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1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione

    • Product Name 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione
    • Alias 3-Methoxy-N-Phthalimide
    • Einecs EINECS 627-260-5
    • 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

    628711

    Iupac Name 1-(3-methoxyphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione
    Molecular Formula C11H9NO3
    Molecular Weight 203.19 g/mol
    Cas Number 38055-51-1
    Appearance Off-white to light yellow solid
    Melting Point 130-134°C
    Solubility Soluble in organic solvents such as DMSO and ethanol
    Smiles COC1=CC=CC(=C1)N2C(=O)CC=C2=O
    Inchi InChI=1S/C11H9NO3/c1-15-9-4-2-3-8(7-9)12-10(13)5-6-11(12)14/h2-4,7H,5-6H2,1H3
    Pubchem Cid 3440480

    As an accredited 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed glass bottle containing 25 grams of 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione, labeled with hazard symbols and product details.
    Shipping The chemical **1-(3-Methoxyphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione** should be shipped in tightly sealed containers, protected from moisture and light. It must comply with all applicable regulations for safe transport. Appropriate hazard labeling, cushioning, and secondary containment should be used to prevent leaks or damage during transit.
    Storage **Storage Description:** Store 1-(3-Methoxyphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Ensure the storage area is clearly labeled and access is restricted to authorized personnel. Follow relevant safety and chemical hygiene protocols.
    Application of 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione

    Applications of 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione in Industrial Manufacturing

    As an experienced manufacturer, we supply 1-(3-Methoxyphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione for multiple high-end industrial applications. This specialty intermediate supports targeted synthesis processes in advanced materials, pharmaceuticals, specialty coatings, and agrochemical manufacturing. Below, we illustrate several real downstream application scenarios, detailing regulatory requirements, compositional considerations, processing steps, and end product outputs.

    1. Pharmaceutical Intermediate Synthesis

    Drug manufacturers use this compound as a key building block for custom N-heterocyclic derivatives. It enters synthesis routes for CNS-active molecules and anti-inflammatory drugs. Downstream labs perform stepwise amidation or N-alkylation under controlled conditions. Process monitoring ensures impurity removal to meet pharmacopoeial and GMP requirements. Finished active ingredients must demonstrate batch-to-batch reproducibility, impurity profiles within ICH Q3A/B, and full traceability for regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. Monographs applicable to APIs and intermediates
    • USP General Chapters <795> and <1058>
    • 21 CFR Part 211 (US FDA GMP)

    Typical usage ratio

    • Dosage in final molecular assembly 0.4–0.7 molar equivalents, adjusted for reaction kinetics and by-product formation
    • Intermediate charge determined via stoichiometric calculation based on API synthesis pathway

    Downstream process integration

    • Introduced in initial N-heterocycle formation step
    • Participates in condensation or reductive amination in dedicated reactor vessels
    • Intermediates undergo purification via crystallization or column chromatography
    • API isolation follows validated GMP protocols post-functionalization

    Final product types

    • CNS disorder APIs (e.g., anticonvulsants, anxiolytics)
    • Anti-inflammatory pharmaceutical actives
    • Custom small-molecule drug candidates for clinical R&D
    • Medical research reagents

    2. Agrochemical Active Ingredient Manufacturing

    Agrochemical producers utilize this heterocyclic imide as a coupling reagent in synthetic routes for herbicides and selective insecticides. It serves as a precursor for molecules containing aryl-imide substructures, which increase environmental persistence and biological target activity. Manufacturing plants precisely control ratio and order of reagent addition regarding environmental safety and occupational hygiene. Finished technical-grade actives must fulfill international pesticide registration quality specifications.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • China NY/T 1977 – Pesticide Quality Standards
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 for manufacturing consistency

    Typical usage ratio

    • 5–12% of total raw reactant mass, fine-tuned based on desired substitution and downstream processing requirements
    • Higher ratios support increased yield for multi-step functionalizations

    Downstream process integration

    • Entered after base hydrolysis and acid activation of parent compounds
    • Participates in catalytic coupling using batch or flow reactors
    • Enables downstream chlorination or alkylation steps for activity enhancement
    • Solvent exchange and phase separation ensure consistent active concentration

    Final product types

    • Technical-grade herbicide actives
    • Selective insecticide intermediates
    • Pre-formulated pesticide blends
    • Research-only agrochemical leads

    3. Advanced Materials Synthesis for Functional Polymers

    Functional polymer manufacturers use this molecule to introduce methoxy-aryl-imide units into specialty polyimide chains for high-performance applications. Incorporation modifies electrical insulation and chemical resistance for electronic device casings and aerospace composite films. Polymerization systems precisely meter imide additive, adjusting temperature and reaction time to maintain desired molecular weight distribution and process safety. Final polymer sheets or coatings meet stringent dielectric, mechanical, and purity requirements for device assembly.

    Industry compliance standards

    • IEC 60216 for electrical insulating materials thermal endurance
    • REACH Registration, Evaluation, Authorization, and Restriction of Chemicals (EU)
    • RoHS Directive 2011/65/EU (limiting hazardous substances)
    • UL 94 for flammability of plastic materials

    Typical usage ratio

    • 1.5–4.0% by weight of total polyimide monomer feed
    • Adjusted based on targeted dielectric and flexibility properties

    Downstream process integration

    • Dosed into polycondensation reactors after primary dianhydride and diamine introduction
    • Polymerization under controlled N2 atmosphere to manage oxidative side-reactions
    • In-process viscosity monitored to control imide segment integration
    • Roll-to-roll casting for composite film fabrication

    Final product types

    • High-temperature wire insulations
    • Flexible dielectric films for electronics
    • Aerospace composite laminates
    • Specialty adhesive tapes

    4. Specialty Coatings and Surface Modification

    Coatings producers employ this imide derivative to create methoxy-substituted N-heterocycle units on surfaces, supporting chemical resistance and UV-stability in end-use coatings. Typical applications include protective lacquers for engineered metals and functional primers for plastics. Formulators carefully control pre-polymer cross-linking, pH, and film formation parameters. Final coat films undergo inspection for hardness, solvent resistance, and UV-aged color stability, verified against application-specific test protocols.

    Industry compliance standards

    • ASTM D3363 for film hardness of organic coatings
    • ISO 12944 for corrosion protection of steel structures by protective paint systems
    • EN 927-6 for artificial weathering and UV exposure tests
    • OECD 301 series for biodegradability assessment

    Typical usage ratio

    • 1.0–2.5% solids content in formulated coating slurry
    • Ratio adjusted to balance physical performance and economic yield

    Downstream process integration

    • Added at pre-polymer blending stage before dilution and cross-linker addition
    • Micronized for dispersion stability and uniform film formation
    • Curing performed in forced-air ovens between 80–160°C
    • Film thickness and adhesion tested post-application

    Final product types

    • Industrial protective lacquers (metal casings, machine enclosures)
    • UV-stable coatings for building facades
    • Primer layers for automotive plastics
    • Functional anti-corrosion paint systems
    Free Quote

    Competitive 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione: A Manufacturer’s Perspective on Reliability, Purity, and Application

    Grounded in Experience, Driven by Precision

    Working hands-on every day with core intermediates, I’ve learned that progress does not hinge on shortcuts or broad claims. In the pursuit of cleaner and more reliable syntheses, 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione proves itself by delivering consistently. This compound, sometimes referred to in industry channels as 3-Methoxyphenyl maleimide, forms the backbone of advanced organic synthesis in industries where reliability, yield, and purity are non-negotiable.

    From the Reactor Vessel to the Bench: Product Origins and Focus

    We don’t just source intermediates and relabel drums. Our process starts in our own reactors, where tightly defined conditions draw the line between acceptable and outstanding. Each batch of 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione goes through repeated purification cycles until we see a consistent product on our HPLC chromatograms. Imbalances in parameters like stir rate, reaction temperature, or the addition sequence can shift impurity profiles. Heading off issues like colored byproducts or off-specification melting points requires an operator who knows the difference by sight and smell, not just numbers on a screen.

    Consistent Quality: Not Just a Slogan

    I have stood beside teams troubleshooting a reactor mid-batch, so I know that the phrase ‘high purity’ means little if it doesn’t line up with the application. 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione produced here regularly achieves GC/LC purities exceeding 99%. Every stage, from raw material assessment to final packaging, sits under a dedicated QA system—one developed after years of catching subtle issues the first time, not after a customer sends product back. Moisture content, trace solvents, and minor contaminants all take center stage because final users notice when they add grams or kilos to their reactions.

    Visually, the product presents as a pale yellow to light beige solid. Product quality isn’t just optical though. Our regular GC and NMR checks confirm the absence of persistent side-products and halogen residues. Once, a single barrel with slightly elevated water content triggered an entire week’s worth of follow-up because we’d rather catch the anomaly here than see it fail in someone else’s hands.

    How 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione Stands Apart

    Chemistry rarely gives two compounds the same story, even with similar structures. This maleimide-based intermediate brings together the electronic effects of a methoxy group with the reactive imide function, turning an otherwise standard synthon into a versatile building block. Its particular reactivity profile gives streamlined pathways in cross-coupling, Diels-Alder chemistry, and targeted derivatization, unlike more heavily substituted or unsubstituted analogues.

    Compared with plain maleimide, the 3-methoxyphenyl variant displays altered solubility in common reaction solvents—a serious consideration for large scale runs. We don’t rely on speculation or datasheet entries. Instead, we gather feedback from kilo-lab to full-scale batches, monitoring yields, side-product formation, and final product color. One customer using a para-substituted alternative experienced unpredictable purification behavior. Shifting to our 3-methoxy analog led to easier separations and fewer colored impurities. This wasn’t just luck; it reflects how nuanced changes in aromatic substitution shift both electrophilicity and nucleophilicity at the functional core.

    Purpose-Driven Design: Where and Why 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione Gets Used

    As a building block, this compound does not act as a placeholder. Medicinal chemistry teams seek out its unique profile for structure-activity relationship studies. Its methoxy substitution patterns expose small but repeatable bioactivity shifts in lead series. Scale-up for agrochemical testing has shown steady yields from gram all the way up to multi-kilo campaigns, saving months of development time.

    Polymer chemists draw on its maleimide backbone for cycloaddition-driven cures and crosslinks. I’ve watched materials engineers use it where standard maleimides wouldn’t give the required flexibility or tunable curing speeds. Substitution at the meta position on the ring allows just enough adjustment to attain precise mechanical outcomes without losing the oxidative stability typically associated with this family. Years ago, one partner used the unsubstituted analog and ran into shelf-life instability—the methoxy-functionalized material outperformed it by seasons, not just weeks.

    Specifications Shaped by Application

    Specification-making in a working synthesis lab keeps us honest. A product that misses the mark on melting point, ash content, or even particle size can ruin an entire week of bench work. Our methodology doesn’t chase the lowest cost synthesis route. Instead, it pursues batch records and histories so you know exactly what to expect. Average melting point falls consistently in the 118–122°C window, with residual solvents tightly controlled below regulatory limits. Each lot ships with fully traceable documentation, connecting every lab result to specific hardware and operator teams.

    Through years of partnership with both multinational formulators and focused startup ventures, we have built out multiple grade options. Most teams using the product for library synthesis gravitate toward our ‘research grade’—minimum 99% purity, clear NMR peaks, and sub-percent water. Production groups scaling into hundreds of kilos choose a bulk grade, sacrificing little on purity while gaining consistency lot to lot. Our own staff routinely puts aside product that lands on the lower end of the acceptable purity or shows color outside the designated range.

    Handling and Storage: Lessons Learned on the Shop Floor

    No two storage solutions work the same, but direct exposure to humidity or poorly vented drums increases the risk of clumping or subtle hydrolysis. Keeping the product in sealed, inert packages at moderate temperatures keeps it as free-flowing and easy to handle as possible. Packed at our site, prebagged in high-barrier foil with desiccant, drums open only once at the user’s lab. This process comes from more ruined batches than I can count, always teaching us to respect the little details that underlie safe, consistent deliveries.

    Anecdotal advice based on lab and pilot plant experience: jobs that transition from bench to pilot runs should always rely on the same packaging class across the board. Over the years, feedback from customers sticking to our original foil-pouched design, as compared to generic plastic, have reported the least variance in downstream test results—especially when hydration-sensitive pathways are in play.

    Addressing Real-World Challenges

    Unexpected shortfalls, lengthy recrystallizations, drum-to-drum variability—these are not stories you hear from PowerPoint slides. Many commercial buyers come to us after seeing spotty yields or complicated waste profiles from substituted maleimides made offshore or re-sold several times. We use our in-house QC data not just as a marketing pitch, but as a self-check. Once, a full twenty-kilo consignment failed because it showed faint but persistent halogen residues. We pulled the lot from circulation and re-trained our shift on batch cleanup procedures, guided not by some outside audit but by what our partners really encounter in lab and plant.

    Our plant operators, chemists, and QA group approach incoming feedback as the next process improvement target. Concerns on trace metals led us to install additional purification columns. Requests for smaller, more manageable unit operations pushed our packing operators to offer drum-to-pail split-offs with batch tracking. Real solutions don’t stop at a signed delivery note—they echo in the next round of improvements, new analytical procedures, and fine-tuned shipment systems.

    Environmental Responsibility: More Than Regulatory Talk

    Sustainability is not marketing fluff here. Each step of manufacturing and purification gets weighed against energy and waste minimization targets. Where we once vented certain processing gases, we now reclaim and scrub. Batch solvents filter and recycle back through our process plant, cutting both material costs and environmental impact.

    Handling 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione at scale means being pragmatic. We operate under strict compliance with current chemical regulations. Every waste stream and handling procedure comes under regular review, informed by our ongoing internal risk assessments and lessons learned across years of scale-ups and product launches.

    Meeting Evolving Customer Demands

    Innovation in fields like pharmaceuticals, performance materials, and specialty coatings continues to move target requirements. Shorter project timelines, ever-tightening purity needs, and stricter documentation standards flow straight from the laboratory through to factory floor. By processing and packing every lot in-house, we’re able to modify processes at the customer’s suggestion, not months later, but in the next manufacturing run. Recently, a shift to lower trace metal content, driven by a partner’s drug discovery program, led us to re-examine entire segments of our in-process sampling protocol.

    Technical teams ask questions based on practical hurdles, so we meet these face-to-face. Instead of one-size-fits-all grade descriptions, we tailor analytical efforts to focus on the minute differences that drive downstream outcomes. Some groups want expanded NMR datasets; others lean on fast, digital lot release summaries for cGMP documentation. Our flexibility comes not from burnt-out operators or remote-owned warehouses, but from chemists and operators invested in the same batch records as our end users.

    Learning from the Field: User Feedback as Product Driver

    Early on, we operated based on what we thought customers needed. Years in, direct, candid feedback shapes how we test every shipment. An instance of low solubility in a DMF-based transformation prompted us to revisit crystallization and drying parameters as routine checks for each lot. Collaborators pointed out process bottlenecks—on-site troubleshooting led us to multiple incremental refinements.

    First-hand experience echoes just as loudly as benchmark data. Consistent feedback from both pilot and industrial lines flagged subtle variances in product homogeneity—feedback we used to tighten milling tolerances and particle cut-off screens, driving down clumps and improving flow. Instead of waiting for outside complaints, we keep lines of communication open, fostering direct ties to those putting kilos of our product through real synthetic challenges.

    The Importance of Trust in High-Stakes Chemistry

    An intermediate like 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione does not sell based on spreadsheet pricing alone. Trust is built at every point—clear identification, batch reproducibility, and the absence of show-stopping contaminants. Researchers and production chemists work under pressure to deliver, and our job is to maintain consistency, so their runs do not stall. Transparency about specification changes, direct lab support, and ownership of every batch record fosters a working relationship built to last through the unexpected.

    Rather than promising the moon, we let direct results and our growing body of real-case customer success stories speak for what this product and our approach can do.

    Summary of Our Commitment

    Years of hands-on experience in chemical manufacturing taught us that every batch and every delivery tells its own story. With 1-(3-Methoxyphenyl)-2,5-Dihydro-1H-Pyrrole-2,5-Dione, we make sure that story is one of rigorous preparation, consistency, and partnership between manufacturer and user. Each lot leaves our site after passing tough standards not imposed by an outside template, but drawn from real-world challenges, failures, and improvements. This approach produces the kind of reliability that our customers notice—less downtime, fewer redos, and more successful innovation.

    By focusing on transparent, fact-based quality control, listening to practical user feedback, and adapting methods on the back of lived manufacturing experience, we keep this intermediate as ready for tomorrow’s breakthroughs as today’s scaling demands. For teams working at the boundary of what’s possible in synthesis and product development, the difference does not just lie in the material—it’s in the people, the process, and the lessons built over years on the plant floor.