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HS Code |
457034 |
| Product Name | 3,5-Dibromotoluene |
| Cas Number | 118-79-6 |
| Molecular Formula | C7H6Br2 |
| Molecular Weight | 249.93 |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | 4-6 °C |
| Boiling Point | 224-226 °C |
| Density | 1.863 g/cm3 |
| Refractive Index | 1.605 |
| Flash Point | 91 °C |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water, soluble in organic solvents |
| Smiles | CC1=CC(=CC(=C1)Br)Br |
| Inchi | InChI=1S/C7H6Br2/c1-5-2-6(8)4-7(9)3-5/h2-4H,1H3 |
| Storage Conditions | Store at room temperature, away from light |
As an accredited 3,5-Dibromotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3,5-Dibromotoluene is securely sealed in an amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 3,5-Dibromotoluene is shipped in tightly sealed containers to prevent leaks and protect from moisture. It should be stored and transported in a cool, dry, well-ventilated area, away from incompatible substances. Handling requires appropriate labeling as hazardous material, and all relevant regulations for flammable and potentially harmful chemicals must be followed. |
| Storage | 3,5-Dibromotoluene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Store away from direct sunlight, heat, and moisture. Proper chemical storage cabinets, clearly labeled, are recommended to prevent accidental contact, spills, or environmental contamination. |
Applications of 3,5-Dibromotoluene in Industrial Manufacturing3,5-Dibromotoluene plays a key role as an intermediate in several high-value chemical manufacturing processes. Its brominated aromatic structure allows precise reactivity control, facilitating the synthesis of advanced materials and specialty chemicals required by multiple industries. Below we detail major industrial applications, listing regulatory requirements, specific usage ratios, unique process roles, and representative end products for each sector. 1. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)Major agricultural chemical formulators use 3,5-dibromotoluene as a core building block in synthesizing select triazole and pyrazole crop protection active ingredients. The molecule introduces site-selective bromine functionalities, supporting key transformations through metal-catalyzed coupling and substitution processes. Regulatory authorities require source traceability and control of halogenated byproducts at every step of this intermediate’s application. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate ManufacturingAdvanced pharma syntheses use 3,5-dibromotoluene to introduce controlled bromine positions in aromatic frameworks for APIs, especially in early-phase process R&D. Its use allows selectivity in metalation reactions, supporting both scale-up safety and reproducibility in multi-kilogram GMP batch operations. Process chemists depend on its purity and batch-to-batch consistency to minimize genotoxic impurities and meet regulatory standards for final dosage forms. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemicals (OLED and Liquid Crystal Intermediate Production)Manufacturers of advanced display materials depend on 3,5-dibromotoluene for the synthesis of custom aromatic species required in OLED emitter layers and liquid crystal molecules. Its dual ortho-bromine pattern enables precise carbon-heteroatom linkages, supporting high-purity electronic-grade intermediates for downstream functionalization. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymers and Advanced Material PrecursorsChemical companies and research groups employ 3,5-dibromotoluene to construct specialty polymers and advanced resins via targeted functional monomer synthesis. Its reactivity with borylated or stannylated partners enables custom polymer architectures with controlled electronic or thermal properties, crucial for membranes, coatings, and composite matrix development. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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The pace of modern chemistry keeps accelerating, with researchers always searching for materials that allow new possibilities in synthesis. In our manufacturing plant, we encounter the need for quality-controlled halogenated aromatics every single day, and among them, 3,5-Dibromotoluene has established itself as a building block with real utility. As the producer, watching it move from crude to carefully purified batches, I have seen what makes this compound fit both lab and industrial scales, especially in industries where margins for error stay razor-thin.
We don’t approach 3,5-dibromotoluene as just another molecule. Yes, it begins simply enough—our starting material is toluene, meeting high purity standards from the beginning, and bromination occurs under rigorously monitored conditions. The final material achieves the white-to-off-white crystalline appearance that allows easy visual checks during QC, but the critical assurance comes from the gas chromatography and NMR analysis we perform. We routinely hit a purity mark of above 98%, keeping residual mono-bromotoluenes and polybrominated byproducts below quantifiable limits. Purity is not simply a marketing point; downstream users in pharma and electronics experience costly shutdowns if contamination sneaks through—manufacturing cuts no corners here.
Each lot receives its own traceability from reactor all the way to customer delivery. Documentation is not an afterthought—we log exact batch times, reaction temperatures, and purification parameters, because inconsistency at this stage causes headaches for anyone relying on predictable performance downstream.
Our experience tells us that 3,5-dibromotoluene enjoys repeat orders not just for being “another” dibromotoluene. Other isomers like 2,4-dibromotoluene or 2,6-dibromotoluene see use, but do not substitute for certain transformations. Research chemists appreciate the meta-relationship between the bromines, which gives unique selectivity in cross-coupling reactions such as Suzuki-Miyaura or Stille couplings. You gain a pattern of reactivity that ortho or para isomers simply do not provide.
For us, customer feedback makes clear why this product draws attention from several sectors. Agricultural developers create advanced fungicides and herbicides using 3,5-dibromotoluene as a core fragment, taking advantage of its substitution pattern for step-efficient synthetic routes. Not only agrochemicals, but electronics manufacturers value its methodical response in synthesizing specialty materials for OLEDs or advanced polymers. Researchers tackling staggered ring-building often report that this isomer’s reactivity offers chances that 2,4- or 2,6- counterparts cannot match.
From the shop floor to the packaging area, our workers deal with 3,5-dibromotoluene daily. Its physical characteristics allow efficient transport and handling—solid at ambient conditions, with melting points stable around 51–52°C, and a molecular weight easily factored into precise reaction design. Our standard drum and bottle packaging prevent absorption and contamination. Critical for scale-up teams, no unusual pressure or humidity sensitivity disturbs routine operations; storage in a dry room suffices for months without any drop in spec.
Many users encounter the same dilemma: cost needs to stay reasonable, but reliability can never slip. Our plant’s continuous flow setup accommodates kilogram-to-ton production, allowing short turnaround for process tweaks driven by customer need. Every lot passes through drying and sieving steps—residues from solvents or fine dust interfere with both analytical and synthetic steps, so our plant technicians keep a close eye, adjusting filtration, or drying times if a batch doesn’t meet our internal benchmarks.
In this industry, isomer differences translate into real-world results. Some resellers and generalists do not see these distinctions, but our chemists know the positioning of the two bromines on the aromatic ring impacts nearly every kind of downstream transformation. 3,5-dibromotoluene gives access to selective and predictable functionalization. Synthetic methods designed for ortho- or para-substituted aren’t simply interchangeable because the electronic and steric effects don’t map one-to-one.
In nucleophilic aromatic substitution, meta-oriented bromines in the 3,5-position resist displacement compared to the ortho or para isomers, affecting choice of catalyst, temperature, and solvent. Customers aiming at multi-step synthesis can design divergent pathways uniquely allowed by this isomer. Suppliers who only offer bulk halogenated benzenes without attention to such details miss the mark for these research and commercial users who rely on position-specific products.
Cost differences emerge too. Other isomers may arise as byproducts, but isolating and purifying the 3,5- form demands optimized processes; we minimize losses and optimize yields by careful reaction control. All of this comes from running these reactions at scale: we see which variables, such as feed rates or reaction temperature, give the cleanest isomeric ratios, and we design our workflow accordingly.
Chemical development doesn’t stop with the academic world or bench-scale labs. Demand for higher volumes, lower impurity levels, and greater traceability led us to invest in continuous improvement. In-house monitoring lets us tweak batches for new applications or to meet stricter impurity thresholds from regulatory bodies. Once, a major client in Germany required trace levels of polybrominated impurities be reduced below 0.05%. That challenge drove us to retrofit purification units with extra crystallization steps, and the process improvements now benefit all future customers.
With each load, we ship a supporting COA with lot-specific NMR, GC, and, on request, trace metal analysis. In our discussions with downstream partners, these records speed their regulatory submissions and release times. By keeping in direct contact, feedback on usability, color, and analytical results gets shared and acted on, closing the loop between production and end use.
Sometimes new applications push the limits of what our current process delivers. A startup developing antifouling coatings needed ultra-low halide contamination, far stricter than anything previously requested. Rather than insisting on our standard specification, we developed a pilot run using activated carbon and acid-wash steps borrowed from pharmaceutical purification. In this way, being the producer, not simply the supplier, meant that we could take immediate action, involve our R&D chemists, and get a pure enough batch into testing within weeks.
When a pharmaceutical manufacturer faced batch-to-batch color differences, our team traced this back to barely-perceptible byproduct formation during bromination. Fine-tuning reaction monitoring and employing in-line colorimetric QA ensured uniform appearance every shipment. Making small changes like this isn’t always possible in trading scenarios or with long supply chains—an in-house manufacturing approach gives real flexibility and fast iteration to meet customer needs.
Growing environmental scrutiny affects every stage. 3,5-dibromotoluene’s bromination involves handling of molecular bromine, which requires best-in-class containment and neutralization systems. In our facility, waste streams go through multi-stage quenching and off-gas scrubbing. We constantly monitor wastewater bromide content and have invested in thermal treatment for safe disposal. This attention matters: local authorities regularly audit both our procedures and output, and every certification or report is based on practical compliance, not theoretical claims.
By collaborating directly with end users—especially those in pharma and agro—input on required impurity thresholds and documentation is used to refine processes. Our methods have been updated over the years to keep up with demands not just for product quality but also for minimal environmental impact. Lessons learned from each regulatory inspection get applied immediately, and open-door policy for audits means we stay ready for any check, anytime.
Producers with hands-on experience see how each halogenated aromatic offers different advantages. A simple switch from 3,5- to 2,4-dibromotoluene can derail an entire reaction pathway. In our plant, our synthesis of the meta isomer uses toluene under strictly measured bromination times and temperatures, producing a significantly cleaner product compared to para-oriented processes. Customers trying to synthesize ligands, functionalized aromatics, or specialty electronic materials rely on these differences. A typical conversation with a user designing ligands for cross-coupling reactions often ends with their confirmation that the 3,5-isomer delivers the regioselectivity required for challenging assemblies.
Pure bromotoluenes also serve as precursors for boronic acids and other organometallic derivatives. During catalyst screening, our colleagues in customer R&D repeatedly note that 3,5-dibromo derivatives perform more reliably under Pd-catalyzed conditions, with higher overall yields and selectivity during functionalization. This performance edge underlines why synthesizing the correct isomer, free from cross-contamination, remains so important.
Other manufacturers with different workflows sometimes struggle with control over side product formation, but keeping the process in-house lets us manage the entire workflow from raw feedstock to crystal isolation and packaging. Traceability follows every batch—each drum, bottle, or sample is tied to a single batch by date, not only a lot number—so investigating or troubleshooting rarely leaves us in the dark.
Every chemical plant faces problems: equipment fouling, unexpected color shifts, varying yields from different raw material lots. With 3,5-dibromotoluene, getting reproducible crystallization remains the trickiest part. If the fine details of cooling rates or solvent choice shift even a little, one batch could grow oversized crystals leading to packing problems, while another forms fine powder prone to dust generation. Regular communication with our packaging and shipping teams led to reproducible filtration and drying cycles that minimize issue frequency.
A client once needed bulk shipments with carefully controlled particle size. Instead of rejecting the order out of hand, we reconfigured our drying and sieving line, installing a new classifier and rotating dedicated teams to monitor output. This led us to develop in-house standard operating procedures that continue to guide our staff. Unlike third-party traders, we don’t run to outside tollers or subcontractors—if a challenge pops up, it’s our own crew figuring out and fixing the problem.
The performance of the final user’s product often hinges on the reliability of the raw chemical. We’ve heard from electronics manufacturers whose devices failed due to off-spec halogen impurities from off-brand dibromotoluenes. Every time we revisit our production and testing thresholds, it’s with this in mind: a failed batch leads to downtime, wasted resources, and—most importantly—loss of trust. Reputations in this business travel faster than freight, and the only way to maintain them is work that holds up to scrutiny, every batch, every shipment.
All downstream analytical data from customers—whether HPLC, GC-MS, or NMR—comes back to us and we log it, trend reports over time, and adapt. Real-world performance sometimes reveals issues not apparent from standard release testing. Direct interaction with end users speeds problem-solving, often allowing process tweaks from batch to batch and catching minor deviations before they become larger quality issues.
For decades, we have learned that listening to end users pays off in more than sales. Practical feedback, sometimes delivered in blunt language, often points to details missed by generic QC checks. A synthetic route may fail not because of nominal purity, but due to trace polar impurities not picked up by standard tests. By opening channels for feedback and rapid batch adjustment, we keep our product performing beyond minimum spec—even updating COAs or adding additional analysis as requested, without bureaucratic delays.
University researchers and industrial clients bring new challenges. Sometimes they need experimental samples outside standard sizes, or a quick turn on a modified specification not listed on any website. Having full vertical integration, from kilogram to multi-ton scale, lets us respond quickly, because our own team controls every step. In some cases, we have adopted novel synthetic routes or purification strategies to help with application-specific challenges. Not many can say this; open dialogue between chemist and customer turns one-off solutions into ongoing improvements.
Chemical innovation shows no signs of slowing down. Our position as the actual producer puts us in contact with the real-life issues faced across research, pharmaceuticals, electronics, and materials science. The requirements change—sometimes driven by new regulations, sometimes pushed forward by customer innovation—so we adapt manufacturing accordingly. Feedback loops with R&D, quality, and environmental compliance keep the process dynamic, so what we deliver isn’t static, but tailored by the demands of present and future users.
With ongoing investments in both technology and people, production efficiency and sustainability move in tandem. Chemistry doesn’t reward shortcuts. Every change made, every update to process, ties back to consistency, reliability, and trust—the values held by those who actually produce what they sell. For those looking to build new molecules, materials, or medicines, we stand ready with insight and product to match.