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4-Bromo-2-Nitroaniline

    • Product Name 4-Bromo-2-Nitroaniline
    • Alias 4-Bromo-2-nitrobenzenamine
    • Einecs 214-482-7
    • 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

    718499

    Chemicalname 4-Bromo-2-nitroaniline
    Casnumber 13125-82-1
    Molecularformula C6H5BrN2O2
    Molecularweight 217.02 g/mol
    Appearance Yellow to orange solid
    Meltingpoint 135-140 °C
    Density 1.82 g/cm3 (approximate)
    Solubilityinwater Slightly soluble
    Purity Typically ≥98%
    Smiles NC1=CC(Br)=C(NO2)C=C1
    Inchikey KGJPGRPBWMIDGR-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Amber glass bottle with secure cap, labeled "4-Bromo-2-Nitroaniline, 25g," hazard symbols, handling instructions, and supplier information.
    Shipping 4-Bromo-2-nitroaniline is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It is classified as hazardous, requiring appropriate labeling and documentation. During transportation, use secondary containment and follow all regulatory guidelines for handling toxic, potentially combustible chemicals. Personal protective equipment is recommended during unpacking and use.
    Storage 4-Bromo-2-nitroaniline should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, excessive heat, and direct sunlight. It should be kept separate from strong oxidizing and reducing agents, acids, and bases. Label the container clearly, and ensure proper handling with appropriate personal protective equipment to prevent exposure.
    Application of 4-Bromo-2-Nitroaniline

    Applications of 4-Bromo-2-Nitroaniline in Industrial Manufacturing

    4-Bromo-2-nitroaniline serves as a critical intermediate for multiple specialty chemical sectors, contributing to precision synthesis and high-value downstream products. As a direct manufacturer, we provide this material to leading players in controlled and regulated industries that demand process consistency, reproducible traceability, and trace impurity minimization. Below, we outline the established application segments where our product integrates into technical processes and final manufacturing workflows.

    1. Synthesis of Azo Dyes for Specialty Textile Applications

    Textile dye manufacturers utilize 4-bromo-2-nitroaniline to synthesize specific mono-azo and diazo dye classes responsible for bright, long-lasting yellow and orange shades in technical fabric treatments. The compound undergoes direct diazotization and subsequent coupling to aromatic phenols or naphthols, producing dyes capable of withstanding repeated industrial laundering, sunlight exposure, and chemical agents. Accurate metering and stringent process controls ensure that final color strength, wash fastness, and toxicity profiles strictly align with textile sector requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • European REACH Regulation (EC) No 1907/2006
    • ZDHC MRSL (Manufacturing Restricted Substances List)
    • ISO 105-B02: Textiles—color fastness to artificial light

    Typical usage ratio

    • 0.2–0.8 molar equivalents relative to the diazotization base component; precise ratio depends on chromophore intensity and target batch size.

    Downstream process integration

    • Direct input into the diazotization reactor followed by in-situ coupling step; integrated into reaction streams under controlled pH and temperature, prior to final dye precipitation.

    Final product types

    • Acid dyes for nylon and wool fibers
    • Direct dyes for cellulosic fabric
    • Disperse dyes for polyester blends
    • Sulfonated dyes for high-performance technical textiles

    2. Production of Pharmaceutical Intermediate Compounds

    Chemical manufacturers in the API (Active Pharmaceutical Ingredient) value chain employ this raw material to construct halogenated and nitro-substituted aniline intermediates, enabling selective synthesis of key pharmaceutical scaffolds. Downstream users conduct hydrogenation or reduction reactions to introduce amino functionalities at late stages, whereby trace levels of process impurities must remain within pharmacopeia-defined limits. Consistency in supplied material directly impacts reaction yield and pharmaceutical batch validation results.

    Industry compliance standards

    • EudraLex Volume 4 (EU GMP Guidelines)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary)
    • Chinese Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.05–0.15 molar equivalents relative to final API target; ratio adjusted per reaction stoichiometry and impurity control strategy.

    Downstream process integration

    • Introduced at early or intermediate step during multi-stage organic synthesis; undergoes selective reduction or substitution steps under inert atmosphere, followed by purification and isolation.

    Final product types

    • Intermediate compounds for antihypertensive drug synthesis
    • Precursors to anti-infective agents
    • Building blocks for non-steroidal anti-inflammatory drug (NSAID) derivatives
    • Phenylhydrazine derivatives used in research-scale medicinal chemistry

    3. Agrochemical Active Ingredient Manufacturing

    Producers of crop protection agents—including specific herbicides and fungicides—use this nitroaniline derivative to introduce halogen functionality and electron-withdrawing groups into the molecular backbone of active substances. Its reactivity provides targeted selectivity during chlorination, alkylation, or cyclization steps, directly affecting efficacy and environmental degradation profiles of final agents applied to crops. Strict feedstock qualification and batch homogeneity reduce variability in field application results.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • BPR (Biocidal Products Regulation, EU 528/2012)
    • ISO 9001:2015 (Quality Management Systems for Agrochemicals)
    • China GB 2763—National Food Safety Standard for Pesticide Residue Limits

    Typical usage ratio

    • 5–20% by weight in technical concentrate formulations; optimized during pilot and scale-up syntheses to balance activity and downstream yield.

    Downstream process integration

    • Charged at the intermediate synthesis reactor prior to functional group transformation; transitions into formulations after isolation, quality testing, and micronization.

    Final product types

    • Sulfonylurea herbicide intermediates
    • Protective fungicide scaffolds
    • Biphenyl-based plant growth regulators for niche crops
    • Precursor to selective weed control agents

    4. Polymeric Colorant and Pigment Precursor Manufacturing

    Advanced plastics and pigment processing plants utilize this chemical as a colorant precursor, particularly when synthesizing brominated azo pigments or functionalized polyolefins containing color-fast moieties. The material enters as a nucleophile or coupling agent in polymer-grafting or batch suspension polymerization, contributing to batch-to-batch uniformity required for automotive components, injection-molded consumer goods, and architectural plastics. Color consistency and regulatory purity remain focal points during downstream processing.

    Industry compliance standards

    • EN 71-3:2019 (Safety of Toys—Migration of Certain Elements)
    • EU Directive 2009/48/EC (Toy Safety Directive)
    • UL 94 (Safety for Flammability of Plastic Materials)
    • FDA 21 CFR 177 (Indirect Food Additives: Polymers)

    Typical usage ratio

    • 0.1–2% by total polymer batch weight; adjusted according to pigment loading efficiency and targeted opacity in molded parts.

    Downstream process integration

    • Blended into polycondensation or extrusion reactors during pigment synthesis, before compounding or extrusion with base resins; integrated under controlled agitation to prevent agglomerate formation.

    Final product types

    • Brominated azo pigments for plastics
    • Color masterbatches for thermoplastic polymers
    • Molded automotive interior/exterior parts
    • Architectural cladding panels with embedded colorants
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2-Nitroaniline: Our Experience as a Direct Producer

    Bringing Practical Chemistry to Industry

    After years of hands-on synthesis in our production facility, we've learned a thing or two about what 4-Bromo-2-Nitroaniline brings to the table. This aromatic compound, known in the lab by its straightforward structure—a bromine and a nitro group sitting on the aniline ring—doesn’t make the most headlines, but its value is clear in the courses of both innovation and scale-up, especially for downstream applications. Our team focuses on consistent output and reliability, supporting clients in areas from specialty dye intermediates to niche pharmaceutical building blocks.

    Product Highlights and Why It Matters

    Our 4-Bromo-2-Nitroaniline, sometimes referenced as model 5-02BN, enters the scene with a keen reputation in the chemical marketplace. It’s recognized by its clean, orange-yellow crystalline appearance, carrying a purity that we ensure surpasses 99% during each batch QC audit. The melting point lands between 134-137°C in our experience, a range we steadily hit thanks to diligent process control. Our own methods prioritize not only purity but also the reduction of trace impurities that can quietly cause problems downstream, especially halogenated or oxidized by-products.

    Users working in the synthesis of azo and disperse dyes find the compound particularly dependable. The combination of the electron-withdrawing nitro and bromine substituents create a structure primed for further reactions, especially nucleophilic substitutions. In our conversations with dye chemists, a clear message comes through: clean starting material minimizes unexpected chromatic shifts or performance faults in the final pigment.

    On the pharmaceutical synthesis side, we engage with scientists who appreciate 4-Bromo-2-Nitroaniline’s reactivity. For those building complex molecules, the predictability of our material’s reactivity reduces troubleshooting, time, and reprocessing costs. We continuously keep this feedback loop open with customers who often share reaction yields or impurity profiles back with us, which we use to drive tighter controls and better process parameters in our own plant.

    How Our 4-Bromo-2-Nitroaniline Stands Apart

    In scaling up production, we’ve faced the variables that smaller syntheses gloss over, and we see where some vendors cut corners. Process waste, precursor purity, and even equipment material (glass vs. stainless steel) can influence the end material. Some manufacturers accept chloride or oxidized aniline residues as within "allowable limits." We set our internal bar well above generic specs, aiming to eliminate false positives during customer HPLC analysis.

    Packing also makes a difference, especially for air- and moisture-sensitive intermediates. Our pack-out happens in a controlled, low-humidity environment, with sealed, UV-resistant drums or bags to preserve the crystal structure and color. Nothing frustrates end-users more than opening a shipment and seeing visible spots or off-odors. While many resellers transfer bulk product into their own packaging, introducing risk of contamination or degradation, our QC teams handle product through every stage in-house.

    Beyond Purity: Attentive Customer Support

    Direct communication saves time and misunderstandings. We answer technical inquiries based on actual plant data, whether it’s solubility in a particular organic solvent, recrystallization recommendations, or suggestions for post-processing filtration. Several customers in the pigment industry have remarked that our team’s approach to troubleshooting beats chasing generic responses from trading houses or non-manufacturing reps.

    Formulators working with more sensitive synthetic sequences sometimes run into trace reactivity from poorly washed starting material. Our analytics team utilizes both GC and LC in parallel, flagging even minor contaminants. Over years of supporting diverse applications, we’ve documented how our process tweaks increase downstream batch consistencies, enabling customers to avoid repeated purification steps.

    What You Get Out of Differentiated Quality

    Some companies refine or resell raw imported material with broader impurity bands. We often hear stories about delayed pilot batches or increased off-spec production due to "trivial" differences in starting material. Our approach always starts with solid, consistent upstream chemistry. Structural isomers, inconsistent crystallinity, or fluctuating water content might look subtle on paper but materialize as real pain points in scale-up.

    A few years back, an intermediate manufacturer turned to us after seeing significant lot-to-lot variation with other sources. The client's HPLC profiles showed a shifting tail that caused significant late-stage purification needs. After switching to our material, their process yields stabilized and they reported a measurable drop in rejected batches. That’s not something we orchestrated in theory—our quality hinges on decades of learning from the plant floor, tweaking reaction conditions, updating filtration protocols, and acting on customer feedback.

    Supporting Sustainability and Responsible Sourcing

    Efforts in the past decade have pushed the industry towards responsible footprints. We’ve responded not just to regulation but to the direct requests from partners seeking fewer environmentally problematic by-products. By optimizing our processes for cleaner bromination and reduction steps, waste volumes dropped and workplace exposure risks decreased. Waste streams now pass through multi-stage treatment, cutting the residuals that hit municipal systems. Occasionally, colleagues in R&D work with academic labs to scale up greener process variations, which we then assess for quality and cost impact before plant-wide adoption.

    Supply chain transparency matters more than ever. Rather than outsourcing core chemistry or relying on third-party QC claims, we keep raw material sourcing and quality audits internal, supported by an established relationship with local and regional suppliers. Buyers can trace each lot of 4-Bromo-2-Nitroaniline directly to a documented synthetic batch, with validation data reflecting actual, not theoretical, impurity levels.

    Safe Handling and Long-Term Partnership

    Most customers familiar with aromatic amines and nitro-compounds already follow strict handling procedures. We offer seasoned advice based on firsthand use: nitrogen blanketing for long-term storage, primary use of PTFE-lined containers for aggressive compounds, and regular training updates for on-site staff. Feedback about how customers handle and store our products often circles back into our own operations, so that we can recommend minor but impactful improvements, from improved drum labeling to shelf-life monitoring protocols.

    Training doesn’t stop at our own doors. Clients developing products heavily based on 4-Bromo-2-Nitroaniline have at times consulted with us as new formulation chemists come aboard. Our staff has conducted on-site walk-throughs to help partners optimize process sequences, reduce operator risk, and tighten documentation—from intake all the way through to application in customer facilities.

    Comparing to Alternatives and Derivatives

    4-Bromo-2-Nitroaniline stands alongside related aniline derivatives, such as 2-Bromo-4-Nitroaniline or even simple 2-Nitroaniline. Each compound exhibits different resonance effects, impact on reactivity, and solubility profiles. For manufacturers that’ve tried to substitute one for another, the resulting impacts aren’t always apparent until late in the process. Swapping out the bromine or repositioning the nitro group frequently alters coupling chemistry, especially during dye or pigment preparation, risking mismatched color fastness or reduced synthetic efficiency.

    In production-scale practice, our 4-Bromo-2-Nitroaniline delivers reliable performance that translates into fewer re-works and more predictable yields. While some competitors offer broader product portfolios, few maintain chemical lines with single-digit ppm impurity levels as a standard for each drum, lot after lot. That’s a reflection not just of routine testing but of a culture focused on chemical integrity.

    Challenges and Continuous Improvement

    Everybody in the specialty chemical sector encounters hurdles: fluctuating raw material prices, evolving safety standards, and sometimes unpredictable transport regulations. We manage these realities not just by smoothing out purchasing strategies but by investing where it counts—equipment upgrades, process monitoring, and integrated resource planning. Looking at the specifics of 4-Bromo-2-Nitroaniline production, years of incremental adjustment have shortened cycle times and reduced reprocessing events.

    Unexpected events have their own lessons. A few years back, we faced a batch deviation traced to a faulty condenser that allowed atmospheric ingress during bromination. Instead of glossing over the issue, our team dug in, updated maintenance schedules, and integrated new online monitoring, so every subsequent run could guarantee spec compliance. We don’t pretend every process runs flawlessly, but we document, correct, and adapt based on what we actually see on the production floor.

    Customer-Driven Solutions

    As a direct manufacturer, we aim to offer more than just a price or a drum off the shelf. Over the years, customers have needed bulk packaging for major dye projects, lab-grade vials for analytical method validation, and customized documentation when developing new certifications. We’ve shipped extra lab samples for downstream QC method creation and provided rapid impurity breakdowns when customers encountered contamination elsewhere in their own supply chains.

    End-users also push us to broaden our technical offering. Whether it's a request for compatibility data with a specific solvent system or a side-by-side comparison with another halogenated aniline, we either draw on our in-house experience or dial in our analytics team for an answer. These efforts build tighter relations and foster mutual trust—a dividend regular trading agents rarely provide.

    Closing the Gap Between Plant and Application

    Ultimately, we don’t view manufacturing as a separate step from the goals of research chemists or process engineers. Our own lab spends just as much time learning about use cases and synthetic routes as we do fine-tuning our reactors. We frequently send out batch-specific COAs reflecting real-time analytical results, not simply generic past data. This transparency helps our partners develop their own processes with confidence, speeding new product introduction.

    While 4-Bromo-2-Nitroaniline isn’t the flashiest molecule, building trust through consistent quality, practical support, and direct communication matters more than ever. We welcome technical dialogue, whether a partner wants to tweak crystal size distribution or verify environmental compliance details. Each production run draws not just on textbook chemistry, but on real-world experience that can’t be swapped out or cut and pasted.

    Sharing knowledge openly drives progress for everyone using our compounds, from the world’s leading laboratories to specialty production lines producing tomorrow’s pigments, drugs, and advanced materials. Whether you’re running gram-scale experiments or servicing multi-ton dye customers, we deliver the reliability and integrity that only a focused, hands-on manufacturer can guarantee.