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3-Bromo-5-Chlorobenzonitrile

    • Product Name 3-Bromo-5-Chlorobenzonitrile
    • Alias 3-Bromo-5-chloro-o-cyanobenzene
    • Einecs 610-003-5
    • 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

    216221

    Chemicalname 3-Bromo-5-Chlorobenzonitrile
    Casnumber 57410-19-6
    Molecularformula C7H3BrClN
    Molecularweight 216.47
    Appearance Off-white to light yellow solid
    Meltingpoint 78-82°C
    Boilingpoint 296°C
    Density 1.68 g/cm3
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Smiles C1=C(C=C(C=C1Br)Cl)C#N
    Inchi InChI=1S/C7H3BrClN/c8-6-1-5(4-10)2-7(9)3-6/h1-3H
    Synonyms 3-Bromo-5-chloro-1-benzenecarbonitrile
    Storageconditions Store at room temperature, tightly sealed, away from light

    As an accredited 3-Bromo-5-Chlorobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "3-Bromo-5-Chlorobenzonitrile, 25g" with hazard symbols, product code, and tightly sealed screw cap.
    Shipping 3-Bromo-5-Chlorobenzonitrile is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. It is classified as a hazardous material and should be transported according to local and international regulations, with appropriate labeling and documentation. Handle with care, and store in a cool, dry, well-ventilated area upon arrival.
    Storage 3-Bromo-5-Chlorobenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, moisture, and sources of ignition. Keep it separated from incompatible substances such as strong oxidizers, acids, and bases. Store at room temperature and ensure the storage area is clearly labeled and equipped for chemical safety.
    Application of 3-Bromo-5-Chlorobenzonitrile

    Applications of 3-Bromo-5-Chlorobenzonitrile in Industrial Manufacturing

    As a specialized producer of 3-Bromo-5-Chlorobenzonitrile, we supply this intermediate to multiple downstream sectors where precise chemical functionality and strict compliance are required. The following sections outline advanced industrial uses in pharmaceutical, agrochemical, dye, and polymer industries, with detailed guidance on regulatory frameworks, in-process roles, formulation ratios, and the nature of resulting products.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical manufacturers utilize 3-Bromo-5-Chlorobenzonitrile as a building block for synthesizing drug molecules, particularly within the anti-inflammatory and central nervous system (CNS) categories. The aryl nitrile backbone allows for selective halogen exchange, coupling, and subsequent transformation into bioactive heterocycles. Reactors integrate 3-Bromo-5-Chlorobenzonitrile during early-stage API assembly, following GMP protocols and multi-step synthesis pathways. Process engineers control addition rates and monitor conversion using in-line analytical techniques to ensure batch consistency.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) (ICH Q7, US FDA, EU GMP)
    • USP, EP, JP for drug substance quality
    • REACH Annex XVII – hazardous substance management
    • DMF support for regulated markets

    Typical usage ratio

    • Ranging from 0.2 to 0.8 molar equivalents versus target heterocycle or core structure, adjusted by desired yield and side reaction minimization

    Downstream process integration

    • Enters the primary condensation or Suzuki-Miyaura coupling step as halogenated arene
    • Undergoes further nitrile group modification in subsequent steps
    • Role as a platform intermediate for diversification before final API crystallization

    Final product types

    • Benzimidazole series CNS drugs
    • Selective kinase inhibitors
    • Tricyclic antidepressants precursors
    • Anti-inflammatory pharmaceutical actives

    2. Key Intermediate for Agrochemical Formulation

    Leading crop protection companies employ 3-Bromo-5-Chlorobenzonitrile for synthesis of nitrile-containing herbicides and fungicides. The dichloro and bromo substitution pattern contributes to high selectivity and bioactivity when constructing phenoxy or pyridine-based agrochemical actives. Chemists introduce the material during the Grignard reaction or across amination steps, maintaining full traceability and compliance with EPA and global agrochemical standards.

    Industry compliance standards

    • FAO/WHO JMPR pesticide specification and evaluation
    • US EPA 40 CFR part 180 (tolerance for residues)
    • ISO 9001 production quality management
    • REACH registration for export to Europe

    Typical usage ratio

    • Typically 0.15–0.45 mol per mol final active ingredient, adjusted based on desired halogenation and final molecule design

    Downstream process integration

    • Added during functional group introduction of advanced intermediates
    • Participates in nucleophilic aromatic substitution reactions
    • Serves as structural precursor in the stage before esterification or final chlorination

    Final product types

    • Nitrile-containing herbicides (e.g., bromoxynil analogs)
    • Triazole fungicide building blocks
    • Novel seed coating agents
    • Intermediate for selective insecticides

    3. Chromophore Construction for Performance Dyes

    Producers of specialty and performance dyes incorporate 3-Bromo-5-Chlorobenzonitrile to synthesize complex aromatic dye precursors, specifically for applications demanding improved lightfastness and chemical resistance. The dual halogen and nitrile functionalities yield chromophore segments for disperse, acid, and reactive dye portfolios. Manufacturers dose at carefully controlled stages to drive selectivity in palladium-catalyzed cross-coupling and Friedel-Crafts acylation reactions, tracking conversion with colorimetry and HPLC.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – textile chemical safety
    • ZDHC MRSL for restricted substances
    • EN 71-3 pigment migration limits (for toys/textiles)
    • REACH SVHC reporting

    Typical usage ratio

    • Used at 5–15% molar ratio relative to total chromophore mass, depending on target shade and fastness requirements

    Downstream process integration

    • Integrated at the initial aromatic coupling or nitrile activation stage
    • Reacted under controlled pH and catalyst selection for maximal yield
    • Subjected to subsequent sulfonation or amino group introduction before granulation

    Final product types

    • Disperse dyes for polyester fibers
    • Functional pigments for automotive coatings
    • Reactive dyes for cotton textiles
    • High-durability printing inks

    4. Monomer Functionalization in Specialty Polymers

    High-performance polymer manufacturers access 3-Bromo-5-Chlorobenzonitrile for its role as a halogenated aromatic monomer precursor. The molecule supports unique chain-extension and cross-linking properties in engineering resins and specialty coatings. In industrial batch polymerization, operators introduce this monomer at the oligomer coupling phase, optimizing ratios to balance mechanical performance, chemical resistance, and processibility. The halogen pattern aids in further modification and expands copolymer design latitude.

    Industry compliance standards

    • ISO 9001 process traceability
    • UL 94 flammability testing for plastics
    • RoHS Directive (2011/65/EU) for restricted halogen content
    • REACH Annex XIV for polymerization auxiliaries

    Typical usage ratio

    • Introduced between 2–10% by mole in aryl polymer backbones; specific content depends on application property targets and downstream processing equipment

    Downstream process integration

    • Supplied to the chain-termination or cross-linking reactor stage
    • Functions as a copolymerizable segment for high glass transition temperature formulations
    • Incorporated after initiator addition under controlled temperature curves

    Final product types

    • High-performance polyarylenes
    • Solvent-resistant coatings
    • Advanced electrical insulation compounds
    • Flame-retardant plastic housings
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    Certification & Compliance
    More Introduction

    Understanding 3-Bromo-5-Chlorobenzonitrile: From Bench Chemistry to Industrial Application

    Meeting the Real Needs of Synthetic Chemistry

    3-Bromo-5-Chlorobenzonitrile features in countless specialized syntheses. In facilities that handle halogenated aromatics every day, its value has grown more pronounced in the last decade. As the manufacturer, we have watched the shift in demand from simple monochlorinated benzonitriles toward analogs like this one, carrying both bromine and chlorine. This double substitution stems from increased complexity in target molecules—pharmaceutical intermediates, novel agrochemicals, and advanced materials that keep coming out of the research pipeline.

    Why Structure Matters

    Our product—known in our catalog as 3-Bromo-5-Chlorobenzonitrile, molecular formula C7H3BrClN—combines an electron-withdrawing nitrile with two distinct halogens. In practice, this substitution pattern allows fine-tuned activation on the benzene ring. This contributes to the selective reactivity highly prized in cross-coupling reactions, nucleophilic aromatic substitution, and functional group transformations.

    The placement of substituents—bromine at the third position and chlorine at the fifth—changes everything about how this molecule participates in downstream processes. The differences come out clearly during catalytic couplings. Bromine's reactivity toward palladium serves as a reliable entry point for creating new C–C bonds. Chlorine at the 5-position offers extra versatility; it can remain as a handle for late-stage modifications or be exchanged under catalytic conditions, depending on the end goal. Our scale-up team has handled every combination of these transformations, so we've seen the impact of each atom.

    Manufacturing Insights: Control at Every Step

    Producing halogenated benzonitriles comes with its hazards and technical hurdles. We draw from decades of process optimization to keep bromination and chlorination selective and clean. Each batch starts with carefully sourced feedstock, often tracked to within a few parts per million impurities. The key is preventing overhalogenation and unwanted isomer formation—mistakes here lead to purification headaches.

    Many customers outside the chemistry world underestimate the difficulties in getting just the right substitution pattern, without generating symmetrical byproducts. In the lab, this often happens as a single flask reaction, but on kilo and ton scales, heat transfer, solvent loading, and reagent purity must be monitored continually. Our analytical QC doesn't only confirm correct structure; it scrutinizes trace impurities likely to affect later synthetic steps. That transparency translates to fewer unknowns for customers downstream.

    Purity and Consistency—What End-Users Notice Most

    Every project starts with reliable raw materials. Slight variations in impurity profile can spell disaster for scale-up in active pharmaceutical ingredient discovery or a new crop-protection compound. Our typical material offers purity well above 98.5 percent by HPLC, often higher. More crucially, we look beyond simple purity numbers. We track moisture, residual halides, and organic residues left over from incomplete conversion. The few tenths of a percent we eliminate at our plant prevent trouble as these molecules cycle through further reagents in someone else's lab.

    These control measures aren't just academic. Several clients have sent us chromatograms from prior suppliers, showing ghost peaks or inconsistent baseline drift. Inconsistencies turn into failed reactions, wasted resources, or analytical speculation. We keep our production campaigns tightly aligned, taking feedback straight from synthetic groups fixing bottlenecks, not just from paper specifications.

    Differences from Simpler Halobenzonitriles

    Compared to single-halide analogs, this product brings a broader reactivity spectrum. Many follow conventional wisdom and reach for either 3-bromobenzonitrile or 3-chlorobenzonitrile, depending on compatibility with catalysts or desired selectivity. But this specific double-halide profile proves vital in multistep synthesis, especially where orthogonal transformations matter. The presence of both bromine and chlorine on the ring permits selectivity control rarely achievable with single halogen derivatives; bromine reacts first, leaving the chlorine untouched for sequential transformations.

    Applications in complex molecule synthesis—particularly heterocycles, functionalized arenes, or substituted pyridines—often require this nuanced control. Research teams developing kinase inhibitors, fungicides, or OLED precursors appreciate the advantages. They can string together steps where bromine acts as a leaving group in Pd-catalyzed couplings, with the chlorine reserved for late-stage introduction of polar fragments or deuterium labeling.

    On the manufacturing side, differences count for more than just chemical reactivity. Waste profile, solvent compatibility, crystallization behavior, and shelf stability all shift when both halogens are present. Our formulation expertise addresses these differences directly, ensuring stability from production through shipping—something customers in hot or humid climates notice most.

    Applications: More than Just a Starting Material

    Aside from serving as a precursor, 3-Bromo-5-Chlorobenzonitrile finds use in places mainstream chemical catalogs don’t mention. We've watched it integrated into custom photoresist molecules, sensors, and as a nucleating core during advanced material development. In some veterinary actives, its chemical framework persists through half a dozen transformations, carrying substituents into positions difficult to access by direct substitution.

    We have ongoing partnerships with academic groups studying its role in heterocycle construction, as well as industrial teams patenting new insecticides and nematicides. In one recent collaboration, a specialty electronics company trialed our high-purity lots in the development of new charge-transport materials. Halogen patterns changed charge mobility in a surprising way, underscoring why fine control at the manufacturing level still matters—often right up to the commercial launch stage.

    Some end-users have designed divergent routes for kinase inhibitor libraries, using the selective cross-coupling properties of this compound to introduce complex aromatic sidechains. The production-level feedback we receive often leads to minor adaptations in reaction setup or solvent swaps, pushing forward the broader field of drug and agrochemical discovery.

    Supporting Solutions for Real-World Challenges

    Requests for custom particle size come up frequently, especially for users with flow chemistry setups or highly automated reactors. Coarse and fine crystalline lots behave very differently in high-shear vessels or continuous stirred tank reactors. Our facilities run multiple milling and sieving operations, backed by in-house physical property testing, because we've learned—always through direct reports—how crucial flowability and weight dosing stability become at large scale.

    Shipments sometimes travel weeks across continents in varied climates. We use packaging designed for halogenated organics: lined drums, moisture-absorbing liners, and desiccants. Our own logistics team coordinates cold-chain shipments upon request, particularly for highly moisture-sensitive lots or during the humid part of monsoon seasons. These steps cut down the occurrence of degraded material on arrival—an all-too-common event that wastes time and derails schedules.

    Feedback Loops Drive Product Refinement

    Product development doesn’t happen in a vacuum. We listen directly to synthetic chemists—the people troubleshooting stalled reactions or trying to squeeze another percent out of yield. Improvements in purity, adjustments to crystal habit, or tighter control over halide ratios arise from these dialogues. Once, a group scaling up a new process pointed out recurring analytical artifacts; that led our process engineers to re-examine a final wash, leading to a new solvent system that reduced a stubborn trace contaminant by half.

    Some feedback centers around ease of dissolution or compatibility with novel solvent systems engineered for green chemistry standards. That spurred changes in our drying protocols, cutting down on residual solvents and guaranteeing faster dissolution in customer screening setups. We learned early on that what reads “acceptable” in-house can send a very different signal on an unfamiliar machine a thousand kilometers away.

    These tweaks don’t just boost our reliability—they support budding research, pilot plant campaigns, and full commercial launches built on the backbone of reliable, fit-for-purpose inputs.

    Looking Ahead: Evolving with Industry Needs

    The landscape for specialty benzene derivatives keeps evolving. In our experience, what’s routine in the lab quickly becomes a bottleneck—or a breakthrough—in manufacturing. "Standard grade" becomes obsolete the moment a customer starts pushing reactions toward higher efficiency or regulatory thresholds for impurity levels tighten. We have to keep anticipating change. As green chemistry shapes process design and regulatory agencies focus on trace contaminants, our operation adapts.

    Adoption of in-process monitoring allows us to follow reaction progress directly and avoid waste. Each step, from bromination to crystallization, gets checked by HPLC, GC, and NMR. We built redundancy into these checks because we’ve seen, over time, that small errors escalate when scaled. Investing in real-time QA, rather than relying solely on endpoint batch testing, lets us catch issues before they reach our clients’ doors.

    The drive toward sustainable chemistry has not bypassed this compound. Some researchers now ask about greener brominating reagents, lower solvent footprints, and recyclable wash streams. Over the years, we’ve piloted alternative synthetic routes and designed new mother liquor recycling systems. All this makes the process cleaner, lowers cost, and—critically—addresses the evolving expectations of our most forward-looking partners.

    Real-World Reliability Matters

    There are hundreds of suppliers listing similar names and catalog numbers, but a world of difference exists between a reliable product and an unpredictable one. Consistency batch after batch is where real manufacturing makes its mark. Over time, researchers who face fewer compound failures, cleaner baselines, and easier purification recognize the value in reliability. We see repeat clients cite direct cost savings in avoided re-screens and more predictable pilot plant runs due to these seemingly minor improvements.

    We hold ourselves to accuracy, not just on paperwork but in the results our customers report back. Some documentation comes shaped by regulatory requirements—full analytical traceability, batch records, and origin data. We see compliance not as a box-ticking exercise, but as a guarantee that production choices stand up to audit and replication. For industries with million-euro pilot plant investments riding on a single key intermediate, these details matter far more than price per kilogram.

    Supporting Sustainable and Efficient Synthesis

    Using 3-Bromo-5-Chlorobenzonitrile isn't only about making desired molecules; it's also about the efficiency and safety of doing so. Our optimized processes produce less halogen waste per kilo than earlier approaches. In the last few years we’ve implemented solvent recovery not just to save costs, but to cut environmental impact. This kind of reduction in waste and emissions benefits our own bottom line and advances the cause of cleaner chemistry across the field.

    In situations that call for zero-residue, low trace impurities, or complaint-resolution data, we open up our documentation. Full batch records, trace impurity profiles, and historic process logs can be made available for partner review. Full transparency means customers understand what they receive—and more importantly, why a product performs the way it does. Customers working in regulated or high-scrutiny markets find these disclosures crucial when scaling products and filing regulatory dossiers.

    Collaborating for Progress

    No manufacturer works in isolation. Our progress comes from building on the successes—and even the headaches—of researchers around the globe. Direct partnerships, pilot plant troubleshooting, and regular feedback lead to iterative improvements that serve as the foundation for each batch. Product orders often come with a request for innovation: a slightly different crystalline form, an adjusted solvent profile, a new packaging method. These small tests compound over time, advancing everybody’s capabilities.

    Chemists looking to push the boundaries of aromatic functionalization, electronic material design, or next-generation crop protection see substantial returns from reliable starting materials. While the world of fine chemicals races ahead with AI-designed molecules and continuous manufacturing, success still hinges on the basic building blocks and the expertise to make them work. Our business stands on supplying those high-standard starting points, listening, adapting, and delivering with the needs of real-world chemistry at the forefront.