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2,6-Dichloro-4-Fluoroaniline

    • Product Name 2,6-Dichloro-4-Fluoroaniline
    • Alias 2,6-Dichloro-4-fluoro-1-aminobenzene
    • Einecs 629-723-0
    • 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

    733978

    Product Name 2,6-Dichloro-4-Fluoroaniline
    Molecular Formula C6H4Cl2FN
    Molecular Weight 180.01 g/mol
    Cas Number 700-36-7
    Appearance Light yellow to beige crystalline solid
    Melting Point 64-68°C
    Boiling Point 251-253°C
    Density 1.48 g/cm3 (approximate)
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Flash Point 111°C
    Storage Temperature Store at 2-8°C
    Chemical Structure ClC1=CC(=C(N)C=C1F)Cl
    Synonyms 2,6-Dichloro-4-fluoroaniline; 2,6-Dichloro-p-fluoroaniline
    Ec Number 616-178-3

    As an accredited 2,6-Dichloro-4-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 2,6-Dichloro-4-Fluoroaniline is supplied in a sealed, amber glass container with a secure screw cap.
    Shipping 2,6-Dichloro-4-Fluoroaniline is shipped in tightly sealed containers, protected from moisture and light. The chemical should be labeled according to regulatory standards, with appropriate hazard warnings. Transport is typically via ground or air freight under controlled conditions, complying with relevant safety and environmental guidelines for handling hazardous substances.
    Storage 2,6-Dichloro-4-fluoroaniline should be stored in a tightly closed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep away from heat and direct sunlight. Ensure containers are clearly labeled and protected from physical damage. Use secondary containment to prevent spills, and store away from food and drinking water.
    Application of 2,6-Dichloro-4-Fluoroaniline

    Applications of 2,6-Dichloro-4-Fluoroaniline in Industrial Manufacturing

    2,6-Dichloro-4-Fluoroaniline serves as a critical intermediate in several high-value chemical manufacturing sectors, supporting rigorous industry standards in downstream synthesis and enabling consistent quality for specialized end products. Our expertise as the original manufacturer supports precise integration into advanced chemical processes to meet industrial demand for pharmaceutical, agrochemical, dye, and pigment synthesis.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Our material finds essential application during the targeted synthesis of key heterocyclic building blocks for regulated API production. Medicinal chemistry teams use its aromatic substitution profile to selectively introduce halogenated motifs into pyridine and quinazoline scaffolds, a requirement for controlled drug development pipelines. Integration occurs after initial skeleton assembly, maximizing batch yield and downstream compound purity. Process engineers optimize loading based on reactivity toward amination or coupling partners, with tight in-process quality controls to support compliance and minimize impurity carryover.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) — ICH Q7
    • United States Pharmacopeia (USP) for APIs
    • ICH Q3A (Impurities in New Drug Substances)
    • EU EMA Pharmaceutical Guidelines

    Typical usage ratio

    • 5–18% molar ratio in step-growth synthesis, adjusted for target heterocycle substitution pattern and scale-up yields

    Downstream process integration

    • Charged after core ring structure assembly during halogenation or nucleophilic aromatic substitution steps; filtered and purified before API crystallization

    Final product types

    • Anti-cancer molecules (e.g., kinase inhibitors, tyrosine analogues)
    • Antiviral agents
    • Central Nervous System (CNS) drug intermediates

    2. Agrochemical Active Ingredient Manufacturing

    Plant protection product manufacturers rely on 2,6-Dichloro-4-Fluoroaniline to build selective herbicide and insecticide actives requiring robust halogen substitution for target specificity and soil persistence. It enters the formulation at the pre-condensation stage for coupling with sulfonylureas or triazine derivatives, ensuring consistent molecular integrity. Quality control teams monitor impurity levels and in-process stability at every batch to meet statutory residue and environmental safety benchmarks in global crop protection markets.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • REACH (EC No 1907/2006) Regulation for agrochemical intermediates
    • ISO 9001:2015 for process management
    • EPA FIFRA standards for restricted-use chemicals

    Typical usage ratio

    • 8–14% by total reactant mass in active ingredient synthesis, with adjustment for crop-specific efficacy and target compound purity

    Downstream process integration

    • Incorporated prior to cyclization or amidation for active core assembly; recovered intermediates pass through solvent exchange and multi-stage filtration

    Final product types

    • Selective herbicides for corn and rice
    • Insecticidal active substances (e.g., neonicotinoids, pyrazoles)
    • Fungicide intermediates

    3. Dye Intermediate for High-Fastness Dyes

    In the specialty dye sector, 2,6-Dichloro-4-Fluoroaniline enables controlled aromatic amine input for the synthesis of high-performance azo and anthraquinone dyes. Colorant producers favor its electron-withdrawing properties to achieve deep shade and enhanced lightfastness for synthetic fiber applications. The compound is introduced during diazotization or coupling steps with precisely timed pH and temperature control. Precise batch dosage and rigorous monitoring of residual halide enable compliance with textile industry heavy metal and aromatic amine limits.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textiles
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) – Version 3.1
    • ISO 105 E04 for color fastness
    • REACH Annex XVII restricted amines list

    Typical usage ratio

    • 3–8% by weight within the coupling component of dye synthesis, nuanced by target pigment intensity and molecular backbone

    Downstream process integration

    • Added at the start of the diazotization reaction for controlling amine reactivity; reaction progress monitored via UV-vis spectrocopy until desired conversion is achieved

    Final product types

    • Disperse dyes for polyester and acetate fibers
    • Reactive dyes for cotton blends
    • High-fastness textile pigments

    4. Pigment Intermediate for Performance Coatings

    Manufacturers of advanced coatings use our raw material as a key intermediate for the synthesis of specific halogenated pigments. Its molecular structure helps develop superior exterior durability and weather resistance in architectural and automotive finishes. The compound is introduced in the first step of the pigment synthesis route, reacting with phthalic anhydride or chlorinated benzene frameworks. Downstream, processors implement multi-stage purification before particle milling, supporting compliance with international pigment migration and extractable content guidelines.

    Industry compliance standards

    • EN 71-3 (Safety of Toys: Migration of certain elements)
    • ASTM D7723 (Standard for Pigments and Extenders)
    • ISO 14001 Environmental Management System for coatings
    • VOC directives for solvent-based coatings (Directive 2004/42/EC)

    Typical usage ratio

    • 7–12% by weight relative to total pigment-forming reactants, tuned per chromophore color and physical property performance

    Downstream process integration

    • Introduced during the nucleophilic coupling stage for intermediate pigment complexation; followed by filtration, thermal stabilization, and jet-milling

    Final product types

    • High-durability exterior architectural paints
    • Automotive OEM coatings
    • Industrial powder coatings
    Free Quote

    Competitive 2,6-Dichloro-4-Fluoroaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,6-Dichloro-4-Fluoroaniline: Manufacturer’s Perspective on a Precision-Crafted Chemical Building Block

    Supporting Advanced Chemistry With 2,6-Dichloro-4-Fluoroaniline

    Over decades spent engineering chlorofluoroaromatic compounds, the unmistakable challenge lies in controlling both reactivity and purity at scale. Few molecules highlight this balance as clearly as 2,6-Dichloro-4-Fluoroaniline. We’ve seen it evolve from a specialty intermediate known to only a handful of researchers to a foundation for pharmaceutical and agrochemical production lines worldwide.

    Our team has poured expertise into fine-tuning every part of the process, beginning with raw chlorinated anilines and progressing through careful halogenation. This approach isn’t a shortcut. Sourcing high-purity materials will always trump superficial batch yields for those working at industrial volumes. Impurities in precursor materials often pass unnoticed until late-stage synthesis. They show themselves in color, odor, or the unpredictability of subsequent coupling reactions. We audit every drum entering the plant. Maintaining this standard over thousands of kilograms per year takes time, resources, and plenty of grit.

    Specification Overview and Manufacturing Rationale

    The final crystalline solid passes extensive analytical testing: chromatographic purity, water content, identification of by-products, and the precise melting point. Experienced operators can spot color shifts at a glance—subtle off-white hints often suggest incomplete dehalogenation or trace by-products from the upstream halide sources. As a manufacturer, we invest in both automated instrumentation and well-trained staff to recognize these fingerprints the moment they appear. Laboratory spectroscopies such as GC-MS and NMR verify our work but seldom replace the sensitivity of a bench chemist’s nose and eyes, especially during critical scaling runs.

    Knowing where product specification ties directly to end-user success brings a sense of responsibility. Pharmaceutical teams may specify ultra-low residual solvents, limiting exposure risk in active ingredient production. Agrochemical lines demand homogeneity across ton-lot batches to avoid surprise results in field trials. We approach each demand with the same consistency, whether the batch fills a single lab order or stocks a multi-year strategic inventory.

    Every Gram Counts in Medicinal and Crop Synthesis

    Chemists and engineers reach for 2,6-Dichloro-4-Fluoroaniline not for simplicity, but rather for its reactivity and selectivity. Fluoroaniline cores permit stepwise modifications across several positions on the ring. The substitution of chlorine at C2 and C6 blocks unwanted side reactions, channeling reactivity where it’s actually needed. This seemingly modest molecule permits elaborate downstream coupling or cyclization chemistry impossible with unsubstituted analogs. Over repeated cycles, these benefits show up most in the cost per kilogram of finished API or formulated active.

    Our close involvement with end-application users has shaped many decisions about particle sizing, free-flowing granule form, and shipment packaging. Early in our production history, we shipped mostly in steel drums. These days, improved moisture-barrier linings and composite bags meet modern GMP logistics. Our storage conditions—temperature, humidity, headspace control—ensure product arrives unchanged, even after months at sea or in warehouse limbo. Engineers learn quickly that savings at the plant are lost if material spoils on the shelf or reacts prematurely en route. Chemical integrity does not tolerate shortcuts.

    Differences Making a Measurable Impact

    A direct comparison with mono-chlorinated or non-fluorinated anilines highlights two main gaps: reactivity and downstream safety. With two ortho-chlorine atoms, 2,6-Dichloro-4-Fluoroaniline maintains resistance to oxidative degradation or substitution in harsh conditions. The fluorine substituent at the para position subtly tunes electron density, moderating reactivity without sacrificing activation ease. Competing analogs often yield unpredictable isomer mixtures or require additional purification, draining time and resources.

    Many downstream routes, especially in urea and amide couplings, rely on this selectivity. When hundreds of metric tons hinge on consistent output, even minor improvements in yield or product quality stack up to serious cost savings. These characteristics also explain the demand surge over the past decade from both pharmaceutical innovators and generic manufacturers racing to optimize cost-of-goods.

    Practical Knowledge From Daily Manufacturing

    Continuous synthesis at scale does not always track perfectly with academic literature. We know firsthand how subtle shifts in impurity profiles, aging of catalyst beds, or solvent selection ripple through an entire month’s output. Our internal process engineers write detailed logs and collect samples from every production lot. These samples feed a library that lets us quickly troubleshoot any shift in quality. Early in our experience, we learned that keeping close tabs on these records prevents costly reruns and reputation damage.

    No process—especially one involving halogen handling—is without hazards. Aniline derivatives generate strong odors, and volatile by-products often find their way into ventilation and waste streams. Over the years, we implemented state-of-the-art scrubbers and containment measures, setting benchmarks that raised the expectations for environmental stewardship in our region. Discharge regulations have tightened, but we’ve turned compliance into an internal competition. Less waste and fewer emissions mean greater operational efficiency and stronger trust with both local communities and regulators.

    Meeting the Evolving Needs of Research and Industry

    The world keeps changing and so do the demands for intermediates. A decade ago, most requests focused on gram-to-kilogram scale for early-stage synthesis. Today’s largest requests often come directly from global partners committed to multiple sites and multi-year rollouts. Our team has adapted by upgrading reactors, automating key transfer steps, and refining purification columns. This operational muscle means faster turnarounds and fewer batch failures.

    Trained chemists and junior engineers regularly rotate through every stage of our line, building not just skill in routine operation, but also the judgment needed for rapid troubleshooting. Keeping lines running through holidays, weather events, and the highs and lows of global supply chains demands a level of coordination few outside the industry fully appreciate. Every member—lab technician, loading operator, shift supervisor—plays a role in keeping the molecule flowing.

    Direct Hands-On Quality Assurance

    A single contaminated batch discovered late can mean thousands of dollars down the drain and the loss of customer partnership. That’s why we tie every shipment to its Certificate of Analysis, unique batch ID, and reserve ample retained samples for post-delivery technical support. If a customer faces an off-spec issue, our technical teams dive into the archived details to identify the source. No generic answers—just data and transparent troubleshooting.

    Over the years, satisfaction grows not just from volume shipped, but from hearing positive feedback when our product gives a smoother path in scale-up or results in one less purification step. Trust develops person to person, built on reliability and expertise rather than marketing slogans. We take pride in being the line between laboratory vision and industrial reality.

    Trends and Expectations Shaping Production

    Regulatory attention on aromatics—especially those bearing multiple halogens—has shaped new production priorities. Concerns about persistence and bioaccumulation have prompted R&D projects looking for green chemistry alternatives or superior process controls. As manufacturers, we keep up with pending rules and partner with external auditors to measure our responses. Routine internal audits now dovetail with customer-driven demand for tracing every raw material from origin to shipment.

    It’s not just about safety data sheets or GHS labeling—it’s about sharing practical insights on handling, storage, and best practices so partners avoid incidents and maintain predictable output. We regularly update our guidance, drawing from first-hand incidents: a valve leak on a cold winter morning, a mix-up with secondary containment drums, an unexpected polymerization during pilot trials. Turning these “lessons learned” into safer, more efficient production cycles keeps quality front-and-center.

    Building Better Partnerships, Not Just Chemicals

    Long-term supply partnerships depend on more than price and paperwork. Our most valued clients return because they have experienced problem-solving and plain honesty from our side of the table. Should there be a hint of irregularity—a batch not matching visual expectations, a test below spec—our field teams reach out with real-time updates and offer replacement timelines. The chemistries involved in 2,6-Dichloro-4-Fluoroaniline production do not forgive errors or neglect. We have grown results-focused; mistakes do not get swept under the rug, and every error, no matter how minor, leads to a tangible response.

    Globalization has shattered old models of insulation from world events. Supply disruptions, port closures, and energy crises reverberate across the supply chain. We serve clients that demand not just logistical agility but transparency and the assurance that backup plans stand ready. Our strategic inventory decisions reflect decades of shipping experience and a deep respect for customer timelines.

    Continuous Learning and Shared Outcomes

    Process chemistry never sits still. Each season brings new routes to purer product, new means to drive down manufacturing residues, and new catalysts promising higher yields with lower waste. Our investment in R&D draws directly from these cycles of improvement, blending seasoned operator judgment with computational models and emerging green chemistry routes. Many of our own best process tweaks have come from collaboration with customer R&D: a single phone call, a request for a custom grade, a challenge to lower a specific impurity below trace detection. These conversations feed back into our plant as drivers for evolution.

    We commit to documentation that does not just meet compliance audits, but also arms partners with the facts and troubleshooting history they need. Our archive has allowed clients to resolve API quality complaints simply by pulling batch records and impurity profiles. Transparency avoids making the same mistake twice.

    Why Manufacturing Experience Matters

    Our credibility lives in getting the hard details right: zero shortcuts to remove off-odor, structure verification at every lot, comprehensive impurity mapping, and rapid trace analysis during incidents. It’s easy to promise tight specs; it’s harder to defend them year after year against shifting global markets and raw material hiccups. Our workforce counts years of hands-on experience, with mid-level operators growing into expert troubleshooters trusted by global buyers.

    Guiding the next generation means investing in their growth, not just assigning them routine tasks. We see value in cross-training, bringing fresh eyes to longstanding problems, and building a workforce not just focused on the present campaign, but on broader industry trends like digitization, energy efficiency, and sustainability metrics. These human investments show up in every pristine batch of 2,6-Dichloro-4-Fluoroaniline shipped, and they underpin our confidence that we meet the expectations of clients, regulators, and the communities that live near our plants.

    Understanding What Sets Our 2,6-Dichloro-4-Fluoroaniline Apart

    Not all products on the market match expectations of high-throughput synthesis, shelf stability, or low volatile residue. Our internal batch records and field performance stories consistently report higher reactivity control and cleaner downstream processing than generic alternatives. Industry users have reported fewer unexpected by-products in scale-up—confirmed by direct bench comparisons against mono-chloro or non-fluorinated anilines.

    Consistency is often the unspoken trait partners demand most. Over countless cycles, the strict analytic chase—whether by NMR, GC-MS, HPLC or TLC—keeps our lineups tight batch after batch. We recognized early how a flawless chain of custody leads to traceability: simple transit monitoring, tamper-evident closures, and robust back-up stocks all feed into superior experience for buyers with demanding timelines and compliance reporting.

    Standing Behind Our Chemicals and Our Word

    As direct manufacturers, our core confidence never grows stale. Each order is more than raw tonnage—it represents an unbroken link of technical trust. Experienced teams oversee every kilo from the first halogenation vessel to sealed packaging. Supplier reputation still rests on reliability, shared insights, and a steady drive to go past routine compliance into the realm of long-term quality.

    The lessons learned from working directly with industrial and laboratory partners have elevated our standards and helped build a pipeline that delivers not just molecules, but results. This spirit of partnership—made real through technical support, transparent documentation, and ongoing innovation—forms the backbone of our approach to 2,6-Dichloro-4-Fluoroaniline and every other compound that leaves our gates.