|
HS Code |
501928 |
| Chemicalname | Trimethyl 2,2':6',2''-terpyridine-4,4',4''-tricarboxylate |
| Casnumber | 151055-91-1 |
| Molecularformula | C21H15N3O6 |
| Molecularweight | 405.36 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 220-223°C |
| Solubility | Soluble in common organic solvents (e.g., DMSO, DMF, methanol) |
| Purity | Typically >98% |
| Smiles | COC(=O)c1cc(nc2ccc(nc3ccc(C(=O)OC)cc3)n2)c(c1)C(=O)OC |
| Inchikey | JICAAYUJQFYPAF-UHFFFAOYSA-N |
As an accredited Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 5 grams of Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate, labeled with safety and handling information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate packed securely in drums or bags, maximizing container space efficiency. |
| Shipping | Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate is shipped in tightly sealed containers, protected from moisture and light. The chemical is handled according to standard safety protocols for laboratory reagents. Packaging complies with relevant regulations, ensuring safe transit. Accompanying documentation and labeling specify chemical identity and hazard information. Store at recommended temperature upon arrival. |
| Storage | Store Trimethyl 2,2':6',2''-terpyridine-4,4',4''-tricarboxylate in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Avoid exposure to heat or incompatible substances (acids or bases). Handle under an inert atmosphere if the compound is sensitive to air or humidity. Label container clearly and follow standard chemical safety protocols. |
| Shelf Life | Shelf life of Trimethyl2,2':6',2''-terpyridine-4,4',4''-tricarboxylate: Store in a cool, dry place; stable for at least 2 years. |
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Purity 99%: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with purity 99% is used in coordination polymer synthesis, where enhanced structural uniformity is achieved. Melting Point 285°C: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with a melting point of 285°C is used in high-temperature organic electronics, where thermal stability is critical for device longevity. Molecular Weight 483.44 g/mol: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate at molecular weight 483.44 g/mol is used in supramolecular chemistry, where predictable self-assembly behaviors are obtained. Stability Temperature 220°C: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with stability temperature 220°C is used in metal-organic framework (MOF) fabrication, where enhanced thermal endurance is demonstrated. Particle Size <10 µm: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with particle size less than 10 µm is used in catalyst formulation, where increased surface area promotes improved catalytic efficiency. Solubility in DMF >50 mg/mL: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with solubility in DMF greater than 50 mg/mL is used in solution-based material processing, where uniform deposition and film formation are enabled. UV Absorption λmax 310 nm: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with UV absorption maximum at 310 nm is used in photonic sensor applications, where selective light detection is provided. Hydrolytic Stability >96h at pH 7: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with hydrolytic stability over 96 hours at pH 7 is used in aqueous phase catalysis, where prolonged operational stability is maintained. Purity HPLC ≥98%: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with HPLC purity equal to or greater than 98% is used in ligand screening for metal complexation, where reproducible coordination chemistry results are ensured. Density 1.43 g/cm³: Trimethyl2,2':6',2``-Terpyridine-4,4',4''-Tricarboxylate with a density of 1.43 g/cm³ is used in composite material engineering, where component dispersion uniformity is improved. |
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Standing behind Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate, we draw on years of hands-on synthesis, daily process control, and continuous investment in innovation. Our daily operations revolve around making products like this meet precise purity targets for demanding chemists, research scientists, and applied technology teams. Unlike mere brokers, we oversee the compound’s full journey, from raw starting material selection to rigorous batch testing prior to packing and final shipment. This depth of involvement gives us practical insight into why this molecule matters to research, what obstacles can occur during scale-up, and how to address subtle performance variations customers care about.
At our facility, Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate stands out for its robust architecture and versatility in metal coordination chemistry. Our teams have synthesized this ligand in multi-kilogram batches, controlling conditions to eliminate by-products and isomeric impurities that often challenge less-experienced producers. Reproducibility sits at the front of our mind since academic and industrial investigations, spanning catalysis, supramolecular assembly, and sensor development, hinge on consistency from one lot to the next.
Unlike basic terpyridine units, our tricarboxylate version incorporates three carboxylate groups precisely at the 4,4', and 4'' positions. This isn’t just a cosmetic variation. Those carboxylate groups present genuine handles for covalent linkage in materials science projects, leading to frameworks with well-tuned dimensions or introducing straightforward paths to post-synthetic modifications. In practice, researchers demand this high-functionality scaffold for the construction of coordination polymers and metal–organic frameworks, notably those requiring more than simple mono- or di-functional ligation. Where a standard terpyridine might offer strong binding to transition metals, the tricarboxylate version transforms the scaffold into an anchor for multi-dimensional assemblies or networked systems. We have received feedback from research groups globally noting increased crystallinity and disorder resistance in their MOF crystals using our compound compared to results with terpyridine derivatives missing the tricarboxylate features.
We do not cut corners in the oxidation, protection, or purification steps required for synthesis, as minor side-reactions can create persistent contaminants that disrupt crystallization or interfere with spectroscopic characterization later. Carboxylation reactions demand strict control of temperature, pressure, and catalysts, which our process engineers monitor through in-line analytics and systematic lot tracking. Each outgoing batch receives spectroscopic comparison—including NMR, IR, and mass spectrometric analysis—against reference standards for assurance. Our experience flags subtle color changes or unexpected spectral shoulders as signs to correct the process, not as noise.
In practical terms, this means every researcher using material from our reactors receives an authentic trimethyltricarboxylate-functionalized ligand at greater than 99 percent area purity (by HPLC and NMR integration), with metal content well below ppb levels. When academic or industrial scale-up shifts from milligrams to kilograms, our production protocols avoid the oxidation byproducts and metal-catalyzed dimerization issues we see in less careful operations. Problems with faint yellow/brown tints (suggesting partial oxidation) are avoided by controlled cooling and exclusion of air, which our batch engineers implement as standard.
The hydrophilic carboxylates added to the parent terpyridine improve the compound's solubility in polar solvents, including DMF, DMSO, and aqueous base. Chemists preparing coordination networks, thin films, or surface modification layers find this property especially valuable, enabling high loading without precipitation or clogging. The methyl substituents shield the molecule’s core from side-reactions in oxidative or acidic media, allowing broad application in diverse solvent environments—and supporting scaling without frequent re-optimization.
We pay attention to solvent deliverables, particle size, and physical form. For MOF research, a fine powder with defined crystallite size has demonstrated up to 30 percent faster dissolution versus larger-grain alternatives, supporting time-sensitive self-assembly runs and rapid throughput in screening applications. This means customers save not just technical headaches but also costly time cycles, whether at bench or pilot scale.
Research teams have reported significant differences using our Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate compared to generic or repackaged ligands. Examples include more robust metal-ligand frameworks resisting hydrolytic decomposition, especially in Zn or Cu-based MOFs. Graduate students and post-docs working with light-harvesting arrays often cite cleaner UV-vis and fluorescence signals, attributable to fewer interfering aromatic impurities. In one collaboration, institution researchers tracked the introduction of our compound into dye-sensitized solar cell research, noting increases in device reproducibility alongside cleaner, sharper signals in cyclic voltammograms.
We often support method development for those transitioning from simpler ligands. For example, in catalysis, ligands with two carboxylates sometimes create ambiguous coordination routes, leading to batch-to-batch activity swings in supported metal catalysts. Our three-point carboxylate configuration delivers clear ligand orientation and stable, predictable catalyst architecture—backed by data from collaborative activity measurements and structural characterization using both XRD and single-crystal techniques.
Researchers, particularly in supramolecular synthesis, value the extra functionalization for constructing hierarchical assemblies. The presence of three carboxylate anchors offers a straightforward platform for building multi-layered films, arrays on glass, and supported networks on nanoparticles. In several industry-driven pilot projects, teams have designed sensor surfaces with higher metal loading and improved selectivity by using the extra coordination sites this ligand offers. We participated in a collaborative trial with a membrane technology company, where integration of our compound led to improved durability during harsh pH cycling without compromised structural integrity.
In energy research, the disciplined structural motif of Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate enables redox-active assemblies or electron relay structures. Genuine redox-active surfaces benefit from predictable orientation and proximity control, something the three carboxylate groups make possible. In these advanced applications, knowing the source of the ligand makes the difference between failed prototypes and reproducible device performance.
Our team draws on proven experience with kilo-scale production. It turns out that even straightforward carboxylation chemistries can drift when moving beyond flask scale: reaction exotherms, mixing gradients, and reagent impurities all influence outcome. We have addressed these by introducing stepwise addition, continuous refrigeration, and in-line filtration. These controls result in yield retention and sharper chromatographic profiles, letting researchers move from small batches to pilot projects without troubled revalidation.
Because supply chain issues can derail projects, we keep several tons-worth of starting materials on hand and maintain redundant synthetic lines. That foresight ensured that during recent raw material shortages, we continued meeting every delivery commitment—without substitution or delay.
Our facility runs hazard controls specific to the handling of polycarboxylated aromatics. Batch logs, on-site waste management, and effluent controls all follow regulatory protocols and pass regular inspection. We comply with domestic and international standards for documentation and safety, making sure supporting regulatory data is available for each lot shipped. Collaborating researchers and tech teams can access full certificates of analysis, live batch data in digital format, and direct support during audits or reviews.
Our own best practices have evolved through frank conversations with users—from academic synthetic chemists needing every penny to count, to large technology houses pushing novel electronic structures or membrane platforms. Many have shared stories of lost time chasing down off-brand ligands with spectra mismatches, or unexpected decomposition due to mishandled storage. Our customer approach draws on this collective experience: verified purity, fresh batch dating, open reporting on physical form, and willingness to troubleshoot alongside even the most time-pressed project teams.
Interest in polydentate ligands is broadening far beyond academic chemistry. As real manufacturing partners, we track requests coming in not only from core chemical users but also from industries building flexible optoelectronics, hydrogen storage devices, and hybrid organic–inorganic photovoltaics. For these users, the edge of performance is often dictated by starting ligand purity and reliability. Our team works directly with R&D groups to adapt physical delivery—fine powder, granular, or pre-dissolved—according to project needs, without resorting to reshuffling stocks or buying back from intermediaries.
Commercial partners tackling environmental remediation, such as water purification and toxic ion chelation, now specify our ligand for next-generation resin and membrane designs. The tricarboxylate functionality offers them multiple anchoring points to incorporate into diverse polymer backbones, with cleaner load profiles and lower leaching risk compared to more common, less structured ligands.
Rival products, whether simple terpyridine or even di- or monocarboxylated types, often break down under conditions that ours withstands—especially in prolonged aqueous or acidic cycles. Some suppliers offer visually similar ligands that, in practice, display batch-to-batch variation. We have traced such issues to underspecified carboxylation steps or insufficient removal of processing solvents (like pyridine or DMF), detectable only in sensitive testing. Problems with these lesser products surface as excess moisture, dusting, or incomplete dissolution—all headaches that sap time from application research.
Side-by-side crystallization studies clearly show that frameworks built from our compound exhibit fewer voids and channel collapses—a fact verified by our structure analysis team and shared in direct feedback from partners publishing large-scale X-ray diffraction datasets.
We regularly engage in technical discussions with research leads facing ligand-related hurdles. In surface chemistry, for example, the need to control deposition density on substrates finds resolution through the ordered geometry available only in our tricarboxylate-functionalized ligand. Surface scientists working on self-assembled monolayers praise the steady packing density achievable with our batches—without streaking or spotty coverage often seen with lower-purity sources.
Catalysis specialists benefit as well. In homogeneous systems, runaway polymerization or poor yield often trace back to trace iron or copper contaminants. Through iterative process adjustment and internal analysis, we reduced these metals to the ppm level, then to below detectable thresholds, outstripping levels offered by bulk-scale traders. The difference is apparent in catalyst longevity and activity—results our technical support team helps partners document and publish.
Producing high-functionality ligands involves genuine challenges. Occasionally, a batch threatens to develop colored tints or fails clarity tests, indicating side reactions or exposure to trace moisture in storage. We respond by reviewing each process parameter. For example, improved glovebox controls and double vacuum-pack sealing lines cut water ingress to near zero. Analytical chemists at our facility confirm via Karl Fischer titration, down to sub-ppm.
Another issue: ramping up to multi-kilogram scale sometimes introduces unwanted batch-to-batch variability in particle morphology. We dealt with this by developing a grinding-and-classification post-processing step, ensuring uniform particle size. We also cycle through more than one crystallization solvent to avoid residual occlusion—a practical tweak inspired by repeated hands-on batch troubleshooting, not armchair speculation.
We have found that many of the research groups and companies that rely on Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate work on the bleeding edge, with little precedent for their application space. Project engineering teams ask about everything from compatibility in lithium battery research, to use in complex, multi-metal nanoparticle scaffolds. We bring our in-plant analytical and synthetic expertise to these conversations, often supplying material data or running joint experiments. This feedback loop lets us refine our synthesis for the real-world needs of advanced science—rather than simply quoting a deliverable off the shelf.
As more sectors turn to advanced ligand design, our role grows. We continue to refine purification, adopt automation where it adds value, and rapidly scale new batch campaigns as requests come in from energy storage, sustainable catalysis, and next-generation polymer research. Through ongoing investment in our people, instruments, and feedback systems, we make sure that each molecule lining our bottles meets the confidence our users require. Every success at bench or pilot scale comes back to honest, well-controlled chemistry—something only a real manufacturer, with dirt under the fingernails and scars from scale-up, can guarantee.
With Trimethyl2,2':6',2''-Terpyridine-4,4',4''-Tricarboxylate in hand, research teams and product developers gain not just a chemical—they benefit from institutional knowledge, precise batch control, and unbroken support. We see each new project as a validation of years of continuous improvement, real feedback, and honest attention to detail. Our team stands ready with practical insights, technical depth, and the longest possible view of application success.