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2-Chloro-5-Fluoronitrobenzene

    • Product Name 2-Chloro-5-Fluoronitrobenzene
    • Alias 2-Chloro-5-fluoro-1-nitrobenzene
    • Einecs 223-419-0
    • 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

    158976

    Cas Number 3209-22-1
    Molecular Formula C6H3ClFNO2
    Molecular Weight 175.54
    Iupac Name 2-chloro-5-fluoro-1-nitrobenzene
    Appearance Pale yellow solid
    Melting Point 40-43°C
    Boiling Point 251°C
    Density 1.527 g/cm³
    Solubility In Water Insoluble
    Flash Point 104°C
    Smiles c1cc(F)ccc1N(=O)Cl
    Pubchem Cid 210724
    Synonyms 2-chloro-5-fluoronitrobenzene; 1-chloro-4-fluoro-3-nitrobenzene

    As an accredited 2-Chloro-5-Fluoronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2-Chloro-5-Fluoronitrobenzene, sealed with screw cap, labeled with hazard and identification information.
    Shipping 2-Chloro-5-Fluoronitrobenzene is shipped as a hazardous material. It must be packed in tightly sealed, labeled containers that comply with local and international regulations. During transport, appropriate temperature, ventilation, and protective measures are required to prevent leaks, spills, or exposure. Shipping documentation should indicate hazardous classification and safety instructions.
    Storage 2-Chloro-5-Fluoronitrobenzene should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from direct sunlight, heat, and sources of ignition. Keep away from incompatible substances such as strong acids, bases, and reducing agents. Ensure proper labeling and store separately from food and feed. Use secondary containment to prevent spills or leaks.
    Application of 2-Chloro-5-Fluoronitrobenzene

    Applications of 2-Chloro-5-Fluoronitrobenzene in Industrial Manufacturing

    2-Chloro-5-Fluoronitrobenzene serves as a critical building block in multiple specialty chemical sectors. As a manufacturer, we supply this intermediate for specialized syntheses pursued by agrochemical, pharmaceutical, materials science, and pigment industries. Its unique substitution pattern supports selective downstream reactions, driving value in high-purity, performance-driven end markets.

    1. Crop Protection Active Ingredient Synthesis

    Producers of advanced herbicides and insecticides integrate 2-Chloro-5-Fluoronitrobenzene during key aromatic substitution steps. The molecule’s electron-withdrawing groups permit controlled nucleophilic displacement, crucial for preparing precursor scaffolds in pyridine- and phenoxy-based pesticides. Technical teams use this intermediate when specifying fluorinated aromatic backbones for systemic and contact agents, supporting high selectivity toward target pest species and resilience in field conditions. Our material’s purity minimizes downstream purification burdens, streamlining overall campaign output.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No. 1907/2006
    • Regulation (EC) No 1107/2009 for EU plant protection products

    Typical usage ratio

    • Commonly 0.8–1.2 molar equivalents relative to aromatic ring precursors; ratio adjusted based on final molecule structure and reactivity.

    Downstream process integration

    • Introduced in batch or continuous reactors during halogen exchange, reduction, and amination phases to construct active pesticide intermediates.

    Final product types

    • Herbicide technical concentrates
    • Insecticidal active substances
    • Seed treatment chemical bases
    • Pre-formulated crop protection mixtures

    2. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical manufacturers employ this compound for constructing fluorinated aromatic fragments in active pharmaceutical ingredients, particularly in anti-inflammatory, anti-infective, and oncology candidates. It participates in nucleophilic aromatic substitution and catalytic reduction steps leading to amine or aniline derivatives, which serve as API cores or key side chains. Our manufacturing process ensures low levels of residual impurities — critical for downstream crystallization, chiral resolution, and GMP batch production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. relevant monographs (for intermediates where applicable)
    • 21 CFR Parts 210/211 (cGMP for Finished Pharmaceuticals)
    • EMA Guideline on the Chemistry of Active Substances

    Typical usage ratio

    • Use at 1.0 molar equivalent for substitution or reduction steps, sometimes 1.1–1.3 to drive completion depending on downstream purification strategy.

    Downstream process integration

    • Added during protected aromatic amination/reduction stages and as an electrophilic arene in C-N and C-O coupling reactions within multi-step API synthesis.

    Final product types

    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Fluorinated aromatic cores in kinase inhibitors
    • Precursors for CNS-active pharmaceutical compounds
    • Contract-manufactured active intermediates under GMP control

    3. Specialty Dye and Pigment Synthesis

    Pigment manufacturers select this fluoronitrobenzene as a targeted precursor in synthesizing high-stability azo and anthraquinone dyes. Its dual halogen and nitro substitution pattern allows for precise regiochemical control during diazotization and subsequent coupling steps with amines or phenols, facilitating chromophore design for lightfastness and solvent resistance. Our stringent control of trace contaminants supports high tint strength and consistent shade reproducibility for industrial colorants.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile applications)
    • EN 71-3 Safety of Toys (colorant safety in toys and packaging)
    • ISO 21461:2012 (polycyclic aromatic hydrocarbons in dyes)
    • REACH Annex XVII for restricted chemical substances

    Typical usage ratio

    • Ranges from 0.5–2.0 molar equivalents based on coupling partner and target dye depth; can be varied to control shade and purity.

    Downstream process integration

    • Incorporated in primary diazotization reactions, typically as the electrophilic arene, before azo-coupling or reduction to amine intermediates.

    Final product types

    • Synthetic azo pigments for plastics and coatings
    • High-purity specialty dyes for textiles
    • Industrial color concentrates for printing ink systems
    • Automotive and OEM paint pigments

    4. Advanced Material Monomer and Precursor

    Materials science companies utilize 2-Chloro-5-Fluoronitrobenzene as a functional monomer precursor for engineering specialty polymers, particularly in high-performance coatings, membranes, and electronic material films. The presence of fluorine and nitro substituents offers tailored reactivity for crosslinking and solution processability, supporting tight specifications for dielectric and chemical resistance properties. Our high-conversion product quality enables direct incorporation in solvent-based and melt mixing polymer synthesis platforms.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management System (for advanced polymer synthesis sites)
    • RoHS Directive 2011/65/EU (electronic applications restriction)
    • ASTM D2563–20 for polymer purity and test methods
    • REACH SVHC declaration (for non-hazardous downstream use)

    Typical usage ratio

    • Usually 5%–15% by weight relative to total monomer feed in advanced polymer backbones; optimized according to target mechanical and dielectric properties.

    Downstream process integration

    • Charged during prepolymerization or post-functionalization stages in both batch and continuous reactor formats, with further chemical modification as needed prior to polymerization.

    Final product types

    • Membrane films for separation and filtration
    • Specialty high-durability coatings for electronics
    • Dielectric materials for printed circuit boards
    • Functionalized polymer intermediates for research and development
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    Certification & Compliance
    More Introduction

    Innovating With 2-Chloro-5-Fluoronitrobenzene: A Manufacturing Perspective

    As a direct manufacturer, our relationship with 2-Chloro-5-Fluoronitrobenzene starts at the reactor and extends out to our partners in pharmaceuticals, agrichemicals, and advanced materials. Every kilogram that leaves our plant represents a series of choices—raw material sources, reaction optimization, strict control on impurities, and deep understanding of how this compound makes a difference in modern chemical synthesis.

    Focusing on Quality: Our Manufacturing Approach

    2-Chloro-5-Fluoronitrobenzene carries a unique dual halogen signature—chlorine and fluorine atoms flanking a nitrobenzene ring. What sounds simple has enormous impact. Precision during chlorination and fluorination steps is everything. Inconsistent process control leads to byproduct build-up, unpredictable downstream reactions, and headaches for anyone using this building block to make advanced intermediates. In our production, real-time analytics guide every batch. We manage exotherms, monitor halogen concentrations, and confirm product identity with NMR and GC-MS before release. Experience has taught us there’s no substitute for vigilance, especially when downstream users rely on predictable purity and performance.

    Understanding the Model and Grades

    2-Chloro-5-Fluoronitrobenzene appears in the trade as “5-Fluoro-2-chloronitrobenzene” or by its CAS number: 367-21-5. Our standard model covers high-purity (≥99%) for pharmaceutical and advanced intermediate synthesis, targeting applications where trace contaminants cannot be tolerated. For some agricultural clients, a specification closer to 98% keeps production costs controlled, as their subsequent reactions tolerate trace organics without compromising yield or efficacy. We never compromise on critical ions or volatile impurities. Over the years, it became clear that rigorous quality assurance prevents costly recalls and process halts down the chain. By working directly with our clients' chemists, we learned first-hand that one odd peak in a chromatogram can throw a whole project off schedule. That’s why our lab team reviews every lot, not just for identity, but for subtle signs of side reactions—something off-the-shelf material or generic intermediates rarely deliver.

    Handling and Storage—More Than Just a Warehouse Concern

    Years in this business showed us: not every kilo moves from plant to production line in a day. Shipping to a partner across the continent, or storing raw supplies for longer periods, puts stress on both the product and the supply chain. 2-Chloro-5-Fluoronitrobenzene requires cool, dry, and tightly sealed storage to keep the aromatic ring from slow degradation or contamination. Moisture and heat encourage hydrolysis of the halogens and reduction of the nitro group. We invested heavily in packaging technology—multi-layer drums under nitrogen, anti-static liners, and robust tracking systems enable us to stand behind shelf-life claims with real data. Chemists and plant managers who have seen the fallout from degraded intermediates know that small lapses in storage quickly become big problems in yield, quality, or downstream worker safety. We saw early on that transparency about shelf life, packaging integrity, and routine testing before shipment makes a real difference in operational reliability for every facility that relies on our material.

    Application Insights: Bridging R&D and Industrial Scale

    Our involvement doesn’t end at the drum door. 2-Chloro-5-Fluoronitrobenzene earns its keep in Suzuki couplings, aromatic substitution reactions, and as a tailored precursor for sulfonamides and fluorinated aromatic drugs. The presence of both chlorine and fluorine brings flexibility and selectivity. In nitroaromatic chemistry, those electron-withdrawing groups on the ring make it a selective partner in nucleophilic aromatic substitution (SNAr) and metal-catalyzed cross-couplings. Our feedback loop with pharmaceutical processors showed us that the difference between a successful scale-up and a stalled pipeline often hangs on consistent reactivity—not only purity, but tight specification of isomer ratios, known impurity profiles, and batch-to-batch reproducibility. In real client cases, featureless literature-grade samples failed to deliver comparable yields to our high-specification batches, underscoring for us that “purity” isn’t a number alone—it is about process transparency, repeatability, and a robust set of analytical controls. Big investments in QA, traceability, and process feedback allowed us to support innovators scaling an R&D process to pilot or full-scale manufacture. We saw our partners succeed when they stopped worrying about their starting materials and focused on real innovation at the target molecule stage.

    Comparisons With Related Halonitrobenzenes

    We have produced a full range of halonitrobenzene derivatives—monofluoro, mono-chloro, and various mixed halogen analogs. Minor changes in the halogen pattern bring major shifts in reactivity, solubility, and downstream process compatibility. Direct clients noticed that 2-Chloro-5-Fluoronitrobenzene, compared to its mono-substituted relatives, grants a way to fine-tune intermediate formation and side reactions. In some cases, dropping the chlorine improves solubility and speeds up certain nucleophilic reactions, but sacrifices selectivity and may boost unwanted reduction pathways in complex molecule synthesis. On the other hand, dual-halogenated intermediates often reduce waste, lower catalyst spend, or permit milder conditions in couplings. The right choice always depends on the precise downstream chemistry, but our experience building dozens of related compounds allows us to steer project teams toward the right material—sometimes suggesting a switch after joint analysis of step yields, isolation challenges, and waste generation.

    Another important distinction comes from impurity carryover. Many common suppliers chase bulk volume above all, meaning higher levels of regioisomeric contamination and ring-halogen scrambling, both of which can confuse downstream functionalization steps or cross-couplings. By keeping synthesis routes optimized and limiting time at elevated temperatures, we control these issues from the start. Talking directly with medicinal chemists using our product, we learned that seemingly “small” contaminants actually poison Pd or Ni catalysts or lead to hard-to-separate byproducts. The devil hides in the details, so we built our process around ultra-clean conditions, timely quenching, and rapid-to-analysis sampling. That way, we can confidently advise technical staff in the field: if you’re seeing capricious reaction behavior, start by checking upstream raw material purity and let’s discuss ways to close these gaps together.

    Safety, Sustainability, and the Modern Chemical Supply Chain

    Handling nitroaromatics is never a casual task. Our operators work in enclosed, ventilated systems, and we rigorously track waste. Knowledge from two decades of plant improvements shapes our protocol: not only minimizing operator exposure and environmental emissions, but streamlining workflows to reduce energy and solvent demand at every step. Our plant operates in a region with strong environmental oversight, and we adopted closed-loop waste capture and off-gas scrubbing from early on. Experience has shown that long-term partners care deeply about this—trace organics leaving the site become tomorrow's liabilities or regulatory headaches. Stories across the industry reinforce this point. Companies that cut corners on waste or ignore best practices wind up facing not only fines, but also brand damage and loss of supplier trust. By investing up front in robust abatement and closed-system handling, we minimize risks for everyone downstream.

    On the sustainability front, halogenated nitrobenzenes raise real concerns. Sourcing fluorinated feedstocks responsibly, ensuring byproducts don’t leave the plant uncontrolled, and continuously reviewing solvent selection makes a difference both for compliance and for stewardship. We spent years replacing high-toxicity solvents in favor of cleaner options, investing in energy recovery, and recycling every possible process stream.

    Supporting Innovation: Working Directly With Users

    Making 2-Chloro-5-Fluoronitrobenzene at industrial scale opened our eyes to the shifts in end-use innovation each year. From medicinal chemistry—where a halogen arrangement can dictate selectivity, stability, or side-chain attachment points—to materials science research into smart polymers or specialty electronics, our job goes beyond “product supply.” Most of our advances came from listening to technical teams, both at established firms and startups pushing boundaries. We have seen breakthrough drugs hinge on using this aromatic platform as a core building block. On the materials side, certain clients pushed us to develop ultra-low moisture grades and define new specifications that did not exist before. Every year brings new requests—sometimes for tighter particle size control, sometimes for blends with other intermediates to cut handling costs, sometimes for custom blend packaging to speed up pilot scale tests. Our ability to act quickly, to run pilot batches and customize specs, sets us apart from major traders working at arm’s length.

    In several projects, a new synthetic step or novel catalytic system demanded only the purest dual-halogen profile. We joined forces to tweak process parameters, pilot new purification techniques, and even help design analytical workflows so that the receiving lab could monitor their key performance indicators easily. This hands-on technical partnership means less guesswork, smoother technology transfer, and more robust intellectual property protection for teams working at the cutting edge.

    Looking Forward: Real-World Challenges and Solutions

    Sourcing specialist intermediates such as 2-Chloro-5-Fluoronitrobenzene demands more than just a purchase order and an MSDS sheet. Users want confidence in continuity and consistency, especially as regulatory eyes tighten globally. We weathered disruptions in fluorine raw materials during global transport disruptions. We built up regional partnerships for supply-chain resilience, going so far as qualifying multiple raw suppliers and keeping buffer stocks despite rising warehouse costs. Forecasting demand is part fact, part gut-feel, and learning from direct dialog with each technical buyer in real-time keeps us ahead of the curve. COVID-era volatility drove this point home for us: plants that plan for disruption last longest, and customers who value partnership, not just price, keep their lines running when the commodity market stalls.

    As regulations change—beyond REACH and GHS, broader environmental and safety overlays—having a direct line to the synthesis and analytics teams upstream gives our partners a real edge. Emerging requirements around halogen content in waste, permitted emissions, and new limits on persistent organic pollutants shifted our internal targets well ahead of compliance deadlines. We built audit trails for each batch, real-time certification datasheets, and line-by-line impurity logs available to our clients, because audit-readiness can swing contracts in moments where supply chains are stretched thin and trust becomes currency. Every time our partners sail through an inspection, we see tangible proof that working directly with the manufacturer, not a middleman, changes outcomes at the ground level.

    In Practice: Partnership, Know-how, and Reliable Delivery

    Decades of manufacturing 2-Chloro-5-Fluoronitrobenzene taught us that true value lies in understanding needs, not just filling orders. We have met researchers who needed near-zero moisture content for a critical coupling, and process engineers struggling to separate close-boiling impurities on pilot scale. We sat with teams troubleshooting byproduct formation, leveraging our on-site analytical resources and production know-how to resolve issues in days, not weeks. In close collaboration, several clients gained efficiencies by adjusting reagent order or optimizing quenching steps in their process, possible only because of our real-world feedback, not theoretical knowledge from afar.

    The chemical industry marches forward on precision, reliability, and respect for the role each intermediate plays. By focusing on direct relationships, transparent, data-driven manufacturing, and a commitment to supporting innovators, we saw our 2-Chloro-5-Fluoronitrobenzene become more than just a reagent. It became part of the solution for advanced pharmaceuticals, crop protection molecules, specialty materials, and beyond. Looking ahead, we stand ready to share our experience, tackle tomorrow’s challenges, and fuel the discoveries our partners will invent with this versatile intermediate, batch by carefully engineered batch.