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4-Chloro-3-Nitropyridine

    • Product Name 4-Chloro-3-Nitropyridine
    • Alias 4-chloro-3-nitro-pyridine
    • Einecs 629-08-3
    • 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

    987251

    Chemical Name 4-Chloro-3-Nitropyridine
    Molecular Formula C5H3ClN2O2
    Molecular Weight 158.55 g/mol
    Cas Number 5470-19-5
    Appearance Yellow to brown solid
    Melting Point 76-80°C
    Density 1.53 g/cm³ (estimated)
    Solubility In Water Slightly soluble
    Smiles C1=CN=CC(=C1[N+](=O)[O-])Cl
    Inchi InChI=1S/C5H3ClN2O2/c6-4-1-2-7-3-5(4)8(9)10/h1-3H
    Pubchem Cid 10682163

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

    Packing & Storage
    Packing Amber glass bottle labeled "4-Chloro-3-Nitropyridine, 25g" with hazard symbols, CAS number, batch info, tightly sealed screw cap.
    Shipping 4-Chloro-3-nitropyridine is shipped in tightly sealed containers to prevent moisture and air exposure. It is classified as a hazardous chemical, requiring appropriate labeling and documentation. Transport must comply with local and international regulations for hazardous materials, ensuring safe handling and storage to prevent spillage, contamination, or accidental release during transit.
    Storage 4-Chloro-3-nitropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing or reducing agents. Protect it from moisture, direct sunlight, and sources of ignition. Clearly label the storage container, and ensure access is limited to trained personnel. Use appropriate secondary containment to prevent spills.
    Application of 4-Chloro-3-Nitropyridine

    Applications of 4-Chloro-3-Nitropyridine in Industrial Manufacturing

    4-Chloro-3-Nitropyridine serves as a critical intermediate in several advanced industrial sectors, supporting the synthesis of specialized compounds where stringent compliance, precise formulation dosing, and proven process integration define every manufacturing stage. Our expertise in large-scale production guarantees consistent supply and reliable quality for your validated downstream formulations. Below, we detail the core application scenarios where this raw material anchors modern product portfolios.

    1. Agrochemical Intermediate for Pyridine-Based Herbicides

    Downstream producers use 4-Chloro-3-Nitropyridine in synthesizing selective herbicides based on pyridine scaffolds, delivering targeted crop protection agents. In this pathway, the intermediate integrates via nucleophilic aromatic substitution, followed by further functionalization steps, aligning with evolving regulation on pesticide residues and manufacturing traceability. Adjustments in loading levels depend on the specific herbicide precursor being targeted and reactor scale. Finished plant protection products must pass rigorous ecotoxicological and crop safety assessments prior to commercialization.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • European Union Regulation (EC) No 1107/2009
    • US EPA Pesticide Registration Requirements
    • ISO 9001 Quality Management Systems

    Typical usage ratio

    • Ranges from 0.8 to 1.1 molar equivalents per target pyridine-based herbicide precursor, adjusted based on intended selectivity and production yield optimization studies

    Downstream process integration

    • Introduced during the aromatic substitution step; integrated under controlled temperature and solvent conditions to ensure full conversion before further cyclization or derivatization

    Final product types

    • Post-emergence herbicide concentrates
    • Premix granules for broadleaf weed control
    • Selective herbicide formulations for sugar beet and cereal crops

    2. Pharmaceutical Intermediate in Active Ingredient Synthesis

    This compound is regularly specified as a halogenated pyridine source during the construction of drug molecules targeting central nervous system and anti-infective therapies. Downstream plants employ it in sequential nitration, reduction, or substitution reactions to access key intermediates conforming to current good manufacturing practice (cGMP). The precise ratio varies with the synthetic route, and every batch is documented to global pharmacopoeial and regulatory filing standards. Final APIs undergo thorough characterization, with all impurities and by-products traced to the original lot materials.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • FDA and EMA Drug Master File (DMF) Registration Procedures

    Typical usage ratio

    • Typically 1.0 equivalent per target API intermediate; stoichiometry finely tuned based on process validation and impurity profile requirements

    Downstream process integration

    • Fed as a controlled reagent into the pyridine nucleus assembly stage, accompanied by real-time analytical monitoring to ensure complete conversion and minimal side product formation

    Final product types

    • API intermediates for CNS-active agents (e.g., epilepsy, depression drugs)
    • Building blocks for fluoroquinolone antibiotics
    • Intermediates for anti-infective injectable drugs

    3. Dye Intermediate for Specialty Pigment Synthesis

    Producers in the colorant industry utilize this compound for constructing nitrogen-containing heterocyclic dyes, especially those targeting high fastness requirements. Its high reactivity profile enables effective coupling in the early stages of pigment condensation, imparting durability and light stability to the final dye structure. Usage quantities are selected according to the chromophore design and the presence of auxiliary coupling components, and all pigment batches are scrutinized under stringent product safety and workplace exposure directives.

    Industry compliance standards

    • REACH (EC 1907/2006) Annex XVII for hazardous substance registration
    • ISO 6503 Textile Colorfastness Testing
    • Oeko-Tex Standard 100 for textiles safety
    • EN 71-3 Safety of Toys migration standards (where relevant)

    Typical usage ratio

    • 0.5–1.2 equivalents per mole of coupling agent; the precise value set by target hue and batch scale optimization

    Downstream process integration

    • Dosed during the initial pyridine chromophore ring construction; timing and sequence are strictly defined to secure pigment granule homogeneity and defect-free molecular structure

    Final product types

    • High-stability textile dyes
    • Plastic-compatible pigments for engineering resins
    • Specialty inks for industrial printing applications

    4. Advanced Material Modifier for Electronic Chemical Synthesis

    In the electronics industry, this intermediate becomes critical in the preparation of functionalized pyridine-based molecules for display and printed circuit board (PCB) materials. It participates in halogen-exchange and controlled substitution to yield custom heterocyclic electron transport agents and charge modification additives. The working dose is closely regulated according to polymer blend ratio or surface treatment design, and the integration sequence is aligned with sector-specific reliability and purity benchmarks to avoid conductivity defects.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IPC-4101B Specification for Base Materials for Rigid and Multilayer PCBs
    • UL 94 Flammability Classification
    • ISO 14001 Environmental Management System (for chemical handling)

    Typical usage ratio

    • Employed at 0.1–0.5% w/w of total blend for charge modification additives; adjusted based on required electronic performance parameters and purity mandates

    Downstream process integration

    • Added at the pre-polymerization or resin compounding stage within inert-atmosphere reactors; sequencing and mixing speeds are specified to ensure defect-free dispersion in electronic-grade material matrices

    Final product types

    • High-frequency PCB boards
    • OLED and display panel conductive layers
    • Semiconductor process auxiliaries
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    Certification & Compliance
    More Introduction

    Introducing 4-Chloro-3-Nitropyridine: A Reliable Choice in Fine Chemical Manufacturing

    Understanding the Value of 4-Chloro-3-Nitropyridine in Chemical Synthesis

    Over the years, we have made various pyridine derivatives, but 4-Chloro-3-Nitropyridine stands out for its stability and reactivity in targeted transformations. Our team specializes in developing synthesis pathways that use this compound as a versatile intermediate. In daily operations, companies in the pharmaceutical, agrochemical, and material science sectors rely on this compound's consistent performance. The difference it makes in downstream products stems from a well-tuned chlorination and nitration process refined through repeated scale-up and optimization.

    We produce 4-Chloro-3-Nitropyridine under strictly controlled manufacturing conditions, beginning with a high-purity pyridine core and precise reaction steps. This approach minimizes unwanted byproducts. Each batch consistently demonstrates narrow product distribution, a result of both process engineering and decades of technical refinement. After synthesis, our purification methods—developed through feedback and pilot data—secure a crystalline product with reliable handling properties. This helps downstream users avoid complications in their own processes that can arise from batch-to-batch inconsistencies.

    Product Model and Characteristics

    Commercial quantities of our 4-Chloro-3-Nitropyridine typically match CAS number 2297-85-6, offered in bulk crystalline form or smaller packs for R&D use. Our most common lot sizes match the demands of process development and large-scale active pharmaceutical ingredient campaigns—these logistical arrangements come from direct conversations with clients facing real production targets.

    Specifications matter, especially because customers use this chemical for applications sensitive to trace metal content or unwanted halogenated pyridines. Each lot undergoes a full suite of analytical checks, including HPLC, GC, and titration, to verify that both assay and impurity levels stay well within the acceptable limits for scalable synthesis. Over years of practical shipments, we found that water content can affect downstream reactivity, so we package with moisture-barrier materials and monitor for residual solvents and loss on drying. During method development, we consult closely with users optimizing reaction conditions such as nucleophilic substitution or Buchwald–Hartwig coupling, since reaction outcomes often hinge on small impurity differences.

    Applications Across Industries

    In the past decade, research teams working on pharmaceutical building blocks have adopted 4-Chloro-3-Nitropyridine for selective coupling reactions, particularly where regioselectivity and halide activation patterns control the next synthetic step. We also hear from agricultural chemistry labs scaling up new crop protection agents who need consistent chlorinated pyridines for their synthetic strategy. For these customers, known impurity profiles reduce the number of unexpected downstream products and can ease regulatory submissions by preventing unidentified process impurities.

    4-Chloro-3-Nitropyridine also patches a gap in certain dye and material applications. Some clients use it to introduce nitro or chloro functionality into heterocycles, which add specific optical properties or electron-withdrawing characteristics to the target molecule. Our experience tells us that switching from unstable or impure intermediates delays both scale-up and commercial launch, so specifying solidly validated intermediates speeds up new product introduction. Consistent product form—typically off-white or light yellow crystalline solid—not only eases transfer but also signals process adherence.

    Key Differences from Other Pyridine Derivatives

    We see important distinctions between 4-Chloro-3-Nitropyridine and related products in daily plant operations and customer feedback sessions. The location of both the chloro and nitro group on the pyridine ring offers distinct advantages over mono-substituted pyridines or isomeric nitro compounds. Our process chemists report that the 4-chloro position often reacts more cleanly in nucleophilic aromatic substitution, freeing up synthetic strategies not possible with pyridine rings bearing the nitro substituent in other positions. Nitro group placement at the 3-position tunes electron density, which helps partners design more selective coupling routes. In comparison, 2-chloro- or 3-chloro-nitropyridines often present different reactivity, with less predictable byproducts or lower product yields.

    In customer troubleshooting calls, we find that switching to this isomer solves issues caused by ortho substitution, which can interfere with metal-catalyzed reactions. Substitution patterns in pyridines often control crystal habit, which in turn affects handling and shelf life. Over time, our lab and plant technicians have evaluated storage and application data, limiting exposure to moisture and light, since certain pyridines degrade or discolor more rapidly. Our supply-chain teams relay these stability data to regular customers, helping them match storage protocols to real-world shipping conditions.

    Meeting High-Purity Demands with Reproducibility

    In practice, our 4-Chloro-3-Nitropyridine process balances synthetic throughput and impurity control. Fine-tuning reaction times and temperatures can shift selectivity, and our operators run regular analytical tests to make sure each batch meets set criteria. No process runs perfectly forever; we spot unwanted byproducts or color changes early through in-process analysis, then feedback those results into daily operation meetings. Years of batch records and customer usage reports guide our specifications, rather than arbitrary or generic guidelines. Product performance in catalytic couplings or direct functionalizations drives which lot acceptance criteria matter most.

    Teams developing APIs request detailed impurity documentation, so we retain thorough analytical records and offer support for method adaptation or validation. Our R&D chemists have run the compound through reaction sequences like Suzuki, Sonogashira, and Stille couplings, supplying customer technical teams with step-by-step data. In practice, chemists synthesizing complex heterocycles or fused ring systems require predictable results across kilo- and ton-scale lots. We keep archives of batch recovery, yield, and waste stream composition, not only for process control but also for environmental and regulatory audits. Our long-term partners appreciate this proactive transparency, as it reduces both risk and regulatory rework.

    Handling, Storage, and Safety Built on Experience

    Years in production have taught us that every aspect of a nitro- and chloro-containing pyridine needs close monitoring. We train staff to respect the hazards—these compounds demand proper PPE, fume extraction, and storage away from reducing agents. Real-world incidents, including spills or thermal runaways, prompt regular review of packing protocols and emergency drills. Our warehouses store the product in clearly labeled, robust containers, supported by climate control where elevated summer temperatures risk softening plastics or caking the solid. Clients rely on packaged lots that survive multi-continent transport, so we design packaging for vibration and moisture control, not only for shelf stability but to avoid safety incidents caused by bin rupture or overpressure.

    Throughout the years, regulators worldwide have tightened shipping rules for nitro- and halogenated aromatics. We consult regularly with both shipping partners and hazardous material experts, adjusting labeling and documentation packages. Customers leverage our experience to draft or update their own risk protocols and train their handlers. The more we share hands-on storage and transport data, the fewer delivery issues our partners face, reducing both costly delays and incident risk. This results in fewer rejected lots and a tighter overall supply chain.

    Supporting Upstream Innovation

    Over years of customer interaction and in-house development, we have seen 4-Chloro-3-Nitropyridine catalyze research in medicinal chemistry, pest control, and electronics. In-house formulation teams often share breakthroughs made possible by the confident use of this stable, well-characterized intermediate. Many key breakthroughs stem from having a dependable starting point for new synthetic routes. Teams building libraries of new small molecules for screening often trace reliable reaction yields to pure, well-handled intermediates.

    For projects constrained by process time, access to a ready supply of 4-Chloro-3-Nitropyridine often makes the difference between missing and meeting a project milestone. Over the years, we have worked with purchasing staff who learned firsthand the pain of batch delays from off-spec materials. In the past, chemists sometimes accepted mixed-source intermediates and ended up redoing multistep syntheses—valuable time lost. Our process data and customer feedback show that consistent supplier relationships and in-depth quality data keep these projects on track and within budget.

    Environmental Stewardship and Regulatory Perspective

    Our focus on nitro- and halo-pyridine synthesis aligns with modern calls for cleaner technology. Traditional routes to 4-Chloro-3-Nitropyridine sometimes led to excess acid effluent or nitrophenolic waste, which could challenge local discharge regulations. Our environmental and process engineers adjust reaction workups with solvent recoveries, closed-reactor systems, and selective crystallization. Batch documentation includes steps to minimize waste and control vented organics. We take regulatory shifts seriously, adapting plant and supply protocols as new guidance emerges, drawing on lessons learned from compliance drives in China, India, Europe, and North America.

    For many customers, a strong compliance and documentation record isn’t just about meeting internal standards—it speeds up product registration and market approval. The more complete our impurity and trace metal profiling, the fewer questions arise from pharmacopoeia submissions or new chemical notifications. We keep up with changing regulatory lists and actively test for emerging contaminants flagged by authorities. These efforts cut down on last-minute scrambling to meet certificate requirements or address unforeseen inspection questions. Our site audits, conducted by both third-party and customer teams, routinely review handling logs, chemical traceability, and staff training—building trust through repeated, documented performance.

    Collaboration With Downstream Partners

    The complexity of scale-up chemical manufacturing doesn’t stop with finished product. We have close working relationships with technical teams at many major downstream manufacturers. Sharing pilot data for reaction conditions, hydrogenation studies, and impurity fate streamlines the adoption of 4-Chloro-3-Nitropyridine in new synthetic routes. Shared troubleshooting has led to innovations in filtration, storage, and secondary process optimization. This responsive feedback cycle is just as important to the advancement of chemistry as any single spectral certificate or product spec sheet.

    We encourage customer site visits, virtual audits, and method review sessions. Direct feedback has improved not only our physical product but also the service and documentation that comes with it. Site-specific handling guides—created with input from scale-up and pilot operators—highlight potential mixing pitfalls, safety interlocks, or side reaction risks that generic guides overlook. Our teams remain flexible, open to process adaptation or packing modifications shaped by real-world needs, not abstract process theory.

    Instrumental Role in Modern Chemistry

    4-Chloro-3-Nitropyridine often goes unnoticed outside research or process chemistry circles, yet its presence weaves through many end-use products and research milestones. In pharmaceutical development, it speeds up route scouting by opening new reaction channels and enables diversification by providing a robust point for further functionalization. By learning from hundreds of pilot campaigns, we’ve tailored production to better support chiral ligand synthesis, anti-infective projects, and advanced materials. This role stems from careful attention to both purity and supply reliability, creating a multiplier effect in our partners’ R&D and commercial projects.

    Clients developing agrochemical actives tell us that well-characterized pyridine intermediates can mean faster registration and reduced regulatory friction. Whether supporting a fast-moving startup or a large multinational, we align shipping windows, batch documentation, and impurity data to meet evolving demands. Success in late-stage project scale-up today reflects preparation and continuous improvement built into our supply network and plant routines. We respond directly to each market’s shifting technical requirements, bringing lessons from one industry vertical to benefit the next.

    Continual Improvement Through Real-World Experience

    No chemical production process remains static, especially at the specialty level. Every campaign teaches new lessons—about seasonal solvent purity shifts, impacts of raw material changes, and the need for nimble logistics. We draw on both seasoned plant technicians and actively publishing chemists to identify improvement points. If a persistent impurity slows down a customer’s process, we build trial production runs to test modified crystallization or post-processing. Over years of requalifications and market expansions, we’ve invested in analytical upgrades and new reactor automation with one clear aim: deliver the robust, reproducible intermediate that modern chemistry demands.

    The challenge of consistent supply and application of 4-Chloro-3-Nitropyridine reflects the complexity of fine chemical manufacturing as a whole. Our daily commitment, from plant operator to quality engineer to shipping agent, revolves around one core value—reliable support of our partners’ innovation. Every improvement in packaging, purity, or documentation translates downstream, shortening project cycles and safeguarding both products and people. Our work with this unique pyridine derivative continues to teach us that excellence in intermediate production builds the foundation for new discoveries, strong customer trust, and long-term chemical industry progress.