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HS Code |
325099 |
| Iupac Name | 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine |
| Molecular Formula | C13H8F2IN3 |
| Molecular Weight | 371.13 g/mol |
| Appearance | Solid (expected, detailed form may vary) |
| Smiles | Fc1ccccc1CN2C(=N)C=C(F)C3=NC=NC23I |
| Inchi | InChI=1S/C13H8F2IN3/c14-9-4-2-1-3-8(9)7-19-11-5-10(15)12-13(18-11)16-6-17-12/h1-6H,7H2 |
As an accredited 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 1 gram of 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine, securely sealed and labeled. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine securely packed in drums, maximizing container capacity and safety. |
| Shipping | The chemical **5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine** is shipped in a tightly sealed container, labeled according to regulatory requirements. It is handled as a hazardous material, often shipped via priority courier with temperature control and protective packaging to prevent contamination or degradation during transit. Shipping complies with all chemical safety regulations. |
| Storage | Store **5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine** in a tightly sealed container, protected from light and moisture. Keep at 2–8°C in a cool, dry, well-ventilated area, separate from incompatible substances such as strong oxidizers. Clearly label the container, and handle under a fume hood with appropriate PPE. Avoid prolonged exposure to air. |
| Shelf Life | Shelf life: Store 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine at ≤4°C, protected from light and moisture; stable for 2 years. |
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Purity 98%: 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced byproduct formation. Melting point 172°C: 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine with a melting point of 172°C is used in solid formulation development, where it provides thermal stability during processing. Stability temperature up to 120°C: 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine stable up to 120°C is used in medicinal chemistry research, where it allows for robust reaction conditions without decomposition. Particle size < 10 µm: 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine with particle size less than 10 µm is used in advanced material science, where enhanced dissolution rates are achieved. Moisture content < 0.2%: 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine with moisture content below 0.2% is used in analytical standard preparation, where it maintains precision in quantitative measurements. |
Competitive 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine prices that fit your budget—flexible terms and customized quotes for every order.
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Each kilogram of 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine carries months of focused chemical work performed on the production floor, drawing on practical knowledge developed through dozens of trial runs and careful parameter optimization. We approach synthesis as craftspeople, always chasing higher yields, consistent particle properties, and superior impurity profiles. Beyond equipment and chemistries, people and repeatability matter. Day after day, our production team monitors every batch by sight, by sample, and through data, measuring subtle shifts before they can become issues. Delivering thousands of combined reactor-hours of experience, we understand that there’s only one acceptable batch: the one that meets both industry benchmarks and the standards we set for ourselves. Real quality rests on human judgment and technical depth at every step.
The dual halogenation—fluorine on the aromatic ring, iodine at the third position—distinguishes 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine from its simpler analogs. This combination delivers two strong handles for further manipulation. Fluorine’s presence stabilizes bioactive compounds, increasing metabolic resilience and shifting physicochemical behaviors. The iodine, meanwhile, allows for highly selective cross-coupling or arylation. This skeleton forms an adaptable platform for new molecules whether targeting pharmaceutical scaffolds, crop science leads, or advanced materials. Simply put, chemists value hybridized platforms such as this for offering both chemical flexibility and the ruggedness demanded by development programs.
We standardize this compound to a purity exceeding 98% (HPLC) because downstream users require precision. Our technical teams continuously refine filtration and crystallization sequences to secure consistent physical form and minimal residual solvents. This care in isolation translates to reduced screening cycles for clients developing new molecules. Moisture levels stay tightly controlled, delivering a product free from problematic aggregation or loss of reactivity. The analytical area—ranging from NMR and mass spectroscopy to trace element analysis—runs on well-established SOPs. By tracking minor impurities after every major process change, our teams minimize batch-to-batch variability, giving researchers greater confidence as they move from screening to scale-up phases.
We’ve worked in real plants and know the difference between specifications on paper and the challenges that surface in warehouses or when scaling up reactions. 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine behaves stably under cool, dry conditions, but we advise strict separation from strong oxidants and moisture ingress. Our containers—custom-selected for air- and light-tightness—support global shipments from kilolab up to multiton scale. Chemists appreciate this attention, as just a few hours of atmospheric exposure can trigger subtle degradation, especially impacting complex iodine-bearing heterocycles. We’ve housed every lot in our monitored storage facilities, logging environmental data and running routine reanalyses at scheduled intervals. If a new handling challenge arises in a client’s operation, our technical and logistics teams work together to troubleshoot, rather than leaving problems behind the shipping dock.
Looking across the array of pyrazolo[3,4-b]pyridine derivatives, patterns emerge: parent compounds tend to offer single-point functionalization, limiting exploratory SAR (structure activity relationship) modification in pharmaceuticals or materials research. Adding fluorine atoms at strategic positions, joined with an iodine substituent, opens doors for orthogonal transformations. Take, for example, the versatility a 3-iodo group unlocks in palladium catalysis—this moiety enables direct coupling with a vast selection of aryl, vinyl, or alkynyl species, creating hybrid systems without forcing harsh reaction conditions. In our experience, teams working with drug-like candidates typically turn to such multiple-handle platforms toward the later stages of hit-to-lead optimization, where customizing substituent ladders on aromatic frameworks influences properties like solubility, target selectivity, or environmental fate.
Unlike catalog traders who hand off product without context, we’ve run dozens of continuous production cycles on this molecule, each time logging reaction temperatures, solvent choice impacts, and washing efficacy. Early on, we saw variable batch color and unexplained NMR peaks, traced back to micro-variations in iodine source quality and slight differences in cooling rates. Our response was to implement real-time monitoring and a rigorous incoming material qualification plan, tools developed from time spent on the production floor amid other synthetic pyrazolopyridines. This compound presented filtration and drying challenges, leading our process engineers to collaborate directly with suppliers for improved micronization—reducing clumping during final isolation. Only the hard-won improvements from hands-on work ensure every lot behaves the same, not just in our reactors, but in the benchtop flask of a pharmaceutical or chemical discovery lab.
Researchers experimenting with rapid late-stage derivatizations, radiolabeling, or alkylation steps often confront hurdles tied directly to starting material quality. Over past years, we’ve fielded requests for variant specifications—tighter moisture limits, abnormal solubility characteristics—engineered to suit unique R&D processes. Our technical support doesn’t end at delivery; we welcome technical troubleshooting calls, provide background on observed process oddities, and sometimes even reformulate lots to help a client pass tricky purification stages. This partnership, direct from the manufacturing origin, counteracts the frustration of trace impurity-derived side reactions, saving countless hours at the synthesis bench.
Every customer pushing a new molecule forward expects more than a certificate of analysis. Drawing on regular results from advanced NMR, LC-MS, and elemental analysis, our QA/QC lab investigates anomalies, validates reproducibility, and archives data across years of batch results. For users developing regulatory submissions, reproducible data speed up the paperwork grind and avoid surprises during intermediates or API campaigns. Detailed tracking of trace elements, residual solvents, and even subtle polymorphic forms directly impacts the workability of this material within a complex synthesis or crystallization scheme. Rarely do third-party channels track down-the-line impacts of adapted processes or alternative synthetic routes. Our relationships grow not by pushing volume, but by maintaining data transparency and appreciating every variable that can spell the difference between a successful or failed scale-up.
Responsible chemistry shapes daily decisions. Halogenated intermediates require nuanced waste treatment, both to prevent environmental burden and to avoid costly downstream remediation. We’ve engineered on-site solvent recycling, batch segregation for halide-rich wastes, and partnered with certified handlers for byproduct management. Our sustainability group regularly audits reaction pathway alternatives—not just for process economics, but for long-term impact. For example, optimizing fluorinated raw material consumption not only trims cost but reduces shipping footprint and warehouse risks. Anyone who’s managed real chemistry understands these aren’t abstract goals; each kilogram responsibly made is a direct investment in maintaining future operating licenses and fostering trust with both local communities and oversight agencies.
Demands on intermediates continue to evolve. Ten years ago, a one-size-fits-all offering might suit varied research groups; today, customization—particle size, impurity cutoffs, process solvent choices—prove necessary. Custom-made lots, produced under stringent confidentiality, have increasingly become routine rather than exception. Our data-driven approach, maintained through extensive batch documentation, gives clients the leeway to specify and verify needs as their projects progress. The best results grow from candid, detail-rich dialogue with real manufacturing experts, not impersonal “product lines.”
Medicinal chemists and crop science innovators choose our 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine as a scaffold for building blocks because it fast-tracks the path from concept to small batch pilot. Addition of the fluorine shifts metabolic breakdown in drug candidates, often extending half-lives or tuning receptor profiles. Material scientists pursue high-performance heterocycles for electronic, luminescent, or photonic research, recognizing the stability and reactivity keyed by this skeleton. In many projects, the margin between success and costly revision narrows to the smallest impurity level or the consistency of a halide substituent. By watching real feedback loops from both R&D and plant environments, we streamline synthesis for real-world application, rather than chasing textbook metrics alone.
Improvement didn’t come overnight. Early production attempts highlighted the tendency for incomplete halogen exchange, leading to downstream purification challenges and loss of yield. The solution came from reengineering agitation and temperature staging, tuning reaction kinetics so costly starting materials ended up where they belonged: in the product drum. Maintaining this process advantage required close cooperation across synthesis, purification, and auxiliary teams. Years of managing similar heteroaromatic families equipped every shift operator and technical specialist to predict difficulties—seasonal humidity swings, container failures, and even unplanned plant outages—before trouble could escalate. Today’s process embodies those learnings, achieving not only strong technical results but a predictably safe operating window as well.
For every compound we manufacture at this complexity level, regulatory compliance, worker safety, and comprehensive documentation become core priorities. Regular process hazard reviews are second nature. Engineers walk production lines to review every step for both known and as-yet-unseen risks. Internal auditors compare every drum shipped with archival records, confirming traceability and legal alignment. Our reporting system draws on both industry best practices and lessons learned from the rare instances where documentation once lagged behind actual process improvements. In regulated markets, these habits shorten timelines and reduce the headaches that can accompany unexpected audits or global customs inquiries.
Sourcing reliable, high-quality iodine and fluorinated precursors created unanticipated bottlenecks during the past few years of global supply chain volatility. Rather than chase lowest bids, we built tight partnerships with upstream manufacturers, sometimes taking on inventory to buffer supply chain shocks. On-site, we created real-time adaptation plans—swapping out certain non-critical reagents, lengthening campaign schedules, or running alternative process steps as needed. By keeping direct lines open with both suppliers and downstream partners, we maneuvered around shipment delays and price surges while always putting consistent quality at the center. Flexibility earned on the plant floor still proves the best antidote to supply disruption.
A well-made intermediate can tip the balance in R&D toward creative risk-taking. By anchoring research teams with predictable, high-purity 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine, we see teams delve deeper into lead optimization, conjugation strategies, and metabolic tuning. Some customers in biopharma pressed us to adapt packaging and logistics for rapid screening runs; others wanted extended support troubleshooting new catalytic couplings. We treat every order as the start of a project collaboration, bringing chemical manufacturing out from behind the curtain and into open technical dialogue. Our practical, technical background in bringing this molecule from laboratory concept to scalable reality helps research teams conserve time and resources—whether their end goal sits in the clinic or the marketplace.
Real manufacturing advantage stems from continuous investment in process analytics, skilled people, and transparent operations. Every generation of chemists asking us for 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine finds new questions—and in turn, challenges us to improve or adapt. We welcome that push, knowing each request brings more insight on formulation practices, reaction schemes, and reliability thresholds. Our future projects are already taking shape based on the practical experience, cumulative feedback, and technical wisdom born from making this compound part of scientists’ toolkits worldwide. Experience teaches that the right technology, handled by the right team, unlocks not only better chemical output but a stronger foundation for any ambitious project.