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HS Code |
711480 |
| Product Name | 4,4'-Dichloro-3,3'-bipyridine |
| Cas Number | 76145-81-6 |
| Molecular Formula | C10H6Cl2N2 |
| Molecular Weight | 225.08 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 139-143 °C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | Clc1cc(nc(c1)c2nccc(c2)Cl) |
| Synonyms | 3,3'-Bipyridine, 4,4'-dichloro- |
| Storage Temperature | Store at 2-8°C |
| Ec Number | 214-360-5 |
As an accredited 4,4'-Dichloro-3,3'-bipyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical, 4,4'-Dichloro-3,3'-bipyridine, is packaged in a 25-gram amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | A 20′ FCL (Full Container Load) can safely accommodate approximately 13–14 metric tons of 4,4'-Dichloro-3,3'-bipyridine, securely packaged. |
| Shipping | 4,4'-Dichloro-3,3'-bipyridine is shipped in tightly sealed containers, compliant with chemical safety regulations. It should be packaged to prevent moisture or light exposure, labeled appropriately, and transported as a hazardous material if applicable. Handle with care, avoiding extremes of temperature and physical damage during shipping to maintain product integrity and safety. |
| Storage | **4,4'-Dichloro-3,3'-bipyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances, such as strong oxidizers. Keep it away from heat and moisture sources. Use secondary containment to prevent spills, and label the storage area clearly. Access should be restricted to trained personnel using appropriate personal protective equipment (PPE). |
| Shelf Life | 4,4'-Dichloro-3,3'-bipyridine typically has a shelf life of 2-3 years if stored in a cool, dry, airtight container. |
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Purity 98%: 4,4'-Dichloro-3,3'-bipyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reproducibility in target compound production. Melting point 141°C: 4,4'-Dichloro-3,3'-bipyridine with a melting point of 141°C is used in controlled-temperature organic reactions, where it maintains phase stability during catalytic coupling. Particle size <20 μm: 4,4'-Dichloro-3,3'-bipyridine with particle size below 20 μm is used in homogenous catalyst formulations, where it enhances dispersion and reactivity. Moisture content <0.5%: 4,4'-Dichloro-3,3'-bipyridine with moisture content under 0.5% is used in moisture-sensitive cross-coupling reactions, where it prevents product hydrolysis and degradation. Stability temperature up to 200°C: 4,4'-Dichloro-3,3'-bipyridine stable up to 200°C is used in high-temperature synthesis processes, where it retains structural integrity and prevents decomposition. Residual chloride ≤0.1%: 4,4'-Dichloro-3,3'-bipyridine with residual chloride less than 0.1% is used in electronic material manufacturing, where it minimizes ionic contamination for improved device performance. Assay (HPLC) ≥99%: 4,4'-Dichloro-3,3'-bipyridine with assay by HPLC greater than or equal to 99% is used in advanced material research, where analytical purity supports reliable experimental outcomes. Heavy metals ≤10 ppm: 4,4'-Dichloro-3,3'-bipyridine with heavy metals content below 10 ppm is used in fine chemical production, where it reduces risk of metal-induced side reactions. |
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There’s a canvas of chemicals that rarely make headlines, but anyone who has spent years in research labs knows products like 4,4'-Dichloro-3,3'-bipyridine matter far more than slick marketing campaigns or splashy packaging. This compound makes crucial steps possible in organic synthesis, especially in the design of advanced materials, agrochemicals, and pharmaceuticals. Years working with chemical intermediates taught me that the right reagent can speed up development or quietly derail a whole project. 4,4'-Dichloro-3,3'-bipyridine holds significance because of its balance of reactivity and reliability in synthesis.
Taking a closer look at 4,4'-Dichloro-3,3'-bipyridine, this bipyridine derivative features two chlorine atoms on the 4 and 4' positions, which switches up its reactivity profile and makes it distinct from regular 3,3'-bipyridine. I’ve worked on projects where this difference defined the project’s outcome. Those extra chlorines modulate electron density, making cross-coupling reactions more efficient and selective compared to other substituted bipyridines. Colleagues in medicinal chemistry often talk about how targeted halogenation can open doors to new lead candidates, and this is one of those compounds you’ll see again and again in retrosynthetic analyses for that reason.
The technical specifications of 4,4'-Dichloro-3,3'-bipyridine often reflect the high purity demanded by modern research. Quality batches usually show a purity of 98% or above by HPLC, sometimes edged even higher for critical experiments. Physical appearance falls in a fine, off-white to light beige powder, and its stability under ambient conditions translates into smoother storage and less worry about rapid degradation or dangerous outgassing. In my experience, shelf stability means fewer headaches during inventory reviews or restocking—time is precious, and so is knowing your stockroom won’t let you down due to sensitivity issues.
Lending itself to Suzuki-Miyaura and other palladium-catalyzed couplings, 4,4'-Dichloro-3,3'-bipyridine can build a scaffold core for ligands, functional materials, or preclinical drug candidates. This isn’t a luxury; it’s a necessity in most up-to-date labs. We don’t see 3,3'-bipyridine derivatives used solely for academic curiosity—industry teams depend on these to move from hypothesis to scaled product. From my own bench time, adding extra halides speeds up the pace, reducing the number of protection and deprotection steps. Any fellow synthetic chemist who’s wrestled with multi-step purifications knows why this is a key win. The core structure resists overreaction, giving more predictable yields during scale-up. Since industry processes often measure costs in seconds and cents, this adds up quickly in the big picture.
Most Kilo-lab and pilot plant teams will echo what I’ve noticed: using a derivative like 4,4'-Dichloro-3,3'-bipyridine means smoother purification, less byproduct, and easier tracing of impurities. Instead of hunting down unidentified peaks on an HPLC, chemists work with a more controlled reaction matrix. This translates directly to better documentation and traceability, a critical demand in regulated industries from pharmaceuticals to crop science.
People sometimes underestimate just how different two similar-seeming compounds can be. I’ve handled both the 3,3'-bipyridine and 4,4'-dichloro analog in the same year; the difference in reactivity shapes the entire workup procedure. Simple bipyridine may suit a teaching lab or a basic heterocycle screen, but pushing toward industrial or advanced research targets, the dichloro variant pulls ahead. Chlorine atoms tune the aromatic system, and this small tweak gives downstream users more control over selectivity and the option to introduce further substituents at later points. This is critical in pharmaceuticals, where metabolic pathways or environmental breakdown must be modeled with precision.
Other halogenated bipyridines exist, but experience shows that the dichloro variant sits in a sweet spot: less aggressive than some fluorinated relatives, yet more reactive than unsubstituted or monohalogenated types. Comparing head-to-head in cross-couplings or N-oxidation, 4,4'-Dichloro-3,3'-bipyridine tends to offer smoother conversions and less troublesome isolation. This saves on solvents, cuts down on purification steps, and reduces the load on analytical teams. Over the course of multi-year projects, these efficiencies multiply. Fewer failed batches translate into tangible budget relief and less lost time for research teams or production operators.
Working with organohalides calls for attention to safety. Early in my career, I gave too little thought to this, until a near-miss with a poorly ventilated flask of a chlorinated heterocycle reminded me never to cut corners. 4,4'-Dichloro-3,3'-bipyridine doesn’t release the dangerous fumes some other halide derivatives do, but treating it respectfully is not negotiable. Standard lab PPE and good ventilation keep things straightforward. Any advanced research lab with established protocols will handle this with ease. One of the subtler benefits is its predictability under typical temperatures and pressures—rarely have I had to deal with unplanned decomposition or runaway reactions using this compound. This matters for teams trying to keep tight project timelines.
Disposal is another important part of the story. Chlorine-containing organics demand proper waste processing. The extra time spent logging and neutralizing these isn’t glamorous, but it matters for the environment and for the lab team’s credibility. Experience tells me that using high-quality, well-documented material makes routine audits and regulatory compliance far easier. Certified suppliers now offer comprehensive documentation, including COAs, which provide the necessary data for internal quality processes. In regulated industries, gaps in documentation can shut down production lines. Using a trusted supply chain partner cuts down on these risks.
People think chemical intermediates are abstract, but 4,4'-Dichloro-3,3'-bipyridine ends up adding value in places most folks never see. Catalysts made from this backbone find their way into major industrial hydrogenation or oxidation steps. Its use as a building block for ligands isn’t just a matter of academic achievement; plant-scale operators lean on these structures in metal separation processes and catalysis. Looking at the numbers, global research pushes toward more specialized ligands and functionalized bipyridines every year. Companies seeking competitive advantage in asymmetric synthesis or crystal engineering often rely on the predictability and accessibility of the dichloro derivative.
Colleagues in agricultural chemistry draw on 4,4'-Dichloro-3,3'-bipyridine for pre-clinical synthesis of novel pesticides or herbicides. Modern crop protection demands less persistent, highly selective agents, and making this possible requires reliable intermediates. Over the last decade, the demand for such tailored pyridine derivatives has grown, tracking with an uptick in patent filings using these frameworks. Years working in early-phase pharmaceutical research brought me into contact with teams screening dozens of derivatives for target inhibition or transport properties. The dichloro-substituted bipyridine consistently appeared in successful lead scaffolds. As pharmaceutical R&D budgets expand in Asia and North America, demand for intermediate-grade material with consistent properties only looks set to climb.
Graduates entering the job market tend to overlook the practical consequences of a loose specification. Run a trial with even a slight impurity or batch inconsistency, and weeks of work go up in smoke. 4,4'-Dichloro-3,3'-bipyridine offers a track record of specification reliability. Batches with moisture content below 0.5% by Karl Fischer titration and clear NMR spectra reduce the risk of side reactions and make product qualification a routine step. Small details like particle size—and whether the supplier can guarantee < 100 microns for proper dissolution—make a world of difference on pilot plant scale. I’ve seen teams lose days to poorly characterized starting material, only to end up returning to a more reliable dichloro derivative.
Industry-academia collaborations often bring together different attitudes to documentation and QC. Smaller research groups sometimes worry about investing in higher purity intermediates. My view, shaped by watching both cost-conscious and high-throughput teams, is that small investments in higher-grade materials usually pay off big in time savings and certainty, sparing projects from troubleshooting batch-to-batch variability.
Other bipyridines compete for space in chemical catalogs—some with nitro, amino, or different halogen substitutions. Each alternative comes with trade-offs. Nitro groups can increase electron withdrawal but introduce regulatory headaches and increase handling risk. Fluorinated analogs sometimes push reactivity too aggressively, causing side products that clog up downstream processing. The 4,4'-dichloro structure brings enough activation, without going so far that it creates instability or tox risk. I’ve lost count of the times a project meant to use a cheap analog ended up reverting to the dichloro form after pilot results showed inconsistent quality.
Users in materials science point out another practical bonus: dichloro bipyridine aids in the structure-property relationship studies for OLEDs and organic semiconductors. This matters as the world heads toward better, low-power displays and lighting. Teams racing to improve electron transport in thin films need intermediates they can trust—materials science is plagued by dead ends, and starting with a dependable building block moves projects forward.
In the broader market, buyers evaluate cost versus value, but in my own work, a reagent that shaves off a couple purification steps or raises process yield by a few percent ends up paying for itself. Time and process stability count for more in the field than price tags ever disclose.
Sourcing high-quality chemicals is not just a box to check; it forms a feedback loop with project momentum. In the earlier days of my career, inconsistency in supply led to weeks lost to troubleshooting. Changes in appearance, unidentified by IR or NMR, flagged unresolved supplier issues. Now, more suppliers use traceable batch-control systems, giving researchers real confidence in their starting material. That matters for labs that handle sensitive ligands or chase patentable IP. Secure, predictable resupply supports researchers who need to repeat experiments for journals or audits.
Lab managers increasingly screen suppliers by their documentation, transport guarantees, and global reach. Experience working between North American and Asian labs underlines how crucial reliable lead times and product stewardship become in multinational projects. Researchers can budget time more effectively, focus on their real intellectual work, and rely on fewer late-night phone calls to chase urgent shipments.
Lab coursework that uses high-purity bipyridine derivatives teaches students the right habits early. I’ve mentored more than a few students who learned the pitfalls of inconsistent materials in a course that skipped on chemical quality. Watching their transformation after working with a top-tier compound speaks volumes about the value of reliable inputs. Students see that chemistry requires not just good designs but thoughtful material choice.
Undergraduate and graduate educators can prepare students for real-world chemistry by exposing them to industrial-grade reagents like 4,4'-Dichloro-3,3'-bipyridine. This gives them a clearer understanding of how professional research operates—and why documentation, quality, and safety protocols are integral to scientific responsibility.
The next steps to strengthen 4,4'-Dichloro-3,3'-bipyridine’s supply chain involve better real-time documentation, strengthened collaboration across the research-to-production cycle, and more open sharing of analytical verification. Laboratory information management systems (LIMS) can help track impurities and performance metrics across batches, and integrating supplier QC data with in-house records provides continuity for large-scale projects. Over the last decade, a handful of suppliers adopted transparent digital systems, letting users access up-to-date certificates and batch histories. When I participated in a cross-border research initiative, this kind of transparency allowed teams on three continents to remain tightly aligned.
Chemicals like 4,4'-Dichloro-3,3'-bipyridine benefit as supply networks prioritize ethical and traceable sourcing. Programs that invest in greener synthesis or solvent reduction point toward a lower environmental footprint. I have seen positive results in institutions where waste minimization is standard procedure, including targeted recycling of halogenated organics through specialized units. Research grant programs should support labs in testing and reporting greener pathways for key intermediates, driving real market change.
Building stronger direct communication between suppliers and research organizations fosters early flagging of demand spikes or regulatory changes. My experience tells me this reduces the panic that comes when regulations or supply disruptions hit. Labs piloting new compounds can benefit from supplier partnerships that include up-front analytical and regulatory data flows. Participating in professional networks and standards-setting consortia makes sense for industry and academia alike, broadening access to best practices in both quality and safety. This kind of engagement, built on years of trust and evidence, helps the whole research community move forward on solid ground.
The story of 4,4'-Dichloro-3,3'-bipyridine offers a window into how unsung chemical intermediates shape real results at the bench, on the production line, and in global supply chains. Working in chemistry long enough reveals that success rarely hinges on high drama; it’s more likely to rest on careful choices and honest assessment of what works. Products like this dichloro bipyridine loom large wherever teams demand progress without compromise. As regulatory and market pressures grow, the basics—high-quality supply, open data practices, and practical hazard management—will only rise in importance. Investing in trustworthy products puts chemistry teams in a strong position to invent, deliver, and, above all, safeguard the future of their work and their world.