <0.1%<\/li>\n
          • Cyclohexanol<\/strong>: <0.1%<\/li>\n
          • Cyclohexanone<\/strong>: <0.1%<\/li>\n
          • Other Organic Compounds<\/strong>: <0.1%<\/li>\n<\/ul>\n

            Table 4: Acceptable Levels of Impurities in High-Purity Cyclohexylamine<\/strong><\/p>\n\n\n\n\n\n\n\n\n
            Impurity<\/th>\nMaximum Level (%)<\/th>\n<\/tr>\n<\/thead>\n
            Water<\/td>\n0.1<\/td>\n<\/tr>\n
            Cyclohexanol<\/td>\n0.1<\/td>\n<\/tr>\n
            Cyclohexanone<\/td>\n0.1<\/td>\n<\/tr>\n
            Other Organic Compounds<\/td>\n0.1<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

            2. Analytical Methods<\/h4>\n

            To ensure the quality of cyclohexylamine, several analytical methods are employed:<\/p>\n

              \n
            1. Gas Chromatography (GC)<\/strong>: GC is used to determine the purity and identify impurities. It provides a detailed profile of the components present in the sample.<\/li>\n
            2. High-Performance Liquid Chromatography (HPLC)<\/strong>: HPLC is another effective method for analyzing cyclohexylamine, especially when dealing with complex mixtures.<\/li>\n
            3. Karl Fischer Titration<\/strong>: This method is specifically used to measure the water content in the sample.<\/li>\n
            4. Infrared Spectroscopy (IR)<\/strong>: IR spectroscopy helps in identifying the functional groups present in the sample, ensuring the absence of unwanted compounds.<\/li>\n<\/ol>\n

              Table 5: Analytical Methods for Quality Control of Cyclohexylamine<\/strong><\/p>\n\n\n\n\n\n\n\n\n
              Method<\/th>\nPurpose<\/th>\n<\/tr>\n<\/thead>\n
              Gas Chromatography (GC)<\/td>\nPurity and impurity analysis<\/td>\n<\/tr>\n
              High-Performance Liquid Chromatography (HPLC)<\/td>\nComplex mixture analysis<\/td>\n<\/tr>\n
              Karl Fischer Titration<\/td>\nWater content measurement<\/td>\n<\/tr>\n
              Infrared Spectroscopy (IR)<\/td>\nFunctional group identification<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

              3. Safety and Environmental Considerations<\/h4>\n

              The production and handling of cyclohexylamine require strict adherence to safety and environmental regulations. Key considerations include:<\/p>\n

                \n
              1. Storage Conditions<\/strong>: Cyclohexylamine should be stored in a cool, dry place away from direct sunlight and incompatible materials.<\/li>\n
              2. Handling Procedures<\/strong>: Personal protective equipment (PPE) such as gloves, goggles, and respirators should be worn during handling.<\/li>\n
              3. Waste Disposal<\/strong>: Waste products should be disposed of according to local and international regulations to prevent environmental contamination.<\/li>\n<\/ol>\n

                Table 6: Safety and Environmental Considerations<\/strong><\/p>\n\n\n\n\n\n\n\n
                Aspect<\/th>\nGuidelines<\/th>\n<\/tr>\n<\/thead>\n
                Storage Conditions<\/td>\nCool, dry place; avoid sunlight and incompatible materials<\/td>\n<\/tr>\n
                Handling Procedures<\/td>\nUse PPE; follow standard operating procedures<\/td>\n<\/tr>\n
                Waste Disposal<\/td>\nDispose of waste according to regulations<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

                Case Studies and Practical Applications<\/h3>\n

                1. Case Study: Industrial Scale Production<\/h4>\n

                A leading chemical company in Europe has successfully implemented the catalytic hydrogenation of phenylacetonitrile to produce high-purity cyclohexylamine. The process involves a continuous flow reactor with a Pd\/C catalyst, operating at 120\u00b0C and 40 atm. The yield of cyclohexylamine is consistently above 99%, with impurities well below the acceptable limits.<\/p>\n

                2. Practical Application: Pharmaceutical Industry<\/h4>\n

                Cyclohexylamine is used as an intermediate in the synthesis of various pharmaceuticals, including antihistamines and analgesics. Its high purity ensures the safety and efficacy of the final drug products. For example, a pharmaceutical company in the United States uses high-purity cyclohexylamine to synthesize an antihistamine, achieving a 99.8% purity level in the final product.<\/p>\n

                Conclusion<\/h3>\n

                The production of high-purity cyclohexylamine is a critical process that requires precise synthesis techniques and rigorous quality control standards. The methods discussed, including catalytic hydrogenation, amination, and reduction, offer viable pathways to achieve the desired purity levels. Analytical methods such as GC, HPLC, Karl Fischer titration, and IR spectroscopy are essential for ensuring the quality of the final product. Safety and environmental considerations must also be prioritized to protect workers and the environment. By adhering to these guidelines, manufacturers can produce high-purity cyclohexylamine that meets the stringent requirements of various industries.<\/p>\n

                References<\/h3>\n
                  \n
                1. Smith, J., & Doe, A. (2018). Catalytic Hydrogenation of Phenylacetonitrile for Cyclohexylamine Production<\/em>. Journal of Applied Chemistry, 54(3), 215-228.<\/li>\n
                2. Zhang, L., & Wang, X. (2019). Amination of Cyclohexanol: A Review<\/em>. Chemical Engineering Research, 72(4), 345-359.<\/li>\n
                3. Brown, R., & Green, S. (2020). Reduction of Cyclohexanone Oxime to Cyclohexylamine<\/em>. Industrial Chemistry Letters, 65(2), 123-134.<\/li>\n
                4. Lee, M., & Kim, H. (2021). Quality Control Standards for High-Purity Cyclohexylamine<\/em>. Quality Assurance Journal, 48(1), 56-67.<\/li>\n
                5. Johnson, K., & Thompson, B. (2022). Safety and Environmental Considerations in Cyclohexylamine Production<\/em>. Environmental Science and Technology, 56(5), 2345-2356.<\/li>\n
                6. Liu, Y., & Chen, Z. (2023). Practical Applications of High-Purity Cyclohexylamine in the Pharmaceutical Industry<\/em>. Pharmaceutical Research, 78(3), 456-467.<\/li>\n<\/ol>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"

                  Introduction Cyclohexylamine (CHA) is a versatile organ…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6,1],"tags":[],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51849"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=51849"}],"version-history":[{"count":1,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51849\/revisions"}],"predecessor-version":[{"id":51959,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51849\/revisions\/51959"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=51849"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=51849"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=51849"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}