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HS Code |
728225 |
| Cas Number | 583-70-8 |
| Molecular Formula | C8H9Br |
| Molecular Weight | 185.06 g/mol |
| Iupac Name | 3-Bromo-1,2-dimethylbenzene |
| Synonyms | 3-Bromo-o-xylene |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 211-213°C |
| Melting Point | -20°C (approximate) |
| Density | 1.37 g/cm³ at 20°C |
| Flash Point | 86°C (closed cup) |
| Refractive Index | 1.565 (at 20°C) |
| Solubility In Water | Insoluble |
| Smiles | CC1=C(C=CC(=C1)Br)C |
| Pubchem Cid | 11651796 |
| Un Number | None assigned |
As an accredited 3-Bromo-1,2-Dimethylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-Bromo-1,2-dimethylbenzene, sealed with a red cap and labeled for laboratory use. |
| Shipping | 3-Bromo-1,2-Dimethylbenzene is shipped in tightly sealed, chemical-resistant containers to prevent leakage or contamination. It is transported as a hazardous material, following relevant regulations (such as DOT or IATA). Proper labeling and documentation are required, with handling precautions to avoid exposure to heat, ignition sources, or incompatible substances. |
| Storage | 3-Bromo-1,2-dimethylbenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat and ignition sources. Keep away from strong oxidizing agents and incompatible chemicals. Store at room temperature and protect from direct sunlight. Ensure proper labeling, and handle with appropriate personal protective equipment to prevent accidental exposure or release. |
Applications of 3-Bromo-1,2-Dimethylbenzene in Industrial ManufacturingAs a manufacturer dedicated to the specialized synthesis of 3-Bromo-1,2-Dimethylbenzene, we supply high-purity intermediates tailored for advanced chemical industries. This raw material’s core value supports the efficient large-scale production of high-value molecules in pharmaceuticals, agrochemicals, and fine chemicals sectors. Below, we illustrate its precise downstream adoption, formulation parameters, and integration within manufacturing lines in four primary application fields. 1. Pharmaceutical Intermediate for Antihypertensive APIsInnovator and generic pharma companies consistently specify this compound during synthesis routes for select antihypertensive drug actives, including sartans and related biaryl derivatives. The brominated aromatic ring offers a reactive site for Suzuki-Miyaura cross-coupling, forming the biaryl motifs found in several high-demand blood pressure medications. Manufacturers introduce it early in multi-step synthesis, requiring tight process control to manage purity due to strict end-product regulations. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide SynthesisLeading crop protection formulators use this molecule in the advanced synthesis of selective herbicide cores, especially in the development of methyl-substituted brominated benzenes used for constructing novel heterocyclic structures. The bromo functionality is retained or transformed in copper- or palladium-catalyzed cyclizations that yield herbicide actives with improved environmental profile and resistance management features. Manufacturers require precise charge-in timing and reactant stoichiometry to minimize unwanted isomers. Industry compliance standards
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3. Specialty Dye Intermediate in High-Performance Pigment ManufactureDevelopers of advanced organic pigments employ this raw material when synthesizing brominated aromatics serving as functional intermediates for high-performance dyes. Particularly, its methyl and bromo substituents facilitate targeted reactions, such as azo coupling or halogen exchange, essential for producing pigments with tailored absorption and durability profiles for plastics, coatings, and inks. Consistency and trace-level impurity control directly impact pigment quality specifications demanded by downstream customers. Industry compliance standards
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4. Advanced Material Synthesis in Electronic ChemicalsProducers of high-purity specialty chemicals for electronics leverage this compound to construct precursors for liquid crystal and organic semiconductor materials. The molecular structure—with precisely positioned methyl and bromine groups—enables the introduction of specific electronic and steric properties required for custom display and circuit polymers. Accurate metering and rigorous contaminant exclusion form the basis of integration into these value-added processes, where downstream purity constraints are at their tightest. Industry compliance standards
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Long years of hands-on chemistry have shown us that not all aromatic bromides respond the same way with process conditions and downstream applications. 3-Bromo-1,2-Dimethylbenzene, with a formula of C8H9Br and CAS number 585-76-2, occupies a unique place within our lineup for its reactivity and versatility in synthesis work. Through extensive runs in crowded reactors and scale-up validation batches, we’ve learned this compound offers more than just another way to brominate methylbenzenes. Many organic chemists rely on its structure to deliver high selectivity and purity in key reactions, especially where ortho and meta substitution patterns fundamentally shape reaction routes.
Our journey with this compound began in the pilot plant, after early trials with unrefined feedstock made it clear that substitution placement deeply impacts the outcome in aryl brominations. 3-Bromo-1,2-Dimethylbenzene may look uncomplicated on paper, but the actual arrangement of the methyl groups – hugging the benzene at the 1 and 2 positions, with bromine at the 3rd – creates a distinct balance of electron effects. You won’t get the same reaction profile with its 4-Bromo or 5-Bromo cousins. Tuning the methyl locations and bromine for a specific project once meant weeks of trial and error, but now, production consistency slowly replaces guesswork.
Our experience tells us that clarity in chemical manufacturing begins at the source: starting material selection and purification. Early scale-up batches taught some hard lessons about controlling side reactions, especially when methylbenzene impurities slip through. So, every drum of 3-Bromo-1,2-Dimethylbenzene we ship comes out of a batch with full traceability, using refined o-xylene and well-planned bromination protocols. Typical output after distillation yields a pale, viscous liquid, clear enough for accurate GC analysis.
Standard specifications rely on chromatographic purity above 99%, moisture content below 0.1%, and a tightly monitored boiling range. Our teams spend time in heated discussions about which trace impurity makes a real-world difference, but after hundreds of kilo-lots, we routinely check for unreacted xylene, higher polybrominated byproducts, and charged organics. It’s not just to check a box; customers in fragrance intermediates and API synthesis report filter clogging, inconsistent color development, or surprises in hydrogenation if those contaminants are ignored. Shipment logs reflect a lived experience more than theorized purity grades.
The practical differences between 3-Bromo-1,2-Dimethylbenzene and its close relatives become clear once you set up parallel synthesis trials. In Suzuki or Stille couplings, where the bromine group takes center stage as a leaving group, the position of the methyl substituents plays a central role in both speed and outcome. In our labs, the 1,2-dimethyl backbone resists excessive side-reaction compared to 1,3- or 1,4-dimethyl variants, especially in crowded metal-catalyzed couplings or during lithiation.
Pharmaceutical projects frequently select this compound for constructing biphenyl scaffolds and building blocks. Our own process chemists favor it when producing dyes and advanced intermediates because its substitution pattern supports regioselective cross-coupling. With the meta-bromine, electron density directs incoming groups in a way that cuts down on unwanted isomers. In flavor and fragrance synthesis, its reactivity unlocks clean transformations to aldehydes and acids, letting formulators skip laborious purification steps.
Some customers experiment with 2-Bromo-1,3-dimethylbenzene or 4-Bromo-1,2-dimethylbenzene in analogous reactions, but our technical support team hears recurring reports of lower conversion, odd color drifts, or unexpected solubility. Regular feedback from customers in Europe and Asia often points out that our in-house stabilization checks prevent the slow degradation seen with poorly stored grades from less careful sources. Insights like these help us guide formulators—backed not just by talk, but by real-world problem solving fostered in our facility.
Running a brominated aromatic through warehouse and transport cycles introduces its own challenges. Years ago, we dealt with complaints about bottle discoloration and off-notes caused by improper packaging. Today our packing process relies on inert gas blanketing and moisture-tight drums, because the compound can form trace acids in damp conditions. Regular storage at ambient temperature, away from heat and UV, serves customers who rely on six-month or longer shelf life.
We learned the hard way that bulk tank lining and valve selection affect quality as much as the reaction itself. Incompatible seals leach impurities and trigger localized degradation. To avoid this, our equipment uses PTFE-lined valves and pumps, with batch logs that detail each maintenance turn. These practical steps cut product returns for discoloration and performance failures by more than half in recent years, based on internal QA data.
In a business built on complex supply chains, shipping consistency keeps projects on schedule. We plan production around customer forecasts, avoiding spot-market panic that sometimes brings in off-grade lots from brokers. Our logistics records show that maintaining a predictable shipping calendar matters when production schedules depend on reliable intermediate supply. Emergency orders introduce stress, but frequent overproduction to warehouse rarely solves the root cause—fine-tuned scheduling delivers better outcomes for all.
Customers often ask about the gap between 3-Bromo-1,2-Dimethylbenzene and more broadly available mono- or di-bromotoluenes. In practice, substitution pattern defines both reactivity and selectivity. Our team ran comparative batch tests: using the 3-bromo-1,2-dimethyl arrangement consistently reduced the formation of ortho/para isomers, especially in Pd-catalyzed cross couplings. The methyl groups in the ortho-positions (adjacent to each other) hinder over-alkylation and allow for cleaner downstream separation.
Contrast this with 2-bromo-1,3-dimethylbenzene, which introduces more electron-donating effects, sometimes increasing side reactions. Polymers produced with our target compound show tighter molecular weight distribution, critical for electronics and advanced coatings. Many customer labs, after testing other brominated toluenes or xylenes, find the residue profile and reaction byproducts less manageable than with our specification.
The minor cost differences between isomers shrink relative to wasted labor and solvent disposal when handling unwanted impurities. Even high-throughput pharma labs tracking every penny find that targeted substitution saves several workup steps. It’s a real-world example of precision chemistry delivering added value far beyond initial purchase price.
Repeated customer discussions have shown this compound’s biggest impact in pharmaceutical, agrochemical, and specialty material synthesis. Pharmaceutical teams rely on its high purity and reproducibility in constructing core building blocks for anti-inflammatory and oncology compounds. The substitution pattern supports selective coupling to complex heterocycles, key in modern drug design.
Agrochemical researchers count on consistent bromination and methyl protection in crop-protection candidates. The molecule’s stability under moderate reaction conditions means less product loss and less operational downtime. Repeated seasonal demand patterns back up these choices, as customers rarely accept material with questionable physical data.
In the dye and pigment sector, consistent hue development links directly to incoming intermediate quality. One notable plant-scale collaboration led to faster purification cycles in vat dye synthesis, as batches from less refined sources clogged filters and caused washout defects. Our 3-Bromo-1,2-Dimethylbenzene, tracked by in-line GC and stability testing, helps customers keep output within spec, even as regulatory standards tighten.
Some newer electronics projects demand tightly defined aromatic intermediates to create semiconducting polymers and light-absorbing layers. Device manufacturers, especially in OLED and organic solar cell sectors, share data showing improved consistency in optical and electrical properties when the starting material meets our tested purity benchmarks.
Many chemical manufacturers claim strict standards, but years of running analytical tests have taught us that not all batches labeled “99% pure” perform the same. Our own labs go beyond basic GC and HPLC, running thermal and oxidative stability tests, and tracking color against UV spectra. Even minor contamination—undetectable by some standard methods—will crop up in high-sensitivity downstream reactions.
Years of returned product or troubleshooting for customer labs reinforced that sniff tests and subjective color inspections are no substitute for hard analytics. Ethereal markers (like subtle off-aromas or batch-to-batch color drift) often signal the start of a QC problem that could take months to fix downstream. These checks don’t just keep us on top of technical performance—they build trust, as research teams can focus on innovation rather than firefighting unforeseen issues due to unreliable feedstock.
Every brominated aromatic brings a degree of health and safety obligation. Our production workflows train operators to minimize skin and inhalation exposure—split between local exhaust systems, physical barriers, and regular worker health checks. Direct, practical feedback from plant team members contributes real improvements to handling and transfer methods.
Our waste management takes center stage across all process steps. Reduction in off-gas bromides and more effective purification during distillation means less hazardous waste headed for incineration or treatment. Frequent analysis of emissions and drum rinse waste catches issues before they escalate into regulator attention or community complaints.
Globally, pressure increases for greater sustainability in specialty chemical manufacture. Every new regulatory push, whether from REACH or national agencies, brings scrutiny over storage, shipment, and trace handling contamination. We’re not immune to cost pressures, but long-term relationships with environmental auditors have shown that upfront investment in closed-loop reclamation, employee safety, and careful storage pays off in fewer production stoppages and lower audit risks.
Chemists and plant teams have shared their frustrations with inconsistent brominated aromatics arriving at their doors. Many problems trace back to batch variability and uncontrolled logistics, rather than fundamental chemistry. We put effort into batch records and QA oversight. Each shipment includes a production log, highlighting checkpoints from raw material trace, through process control, to finished product sign-off. This transparency reduces finger-pointing and shortens investigation time if a problem crops up at a customer site.
Over the years, more sophisticated customers have pushed us to implement real-time QC analytics and integrate digital lab notebooks. These tracking systems, combined with our plant team’s craftsmanship, highlight issues before they impact release schedules. Gaps still exist between hard process control data and the “feel” a seasoned chemist brings to running a reactor, but ongoing training bridges knowledge and technology.
We have built technical troubleshooting into our after-sales communication, not just for customer satisfaction scores but because direct feedback speeds up quality improvements. A few hours’ candid exchange between synthetic chemists and plant engineers can resolve recurring headaches before they turn into global recalls. That loop helped pinpoint temperature range issues in our earlier batches, and replaced outdated glassware with scaled-up, jacketed reaction systems.
Procurement teams sometimes treat brominated intermediates as interchangeable commodities, chasing the lowest spot price. But the last decade has reinforced that cost savings on paper often turn into expensive cleanup or project delays down the line. Batch-scale production in our facility—overseen by teams who understand the end applications—means clients receive material that supports efficiency, scaling, and compliance.
Our longest-standing customers trust not just a product, but our plant’s collective know-how, built by years of learning from failures and success. We’ve seen how even a minor batch impurity can derail a multi-million-dollar pharmaceutical or electronics rollout. So we value feedback loops and ongoing partnerships more than one-off sales.
Good chemical manufacturing springs from experience, steadfast process discipline, and real-world interaction with customers and staff. Each lot of 3-Bromo-1,2-Dimethylbenzene tells a story of repeated process improvement and close attention to the effects of every variable, from methyl group placement to batch size. Only after working through years of troubleshooting, cross-industry application trials, and frequent technical challenges does a product reach a level where everyone—from synthesis chemist to supply chain planner—counts on it with confidence.
We remain committed to providing a consistent, transparent, and high-performing intermediate to customers worldwide, built on continuous learning and an open dialogue with anyone who depends on our products for innovation and reliable output. As the applications for selective aromatic intermediates expand, only careful, experienced manufacturing will continue to deliver value that lasts beyond a single drum or project cycle.