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HS Code |
798979 |
| CAS_number | 583-53-9 |
| Molecular_formula | C6H4Br2 |
| Molar_mass | 235.90 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting_point | −3 °C |
| Boiling_point | 224 °C |
| Density | 1.98 g/cm³ |
| Solubility_in_water | Insoluble |
| Flash_point | 96 °C |
| Refractive_index | 1.595 (20 °C) |
As an accredited 1,2-Dibromobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,2-Dibromobenzene is supplied in an amber glass bottle, securely sealed, containing 500 mL, with hazard labeling and safety information. |
| Shipping | 1,2-Dibromobenzene is shipped in tightly sealed, corrosion-resistant containers to prevent leaks and exposure. It is classified as a hazardous material, requiring labeling and documentation per transport regulations. Transport must ensure the chemical is kept away from heat, strong oxidizers, and incompatible substances, with secure, upright placement throughout transit. |
| Storage | 1,2-Dibromobenzene should be stored in a tightly closed, clearly labeled container in a cool, dry, and well-ventilated area, away from sources of ignition, acids, strong oxidizers, and direct sunlight. Keep it away from incompatible materials and moisture. Use chemical storage cabinets designed for hazardous organic chemicals, and ensure appropriate safety measures, such as spill containment and secondary containment, are in place. |
Applications of 1,2-Dibromobenzene in Industrial Manufacturing1,2-Dibromobenzene serves as a critical intermediate in diverse industrial fields where its reactivity supports high-value synthesis. As a direct manufacturer, we supply consistently controlled quality for demanding downstream conversion and compounding processes in established chemical sectors. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers incorporate 1,2-dibromobenzene in the preparation of active pharmaceutical ingredients and advanced intermediates, particularly for small-molecule APIs requiring ortho-disubstituted aromatic moieties. Nucleophilic substitution and cross-coupling processes use this building block to introduce brominated aromatic segments that cannot be efficiently assembled in later synthetic steps. Its application is central in the multi-step production of several antihypertensive and antineoplastic agents, where regioselective transformation and halogen exchange must conform to cGMP synthesis protocols under validated batch controls. Industry compliance standards
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2. Agrochemical Active Ingredient ProductionLeading agrochemical producers deploy 1,2-dibromobenzene in the synthesis of highly engineered pesticide molecules and herbicide intermediates where ortho-disubstituted patterns dictate biological activity. The presence of bromine atoms supports both direct field efficacy and process selectivity during aryl-to-aromatic substitution. It enters strictly monitored process trains where batch-to-batch traceability is required to align with local and international agrochemical manufacturing statutes. Strict in-process controls, including quantitative halide analysis, are maintained throughout conversion into biocidal or weed control end products. Industry compliance standards
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3. Organic Electronic Material and Liquid Crystal PrecursorManufacturers in the organic electronics sector utilize 1,2-dibromobenzene as a starting material for synthesis of functionalized aromatics used in advanced display technologies and specialty polymers. Cross-coupling reactions such as Suzuki and Ullmann allow efficient aryl-aryl bond construction, crucial for producing high-purity organic semiconductors and nematic liquid crystal intermediates. The input is managed within closed systems to meet trace impurity thresholds and must conform to electronic-grade quality guidelines for downstream melters and deposition. Industry compliance standards
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4. Synthesis of Specialty Dyes, Pigments, and Photographic ChemicalsDye and pigment producers rely on 1,2-dibromobenzene for the formation of highly conjugated and color-intensive aromatic rings where ortho substitution patterns alter chromophore absorption. It enters azo, anthraquinone, and phthalocyanine colorant synthesis, supporting not only the precise hue adjustment but also ensuring compatibility with optical, textile, and photographic applications. The compound must meet end-use specific metal, halide, and volatility limits and serves in integration steps preceding sulfonation or metallization. Industry compliance standards
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5. Flame Retardant Intermediate ManufacturingProducers in the flame retardant field introduce 1,2-dibromobenzene to prepare aromatic bromine-rich intermediates. These compounds contribute brominated segments essential for achieving target thermal and oxidative stability in finished FR polymer systems. The manufacturing process emphasizes control over side-reaction products and specification of residual bromine content, as raw material consistency directly impacts efficiency in downstream extrusion or blending with base resins like polyolefins and polyamides. Industry compliance standards
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Competitive 1,2-Dibromobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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Anyone who has spent time in a chemical manufacturing plant comes to recognize certain aromatic halogenated compounds by their unmistakable impact on lab benches, process pipelines, and finished products. 1,2-Dibromobenzene has built up a reputation based on decades of consistent reactivity, structural stability, and focused utility across many industries. Working with this material day in, day out presents real lessons on what can go right or wrong, what customers expect, and where it earns its place as a go-to intermediate.
Our own manufacturing operation runs a dedicated line for 1,2-Dibromobenzene, often referred to as ortho-dibromobenzene. We produce this colorless to pale yellow liquid by direct bromination of benzene—controlling temperature, stoichiometry, and catalytic efficiency with closed-loop monitoring. Each batch faces precise gas chromatography–mass spectrometry analysis, which enables our process to reach consistently high purities as demanded for downstream users in pharmaceuticals and specialty chemicals.
Most buyers recognize 1,2-Dibromobenzene from its CAS number or molecular formula (C6H4Br2), but behind these details sits a benzene ring with two adjacent bromine atoms. These features lead to intense discussions between chemists, engineers, and purchasing teams regarding reactivity or compatibility with other reactants. This compound is seldom handled in isolation. In our experience, customers ask specifically for ortho-isomer when seeking selective halogenation results, as substitution patterns can dramatically affect overall synthesis outcomes. We routinely get requests requiring precise ortho control, because even a small amount of the meta (1,3-) or para (1,4-) isomers can introduce complications during scale-up or catalyst performance.
We get frequent questions about batch documentation, with specifications including purity levels—often exceeding 99%—as well as moisture content and trace halide analysis. Not every application tolerates the same impurity profile. Agrochemical manufacturers, for example, trust our 1,2-dibromobenzene for its record of clean transformation into more complex compounds, avoiding downstream fouling or catalyst poisoning. They rely on sharp melting and boiling points that come only from tight process controls.
Every tank and drum leaving our facility comes with spectral printouts and lot traceability. Some clients require further customization, such as specific stabilizer additives or container linings to prevent micro-impurities during extended storage. Synthetic route efficiency can collapse if these subtle details go unnoticed. Our operations team learned early to never dismiss a client’s requirement as unnecessary. Even small deviations in column separation or storage conditions have ripple effects for bulk users, especially when transitioning to continuous production.
It is easy to find basic descriptions of 1,2-Dibromobenzene’s role in the synthesis of pharmaceuticals, dyes, and organic intermediates. After years on the production floor, supplying large and small end-users, we see trends that textbooks only hint at.
On the pharmaceutical side, 1,2-dibromobenzene is sought for its ability to act as a versatile aryl halide building block. Researchers and process chemists value its ortho-bromo arrangement, which unlocks routes for Suzuki-Miyaura coupling, nucleophilic aromatic substitution, and Grignard reagent formation. Customers developing antineoplastic agents and new active pharmaceutical ingredients request our batches based on documented reliability—especially when moving from pilot to full-scale campaigns. The ortho-dibromo structure reduces the risk of unwanted rearrangements or by-product formation during multi-step synthesis.
The dye and pigment industries depend on consistent halogenated benzenes for stable color development, lightfastness, and compatibility with next-generation polymer blends. Our technical teams help clients integrate 1,2-dibromobenzene in vat dye, azo pigment, and high-performance ink manufacturing. Experience shows that wide batch-to-batch variability leads to unpredictable hues or shifts in color strength once the materials reach customer plants. Maintaining this consistency is only possible through a feedback loop with customers and strict, on-site analytical control.
Aside from major industry sectors, fine chemical makers choose this product for its ease of functional group conversion. Whether crafting specialty monomers, targeting unique bromoarene structures, or building blocks for organometallic catalysts, they value reproducible halogenation patterns. In every case, the impact of even trace contaminants can undermine catalytic cycles or reaction yield. We continually test our product for potential interfering constituents such as monochlorinated by-products or isomeric dibromobenzenes, as missed impurities become costly at the kilo or ton scale.
1,2-Dibromobenzene competes with other dibromobenzenes (meta and para), as well as the wider family of chlorinated and fluorinated benzenes. Our team has seen researchers try to substitute these alternatives in bench work, only to face mixed or outright failed results. Ortho-dibromo compounds deliver a unique electron-withdrawing effect and steric outcome, influencing reactivity in ways neither the meta nor para isomers match. Our staff often fields questions about using less expensive 1,4-dibromobenzene, but experience shows the ortho product delivers more predictable coupling in specialized syntheses, especially involving ortho-functional group proximity reactions. Small differences in bromination position mean large-scale recalibration, disrupting ongoing campaigns, and additional costs.
Compared to monochlorobenzene or 1,2-dichlorobenzene, the dibromo analog provides increased molecular weight, a higher boiling point, and different electronegativity. These features alter its behavior in separation and purification schemes or when acting as a reaction intermediate. For polymer scientists, ortho-dibromobenzene falls within a sweet spot: reactive enough for coupling, stable during storage, and easy to track spectroscopically. Our historical sales data reveal that many users return to this chemical after trying more aggressive or less selective halogenated compounds, simply because their final product quality takes a hit with substitutes.
Each product in the halogenated benzene family has niche advantages. In our experience, 1,3-dibromobenzene sees limited use in coupling reactions intended for symmetrical products or in sites with less steric hindrance. Likewise, para-dibromobenzene serves best for high-symmetry applications, but for any task where ortho-stereochemistry is crucial—such as building block design or catalysis innovation—clients invariably return to the 1,2-isomer.
Manufacturing 1,2-dibromobenzene above the kilo scale brings unique challenges. Our operators navigate bromine handling risks, strict environmental controls, and precision on reactor temperature. Tolerances run tight. Unmonitored trace contamination can undermine months of customer trial work, potentially derailing product launches or regulatory filings. It takes continuous investment in analytical technology and staff training to reduce batch variation, document all in-line adjustments, and certify each shipment.
Clients sourcing for research may tolerate wider specification ranges, but multinational buyers or highly regulated fields require confidence in every ton. Our plant designed extensive process validation steps to pass regulatory, environmental, and logistics audits. Any deviation in raw material supply or waste disposal impacts production cost and client satisfaction. In regions with changing regulatory standards for halogenated compounds, we actively monitor rules for both workplace safety and downstream environmental impact, ensuring that our product keeps pace with evolving customer expectations.
Logistics plays a large role at scale. Even top-quality 1,2-dibromobenzene loses value when storage or transport practices lapse. We have witnessed spilled drums and container failures add to reclamation bills, slow down customer lines, or, worse, require batch requalification. Lessons learned from real incidents prompted us to collaborate with packaging engineers and logistics teams to select drum linings, seals, and labeling practices that withstand long-distance shipment through multiple climates and warehousing environments.
The market for organobromine compounds continues to tighten, as bromine prices fluctuate and environmental regulations evolve. Our manufacturing teams face the reality that cost-sensitive clients sometimes seek alternatives or dilute dibromobenzene with other aromatics. But from long-term supply relationships, we know that premature switching often introduces greater risk—lead time volatility, process instability, and material failure—overshadowing nominal cost savings. We track the global bromine market closely, invest in supply chain resilience, and focus on keeping product delivered on time despite volatility, preventing costly plant shutdowns at our customers’ facilities.
New uses for 1,2-dibromobenzene keep emerging in materials science, particularly where reactivity and positional control matter. We see project teams developing advanced coatings, specialty resins, and new organic semiconductors request detailed impurity breakdowns and custom packaging for pilot lots. In a field where reproducibility is paramount, our ability to provide high and consistent purity, storage stability, and transparent technical support earns loyalty and longer-term business.
The path from order placement to successful application never follows a straight line. Teams of scientists, engineers, and procurement officers regularly contact us to troubleshoot reactivity, volatility, or downstream compatibility issues. For example, a customer scaling from a 2-liter lab synthesis to a 2000-liter plant run may find dissolved oxygen or trace moisture suddenly becomes a limiting factor. Our technical support staff, many of whom have worked in process development themselves, engage in these conversations, review chromatograms, and suggest handling protocols or reformulation options. Sharing lessons learned, rather than reciting isolated facts, advances both our customers' projects and our own process innovation.
The learning goes both ways. Each client’s production setup, analytical method, and product requirement reveals new challenges, often prompting us to refine air exclusion procedures, update in-process filters, or invest in advanced purification steps. This responsive approach, drawn from actual issues faced at the bench or on the shop floor, shapes both our current offering and our future plant modifications.
As scrutiny rises on brominated aromatics, environmental compliance sits front and center for manufacturers. Our operation maintains stringent effluent control, volatile organic compound abatement, and closed-loop recycling—core elements for continued production in tightly regulated jurisdictions. Lowering the environmental impact of both product and process has become a shared goal with our largest customers, who incorporate life cycle analysis and green chemistry targets into purchasing decisions and process audits.
Certifications and audit-ready documentation demonstrate commitment, but it is ongoing investment and transparency that sustain real progress. We routinely invite customers for site visits and audits, opening our quality, safety, and environmental systems up for shared review and collaborative improvement. Feedback from these interactions uncovered areas for further reduction in bromine losses, greater thermal efficiency, and more standardized waste management.
Industry standards for purity and safety continue to tighten. Rather than reacting to regulatory changes, our plant trains staff in upcoming compliance requirements, partners with environmental agencies, and works to foster a culture where process optimization goes hand-in-hand with safety and sustainability.
Rapidly shifting customer requirements, emergent technologies, and tighter regulations comprise the landscape chemical manufacturers navigate each year. In the past five years, our biggest challenges in 1,2-dibromobenzene production linked to raw material bottlenecks, stricter hazardous waste control, and nuanced customer specs not seen even a decade ago. Solutions require open communication—not just between production and sales, but right through to the customers’ process chemists and regulatory teams.
In direct consultation, customers flagged bottle-necking at their dosing and unloading stations, as well as issues with transition metal catalysis stemming from subtle impurities. Together, we adjusted filtration protocols, modified drum designs, and provided sample splits for pre-qualification, smoothing large-scale transitions that would have otherwise delayed launches.
Forward-looking customers increasingly request green production methods, reduction of hazardous by-products, and lower energy footprints. Our pilot projects now routinely assess opportunities for bromine recovery, solvent recapture, and energy integration. This persistent effort in process improvement not only addresses regulatory pressures but also cuts costs and improves workplace safety.
Research is underway exploring selective catalytic bromination and continuous flow chemistry, both approaches which may improve future yield, lower waste, and stabilize prices for end-users. Transparent sharing of pilot data with select customers lets us align process development with market needs—another example of how sustained manufacturer-customer partnerships drive progress.
Over years spent producing, refining, and supplying 1,2-dibromobenzene, we have learned that trust and communication eclipse any technical description. Customers seek more than raw material; they look for a manufacturer whose day-to-day experience, technical problem-solving, and willingness to improve impacts their products and bottom line. Each drum, each lot, bears the mark of countless adjustments and lessons—earned not just in our own plant, but in cooperation with everyone who relies on our 1,2-dibromobenzene to deliver results across pharmaceuticals, dyes, materials science, and beyond.