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3,5-Dibromobenzonitrile

    • Product Name 3,5-Dibromobenzonitrile
    • Alias 3,5-Dibromobenzenecarbonitrile
    • Einecs 254-917-7
    • 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

    877000

    Chemical Name 3,5-Dibromobenzonitrile
    Cas Number 6265-58-9
    Molecular Formula C7H3Br2N
    Molecular Weight 276.92
    Appearance White to off-white solid
    Melting Point 87-91°C
    Density 2.17 g/cm3
    Solubility Insoluble in water
    Smiles C1=CC(=CC(=C1Br)C#N)Br
    Inchi InChI=1S/C7H3Br2N/c8-6-1-5(4-10)2-7(9)3-6/h1-3H
    Pubchem Cid 156969

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

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed, with a white screw cap and labeled "3,5-Dibromobenzonitrile, 98%," hazard symbols included.
    Shipping **3,5-Dibromobenzonitrile** should be shipped in tightly sealed containers, protected from moisture and sunlight. Classified as hazardous, it must comply with relevant regulations (such as DOT, IATA, or IMDG). Appropriate labeling and documentation are required, and transport should be by authorized carriers trained in handling chemicals to ensure safety and compliance.
    Storage 3,5-Dibromobenzonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Store at room temperature, and avoid moisture to prevent hydrolysis. Proper chemical labeling and access control are essential to ensure safe storage and handling.
    Application of 3,5-Dibromobenzonitrile

    Applications of 3,5-Dibromobenzonitrile in Industrial Manufacturing

    As a direct manufacturer, we supply 3,5-Dibromobenzonitrile to leading producers in pharmaceutical, agrochemical, specialty chemical, and advanced materials sectors. The following downstream applications represent core industrial uses, each with specific formulation requirements, compliance frameworks, and integration practices unique to our B2B clientele.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical API producers use 3,5-Dibromobenzonitrile as a building block in the synthesis of active pharmaceutical ingredients, especially in the preparation of molecules with substituted aromatic rings. Production often involves nucleophilic aromatic substitution or palladium-catalyzed coupling reactions, where precise stoichiometric control is necessary due to the reactivity of the dibromo and nitrile functionalities. Reaction streams may require closed handling to comply with GMP guidelines and risk assessments for API impurity control. Our batches meet GMP-related documentation and are traceable, with QC supporting multi-kilo custom manufacturing campaigns.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Volume 4 Part II
    • US FDA 21 CFR Parts 210/211
    • USP/NF monographs (where related intermediates are included)

    Typical usage ratio

    • 0.8–1.2 molar equivalent per final API molecule; ratio adjusted for process yield and impurity control

    Downstream process integration

    • Charged at the aromatic coupling or functional group introduction step during small-molecule synthesis

    Final product types

    • Antineoplastic agents
    • Central nervous system actives
    • Specialty intermediates for custom synthesis CDMOs
    • End-use prescription pharmaceuticals

    2. Agrochemical Active Ingredient Manufacturing

    Crop protection manufacturers integrate 3,5-Dibromobenzonitrile for synthesis of brominated aromatic intermediates that serve as core structures in fungicide and herbicide actives. Its high specificity for aromatic substitution chemistry enables selective production of target molecules, especially where high purities and minimal byproduct formation are critical for downstream environmental toxicology profiles. We supply consistent quality suitable for continuous and batch processing. All supply aligns with compliance monitoring for trace residuals in agricultural actives.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice
    • REACH Regulation (EC) No 1907/2006 (Europe, for intermediates)
    • EPA 40 CFR Part 158 (Data requirements for pesticides, USA)

    Typical usage ratio

    • 20–40% w/w of aromatic core in stepwise synthesis of actives; adjusted for impurity limits and step conversion

    Downstream process integration

    • Fed directly into the aromatic halogenation or functionalization stage before condensation with bioactive side chains

    Final product types

    • Brominated fungicide intermediates
    • Herbicide precursor compounds
    • Custom pesticides for contract production
    • Bulk crop protection chemicals

    3. Liquid Crystal Material Production for Displays

    Advanced material manufacturers in the liquid crystal industry utilize 3,5-Dibromobenzonitrile to produce highly oriented aromatic compounds with tailored electronic properties for display applications. Its unique halogen and nitrile substitution pattern allows elaborate cross-coupling reactions to introduce functional groups necessary for display-grade liquid crystal molecules. Quality control emphasizes extremely low metallic or organic impurities, as minor variations impact optical clarity and dielectric anisotropy. All manufacturing aligns with QC requirements for mass production in TFT-LCD and OLED supply chains.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for downstream use in electronics)
    • IEC 61249-2-21 restrictions on halogen content (electronics material supply)
    • ISO 9001:2015 quality management system (specialty material supply)
    • Customer-specific display industry purity standards

    Typical usage ratio

    • 5–25% by weight in precursor formulations for mesogenic compound production; level set by molecular design and chain length

    Downstream process integration

    • Introduced during the main coupling or condensation reaction to build the central aromatic core of the liquid crystal compound

    Final product types

    • TFT-LCD liquid crystal mixtures
    • OLED display materials
    • Specialty optical films
    • Photonic intermediate components

    4. Specialty Polymer Intermediate Preparation

    Polymer manufacturers require 3,5-Dibromobenzonitrile as a functional monomer source in the synthesis of specialty polyarylenes and high-performance copolymers. Its difunctional reactivity supports step-growth condensation or Suzuki-Miyaura-type coupling, where precise control over chain propagation and aromatic distribution is important for downstream mechanical and thermal properties. We provide material with tight particle size specification and high purity to prevent polymerization inhibition and ensure batch reproducibility.

    Industry compliance standards

    • ISO 14001:2015 environmental management for chemical handling
    • EN 10204 3.1 material certification (for engineering polymers)
    • Customer specifications for polyarylene batch release
    • REACH Article 3 for polymer intermediates registration (EU)

    Typical usage ratio

    • 10–35 mol% relative to total monomer charge, based on desired copolymer structure

    Downstream process integration

    • Feedstock supplied to the reactor as the primary aromatic unit during controlled polymer chain formation

    Final product types

    • High-temperature thermoplastics
    • Aromatic polyamide copolymers
    • Electronic encapsulation materials
    • Custom engineering plastics
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    Competitive 3,5-Dibromobenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3,5-Dibromobenzonitrile: Practical Advantages and Real Manufacturing Experience

    Understanding the Role of 3,5-Dibromobenzonitrile in Modern Chemistry

    3,5-Dibromobenzonitrile is a specialty intermediate with a reputation for reliability in process chemistry circles. Having worked hands-on with such nitrile compounds in our facilities, it’s become clear why customers gravitate toward this exact model—neither overly commoditized nor so niche that availability becomes a problem. Our product stands out for consistency, pulled straight from controlled reaction systems maintaining strict temperature and feed protocols. This attention to process is not just checklist compliance; it’s ingrained in the way we run the plant.

    Real Specifications, Not Marketing Claims

    Chemically, 3,5-dibromobenzonitrile carries the molecular formula C7H3Br2N and a molecular weight of 276.92. For many manufacturers, these data points are easy to copy-paste, but our interest lies in why they matter. The two bromine atoms on positions 3 and 5 of the aromatic ring provide targeted reactivity for subsequent couplings or substitutions. Unlike mono-substituted benzonitriles or isomeric products, this specific substitution pattern delivers more controlled synthetic outcomes, particularly in agrochemical and pharmaceutical routes.

    As professionals who support dozens of kilo-to-ton batches each year, we pay close attention to more than just the assay. Purity influences the success of the downstream step, so we keep impurity profiles tight, frequently achieving purity above 98 percent by HPLC, with moisture levels under 0.5%. The stability profile makes storage simple, opening the door to smooth inventory management even across seasons.

    From Production to Application: Insights from the Production Floor

    We’ve handled several aromatic nitriles through the years, but the demand for 3,5-dibromobenzonitrile has grown for solid reasons. Its use as a building block for active ingredients in crop protection and specialty pharmaceuticals sets it apart from standard benzonitriles. In our experience, this is not a one-trick intermediate: contract R&D groups reach out for 3,5-dibromobenzonitrile during custom syntheses aimed at fine-tuning halogenation or achieving advanced intermediates in API development. Its high selectivity in Suzuki or Buchwald couplings makes it an engineer’s choice for scaling batches with predictable yields.

    We’ve tracked returns from our own customers, and when switching from similar products like 4-bromobenzonitrile or 2,6-dibromobenzonitrile, chemists point to less byproduct formation and fewer purification headaches. Essentially, this is not just another product from the catalog—it fills a real process gap for both inventors and manufacturers.

    Making and Maintaining Quality Without Compromising Safety

    On the floor, scaling from a 20-liter glass reactor to full-scale plant vessels often exposes flaws in synthetic concepts. We bring practical operating experience with 3,5-dibromobenzonitrile’s synthesis; our bromination step is tightly monitored, minimizing excess reagent and limiting formation of polybromo byproducts. This approach keeps both waste output and environmental load modest. Nitrogen sweep lines and proper venting keep workers out of harm’s way. Years of refining our route mean downstream workups are simpler, leading to fewer batch failures and better lot-to-lot consistency. Reliable yields have kept customers returning year after year.

    Many in the field underappreciate the challenge of working with halogenated aromatic compounds. Brominated intermediates, including this one, require careful handling and specialized waste treatment. We patrol for worker exposure and maintain separation from sensitive process streams, as even trace cross-contamination poses setbacks during scale-up. Emphasizing control in every transfer and filling step, we avoid costly product holds—a difference felt where it matters.

    Why 3,5-Dibromobenzonitrile Outperforms Close Relatives

    Comparisons with similar intermediates pop up frequently at trade meetings. Ask a chemist to choose between 3,5-dibromobenzonitrile and its close cousins, and you’ll hear about the advantages in coupling chemistry and step economy. Mono-halogenated products might look less expensive on paper, but they lack the symmetry and activation needed for smoother follow-up reactions. We’ve seen repeat clients who tried more generic nitriles return to 3,5-dibromobenzonitrile, reporting fewer side products and less effort in column separations, saving time for their production teams. The doubly brominated nature also enables unique substitution patterns, especially in the construction of regulated actives for the pharmaceutical and agrochemical fields.

    During pricing discussions, we’ve noticed that customers familiar with high-purity nitriles understand that savings often come from tight controls—not only at the raw material stage but in the way the plant is run. Our experience shows that a well-made batch of 3,5-dibromobenzonitrile saves hours downstream. That efficiency has tangible value.

    Addressing Common Challenges: Production Hurdles and Solutions

    Challenges with 3,5-dibromobenzonitrile often look similar across manufacturers. The top concerns involve side-reactions during aromatic halogenation and proper quenching of hazardous reagents. There is no shortcut; temperature control and real-time analytics do the heavy lifting. We discovered early that process deviations tend to cause impurity build-ups, affecting not only current production but future cleanouts.

    Few outsiders realize that halogenated byproducts bring potential for environmental regulatory headaches. Our solution anchors itself in process monitoring and the use of closed-system filtrations and specialist scrubbers. Regular worker training and a culture of open reporting keep us on top of safety notifications, allowing us to refine cleaning protocols and improve yields instead of firefighting compliance issues weekly.

    Another issue surfaces in storage and shipping. Older materials sometimes degrade if mishandled. Limiting transit times, using sealed drums, and providing customers with clear, experience-backed guidelines takes the guesswork out of stocking. Long-term partnerships with trucking and warehousing outfits who understand chemical hazards also help prevent avoidable incidents.

    Downstream Impact in Customer Operations

    It’s in the follow-on chemistry that 3,5-dibromobenzonitrile demonstrates its true worth. Many clients in medicinal chemistry, process-development, and contract manufacturing settings rely on successful heteroatom substitutions or complex migrations. We’ve taken calls where a project’s entire timeline swung on material quality—one off-note lot introduced delays of weeks due to tough purification. Through documented process data and traceable batch records, our teams can pinpoint process variables responsible, making it possible to adjust and resupply with the needed performance.

    Our labs coordinate with external QC teams, providing technical insights beyond the standard COA. This collaborative problem-solving has built a trust level we’re proud of; scientific dialog beats marketing any day. Some of our closest relationships started from a call about process troubleshooting, where real data—not brochure terms—mattered most.

    Meeting Compliance, Supporting Sustainable Practices

    Policy shifts continue to push the chemical sector hard on compliance and sustainability. Brominated aromatic intermediates draw scrutiny due to their persistence, driving manufacturers to fine-tune not just reactions but also waste and solvent management. For us, this means ongoing work in selective reagent use, recycling spent solutions, and keeping transporters up to date on new safety requirements. This hands-on experience navigating regulation changes helps customers avoid shipment disruptions or customs complications.

    Our teams attend both regional and international workshops on environmental stewardship and green chemistry; these aren’t box-ticking exercises. Direct interaction with peer plants has led us to share and implement best practices—especially in emission control and effluent treatment. Strong relationships with trusted auditors let us react quickly to new expectations, tweaking protocols as necessary.

    Applying this philosophy to 3,5-dibromobenzonitrile means tracking spent reagents closely, using carbon-based traps for airborne residue, and running closed-loop water systems. We review procedure logs monthly and regularly invest in plant upgrades when technology improves. Over the last five years, such investments have reduced non-conformities on environmental scoresheets and minimized unplanned maintenance.

    Supporting Discovery, Scale-Up, and Customization

    Unlike traders or resellers, we interact daily with chemists who know the costs of failed syntheses and wasted time. Our technical bench answers challenging questions, from custom particle sizes to supporting analytical documentation adjusted for regulatory filings. Customization requests—such as adjusting impurity specs for pre-clinical use or blending special antioxidant packs into batches for longer shelf life—come from frequent, practical feedback.

    We maintain in-house analytical stations and pilot lines for quick scale-up tests. Insights from these runs feed directly into the main production routines. Over time, this practice has allowed us to cut development cycles and help clients move promising leads closer to registration or market launch.

    The knowledge gained from troubleshooting failed scale-ups in the early days became the backbone of our current practices. We make every reasonable effort to share lessons learned with our partners, knowing that a product’s reputation travels faster by word of mouth than in any brochure.

    Supply Strategy: Mitigating Disruptions and Building Resilience

    Recent global logistics challenges have tested every chemical producer. Shipping delays, port slowdowns, and vessel shortages put just-in-time concepts to the test. Our approach involves clear forecasting, regular communication with raw material producers, and a stock policy built for resilience. We maintain inventory buffers of 3,5-dibromobenzonitrile based on direct sales forecasts—not historical data alone. This method let us weather price spikes in key raw materials without putting our clients on allocation.

    Each season, the purchasing team reviews supply chain health with our field staff. In years where bromine prices suddenly rose, we leveraged our experience to open parallel sources and kept our customers informed. This proactive communication avoided panic purchasing or sudden price jumps, protecting ongoing projects.

    Strong working relationships with domestic and overseas shipping partners keep documentation moving, while a dedicated team tracks transit in real time and flags potential incidents before they can escalate into setbacks.

    Collaborative Development and Technical Feedback Loops

    Chemistry is rarely static, and neither are customer requirements. Over the past decade, we’ve supported collaborative projects for advanced material synthesis, specialty dye intermediates, and emerging pharmaceutical leads. Customers share their process challenges, whether around solvent compatibility or reaction scale-up. Our analytical teams respond with real measured data, stability results, and process suggestions founded on direct run experience.

    A few years ago, a client needed a non-standard variant of 3,5-dibromobenzonitrile with less than 0.1% moisture content for a particularly sensitive application. Our in-house R&D retooled drying and packaging, making it possible to deliver the right batch and save the end synthesis. This type of responsiveness comes from accumulated know-how, not just off-the-shelf answers.

    Joint troubleshooting—sharing failures and rethinking process parameters—keeps everyone in the loop. In one case, a large-scale user required a tweak to particle distribution for automated handling. Within a month, plant trials produced a specification that not only met but improved their throughput compared with the previous setup.

    Real Value: More Than Just a SKU

    It’s easy to forget the difference direct manufacturing brings in a world full of intermediaries. When supply chains are tight, the ability to answer specific technical questions, adjust batch schedules, or support a regulatory review stands out. Years of practical manufacturing experience have taught us the importance of discipline, communication, and an openness to feedback. At its core, delivering 3,5-dibromobenzonitrile is not about filling orders; it’s about establishing trust, batch by batch.

    As we reflect on the day-to-day practicalities, from safe handling to seamless transport and customer dialogue, our ultimate measure of success comes from productive, long-standing relationships with formulation houses, custom manufacturers, and research-driven clients. Every request for discussion or improvement offers a fresh learning opportunity, guiding refinements in the way we produce and deliver what has become an essential intermediate across multiple industries.

    We’ve watched 3,5-dibromobenzonitrile sustain its place in the market not just because of specifications in a brochure, but for its proven ability to unlock efficient, low-impurity synthesis. This track record, made possible by hard-earned production experience, drives us to keep improving—ensuring every batch matches the demands of a changing industry.