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HS Code |
989690 |
| Compound Name | 3,4-Dibromotoluene |
| Molecular Formula | C7H6Br2 |
| Molar Mass | 265.93 g/mol |
| Cas Number | 615-23-0 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 220-224 °C |
| Melting Point | 4-7 °C |
| Density | 1.93 g/cm³ |
| Refractive Index | 1.603 |
| Flash Point | 99 °C |
| Smiles | CC1=CC(=C(C=C1)Br)Br |
| Solubility In Water | Insoluble |
As an accredited 3,4-Dibromotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3,4-Dibromotoluene is supplied in a sealed amber glass bottle with a tight screw cap and hazard labeling. |
| Shipping | 3,4-Dibromotoluene is shipped as a hazardous chemical, typically in tightly sealed containers made of compatible materials. Containers are clearly labeled and protected against breakage. Shipping complies with regulations for flammable liquids and toxic substances, with documentation and handling protocols to ensure safety during transport by road, air, or sea. |
| Storage | 3,4-Dibromotoluene should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and excessive heat. Label the container clearly and keep it away from food and drink. Use proper containment to prevent environmental contamination in case of leaks or spills. |
Applications of 3,4-Dibromotoluene in Industrial ManufacturingAs an original manufacturer, we supply 3,4-Dibromotoluene to downstream industries where it serves as a targeted intermediate in specialty synthesis. The following sectors implement our material in line with recognized compliance, standardized formulations, and controlled production processes to achieve precise end-use performance in advanced industrial goods. 1. Pharmaceutical Intermediate for Sartan Drug SynthesisPharmaceutical manufacturers use 3,4-Dibromotoluene in the synthesis of key benzylic intermediates that form the aromatic framework of angiotensin II receptor blockers, such as valsartan and telmisartan. This process requires consistently pure batches to meet strict impurity specifications and address regulatory audit demands for traceability. Usage concentrations differ based on route optimization and impurity control protocols, with most producers referencing guidance from the originator synthesis patents and adjusting according to batch yields of subsequent coupling or cyclization steps. Industry compliance standards
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2. Agrochemical Synthesis: Pyridine and Pyrimidine DerivativesThe crop protection sector uses 3,4-Dibromotoluene to introduce defined aromatic substitution in the creation of heterocyclic intermediates for advanced herbicides, fungicides, and insecticides. Industrial-scale processes favor this compound’s reactivity in cross-coupling and ring-closure reactions, which are critical for the generation of selectivity-conferring moieties in agrochemical molecules. Industry compliance standards
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3. Specialty Dye and Pigment IntermediateDye and pigment manufacturers incorporate 3,4-Dibromotoluene into complex aromatic frameworks to create custom molecular structures with tailored lightfastness, hue, and solubility for professional textile and industrial coatings. Due to the selectivity of bromination at specific ring positions, this compound offers reliable anchoring points for further azo-coupling, condensation, or oxidation chemistry under scale-up conditions. Industry compliance standards
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4. Fine Chemical Building Block for Performance PolymersIn the specialty polymer sector, downstream producers employ 3,4-Dibromotoluene as a precision monomer for introducing controlled aromatic substitution during the synthesis of high-performance resins. These operations depend on the material’s purity and batch consistency to achieve repeatable reactor conversions during processes such as nucleophilic aromatic substitution or direct azeotropic polymerization, yielding advanced engineering plastics or photoresist polymers for electronics. Industry compliance standards
Typical usage ratio
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Every day on our production lines, our team handles countless kilos of the finished aromatic compounds that shape modern industry. For years, 3,4-Dibromotoluene has played a unique role in our work, requiring precision and consistency with every batch. This molecule may seem straightforward—just a toluene ring with bromines at the 3 and 4 positions—but its subtle differences from related chemicals lead to practical impacts that chemists and manufacturers encounter firsthand.
Chemicals like this rarely make news headlines, but among process chemists and specialty formulators, demand for reliable halogenated toluenes remains high. We’ve observed the influence of even trace impurities on downstream reactions, especially in pharmaceutical synthesis or advanced materials. That’s why the way 3,4-Dibromotoluene is made, purified, stored, and delivered makes a real difference, not just on paper.
The arrangement of bromine atoms on the toluene ring distinguishes 3,4-Dibromotoluene from its 2,3-, 2,4-, and 2,5-isomers. This impacts its reactivity in cross-coupling, nucleophilic substitution, or directed ortho-metalation. On our own lines, we’ve seen how even slight shifts in substitution patterns can create extra steps or headaches during synthesis. The 3,4- isomer offers a specific window for further functionalization, which our clients in agrochemicals and custom synthesis appreciate, especially for structure-activity relationship studies.
We select starting materials carefully—our bromination of toluene relies on optimized conditions to target the 3,4-positions, avoiding the formation of unwanted isomers as much as possible. Technicians keep detailed records on reaction temperature, bromine addition rate, and quenching techniques, because each batch presents its own technical curveballs. In the end, high purity is not just a specification, but something we verify using GC, NMR, and other analytical tools before moving a kilogram off site.
Years of hands-on production have taught us that 3,4-Dibromotoluene behaves differently compared to 2,4- or 2,5-Dibromotoluene—particularly during isolation and purification. This is not immediately obvious from textbooks or catalogs; you notice it after handling dozens of batches. 3,4-Dibromotoluene’s lower symmetry means slightly different melting and boiling points, which affect crystallization and distillation. We train our staff to look for these signs during processing, making adjustments on the fly if purity or yield drops.
These technicalities matter when it comes time to respond to scale-up needs. In a synthesis plant, a trace impurity can snowball at the ton scale, leading to derailments in pharmaceutical building block routes or specialty polymer feedstocks. One example: a client once flagged unexpected byproduct formation when switching from a generic dibromotoluene to our 3,4-isomer. A troubleshooting call and some spectral analysis traced the difference to the subtle electronic effects of the isomer—something you pick up only after close contact with production.
Purity drives quality in specialty chemicals. We’ve seen how chemists working downstream sometimes face stalled reactions from off-brand batches, with purity under 98% or inconsistent isomer proportions. For us, batch-to-batch reproducibility is about more than checking boxes—it’s about supporting teams who depend on our results. Our analytical unit tests each batch with gas chromatography and proton NMR, looking not just for the main product, but also for bromotoluene isomer profiles, possible mono-brominated byproducts, and trace toluene.
Brominated aromatics attract moisture and light over time, especially after long-distance shipping. We use amber glass and lined drums for storage, and our shipping department monitors transit times. By tracking finished product from reactor to loading dock, we ensure what arrives at a customer’s lab bench matches the certificate of analysis that left our hands.
Our customers have told us that this consistency saves weeks in method validation and scale-up, especially for teams in medicinal chemistry or material science who need repeatable building blocks for screening libraries or pilot runs. The confidence in a reliable 3,4-Dibromotoluene means fewer roadblocks when scaling up or troubleshooting.
Choices among dibromotoluene isomers are not just academic. Customers occasionally ask why 3,4- should be chosen over 2,4- or 2,5-, or what challenges arise if someone switches between them. On the plant floor, the extra methyl group and different bromine placements create impacts in reactivity, safety, and even storage. The 3,4- isomer, for example, offers unique sites for further chemical modification, which gives certain syntheses more predictable yields and selectivity. Clients in specialty dyes and intermediates often comment that alternative isomers demand more process steps or lead to byproducts that require intensive separation.
Nobody likes wasting time or resources on extra purification steps. Over the years, our R&D group has worked alongside purchasing teams and chemists to identify the best matches for their project goals before the first drums go out the door. For instance, bromination at the 2,4- positions allows different cross-coupling reactions but limits downstream substitution, while 3,4-Dibromotoluene keeps open specific positions on the ring prime for further chemistry.
There’s also a storied distinction in how these isomers perform in Grignard, Suzuki, or Negishi coupling reactions. Our crew has spent time at customer sites troubleshooting sluggish conversions, and all too often the culprit is a mismatch between the isomer required and what is actually in the drum. We routinely advise on the pros and cons of each isomer. The differences in electron density, boiling points, solubility, and reactivity aren’t mere theory—they become practical experience during every synthesis run.
Safety around brominated aromatics has changed since we opened shop. Old habits die hard, but training remains constant. 3,4-Dibromotoluene demands care around high temperatures during distillation. Over the years, we’ve optimized our heat transfer and inert atmosphere protocols, not only to protect workers but also to minimize decomposition or side reactions. Logistics and storage teams have refined container schedules to minimize moisture exposure and light-induced breakdown, keeping the product stable and lessening batch rejections.
Our operations prioritize direct, regular safety training for everyone—no exceptions, from new hires to long-time crew. All brominated products receive secondary containment and dedicated transfers. We learned the hard way that improper drum sealing can lead to not only safety risks but also expensive product loss due to permeation or hydrolysis, especially during long ocean transits. Attention to detail and routine investment in upgraded containment saves everyone time and money in the end.
3,4-Dibromotoluene shows up most where high-purity substituted aromatics form the backbone of new molecular entities. Agrochemical developers use it as a scaffold for selective herbicide and fungicide chemistry, while pigment chemists rely on its reactivity profile for bright, stable dyes. Pharmaceutical teams value its reliability during the construction of intermediates, reducing time spent on purification or troubleshooting.
Even beyond R&D, several clients use our product in custom manufacturing campaigns, trusting bulk shipments to perform as consistently as smaller research-grade lots. Our batches have supported new fragments for polymer science and specialty coatings. Practical results from customers—such as higher reaction yields or faster throughput—keep us focused on confirming specs and upping our process control game.
We learn the most from troubleshooting calls or feedback sessions from users. For example, one customer in fragrance intermediates flagged discoloration and unexpected off-notes traced back to trace impurities—a reminder for us to review quenching and workup steps yet again. Another client in fine chemicals pointed out a difference in solubility depending on their solvent system, which led to improvements in our drying and packaging process.
We’ve invested in direct lines of communication with our main users, integrating customer experiences right into our process reviews. This means not just tweaking reactor setups, but drilling down into each complaint or compliment, looking for insight. Sometimes the best advice comes not from a laboratory manual but from an engineer who’s run the same reaction 100 times and knows what to expect.
A customer-focused approach grows stronger when coupled with honest documentation. For us, this means tracking and sharing batch-specific information: purity data, moisture content, isomer distribution, and any anomaly encountered. Partners who use our 3,4-Dibromotoluene on high-value projects need this transparency for their regulatory and scale-up steps, and we see fewer surprises or rejected lots as a result.
There is no static method in chemical production; continuous improvement is as much necessity as principle. Over the years, our process specialists have tweaked everything from bromination timing to waste minimization protocols. Reducing side products cuts down not only cost but also waste disposal—a growing challenge as environmental controls grow tighter. We’ve piloted changes in solvent recovery and reducing rinse water, and even these incremental improvements add up fast when multiplied across hundreds of runs.
Our facility abides by best practices for emissions control and responsible waste management. Technicians monitor effluent streams and emissions. A big step forward recently involved updating containment and scrubbing systems for off-gassing during bromination, which keeps both the workspace safer and our neighbors happy. There’s pride in running a plant where attention to detail ensures product quality, worker safety, and environmental care, all together.
Regulatory expectations around brominated organics also mean transparent documentation and traceability. Our documentation team preps batch records and compliance documentation that follow every container, giving downstream users peace of mind over sourcing and composition. This is not a tick-box bureaucratic exercise, but something born from years of audits, customer requests, and our own wish to see safer practices industry-wide.
Procurement officers and project chemists often wrestle with choosing the right dibromotoluene isomer, balancing price, specifications, and supply reliability. Our advice—rooted in cycles of feedback, process setbacks, and hard-earned fixes—is to start conversations early. Direct collaboration between supplier and R&D or manufacturing ensures the right product in the right format, minimizing headaches mid-project.
We’ve seen how miscommunications—say, an order meant for 3,4- inadvertently filled with 2,4-—translate into lost cycles of troubleshooting, lower yields, or even regulatory hurdles if the incorrect material makes its way into a file. Our order-entry crew reviews every specification for clarity, cross-checks with the plant floor, and maintains reference samples for each batch. Reproducibility matters as much for us as for clients downstream; that commitment comes from years of rolling up our sleeves at production scale.
For those venturing into new applications, our technical support shares cautionary tales and best practices, drawing on both positive and negative outcomes from years of market experience. Often, the difference between a struggling synthesis and a streamlined one comes from something simple—an adjusted drying step, an earlier detection of a minor impurity, or improved packaging to prevent off-gassing in transport.
3,4-Dibromotoluene stands as one of the cornerstones of our specialty product line. Its ongoing relevance comes not only from its chemical properties but the dependability built from decades of production, troubleshooting, and partnership with expert users. As markets evolve—demanding more high-value intermediates for pharmaceuticals, electronics, and advanced materials—experience in managing the idiosyncrasies of this compound will remain an advantage.
We continuously invest in our people, infrastructure, and process control systems, knowing that no document or certificate entirely substitutes for years of hands-on expertise. Feedback loops with our users sharpen our edge, and we remain open to suggestions, audits, and collaboration. Our commitment lies in supplying 3,4-Dibromotoluene that meets more than just technical data: it must perform reliably for every user and every application.
This is a story not just of one molecule, but of a manufacturing team working behind the scenes to keep complex supply chains running smoothly. Every batch leaving our facility carries the accumulated lessons and pride of people who’ve made specialty chemistry their work and passion.