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HS Code |
647935 |
| Iupac Name | dichlorobis(2,2'-bipyridine)nickel(II) |
| Alternative Name | Nickel(II) dichloride 2,2'-bipyridine complex |
| Chemical Formula | C10H8Cl2N2Ni |
| Molecular Weight | 301.79 g/mol |
| Cas Number | 14483-06-6 |
| Appearance | Green crystalline solid |
| Melting Point | 235 °C (decomposes) |
| Solubility | Soluble in polar organic solvents |
| Coordination Geometry | Square planar |
| Oxidation State Of Nickel | +2 |
As an accredited Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 5-gram amber glass bottle, sealed with a screw cap, labeled with the chemical name and hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2): Secure, sealed, labeled drums/pails, max 20-foot container, following chemical safety regulations and export compliance. |
| Shipping | The shipping of Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- complies with regulations for hazardous chemicals. It is securely packaged in sealed containers and clearly labeled with hazard warnings. Transport is conducted via approved carriers, ensuring environmental containment and personnel safety as mandated by relevant local and international guidelines. |
| Storage | Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect it from light and moisture. Follow appropriate chemical storage protocols and ensure that only trained personnel handle and access the storage area. |
| Shelf Life | Shelf life: Stable for at least 2 years if stored in a cool, dry place, protected from moisture and light. |
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Catalyst: Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- with 98% purity is used in homogeneous catalysis for organic synthesis, where it enhances reaction selectivity and yield. Complex stability: Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- with high ligand stability at 25°C is used in coordination chemistry studies, where it ensures reproducible complex formation. Oxidation state: Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- featuring a stable Ni(II) oxidation state is used in redox-active material development, where it provides consistent electrochemical performance. Solubility: Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- with good solubility in polar organic solvents is used in solution-phase reaction protocols, where it allows uniform catalyst dispersion. Melting point: Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- with a melting point of 320°C is used in thermally stable catalyst systems, where it maintains activity under elevated temperatures. Particle size: Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- with a particle size of <10 μm is used in fine chemical manufacturing, where it offers rapid dissolution and high reactivity. |
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Nickel complexes with 2,2'-bipyridine ligands have made a real mark in catalysis and R&D. As a manufacturer involved directly in the hands-on synthesis of Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)-, we have observed the increased demand for this specific compound, especially from academic and industrial researchers. Many inquire about its advantages compared to basic nickel salts and other nickel-bipyridine derivatives. Here we explain what sets it apart and why research groups prefer this particular complex.
Years of batch-after-batch production clarify one thing: careful crystal engineering and stoichiometric control determine both reactivity and practical value. Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)-, typically with molecular formula C10H8Cl2N2Ni, shows both air-stability and solubility in polar organic solvents, traits not always found in cheaper nickel(II) chloride options. The deep color reflects the strong ligand field induced by bipyridine coordination, which produces a more predictable electronic environment for transition-state control.
While producing this compound, we focus on rigorous purification. Most end uses call for high-purity material—both in terms of metals analysis and ligand content. Trace metal contamination, especially from competing cations, often torpedoes reaction outcomes. Each lot receives elemental analysis, FTIR, and, for certain clients, XRD confirmation of structure. There’s no shortcut to consistency; we’ve seen how even minor process deviations cause undesirable reaction byproducts or lower yields for end-users.
Colleagues in both academic and corporate labs often pick this complex for cross-coupling, polymer precursor modification, and redox catalysis. In these sectors, routine nickel salts struggle due to questionable stability and vague ligand field effects. Adding bipyridine offers site-specificity and stabilizes the oxidation state, especially for sensitive transformations like Kumada and Negishi couplings or C–H activation. The preformed coordination bond in this complex provides better entry into controlled mechanistic cycles, leading to repeatable results batch after batch—not only in the literature, but also in scale-ups.
While nickel(II) chloride works in some settings, many customers have told us about unrepeatable results and catalyst decomposition. Switching to our bipyridine complex, they’ve shown us NMR yields and chromatograms that finally match published results. This is no minor detail; research cycles waste months when a complex doesn’t deliver cleanly from the start. Often, control experiments using only nickel(II) chloride as the catalyst return only trace product, with unwanted side reactions. Our product’s shelf-stability matters too, with customers storing it outside gloveboxes for weeks without observing breakdown.
Doing in-house side-by-side tests and following up on customer feedback, we’ve noticed distinct differences depending on ligand structure and counterions. The (SP-4-2) isomer arrangement creates predictable coordination geometry and reactivity. For chemists exploring other bipyridine analogs or alternate halide counterions (like bromide or iodide), reaction rates drop or side-product profiles increase. We’ve isolated and analyzed the off-spec materials to confirm this trend in our QC labs.
Some competitors offer similar ligands, but rigorous checks reveal differences in purity. The challenging point often comes from incomplete chloride exchange or trace ligand impurities. Analysts in our quality team routinely separate color fractions from post-synthesis mother liquids. Impure fractions show expanded peaks or impurity signatures in both NMR and mass spectrometry analyses. These details matter because they directly affect the selectivity of nickel-catalyzed reactions, where our customers want clean, single products at scale.
Many years in the chemical industry taught us to keep direct communication with R&D customers. Larger players audit our production records and require batch-specific documentation, showing not only the synthetic history but also solvent origins, drying methods, and waste elimination steps. Satisfying demand at scale depends on repeatable process protocols. Every team member receives training on handling and isolating nickel species; we immediately document and log any outlier during synthesis or workup. Periodic spectral archiving maintains traceability, so customers can review data linked to a particular shipment.
We’ve noticed a growing expectation from laboratories in varied sectors: electronics, pharmaceutical intermediates, polymer research, and green chemistry. Where once simple nickel salts satisfied these sectors, modern research forces upgrades to more defined coordination complexes. Our plant’s investment in dedicated reactor lines, separate filtration, and packing setups stems from customer feedback pointing out the consequences of cross-contamination or inconsistent hydration states. There are no workarounds for precision; in nickel coordination chemistry, detail rules outcome.
Labs working day-to-day with this complex value stability more than labels might suggest. Unstabilized nickel compounds have a tendency to absorb water, form unknown hydrates, and show unwanted color changes that hint at hydrolysis. Our product, as delivered, resists this kind of drift. Technicians at our facility document powder flow, moisture pick-up, and solvent compatibility not only at shipment but through extended shelf tests. Controlled drying and nitrogen blanketing lower risk during transit and storage, and we regularly review these measures based on customer feedback.
We designed our packaging with hands-on users in mind, hearing too many times about broken glass vials and caked-up powders from previous suppliers. Providing resealable high-barrier pouches and clear labeling avoids confusion in multi-user settings—a must for busy shared facilities and university stockrooms. Customers who scale up to multigram or kilogram quantities access customer-matched packaging and certificates, which saves time matching purchase records with research batches.
Unlike bulk commodity chemicals, specialty nickel complexes see most use in emerging areas—new bond-forming reactions, ligand screening for catalysis, advanced materials synthesis, and electrochemical innovations. Direct conversations with researchers and long-term supply partners reveal where the compound shifts outcomes. Many mention that standard nickel salts, especially hydrate forms, lead to inferior selectivity or require pilot studies for every new ligand or substrate class. In comparison, the bipyridine nickel complex lets them plug directly into literature protocols with minimal adaptation, increasing productivity and decreasing troubleshooting.
Startups and universities working on photoredox catalysis or C–C coupling have shared notebooks and spectra confirming increased turnover numbers with our product. Even beyond academia, customers in advanced battery R&D and specialty polymer synthesis require reproducible metal-ligand complexes. The bipyridine motif, with its rigid chelation and electronic donating properties, makes for uniform reaction cycles. Synthetic users benefit from lower metallic waste and higher product yields as a result of cleaner catalysis. Precise ligand geometry, as seen here, better survives reaction stress and repeated charge cycles, which is essential in electronics development.
Feedback from research chemists confirms that small impurities—whether residual solvents or trace transition metals—skew results far more than theoreticians predict. Routine spot-checks on competitor material reveal contamination that isn't listed in certificates. Across thousands of runs in customer labs, failed reactions occur disproportionately with low-grade feedstocks. Pure product translates into stronger publications, intellectual property gains, and faster scaling. Repeat customers often value supply partnerships over marginal price discounts, having learned that reliable performance pays off by minimizing downtime and eliminating repeat work.
Even suppliers who claim identical product names might not provide identical results; our own comparative trials and dissolution studies reveal changes in reaction profile driven by source. Consulting with remediation and manufacturing teams, we have isolated key points in our synthesis to secure a clean product: selected bipyridine lots, careful chloride dosing, minimized exposure to air during workup, and closed-system drying. Each adjustment over the years reflects lessons not from handbooks but from returned material and in-process complaints.
Industrial partners and regulatory-conscious researchers often ask about our waste minimization and safe handling steps. We upgraded procedures to capture nickel metal and ligand residues, tracking them with in-house elemental analysis. As nickel compounds raise environmental and health concerns if mishandled, close work with safety teams ensures full documentation and waste treatment. On request, we provide solvent-usage reports for green chemistry programs and label compliance. Material sent abroad follows international transportation guidelines, including full shipment logs and declared metal content.
Several customers told us about near-misses with damaged or leaking containers from other suppliers. To address these worries, we perform routine package drop-tests and secondary containment packing. This keeps hazardous exposure low in transit and simplifies unpacking at research sites. Our storage guidance also emphasizes low humidity and absence of competing halides, as these conditions best preserve the defined nickel-bipyridine structure. Safe chemical workflows include ample warnings, and we listen closely to feedback from EHS officers adapting our product to sensitive work environments.
In practice, R&D users often grapple with unexplained color drift, catalysis drop-off, and batch variation. Instead of scripted answers, we trace these to ligand aging, metal-ligand dissociation, or unsanctioned process substitutions. On occasion, we send technical staff to customer sites to verify lab conditions or review failed batch histories. Diagnosis sometimes means identifying humidity or pH excursions during a late-night workup, or catching a user mistaking hydrate for anhydrous forms.
A common workaround seen in competitor products—relying on “one size fits all” nickel complexes—rarely works when research pushes at frontiers. Our approach matches form to function, ensuring each gram contains the intended stoichiometry and coordination. Labs aiming for scale notice quickly if a material underdelivers; signals include higher byproduct rates and unstable yields. Hands-on troubleshooting, along with ongoing technical support, ensures that purchasing managers and bench chemists can expect more than a generic supply chain experience.
Research directions point toward greater automation, tighter analytical control, and more robust ligand-metal combinations. As sustainable synthesis advances, chemists call for lower energy input not only at the reactor, but during upstream chemical manufacture. We invested in cleaner purification cycles, reduced solvent use, and energy-efficient drying lines to meet these demands. The product, in its (SP-4-2) configuration, lends itself to these modern production methods, as its structure allows high-yield purification under mild conditions.
Researchers interest in continuous-flow and automated synthesis favor this complex for its solubility and handling characteristics. Pure, reproducible feedstocks remain vital in these advanced technologies. For battery and electronics researchers, longer-term cycling and stability matter more now than ever. As feedback loops from users reach our technical group, we adjust our formulas or packaging in response—never locking ourselves into obsolete practices.
There’s a visible shift in expectation. End-users, whether principal investigators or industrial R&D managers, want deeper product provenance, precise analytical backing, and, above all, honest partnership from producers. Direct feedback structures our batch review meetings. What we learn from the laboratory floor shapes the next update to our documentation and the physical processes inside our reactors.
From our daily work at the reactor, through hours in the analytical suite, to late calls with troubleshooting researchers, experience has taught us the value of the right nickel complex for the right problem. Novel bond formation, new materials, and precision catalysis all demand reliability and reach in every gram of product. Advanced synthesis depends on clearly characterized, stable compounds like Nickel,(2,2'-bipyridine-κN1,κN1')dichloro-,(SP-4-2)- delivered with transparency and technical depth.
Our compound supports chemists targeting new synthetic space, striving for repeatability and accelerating from small to larger scales. Serving this community means focusing on the details others skip: real-world purity, careful handling steps, verified batch data, and a willingness to learn from each purchase and application. Users who value experience-driven supply, coupled with openness to feedback, build lasting research progress, one reaction at a time.