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4-Chloro-1,3-Benzenediamine

    • Product Name 4-Chloro-1,3-Benzenediamine
    • Alias 4-Chlorobenzene-1,3-diamine
    • Einecs EINECS 209-353-6
    • 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
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    Specifications

    HS Code

    377743

    Cas Number 95-83-0
    Molecular Formula C6H7ClN2
    Molecular Weight 142.59 g/mol
    Iupac Name 4-chlorobenzene-1,3-diamine
    Appearance Grayish to brownish solid
    Melting Point 131-134°C
    Density 1.30 g/cm³ (approximate)
    Solubility In Water Slightly soluble
    Flash Point 177°C
    Synonyms 1,3-Benzenediamine, 4-chloro-; 4-Chloro-m-phenylenediamine
    Pubchem Cid 7542

    As an accredited 4-Chloro-1,3-Benzenediamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Chloro-1,3-Benzenediamine (25g) is packaged in a sealed amber glass bottle with a safety cap and hazard labeling.
    Shipping 4-Chloro-1,3-Benzenediamine is typically shipped in tightly sealed containers to prevent moisture and air exposure. It should be transported according to local and international hazardous material regulations, usually as a Class 6.1 toxic substance. Proper labeling, documentation, and protective measures are required to ensure safe handling and delivery.
    Storage 4-Chloro-1,3-benzenediamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as oxidizers and acids. Keep the chemical away from sources of ignition and moisture. Proper labeling, secondary containment, and access limited to trained personnel are recommended to ensure safe storage procedures.
    Application of 4-Chloro-1,3-Benzenediamine

    Applications of 4-Chloro-1,3-Benzenediamine in Industrial Manufacturing

    We supply 4-Chloro-1,3-benzenediamine directly from our dedicated production lines for multiple advanced chemical manufacturing sectors. As a qualified upstream manufacturer, we maintain rigorous quality assurance and formula traceability across every batch used in specialty industrial processes. Below, we provide a comprehensive overview of specific downstream applications, focusing on strictly verified use cases supported by regulatory and market evidence.

    1. Synthesis of High-Performance Polymeric Materials (Polyamide and Polyimide Sectors)

    4-Chloro-1,3-benzenediamine serves as an essential aromatic diamine monomer in the synthesis of specialty polyamides and polyimides, valued for its chlorine substitution, which improves flame resistance and mechanical stability. Direct integration into polymerization feeds permits the industrial production of advanced films and resins for demanding electrical and aerospace applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for industrial polymers
    • RoHS Directive 2011/65/EU (limiting hazardous substance content in finished goods)
    • REACH Regulation (EC) No 1907/2006 substance registration and use notifications
    • ASTM D4066 for polyamide compounds

    Typical usage ratio

    • 3–12% by molar proportion in monomer feedstock; optimizable based on target thermal or mechanical properties of polymer; higher loading for increased flame retardancy

    Downstream process integration

    • Charged to the diamine feed tank; condenses with dianhydride or diacid chlorides during controlled polycondensation; maintained under inert or vacuum atmosphere; final polymer solution cast or spun as film or fiber

    Final product types

    • Polyimide films (flexible printed circuit substrates, aerospace insulation)
    • High-performance polyamide molding resins (automotive under-hood components)
    • Insulating varnishes for electrical and electronics industry
    • Heat-resistant engineering plastics

    2. Synthesis of Agrochemical Active Ingredients

    As a key intermediate, 4-Chloro-1,3-benzenediamine enters multi-step syntheses for certain urea, triazine, and other heterocycle-based agrochemical actives. The chlorine substituent supports target molecule synthesis while the diamine motif enables ring closures or coupling, crucial for herbicide and fungicide innovation. Our material ensures reliable batch purity for reaction scalability and downstream performance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Good Manufacturing Practice (GMP) for crop protection active substances
    • ISO 9001:2015 for manufacturing quality systems in agri-inputs
    • REACH notification obligation for export/import within EU

    Typical usage ratio

    • Varies from 0.2–1.5 molar equivalents based on synthesis step and active ingredient structure; reaction yield optimization may adjust ratio slightly

    Downstream process integration

    • Incorporated as a building-block in closed vessel batch synthesis; reacts via amination, nucleophilic substitution, or condensation to form key precursors; intermediates isolated and further processed by cyclization or functional group transformation

    Final product types

    • Precursor intermediates for selective herbicides
    • Key units for certain contact fungicides
    • Synthesis intermediates for insecticide active substances
    • Custom building blocks for contract research agrochemicals

    3. Dye and Pigment Intermediate for Specialty Colorants

    This aromatic diamine forms critical azo and heterocyclic intermediates in colorant manufacturing, particularly for synthetic dyes used in technical textile and industrial coatings. The para-chloro group contributes to lightfastness and chemical resistance, while the diamine function allows versatile coupling and diazotization for tailored pigment synthesis routes.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100 for textile chemical inputs
    • ISO 9001:2015 Quality Management (colorant sector)
    • REACH Annex XVII for restricted aromatic amines content in end-use dyes
    • GMP for colorant intermediates (where exported for food-contact textile dyes)

    Typical usage ratio

    • Used at 0.5–2.1 mole equivalents in diazo-coupling stages, adjusted based on targeted shade intensity and desired fastness properties

    Downstream process integration

    • Introduced during diazotization step; coupled with aromatic or heterocyclic partners in controlled temperature and pH reactors; post-treatment steps for purification, filtration, and crystallization of pigment intermediate

    Final product types

    • Azo dye intermediates for synthetic textile coloration
    • Technical colorants for coatings and paints
    • Specialty pigments for plastics compounding
    • Base components for inkjet and industrial printer inks

    4. Pharmaceutical Intermediate in API Synthesis

    The diamino-chloro motif in 4-Chloro-1,3-benzenediamine underpins multiple steps in pharmaceutical intermediate routes, including functionalization of small-molecule APIs and chiral catalyst frameworks. Controlled production supports high-purity integration for downstream GMP-compliant operations, targeting both generic and innovative therapeutic molecules.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient manufacturing
    • Ph. Eur. (European Pharmacopoeia) specification for raw materials
    • USP General Chapter <1078> for chemical process intermediates
    • ISO 9001:2015 for quality system operations

    Typical usage ratio

    • Used at 0.4–1.0 molar equivalents depending on the synthetic route and purity grade; ratios tailored based on total conversion requirement at each stage

    Downstream process integration

    • Charged as early-stage intermediate, often involved in catalytic amination, condensation, or building block assembly; followed by isolation, purification, and conversion to advanced intermediates or API core structures

    Final product types

    • API intermediates for anti-infective compounds
    • Key synthesis units for anticancer drug candidates
    • Precursors for neuroactive pharmaceutical agents
    • Ligand frameworks for active catalyst libraries used in chiral drug development

    5. Corrosion Inhibitor Synthesis for Industrial Water Treatment

    The structure of 4-Chloro-1,3-benzenediamine makes it a favored choice in producing organic corrosion inhibitor molecules designed for industrial cooling systems and closed circuit water loops. Its functionality enables formation of strong corrosion-resistant complexes, extending system lifespan under heavy process conditions in power plants and refineries.

    Industry compliance standards

    • ANSI/AWWA B600-22 standard for water treatment chemicals purity
    • ISO 9001:2015 for water treatment product manufacturing
    • REACH registration for corrosion inhibitor actives
    • Applicable national environmental protection regulations (e.g., US EPA 40 CFR 141)

    Typical usage ratio

    • 1.0–5.0% in final inhibitor molecule synthesis; exact percentage adjusted to target inhibitor species and desired field dose rates

    Downstream process integration

    • Reacts as a nucleophile during organic synthesis sequences for corrosion inhibitor production; final product isolated, formulated, and quality-tested before dispatch to end-users

    Final product types

    • Organic corrosion inhibitor actives for closed water systems
    • Additives for cooling tower chemical packages
    • Concentrates for oilfield water management
    • Industrial circulation water treatment blends
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    Certification & Compliance
    More Introduction

    4-Chloro-1,3-Benzenediamine: Built for Consistent Performance

    Anyone in the chemical sector knows how small tweaks in a molecule can make a world of difference down the production line. Over our years manufacturing 4-Chloro-1,3-Benzenediamine, we’ve seen its impact firsthand, particularly in the dyes and pigment industries, specialty polymers, and advanced intermediates. This product, known sometimes by its CAS number 95-83-0, features a benzene ring with both amino and chloro substitutions. The position of those groups shapes its performance, applications, reactivity, and safety handling. We’ve learned that understanding these differences goes a long way toward better products and smoother manufacturing runs.

    What Consistency Adds to Manufacturing Reliability

    On paper, this compound might look similar to other chloro-benzenediamines or even simple phenylenediamines. Once you move from specs to vats and reactors, though, real distinctions appear. Our customers producing advanced dyes rely on this molecule's reactivity, which sits between standard phenylenediamines and more heavily substituted analogues. Too much chlorine and the material stays stubbornly unreactive; too little and you invite side reactions, loss of yield, or even product off-colors.

    In our operations, attention lands squarely on purity. A typical shipment leaves our lines hitting a minimum purity threshold—usually above 99 % by HPLC. Moisture, trace organic byproducts, or variability in raw material quality can amplify issues in downstream synthesis. Impurities might look like minor technical data, but time in the plant has shown they affect both color quality for dyes and polymer properties in resins. Over the years, direct feedback from users has made us tighten controls over the % of isomers present—a minor change that visibly cuts defect rates.

    Physical Characteristics Shape Downstream Uses

    4-Chloro-1,3-Benzenediamine appears as an off-white to light beige solid, often forming fine crystalline powder at room temperature. This seems simple enough, but the way the fine particles behave during mixing and charging to reactors demands attention. Caking, dusting, or uneven blending can lead to downtime or inconsistent batch results. We've worked closely with operators to improve handling. Packing density, particle size control, and storage recommendations all come out of this real-world, plant-level experience. Many plants prefer material packed in polyethylene-lined fiber drums, which reduce moisture ingress and prevent unnecessary handling-related loss or contamination.

    Moisture control means more than just preventing clumping. Absorbed water can alter reactivity, raising the risk of unpredictable yields. In high-precision textile dye production or electronics-grade resin synthesis, this subtle variable means product passes or fails final QA. We invest time not just in drying, but in fast, dry, and protected filling lines that maintain the integrity of every batch.

    Comparisons with Other Benzenediamines

    Practical experience shows why plant and lab teams pick 4-Chloro-1,3-Benzenediamine over alternatives. For example, take 1,4-phenylenediamine—often cited in similar circles. The 4-chloro, 1,3 positioning of amino groups in our product blocks undesired side reactions common in 1,4 or 1,2 analogs. Fewer side products simplify purification, raise yields, and in some applications, lower ash or residue in final materials.

    On the other hand, 2-chloro substitution offers different reactivity, sometimes leading to alternate by-product profiles or slower reaction kinetics. Over time, customers have shared with us that the 4-chloro substitution in the 1,3 positions gives the cleanest results when targeting core chromophore frameworks in dyestuff chemistry or building higher-performance monomers for special polymers. It's the reactivity, selectivity, and cleaner downstream processing that pushes formulators our way after trial runs with related molecules.

    A newer application area—monomer production for specialty coatings—highlights another difference. During oxidative polymerization, 4-Chloro-1,3-Benzenediamine gives polymers with improved chemical resistance compared to those using unsubstituted diamines. Chlorine at this particular ring location appears to discourage crosslinking faults, which boosts durability. That's not a deduction from textbooks; it's based on failed and successful pilot batches our technical team debriefs with end customers.

    Sourcing, Traceability, and Supply Chain Challenges

    On the sourcing side, no factory escapes the ripple effects of raw material volatility. Over the past decade, we’ve weathered supply shocks linked to feedstock changes, regulatory pressure, and global transport bottlenecks. For 4-Chloro-1,3-Benzenediamine, the key feedstock remains aniline or its derivatives, so we maintain diversified procurement contracts with trusted partners. Closely monitoring intermediate prices means less chance of nasty surprises for our downstream users.

    No single producer runs out of challenges. For instance, we've learned to plan ahead for warehousing across seasons, as even small humidity swings can quietly degrade quality. Regular, independent analysis backs up every lot we release, and our commitment to supply-chain traceability translates into detailed batch records available for customer audit. This isn’t just for compliance—it provides assurance. If a plant faces an unexpected yield drop or finished product issue, we can pinpoint potential sources fast.

    Impact on Dye Manufacturing and Performance

    4-Chloro-1,3-Benzenediamine often forms the backbone of azo and anthraquinone dye synthesis. The chloride group helps direct substitution patterns on the aromatic ring, which strongly affects the hue, lightfastness, and wash durability of the final dye. In textile dyehouses, even small shifts in substitution order create costly rework or waste gallons of water. Our process parameters focus on minimal batch-to-batch variation, so dye formulators can count on repeatable performance in their large runs.

    Direct feedback from end users matters. Some of our dye customers run continuous audits and color matching at scale. Failures in shade consistency mean rejected lots, contractual penalties, and wasted resources. By keeping our own test standards aligned with those in their plants, we stay ahead of complaint cycles—solving small issues before they cascade into lost sales.

    An often-overlooked point: the role of trace impurities in downstream dye stability. A few years back, one major customer reported increased fading and irregular chroma in certain high-value red dyes. Working together, we tracked the culprit to sub-ppm levels of isomeric byproducts in the aromatic starting material. After refining our purification process—at no small operational cost—those complaints dropped off. It underscores how tight control at the start means fewer headaches later down the line.

    Role in Specialty Polymers and Coatings

    Beyond colorants, 4-Chloro-1,3-Benzenediamine finds ongoing demand as a chain extender or crosslinker in polymer synthesis. Its chemical structure introduces rigidity and defined electron-donating properties on the aromatic backbone. This translates to enhanced chemical and wear resistance in industrial coatings and engineered plastics. We focus on delivering a granular or powdered product that disperses smoothly in polymer matrices, minimizing hot spots and potential localized degradation.

    Feedback from industrial clients in the coatings sector often points to one in-plant pain point: slow or incomplete curing due to off-ratio mix of reactants. Our technical support teams discuss not only typical assay and moisture results but also suggest optimal addition protocols based on decades of customer-run trials—shortening learning curves and reducing production scrap.

    As advanced composites and specialty elastomers move toward lower-VOC and higher-performance chemistries, the need for reliable, highly pure diamines increases. Not all plants have equal capacity to refine or treat off-standard lots, so we’ve made a point to over-deliver on analytical support. Our batch certificates track minor impurity trends over time, which helps strategic buyers adjust pre-polymer dosing in real time. Attention to these details only comes from deep and regular exchanges with plants whose yields depend on getting the small stuff consistently right.

    Environmental and Safety Commitments Drive Innovation

    Making 4-Chloro-1,3-Benzenediamine safely starts with strict production controls. Aromatic amines—especially those with halogen substituents—pose documented health and safety risks if managed poorly. Following decades of regulatory tightening, we’ve shifted to modern closed-loop systems, with multi-stage scrubbers and dedicated waste treatment lines. Air and water emissions are monitored continuously, and operational teams receive direct, scenario-based safety training.

    Years back, waste chlorinated amine byproducts raised concern for both local regulators and global buyers. We responded with both process redesign and investment in recovery technologies. Now most of our production waste gets repurposed as lower-value intermediates or internal energy sources, instead of leaving our site as treatable hazardous waste. Not every plant reaches zero waste, but the push to recover more material and minimize exposure risks has become integral to our daily work.

    Customer feedback led us to phase in lower-dust formulations and simpler pack formats. A well-sealed drum or bag reduces handling exposures on end-user sites. Shared audits with large accounts—sometimes involving joint process hazard analyses—have driven us further to anticipate problems before they balloon into regulatory headaches or unexpected plant shutdowns.

    Quality Control: Beyond the Certificate of Analysis

    The standard Certificate of Analysis (CoA) forms the bedrock of trust in most chemical transactions, but the numbers only tell part of the story. We believe in tying those numbers back to real-world use conditions. Real certainties come from repeated collaboration with users who share how material performs in their unique setups. Our in-house analytical lab maintains multiple HPLC and GC-MS runs on each batch, but we augment those results with external verification—especially where regulatory bodies demand extra diligence.

    Insight gained from plant feedback loops continues to change how we work. In several markets, requests for lower trace metals prompted us to overhaul filtration protocols and install screening for nickel, cobalt, and copper at previously overlooked points. While old CoAs would have satisfied historical specs, modern buyers expect traceability and transparency throughout the chain.

    Traceability work goes beyond the laboratory. We maintain a living batch record system, tying each lot number back to individual reactor cycles, operator logs, and intermediate reagent sources. In case of any downstream incident—like a sudden spike in off-standard dye lots—we can rapidly reconstruct each variable involved. This traceable, accountable process flow forms a backbone of trust for customers seeking not only regulatory compliance but maximum process predictability.

    Process Improvements and Continuous Learning

    Long-term production of 4-Chloro-1,3-Benzenediamine taught us that no process stays optimal. As new applications emerge—in battery binders, specialty surfactants, or bioactive compounds—the property demands change. We invest in continuous small-scale piloting, often working in parallel with university and client pilot labs. Experience shows that early-stage engagement results in faster scale-up, fewer quality headaches, and better cost control for all involved.

    Recent years brought in more digital monitoring: in-line sensors, batch event logs, and predictive maintenance. Not every technology delivers, but a few have directly cut batch failures. For example, real-time pH and ORP readings in diazotization steps allow us to adjust feed rates before runaway reactions can start. These measures go beyond simple compliance—production stays consistent, and downstream complaints shrink.

    Learning from errors forms another vital tradition. Not every batch hits the mark. Transparent root-cause analysis and published error reports help foster both internal skill development and external trust. Customers value suppliers who admit shortfalls, identify root causes, and close the loop with permanent fixes.

    Future Outlook: Meeting Evolving Demands Together

    Looking ahead, growth in eco-friendly dyes and performance plastics will continue to expand the uses for 4-Chloro-1,3-Benzenediamine. Customers expect not only technical reliability but responsible sourcing and full lifecycle analysis. Our own team tracks regulatory shifts on persistent organic pollutants and advances in biodegradable polymer uses. By staying plugged into these developments—and by listening carefully to customer needs—we aim to stay ahead, not just react.

    Our experience shows real value emerges through dialog over decades, not just at order time. We invite open technical, sourcing, and safety conversations with every customer—new or long-term. No web page can carry the whole story, but these highlights reflect what time in chemicals teaches: details make products, and relationships maintain both performance and progress.

    The Manufacturer’s Perspective: Built from Experience

    From the first reactors years ago to the advanced quality systems in use today, our approach to 4-Chloro-1,3-Benzenediamine has changed with the industries that rely on it. Value doesn’t come from just hitting a spec or delivering a drum—it’s about delivering reliability, consistency, and service at every plant gate. Those qualities don’t show up on a CoA, but they shape everything from pigment vibrancy in clothing to product durability in new polymers. More importantly, they lower risk and support growth for innovators along the value chain.

    Decades of close work with formulating chemists, plant managers, and sourcing professionals convinced us there are no easy substitutes for genuine experience. Through every technical challenge and regulatory change, shared experience with demanding users forged improvements. We do not set out to mimic the field—we learn from it, produce to meet it, and welcome every opportunity to help customers reach higher standards with every kilogram shipped.