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4-Nitro-N-Methylphthalimide

    • Product Name 4-Nitro-N-Methylphthalimide
    • Alias N-Methyl-4-nitrophthalimide
    • Einecs 221-838-6
    • 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

    235484

    Chemical Name 4-Nitro-N-Methylphthalimide
    Molecular Formula C9H6N2O4
    Molecular Weight 206.16 g/mol
    Cas Number 5718-50-1
    Appearance Yellow crystalline solid
    Melting Point 200-204°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.50 g/cm³ (approximate)
    Boiling Point Decomposes before boiling
    Storage Conditions Store in a cool, dry place, tightly closed
    Purity Typically ≥98%
    Smiles CN1C(=O)c2cc(ccc2C1=O)[N+](=O)[O-]

    As an accredited 4-Nitro-N-Methylphthalimide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled “4-Nitro-N-Methylphthalimide, 25g,” with hazard symbols, lot number, and manufacturer’s details; securely sealed.
    Shipping 4-Nitro-N-Methylphthalimide should be shipped in tightly sealed, chemical-resistant containers, protected from light, moisture, and physical damage. Comply with local, national, and international chemical transport regulations. Label as a hazardous material if required, and include proper documentation and safety data sheets. Ship at ambient temperature unless otherwise specified.
    Storage **4-Nitro-N-Methylphthalimide** should be stored in a tightly sealed container, away from direct sunlight and sources of ignition. Keep in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong reducing agents. Ensure proper labeling and secondary containment to prevent accidental release. Follow all relevant institutional and safety guidelines for hazardous chemical storage.
    Application of 4-Nitro-N-Methylphthalimide

    Applications of 4-Nitro-N-Methylphthalimide in Industrial Manufacturing

    As a direct manufacturer of 4-Nitro-N-Methylphthalimide, we distribute this specialty compound to global processors in diverse chemical sectors. Our production processes align with advanced quality systems to ensure reliable performance in critical end-use applications. The following sections detail this raw material’s integration into established downstream industries.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use 4-Nitro-N-Methylphthalimide for the preparation of complex heterocyclic scaffolds. It serves as a nitrated building block in the multi-step synthesis of active pharmaceutical ingredients, including specific anticonvulsants and antineoplastic drug molecules. Handling protocols require precise stoichiometric calculation to prevent impurities during condensation and reduction stages. Large-scale reactors require thorough quality validation to achieve GMP-compliant outputs, minimizing risks of carryover residues from intermediate transformation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF and EP monographs for finished APIs
    • FDA 21 CFR Part 211 for finished pharmaceutical products
    • ISO 9001:2015 certified QC systems for intermediates

    Typical usage ratio

    • 0.2–0.8 molar equivalents per synthesis batch, adjusted based on target API structure and by-product pathways

    Downstream process integration

    • Charged as a starting material in reaction vessels for nitration and cyclization
    • Undergoes catalytic reduction in the intermediate isolation phase
    • Subjected to solvent exchange before further derivatization

    Final product types

    • Hospital injectable oncology preparations
    • Oral solid-dosage anticonvulsant tablets
    • Precursor compounds for research-grade kinase inhibitors

    2. Agrochemical Synthesis

    Downstream agrochemical producers incorporate 4-Nitro-N-Methylphthalimide in the manufacture of selective herbicide compounds, primarily those containing phthalimide or structurally related functional groups. The nitro functionality supports controlled ring opening and substitution necessary for the synthesis of targeted active ingredients. QC labs monitor for isomeric impurities during formulation, and downstream blending facilities use automated weighing for precision dosing. Typical process arrangements integrate this material at the pre-formulation stage prior to active ingredient crystallization.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • EPA 40 CFR Part 180 for pesticide residue compliance in finished products
    • REACH Regulation (EC) No. 1907/2006 registration
    • ISO 17025 accreditation for in-process QC laboratories

    Typical usage ratio

    • 0.1–2.5% w/w based on crop-specific herbicide formulation and required mode of action

    Downstream process integration

    • Integrated at initial mixing in pre-reactor tanks
    • Participates in condensation and subsequent functionalization steps
    • Filters and isolates as an intermediate before final blend-in with adjuvants

    Final product types

    • Granular and suspension-concentrate selective herbicides
    • Industrial weed management liquid formulations
    • Custom agricultural chemical intermediates

    3. Dyes and Pigments Manufacturing

    Producers of specialty organic pigments and dyes employ 4-Nitro-N-Methylphthalimide as a key intermediate for phthalimide-based chromophores. Its electron-withdrawing nitro group enables controlled coupling reactions and enhanced tinctorial strength in subsequent products. Batch operations require tight process control to regulate temperature and pH, reducing by-product coloration. The material is added to reaction kettles during azo coupling and is further processed through filtration and drying before conversion to pigment dispersions.

    Industry compliance standards

    • EN 71-3 (Safety of Toys – Migration of Certain Elements) for pigments used in toys
    • ISO 9001-certified pigment production sites
    • U.S. TSCA compliance for dye intermediates
    • China GB 9685 for pigment use in food-contact plastics (where relevant)

    Typical usage ratio

    • 0.5–3.0% w/w relative to finished pigment mass, as determined by required color intensity

    Downstream process integration

    • Entered at batch dye-coupling or pigment synthesis vessel
    • Subjected to reflux under monitored conditions
    • Filtered, dried, and milled pre-blending into dispersions

    Final product types

    • Solvent dyes for plastics and coatings
    • High-purity organic pigments for automotive applications
    • Textile printing ink concentrates

    4. Specialty Polymer Additive Production

    Advanced material producers use this phthalimide derivative as a synthesis precursor for high-performance polymer additives. It supports modification of imide-based polymer backbones, enhancing flame retardance and thermal stability in engineering plastics. Input ratios are determined by targeted molecular weight and chain-end functionality. The feedstock enters compounding extruders or batch reactors in controlled quantities, and post-modification QC involves spectroscopic confirmation of structural integration.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • RoHS Directive 2011/65/EU limiting hazardous substances in end-use polymers
    • ISO 14001 environmental compliance for polymerization facilities
    • OEM tier-one supplier qualification for automotive or electronics polymers

    Typical usage ratio

    • 0.2–1.5% by mass of total monomer feed for polymer property modification

    Downstream process integration

    • Dosed into polymerization reactor with other monomers and catalysts
    • Participates in co-polymerization or post-polymerization modification
    • Downstream blending in masterbatch or compound systems

    Final product types

    • Flame-retardant engineering plastics
    • High-temperature resistant wire and cable insulation
    • Specialty polymer masterbatches for auto and electrical sectors

    5. Research & Development of Fine Chemical Intermediates

    Global fine chemical companies and research institutes rely on 4-Nitro-N-Methylphthalimide for targeted molecule construction in pilot and custom-synthesis projects. Its nitro-substituted aromatic structure forms the basis for a wide range of imide and aniline derivatives through reduction, substitution, and ring-opening steps. Highly controlled laboratory or kilo-scale reactors utilize precise weighing and high-purity lots. Post-reaction purification often involves preparative chromatography and advanced analytical characterization.

    Industry compliance standards

    • ISO 17025 accreditation for analytical chemical testing laboratories
    • Internal SOPs for chemical handling and waste management
    • REACH pre-registration for R&D substances in the EU
    • OSHA 29 CFR 1910.1450 for laboratory chemical hygiene

    Typical usage ratio

    • 0.05–1.0 mol per lab batch, adjusted to molecular target and scale

    Downstream process integration

    • Reagent in single or multi-step synthesis for custom intermediates
    • Integrated at the nitration, reduction, or alkylation step of synthesis
    • Prepared for downstream functional group transformations

    Final product types

    • Exploratory small-molecule intermediates
    • Structural reference standards for analytical labs
    • Custom reagents for project-based molecule design
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    Certification & Compliance
    More Introduction

    4-Nitro-N-Methylphthalimide: Experience from the Manufacturer’s Workbench

    4-Nitro-N-Methylphthalimide stands out as a niche but dependable intermediate in the toolbox for custom synthesis, dye manufacture, and specialty chemical production. As a manufacturer with two decades spent listening to what chemists and process engineers expect from phthalimide derivatives, I’ve watched this material perform inside a production line that values both purity and predictability.

    Producing 4-Nitro-N-Methylphthalimide: What We've Learned

    The core of 4-Nitro-N-Methylphthalimide’s performance lies in the quality of the raw inputs and tight process control. In our plant, the synthesis starts with phthalic anhydride as the base and a careful sequence of nitration and methylation. Sensitive handling during nitration determines the whole fate of the product quality — too hasty, and you’ll cram in unwanted isomers; too slow and batch stability drops off.

    Our engineers observed that the methyl group on the imide nitrogen brings a distinct profile to the molecular structure. In a reaction vessel, that little group means higher selectivity during condensations and lower by-product generation versus the classic 4-nitrophthalimide. There’s no theory here, only what results say: reactions with certain aromatic amines run cleaner, limiting tar formation and unwanted secondary nitro compounds that drag on purity.

    We check each lot by high-performance liquid chromatography (HPLC) and melting point analysis—down to single-digit ppm impurities. Each batch typically shows pale yellow crystalline appearance, solid at room temperature, and remains stable when stored away from sunlight and moisture. The actual figures from our recent output displayed a melting point consistently above 190°C, which speaks for the structural consistency.

    Many products flow through our drums and hoppers, but when I visit the intermediate staging area, the sharp crystalline habit of 4-Nitro-N-Methylphthalimide always signals reliability. It pours evenly, stores without caking, and resists hydrolysis—a trait not every phthalimide-based nitro compound can claim.

    The Chemistry Driving Application Choices

    Clients from colorant synthesis, pharmaceutical research, and organic electronics often call to confirm nuances in the molecular reactivity they’ll find with this nitrophthalimide. Over years of collaboration, we’ve noticed that methyl substitution at the imide group confers both steric and electronic effects. In downstream use, this translates to faster amination and less chance for side-chain splitting, which keeps yields on track and waste streams cleaner.

    A frequent application draws on its role as a precursor for specialty pigments. The 4-nitro group activates further substitutions at ring carbons, making the molecule attractive for custom azo dye work. In pharmaceutical intermediate work, a trusted trick involves using it in nucleophilic aromatic substitution—something that benefits from both the activating effect of the nitro group and the steric shielding from methyl substitution.

    Our regular users tell us their work benefits from the chemical’s sturdiness under both alkaline and mildly acidic conditions. This enables multistep syntheses where pH fluctuates, but the intermediate needs to hold up without breaking down or discoloring. Some have reported process cycles that run back-to-back for days, all drawing from the same stock, without seeing decomposition or significant product darkening.

    Comparing Performance with Other Phthalimides

    A seasoned operator spots differences between nitrophthalimide derivatives on the production floor. Run two synthesis batches side by side—one with 4-nitrophthalimide, one with 4-nitro-N-methylphthalimide—reagent demands and post-reaction work-up diverge. With 4-Nitro-N-Methylphthalimide, byproducts like dinitro-compounds remain minimized. The methyl group tempers reactivity, making purification steps more forgiving, and downstream filters clog less.

    Customers that tried switching from the parent nitrophthalimide to this methylated version tell us extraction and crystallization steps get faster. Less sticky impurities collect in evaporation dishes, and product color remains brighter. There’s less cleaning needed between batches, which means the plant runs smoother.

    One headache with some other derivatives—especially unsubstituted phthalimides—is the tendency to hydrolyze during aqueous steps. 4-Nitro-N-Methylphthalimide shrugs off moisture under neutral and slightly basic conditions, letting longer reactions run without yield loss. We’ve even had clients move from inert gas blanket processes down to standard venting—feedback that saves money and reduces complexity in plant setups.

    Our own team ran storage tests comparing this compound with 4-nitrophthalimide and 3-nitrophthalimide stocks over six months. We logged less than 0.5% loss in purity for the methylated version kept in sealed drums at ambient humidity, compared with upwards of 2% loss for the non-methylated batch. That real-world durability keeps batch records tight and lowers re-inspection costs.

    Process Feedback from Real-World Applications

    Over the last few years, the growth in demand for custom dyes and electronic intermediates led several mature plants in the sector to redesign their workflows around intermediates like 4-Nitro-N-Methylphthalimide. One dyestuff maker, based in East Asia, reported that after adopting our product for their anthraquinone dye range, they shaved reaction times by over 10% and returned improved pigment clarity. The reduced need for batch washing and less colored filtration cake meant less solvent usage—a bottom-line saving few engineers ignore.

    Pharmaceutical researchers face a different set of priorities. Our European partner, specializing in exploratory small-molecule synthesis, explained that methyl-substitution allows milder deprotection conditions. Their route from the phthalimide intermediate to an amine endpoint slashed deprotection time nearly in half compared to processes that use unsubstituted analogues. They found contaminant profiles easier to manage, particularly in late-stage chromatographic separation.

    In electronics, a customer specializing in organic field-effect transistor materials optimized their process using this intermediate. They noted that the product’s chemical predictability leads to better reproducibility in thin-film deposition, and this keeps batch-to-batch performance tight—a key issue for materials entering production for test runs and scale-up.

    We supply both regular drummed lots and custom, small-quantity packaging for those with pilot-scale needs. This dual approach grew from active dialog with industrial and research customers—one size rarely fits all, and nothing frustrates a process engineer more than large, inflexible minimum order sizes.

    Quality Control and Safety Matters from the Manufacturing Floor

    Every lot that leaves our plant walks a gauntlet of checks. Many buyers ask how we guard against contamination and unexpected byproducts. Realistically, maintaining batch-to-batch consistency requires configuration of closed systems for nitration and a continuous sampling protocol. We use both chemical and spectroscopic tests at each phase.

    There’s value in traceability. We record lot numbers down to every drum and maintain a sample archive, in part because researchers sometimes need to revisit analytical details months after shipment. Our team insists on transparent communication—when we spot unusual minor peaks by HPLC, we investigate and communicate straight back to our customers, no matter how small the anomaly may appear.

    Worker safety deserves mention. The reaction environments for nitration can push temperatures, and even with good automation, vigilance pays off. Over the years, we improved ventilation, switched to less aggressive acid sources for certain steps, and invested in reactor safety controls. No shortcut presents itself; real trust is built batch by batch, with documented safe operation.

    Storage, Transport, and Handling Notes

    The chemical itself ships well. Stable at ambient temperatures, it doesn’t require special insulation or refrigerated transport except in long-term ocean freight, where risk of moisture exposure or excessive heat matters. Our standard drums include moisture-barrier liners for overseas customers.

    Day-to-day handling rarely brings problems: the compound doesn’t exude significant dust and isn’t volatile or hygroscopic. Nevertheless, our floor guidelines keep protective gear on workers because fine powder always presents some inhalation risk. For larger customers, we suggest batch-specific handling advice based on their process temperatures, solvent choices, and throughput rates.

    Disposal and emission control matter more now than ever. We maintain a take-back program for expired or off-spec lots, encouraging circular disposal—even if this eats into margins, the environmental case remains clear. Users running aqueous work-up processes have shown effluent levels for this compound's trace residues remain below typical industrial thresholds for nitro organics, as long as plant controls adhere to core guidelines on pH and temperature.

    Outlook: Challenges and Improvements in Manufacturing and Use

    A few recurrent issues arise. Scaling up production for large-volume orders sometimes tests the limits of our continuous-feed reactors. To avoid surprises, we invested in real-time process monitoring, logging temperature, pressure, and impurity levels throughout each reaction. This reduces risk of off-spec product and supports rapid course correction—no reliance on “after-the-fact” troubleshooting.

    Some stages of manufacture still rely on careful labor input, especially during raw material charging and product isolation. Over time, we’ve installed semi-automated conveyors and dust-control filtration to keep worker health protected and loss to a minimum. We believe hands-on monitoring from experienced chemical operators, paired with smart automation, gets better results than full automation with no human oversight.

    On the demand side, customers increasingly request documentation for sustainability and regulatory status. We keep tightening our documentation and lifecycle analysis, collaborating with industry groups to benchmark energy, water, and waste profiles. We regularly welcome customer audits, and even brainstorm new uses for secondary streams resulting from the synthesis.

    Shipping logistics strain global chemical supply chains, so we maintain production buffers when possible and work with forwarders trained to handle specialty chemicals. We avoid transshipment where possible, aiming for direct routes and reduced risk of cross-contamination or handling mishaps.

    Listening to Feedback: What Our Partners Teach Us

    Some of the most useful innovation stems from direct user conversation. Only last quarter, a specialty dyes customer pointed out that their own test runs with slightly altered solvent ratios drove up yields by two percent, using our 4-Nitro-N-Methylphthalimide as a core building block. Rather than waiting for a formal complaint or service request, we ran a duplicate of their process at bench scale and confirmed the gain—then tipped off our broader user base.

    A recurring improvement suggestion from pharmaceutical groups focused on analytical transparency. We now include additional spectral data (NMR and FTIR) alongside the regular chromatography, because for customers in drug research, even a ppm-level impurity profile influences process validation. Fast feedback loops between our analytical team and our clients make this possible.

    We also learned a lesson from a purchasing manager, who flagged a batch that arrived slightly off-color due to a logistics glitch—a humidity spike pierced a drum liner. She requested extra humidity monitoring stickers on each drum, a simple change that’s now policy across all our ocean shipments.

    Chemical manufacturing isn’t faceless. The improvements that matter often grow from pointed feedback, careful critiques, and ideas from those further down the value chain. Our manufacturing experience with 4-Nitro-N-Methylphthalimide tracks this learning curve, shaped by years of close technical collaborations and an open-door policy for customer site visits and process reviews.

    Conclusion: Choosing 4-Nitro-N-Methylphthalimide from the Manufacturer’s Perspective

    The story of 4-Nitro-N-Methylphthalimide highlights a pattern—chemical intermediates rarely sit still. As manufacturing challenges shift and application fields evolve, those who produce and use this compound pay tangible dividends from connection and shared experience. Direct feedback from floor operators and process chemists shaped how this product is made, shipped, and improved over time.

    Choosing this intermediate goes beyond scanning a technical data sheet. The difference lies in knowing its idiosyncrasies, handling its quirks, and making batch-by-batch refinements informed through hands-on production and honest customer dialog. From diagnostics in our analytic lab to process tweaks born from user innovation, this chemical serves as a reminder that production and application both benefit from candor, scrutiny, and constant improvement.