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HS Code |
825326 |
| Chemical Name | N-Phenylmaleamic Acid |
| Cas Number | 3164-60-1 |
| Molecular Formula | C10H9NO3 |
| Molecular Weight | 191.18 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 200-204 °C |
| Solubility | Slightly soluble in water |
| Boiling Point | Decomposes before boiling |
| Density | 1.35 g/cm3 (estimated) |
| Iupac Name | 2-(phenylamino)but-2-enedioic acid |
| Pubchem Cid | 2833946 |
| Smiles | C1=CC=CC=C1NC(=O)C=CC(=O)O |
As an accredited N-Phenylmaleamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | N-Phenylmaleamic Acid, 25g, packaged in a sealed amber glass bottle with a tamper-evident screw cap and clear labeling. |
| Shipping | N-Phenylmaleamic Acid should be shipped in sealed, chemically-resistant containers, clearly labeled, and protected from moisture and incompatible substances. It must comply with relevant transportation regulations and be accompanied by a Safety Data Sheet (SDS). The package should be handled with care, avoiding excessive heat, direct sunlight, and physical damage during transit. |
| Storage | N-Phenylmaleamic Acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent spills or accidental exposures. Use only with appropriate personal protective equipment (PPE). |
Applications of N-Phenylmaleamic Acid in Industrial ManufacturingN-Phenylmaleamic Acid supports key chemical transformations and niche polymer modifications within several mature manufacturing segments. As an experienced manufacturer, we focus on its integration into chemical synthesis, agriculture intermediates, specialty polymer additives, and water treatment chemistry, ensuring precise compliance and process control at each step. 1. Organic Synthesis Intermediates for PharmaceuticalsPharmaceutical manufacturers use N-Phenylmaleamic Acid as a strategic building block during the synthesis of maleimide and phthalimide derivatives, which act as critical intermediates for APIs such as anti-inflammatory, anti-viral, and CNS-active molecules. The amide function and aromatic ring enable selective cyclization and coupling steps, supporting scale-up with controlled impurity profiles. Manufacturers incorporate this material directly into their step-growth or batch processes following Green Chemistry principles and ICH Q7 GMP. Attention centers on solvent choice and reaction parameters to reduce byproduct formation and facilitate high-yield isolations, resulting in stable intermediates and further downstream transformations. Industry compliance standards
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2. Agricultural Chemical IntermediateProducers of agricultural fungicides and plant protection compounds introduce N-Phenylmaleamic Acid during the synthesis of maleamic- and maleimide-derived agrochemicals. Its controlled reactivity and defined aromatic functionality facilitate preparation of bioactive heterocyclic derivatives at the pre-formulation stage. Formulators utilize the acid in condensation reactions and heterocycle ring closures, supporting synthesis purity and compliance with international agrochemical guidelines. Rigorous QC on residuals and content uniformity occurs prior to downstream blending, and handling aligns with FAO and EPA-published manufacturing protocols. Industry compliance standards
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3. Functional Monomer Modifier for Specialty PolymersSpecialty polymer manufacturers add N-Phenylmaleamic Acid as a functional comonomer or as a chain-end modifier during the synthesis of performance resins. The aromatic amide moiety improves compatibility and adhesion in maleic anhydride copolymer matrices, enhancing heat resistance and chemical stability of the finished resins. Typical operation occurs in solution or suspension polymerization, with real-time monitoring of conversion ratios and molecular weight distribution. Downstream processes focus on precisely dosing the acid to tailor polymer properties, meeting performance targets for niche engineering plastics, adhesives, and specialty polyimides for electrical and high-temperature end uses. Industry compliance standards
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4. Cross-Linking Agent in Water Treatment PolymersN-Phenylmaleamic Acid acts as a cross-linking co-monomer in manufacturing specialty flocculant polymers for industrial and municipal water treatment. Its aromatic structure strengthens the polymer network and enhances selective adsorption sites. Process engineers add the acid during aqueous solution polymerization, closely regulating pH and initiator levels to ensure product consistency and regulatory compliance. The resulting polymers show increased effectiveness in contaminant binding and sludge dewatering applications. Industry compliance standards
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