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HS Code |
918046 |
| Iupac Name | 6-chloro-1H-pyrazolo[3,4-b]pyridine |
| Cas Number | 37143-73-8 |
| Molecular Formula | C6H4ClN3 |
| Molecular Weight | 153.57 |
| Melting Point | 218-222°C |
| Appearance | Off-white to light yellow powder |
| Solubility | Slightly soluble in water |
| Smiles | Clc1ccc2n[nH]cc2n1 |
| Inchi | InChI=1S/C6H4ClN3/c7-4-1-2-5-6(10-4)8-3-9-5/h1-3H,(H,8,9,10) |
| Pubchem Cid | 2829805 |
As an accredited 1H-pyrazolo[3,4-b]pyridine, 6-chloro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package features a sealed, amber glass bottle, labeled with hazard symbols, reagent details, and clear "1H-pyrazolo[3,4-b]pyridine, 6-chloro-" identification. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 1H-pyrazolo[3,4-b]pyridine, 6-chloro- involves secure, bulk packing and safe transport in a 20-foot container. |
| Shipping | The chemical 1H-pyrazolo[3,4-b]pyridine, 6-chloro- is shipped in tightly sealed, chemical-resistant containers with clear labeling. It is transported under ambient or specified temperature, adhering to relevant safety and regulatory guidelines. Shipping documentation includes hazard information, and handling is performed by trained personnel to prevent leaks, spills, or exposure. |
| Storage | 1H-pyrazolo[3,4-b]pyridine, 6-chloro- should be stored in a tightly sealed container at room temperature, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep away from heat, sparks, and incompatible substances such as strong oxidizing agents. Properly label the storage container and use appropriate personal protective equipment (PPE) when handling. |
| Shelf Life | 1H-pyrazolo[3,4-b]pyridine, 6-chloro- typically has a shelf life of 2–3 years when stored in a cool, dry place. |
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Purity 98%: 1H-pyrazolo[3,4-b]pyridine, 6-chloro- with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal yield and minimal by-product formation. Molecular weight 167.56 g/mol: 1H-pyrazolo[3,4-b]pyridine, 6-chloro- with molecular weight 167.56 g/mol is used in medicinal chemistry research, where accurate molecular sizing allows precise dose calculations in drug formulation. Melting point 172°C: 1H-pyrazolo[3,4-b]pyridine, 6-chloro- with melting point 172°C is used in solid-state formulation studies, where thermal stability enhances compound integrity during processing. Particle size <10 μm: 1H-pyrazolo[3,4-b]pyridine, 6-chloro- with particle size <10 μm is used in high-performance chromatography, where fine particle distribution improves resolution and analytical accuracy. Stability temperature up to 150°C: 1H-pyrazolo[3,4-b]pyridine, 6-chloro- with stability temperature up to 150°C is used in high-temperature reaction screening, where sustained stability prevents degradation during thermal processing. Water solubility <0.1 mg/mL: 1H-pyrazolo[3,4-b]pyridine, 6-chloro- with water solubility <0.1 mg/mL is used in hydrophobic drug screening, where low solubility supports targeted delivery system development. |
Competitive 1H-pyrazolo[3,4-b]pyridine, 6-chloro- prices that fit your budget—flexible terms and customized quotes for every order.
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Decades in the fine chemical sector have taught us that nothing slows research and development like unreliable intermediates. So, we set out to support labs and production teams that can't afford unnecessary downtime by refining our approach to synthesizing 1H-pyrazolo[3,4-b]pyridine, 6-chloro-. Before this product joined our catalog, orders for similar heterocyclic compounds always came with a list of frustrations from our partners: unstable moisture profiles, inconsistent purity, lack of process transparency, or batch-to-batch drift. Chemists grow tired of repeated troubleshooting because their building block doesn't perform the same way twice. At our plant, we decided it's more useful to put rigorous, hands-on control at the center of every step—purity, crystal form, particle load, and dry handling. Process improvement isn’t abstract to us: it’s a hands-dirty business involving solvent recovery runs, recrystallization trials, and endless analytics panels. Instead of relying on contract blending, we rebuilt key segments of the synthesis workflow. Many nights were spent optimizing isolation, switching up halogen sources, and tuning purification to handle the sensitivities of the pyrazolopyridine core.
1H-pyrazolo[3,4-b]pyridine, 6-chloro- carries a unique signature that stands out in any catalog of fused heterocycles. At the atomic level, the structure integrates both pyrazole and pyridine rings with a strategically placed chlorine, causing distinct reactivity in further syntheses. Our chemists appreciate the tight arrangement of nitrogen atoms, which brings versatility in building broader libraries for pharma, agrochemical, and specialty materials development.
Over the years, our R&D team received requests to modify substitutions or introduce halogen variation into fused-ring systems, aiming to push biological activity profiles or modify solubility. Through our own testing and upstream research partnerships, we’ve seen 6-chloro- substitution emerge repeatedly as a robust scaffold for kinase inhibitor research, crop protection agents, and diagnostic probe development. Scientists appreciate both the electronic effects chlorine brings to the core and the options for selective transformations downstream. We keep purity thresholds high—routine QCs confirm levels at or above the area percent standard trusted in GMP-targeted work. Whether a client scales to kilogram lots or requests pilot grams, we maintain clear traceability and stability checks to avoid hiccups under scale-up or during analytical characterization.
It can be tempting to focus just on chemical reactivity when assessing a compound, but actual bench performance depends on every upstream variable. Chromatography and melting point may serve as quick diagnostics, yet the true test comes after repeated synthetic cycles—where impurities accumulate, filtration slows, or color drifts. With 1H-pyrazolo[3,4-b]pyridine, 6-chloro-, our QC technicians dig deep to screen not only for the main product, but also track regional impurities like hydrolyzed side-products, over-halogenated variants, or trace solvents. In early production, we saw how small lapses in process water management or workup speed caused material to fail HPLC. Instead of writing off these losses, we invested in in-line monitoring and automated drying logistics, refining both the process and the culture around reliability.
Feedback from pharmaceutical partners underscored the need for lot-to-lot reproducibility. Time is money, and neither major nor minor batch shifts go unnoticed in a regulatory environment. We have integrated batch record systems and periodic stability monitoring, avoiding sudden downgrades or out-of-spec deliverables. Clients with shelf-lifetime concerns find it useful that our compound resists hydrolysis and remains chemically inert during regular storage, provided basic precautions for moisture and light are followed. This gives them more flexibility to aliquot, store, and dose as their own workflow demands.
Most inquiries about 1H-pyrazolo[3,4-b]pyridine, 6-chloro- come from research groups, medicinal chemists, or specialty chemicals developers working on tight timelines. Researchers in pharma use it as a core fragment for kinase inhibitor synthesis. The halogen’s position gives selective handle for further functionalizations, whether by Suzuki cross-coupling, nucleophilic aromatic substitution, or radical addition. Over the last few years, requests have risen from agrochemical labs seeking to expand biological screens for pest resistance and environmental safety. We track conversations with our collaborators, and keep our technical team available for troubleshooting any challenge: unexpected behaviors in pilot reactions, compatibility with bespoke reagents, or ampule preparation for particularly moisture-sensitive procedures.
Academic customers sometimes seek advice about handling or analytical techniques. We share best practices learned inside our own facility. For instance, we recommend setting aside a dry-room bench for portioning the compound to avoid unnecessary hydration. HPLC can easily resolve the product’s main peak; for labs without UHPLC, standard silica column purification typically separates any over-chlorinated side products. Our technical results suggest good shelf-life with proper storage, and we flag any process changes to our partners who must submit documentation to regulators. We also routinely run stress tests to confirm solubility in common organic solvents including DMSO and acetonitrile, supporting those working in both route scouting and bioassay prep.
Anyone with experience sourcing heterocyclic intermediates has encountered the headaches caused by origin drift or split-lot production. Many suppliers source from blended or repacked product, leading to surprises: variable particle size, retained solvent, or shifts in melting behavior. We build our material from the ground up, maintaining full traceability from raw reagents to each finished batch. Our operators don’t farm out steps or add bulking agents; every batch receives full in-house analytics. That means customer labs receive the identical certificate of analysis, and results hold up whether repeated in Boston, Basel, or Bangalore. Our clients no longer waste hours running their own side-by-side screens for off-target contaminant signals.
Frequent complaints in the market concern ambiguous documentation or inconsistent packaging. In our supply chain, we keep packaging stable, use custom-lined drums or bottles as required for air- and light-sensitive deliveries, and disclose all relevant handling notes. By discussing best storage options openly, we help users prevent accidental exposure or spoilage. We also engage directly when researchers hit roadblocks with our product—whether troubleshooting off-target side reactivity or chasing obscure analytical artifacts. After hundreds of feedback rounds, we adjust production variables based on field reports, which in practice means fewer retests and more hassle-free syntheses downstream.
Any producer of specialized building blocks today works with the reality of regulatory oversight and stricter environmental responsibilities. The market no longer tolerates vague sourcing, nor can any manufacturer afford to ignore new compliance pressures. Our facility is built around solvent recycling, secondary containment, and strict process control. By choosing halogen sources that minimize hazardous byproducts and implementing scrubbers for exhaust streams, we reduce the environmental load associated with 6-chloropyrazolopyridine synthesis.
We document our compliance practices for customers in regulated industries—pharma, agro, and materials R&D—where audits or regulatory filings are routine. On-site, we keep lot retention samples for back-checking if any downstream concern arises, ensuring both quality and accountability. Researchers submitting investigational new drug applications tell us that accessible documentation reduces their own paperwork burden. We treat any flag from downstream users as a trigger for root-cause analysis at the source, rather than passing blame or deflecting responsibility.
Just a few years back, small-batch chemical producers rarely looked beyond immediate demand. Times have changed. More teams push the boundaries of complex molecule synthesis, and new therapeutic targets continue to emerge. The research community now expects higher-purity, scalable intermediates ready for on-demand deployment. Because 1H-pyrazolo[3,4-b]pyridine, 6-chloro- features a fused, nitrogen-rich system, it serves as a critical launchpad for exploring new chemical space. By refining parameters—base equivalents, solvent types, temperature ramps—our engineers squeeze out higher yields and minimize batch-to-batch drift.
Direct requests from innovative clients have brought us into projects extending beyond pharma. We’ve seen this core ring system leveraged in OLED materials screening, enzyme probe construction, and analytical standard sets for environmental screening tools. Each new application brings fresh technical challenges: solubility in nonpolar carrier fluids, improved stability under field conditions, or compatibility with novel catalysts. Our solution involves an open channel between the bench and the customer. What begins as a technical service request sometimes triggers a process overhaul or a shift in purification approach for future lots.
Supplying 6-chloropyrazolopyridine goes beyond just shipping containers. Our credibility in the sector comes from taking ownership of every interaction—from the initial inquiry, through scale-up planning, to data sharing with regulatory teams. Upstream control, user-friendly support, and honest answers about materials performance keep our partners coming back. Beyond large multinational accounts, we also hear regularly from small startup teams in early-stage pipeline development and university programs embarking on grant-backed investigations. Across all users, a single theme dominates: researchers want a reliable, high-performing intermediate that matches published specs without surprises.
Direct feedback makes a huge difference. Academics sometimes consult us specifically to troubleshoot novel applications, such as coupling with new heterocycles or adapting workup for trickier downstream conditions. We respond not with generic stock advice, but with observations from our plant—what we’ve seen work (or fail) under parallel conditions, actual yield outcomes, or pitfalls to dodge. Our support helps labs plan better, whether adapting for glovebox procedures, rapid heating schedules, or alternative solvent systems.
Many advances in chemical manufacturing have come from embracing incremental, hands-on improvements. New tools, smarter reactors, in-line analytics, and fully tracked documentation transform what seemed like a commodity intermediate into a robust research ally. With 1H-pyrazolo[3,4-b]pyridine, 6-chloro-, our facility has committed to continuous improvement: reducing trace impurity profiles, extending stability under harsh storage, and customizing particle sizing or crystallinity as customer projects demand.
Technical partners have reached out for custom variants and process adaptation. Our willingness to engage at the process level, whether for specialized halogen patterns, isotope labeling, or batch traceability, stands as a core value. Over the years, this investment in open collaboration earns strong relationships and repeat business as product requirements evolve alongside scientific frontiers.
The learning curve with 6-chloropyrazolopyridine synthesis ran steep at the very beginning, even with experienced chemists at our disposal. Solvent choices impacted not just yield but also crystallinity and filtration speed. Process-side contamination from impure feedstocks drove us to invest in higher-level analytical tracking. Sometimes, batch failure meant late nights in the lab—running controls, deciphering NMR traces, tracking micro-impurities through LCMS. This hands-on troubleshooting brought more process insight than a stack of technical papers ever could.
Over time, new grades and variants emerged at the request of researchers aiming to reach next-tier targets in enzyme inhibition or receptor binding studies. These requests brought fresh technical challenge, as shifts in substitution pattern needed new purification approaches. We welcomed these feedback loops, since each insight from users in the field translated into fewer production hiccups for all future lots.
The demand for robust, high-purity 1H-pyrazolo[3,4-b]pyridine, 6-chloro- continues to grow as industry and academic priorities shift. We expect to see even greater emphasis on digital traceability, green production practices, and adaptive formulation based on diverse user needs. Our manufacturing team remains ready to adapt, optimize, and share knowledge with every client, never taking short-cuts that might compromise bench or pilot plant results.
Our history with this compound shows that a strong product foundation comes from ownership—control over every reaction, drying run, packaging step, and validation test. Through attentive listening, technical openness, and a willingness to adapt, we have built our reputation on meeting the real-world needs of researchers pushing at the edges of chemical and biochemical discovery.