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N-Phenylmaleamic Acid

    • Product Name N-Phenylmaleamic Acid
    • Alias NPMA
    • Einecs 246-998-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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).
    Application of N-Phenylmaleamic Acid

    Applications of N-Phenylmaleamic Acid in Industrial Manufacturing

    N-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 Pharmaceuticals

    Pharmaceutical 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monographs for pharmaceutical excipients and intermediates
    • REACH and GHS labeling for chemical safety

    Typical usage ratio

    • 0.2 to 1.0 molar equivalents relative to target maleimide intermediate; ratio adjusted by desired yield, solvent system, and downstream coupling requirements

    Downstream process integration

    • Batch-fed or continuous addition in amide ring formation/SNAr coupling reactions
    • Crystallization and purification post-condensation
    • Integration into multi-step synthetic routes for API manufacturing
    • Direct transfer into closed-system hydrogenation or cyclization units

    Final product types

    • Maleimide-based APIs (e.g., CNS actives, immunomodulators)
    • Phthalimide intermediates for specialty actives
    • Process-certified starting materials for global pharmaceutical companies
    • Regulatory-compliant intermediates for generic drug manufacturing

    2. Agricultural Chemical Intermediate

    Producers 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

    • FAO Specifications for Plant Protection Products Manufacturing
    • US EPA 40 CFR Part 158 (Agrochemical Data Requirements)
    • REACH and CLP chemical registration for agrochemical precursors
    • ISO 9001-certified QC for pesticide production

    Typical usage ratio

    • 5–15% of total active intermediate mass basis, based on downstream reaction stoichiometry and product-line composition requirements

    Downstream process integration

    • Fed into closed reactors for condensation and cyclization
    • Inline monitoring for amide conversion and purity checks before formulation
    • Cleaning validation to prevent cross-contamination in multipurpose plants
    • Batch documentation for traceability and residue assessment

    Final product types

    • Maleimide-derived fungicide active ingredients
    • Heterocyclic pesticide intermediates
    • Raw materials for broadleaf herbicide synthesis
    • Finished chemical crop protection agents compliant with EU and US regulations

    3. Functional Monomer Modifier for Specialty Polymers

    Specialty 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

    • ISO 9001:2015 for quality management in polymer production
    • TSCA (Toxic Substances Control Act) polymer exemption requirements (USA)
    • RoHS and EN 14582 for restricted substances in electrical/electronic components
    • REACH Annex XVII for monomer and additive restrictions in EU

    Typical usage ratio

    • 0.5–5% by weight of total monomer feed, depending on targeted mechanical properties, thermal stability, and compatibility requirements

    Downstream process integration

    • Dosed to the polymerization kettle during monomer charge sequence
    • Real-time spectroscopic monitoring for copolymer incorporation
    • Chain-end capping and dispersibility adjustment in molten resin phases
    • QC sampling for residual monomer and polymer matrix uniformity

    Final product types

    • Heat-resistant polyimide films
    • Maleimide-modified resins for laminates
    • Specialty adhesives for electrical assembly
    • Compounded engineering plastics for automotive and aeronautics

    4. Cross-Linking Agent in Water Treatment Polymers

    N-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

    • ANSI/NSF Standard 60 for Drinking Water Treatment Chemicals
    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)
    • ISO 14001 for Environmental Management in production
    • REACH SVHC screening for polymer raw materials

    Typical usage ratio

    • 0.1–2.0% by weight in polymer feed, adjusted by downstream requirements for cross-link density, floc strength, and performance in local water chemistries

    Downstream process integration

    • Inline metering into aqueous polymerization reactors
    • Blending with acrylamide or acrylate monomers under controlled temperature
    • Post-polymerization purification and formulation as dry or liquid flocculant products
    • Performance testing for contaminant removal efficiency

    Final product types

    • Industrial sludge dewatering agents
    • Drinking water grade flocculants
    • Wastewater clarifiers for municipal facilities
    • Custom floc polymers for mining or oilfield water treatment
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