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HS Code |
759361 |
| Iupac Name | 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine |
| Molecular Formula | C30H39N3 |
| Molecular Weight | 441.65 g/mol |
| Cas Number | 124729-97-3 |
| Appearance | White to off-white solid |
| Melting Point | 123-126 °C |
| Solubility | Soluble in organic solvents (e.g., chloroform, dichloromethane) |
| Smiles | CC(C)(C)c1cc(nc(c1)c2cccc(n2)c3cccc(n3)c4cc(ccn4)C(C)(C)C)C(C)(C)C |
| Inchi | InChI=1S/C30H39N3/c1-30(2,3)25-16-28(19-26(17-25)32-22-10-7-13-34-28)27-18-29(20-23(31-27)21-24(27)31)33-14-8-11-35-29/h7-8,10-11,13-14,16-21H,9,12,15H2,1-6H3 |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at 2-8 °C, protected from light |
| Usage | Ligand in coordination chemistry and catalysis |
| Density | 1.12 g/cm³ (estimated) |
As an accredited 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5-gram amber glass bottle, tightly sealed with a screw cap, and labeled for laboratory use. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** Holds approximately 5–7 metric tons, packed in 25 kg fiber drums, safely secured for international shipping of this chemical. |
| Shipping | **Shipping Description:** 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine should be shipped in a tightly sealed container under ambient temperature, protected from light and moisture. Ensure compliance with all local, national, and international chemical transport regulations. Handle with appropriate personal protective equipment. Not classified as hazardous for transport under most guidelines (verify with current SDS). |
| Storage | **Storage:** Store 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine in a tightly sealed container under inert atmosphere (nitrogen or argon) and keep it in a cool, dry place, away from direct light and moisture. Avoid exposure to strong oxidizing agents. Store at ambient or lower temperatures, following manufacturer’s recommendations, and ensure proper labeling to avoid contamination or degradation. |
| Shelf Life | Shelf life of 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine is typically two years when stored cool, dry, and protected from light. |
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Purity 98%: 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine with Purity 98% is used in homogeneous catalysis, where high purity ensures consistent catalytic performance and reproducible yield. Molecular Weight 432.65 g/mol: 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine with Molecular Weight 432.65 g/mol is utilized in coordination complex synthesis, where precise stoichiometry enables optimal ligand-to-metal binding ratios. Melting Point 155°C: 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine with Melting Point 155°C is applied in thermally robust polymer formulations, where high melting point improves thermal stability of the final product. Particle Size <50 µm: 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine with Particle Size <50 µm is used in inkjet ink formulations, where fine particle size enhances dispersion and prevents nozzle clogging. Stability Temperature up to 200°C: 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine with Stability Temperature up to 200°C is used in electrochemical sensor design, where elevated stability ensures long-term sensor durability and accuracy. Solubility in Acetonitrile >50 mg/mL: 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine with Solubility in Acetonitrile >50 mg/mL is utilized in transition metal complex preparation, where high solubility ensures uniform ligand incorporation. |
Competitive 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch of 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine we synthesize goes through the hard-earned process improvements and quality controls that only come from repeated hands-on manufacturing. Over years in production, we’ve learned that the needs of researchers and industrial partners don’t rest on paper specs, but rely on reliability and consistency in lab and pilot plant results. Our experience tells us technical performance in ligands can influence both the direction of R&D and the feasibility of scale-up in coordination chemistry, catalysis, and material science.
The model we’ve established for this compound brings forward a careful synthesis route developed from thousands of real-world scale reactions. Our standard offering delivers 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine at a high assay, sustained by advanced purification methods that eliminate trace impurities affecting complex formation and reactivity. From our perspective, batch consistency doesn’t stem from a catalog promise. It shows up in the trace metal tests, in the NMR and HPLC traces, and in the way crystals form under the microscope.
This tritert-butyl functionalized terpyridine sets itself apart with enhanced steric hindrance at the 4,4',4'' positions. The structural bulk influences the electron-donating character and coordination geometry in metal–ligand assemblies. This feature, in our experience, enables selectivity and performance in fine-tuned homogeneous catalysts, OLED emitter prototypes, and functional supramolecular architectures.
We supply this terpyridine directly to hands-on chemists whose priorities evolve with shifting application demands. Batch feedback from academic laboratories and industrial R&D teams has shown that our controlled process preserves the t-butyl substitution without side products. We use reagents and solvents that meet high-purity standards, and when challenges arise—such as problems with ligand stability or trace contamination—our production teams troubleshoot directly at the reactor, not through remote troubleshooting.
Even a small deviation in the t-butyl group’s placement or a minor impurity can impact self-assembly, coordination stability, or photophysical results. We have spent years identifying and correcting such issues, such as adjusting the work-up to avoid residual halide or refining our solid-phase drying to limit peroxide formation. This approach exceeds what generalized distribution channels can provide because our product testing aligns with the exacting standards of coordination chemists who look beyond a simple CAS number.
We see our 4,4',4''-Tris(2-methyl-2-propanyl)-2,2':6',2''-terpyridine as a toolkit component for synthetic and applied chemists, not just a line in a catalog. We monitor customer feedback on crystallization behavior, metal binding, and even the way the compound dissolves under routine conditions. These fine points influence success in creating iridium, ruthenium, and lanthanide complexes that serve as functional materials and catalysts.
Some researchers turn to this ligand for sterically-protected coordination spheres, aiming for improved selectivity or photostability. Others use it as a leverage for creating large supramolecular assemblies where less protected terpyridines tend to lead to competing side reactions or aggregation. Over time, real-world reports inform our ongoing process improvements and QC benchmarks.
In the layered world of terpyridines, not all derivatives function interchangeably. This particular molecule provides a unique mix of electronic and steric effects. It stands apart from unsubstituted analogs by reducing unwanted side coordination and aggregation issues. Compared with other alkyl-substituted terpyridines, the t-butyl groups in our product confer both increased solubility in organic solvents and strong resistance toward oxidation during catalysis—a critical feature for researchers facing air- or moisture-sensitive synthetic challenges.
Compounds with fewer or smaller substituents often yield reduced selectivity for specific coordination geometries, leading to mixtures or less stable complexes. Our customers have demonstrated that using this tritert-butyl-functionalized ligand, they can drive reactions toward mononuclear over polynuclear species, essential in high-value catalyst applications. The result in the real world has been cleaner NMR spectra, higher isolated yields, and simpler product purification.
From the manufacturer’s bench, we recognize that product differences manifest not in advertising, but in application. For example, university teams using this ligand as an acceptor for metallosupramolecular assembly report sharper, more reproducible results. In the OLED field, its bulky tert-butyl substituents minimize non-radiative decay by preventing unwanted π–π stacking and aggregation, translating to higher luminescence and greater material stability.
These empirical successes come from direct application, not conjecture. Process scalability also improves because tert-butyl protection guards the core terpyridine ring against undesired side reactions during metal complex formation. As a result, the product simplifies reaction workups, reduces side product formation, and extends the operational window for sensitive transitions.
Terpyridines serve as workhorse ligands, and modifications often build an edge into chemists’ projects. Our clients who compare the tritert-butyl group ligand with standard unsubstituted terpyridines notice distinct operational benefits. The lack of reactivity at the 4,4',4'' positions blocks pathway to side products where other ligands fail. It also means the same ligand performs robustly in both small- and larger-scale syntheses.
One major divergence lies in solubility in polar and non-polar media. Researchers synthesizing metal complexes on gram or kilogram scale appreciate that tritert-butyl groups impart easier phase separation, minimize emulsions during extractions, and lower tendency for oily by-product formation. In our observations, this directly affects throughput and labor costs at the plant floor, reducing the number of washes needed for isolation and bringing consistency to recrystallization or precipitation.
Maintaining consistency across lots—batch-to-batch and gram-to-kilogram—relies on direct process oversight. We exhaustively map out each variable that could drift over time. Our workers measure particle size distribution, monitor the color evolution in each batch, and log deviations in intermediate purity after every step. When unexpected behavior crops up, such as slower crystallization or off-color solutions, our workflow allows us to adjust conditions on the fly.
Every customer report, even remarks about odor or how powders settle during shipping, informs incremental improvements. This is a street-level reality for manufacturers—minute issues eventually amplify mismatches between lab and scale. We integrate direct feedback channels, so those using our ligand in critical applications play a key role in future process upgrades.
As a direct manufacturer, our main concern after quality centers on sustained supply. We maintain multi-reaction lines for the terpyridine core, and we pre-stock necessary precursors on-site after vetting each supplier batch for contaminants and post-synthetic modifications. Redundancy safeguards against unexpected raw material shortages or delays; our production network stays lean by forecasting downstream demand fluctuations. Efforts focus both on raw input consolidation and on owning every synthesis step internally.
Our warehouse and process scheduling revolve around real-time communication between floor teams and logistics engineers. Rather than spinning up a reaction on a speculative order, we confirm shelf availability and shipping lead time daily. Any client forecasting a large project or a multi-phase synthesis gets our advance notice and honest timeline, not just a standard “available” flag on a digital platform.
The handling and storage of this ligand present practical challenges that become evident as quantities increase. Tert-butyl substituents protect against some forms of oxidative degradation, extending shelf life, but strict exclusion of light and atmospheric moisture further prolong stability, especially for customers who stock this product for months instead of weeks. Our packaging methods use inert nitrogen blanketing and moisture-impermeable liners, and each package size—from small sample vials to industrial drums—receives stability testing to confirm no cross-contamination or decomposition over time.
Production teams integrate these safeguards not from theoretical protocols, but because returned lots and customer-reported issues over the years have shown the pitfalls of cut corners in packaging. Technicians spot-check fill weight, monitor closure integrity, and update quality logs to track product movement from synthesis line through final sealing.
Sustainable chemistry comes from practical improvements on the factory floor. Our process, refined for this ligand, cuts down excess solvent consumption through aggressive recycling and distillation controls. Spent acids and bases from the t-butylation steps go through closed-loop neutralization and filtration before disposal. When we mapped out emissions and waste flow, we noticed opportunities to reclaim solvent at every step, which had knock-on effects in both cost savings and reduction in total site emissions.
Our research group collaborates with users to determine the lowest feasible impurity profile, allowing for easier downstream purification in client operations. This cuts secondary waste—spent silica, contaminated water, used cartridges—from the overall application process. It isn’t a perfect system, but our experience indicates that these small cumulative changes drive down total environmental footprint.
Industry standards evolve, especially across different continents. From our location, we’ve learned the hard way what constitutes a “clean” batch for regulatory submissions, both in academic research and industrial filings. Large end-users often require documentation packages that describe not only the synthetic route but also the rigorous analytical support behind every lot—NMR, LC-MS, IR, and elemental analysis. We maintain full data records for every batch, accessible for client audits or regulatory reviews, and comply with requirements as they increase or shift.
Comprehensive traceability isn’t just a paperwork exercise for us. When downstream users submit grant reports or patent filings, supporting purity and origin documentation strengthens both their outcomes and our client relationships. In our daily work, we approach these records as essential extensions of hands-on manufacturing, not as bureaucratic overhead.
The experience gained from dozens of industrial projects drives improvements in reproducibility and cost. Early on, unreliable t-butylation led to batch impurities. We faced challenges with exothermicity in scale-up, which prompted special reactor cooling cycles and staged reagent addition. Later, we encountered unexpected difficulties with purification, which prompted custom column packing and real-time fraction collection. These lessons converted into precise process controls we apply in every run.
The market for tritert-butyl terpyridine isn’t static. New user applications, including in photoredox catalysis and responsive polymers, feed back into our development pipeline. As custom ligand requests arise, we adapt by testing modified synthetic routes or purification options, aiming to retain the reliability that defines our core product line. Those who repeatedly use our material for sensitive or regulatory-driven synthesis have influenced the grading standards and characterization work we perform daily.
Our years spent manufacturing this terpyridine derivative have shown us the real-world meaning of quality and process control. Consistency comes not just from a finished powder or crystalline product, but from every line operator, every scientist at the QC bench, and from the skilled feedback of hundreds of end-users. We see the process as a living workflow, refined by each batch and project requirement.
Chemists come to us for reliability—a quality rooted in repetitive cycles of testing, feedback, and practical adjustment. Whether users deploy our ligand in large-scale catalyst builds, high-throughput screens, or fundamental coordination chemistry, they benefit from process transparency, detailed analytics, and open communication lines. Every challenge raised, every report of a sticky purification or a change in reactivity, feeds back into our system.
Our confidence in this product does not rest on catalog blurb or marketing lingo. It’s woven into the years of cumulative manufacturing trial, customer transparency, and small gains that come from listening to the real working world of scientific researchers. That, more than any synthetic route or technical data point, shapes why we believe this ligand stands apart.