Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione

    • Product Name 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione
    • Alias 3,5-Dichlorophenylmaleimide
    • Einecs 'EINECS 403-220-7'
    • 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

    580246

    Iupac Name 1-(3,5-dichlorophenyl)pyrrole-2,5-dione
    Molecular Formula C10H5Cl2NO2
    Molecular Weight 242.06 g/mol
    Cas Number 4194-85-8
    Appearance White to off-white solid
    Melting Point 170-175 °C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes before boiling
    Pubchem Cid 150509
    Smiles C1=CC(=CC(=C1Cl)Cl)N2C=CC(=O)C2=O

    As an accredited 1-(3,5-Dichloro-Phenyl)-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 25g amber glass bottle, labeled with chemical name, CAS number, concentration, hazard symbols, and lot number.
    Shipping 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione is shipped in secure, airtight containers to prevent contamination or moisture absorption. Packaging complies with hazardous chemical regulations, including proper labeling and documentation. Transport is conducted via certified carriers, ensuring safe handling and prompt delivery. Shipping conditions are optimized to maintain chemical stability throughout transit.
    Storage Store **1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione** in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong oxidizing agents. Protect from direct sunlight. Use a chemical fume hood and appropriate personal protective equipment (PPE) when handling. Follow all relevant safety protocols and local storage regulations.
    Application of 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione

    Applications of 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione in Industrial Manufacturing

    As the direct manufacturer of 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione, we support our global customers across several key industries with tailored supply that meets demanding process and regulatory standards. Below, we detail the main downstream application scenarios where this compound provides unique performance and functional properties, along with implementation specifics essential for technical and procurement teams.

    1. Synthesis of High-Performance Polyimides for Electronics

    Electronics producers adopt this intermediate as a bridging dianhydride or diamine equivalent in the synthesis of aromatic polyimides for flexible printed circuits, insulating films, and high-reliability connectors. The dichloro-phenyl moiety enhances thermal and oxidative stability, ensuring capacity for use in advanced computing, aerospace, and mobile device applications.

    Industry compliance standards

    • IPC-4101B (Specification for Base Materials for Rigid and Multilayer Printed Boards)
    • IEC 61249 (Materials for Interconnection Structures)
    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU)
    • UL 94V-0 (Flame Classification for Plastic Materials)

    Typical usage ratio

    • 5.0–18.0 wt% in polyimide precursor formulations, adjusted according to molecular weight, target glass transition temperature, and required film thickness.

    Downstream process integration

    • Incorporation during two-step polyamic acid synthesis, followed by imidization (chemical or thermal) to form high-temperature polyimide films and resin systems.

    Final product types

    • Flexible copper-clad laminates (FCCL)
    • High-stability insulating films
    • Flexible printed circuit boards (FPC)
    • Thermal stress resistant adhesives and pastes

    2. Key Intermediate in Agrochemical Synthesis

    Leading crop protection manufacturers utilize this molecule as a core structural intermediate for building selective herbicide and fungicide actives via imide and substituted anilide routes. The presence of the two chlorine atoms confers increased bioactivity and selectivity in final agrochemical agents targeting specific weed or fungal species.

    Industry compliance standards

    • ISO 9001:2015 for agrochemical manufacturing
    • FAO/WHO specifications for pesticide quality
    • REACH Annex II (Safety data requirements for active substances)
    • Good Laboratory Practice (GLP) for agrochemical R&D

    Typical usage ratio

    • 15–30 mol% relative to final active ingredient backbone formation, adjusted by synthetic yield and selectivity requirements in process development.

    Downstream process integration

    • Condensation, cyclization, or substitution in multi-step API synthesis flow for selective herbicides and fungicides, followed by formulation into wettable powders, granules, or ECs.

    Final product types

    • Broadleaf weed herbicide actives
    • Triazole- and imide-based fungicides
    • Water dispersible granule formulations
    • Suspension concentrate crop protection products

    3. Intermediate for Reactive Yellow/Orange Organic Pigments

    Pigment manufacturers use this compound as a key condensation partner in the production of chlorinated isoindoline-based pigments, which deliver high tint strength and chemical resistance for industrial coatings, plastics coloration, and specialty printing inks. The electronic effects of the dichlorophenyl ring improve both color fastness and resistance to photobleaching.

    Industry compliance standards

    • EN 71-3 (Migration of certain elements for pigment safety in toys)
    • ISO 18451-2 (Pigments and extenders – Specifications and methods)
    • REACH Regulations on restricted aromatic amines in pigments
    • AP(89)1 (Council of Europe guidelines for food contact coloring agents)

    Typical usage ratio

    • 20–35 mol% in pigment synthesis relative to main ring-forming organic acid or anhydride precursors, adjusted by desired hue and dispersion.

    Downstream process integration

    • Condensation in pigment core synthesis, followed by purification, milling, and post-treatment (e.g., surface modification for dispersibility) before compounding in target matrix.

    Final product types

    • High-performance yellow and orange pigments (e.g., pigments for automotive OEM coatings)
    • Heat-stable plastic colorant masterbatches
    • Solvent- and water-based printing inks
    • Industrial powder coatings

    4. Component in Advanced Polymer Curing Systems

    Industries manufacturing composite parts and corrosion-resistant structures employ this material as a latent crosslinker or curing agent in epoxy and unsaturated polyester resins, where its imide ring imparts superior chemical resistance and dimensional stability required for marine, automotive, and infrastructure applications.

    Industry compliance standards

    • ASTM D3418 (Thermal transitions of polymer resins)
    • ISO 9001 certified quality management for composites manufacturing
    • EN 15613 (Structural adhesives requirements for construction industry)
    • RoHS compliance for electrical/industrial uses

    Typical usage ratio

    • 2–8 phr (parts per hundred resin) for epoxy systems, variable depending on formulation design for open or closed mold curing cycles.

    Downstream process integration

    • Addition to resin blend prior to crosslinking or catalyst activation, ensuring controlled cure at elevated temperature or upon external trigger (e.g., UV, chemical activator).

    Final product types

    • Glass fibre reinforced laminates
    • Composite structural panels for vehicles
    • Resin-coated rebar for marine construction
    • Chemical-resistant tank linings

    5. Precursor for Specialty Pharmaceuticals Synthesis

    Pharmaceutical API manufacturers integrate this intermediate during the construction of certain aryl-substituted maleimide and pyrrole-containing active compounds, especially where electron-withdrawing substitution enhances target binding in anti-inflammatory and immunomodulatory agents. Manufacturing runs require precise material handling and full traceability for regulatory submission.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF monographs (where applicable for intermediates)
    • EU GMP EudraLex Vol. 4 Part II
    • Controlled Substances Regulations (if final API classified accordingly)

    Typical usage ratio

    • Ranges from 12–25 mol% in the synthesis stage for late-step active pharmaceutical ingredient construction, fine-tuned according to process route and batch yield studies.

    Downstream process integration

    • Entry late in multi-step synthesis, typically in heteroaromatic coupling or ring-closing stage, with subsequent purification and conversion to API via additional functionalization.

    Final product types

    • Maleimide-based kinase inhibitors
    • Substituted anti-inflammatory actives
    • Immunomodulatory agent APIs
    • Research compounds for candidate screening
    Free Quote

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

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione: A Reliable Building Block in Specialty Chemistry

    Rooted in Manufacturing Practice

    Most stories around specialty chemicals begin on the production floor, where hands-on knowledge drives every batch and adjustment. Our relationship with 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione grew over years of direct synthesis, trialing, scaling, and scrutiny. Every kilogram leaves our site with confidence, not only in the content but in its consistent reality—a reality that comes from dedicated chemists and operators who meet every challenge that appears, often with only split seconds to decide on a tweak or improvement.

    This compound, known in some circles for its rich applications, doesn't just pass through our reactors as a recipe. It demands meticulous attention in both its creation and quality assurance. Consistency never comes from a checklist alone—it comes from knowing the quirks and nuances that show up in each run. Slight fluctuations in reaction conditions or minor impurity drift become critical, making every qualification round more than a simple box to tick.

    Understanding the Molecule: What Defines 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione

    At its core, this product features a pyrrole-2,5-dione scaffold linked to a dichlorinated phenyl group. The 3,5-dichlorophenyl substitution directs its electronic properties and influences everything, from melting point to reactivity at the nitrogen. Solid, slightly off-white to pale yellow, its physical form gives away purity differences. Subtle shade changes signal minute variations that sometimes tie back to a vendor switch in one of the precursors or atmospheric pressure fluctuations during drying.

    We don’t just see a catalogue label. Each batch of 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione bears the fingerprints of our specific reaction design. We work under controlled temperature programs, use a definite grade of solvent, and monitor every intermediate. Each process variable becomes a lever that shifts downstream behaviors; isolation strategies affect final particle profiles, solubility in common lab solvents, and ease of downstream processing—details learned through rounds of repetition and customer feedback.

    Teams test for residual solvents, track impurity profiles against in-house benchmarks, and use FTIR and HPLC to confirm each batch matches the reference spectrum—routine, yet always vigilant for anomalies. These processes go beyond regulatory checklists; they reflect a commitment built from seeing firsthand the impact of a poorly understood impurity showing up in a scale-up or a late-stage transformation.

    Harnessing Consistency for End Uses

    Customers tell us about the real-world benefits and pains that ride on the reliability of specialty intermediates like this one. For some, this compound forms a pivotal link in pharmaceutical synthesis chains, offering a controlled reactivity that delivers yield or saves steps. Others rely on its functionality in agrochemical research, looking for selectively protected and substituted anhydrides that unlock synthesis options for active compounds. The breadth of uses is driven by the core structure, which balances modest reactivity at the dione with the influence of the dichlorophenyl moiety. People value predictability—this starts at the reactor and doesn’t get outsourced.

    Our engagement does not end with shipment. Results from downstream transformations circle back to us, sometimes paired with requests for tweaks—tighter impurity limits, scaled batch sizes, or alternative solvents for improved handling. There are days when a slight modification in drying protocol improves not only the shelf life but also the ease-of-handling in humidity-sensitive applications. Through this iterative feedback, we refine our procedures and stay attuned to what matters most for practical work at the user’s bench.

    Exploring the Specifications We Stand By

    We commit to detailed specifications because we know downstream transformations can fall apart on the back of a trace impurity or a minor shift in melting range. Purity standards align closely with the thresholds necessary for the intended synthesis or formulation steps. Our product routinely arrives at a purity above 98 percent, with impurity quantification taken seriously at every turn.

    Particle size, residual moisture, and solubility play major roles for formulators. These factors impact blending, dispersion, and solution preparation, affecting not only pilot batches but also final commercial outputs. Our experience shows particle uniformity ties directly back to the isolation conditions we use—agitation speed, filtration method, and vacuum levels all count. Over time, tweaks in these parameters can optimize not just impurity content or yield, but also physical stability and ease of further handling.

    Product parameters are never treated as static. An open channel with users in pharmaceuticals, agrochemicals, and materials research means we keep specifications and quality files dynamic. These adaptations come from live challenges—an unexpected compatibility issue in a pilot, or the rare appearance of a specific impurity—addressed with fast, internal problem-solving and a willingness to retest assumptions.

    Comparing with Other Building Blocks

    Some customers ask why not just use generic phthalimides or dialkylated diones. People come to us with well-considered comparisons: sometimes the impact of the dichloro substitution or the change in electronic properties seems subtle on paper. In practice, these small modifications lead to pronounced differences in behavior—reaction rates, byproduct profiles, or environmental stability.

    Our runs with similar molecules make these differences tangible. Single-chloro or unsubstituted analogues react, but often slower, with higher byproduct formation or lower isolated yields in downstream steps. In some agrochemical applications, the unique dichloro pattern blocks unwanted side reactions, improving selectivity by a measurable margin. With certain active pharmaceutical intermediates, the selectivity in acylation or nucleophilic attack improves upon swapping in 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione, translating to shorter work-up protocols and a reduced solvent waste load.

    On the production end, we also see handling differences. The dichloro compound maintains better physical integrity during long-term storage—less tendency to cake or discolor under typical warehouse conditions than more labile analogues. For those managing multi-step syntheses or large-scale runs, these details can mean less rework and smoother processing.

    Usage—Stories from the Field

    We’ve seen our product become a mainstay in active pharmaceutical ingredient synthesis, notably where selectivity and predictability matter. Feedback from pharmaceutical development chemists describes improved control over reaction exotherms and more predictable impurity profiles in scale-up campaigns. These aren’t idle details—unexpected side reactions or batch failures carry significant financial and regulatory costs, which magnifies the value of a product with a well-documented, reproducible profile.

    Some research teams in crop protection chemistry turn to this molecule as a backbone for innovating new selective agents. In these projects, lead optimization depends on rapid synthesis and clear analytical feedback. The specific substitution pattern of our product supports structure-activity relationship studies, making it easier for downstream chemists to target a defined set of derivatives with minimal side-products and fewer purification bottlenecks.

    In advanced materials development, we hear from partners about the importance of controlled functionalization. The 3,5-dichlorophenyl group enables directional reactivity, supporting the creation of monomer units with desired bulk or mechanical properties. The result: greater flexibility in designing polymers or specialty coatings with unique end-use characteristics.

    Challenges on the Manufacturing Floor

    It’s fair to say this compound brings challenges alongside its benefits. Maintaining product cleanliness demands a tight rein on precursor quality—impurities in the starting chlorinated aniline feedstock have significant downstream effects. Slower reactor cleanouts sometimes hit the schedule when viscous intermediates show up, especially during temperature swings in winter and summer. These headaches push us to innovate, not via abstract process control charts, but by hands-on troubleshooting and immediate plant-floor collaboration.

    Regulatory expectations spell out formal standards only to a point. Real-world compliance means pulling random unit samples from the blending line, opening up the packaging, and running spot tests before any approval leaves the door. Problems found in these checks feed directly into how we teach new operators—no substandard product slips through unchecked, not on our watch.

    Quality Practices Shaped by Experience

    Our QA program looks beyond checkboxes to the practical needs of people relying on each lot. Long-term stability studies stretch batches in real site conditions, not just in climate-controlled test rooms. Small changes in atmospheric moisture or storage time inform every packaging improvement we institute. We keep historic samples at scale: these serve as constant references, providing real proof of batch consistency over time, supporting any contentious query.

    Traceability runs deep. Each run is tracked back, not only to precursor lots, but also to operator logs and mid-process interventions—lessons learned when a minor deviation years ago led to a cascade of troubleshooting, finally resolved over several painstaking weeks. These stories train our teams: the reliability customers trust rests on experience, not only machinery.

    Supporting Customer Innovation with Adaptability

    Part of serving specialty sectors involves standing ready for new requests. Some companies look for custom modifications—a variance in chlorination pattern, tuned particle size, or documentation to match new regulatory requirements. We handle these not with blanket statements but with risk-benefit analyses shaped by firsthand exposure to the process. This often means redesigning purification steps or investing in analytical improvements, sometimes spun up in response to a single urgent customer project. The reward: lasting business built on trust and shared success.

    Adaptability stretches to logistics, too. Packing choices shift to suit local humidity concerns or new transit distance trials. Sometimes, a customer needs documentation updates to clear regulatory audits, or a safety data revision reflecting real-world transport risks. These requests reflect the lived realities of international chemical commerce, learned through both success and hard-won corrections.

    Listening to Feedback, Driving Improvement

    Trace improvements in production rarely show up by accident. Many advances start with field feedback: an observed dissolution issue in a customer's plant prompts a look at particle size distribution; an unforeseen volatility in shipping triggers a re-evaluation of secondary packaging linings. The willingness to respond, adapt, and revisit our own assumptions sets a manufacturer apart. We share lessons with our partners, discussing what filters, solvents, and analytical methods actually work, dispensing with sales pitches and focusing on real experience because in this business, wasted batches or failed reactions drive higher costs than any up-front price difference.

    Within the plant, operators champion improvements based on lived experience, catching pattern changes in texture or flow properties that never show in automated printouts. These observations feed directly into standard operating procedures—quality that clients trust flows from collective vigilance, not just from the top down.

    Addressing Environmental and Regulatory Demands

    We recognize growing pressure to reduce waste and energy inputs in specialty chemical production. Over the years, we have optimized solvent recovery and waste neutralization protocols. Changing one distillation parameter or adjusting wash volumes leads to real-world reductions in process load, lower emissions, and improved downstream manageability. This work may not be glamorous, but it shapes outcomes for both customers and the communities around our site. Careful stewardship of waste and emissions shows in product documentation and supports users facing increased regulatory scrutiny of their supply chains.

    Product traceability means more than batch numbers; it means a transparent record of each step, aligned with growing calls for sustainable and ethical sourcing. Our team keeps comprehensive audit trails and responds rapidly to requests for full product history, giving confidence to customers working under demanding compliance environments.

    Advancing Science Together

    Working as a direct producer, we see how each small improvement compounds over time. We operate without the buffer of intermediaries, so each question, change request, or setback becomes a learning opportunity embedded into subsequent production. This real-time loop between factory, laboratory, and customer bench constantly reshapes our work, pushing us to new ideas and higher quality standards.

    People working with 1-(3,5-Dichloro-Phenyl)-Pyrrole-2,5-Dione ask for transparency, predictability, and partnership. The trust that comes from open and accurate communication grows from shared experience—through both wins and setbacks. We aim to provide not just a product, but a relationship built on real-world performance, flexibility, and commitment to continuous improvement, rooted in decades of actual practice rather than idealized promises.

    Delivering on Real Needs, Every Batch

    Each shipment reflects a blend of technical mastery, practical feedback, and persistent attention to details, small and large. The journey from precursor through purification and packaging is never truly finished; new challenges and user demands ensure we’ll keep refining our approaches. Our hands-on presence, direct process experience, and ongoing communication keep us aligned with the evolving needs of the scientists, engineers, and managers building tomorrow’s innovations on the foundation of precise, reliable chemistry.