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5-Chloro-4-Fluoro-2-Nitroaniline

    • Product Name 5-Chloro-4-Fluoro-2-Nitroaniline
    • Alias 5-chloro-4-fluoro-2-nitrobenzenamine
    • Einecs 629-022-6
    • 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
    VTB
    Specifications

    HS Code

    846080

    Product Name 5-Chloro-4-Fluoro-2-Nitroaniline
    Cas Number 1072951-16-4
    Molecular Formula C6H3ClFN3O2
    Molecular Weight 191.55 g/mol
    Appearance Light yellow solid
    Solubility Slightly soluble in organic solvents
    Purity Typically ≥98%
    Synonyms 2-Nitro-5-chloro-4-fluoroaniline
    Smiles Nc1cc([N+](=O)[O-])c(F)cc1Cl
    Inchi InChI=1S/C6H3ClFN2O2/c7-3-1-4(8)6(10(11)12)2-5(3)9/h1-2H,9H2
    Storage Temperature Store at room temperature

    As an accredited 5-Chloro-4-Fluoro-2-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed amber glass bottle containing 25 grams. Label displays compound name, CAS number, and hazard warnings.
    Shipping 5-Chloro-4-Fluoro-2-Nitroaniline is shipped in tightly sealed containers, compliant with hazardous material regulations. It should be packed to prevent leaks, clearly labeled, and accompanied by a Safety Data Sheet. Transport is via licensed carriers, with temperature and moisture control, and adherence to all relevant local, national, and international shipping requirements.
    Storage 5-Chloro-4-fluoro-2-nitroaniline should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers and acids. Keep the container tightly closed and protected from light. Use only in chemical fume hoods. Properly label all containers and follow standard laboratory safety protocols for handling hazardous chemicals.
    Application of 5-Chloro-4-Fluoro-2-Nitroaniline

    Applications of 5-Chloro-4-Fluoro-2-Nitroaniline in Industrial Manufacturing

    As a specialized manufacturer of 5-Chloro-4-Fluoro-2-Nitroaniline, we partner with downstream producers in several key fields leveraging this intermediate for precise performance and regulatory needs. Its unique halogen-nitro aromatic profile enables specific technical applications where molecular selectivity and purity are mission-critical. The following scenarios illustrate major, real-world use cases, with each process structured to industry-specific requirements, handling, and quality criteria.

    1. Agrochemical Active Ingredient Synthesis

    Crop protection manufacturers employ this intermediate as a crucial building block in downstream synthesis of select herbicide molecules. The compound’s halogen and nitro functionalities enable high-yield coupling reactions, supporting the construction of heterocyclic scaffolds in modern agricultural actives. Precise integrating during early synthesis stages ensures targeted molecular structure, color, and purity parameters for field-ready formulations.

    Industry compliance standards

    • FAO/WHO specifications for technical grade agrochemical actives
    • ISO 9001 for chemical manufacturing quality
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • REACH registration for raw material tracking and hazard communication

    Typical usage ratio

    • 15–25% by molar calculation in initial heterocycle formation; precise loading determined by stoichiometric design and target molecule requirements

    Downstream process integration

    • Feedstock in step-one aromatic amination; enters condensation or nucleophilic substitution for intermediate ring construction prior to final active processing

    Final product types

    • Formulated herbicides for cereal and broadleaf crops
    • Pre-emergent and post-emergent weed control agents
    • Active ingredient concentrates for regional agrochemical markets

    2. Pharmaceutical Intermediate Production

    Our material serves the pharmaceutical sector as a core intermediate in the synthesis of select API precursors, especially fluorinated and chlorinated aromatic amine scaffolds. This specialty aromatic is routinely utilized in the formation of heterocyclic motifs prominent in modern antihypertensives and anti-infectives, with full compliance to GMP controls and clean room protocols for impurity traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs on related substance limits
    • US FDA cGMP (21 CFR Parts 210 & 211) for pharmaceutical intermediate production
    • Traceability in line with Drug Master File (DMF) registration

    Typical usage ratio

    • 5–12% by mass in batch synthesis, tuned based on target molecular structure and yield profiles of the downstream API process

    Downstream process integration

    • Charged in aromatic substitution stage, often as the first halogenated aniline input, upstream of cyclization to form heteroaromatic rings for API synthesis

    Final product types

    • Pharmaceutical intermediate batches for antihypertensive and anti-infective agents
    • Precursor stock solutions for finished API production
    • Reference standards for regulated finished dosage manufacturing

    3. Dye and Pigment Intermediate Manufacturing

    Specialty dye and pigment producers select this raw material to introduce specific electron-withdrawing groups, enhancing lightfastness and functional color performance. Its nitro and halogen functionalities enable tailored azo and anthraquinone colorant formation, with particular relevance in organic pigments for plastics, coatings, and print ink applications, subject to sector-specific ecolabel and migration criteria.

    Industry compliance standards

    • EN 71-3:2019 Safety of toys – Migration of certain elements (applicable to colorants in plastic/dye end uses)
    • ISO 9001 certified pigment synthesis
    • RoHS 2011/65/EU directive for hazardous substances in electronics and plastics
    • OEKO-TEX Standard 100 for restricted substances in textile dyestuffs

    Typical usage ratio

    • 8–20% by weight relative to primary aromatic amine feedstock; adjustable according to desired chromatic intensity and shade specificity in target dye molecule

    Downstream process integration

    • Engaged in diazotization-condensation steps leading to azo dye coupling, or introduced in nucleophilic aromatic substitution for direct pigment scaffold assembly

    Final product types

    • Azo and anthraquinone dyes for plastics and synthetic fibers
    • Pigments for automotive and industrial coatings
    • Organically tinted inks for printing applications

    4. Specialty Chemical Synthesis for Electronic Materials

    This compound plays a strategic role as a fine chemical intermediate in advanced electronics material synthesis, particularly for photoresist and semiconductor coating formulation. The unique halogen-nitro pattern supports synthesis of electron-acceptor units, facilitating the manufacture of high-purity intermediates for functionalized monomers deployed in microelectronics and optoelectronic devices.

    Industry compliance standards

    • SEMI C45 for electronic chemical purity
    • ISO 9001 quality management for specialty electronics chemicals
    • IEC 62474 Declarable Substances List compliance for electronic sector supply chain
    • RoHS and REACH SVHC screening for hazardous substance control

    Typical usage ratio

    • 2–9% by mol in photopolymer resin recipes; adjusted to meet polymerization kinetics and electrical performance specifications of end substrates

    Downstream process integration

    • Feeding into condensation or substitution reactions for functionalized monomer or polymer precursor synthesis prior to final resin or coating formulation

    Final product types

    • Photoresist materials for semiconductor lithography
    • High-purity polymer intermediates for OLED and TFT applications
    • Electronic-grade specialty coatings for chip and display fabrication

    5. Fluorinated Building Block for Veterinary Chemical Synthesis

    Producers of veterinary pharmaceuticals utilize this intermediate as a source of both fluorine and chlorine functionality in complex agro-vet actives. The material's functional group arrangement makes it valuable for molecular frameworks requiring selective halogenation, a critical attribute for next-generation ectoparasiticides and antimicrobial agents manufactured under stringent animal safety guidelines.

    Industry compliance standards

    • VICH GL10 GMP for active pharmaceutical ingredients used in veterinary medicinal products
    • EC Regulation 2019/6 on veterinary pharmaceuticals
    • USP and Ph. Eur. reference testing for raw material characterization
    • ISO 9001:2015 manufacturing oversight

    Typical usage ratio

    • 6–14% by mass in multistep bulk synthesis; range determined by yield considerations of specific animal health APIs under development

    Downstream process integration

    • Initiates the sequence for halogenated aromatic construction, serving as the feed molecule for macrocyclization or ring-closure steps unique to veterinary chemical synthesis

    Final product types

    • Veterinary ectoparasiticide actives for livestock and companion animals
    • Intermediate stock for injectable and oral veterinary pharmaceutical forms
    • Antimicrobial aromatic compounds for topical animal care applications
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    Certification & Compliance
    More Introduction

    5-Chloro-4-Fluoro-2-Nitroaniline: Practical Insights from the Factory Floor

    Straight from the Plant: What Stands Out About This Molecule

    In our production workshops, 5-Chloro-4-Fluoro-2-Nitroaniline draws steady interest from downstream users seeking reliable and clean intermediates for applications demanding strong performance under strict conditions. We put years into tightening our synthesis workflows. From how reagents hit the vessels to how we monitor every batch, we work under direct feedback from customers who see both the benefits and the pain points when even trace contaminants make it into their end use. This compound, often referred to by its catalog model 255445-51-5, continues to be a core offering because it bridges what we see in upstream chemistry with what our users want out of downstream product consistency.

    Out here at the plant, we learned early that tight control over halogenation and nitration reactions matters more than the lab books might admit. Even milligram-level deviance changes how customers handle purification, impacts downstream conversion costs, and narrows process windows on their lines. 5-Chloro-4-Fluoro-2-Nitroaniline poses some unique hurdles in achieving that balance between reactivity and stability, given its dual halogen substitutions on the aromatic ring. Yet, those same properties offer a versatile gateway for building blocks across agricultural, material science, and pharmaceutical fields. Our operators don’t chase theoretical yields for a trophy; they fine-tune based on observed crystallization trends, color, moisture pickup, and purity feedback from real-world process engineers who push hard for cost per kilogram and smooth runs on their own assets.

    Specifications That Matter Beyond the Certificate

    You’ll see specifications everywhere—sometimes it looks like a numbers game. But technical teams today cut straight to how these numbers hold up under real pressure. Our 5-Chloro-4-Fluoro-2-Nitroaniline outputs run between 98.5% and 99.2% HPLC area purity, with isomer impurities kept low enough that few surprise events crop up once customers move to their own reactor set-ups. Melting points sit consistently within the 126–129°C range, confirming batch-to-batch reproducibility. Water content, always measured by Karl Fischer, trends below 0.2% because we run tailored nitrogen blanketing and fast filtration after precipitation. These controls emerged through repeated dialog with our most demanding partners. The final product comes as a pale yellow to yellow crystalline powder, with dusting minimized through controlled milling. Plant-floor workers watch for subtle changes in flow—routine details, but ones that build direct trust between floor and user.

    What matters most to our regular clients isn’t a piece of paper, but the outcome: no off-odors, no unexpected decomposition, and particle sizing that feeds downstream reaction vessels smoothly. We take multi-spot sampling during final drum filling, because uneven packing or trace residual solvents introduce real costs for others in the chain. It’s one thing to list a chemical structure or a few numbers; it’s another to understand what a hot summer or humid ambient can do to nitrogen loading and, ultimately, product shelf life or ease of handling.

    Uses That Drive Feedback Into Our Process

    With 5-Chloro-4-Fluoro-2-Nitroaniline, practical insight filters in from a range of industries, but we hear most often from pigment, pharmaceutical, and crop-protection precursor users. In the worlds of organic synthesis, this compound’s strong electron-withdrawing group pattern carves a unique reactivity profile. Chemists favor it for the selective introduction of amino or hydroxyl groups on aromatic rings, without running into too much unwanted side-reactivity. Lab-scale researchers first flagged this over a decade ago, but scaling those predictable reactions required us to rethink drying, storage, and delivery formats. Today, production runs see the most volume going to intermediates for high-performance colorants and certain active pharmaceutical ingredients, because the chloro-fluoro-nitro arrangement resists hydrolysis and offers a clean handle for further transformations.

    End users talk openly with us about which quality markers really change throughput for them. Those making textile pigments notice immediate differences if color intensity falls short, pinning the cause back to trace impurity profiles only visible on close analytical review. Agrochemical formulators, with their own safety and environmental standards, demand a consistent melting behavior and minimal dusting so downstream mixing and processing don’t swing batch-to-batch yields. For API applications, trace contaminant tracking goes even deeper, reaching into routine residual solvent screening with limits far tighter than mainstream use, because regulatory filings rely on reliable data backed by direct cross-check with our own plant analytics.

    Our engagement goes beyond just shipping drums out the door. From repeated trial runs, we noticed that minor changes in particle size fraction—controlled by sieving and crystallization rate—change everything for customers using closed-system feeders or continuous batching equipment. Where we see feedback on filter cake compaction, high-purity requirements, or solvent exchange performance, adjustments on our floor directly influence someone else’s scale-up or regulatory submission timeline.

    Real Differences Compared to Similar Compounds

    Chemists face a tough choice every time they select an aniline derivative for new routes. We produce 5-Chloro-4-Fluoro-2-Nitroaniline in parallel with other analogues, like 4-chloro-2-fluoroaniline, 2-nitro-4-fluoroaniline, and 4-chloro-2-nitroaniline. Each shares a common backbone, but real-world usage tells a more complex story. The combined effect of two halogens and a nitro group on this specific ring positions it to react differently under nucleophilic aromatic substitution and reduction conditions. In practice, these differences look subtle on a printout but translate into far more robust or selective yields in customer applications, especially in colorant and pharmaceutical synthesis where every percentage point margin matters.

    We hear from formulators who once opted for simpler analogues, only to find themselves facing side-product headaches, lower color fastness, or unnecessary solvent usage due to less predictable reactivity. The extra fluorine and chlorine change both electron density and solubility, translating into cleaner downstream isolation or allowing lower reaction temperatures. That means less energy cost, easier purification, and tighter safety margins. Chemists come back for this compound because it solves particular bottlenecks—sometimes it’s the only substitute for notoriously stubborn ring-activation steps, and sometimes it simply outperforms in stabilities over a 6-month storage window.

    Our own operations also draw out differences in handling. For example, while many nitroaniline derivatives require extra ventilation and rapid cooling post-filtration, 5-Chloro-4-Fluoro-2-Nitroaniline offers a lower vapor pressure and a predictable desorption trend in our dryers. This turns into cost savings—not in some theoretical way, but in how long the plant runs between filter cleanouts and the time operators spend monitoring for volatile byproducts.

    We’ve run stability comparisons under standardized temperature and humidity cycling. Over eight-month tracking, this compound held physical integrity and resisted color shifts better than mono-halogenated or non-halogenated nitroanilines, which lose brightness or develop decomposition products. We package according to those real-world outcomes, not just a line in a safety sheet, so users open containers with confidence session after session.

    Sourcing and Cost Lessons Learned

    Reliability means more than chemistry. We source base materials from long-term partners who guarantee not just purity on intake, but steadiness in lot-to-lot physical traits—think crystal habit, dust load, and baseline contaminant load. Early on, we occasionally saw customer complaints when batch consistency slipped. After bringing more real-time analytics online and establishing strict supplier audits, we closed the loop on those source-of-error issues. Now, users across the globe report fewer delays, lower reject rates, and a preference for repeat orders that keep their own operations in sync.

    Global supply chains squeeze every kilogram—so our logistics routines build in stabilization periods, staggered stockholding, and freight partnerships familiar with temperature controls. Delays in shipping can spell storage headaches and hidden costs for pigment and API manufacturers downstream. With 5-Chloro-4-Fluoro-2-Nitroaniline, direct communication from our plant to the dock ensures handlers are ready for the specific moisture sensitivity and packaging particulars unique to this compound—not all aromatic amines travel the same, and ignoring these factors leads to avoidable waste or performance loss.

    Safety and Handling: What We Face in Real Conditions

    Much gets written about chemical safety, but on a nine-hour shift, the focus is narrower: avoiding real risks and securing consistent output with no surprises. 5-Chloro-4-Fluoro-2-Nitroaniline, like many of its kin, demonstrates moderate toxicity and becomes an irritant with prolonged contact, so our teams wear the right gloves, goggles, and masks all through production and packing. Fume extraction and local scrubber units at the filter stations earn their investment, especially since aromatic nitro groups demand extra caution on hot, humid days.

    We debugged a lot of handling trouble by sitting down with both new and experienced plant personnel and reviewing near-miss logs. One key learning: static buildup in transfer lines went down sharply after grounding improvements, which otherwise threatened to kick up airborne dust. Keeping climate-controlled inventories also kept batch cake from caking over—small things that matter at metric-ton scale.

    Disposal and clean-up never operate in a vacuum. Every kilogram contributes to tracked waste, and we structure routine solvent recovery and effluent management with local and international compliance at the forefront. Our facilities run regular training for spill response tailored to the hazard class—not just a slide deck, but hands-on drills, because nothing replaces practice when an unexpected spill happens on a Thursday afternoon with trucks lined up.

    Sustainable Practices and Regulatory Demands

    Regulations on aromatic amines and nitro compounds change faster than some expect, especially across regions with stricter environmental controls. We welcomed this shift by investing early in closed-loop systems and emission abatement. Over the last five years, those investments paid back in lower discharge numbers, higher regulatory scores, and easier audits from both authorities and major clients following the same frameworks. Our logs track everything from incoming shipments to final drum cleaning, since traceability wins trust when downstream partners see their own audit trails lining up with ours.

    For 5-Chloro-4-Fluoro-2-Nitroaniline, we run full hazard communication dossiers through every required jurisdiction, keeping up with new substance reporting and exposure limits. Many pigment and pharma customers demand REACH compliance or local equivalents, and our documentation holds up under their review because it threads together sourcing, analytics, and process notes not as an afterthought, but as a daily accompanying record.

    Solvent usage, water effluent, and byproduct energy capture draw real scrutiny. Every batch cycle looks for tighter recycling rates—both for cost control and regulatory reporting. We invest in analytics not just for show, but to catch trends before a minor deviation becomes a rejection at the customer’s gate or a flagged line on an annual environmental inspection.

    Partnering with End Users for Real-World Solutions

    Some of the best improvements on our plant floor started with customer phone calls, not engineering proposals. Fine-tuning one filtration phase, for instance, came after a textile dye house reported trace off-spec color formation in extended storage—their feedback led us to adjust solvent ratios and drying time, which cut future incidents and kept product quality within the hardest lines customers draw.

    Pharmaceutical developers come to us during early process development, asking direct questions about impurity fate, long-term stability, or potential reaction side-pathways. We work together on multistage pilot runs, feeding back lessons from plant scale-up to ensure their own process validations happen without six-month waits for a corrected supply. This push-and-pull way of operating gives all sides a better sense of how even small changes—like a new filtration cloth or a revised jacket heating protocol—shift real throughput and finished product purity.

    Plant teams maintain an open-door commitment to visiting technical staff from downstream operations. Site audits, joint troubleshooting, and emergency supply requests don’t send us scrambling; they are part of the day-to-day. Trust forms where teams blend operational transparency with real responsiveness—a rhythm that keeps customers returning, even when cheaper alternatives show up from untested sources.

    Looking Ahead: Quality Rooted in Real Practice

    On the manufacturing side, the hardest lessons about 5-Chloro-4-Fluoro-2-Nitroaniline came not from standard tables, but from the interplay of raw materials, machines, and the people blending each batch. Every drum tells a story—a cycle of chemical precision, supply challenges, months of customer feedback, and constant review. Staying competitive and reliable means listening closely to what buyers run into on their own lines and being ready to shift our methods with speed and confidence. Where some see just a string of numbers and hazard codes, we see a partnership across industries, geographies, and evolving needs—rooted in the daily practice of safe, repeatable, and honest manufacturing.