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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 | 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. |
Applications of 3,5-Dibromobenzonitrile in Industrial ManufacturingAs 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 SynthesisPharmaceutical 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
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2. Agrochemical Active Ingredient ManufacturingCrop 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
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3. Liquid Crystal Material Production for DisplaysAdvanced 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
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4. Specialty Polymer Intermediate PreparationPolymer 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.