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HS Code |
127141 |
| Chemical Name | 2,2'-bipyridine-dichloropalladium (1:1) |
| Molecular Formula | C10H8Cl2N2Pd |
| Molecular Weight | 342.52 g/mol |
| Cas Number | 14221-01-3 |
| Appearance | Yellow to orange crystalline powder |
| Solubility | Soluble in polar organic solvents (e.g., DMF, DMSO, acetonitrile) |
| Melting Point | Decomposes above 250°C |
| Storage Conditions | Store in a cool, dry place under inert atmosphere |
| Purity | Typically ≥98% |
| Application | Catalyst for coupling reactions (e.g., Suzuki, Heck, Sonogashira) |
| Density | 1.86 g/cm³ |
| Coordination Geometry | Square planar around Pd(II) |
As an accredited 2,2'-bipyridine-dichloropalladium (1:1) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle, 5 grams; white printed label showing "2,2'-bipyridine-dichloropalladium (1:1)", batch number, and hazard pictograms. |
| Container Loading (20′ FCL) | 20′ FCL: Securely packed in drums or containers, 2,2'-bipyridine-dichloropalladium (1:1) loaded with moisture protection and clear labeling. |
| Shipping | 2,2'-Bipyridine-dichloropalladium (1:1) is shipped in tightly sealed, inert containers to prevent exposure to moisture and air. Packaging complies with regulations for hazardous materials. The product is typically transported at ambient temperature, with cushioning to prevent breakage, and proper labeling to ensure safe handling during transit. |
| Storage | 2,2'-Bipyridine-dichloropalladium (1:1) should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances (especially strong oxidizers). Keep the container tightly closed when not in use. Store in a designated chemical storage cabinet, preferably under inert atmosphere (such as nitrogen or argon) to prevent degradation by moisture or air. |
| Shelf Life | 2,2'-Bipyridine-dichloropalladium (1:1) is stable for at least 2 years when stored sealed, dry, and protected from light. |
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Purity 99%: 2,2'-bipyridine-dichloropalladium (1:1) with purity 99% is used in Suzuki-Miyaura cross-coupling reactions, where it ensures high product yield and minimal side reactions. Melting Point 310°C: 2,2'-bipyridine-dichloropalladium (1:1) with a melting point of 310°C is used in high-temperature catalytic processes, where it maintains catalyst integrity and operational stability. Particle Size <10 μm: 2,2'-bipyridine-dichloropalladium (1:1) with particle size less than 10 μm is used in homogeneous catalysis, where it improves catalyst dispersion and reaction kinetics. Stability Temperature up to 250°C: 2,2'-bipyridine-dichloropalladium (1:1) stable up to 250°C is used in thermally demanding synthesis, where it enables prolonged reaction times without degradation. Solubility in DMF: 2,2'-bipyridine-dichloropalladium (1:1) soluble in DMF is used in ligand complexation studies, where it facilitates homogeneous solution phase reactions. Molecular Weight 393.5 g/mol: 2,2'-bipyridine-dichloropalladium (1:1) with molecular weight 393.5 g/mol is used in stoichiometric control of organometallic reactions, where precise reagent calculation enhances reproducibility. Moisture Content <0.2%: 2,2'-bipyridine-dichloropalladium (1:1) with moisture content below 0.2% is used in sensitive polymerization reactions, where it prevents unwanted hydrolysis and ensures purity of the end product. Assay ≥98%: 2,2'-bipyridine-dichloropalladium (1:1) with assay not less than 98% is used in pharmaceutical intermediate synthesis, where it provides consistent catalytic performance and reliable batch scalability. Stability in Air: 2,2'-bipyridine-dichloropalladium (1:1) with air stability is used in open-atmosphere chemical processes, where it minimizes the risk of catalyst deactivation by ambient conditions. Trace Metal Impurities <50 ppm: 2,2'-bipyridine-dichloropalladium (1:1) with trace metal impurities below 50 ppm is used in electronic material synthesis, where low contamination preserves semiconductor quality. |
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At our plant, 2,2'-bipyridine-dichloropalladium (1:1) stands as more than just a catalogue item; it’s a staple for synthetic chemists pushing beyond typical cross-coupling boundaries. We stock this catalyst in consistent forms, both in powder and crystalline textures, always prioritizing batch integrity and stability. Customers appreciate the vibrant yellowish tone, a quick indication that our material holds up to the tight standards they expect for high-performance ligated palladium complexes.
Walk into any synthetic lab where new C–C or C–N bonds take center stage, and you’ll find a specific demand for air-stable, robust pre-catalysts. We see orders for 2,2'-bipyridine-dichloropalladium most often from researchers familiar with its shelf stability and reliability in Suzuki, Heck, and Sonogashira couplings. This complex, with one molar equivalent each of bipyridine and palladium dichloride, easily dissolves in acetonitrile or DMF—just what you want for reproducible batch chemistry.
Looking at some of our long-term customers, process chemists in both pharmaceuticals and specialty chemicals count on this material to shorten optimization cycles. The pre-ligated format trims back risks of mismatched stoichiometry or slow initiation, issues that crop up with in situ metal/ligand mix-and-match. Spending less time troubleshooting solubility or activation means they can focus on yield, selectivity, and cost control instead.
Beyond the minimum assay value, each drum passes HPLC and ICP checks to push trace metals and free chloride below the thresholds known to poison reactions. Experts coming from scale-up backgrounds expect these controls because batch-to-batch deviation complicates global regulatory filings or preclinical timelines. Our QC team double-checks for consistent ligand coordination, clear of measurable excess free bipyridine that would otherwise impact reactivity or cause side reactions.
We specify this product to meet the melting range and solubility necessary for process applications. Granular size sits tight so that dusty handling in the fume hood or excessive clumping at pilot scale don’t become a hindrance. Attention to these details keeps downstream analytics straightforward, especially in regulated sectors where impurities can set off red flags during audits.
Our firsthand experience has shown that the choice between preformed 2,2'-bipyridine-dichloropalladium and building your active catalyst in situ impacts the pace of development. A preformed structure saves labor on the benchtop, bringing down error rates under routine glovebox or open-air conditions. Process teams handling multigram or kilogram challenges appreciate the minimized risk of incomplete ligation or the hassle of over-liganding, both of which can spook less experienced chemists.
Some early-career visitors, especially those who stick to standard PdCl2 or Pd(OAc)2 plus bipyridine, often face inconsistent results. They call in for advice after seeing wild fluctuations in conversion or trace metallic residues in product isolations. Our technical support often demonstrates—sometimes over a video call—the more repeatable performance by starting from a well-characterized, pre-ligated material. Unintentional introduction of excess free ligand or water can sour the whole batch; preformed complexes make troubleshooting much more straightforward.
Bench chemists working parallel screens for ligand effects or substrate scope rarely stop and analyze impurity sets but notice right away when low conversion crops up during purification. With this product, the tight control over palladium-to-bipyridine ratio removes excess variables. In the field, that means more focus on substrate compatibility and product proof, less time spent hunting the source of disappointing turnovers.
It’s one thing for a material to work in a 10 mL reaction tube at 80 °C, another for it to handle a 50 L batch with a tricky base or heteroatom substrate. We’ve shipped pallets of 2,2'-bipyridine-dichloropalladium to contract manufacturers handling pre-commercial scale runs; feedback focuses on the absence of batch failures even when changes in operational temperature or solvent choices move from DMSO to acetonitrile. Several industry groups report smoother washing steps and robust catalyst recycling compared to basic palladium salts, cutting back their palladium losses and container residue.
In scale-up, pressure to minimize hazardous waste grows yearly. A side benefit of using a pre-ligated complex stems from easier downstream separation and reduced filtration headaches. Facilities chasing green chemistry benchmarks find that fewer side-products signal less need for post-reaction remediation. Some of our bulk users in OLED and electronic materials synthesis also report sharply reduced metal contamination in their products, smoothing the path to compliance with demanding electronics standards.
Technologists sometimes ask us why we focus on this specific bipyridine ligand. From our vantage point, 2,2'-bipyridine stabilizes the palladium center without introducing steric congestion common in bulkier nitrogen ligands. The chelating bite angle helps tune both activity and selectivity for a wider substrate window. Many of our senior organic chemists comment that, for tough aromatic and heterocyclic couplings where phosphines can get poisoned, this bidentate ligand ensures longer catalyst lifetime.
For sustainability-minded clients, bipyridine-derived palladium complexes avoid problems experienced with trialkylphosphine ligands, like air sensitivity and odor. In the scale-up bay, you can weigh the solid without glovebox fuss or auxiliary equipment, which directly influences operational safety. Our formulations actively avoid excessive ligand so as not to compete for substrate binding or formation of less-reactive species—details that enhance cost control when working with expensive starting materials.
Requests for comparative information often center on the practicalities of switching from separate PdCl2 and ligand combinations, or moving away from phosphine-based complexes. We’ve benchmarked this compound for dozens of proprietary clients over the years. What they tell us: 2,2'-bipyridine-dichloropalladium, unlike plain PdCl2 or Pd(OAc)2, behaves more predictably and reacts quickly, even in air or damp atmospheres. Where alternatives like Pd(PPh3)4 offer high initial activity but decay under repeated heating or exposure, our bipy-Pd complex maintains reactivity across cycles. No need for vacuum sealing or complex storage, making it handy for both research and production lines.
Clients working with ligands like dppe, dppf, or tBu3P see clear trade-offs in reactivity and substrate tolerance. N-heterocyclic carbene complexes, for example, deliver on some challenging coupling partners but at the cost of more complex handling and synthesis. Many high-throughput labs report that bipyridine-based catalysts, our flagship included, give more consistent assay results for patchwork libraries of amines, aryl halides, or boron reagents, with less fuss about solution color changes signaling deactivation.
Experience has taught us to focus on safe, user-friendly packaging. Our bipy-Pd complex resists humidity and does not darken with short-term exposure to air, providing a useful buffer during inventory checks and transport. We avoid extraneous stabilizers since unintended additives sometimes impair catalyst performance in precise pharmaceutical syntheses. Even so, we keep each container lined and marked with distinct batch information. Process engineers know where things can go wrong with dusty, sticky, or lump-prone powders; we pay attention to particle size and free-flowing qualities from drying to packing.
Feedback on storage draws from the realities of bench and warehouse logistics. No ultra-low freezers or inert-atmosphere hoods are necessary. Our staff trains buyers on optimal dispensary practice: store cool and dry, cap tightly after use, and keep away from direct sunlight. Even when batches pause in transportation or sit in queue before usage, degradation stays low, so you get as clean a start as possible every time you weigh out a portion.
Over the years, we’ve invested steadily in refining purification and analysis. Demand from regulated markets—especially drug intermediates—drives our methods. Each production run links back to a robust batch history. Our analytical suite checks for both main and trace impurities missed by less exacting suppliers. This is not just about numbers on a certificate of analysis: it’s the difference between reproducible reactions and rolling the dice on quality, especially under accelerated timelines for early-phase projects.
Some competitors may market generic or repacked versions lacking full disclosure of upstream sources or shipping conditions. Our clients, especially those in regulated or export-focused industries, stress how much this transparency matters if problems arise mid-project. Regulatory filing often requires a complete audit trail. We keep clear records—in-house and on request—so transfer of technology never hits unexplained snags tied to missing provenance or out-of-spec material.
We don’t stop at bulk supply. Collaboration shapes our day-to-day: method development for new transformations, troubleshooting, and training on optimal use. Several customers partner with us early in route scouting for lead molecules or new electronic materials. Real-world projects mean the unexpected happens—an off-color batch, a contaminant trace, a sudden switch in solvent policy. Our technical teams stand ready to help trace root causes, run comparison splits, or adjust support documents for regulatory submissions.
Practically speaking, synthetic chemists and process engineers expect suppliers to know more than just catalog numbers. We track changes in academic literature and patent filings that hint at new applications, so the product never lags behind evolving needs. That edge allows our catalyst to stay in scope, even as reaction methodologies swing toward new sustainability or selectivity targets.
Clients’ input shapes not only our technical sheets, but even the way we package and deliver. For example, routine customer updates uncovered a rising need for smaller batch packaging, so we added more flexible containerization. That lets researchers run pilot and process-scale reactions without sitting on surplus stock or worrying about moisture ingress over long-term storage. Some even requested specific label data, so now we include expanded source and data codes for easier batch traceability.
Requests for specialized particle sizes, higher or lower bipyridine ratios, or custom solvent compatibility have led us to run short custom syntheses. As a manufacturer directly responsible for process and QA, these requests push us to stretch facility flexibility and QC speed—an effort our staff takes real pride in. Our openness to incremental change, driven by day-to-day lab realities, keeps us connected to users instead of chasing abstract “market trends.”
In the current landscape, transparent sourcing and disclosure grow more important. Regulations clamp down on heavy metal residues and demand clearer audit trails. Simple, robust pre-ligated complexes like ours meet regulatory agencies’ need for defined composition and lot-traceable documentation. Companies pressing to reduce palladium in effluents or minimize downstream processing costs gravitate toward our material, both for its purity and straightforward analytical profile.
We audit our own supply chains as part of greener chemistry demands. By optimizing for minimal waste in synthesis and scaling steps, we align with customers aiming for lower total environmental impacts. Feedback on catalyst removal and reuse cycles gets funneled directly to our R&D team, so improvements can reach the next batch. This loop, built on real-world deployment, helps keep us ahead of compliance shifts.
Every month, we field calls from R&D groups running new heterocycle couplings or exploring late-stage functionalization. Failures encountered due to older, variable-quality raw materials often lead these teams to re-run screens using our 2,2'-bipyridine-dichloropalladium. One team working on complex arylated indoles credited the clean reaction profiles to the pre-ligated complex, moving from low, inconsistent yields to clear, high-purity product in fewer steps.
Another client working in the flavor chemicals sector faced color and odor issues with previous catalyst suppliers, which complicated product purification and masked trace artifacts. After switching to our material, their downstream work-up and crystal isolation sped up, with less solvent required to reach regulatory standards. Such case histories underscore the practical gains from consistent, QC-vetted source materials, especially when dealing with cost- or regulation-sensitive products.
From factory to benchtop to post-reaction workup, 2,2'-bipyridine-dichloropalladium (1:1) proves its worth not through overhyped claims but by meeting customers’ real process needs. We don’t pretend our material works in every imaginable scenario, but we do stand behind its performance where reliable cross-coupling catalysts are called for. Years of feedback from users fighting deadline pressure, dealing with tough substrates, or scaling tricky molecules keep us alert to new demands and old pitfalls alike. That insight, rooted in the nuts and bolts of manufacturing and daily problem-solving, shapes every drum that leaves our door.