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HS Code |
562015 |
| Cas Number | 2052-66-2 |
| Molecular Formula | C12H8Br2 |
| Molecular Weight | 327.01 g/mol |
| Appearance | White to pale yellow solid |
| Melting Point | 81-84°C |
| Boiling Point | 346°C |
| Density | 1.69 g/cm³ |
| Solubility In Water | Insoluble |
| Refractive Index | 1.673 |
| Smiles | C1=CC=C(C=C1)C2=CC=CC(=C2)Br |
| Inchi | InChI=1S/C12H8Br2/c13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14/h1-8H |
| Synonyms | 2,2'-Dibromo-1,1'-biphenyl |
| Pubchem Cid | 70924 |
| Ec Number | 218-137-5 |
As an accredited 2,2'-Dibromobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,2'-Dibromobiphenyl is packaged in a 25-gram amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 2,2'-Dibromobiphenyl is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It is classified as a hazardous material and must be transported according to relevant chemical safety regulations, including appropriate labeling and documentation. Shipment typically occurs via ground or air under controlled conditions, avoiding direct sunlight and extreme temperatures. |
| Storage | 2,2'-Dibromobiphenyl should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, well-ventilated area. Store away from sources of ignition, strong oxidizing agents, acids, and bases. Clearly label the container and handle the chemical using appropriate personal protective equipment (PPE) to prevent inhalation, ingestion, or skin contact. |
Applications of 2,2'-Dibromobiphenyl in Industrial Manufacturing2,2'-Dibromobiphenyl serves as a key intermediate in several advanced chemical production chains, supporting high-performance polymers, pharmaceutical synthesis, agrochemical manufacturing, and specialty electronics materials. As the direct manufacturer, we ensure each batch meets strict industry requirements and predictable quality for complex formulation environments. 1. High-Performance Polymer Flame Retardant IntermediatePolymer compounders use 2,2'-Dibromobiphenyl as a core building block in the synthesis of halogenated flame retardants, particularly for polycarbonate, ABS, and polystyrene plastics requiring elevated fire resistance in electrical and automotive applications. Its di-brominated structure provides controlled bromine content that enables effective char formation and inhibits combustion during the final compounding step, supporting stringent regulatory flame standards across global markets without compromising processability or physical properties of the base polymer. Integrators select this molecule specifically for consistent performance in automated extrusion and injection molding lines. Industry compliance standards
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2. Pharmaceutical Synthesis of Biaryl Scaffold DrugsProcess development chemists use 2,2'-Dibromobiphenyl as a coupling precursor for the generation of biaryl motifs during the synthesis of small-molecule APIs, especially via Suzuki-Miyaura and Ullmann-type reactions. Its specific regioisomer enables selective formation of unsymmetrical biaryl cores, important for the design of kinase inhibitors, anti-inflammatory molecules, and selective central nervous system actives. Batch documentation and regulatory traceability remain essential as it enters GMP-compliant multipurpose synthesis plants, where customers require unambiguous source and impurity profiles for regulatory submissions. Industry compliance standards
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3. Agrochemical Precursor for Crop Protection AgentsChemical synthesis plants utilize 2,2'-Dibromobiphenyl as a controlled halogenation intermediate in the manufacture of selective herbicides and fungicides for high-value fruit and vegetable crops. Agrochemical formulators leverage the molecular stability and substitution pattern to generate diaryl substitutes, ensuring controlled release and environmental stability in finished formulations. The starting material must conform to agro-grade impurity limits and provide traceable sourcing documentation for national and export registration processes. Compatibility with large-scale batch and continuous manufacturing always underpins consistent downstream outcomes. Industry compliance standards
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4. Specialty Materials for High-Purity Electronic ChemicalsProducers of liquid crystal monomers and OLED materials incorporate 2,2'-Dibromobiphenyl as a rigid, planar aromatic scaffold for custom synthesis of electronic-grade intermediates. This raw material’s defined substitution is essential for controlled crystal packing, charge transport, and stability under display device operating conditions. Electronic chemical formulators demand documented ultra-trace metal and halogen impurities, as well as full analytical disclosure to support integration into precision thin-film deposition and organic semiconductor processing streams. Quality metrics exceed standard chemical grade expectations, as batch consistency influences device yield and optical clarity. Industry compliance standards
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Experience in manufacturing specialty organic compounds tells us that the devil is always in the details. 2,2'-Dibromobiphenyl, known for its clear structural reliability, remains a cornerstone for research chemists and advanced material development. We synthesize this molecule through a carefully monitored bromination reaction that preserves biphenyl integrity. Our process gives a crystalline solid with high purity, proven by routine HPLC and GC checks. This approach avoids unwanted isomerization, which can complicate synthesis downstream.
Most customers coming through our doors search for a compound that performs consistently, batch after batch. The structure of 2,2'-Dibromobiphenyl means each bromine sits on the ortho position of each benzene ring, making this compound remarkably useful for selective Suzuki and Ullmann couplings. In our own process improvement cycles, we found that starting material purity and controlled reaction temperature play larger roles than reagent brand or country of origin. That experience led us to invest in additional purification steps after final crystallization.
Typically, 2,2'-Dibromobiphenyl comes in a white to off-white crystalline form. Our usual specification requires a purity of not less than 98%, with moisture content held below 0.1%. Each lot gets an infrared spectrum run against our reference file; any variance triggers further analysis. Every customer order receives a certificate listing trace levels of possible polybrominated biphenyls, residual solvents, and heavy metals, giving chemists the data needed for risk assessment and reaction planning. Shipment always includes a batch sample, not just for transparency, but to help our customers confirm that the material meets their own incoming inspection standards.
Even a small difference in substitution pattern can shift reaction outcomes. In biphenyl chemistry, misplaced halogen atoms disrupt coupling sites, and trace isomers often carry through into final products. Our lab team regularly supports customers troubleshooting by confirming both isomeric purity and absence of contaminants. Many academic and scale-up laboratories have moved away from buying through third parties for this very reason. Our manufacturing site has run hundreds of kilograms of this molecule, with many lots destined for pharmaceutical intermediates, liquid crystal research, and high-end polymer projects.
We use a batch process that allows us to keep a close eye on reaction exotherms and ensure that the product forms without over-bromination. Automated data logging helps prove batch consistency for downstream users who need that assurance for regulatory filings. There’s less guesswork when you work with material that’s been handled by chemists rather than just logistics operators. We've heard feedback directly from development managers: having access to source-level information on synthesis and purification steps saves them troubleshooting time, particularly during validation.
Markets offer a whole range of brominated and chlorinated biphenyls. Each isomer carries different risks and rewards. Customers sometimes ask about the difference between 2,2'-Dibromobiphenyl and close analogs, such as 4,4'-dibromobiphenyl or mixed bromo-chloro analogs. The main feature of the 2,2'- compound is its ability to direct further transformations to the para-positions of the rings, opening up synthetic routes not available with para- or meta-substituted analogs. Coupling efficiency and product yields often depend on matching the right regioisomer to the desired end-use molecule.
Material with bromines on both ortho positions tends to react more selectively in nickel- or palladium-catalyzed processes. Our technical service group tracks published data and customer feedback; most reports indicate higher reactivity and selectivity from our 2,2'-Dibromobiphenyl compared to di- or tri-substituted versions, especially in electronic material research. That’s not just marketing language; it's backed up by actual user batch records shared during collaborative process improvement programs.
Manufacturing chemists live with the reality that each organobromine presents health and environmental questions. We've built specialized containment and scrubbing into our facilities just to keep byproducts and dust strictly controlled. The broader chemical industry, especially in specialty manufacturing, sometimes neglects the impact of halogenated intermediates downstream. We bring this up in regular customer meetings, because some production partners need tighter controls than others. It isn’t just a regulatory checkbox; mishandling waste or accidental release can seriously affect worker health and local water supplies. Experience taught us the cost is always lower in the long run if you plan for safe handling up front.
Getting the highest product quality out of each kilogram isn’t about exotic tech or fancy marketing. It comes down to process understanding—both chemistry and engineering. At our plant, we track frequent process data: from bromine source quality to ambient humidity, from operator shift logs to batch log sheets. Long experience tells us that even small excursions outside the spec can hurt yield and reliability, which our downstream customers see in their own product purity or project milestones. If a batch falls shy of our internal release targets for foreign matter or melting range, it doesn’t leave our warehouse.
Years running these reactions have shown us that solvent choice matters as much as catalyst, especially when scaling beyond gram-scale. We stick to a solvent blend that minimizes polysubstitution and keeps workup clean. At one point, we tested alternative, greener solvents with a university partner. The trials showed promise for small-scale runs, but struggled to keep product yield high in drums versus flasks. We keep samples of these trial runs on file, because real progress in green chemistry comes from incremental improvement, not one-off pilot campaigns.
Every manufacturing run includes time for routine safety talks and equipment checks. Halogenated biphenyls like 2,2'-Dibromobiphenyl call for special procedures that go beyond standard organic compounds. The dust, though not overtly toxic compared to older PCB-laden mixtures, still calls for local exhaust and careful glove work on the filter. Solids are never left exposed in open bins; we rely on double-containment hoppers and negative pressure workspaces modeled after industry best practices. Spills are rare because of these steps, but we run regular drills for our shift crews since a process is only as strong as its weakest oversight.
Outside laboratories sometimes ask about how stability and shelf life compare to mixed-halogen biphenyls. Our stability testing shows virtually no change over five years if sealed tightly and kept away from UV light. Crystals that yellow over time usually point to improper storage, not chemical degradation. Routine retesting only takes minutes with our FTIR and DSC systems, so end users never need to wonder about unexpected changes after long-term storage. Customer feedback flagged a propensity for static buildup when dispensing, so we modified our filling equipment to ground and discharge the product more efficiently.
At the bench and in pilot plants, we see researchers draw on 2,2'-Dibromobiphenyl chiefly to build more elaborate aromatic cores. This might mean directed ortho-metalation for pharmaceutical scaffolds, or polymer backbone creation for electronic displays. With access to well-made material, users report fewer purification headaches. That translates to lower solvent usage, less time in the fume hood, and a smoother route to their target molecules. University collaborations have sometimes surfaced unexpected applications, like using this compound as a template in the synthesis of metal-organic frameworks or as a doping precursor in organic electronic devices.
End-to-end traceability gives our partners a leg up during scale up and regulatory review. We share representative production records for major shipments, and subject every lot to multi-stage impurity profiling. This does more than boost customer confidence—it gives us early warning of rare process bugs that might otherwise fly below the radar in outsourced or resold material. On occasion, a sharp question from a customer on impurity formation has led us back to modify a cleaning cycle or reevaluate a filtered waste stream. Strong two-way communication makes both sides better, raising the bar for everyone in the chain.
Making, storing, and shipping 2,2'-Dibromobiphenyl isn’t just a technical task. Every turnaround cycle calls for close coordination between operators, engineers, logistics, and compliance teams. Staff training now covers not only reaction protocol but also personal protective equipment use, incident response, and waste segregation to keep pace with evolving regulations. Regional rules on brominated organics keep shifting, and we track changes by participating in industry groups and regulatory advisories. Preemptively updating our in-house practices has cut the learning curve each time rules change. Partners working in countries with tighter restrictions benefit from this, skipping needless delays at import or customs.
Over time, we've seen creative approaches from our customers across pharmaceuticals, electronic materials, and specialty polymers. Some called for heavier documentation suites for environmental compliance, others asked for help adapting to tighter allowable impurity thresholds. We work through these issues directly—not through intermediaries. On-the-ground experience managing product through the full lifecycle, from raw material to container check-out, gives us unique visibility into the real-world issues that can affect research outcomes. Longstanding relationships with repeat customers arose in part because we share not just a product, but a mutual investment in reducing hassle and raising standards.
Manufacturing specialty halogenated aromatics like 2,2'-Dibromobiphenyl isn’t set-and-forget. Each process review delivers a lesson. Repeated analysis by our own QA group flagged rare byproducts, not visible at the crude isolation stage but detectable by LC-MS in finished material. Actively screening for these byproducts gave us better yield control and improved customer satisfaction on large projects. Even small process improvements—tightening the filtration sequence by a few degrees or drying at slightly reduced pressure—have shown measurable return on product quality. Customers and staff alike push us to keep asking what can be better, not just what meets spec.
We’ve faced logistical constraints, from global transport slowdowns to volatile raw material pricing. Long experience taught us to build flexibility into raw material sourcing and maintain transparent communication channels with both suppliers and customers. When solvent supplies ran tight, we pivoted batch sequencing, keeping core product lines in production while testing minor process tweaks for non-critical runs. This kept our commitments on 2,2'-Dibromobiphenyl delivery even at times when some industry partners faltered.
Process upsets are inevitable in chemical manufacturing. We’ve learned more from a failed batch than from dozens of routine ones. Contamination incidents, though rare, have led to tougher protocols and direct investment in automated monitoring. Customers quickly pick up on issues with batch consistency; only through honest communication and corrective action can long-term trust be built. Improvement doesn’t just mean bringing a production run back into spec, but sharing post-mortem reviews with commercial partners to prevent future headaches on both sides.
Getting feedback from end users in Asia, Europe, or North America often uncovers subtle issues. For example, during a multi-ton project using 2,2'-Dibromobiphenyl as a drug intermediate precursor, a downstream customer reported trace interference in a bioassay protocol. Working together, we reviewed the full impurity profile and traced the culprit to an unexpected brominated stilt arising during scale-up. Addressing such issues requires open files, access to personnel with reaction and analytical expertise, and a willingness to invest time until an answer is found. These lessons rarely make it into catalogs but shape how specialty chemicals like ours actually succeed at the bench.
Emerging markets in organic electronics, biomedical devices, and responsive materials have started specifying tighter purity and documentation standards for intermediate materials. We anticipate customers will continue challenging manufacturers for more granular information, not just on product composition, but also on process safety profiles and environmental documentation. Specific regulatory frameworks around brominated chemicals, such as REACH in Europe, already demand detailed impurity control and waste stream handling procedures. Keeping pace with these requirements forms part of daily workflow for our technical and regulatory staff.
Ongoing work with development partners drives home the point that high-quality 2,2'-Dibromobiphenyl makes innovation faster and more reliable. From OLED displays to new classes of drug molecules, outcomes rely on the small choices and persistent investment that characterize accomplished chemical manufacturing. We expect the pressure for even cleaner, lower-impact bromination methods will grow, led by both environmental regulators and the most progressive development teams. Our plant upgrades focus on both reducing waste and tightening energy management, not just because it checks a sustainability box, but because efficient use of resources and rigorous waste reduction has proven to directly improve product consistency and reliability.
By listening carefully to both technical and regulatory demands, direct manufacturers like us play a central role in enabling next-generation technologies and safeguarding health. It is this daily grind—constant tuning, learning, and open exchange—that underpins the quality and confidence built into every shipment of 2,2'-Dibromobiphenyl that leaves our facility.