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2-Bromo-5-Chloronitrobenzene

    • Product Name 2-Bromo-5-Chloronitrobenzene
    • Alias 2-Bromo-5-chloro-1-nitrobenzene
    • Einecs 221-794-1
    • 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

    935228

    Chemicalname 2-Bromo-5-Chloronitrobenzene
    Casnumber 23518-54-1
    Molecularformula C6H3BrClNO2
    Molecularweight 236.45
    Appearance Yellow crystalline solid
    Meltingpoint 70-73°C
    Density 1.84 g/cm3
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Smiles C1=CC(=C(C=C1[N+](=O)[O-])Br)Cl
    Inchi InChI=1S/C6H3BrClNO2/c7-4-1-2-5(8)6(3-4)9(10)11/h1-3H
    Synonyms 2-Bromo-5-chloro-1-nitrobenzene

    As an accredited 2-Bromo-5-Chloronitrobenzene 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-Bromo-5-Chloronitrobenzene, tightly sealed, labeled with hazard warnings and chemical information.
    Shipping 2-Bromo-5-chloronitrobenzene is shipped in tightly sealed containers, compliant with international hazardous materials regulations. The package is labeled as a hazardous chemical (UN Number appropriate), protected from moisture, heat, and direct sunlight, and transported by trained personnel. Appropriate safety documentation, including SDS, accompanies each shipment to ensure safe handling and delivery.
    Storage **2-Bromo-5-Chloronitrobenzene** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong acids, bases, and reducing agents. Keep the container tightly closed and protected from physical damage. Store at room temperature, away from direct sunlight and moisture. Use appropriate personal protective equipment when handling this chemical.
    Application of 2-Bromo-5-Chloronitrobenzene

    Applications of 2-Bromo-5-Chloronitrobenzene in Industrial Manufacturing

    2-Bromo-5-chloronitrobenzene supports production processes in several specialized sectors requiring halogenated nitroaromatic intermediates. As the original manufacturer, we supply this intermediate to certified customers across the fine chemical, agrochemical, pharmaceutical, and colorants industries for incorporation into high-value formulations.

    1. Synthesis of Agrochemical Active Ingredients

    In modern agrochemical production, manufacturers use this compound to build complex active molecules for selective herbicides and fungicides. It acts as a halogenated aromatic core that enables the controlled introduction of substituents via nucleophilic substitution or reduction. Process chemists typically apply it for nitro group reduction and further coupling reactions, resulting in diversified crop protection agents through scalable technical syntheses.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 (EU plant protection products)
    • ISO 9001:2015 Quality Management
    • FAO/WHO specifications for technical grade active ingredients
    • REACH registration for all supplied volumes

    Typical usage ratio

    • Used at 1.2–1.6 molar equivalents in most halogen exchange or nitro group reduction reaction recipes, with adjustment based on desired ring substitution patterns and proprietary downstream reaction balance.

    Downstream process integration

    • Introduced during the first or second synthesis step as the principal aryl halide substrate; processed under controlled reduction conditions with subsequent coupling or alkylation depending on the targeted active compound.

    Final product types

    • Triazole fungicides
    • Phenoxycarboxylic acid herbicides
    • Benzimidazole pesticides
    • Substituted aniline derivatives for crop protection formulations

    2. Synthesis of Pharmaceutical Intermediates

    Pharmaceutical manufacturers use the compound to generate substituted anilines, an essential step for several APIs, especially in the anti-infective and anti-inflammatory categories. As a key halogenated and nitro-activated platform, it participates in nucleophilic aromatic substitution or catalytic hydrogenation to form pharma-grade intermediates under validated GMP conditions. Integration ensures batch traceability and reproducibility for regulated drug synthesis.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP–NF monograph compliance for final APIs
    • EDQM CEP requirements for pharmaceutical intermediates
    • 21 CFR Part 211 (US GMP)

    Typical usage ratio

    • Applied at 1.0–1.4 molar equivalents, set by the stoichiometry required in selective hydrogenation, amination, or direct substitution protocols, following validated pharmaceutical synthesis documents.

    Downstream process integration

    • Fed directly into the API synthesis route as the initial aromatic precursor, followed by reduction or protected amination, and subsequent derivatization to access target API scaffolds in a CGMP environment.

    Final product types

    • Intermediate for fluoroquinolone antibiotics
    • Anti-inflammatory API intermediates
    • Pain-management drug scaffolds
    • Key building blocks for CNS-active compounds

    3. Development of Azo and Disperse Dyes

    Dye producers utilize this material as an electro-deficient aromatic base to achieve targeted electron-withdrawing substitution patterns required for high-performance azo and disperse dyes. The nitro and halogen substituents provide robust colorfastness and light stability properties after coupling reactions, particularly in textile dyes. Formulators adjust reaction conditions to achieve precise shade reproducibility for synthetic fibers.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • ZDHC MRSL, V.2.0
    • ETAD Code of Ethics
    • China GB/T 7573 for textiles

    Typical usage ratio

    • Applied in the range of 0.6–1.2 molar equivalents per coupling batch in azo condensation or halogen replacement reactions, ratio adjusted based on target chromophore and color strength requirements.

    Downstream process integration

    • Processed in the dye synthesis step as an activated nitroaromatic, before reduction to amine or directly entered into diazotization and coupling to naphthol derivatives or other chromogenic fragments.

    Final product types

    • Disperse dyes for polyester
    • Azo dyes for synthetic fabrics
    • Solvent dyes for plastics and coatings
    • Colorants for technical fiber applications

    4. Manufacture of Specialty Electronic Chemicals

    Electronic materials manufacturers rely on this compound as a controlled halogen and nitro source for functionalizing organic semiconductors, LCD intermediates, and optoelectronic monomers. It enters targeted cross-coupling or halogen-lithium exchange steps to introduce specific donor–acceptor groups, which enhances charge transport and optical absorption in downstream devices.

    Industry compliance standards

    • IEC 61249-2 (Electronic substrate standards)
    • RoHS Directive 2011/65/EU
    • ISO 14001 Environmental Management System
    • IPC-4101 for substrate base materials

    Typical usage ratio

    • Used at 0.8–1.0 molar equivalents per reaction in cross-coupling, adjusted by the desired halogen density and nitro activation level specified in organic device blueprints.

    Downstream process integration

    • Charged at the intermediate synthesis stage, where it is converted via Suzuki or Stille coupling or selectively reduced for further halogen exchange prior to monomerization and copolymerization.

    Final product types

    • OLED intermediate building blocks
    • Luminescent dye precursors for displays
    • Charge-transport agents for solar cells
    • Specialty polymers for microelectronic films
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    Certification & Compliance
    More Introduction

    2-Bromo-5-Chloronitrobenzene: A Commentary from the Manufacturer

    Direct from the Reactor: Realities of Production

    Every chemical that comes out of our plant brings its own challenges and surprises. 2-Bromo-5-Chloronitrobenzene, with its CAS number 39489-76-0, keeps us vigilant with its double halogenation and nitro substitution patterns. Our production process for this compound starts with a focus on consistency, since even the slightest deviation during halogen exchange or nitration can lead to off-spec material. In practice, we have found that temperature control during the halogen exchange step has the most dramatic impact on purity. No batch is exactly like the last one, and that’s where hands-on, daily familiarity with the chemistry pays off. Process technicians can spot an inconsistency in color or aroma faster than any probe or instrument.

    Purity, Particle Size, and the Details That Matter

    Customers use 2-Bromo-5-Chloronitrobenzene mainly as an intermediate for pharmaceutical and agrochemical synthesis, so we pay close attention to residual solvent content and trace impurities. The crystalline nature of this compound allows for filtration and recrystallization steps that give us an edge in controlling particle size and purity in ways that aren’t possible for more oily or amorphous intermediates. Over multiple campaigns, we’ve iterated on washing protocols to reduce inorganic residues that can show up during downstream metal-catalyzed coupling reactions. A critical step: we screen product lots by GC and HPLC to monitor not just the main component, but also low-level byproducts. We route off-spec lots to further purification instead of hoping no one notices traces of 3-bromo-6-chloronitrobenzene or dinitro impurities.

    Typical purity targets for us land between 99.0% and 99.5% by HPLC, depending on the client's end use. Some customers who drive toward active pharmaceutical ingredients demand even tighter windows, where a 0.1% unknown peak triggers a full root-cause analysis. Those requests require close coordination between our lab techs and plant operators to look at solvent selection, batch timing, and drying schedules. Moisture content also comes under scrutiny, especially where the material is sensitive to hydrolysis or where downstream requirements set lower than 0.2% water.

    Small Tweaks, Big Differences

    The dual halogenation in this molecule—bromine at position 2, chlorine at position 5—changes reactivity in unexpected ways compared to isomers like 4-bromo-3-chloronitrobenzene. From experience, we’ve learned that bromine’s position supports more selective cross-couplings, while the nitro group serves as a strong electron-withdrawing group that lets chemists choose selective reduction or further substitution. Colleagues on the pharma intermediates side often mention how 2-Bromo-5-Chloronitrobenzene provides good reactivity for Suzuki couplings, especially when prepping heteroaromatic frameworks.

    If you compare this compound with 4-bromo-1-chloronitrobenzene or the purely chlorinated and nitrated analogs, you see immediate effects on melting point, solubility, and downstream reactivity. We’ve noticed that 2-bromo-5-chloro consistently offers greater solubility in DMF, DMSO, and acetonitrile, making it easier to charge and stir in both bench and plant-scale glassware. That extra solubility also improves process safety, since you don’t end up with stubborn slurries that can clog transfer lines or resist filtration.

    What Sets This Compound Apart Defined by Practice

    The question always circles back to: Why select this compound for synthesis work? As the manufacturer, we see the demand spike when innovators need both high reactivity and the stability of a halogenated nitroarene. Over several production years, our customers have used 2-Bromo-5-Chloronitrobenzene as a building block in insecticides, fungicides, and intermediate steps for advanced pharmaceuticals. The high halogen load translates to downstream options for amination, reduction, and metal-catalyzed reactions that aren’t feasible with other isomers.

    We’ve fielded more than a few custom requests for alternative particle sizing or lower sodium content. The source of sodium, as it turns out, can come from common process aids or work-up steps. Besides, trace metals remain an industry-wide challenge, especially knowing how stringently some regulatory bodies monitor these in API manufacturing. Our investments in trace metal analysis and post-crystallization washing routines give us confidence in what leaves the drum.

    Reliability—Not Just a Buzzword

    No chemical batch lives up to its promise without strict attention to reproducibility, so we benchmark every cycle against historical bests. One frequent feedback point involves color variance. While the ideal 2-Bromo-5-Chloronitrobenzene presents as an off-white to yellow solid, sometimes a faint gray cast or a stronger-than-normal yellow suggests residual byproducts. We take those cues seriously, cutting open filter cakes and sampling all the way down to the bottom. End-users appreciate constant color and flow, as batch-to-batch variability leads to re-optimization of their own processes.

    Our closest customers often visit to audit manufacturing operations in person. During those walk-throughs, the questions revolve less around certificates of analysis and more around real-time observations—how the operators monitor pressure, how the lab interprets HPLC traces, how waste streams are segregated at the source. These on-the-ground realities matter more than any marketing catchphrase ever could.

    Practical Product Details: Loading, Handling, Transport

    Though our product travels extensively, sensitive handling starts at packaging. 2-Bromo-5-Chloronitrobenzene goes straight into lined fiber drums to avoid corrosion from halide traces, and the drums stack better than traditional plastic alternatives. Inside the plant, our operators always work under local exhaust, wearing gloves and using sealed scoops, because the powder stings if inhaled or lingering dust contacts skin. Sensitive compounds like this one deserve no shortcuts—no trainee learns through guesswork; everything’s demonstrated live during onboarding.

    We have learned from hard experience that product temperature on loading must remain tightly regulated. A hot filling leads to condensation, so our drums only accept product after cooling under nitrogen purge. This keeps moisture and atmospheric oxygen out, both of which can cause caking or slow decomposition in storage. We keep pigments and dust to an absolute minimum during packaging, since even a slight orange hue or fine fraction can trigger customer complaints.

    Efficiency in Synthesis: End-User Stories

    Since the beginning of producing this compound, we’ve tracked feedback across many downstream reactions. Pharmaceutical customers find that the bromo and chloro groups align for different activation conditions, allowing for orthogonal synthetic routes—take the bromine for coupling, save the chlorine for late-stage modification, or vice versa. Some process chemists in the agrochemical sector comment that this arrangement helps bypass certain costlier or hazardous chlorination steps.

    Over years, our technical team supports scale-ups by offering insight on solvent compatibility and potential side reactions. For example, during one campaign to scale an aniline derivative, a collaborator noted increased yield variation. Our team traced it back to slight shifts in residual acetic acid from an upstream step—something only direct plant involvement can uncover. In contrast, buying this material from a distributor rarely comes with such detailed process knowledge.

    We’ve seen this compound used as a direct precursor for dense heteroaryl compounds where purity impacts overall project timelines. A pharma customer once shipped us back a batch, demanding trace chlorinated biphenyl quantitation—an impurity we had never considered critical before. That event led us to rethink our trace analysis panel and upgrade our instrument sensitivity, benefiting every subsequent lot. End-user chemistry is always more creative and demanding than any written guideline.

    Safety, Environmental Realities, and Lessons Learned

    While we claim no magic environmental bullet, our production line keeps the focus on responsible handling and waste minimization. Nitration and halogenation each produce side streams that require careful neutralization before discharge. Local authorities run unannounced checks and routinely sample our effluent. This pressure makes environmental compliance part of every tank changeover and line cleaning session.

    Learning from past mistakes, our plant protocols now require double checks on all waste management logs. Small losses—what operators used to call “unaccounted for”—now drive daily audits and have forced us to invest in better solvent recovery equipment. Employees get periodic training in spill containment and first-aid for chemical exposure, shaped by eyewash and safety shower drills. No process can afford to treat safety and environment as afterthoughts.

    Bulk buyers often visit to review materials safety data and site records—they expect no less. Detailed batch histories are maintained, and deviations—however minor—get tracked for months. The approach isn’t about regulatory boxes, but about knowing what’s really in the drum leaving our floor.

    Comparison with Similar Compounds: Why Our Choice Matters

    If you line up common nitrobenzene derivatives, the subtle differences in halogenation pattern make or break certain synthetic routes. 2-Bromo-5-Chloronitrobenzene, with its particular substitution, gives a predictable reactivity profile in cross-coupling chemistry. Compared with 4-bromo-1-chloronitrobenzene, our product delivers faster rates in Buchwald-Hartwig amination, and holds up to stronger bases before degrading. The balance of substitution also helps with regioselective substitutions—veteran chemists prefer our product when looking to avoid scrambling or unpredictable side reactions.

    Compared to unsubstituted nitrobenzenes or those with only one halogen, our experience is that reaction times shorten and fewer purification steps are needed downstream. In practical terms, this means less solvent use, shorter work-up schedules, and, in many cases, better overall yields.

    Perhaps most important, we maintain stable supply chains for both raw materials and site operations. During global market disruptions, that stability has allowed customers to keep their own processes moving without sudden reformulations or costly delays. Our direct engagement with partners keeps us nimble. Feedback isn’t just welcomed—we seek it, because improvements in process or product turn into real benefits not just for us, but also for the industries we support.

    Experience at Scale: The Human Element

    The human element of making 2-Bromo-5-Chloronitrobenzene comes through in every batch. Operators draw on years—sometimes decades—of practical know-how to spot issues where a less experienced eye might gloss over shifts in color or subtle changes in crystallization. Regular team briefings pass on hard-won lessons, like how even a minor tweak in agitation rate can mean the difference between fine crystals and a stubborn lump at the bottom of a reactor.

    Technical support conversations with customers regularly lead to changes in our production line. We’ve updated filtration protocols based on feedback about dustiness or flow, and we work with end-users to offer lot-specific certificates, analytical data, and storage recommendations. Instead of staying locked into our own procedures, we run trial lots for research partners, changing isolation and drying conditions as their results dictate.

    We document, record, and trace back every batch variable, tracking what works, what flops, and what yields the best results for users. In this business, the real breakthroughs come not from standardized protocols, but from arms-length attention and engagement with every detail, no matter how small.

    Working Beyond the Spec Sheet: Insights and Lessons

    Many who first encounter 2-Bromo-5-Chloronitrobenzene see nothing but another mid-spectrum intermediate—a drum of powder waiting to be split and solubilized. Years in manufacturing have shown us how wrong that first impression can be. Every step, from raw material sourcing, through batch charging and crystallization, right up to final drum closure, comes with pitfalls and opportunities for new ideas.

    Constant pursuit of better yields and cleaner profiles drives our improvements. Sometimes the fix is tweaking a reagent charge profile across a five-minute stretch, sometimes it means swapping out glassware rinses that seemed trivial but actually changed the impurity profile. We listen to customer cases where a subtle impurity spikes an off-odor, or a slow-dissolving clump delays bench work. These stories shape how we refine processes and guidelines for the next production run.

    We see our role not as just filling drums with product, but as partners in progress—actively taking lessons from the field and pushing for greater value with every outgoing lot. Whether the aim is higher selective functionalization, or more reliable downstream coupling, we make it our business to keep learning and adapting.

    Setting the Standard—Not Resting on It

    Long-term relationships—and repeat business—are built not on standard certificates but on trust and transparency. That’s been our experience after delivering thousands of kilograms to demanding chemists. We know that surprises in a reaction, setbacks in yield, or delays in delivery all trace back to choices made on our shop floor. Plant managers, technicians, and logisticians engage every day to balance efficiency, safety, and product quality.

    Unresolved challenges always remain: better control over trace byproducts, more sustainable sourcing of starting halides, and new demands customers think up that stretch what anyone believed possible for a “basic intermediate.” We stay open to these developments, ready to update technique, equipment, or even core process flows to continue offering what chemists, engineers, and innovation leaders expect from a manufacturer.

    Closing Thought

    The story of 2-Bromo-5-Chloronitrobenzene is one of detail, partnership, and the day-to-day decisions that add up to industrial progress. As manufacturers, we experience firsthand the realities and responsibilities of turning fine chemicals into reliable tools for science and industry. Every drum dispatched carries not just a product, but a testimony to the discipline, experience, and ongoing curiosity that guides our work. We welcome challenges and the daily chance to do things better, batch after batch, together with the customers who rely on our expertise.