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HS Code |
379261 |
| Cas Number | 615-89-2 |
| Molecular Formula | C7H6Br2 |
| Molecular Weight | 265.93 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 30-33 °C |
| Boiling Point | 243-245 °C |
| Density | 1.864 g/cm3 at 25 °C |
| Solubility In Water | Insoluble |
| Refractive Index | 1.623 |
| Flash Point | 105 °C (closed cup) |
As an accredited 2,5-Dibromotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g brown glass bottle labeled "2,5-Dibromotoluene, 98%." Features hazard symbols and detailed chemical information on the label. |
| Shipping | 2,5-Dibromotoluene is shipped in tightly sealed containers, typically as a solid or crystalline powder. Packaging complies with relevant hazardous materials regulations, ensuring safe transport. Containers are labeled with appropriate hazard warnings and stored in a cool, dry place, away from heat and incompatible substances during shipping to prevent any accidental release or contamination. |
| Storage | 2,5-Dibromotoluene should be stored in a tightly closed, clearly labeled container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and ensure proper containment to prevent leaks or spills. Follow standard chemical storage and safety protocols. |
Applications of 2,5-Dibromotoluene in Industrial Manufacturing2,5-Dibromotoluene plays a critical role in several advanced industrial sectors, where its controlled halogenation pattern supports precise synthesis routes. As a direct manufacturer, we supply this specialty intermediate to downstream partners seeking reliable input for complex chemical transformation. Below, we outline its real-world applications in key industries, supported by formulation data, relevant compliance frameworks, process details, and resulting end products. 1. Agrochemical Intermediates for Advanced HerbicidesChemical manufacturers employ 2,5-dibromotoluene as a tailored intermediate in the custom synthesis of modern herbicidal actives, especially for brominated aromatic scaffolds. Its dual bromine substitution pattern permits highly selective cross-coupling reactions, critical for generating final compounds with improved weed selectivity and environmental stability. Manufacturers commonly adjust the incorporation rate based on the specific downstream halogenation and functionalization sequence, ensuring target compound yield and purity for pre-emergence herbicide formulations. Industry compliance standards
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2. Pharmaceutical Building Blocks (API Synthesis)The pharmaceutical sector uses 2,5-dibromotoluene in the synthesis of advanced aromatic intermediates that serve as precursors to drug substance candidates. Its controlled bromine substitution simplifies the introduction of amine and ether functionalities through nucleophilic aromatic substitution, improving yields in multi-step active pharmaceutical ingredient (API) routes. This intermediate supports compliance with current Good Manufacturing Practices (cGMP) and can be used in both pilot and commercial synthesis settings, especially where precision in aromatic ring substitution dictates downstream bioactivity. Industry compliance standards
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3. Liquid Crystal Monomer Precursor (Display Technology)Producers of specialty monomers for LCD manufacturing integrate 2,5-dibromotoluene as a platform molecule. Its structure facilitates efficient synthesis of mono-substituted and di-substituted biphenyl derivatives, essential for nematic and smectic liquid crystalline phases. Brominated toluidines derived from this intermediate allow precise tuning of electronic and steric effects, enabling formulation engineers to meet stringent panel performance and environmental compliance requirements for high-definition displays. Industry compliance standards
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4. Dye and Pigment SynthesisSpecialty dye and high-performance pigment manufacturers utilize 2,5-dibromotoluene for the custom construction of halogenated aromatic cores, supporting advanced chromophore frameworks. Its bromine pattern enables reliable cross-coupling with arylboronic acids, introducing extended conjugation needed for high durability colorants. These properties are critical for color fastness and weather resistance in technical coatings and specialty ink applications, with batch-to-batch purity essential to meet downstream consistency requirements. Industry compliance standards
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5. Advanced Polymer Building Block (Specialty Engineering Materials)Manufacturers of advanced polymers incorporate 2,5-dibromotoluene as a strategic dihalogenated aromatic monomer in the synthesis of polymers requiring flame retardant or high thermal stability properties. The compound undergoes site-specific polymerization with aromatic diols or diamines, contributing to both polymer backbone rigidity and controlled bromine content. Adjustment of input levels ensures compatibility with desired polymer molecular weight distributions and post-polymerization modification steps, directly impacting end-use performance in electronics, automotive, or aerospace sectors. Industry compliance standards
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As a manufacturer handling aromatic halides daily, there’s value in sharing what really matters about 2,5-Dibromotoluene from the perspective of someone who scales up batches, fine-tunes reaction yields, and answers tough questions about consistency. This is a compound that draws serious attention from fine chemical producers, pharmaceutical researchers, and material scientists who pursue structure-specific outcomes. Our operations focus on a clear, colorless to pale yellow liquid or crystalline solid, meeting rigorous benchmarks around specification, purity, and reproducibility.
Quality in 2,5-Dibromotoluene begins with controlled synthesis. The molecular formula C7H6Br2 means each batch needs exacting process chemistry. We maintain bromine substitutions at the 2 and 5 ring positions—a factor that sets it apart from other isomeric dibromotoluenes, such as 3,5-dibromotoluene or 2,4-dibromotoluene. Mistakes in position mean wasted effort in downstream transformations, especially as even trace levels of off-spec isomers influence the performance of activated methylene derivatives, biaryl intermediates, and cross-coupling reactions.
We run GC-MS and NMR on every lot—without these checks, downstream users risk variable physical properties in their products. The melting point typically sits between 36-39°C, solidifying our internal references. Purity by GC nearly always clocks in above 99%. Water and halide contamination remain critical, so every step of handling, from recrystallization to bottling, gets close monitoring.
All disciplines working with aromatic building blocks ask for reliability. Over decades, we’ve seen 2,5-Dibromotoluene play central roles in Suzuki and Stille couplings. Academic groups and pharmaceutical labs come to us because this isomer unlocks access to selective cross-coupling for functionalized biphenyls and heterocyclic scaffolds. Process chemists building frameworks for active pharmaceutical ingredients report that impurity profiles in their routes improve when starting with our product, since they can trust we’ve eliminated trace regioisomers and low-level polybrominated byproducts. This is one of the big ways experience shapes outcomes.
Manufacturers of electronic materials find 2,5-Dibromotoluene attractive as a starting point for π-conjugated systems, light-emitting diodes, and organic field-effect transistors. This use case calls for a reproducible degree of halogenation to enable efficient further functionalization. Polymerization researchers reaching for precise substitution patterns avoid performance drifts by checking their initial batches’ spectral fingerprint against ours.
Pigment and dye synthesis also benefit, since certain chromophores and colorfast materials trace their origins to these precisely brominated toluenes. Try to swap in a mixed isomer blend, and downstream color performance falters. Consistency in our upstream feed means less rejection of failed lots for our customers.
On the surface, most aromatic dibromides appear nearly identical. A practical maker’s experience says otherwise. The distinct substitution pattern dictates reactivity and ultimately the suitability for further chemical modification. Our operations target only the 2,5-regioisomer. If the process drifts, you get unreacted monobromide, increased 2,4- or 3,5-dibromotoluene, or even polybrominated waste—which ruins yield in Grignard or lithium-halogen exchange conditions downstream. This is the sort of operational discipline that can’t be taught from a catalog sheet.
Our workers operate reactors under inert conditions, monitor bromine feed rates, and check crystallization parameters with each shift. These steps block over-bromination and unpredictable side-product profiles, delivering that repeatable material researchers need for high-throughput screening and sensitive dosage formulations. Compare our outcome to a trader reselling broad-cut bromotoluenes, and the advantage stands clear in both purity and guaranteed substitution pattern.
Packaging also warrants attention. We standardize on amber glass and sealed drums, tailored for air and light sensitivity, especially during warm seasons and for longer-term storage. This practical focus extends material shelf-life and assures that physicochemical integrity stays unchanged from batch release until application. Teams using boronic acid syntheses or coupling chemistry face fewer headaches with blocked reaction sites or hydrolysis byproducts.
Every sector brings distinctive requirements. In pharma and agrochemical discovery, the ability to introduce functional moieties onto a clean aromatic scaffold depends on absolute certainty in initial substitution. Only 2,5-Dibromotoluene allows some routes to close in two or three steps with high yield—switch to a 2,4- or 3,5-isomer, and additional protection/deprotection moves become mandatory, which eats up time and resources. Synthetic chemists rely on succinct, high-throughput methods, especially at scale-up or process validation; they turn to partners who bring a proven record of isomer control.
Performance materials design—such as organic semiconductors—demands not just purity, but also batch-to-batch consistency at the isomer level. Our experience in requalifying every batch for charge transport studies, device prototyping, or optical grade refinement makes a difference. Even the best lab recipe fails if a poorly sourced batch introduces minor, undetectable contaminants. For this reason, our QA includes both classical and spectroscopic analytics, warranted by dozens of satisfied customer audits each year.
Environmental labs exploring halogenated pollutant metabolism request our 2,5-Dibromotoluene to trace specific degradation paths. Isomer-specific fate and transport profiles mean regulatory tests only work with an assured feedstock—no room for doubt about mixture composition. Several projects evaluating persistent organic pollutant analogs have cited our source as the single most reliable reference, because the batch-to-batch GC traces match with published literature.
Experience teaches that fine details make or break a synthesis. Small changes in handling—heat, moisture, packaging—lead to unwelcome impurities. By treating every step with the attention typical of GMP pharma intermediates (without the added cost), we position our 2,5-Dibromotoluene as a foundation-grade intermediate. Customers with downstream sulfonation, amination, or carboxylation steps report improved yields and smoother isolations thanks to our consistent impurity profile.
Bulk and research-scale users ask about long-term stability. Our records show material remains stable in ambient storage for over a year, if kept sealed away from light and excess humidity. Recrystallization on-site allows easy purification for especially sensitive runs requiring ultra-low impurity backgrounds—a request we fulfill for advanced material and biotech startup clients. This one-to-one process knowhow flows from decades of hands-on manufacturing, not just stockroom logistics.
By running our own distillation, bromination, and isolation lines, we guarantee immediate feedback from QC. Failures don’t trickle down third-hand; every worker on the floor receives training in recognizing deviations in product flow, indicating either raw material contamination or reaction drift. These internal checks have helped keep rework rates low and customer returns nearly nonexistent over the past five years.
Bench chemists and industrial process engineers often ask if they can swap 2,5-Dibromotoluene with other brominated aromatics—say, 3,4-dibromotoluene, or monobromotoluene. The short answer: not if regioselectivity matters. The 2,5 positions open clean routes to biaryls or positional cross-couplings. Trying the same trick with a 2,4- or 3,5-substituted analogue changes product sterics and electronic properties. You’re left running extra purification steps, chasing inconsistent GC traces, or risking patent or formulation conflicts.
Certain markets prize 2,5-Dibromotoluene precisely because it isn’t a commodity. Its route-specific nature prevents unwanted byproducts common with other dibromotoluene isomers. Customers coming from a generic supplier often report color, melting point, and coupling issues that disappear after moving to a dedicated manufacturer with stringent isomer control. We’ve documented differences not just in routine analytics, but in ultimate product performance across application domains.
Other brominated intermediates, including tribrominated or chlorinated analogues, bring heavier regulatory burdens and often reduced reactivity in C–C coupling contexts. We’ve learned to minimize regulatory headaches by providing compliant material with full traceability and documentation from raw material lot to finished product outgoing certificates. Fine details translate to confidence on the end-user side, sometimes worth more than any price tag.
Scaling up 2,5-Dibromotoluene involves balancing several hurdles. Managing hazardous raw materials—toluene, bromine, acid catalysts—means careful risk assessment for every new batch. Years of practice have cemented process safety, including redundant vent systems, emergency quenching setups, and solvent recycling to reduce environmental load. These steps cost time and money but prevent both downtime and unsafe workplace incidents.
Waste stream management looms large. By fine-tuning reaction stoichiometry and purification, we cut halogenated organic byproduct content, making aqueous and solid waste easier to handle and treat. Customers increasingly demand sustainability; sharing actual recycling and waste minimization statistics helps buyers build green chemistry credentials into their sourcing. Not every maker can show closed-loop bromine recovery or solvent cycling—capabilities that require significant investment and operational discipline.
Maintaining a motivated, skilled workforce remains as important as technical innovation. Junior operators learn reaction management by shadowing experienced hands—spotting problems in color, viscosity, solid-liquid separation early, well before they show up on paper analytics. This level of vigilance flows from placing crafting chemical materials above chasing volume or sales numbers. The results show in daily process reliability and customer loyalty over decades, not quarters.
Verifying compound identity, purity, and isomer content forms the baseline of our routine. Our team uses GC, FT-IR, and NMR as regular tools, not just regulatory checklists. Several times each month, customers or contract partners request custom packaging, additional purity guarantees, or unique physical forms (powder, flake, solution). We deliver with real-world flexibility because our team understands specific requirements from direct production experience.
Long-term partners appreciate that we document and archive each batch’s analytical data for years, not just weeks. Researchers in pharma, electronics, and specialty chemicals often revisit orders years later, matching their own analytical results to our archive files—saving time and troubleshooting costs. Our feedback cycle means new process insight from customers directly improves future batch production, a win for both sides.
Customers seeking a stable source of 2,5-Dibromotoluene always ask: will the provider maintain consistent quality, traceability, and technical support over multiple runs? By running all operations in-house, we avoid issues seen with relabelers or intermediaries—namely, mixed lots, questionable documentation, or missing technical follow-up. We take responsibility from raw material intake to final QC sign-off.
Users in regulated settings such as pharmaceutical, agricultural, or advanced electronics sectors require not just a product, but a supply chain partner. This means proof of routine testing, audit transparency, and clear communication around any process changes that could influence outcomes. The real difference shows up in user feedback—often coming back to us for repeat work, new sizes, or even collaborative development on routes that use our 2,5-Dibromotoluene as the key node.
Knowledge gained from thousands of kilograms’ worth of runs—successful, failed, and in-between—means recommendations come grounded in years of both success and challenge. We troubleshoot not only our own production, but also customer-side integration, sharing practical advice on solubility, storage, and reactivity picked up through daily genuine practice, not sales scripts.
Scientific and technical fields move quickly; requirements for intermediates like 2,5-Dibromotoluene continue to evolve. Over the past decade, research has called for even tighter impurity control, new analytical benchmarks, faster lead times, and ever more specific variants (such as labeled isotopes or functionalized derivatives). Our response has combined incremental process improvement with investment in analytical capabilities, and partnership with end-users who push the boundaries of what to expect from a chemical supplier.
Sustainability continues to impact choices across chemical supply chains. New initiatives around solvent and bromine recycling, eco-friendly packaging, and reduced footprint logistics only come about with in-house commitment and knowhow. Our colleagues in R&D frequently test green solvents, alternative reaction conditions, and advanced in-line monitoring as part of every production campaign. This approach has cut our waste per batch, improved yield, and driven down corrective actions linked to off-spec product.
By putting production and operational expertise at the center of business, we keep 2,5-Dibromotoluene an accessible and dependable tool for scientific progress. Whether supporting a new pharmaceutical pipeline, building materials for the next generation of electronics, or enabling classic synthetic transformations, we stay firmly rooted in the practical, daily realities of manufacturing—a record measured by outcome, not just output.