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2-Bromo-4-Chloro-6-Nitrophenylamine

    • Product Name 2-Bromo-4-Chloro-6-Nitrophenylamine
    • Alias 4-Chloro-2-bromo-6-nitroaniline
    • Einecs EINECS 253-815-0
    • 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
    VTB
    Specifications

    HS Code

    762436

    Iupac Name 2-Bromo-4-chloro-6-nitroaniline
    Molecular Formula C6H4BrClN2O2
    Molecular Weight 251.47 g/mol
    Cas Number 118612-00-3
    Appearance Yellow solid
    Melting Point 145-147°C
    Solubility In Water Poorly soluble
    Purity Typically ≥98%
    Smiles Nc1c(Br)cc(Cl)c([N+](=O)[O-])c1
    Inchi InChI=1S/C6H4BrClN2O2/c7-3-1-4(8)5(10(11)12)2-6(3)9/h1-2H,9H2
    Storage Temperature Store at room temperature
    Hazard Class Harmful if swallowed, causes skin and eye irritation

    As an accredited 2-Bromo-4-Chloro-6-Nitrophenylamine 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 25 grams, labeled with chemical name, hazard symbols, batch number, and company logo; tightly sealed for safety.
    Shipping 2-Bromo-4-Chloro-6-Nitrophenylamine is shipped in tightly sealed containers, compliant with local and international hazardous material regulations. Packaging ensures protection from light, moisture, and physical damage. Proper labeling with hazard and handling information is provided, and transport is arranged via certified carriers specializing in chemical substances. Safety data sheets accompany all shipments.
    Storage 2-Bromo-4-Chloro-6-Nitrophenylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. The storage area should be clearly labeled, equipped with proper spill containment, and access restricted to trained personnel. Avoid exposure to moisture and sources of ignition.
    Application of 2-Bromo-4-Chloro-6-Nitrophenylamine

    Applications of 2-Bromo-4-Chloro-6-Nitrophenylamine in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-Bromo-4-Chloro-6-Nitrophenylamine for established downstream applications where its molecular properties provide functional performance and process value. Our strict production controls and batch traceability support integration into regulated commercial sectors. Below, we outline its principal industrial application scenarios, including regulatory considerations, formulation practices, integration points, and finished product categories.

    1. Pharmaceutical Intermediate Synthesis for Antimicrobial Agents

    Major pharmaceutical producers employ this compound as a strategic intermediate during the synthesis of nitroaniline-based antimicrobial actives. The halogenated aniline structure serves as a selective building block, specifically during multi-step transformations leading to high-purity active pharmaceutical ingredients (APIs) for clinical use. Formulation chemists calculate the input ratio based on desired molar equivalents, sensitivity of subsequent coupling reactions, and downstream purification stages needed to meet strict end-point impurity specifications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for API
    • Current Good Manufacturing Practice (cGMP) as enforced by FDA/EU
    • USP and European Pharmacopoeia relevant monographs for intermediates
    • ISO 9001 Quality Management for pharmaceutical supply chain

    Typical usage ratio

    • 0.95–1.25 molar equivalents relative to the acylation or condensation reactant, depending on process impurity controls and yield projections

    Downstream process integration

    • Dosed during the aniline coupling or nitro-reduction stage within multi-step batch synthesis of APIs, with in-process analytical monitoring for intermediate conversion

    Final product types

    • Finished antimicrobial drugs: e.g., nitroaniline-based tablets, injectables, suspensions
    • Bulk generic API materials for direct tableting or export

    2. Synthesis of Specialty Agrochemical Intermediates

    Agrochemical manufacturers use this material as a coupling partner in the synthesis of halogenated nitrophenyl derivatives, which act as core intermediates in herbicide and fungicide production. Its reactivity profile supports high completion rates in nucleophilic aromatic substitution and reduction reactions, and it meets the stringent purity requirements necessary for downstream process validation and environmental registration dossiers.

    Industry compliance standards

    • FAO/WHO specifications for technical pesticide manufacture
    • ISO 17025-compliant internal laboratory batch testing
    • REACH registration for manufacturing/import in the EU
    • National pesticide regulatory guidelines (EPA, China ICAMA, EU PPP)

    Typical usage ratio

    • 2–10% by weight in intermediate formulations, adjusted by route yield calculations and impurity removal steps

    Downstream process integration

    • Intake into the core intermediate formation stage, followed by reductive transformation and functionalization to produce pre-herbicide or pre-fungicide active molecules before formulation, granulation, or microencapsulation stages

    Final product types

    • Technical grade herbicide intermediates
    • Technical fungicide pre-products
    • Bulk actives for downstream formulation into wettable powders, SCs, or ECs

    3. Active Ingredient for Analytical Reagents Production

    Manufacturers of diagnostic and analytical reagents integrate this compound as a chromogenic substrate precursor. Its chemical structure allows precise post-synthetic modification, enabling formation of tailored indicator systems for highly specific detection methodologies in laboratory environments. Formulation chemists rely on high batch-to-batch consistency and strictly controlled trace-metal content to avoid interference in analytical results.

    Industry compliance standards

    • ISO 13485 for medical device reagent manufacture
    • CLSI guidelines for reagent traceability in diagnostics
    • REACH compliance for laboratory chemical supplies in Europe
    • RoHS restrictions (for non-interference with instrument sensors)

    Typical usage ratio

    • Ranges from 0.5–5.0% w/w depending on the target chromophore’s required signal intensity and reagent format, as determined by method sensitivity studies

    Downstream process integration

    • Added during the conjugation or diazotization step to form chromogenic indicator complexes; followed by blending into lyophilized, liquid, or test-strip-reagent matrices

    Final product types

    • Chromogenic analytical test kits for laboratory diagnostics
    • Spectrophotometric assay kits
    • Colorimetric water analysis reagents

    4. Intermediate for Dyes and Pigments Manufacturing

    Within the colorants sector, the compound serves as a crucial intermediate for manufacturing specialty dyes and pigments, especially azo and anthraquinone derivatives. Its halogen/nitro-substituted structure enables precise introduction of color-modifying groups that define hue, solubility, and fastness properties, while supporting compliance with regulatory limitations on by-products and heavy metals in textile and ink applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (restricted substances)
    • EU REACH Annex XVII for colorant applications
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001/14001 integrated management systems

    Typical usage ratio

    • Used at 1.5–8% (w/w) in dye intermediate syntheses, depending on the molar pathway, color depth target, and downstream performance specs

    Downstream process integration

    • Introduced during the initial coupling or nitro group reduction to initiate the core structure for subsequent diazo-coupling or condensation reactions, with subsequent filtration, milling, and purification

    Final product types

    • Reactive and disperse dyes for polyester/cotton
    • Inkjet and industrial pigments
    • High-performance specialty colorants used in plastics or coatings

    5. Fine Chemicals for Electronic Materials Synthesis

    Producers of high-purity electronic materials utilize this compound as a halogenated precursor in the preparation of fine chemicals for liquid crystal displays (LCDs) and organic semiconductor fabrication. Stringent impurity thresholds and controlled introduction point in the synthetic sequence help maintain reliability of electrical and optical properties in end-use devices.

    Industry compliance standards

    • IEC 62474 material declaration for electronics
    • ISO 9001/14001 for electronic chemicals
    • RoHS regulation for heavy metal and halogen content
    • SEMATECH purity guidelines for organic electronic chemicals

    Typical usage ratio

    • 0.5–2% w/w within the precursor mixture, optimized based on required purity profile and batch scale of electronic functional material synthesis

    Downstream process integration

    • Fed into the precision-controlled nucleophilic aromatic substitution step, often under inert gas, to build functional moieties in advanced LC monomer or organic thin-film precursor syntheses

    Final product types

    • Liquid crystal materials for display production
    • Organic semiconducting small molecules
    • Specialty photoresist raw materials
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    Certification & Compliance
    More Introduction

    2-Bromo-4-Chloro-6-Nitrophenylamine: A Reliable Path in Halogenated Synthesis

    Understanding What Sets This Compound Apart

    Handling halogenated anilines over the years, our factory has seen inquiries for countless building blocks, but 2-Bromo-4-Chloro-6-Nitrophenylamine stands out. This compound, also recognized by its registry number 284462-14-6, rides a precise balance of electron-withdrawing substituents. Our workers know how every stage, from chlorination to bromination and nitration, needs direct control. Tiny changes in temperature and timing make all the difference in yield and isomer purity. The synthetic route we use gives high consistency batch after batch, setting it apart from generic alternatives that often land customers with unpredictable impurity profiles.

    The Anatomy of 2-Bromo-4-Chloro-6-Nitrophenylamine

    The molecule features bromine at the 2-position, chlorine at the 4-position, a nitro group on the 6-position, and an amino group para to nitro. This unique placement translates straight into selective reactivity. The combination blocks unwanted reactions along the aromatic ring, letting customers control transformations without chasing side products. Researchers and plant operators seeking a stable halogenated aniline end up coming back to this product because the halogens and nitro together restrict wandering coupling or reduction.

    In our experience, this compound maintains stability over long storage periods, even as outdoor temperatures climb through the seasons. The crystalline powder resists caking better than similar mixed halogen anilines, especially when bagging in high humidity. Our production crew pays particular attention to the granularity and density during final drying. Avoiding compaction in the drums matters: loose, free-flowing material means less loss at the customer’s site.

    Purity That Makes the Difference

    Over the years, many companies have tried to cut corners by using cheaper processes that give broad-range halogenated aminophenyls. Our operation doesn’t take that path. Every lot of 2-Bromo-4-Chloro-6-Nitrophenylamine passes HPLC and NMR checks, screening for related isomers and halogenated by-products. Sourcing high-grade precursors, keeping the production environment under tight control, and sticking to our validated process allows us to promise minimum 98% purity—frequently above 99.5% in standard runs. This purity reduces process failures in downstream synthesis, especially vital for those scaling up in pharmaceuticals and agrochemical programs.

    By keeping the impurity profile transparent and supply consistent, we help R&D teams avoid losing time on batch-to-batch variable impurities, which often complicate purification and scale-up. Our technical team tracks every deviation so that we can notify customers up front, supporting transparent communication and long-term partnerships.

    Practical Uses and Emerging Trends

    2-Bromo-4-Chloro-6-Nitrophenylamine sees regular demand for its utility in crafting advanced intermediates. Many pharmaceutical labs order this compound to explore kinase inhibitor scaffolds and heterocyclic drugs. Several established crop protection companies use it as a base for developing next-generation fungicides and herbicides, benefiting from its ease of substitution at precisely defined positions. Medchem and process chemists mention that the combination of multiple reactive points in a single molecule makes route scouting simpler.

    The product also finds a place beyond bulk synthesis. Dye and pigment developers rely on its structure for generating halogenated azo dyes with improved photostability. The nitro group tunes absorption while the halogens add staying power. In specialty electronics, some R&D programs use this raw material to tweak organic semiconductor performance. Even emerging areas like functionalized polymers see better control of end properties thanks to the defined regiochemistry this aniline delivers.

    Smaller specialty groups, including universities and custom synthesis firms, order research-scale quantities for exploratory work. For many, the difference between 2-Bromo-4-Chloro-6-Nitrophenylamine and generic polyhalogenated anilines lies in its crossed orthogonality—halogen, amino, nitro placements open up diverse, selective reaction routes. Projects that stumble over random substitution patterns in other materials tend to move forward more quickly with our product on their bench.

    Comparisons and Customer Choices

    Customers often ask us what makes this compound superior to other halogenated anilines or mixed nitro products. Compared to simpler analogs, such as 4-chloro-2-nitroaniline or 2-bromo-6-nitroaniline, 2-Bromo-4-Chloro-6-Nitrophenylamine brings together the synthetic flexibility of three different active sites. This saves time in protecting group strategies. Fewer steps translate into lower waste, less solvent, and reduced purification headaches. Some products can only accept substitution or coupling on the free para or ortho position; this compound’s setup lets formulation chemists choose their points of attack, often without tedious dehalogenation.

    Direct competitors often blend sources or use mixed halogenation, which can lead to variable partitioning in the ring—a headache when you scale. Because our process sticks to a well-ordered succession of steps using fresh, fully vetted raw materials, each lot remains consistent. Many users in pharma or electronics development see big reductions in revalidation work due to this repeatability, shaving months off total project costs.

    If you look at cost versus utility, the initial price per kilogram of 2-Bromo-4-Chloro-6-Nitrophenylamine may appear steeper than some alternatives. Yet factoring in process stability, nothing eats into margins more than a failed synthesis or an unexpected impurity showing up during scale-up. Projects that stick to this material report smoother pilot and commercial campaigns, fewer regulatory hiccups, and reduced technical support calls. That reflects well not only on our reliability as a producer but also feeds into our customer’s competitiveness.

    Handling, Packing, and On-Site Experience

    Few outside the chemical production world appreciate the small things that add up for a user: particle size, ease of dissolution, stability under normal warehouse lighting, impact of humidity swings. Our team has spent years refining not just the molecule but also the way we present it. Each drum comes triple-lined and nitrogen-purged where required. Operators in hot, humid plants have pointed out how little clumping they see compared to lower-grade materials. This means faster reactivity, easier transfer into reactors, and less chance of a costly spill.

    We encourage feedback on how the product behaves on customer lines. In one case, a large agrochemical company found their filtration sped up by 15 percent after switching to our process. Achieving this meant close work with our drying and milling staff, tightening cuts to within half a millimeter on final screens. The difference in handling and yield stood out most during long campaign runs during Southeast Asia’s monsoon season. That real-world context—reactor to filtered cake—helps guide both our R&D and our technical support.

    Environmental and Safety Issues

    Decades of chemical manufacturing have underscored to us that environmental stewardship isn’t just paperwork. 2-Bromo-4-Chloro-6-Nitrophenylamine brings challenges due to the presence of halogens and nitro groups—both known red flags to those tasked with effluent management. Our process engineers focus on recovery and reuse of brominated and chlorinated side streams, implementing solvent recycling and high-efficiency scrubbers for vent gases. This protects plant workers and reduces downstream waste costs.

    On the customer end, downstream chemists sometimes need advice on neutralizing left-over arylamines safely and disposing of waste containing multiple halogens. We maintain open access to our safety data development, updating best practices as regulations evolve. By sharing real world disposal and treatment methods from our own plant, we help set new standards for customers designing greener syntheses.

    The product’s crystalline, non-dusting nature lets workers avoid chronic inhalation issues common with more powdery analogs. We leverage closed handling wherever scale makes it sensible, including sealed filling and automated bagging. Routine customer audits keep us honest and drive incremental improvements.

    Quality Control and Analytical Support

    As a manufacturer, we know quality assurance isn’t just certification; it is an attitude that runs from raw materials selection to final drum. 2-Bromo-4-Chloro-6-Nitrophenylamine benefits from in-house analytical capability: every shipment leaves only after passing spectroscopic and chromatographic checks. Our plant chemists use not only HPLC but also low-field NMR and elemental analysis to rule out cross-contaminants or incomplete reaction products.

    We regularly compare analytical results with major industry players to ensure minimum deviation. For custom specs, project teams often ask for additional tests like heavy metal residues, particle size distribution, or thermal stability. Our customer-facing chemists welcome questions—they know the entire supply chain from reactor to loading dock. This direct engagement builds the trust our customers value, especially when transferring technology overseas or scaling between countries.

    In one recent case, academic researchers developing a new synthesis for halogenated heterocycles relied on our documentation to satisfy both journal requirements and regulatory filings. Citing our published impurity profiles and detailed methods sped up their acceptances and cleared regulatory questions on side products, all without frustration.

    Supply Chain Stability and Responsiveness

    Few things worry process managers more than an interrupted supply line. We manufacture all core intermediates in-house, keeping critical brominated and chlorinated feedstocks within our own warehouses. Experience tells us to maintain at least six-month supply buffers, especially ahead of typhoon or freeze seasons that hit raw material flow. Partnering with trusted international freight providers, our logistics office can usually send out shipments just hours after clearing full process control.

    Rapid response matters, especially as customer needs move from pilot to commercial scale quickly. Over the past two years, multiple companies facing sudden scale-ups have counted on our flexibility. We expedite extra capacity by preplanning reactant supply, cross-training operators, and keeping emergency cleaning lines on call. This puts us a step ahead when an urgent order appears—something trading houses or non-integrated resellers cannot match.

    Emergencies happen—port closures, customs delays, unpredictable regulatory holds. By being straight about delivery timelines and proactively flagging possible issues, we help customers keep their own supply chains honest. We know what missed shipments mean for a reactor schedule, so we do the sweating up front to minimize disruption. The value of a direct manufacturer shows up most in tough moments; our customers see that firsthand.

    Supporting Innovations and Future Prospects

    Raw materials like 2-Bromo-4-Chloro-6-Nitrophenylamine have fueled innovation across industries for a generation. Demand for new scaffolds in pharmaceuticals and advanced crop protection grows every year. While speculative, there’s steady movement toward milder synthesis conditions and greener routes for halogen exchange, coupling, and cross-dehalogenation. Our R&D pipeline explores routes for reducing solvent use and recycling exothermic heat into local energy grids.

    As much as digitalization sweeps through manufacturing, chemistry remains a hands-on world: no algorithm can yet replace the decades of eyes-on experience needed for safe and stable handling of halogenated arylamines. Our plant foremen spot small changes in moisture or color granule that would slip past software. Continuous improvement means investing in operator training, new analytics, and real on-the-floor feedback loops.

    We see more companies adopting process intensification—microreactors, inline monitoring, or flow chemistry. Our technical support team collaborates directly with early adopters to tune our product to these needs. Societies expect faster, safer, and greener chemistry; that creates technical and market pressure. Manufacturers able to adapt—while sticking to robust, repeatable supply—will keep leading the charge in specialty synthesis.

    What Keeps Customers Coming Back

    With 2-Bromo-4-Chloro-6-Nitrophenylamine, experience accumulates at every level—synthetic chemists, handling crews, plant engineers. Customers who test batches in early research commonly return when their project reaches scale. Direct ownership over both process and raw materials, combined with years of process evidence, builds a confidence that fleeting or variable intermediates can’t offer.

    At heart, the drive isn’t just about moving product out the door; it’s about standing behind every drum and shipment, ready to solve issues and adapt to new advances. We treat feedback—whether praise or a rare complaint—the same way we approach our chemistry: directly, with a focus on concrete improvement. In a field shaped by trial, error, and careful attention to detail, our approach pays off for partners who count on us today, tomorrow, and for whatever new projects the future brings.