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4-Nitro-Isatoic Anhydride

    • Product Name 4-Nitro-Isatoic Anhydride
    • Alias 4-Nitrophthalic anhydride
    • Einecs 221-758-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    365681

    Chemical Name 4-Nitro-Isatoic Anhydride
    Cas Number 610-79-1
    Molecular Formula C8H4N2O5
    Molecular Weight 208.13 g/mol
    Appearance Yellow to orange solid
    Melting Point 219-222 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boiling Point Decomposes before boiling
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C, in a tightly closed container
    Synonyms 4-Nitro-1,3-benzoxazine-2,4-dione

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

    Packing & Storage
    Packing 250g of 4-Nitro-Isatoic Anhydride is packaged in a sealed amber glass bottle with a tamper-evident screw cap, labeled for safety.
    Shipping **Shipping Description:** 4-Nitro-Isatoic Anhydride should be shipped in tightly sealed containers, protected from moisture and light. Handle with care as it is an irritant and potentially hazardous. Ensure proper labeling according to chemical safety regulations, and transport within secondary containment to prevent leaks or contamination. Follow all local, national, and international shipping regulations.
    Storage 4-Nitro-Isatoic Anhydride should be stored in a cool, dry, and well-ventilated area away from heat, ignition sources, and incompatible substances such as strong acids and bases. Keep the container tightly closed and protected from moisture and direct sunlight. Store in a chemical-resistant, labeled container, and follow all relevant safety and regulatory guidelines for hazardous chemicals.
    Application of 4-Nitro-Isatoic Anhydride

    Applications of 4-Nitro-Isatoic Anhydride in Industrial Manufacturing

    4-Nitro-Isatoic Anhydride serves as a critical intermediate for several high-value chemical sectors. Our expertise as a direct manufacturer enables precise control over purity and production consistency, supporting downstream users in pharmaceuticals, dyes, agrochemical synthesis, and advanced materials development. Below, we detail practical application scenarios employed by leading industries.

    1. Pharmaceutical Intermediate for Quinolone Antibiotics

    This material functions as a key intermediate in quinolone drug synthesis, including ciprofloxacin derivatives. Facilities depend on high-purity grades with tight specification windows. The anhydride group enables selective ring closure within multi-step synthetic routes, improving overall yield and reducing side-reactions. Downstream users integrate this intermediate during piperazine or cyclopropylamine functionalization, targeting controlled production runs under strict cGMP and DMF-supported procedures.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP)
    • EDQM CEP requirements (Europe)
    • Chinese Pharmacopoeia specifications (if supplied in China)

    Typical usage ratio

    • 0.8 – 1.2 molar equivalents per target quinolone core; adjusted based on yield optimization and impurity profiles. Final scale-up fixed after pilot batches.

    Downstream process integration

    • Introduced after primary aromatic amine functionalization. Engaged in ring closure before final side-chain derivatization. Processed under anhydrous conditions to maximize selectivity.

    Final product types

    • Ciprofloxacin intermediate compounds
    • Levofloxacin key intermediates
    • Danofloxacin synthesis intermediates
    • Norfloxacin precursor compounds

    2. Advanced Dyes and Pigments Synthesis

    This raw material contributes crucial building blocks in the production of high-stability azo and anthraquinone dyes for textile, ink, and plastic coloration applications. It enables the introduction of nitro and carboxyl functionalities, supporting vivid color performance and improved fastness. In dye production plants, this compound initiates condensation with aromatic amines or phenols, forming chromophores under controlled temperature and pH.

    Industry compliance standards

    • OEKO-TEX Standard 100 requirements for restricted substances
    • REACH Regulation EC 1907/2006 (Annex XVII restrictions)
    • ISO 105-B02 for color fastness testing
    • ZDHC MRSL for textile and leather chemical inputs

    Typical usage ratio

    • 5–20% by weight in dye formulation batches; ratios change according to target chromophore structure and required dye strength per application sector.

    Downstream process integration

    • Undergoes nucleophilic aromatic substitution with secondary amines or phenols. Engaged in sulfonation or diazotization as a precursor step. Controlled addition at specific pH and temperature setpoints.

    Final product types

    • Disperse yellow and red azo dyes
    • Anthraquinone-based pigments for plastics
    • Textile disperse dyes for polyester and acetate fibers
    • High-performance inkjet printer colorants

    3. Agrochemical Synthesis, Including Fungicide Intermediates

    As a core intermediate for select agrochemical actives, this chemical plays a critical role in the stepwise assembly of systemic fungicides and herbicide backbone structures. Downstream users leverage its anhydride ring to couple with substituted anilines or heterocycles, allowing rapid functional group modifications. Technical batch controls focus on impurity minimization to meet international residue regulations on finished crop protection products.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications
    • ISO 9001:2015 Quality Management for production runs
    • Globally Harmonized System (GHS) for labeling and transport
    • EU Regulation (EC) No 1107/2009 for plant protection product registration

    Typical usage ratio

    • 10–50% by weight within the key intermediate stage; dosed based on the molecular design of the end-use active, typically calculated relative to heterocyclic precursor availability.

    Downstream process integration

    • Reacted with functionalized amines under controlled reflux during formation of core heterocyclic intermediates. Incorporated early to middle cascade steps, prior to final esterification or sulfonation.

    Final product types

    • Triazole fungicide intermediates
    • Isoxazoline-based herbicide precursors
    • Plant growth regulator building blocks
    • Pyridine and pyrimidine agrochemical scaffolds

    4. High-Performance Polymer Additive and Specialty Resin Production

    In specialty materials manufacturing, this raw material adds value during the production of engineered polyimides and advanced thermosetting resins. Its functional groups facilitate copolymerization and crosslinking, improving thermal stability and mechanical performance for downstream users in electronics and transportation sectors. Manufacturers meter precise quantities into prepolymer blends, optimizing homogeneous distribution and batch reproducibility under ISO-accredited QC environments.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronics polymer use
    • UL 94 flammability standards for resins
    • ASTM D5207 for polyimide resins in insulating films
    • ISO 9001-certified process control

    Typical usage ratio

    • 3–10% by weight in polyimide or resin matrix formulations; tuning based on molecular weight targets and degree of crosslinking required by the end application.

    Downstream process integration

    • Blended with dianhydrides and diamines during the imidization stage. Added to monomer feed prior to high-temperature polymerization or curing. Batch dosing tightly controlled for reproducibility.

    Final product types

    • Flexible printed circuit protective films
    • High-heat-resistant adhesives
    • Structural composite resins for aerospace
    • Automotive under-hood components based on advanced polymers

    5. Electronic Chemicals for Photolithography

    Our material supports the formulation of specialized photoresist developer chemicals used in semiconductor fabrication. Its nitro-substituted aromatic structure allows precise control over developer solubility and reactivity, translating to sharper imaging and resolution for device miniaturization. Microelectronics clients rely on batch-certified lots for consistent formulation and process repeatability at scale.

    Industry compliance standards

    • SEMI MS4 for photoresist chemical purity
    • ISO 14644-1 cleanroom standards
    • REACH SVHC non-inclusion for EU-based processing
    • IEC 62474 for hazardous substance management in electronics

    Typical usage ratio

    • 0.5–2.0% by weight in photoresist developer formulations; composition depends on target photoresist thickness and light wavelength (i-line, g-line, KrF, ArF).

    Downstream process integration

    • Added during the developer concentrate production step. Dissolved under cold, inert gas conditions with solvent blending. Quality checked for trace impurities and water content.

    Final product types

    • Positive and negative-tone photoresist developers
    • Micro-pattern transfer chemicals for wafer manufacturing
    • Sub-micron lithography etchant blends
    • High-resolution imaging agents for advanced semiconductors

    6. Specialty Chemical Reagent for Analytical Standards

    High-purity grades of this material are essential for analytical reference standard production in pharmaceutical and environmental QC laboratories. Reliable structural identity and low impurity levels support accurate calibration of chromatographic and spectrophotometric methods. End-users depend on full batch traceability, custom packaging, and stability data to meet international laboratory accreditation requirements.

    Industry compliance standards

    • ISO/IEC 17025 for testing and calibration laboratories
    • USP Reference Standard Guidelines
    • EPA Method 8270D for semi-volatile organic compounds analysis
    • GLP (Good Laboratory Practice) principles

    Typical usage ratio

    • Prepared as neat standards (100%) or serially diluted to 0.1–10 ppm in suitable solvents. Used according to validated method sensitivity requirements.

    Downstream process integration

    • Packaged and labeled in sealed ampoules following micro-analysis. Integrated into QC workflows for chromatographic method development, calibration curve building, and proficiency testing.

    Final product types

    • Reference standard kits for HPLC/GC
    • Certified analytical calibration solutions
    • Spectrophotometric calibration markers
    • QC check solutions for pharmaceutical analysis
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    Certification & Compliance
    More Introduction

    Introducing 4-Nitro-Isatoic Anhydride: Experience and Perspective from the Manufacturer

    Anyone who has worked in fine chemical manufacturing knows the importance of precision at every step. 4-Nitro-Isatoic Anhydride, recognized by its CAS number 610-77-9 and chemical formula C8H4N2O5, offers unique advantages for downstream synthesis—especially in pharmaceuticals and advanced material science. From our plant floor, countless batches have been produced, each with tight controls that reinforce our deep experience handling this complex compound. While the basic science behind this yellow crystalline solid may be well documented, the drive to perfect our process is an ongoing task.

    What Sets 4-Nitro-Isatoic Anhydride Apart?

    Anyone can order a chemical. Getting it to meet the exacting needs of your synthesis is another story. 4-Nitro-Isatoic Anhydride isn’t interchangeable with its relatives—its nitro group in the 4-position shifts reactivity in ways a bench chemist can’t ignore. This compound supports versatile transformations: amide formation, heterocycle construction, and selective substitution—all driven by that nitro group’s influence on electronic structure.

    From our production line, the difference between 4-nitro and 5-nitro derivatives reveals itself clearly in purity profiles and reactivity in downstream chemistry. Subtle changes in impurity content can ripple through to affect yields, product color, and even isolation work-ups for researchers. While some broad-specification materials pass a basic assay, we focus on minimizing ortho-substituted analogs and other structural impurities, knowing these can interfere with key pharmaceutical applications.

    Insights from Real-World Manufacturing

    Scaling up 4-Nitro-Isatoic Anhydride is no small feat. Anyone can look up laboratory syntheses, but translating that knowledge to the kilo or ton scale demands serious expertise. In the early days, common problems included hydrolysis during crystallization and nitrate salt formation during purification. These flaws used to push finished product out of specification: off-color crystals, irregular melting ranges, and unexpected side products in downstream users’ reactions.

    With time, process tweaking, and constant feedback from end users, our team has learned to control temperature gradients, solvent composition, and filtration equipment in ways that stabilize the intermediate stages. Nailing down a batch’s final moisture content took years of batch-to-batch comparison and in-process analytics. If you ever spot a faint orange tint in what should be a pure yellow solid, it almost always signals a process misstep back at the nitration or cyclization stage—a lesson hammered home by real experience, not just reading the spec sheet.

    Every batch gets checked for trace acids and metallic contamination, since pharmaceutical clients have strict protocols now that trace impurities trigger regulatory concern. Getting ahead of that curve, we invested in high-resolution chromatography and atomic absorption tools, prompted by requests from major research labs that ran into trouble with generic material from lesser producers.

    Practical Applications: Lessons from the Lab and Plant Floor

    Chemists who have handled 4-Nitro-Isatoic Anhydride know it opens up a world of molecular scaffolds. The nitro group’s electron-withdrawing nature sets it apart when constructing nitrogen heterocycles, making it a staple in the synthesis of active pharmaceutical ingredients (APIs) and pigments. Engineers and lab chemists come to us with synthesis challenges—cutting steps, shortening reaction times, or looking to swap out less stable reagents—and this compound gives them options.

    Most of our output heads to pharmaceutical R&D and intermediate plants, where it serves as a coupling partner, particularly in amide and urea linkages. The high yield and cleaner reactions of the 4-nitro variant cut down on waste streams in scale-up, helping both efficiency and environmental compliance. You can trace our lots through to clinical trial materials and even commercial drug launches—a point of pride echoed in every lot number we assign.

    Outside pharma, the electronics sector values its high purity for specialty dyes and optical brighteners. Our long-time clients have shared stories of failed formulations with generic suppliers: a single misstep in the synthesis pathway means a drop in luminescence, or an off-spec color, or even migration issues in polymer matrices. That’s led to plenty of midnight calls troubleshooting issues that trace back to someone using low-grade starting material.

    Specifications Born from Experience

    Specification writing for 4-Nitro-Isatoic Anhydride is part science, part craft. Academics can run an NMR and call it a day; commercial buyers need assurance that every drum matches last quarter’s performance. Through trial and error, we settled on a melting range that avoids “tailing off” at the edges—a sign of impure side products. We confirm purity at over 98% by HPLC, with moisture content below 0.3% by Karl Fischer titration and residual organic solvents below the most recent regulatory cutoffs.

    More than once, a new customer has complained about “good enough” material from another supplier, only to have their yields drop or their isolates discolor under sunlight. Simple testing for common inorganic impurities—nitrate, chloride, and trace metals—has saved innumerable hours in pilot runs at specialty pharma plants. In our records, the tighter we drove inorganic profiles, the smoother our customers’ runs went. The data supports it every time.

    Particle size matters in process chemistry—especially for automatic feeders and continuous reactors. For years, we battled issues with caking and bridging in shipment, which turned out to be a function of drying time and humidity—not the grinder settings. Once we started controlling atmosphere throughout final fill, the difference in customer feedback was immediate: blocked hoppers became a thing of the past.

    Shelf life has generated controversy in global supply chains, especially when ocean transit times stretch. Some producers don’t flag minor hydrolysis, which triggers reactivity changes after even a few months on the shelf. From years of field feedback (and the occasional emergency reshipment), we built in more robust packaging—triple-layer linings and nitrogen purging—so the material arrives in the same state it left us, whether it crosses a continent or an ocean.

    Safety Considerations: Plant to End User

    Anyone who’s watched a dehydrator puff a cloud of fine yellow powder into the air knows dust control means more than an SOP on paper. 4-Nitro-Isatoic Anhydride demands respect—its inhalation hazard has shaped our plant design, from dedusting cyclones to negative-pressure filter rooms. Over years of operation, we never take safety for granted; it only takes one near-miss to tighten protocols.

    Waste handling gets special attention. Early batches generated a nitrate-rich aqueous stream that traditional plants struggled to treat. Now, we recover and neutralize nearly all process water, reusing it in upstream reaction train steps. Lab users downstream have benefited: less residual nitrate means less opportunity for exothermic surprises in their own reactors.

    Disposal of packaging and cleanup demands caution. Each drum goes out with usage notes drawn from real-life plant experience, not boilerplate text. Downstream users appreciate the candor. We work with research sites to engineer safe handling, sometimes modifying delivery size based on lab capabilities. There’s a big difference between a kilogram bag for a university and a hundred-liter drum for an API plant.

    Comparing 4-Nitro Isatoic Anhydride to Related Compounds

    Working with 4-Nitro-Isatoic Anhydride puts its differences with similar compounds in sharp relief. The 5-nitro isomer gets credit for similar uses, but it reacts differently during ring-opening steps—often less predictably in certain amide bond-forming reactions. Lab tests show faster, more complete conversions for the 4-nitro, which cuts purification steps for most applications. Ask any pilot plant chemist about side reactions and you’ll hear stories about 5-nitro material failing in high-throughput screens.

    Traditional Isatoic Anhydride lacks the power of the electron-withdrawing nitro group altogether. This means slower rates in nucleophilic aromatic substitution, less versatility in downstream heterocycle syntheses, and sometimes the need for harsher conditions. We get inquiries from new users who struggled with older protocols built around the base molecule, only to upgrade to the 4-nitro product and streamline their entire workflow.

    Amino-substituted analogs flip the situation again. Their electron-donating nature usually drives reactivity in the opposite direction: more basic, less stable, and often limited to a different world of chemical synthesis. The bottom line from our vantage point: the 4-nitro variant occupies a sweet spot for building complex molecules under gentle, scalable conditions.

    Regulatory and Quality Perspective Grounded in Practice

    Regulatory scrutiny defines modern fine chemical manufacturing, with pharmaceutical clients leading the charge. Every lot release passes not just classical organoleptic tests—color, crystal habit, odor—but validated analytical runs monitored by independent quality teams. Once, the trace of an unlisted solvent in a small batch prompted a client audit that changed our approach to column maintenance and batch records.

    Audit trails link every process step to a time and operator, and deviations get investigated by people who have watched hundreds of these syntheses unfold. Certification isn’t just paperwork; regulatory authorities demand access to analytical chromatograms and real-world stability data. Our plant now maintains samples from every batch in a climate-controlled archive. We track product evolution under different storage and transport conditions, especially with the growing complexity of global logistics. The hard lessons from early missteps taught us to design for worst-case scenarios, not just the best.

    Pharmaceutical manufacturers expect zero surprises. The evolution of Good Manufacturing Practice (GMP) standards changes how even the bulk suppliers like us operate. We carry out all plant improvements with these realities in mind: cleaner equipment, cross-contamination controls, dedicated lines for multi-step syntheses. This careful approach is born from the trenches, not from marketing.

    Solutions for Supply Chain and User Challenges

    Supply constraints and raw material quality have long shaped our strategy. Sourcing the right nitrobenzene and controlling batch-to-batch consistency presented the greatest difficulty in the first days. Early on, we saw how a single bad shipment upstream could drive upside-down reactivity downstream, so we implemented multi-source procurement for all critical intermediates. Finished product never leaves the plant before a round of impurity profiling and accelerated stability testing.

    Global shipping delays, especially since the pandemic, made shelf-life protection even more important. We answer directly to clients who run into problems from extended transit. That’s driven investments in stabilization—chemical and packaging—to maintain reactivity and minimize hydrolysis, even when a container crosses through summer temperatures or sits in a customs warehouse. Return customers point to this reliability as the main reason for sticking with our brand.

    Problems with scaling are familiar to us as well. As pilot plants switch over to kilo-scale runs, even minor changes in solubility or crystal habit can lead to equipment blockages, filter press clogs, or reactor fouling. We built a feedback loop in our technical support, matching reports of field failures against our operation logs, to tune drying, blending, and packaging parameters. Value comes not from an idealized product but from adaptability and a two-way dialogue with every chemist who uses our product at scale.

    Continuous Improvement: A Manufacturer’s Outlook

    Nobody gets every batch right the first time. Improvements to our 4-Nitro-Isatoic Anhydride come straight from end-users and plant observations. Once, a client flagged residual acidity linked to off-flavors in a downstream drug intermediate. Digging through our logs, we discovered that a slight variation in reactor pressure had led to incomplete cyclization. New sensors and in-process controls addressed the problem within weeks.

    Feedback sometimes comes in the form of repeated trouble tickets: persistent clogging, color shift, drop in assay. Each one has shaped either our process equipment (like closed-loop grinding) or procedural guidance for storage and handling. Rolling out new packaging was never a “top-down” decision; it emerged from toolkits built in response to months of moisture pickup problems on transatlantic shipments.

    We routinely run joint studies with major pharmaceutical R&D departments, taking back samples of off-spec product for root-cause diagnostics. This closed feedback system has shortened our lead times and prompted studies of process contaminants we’d never have caught using standard QC. The result isn’t just a purer product, but a company-wide understanding of why each quality step matters.

    Looking Ahead: Supporting Researchers and Manufacturers

    Our goal remains simple: deliver a reliable, high-purity 4-Nitro-Isatoic Anhydride that won’t add headaches to anyone’s workflow. We do this by staying engaged with the bench chemistry—the nuts and bolts of how the product performs at all stages of application. Every tweak in synthesis aims to minimize environmental footprint, operational risk, and scrap rates.

    As global regulations tighten, every shipment reflects decades of accumulated knowledge. The learning process never ends. Chemists working at scale, whether in biotech or advanced materials, shape how we operate—by sharing both successes and stumbles. Only by drawing from the real experience within our operations and the continual feedback of a far-flung user community can we keep refining our 4-Nitro-Isatoic Anhydride, ensuring that it’s more than a line on the spec sheet but a trusted tool in discovery and production.