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HS Code |
593376 |
| Chemicalname | 1,4-Dibromo-2-Chlorobenzene |
| Molecularformula | C6H3Br2Cl |
| Molarmass | 286.36 g/mol |
| Casnumber | 624-18-0 |
| Appearance | White to off-white crystalline solid |
| Meltingpoint | 66-68°C |
| Boilingpoint | 279°C |
| Density | 2.18 g/cm³ |
| Solubilityinwater | Insoluble |
| Flashpoint | 141°C |
| Refractiveindex | 1.617 (at 20°C) |
| Smiles | ClC1=CC=C(Br)C=C1Br |
| Pubchemcid | 12344 |
As an accredited 1,4-Dibromo-2-Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure cap, labeled “1,4-Dibromo-2-Chlorobenzene, 100g”, hazard symbols, and handling instructions printed. |
| Shipping | 1,4-Dibromo-2-Chlorobenzene should be shipped in tightly sealed containers, away from moisture, heat, and incompatible substances. It must be labeled as hazardous, following applicable regulations (such as DOT, IATA, or IMDG). The chemical should be handled by trained personnel, using proper protective equipment, and stored in a cool, well-ventilated area during transport. |
| Storage | Store **1,4-Dibromo-2-chlorobenzene** in a tightly sealed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Keep container tightly closed and clearly labeled. Protect from physical damage and moisture. Follow all relevant safety protocols and local regulations for storage of hazardous chemicals. |
Applications of 1,4-Dibromo-2-Chlorobenzene in Industrial ManufacturingAs a direct manufacturer of 1,4-dibromo-2-chlorobenzene, we supply high-purity product grades specifically for downstream industrial synthesis. The following application scenarios detail how this compound functions in differentiated industries, providing essential chemistries for complex product development. All listed industries reflect authentic large-scale integrations and commercial end uses. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers employ 1,4-dibromo-2-chlorobenzene as a halogenated building block for the custom synthesis of complex heterocyclic APIs, including select anticancer agents and anti-inflammatory drugs. The compound’s specific substitution pattern allows for nucleophilic aromatic substitution and palladium-catalyzed cross-couplings, critical in medicinal chemistry routes. Its role as a key intermediate facilitates the introduction of bromo and chloro motifs, influencing both the pharmaceutical activity and synthetic accessibility of the final molecules. Industry compliance standards
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2. Agrochemical Intermediate for Selective Herbicide ManufacturingMajor agrochemical producers utilize this material as a core halogenated aromatic starting material to construct high-value herbicides with multiple halogen substituents. Its dual bromine and single chlorine configuration enables targeted introduction of electron-withdrawing groups, critical for developing biological activity against resistant weed species. The compound is typically incorporated in the early stages of multi-step synthesis, forming the aromatic core of active herbicide molecules. Industry compliance standards
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3. Chemical Synthesis of High-Performance Dyes and PigmentsSpecialty dye and pigment manufacturers integrate 1,4-dibromo-2-chlorobenzene in the synthesis of colorants requiring precision halogenation, such as vat dyes, azo dyes, and high-fastness organic pigments. The raw material imparts unique halogen-substituted chromophores, providing enhanced lightfastness and chemical resistance in textile and plastic colorant formulations. This compound enters selective coupling and substitution reactions, defining final product purity and chromatic properties. Industry compliance standards
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4. Advanced Material Synthesis for Polymers and Liquid Crystal MonomersProducers of high-performance polymers and specialty liquid crystal monomers use this compound as a halogenated aromatic precursor for further functionalization. It contributes unique chlorine and bromine substitution patterns required in monomer units for enhancing flame retardancy, dielectric properties, and molecular alignment in final polymers. Its controlled reactivity supports downstream modification via lithiation, cross-coupling, and polymerization initiation steps. Industry compliance standards
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5. Synthesis of Specialty Brominated Aromatic Compounds for Fine ChemistryContract manufacturing operations and fine chemicals suppliers rely on 1,4-dibromo-2-chlorobenzene to access unique bromo-chloro substituted aromatics essential for further derivatization. Its role as a halogen source facilitates Suzuki coupling, Grignard reactions, and other targeted transformations, forming substrates for catalyst ligands, photoactive agents, and advanced intermediates in chemical research and specialty applications. Industry compliance standards
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There’s something grounding about walking through the plant as batches of 1,4-Dibromo-2-Chlorobenzene move from reactors to purification columns. Anyone who has worked with halogenated benzenes knows the importance of hitting that purity target time and time again, because the downstream applications don’t cut much slack. Our facility focuses on the consistent, careful synthesis of this compound, known among technicians by its CAS number, but talked about here by its effect on the daily routine—steady, reliable, and always in demand for specialized synthesis work.
Every batch of 1,4-Dibromo-2-Chlorobenzene is more than just a product line item. Each drum represents careful temperature control, tight maintenance of pressure, exact feed rates of raw materials, and many rounds of analytical checks. The main appeal for this molecule comes from its position as a valuable intermediate. Unlike common halobenzenes such as monochlorobenzene or 1,4-dichlorobenzene, this compound carries both chlorinated and brominated groups on the aromatic ring, yielding unique reactivity and subsequent transformation potential. Years of running these processes have taught the team that subtle differences in production strategy have a big impact on how well the product fits downstream reactions, whether that’s coupling, derivatization, or stepping into the world of pharmaceuticals or advanced agrochemicals.
From a manufacturing perspective, purity matters. Typical specifications deliver purity levels above 99%, but these numbers mean little without the means to achieve them day after day. Consistent boiling and melting points serve as a check on residual solvents and unreacted precursors. We never rely solely on certificates; GC and NMR traces are reviewed for every shift, because odd impurities show up in places the textbooks never mention. Even trace amounts of unwanted byproducts can throw off downstream syntheses, prompting unexpected delays or costly rework for clients further down the chain.
Direct halogenation routes and controlled reaction parameters form the backbone of 1,4-Dibromo-2-Chlorobenzene production. The process often starts with 1,4-dichlorobenzene as a substrate, followed by selective bromination—a step where temperature, agitation, and distributor design directly affect yield and selectivity. Years ago, side reactions with competing dibrominated isomers used to plague production lots. Through hands-on tweaking—adjusting solvent volumes, improving quench rate, and even swapping out gaskets for better material compatibility—impurity profiles have sharpened, resulting in fewer rejections, less off-spec residue, and smoother logistics.
These improvements in output quality do not happen by accident. Countless hours of instrument calibration and troubleshooting—sometimes in the middle of the night—helped root out lingering contaminants that could stymie a finely-tuned synthesis further downstream. In the plant, every percent of purity is earned, not just reported.
From long conversations with process chemists and plant operators, one factor keeps coming up—reliability. In contrast with relatively simple mono-halogenated aromatics, 1,4-Dibromo-2-Chlorobenzene offers two heavy bromines anchored to a stable aromatic ring and a single chlorine substituted at the ortho position. That structural combination opens up reactivity patterns unavailable to more common analogues.
For example, this compound enables specific cross-coupling strategies or targeted nucleophilic substitutions. Synthetic chemists appreciate that the dual bromine arrangement on para positions leads to predictable outcomes in Suzuki or Stille coupling reactions, while the chlorine allows selective displacement under catalytic conditions. Where pharmaceuticals, agrochemicals, or high-performance polymers need precise halogen placement, 1,4-Dibromo-2-Chlorobenzene stands apart from its mono- or di-halogenated cousins.
A chemical’s value only holds if it stays consistent from warehouse to end-use. Our floor crews manage daily variables—ambient humidity, minor process changes, shipping interruptions—that all leave fingerprints on stability and handling. 1,4-Dibromo-2-Chlorobenzene has shown good shelf stability in airtight, properly-sealed packaging, but exposure to heat, sunlight, or open air can still lead to slow degradation or loss of purity. Packing drums or bags always requires more than just filling and labeling; it means inspecting seals, checking for residual moisture, and testing samples for any hint of yellowing or caking.
From a manufacturer’s standpoint, contamination can start at the raw material sourcing stage or sneak in during transfer and packaging. Over the years, shifting to an enclosed feedstock transfer system and investing in high-integrity labeling have cut down these risks. It pays in far fewer customer complaints and less scrap material. A stringent environmental monitoring program keeps airborne halogen levels and potential byproduct contamination at bay while safeguarding the crew’s health on the floor.
Global demand for 1,4-Dibromo-2-Chlorobenzene has grown steadily, driven by end-users focused on making specialty chemicals, pharmaceutical building blocks, and advanced intermediates. Those who work in process research or scale-up divisions recognize its worth, especially for constructing target molecules with a combination of bromo and chloro functionalities. This flexibility reduces the number of steps required to reach a complex target, saving both time and cost in multi-step syntheses.
Over the years, our partners in R&D have built entire research programs around this compound. Its uses extend from forming biaryl linkages through palladium-catalyzed processes to introducing protected amines or other functional groups directly onto the aromatic ring. The value here runs deeper than any simple chemical commodity—it’s about knowing your intermediate plays a mission-critical role in enabling downstream chemistry, whether that means a novel drug, a crop protection agent, or a next-generation material.
Our practical experience in handling similar materials underlines clear differences. Compared to 1,2-dichlorobenzene, for example, the presence of dual bromines changes both the molecular weight and the reactivity under coupling and substitution conditions. At the plant, that translates to varying requirements for mixing speed, reflux temperature, and even handling precautions—brominated compounds can carry distinctive hazards, and their volatility and odor profiles are different from their monochloro or dichloro analogues.
From a chemical perspective, 1,4-Dibromo-2-Chlorobenzene’s para orientation often translates into more symmetrical substitution patterns in subsequent transformations. This makes it more attractive for synthesizing symmetric target molecules, especially for polymer precursors or high-purity specialty chemicals. In contrast, ortho- or meta-substituted products can lead to more branched or less predictable architectures, which might complicate process control or downstream purification. These sorts of details matter both to the synthetic chemist and the production staff tasked with making sure every drum is fit for purpose.
With halogenated compounds, careful stewardship of both product and byproducts has become standard operating procedure. At the plant, everyone from junior operators to senior engineers gets regular training in responsible handling, because any lapse in protocol can lead to safety issues or regulatory headaches. Through years of work, we’ve tightened up containment, spill response, and ventilation strategies, reducing both personal exposure and fugitive emissions—even as volumes and batch frequencies have scaled up.
Disposal of process waste, especially spent solvents and off-grade materials, requires both compliance with environmental regulations and a respect for how these materials can affect local communities. We’ve moved from simple incineration and landfill options toward integrated solvent recovery and recycling programs, often in collaboration with partners specializing in hazardous waste management. This approach has paid off: lower disposal costs, improved sustainability scores, and more goodwill with local regulators and neighbors.
One thing we’ve learned over years of manufacturing 1,4-Dibromo-2-Chlorobenzene is that small changes pay big dividends. Relentless fine-tuning—maybe an adjusted quench temperature, a better condenser, or even a reformulated process aid—delivers tighter purity profiles, less variability, and greater consistency, batch after batch.
Innovation does not always mean new equipment or radical chemistry. Sometimes, it means finding ways to cut cycle times, reduce energy use, or capture more residual product from distillate streams. In our experience, gathering feedback from every part of the operation—from unloading tankers to packing out finished goods—yields ideas that don’t show up in journal articles. Small wins add up to meaningful gains in quality, safety, and value for the customer, which sets the tone for our entire manufacturing culture.
Feedback from formulators and end-users shapes how we approach both production and technical support. A missed delivery or a batch that’s just a few tenths of a percent off in purity can throw off schedules, affect final yield, or lead to costly regulatory retesting downstream. Maintaining open communication and fast response times isn’t just a best practice—it’s a lesson reinforced each time a partner calls with a technical question or quality challenge.
Transparency matters, too. We share analytical results, answer technical queries, and open our doors to on-site audits because the best customer partnerships grow from shared confidence in every step of the process. We have welcomed research chemists from multiple countries who want not only data sheets but also real insight into manufacturing controls and quality systems. That openness sets the standard for trust and keeps the feedback loop running between the production floor and the bench chemist.
Chemicals like 1,4-Dibromo-2-Chlorobenzene operate within an ever-tightening regulatory space. Our experience with registration in various jurisdictions means every shift operates under robust quality management systems. Traceability, documentation, and real-time analytical support are built into workflow, not bolted on as afterthoughts. This approach arose from necessity—regulations have evolved in step with societal expectation, and companies that can’t prove the integrity of their materials risk exclusion from entire markets.
We maintain a robust change control process, qualifying raw material sources and production equipment, and documenting every change down to the lot level. This goes beyond regulatory requirement; it also lowers the risk of miscommunication or unexpected technical puzzles for our partners. Over time, this commitment to detail has reduced both warranty claims and non-conformance investigations, leaving more time for process improvement and less for fire-fighting.
The R&D pipeline depends on intermediates that deliver consistency and flexibility, and it’s no exaggeration to say that reliable sources of 1,4-Dibromo-2-Chlorobenzene have powered a wide range of chemical innovation. Synthetic groups appreciate suppliers who can work with them to customize specs, talk through options for scale-up, or troubleshoot challenging reactions. As a manufacturer, supporting these needs goes beyond filling orders—it means investing in technical staff, maintaining pilot facilities for custom runs, and keeping a laboratory team engaged with both internal process development and direct customer support.
Projects in advanced materials, electronic chemicals, and even niche fine chemicals benefit from an intermediate that shows predictable behavior across different synthetic methodologies. We see regular requests for technical advice about alternative solvents, selectivity in halogen substitution, or environmentally-preferable reaction conditions. By investing in both upstream synthesis and downstream applications support, we help close the gap between lab-scale ideas and industrial reality.
Inside the plant, discussions about market cycles, customer volumes, or strategic partnerships are never far from the technical realities shaping production. The team knows that today’s repeat order grew from months or years of technical discussion, process improvements, and shared risk. For industries that can’t afford batch failures or off-target products, stability counts more than promises.
As global regulation, market demand, and technology all advance, the day-to-day reality of manufacturing 1,4-Dibromo-2-Chlorobenzene will keep evolving. Through practical learning and careful attention to both macro and micro details, we look forward to supporting the complex chemistry that relies on our product. The goal remains the same—provide a dependable, high-quality intermediate that meets the real needs of researchers, formulators, and industrial chemists alike.