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HS Code |
929485 |
| Chemical Name | 1H-Pyrazolo[3,4-b]pyridine, 3-bromo- |
| Molecular Formula | C6H4BrN3 |
| Molecular Weight | 198.03 g/mol |
| Cas Number | 764692-11-7 |
| Appearance | off-white to light yellow solid |
| Smiles | Brc1nn2cccnc2c1 |
| Inchi | InChI=1S/C6H4BrN3/c7-5-4-8-10-6-3-1-2-9-6(4)5/h1-3H,(H,8,9,10) |
| Storage Conditions | Store in a cool, dry place, keep container tightly closed |
| Purity | Typically ≥97% |
| Synonyms | 3-Bromo-1H-pyrazolo[3,4-b]pyridine |
As an accredited 1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 1H-Pyrazolo[3,4-b]pyridine, 3-bromo-, 5 grams: sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Standard 20-foot container, securely packed with 1H-Pyrazolo[3,4-b]pyridine, 3-bromo-, ensuring safe transportation. |
| Shipping | 1H-Pyrazolo[3,4-b]pyridine, 3-bromo- is shipped securely in airtight, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with international transport regulations, including labeling as a laboratory chemical. Shipping is conducted via certified carriers to ensure safe handling, with documentation included for tracking and regulatory compliance. |
| Storage | 1H-Pyrazolo[3,4-b]pyridine, 3-bromo- should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect the compound from moisture and direct sunlight. Handle in accordance with standard laboratory safety protocols, and ensure appropriate labeling to prevent accidental misuse or exposure. |
| Shelf Life | The shelf life of 1H-pyrazolo[3,4-b]pyridine, 3-bromo- is typically 2–3 years when stored in cool, dry conditions. |
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Purity 98%: 1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal by-product formation. Melting Point 187°C: 1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO- with a melting point of 187°C is used in solid-state drug formulation, where thermal stability allows for reliable processing. Molecular Weight 226.03 g/mol: 1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO- with molecular weight 226.03 g/mol is used in chemical library development, where consistent molecular mass ensures compound identification accuracy. Particle Size ≤ 10 µm: 1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO- with particle size ≤ 10 µm is used in high-throughput screening assays, where fine particle distribution improves dissolution rates. Stability Temperature up to 120°C: 1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO- with stability temperature up to 120°C is used in medicinal chemistry research, where thermal resilience maintains structural integrity during reactions. |
Competitive 1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO- prices that fit your budget—flexible terms and customized quotes for every order.
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Every day at our manufacturing plant we handle dozens of building blocks for pharmaceutical and agrochemical synthesis, but few catch the eye quite like 1H-Pyrazolo[3,4-b]pyridine, 3-Bromo-. Years ago, demand for this compound barely registered above background levels, but over the last decade synthetic chemists and project leaders started reaching out for it with growing urgency. This compound slots straight into many modern drug discovery projects and crop protection research streams, and our experience with large-scale synthesis has become a distinct source of value for both us and clients.
The addition of bromine to the 3-position of the pyrazolo[3,4-b]pyridine ring system marks a clear distinction from more common analogs that leave the ring unhalogenated or use other substituents. Under precisely controlled reaction conditions, our team uses proprietary bromination methods to maintain consistency in crystal form and purity, aiming at levels upwards of 98%. We’ve learned through trial and error that batch-to-batch variability in halogenated heterocycles tends to sink research productivity, so our process is built with purity monitoring at every stage.
Over the years, clients have sent us feedback on downstream issues tied to unreacted starting materials or ambiguous chromatographic profiles. Our synthetic protocols evolved to address these, especially in crystallization and filtration. Each kilogram produced gets checked not just with standard HPLC and NMR, but also on scalable reaction repeatability, since our partner labs can’t afford unanticipated side-products blowing up analytical costs.
It’s easy to overlook the function of building blocks if you’re not directly running library synthesis or high-throughput parallel investigations. Yet, switch out a hydrogen for a bromine at the correct location, and suddenly that core structure—previously a bit player—enables a wave of further functionalizations. Our compound sets up Suzuki, Buchwald, and other well-defined coupling reactions, giving synthetic teams a versatile handle for extension work.
We have worked closely with R&D chemists tracking SAR cycles, who emphasize how the right starting scaffold can shave weeks off lead optimization. Many downstream analogs get defined by the robustness of the initial brominated pyrazolopyridine intermediate. Some projects would come to a standstill without this tool in the kit; lackluster or impure supply can turn a workable idea into a dead end. We saw this up close with a CRO using generic supply: after repeated delays, they mapped the root-cause back to inconsistent halogen patterning at the 3-position.
On the factory floor, we judge the end product by factors that speak directly to lab usability. Moisture content, sharp melting point range, and solubility in commonly used polar aprotic solvents matter as much as nameplate assay. Synthetic chemists regularly comment on their needs for predictable handling during scale-up. Fine particulates, wide-melting impurity profiles, or questionable batch histories bring on headaches and rework. Our in-house teams learned long ago that meeting these direct-use criteria determines repeat business.
The 3-bromo addition confers not only the desired reactivity but also unique electronic effects. In cross-coupling setups, we have seen increased reactivity under both standard Pd and Ni catalysis. Over time we’ve fine-tuned specifications and can tune batch attributes (such as particle size and polymorph) per R&D request, though the core product consistently meets pharmaceutical research standards. A few organizations requested analytical support with scale-up, and we walked through parameter variation for them in side-by-side test runs. No off-the-shelf distributor can match such tailored experience in handling a molecule that sits at the intersection of synthetic innovation and practical reliability.
Production challenges never fade. Sourcing reliable brominating agents, controlling by-product profiles, and scaling up without cross-contamination all require steady process revision. Our team invests in new analytical methods; for this compound, lower detection limits for trace halogenated byproducts significantly cut down on customer troubleshooting down the pipeline.
Environmental handling also drives choices we make. Brominated compounds call for attention to waste first and foremost, and we have ongoing projects to upgrade solvent recovery and emissions capture. Having worked through various output grades, we see that on demand for eco-compliance, researchers are ready to pay a premium for transparent, low-impact processes. As legislative checks on halogenated aromatic compounds become tighter in Asia, Europe, and North America, early adoption of these best practices safeguards both our business and clients' regulatory progress.
It’s hard to compare this molecule straight across to other pyrazolopyridines or more generic halogenated intermediates. Unsubstituted 1H-Pyrazolo[3,4-b]pyridines find some use in research, but they can lack the required handle for regioselective transformations in modern design campaigns. The 3-methyl or 3-chloro analogs each fill their own niche, yet the 3-bromo variant unlocks next-stage diversification. The chemoselectivity of the bromo group in metal-catalyzed cross-coupling reactions acts as the principal lever for medicinal chemists who want efficiency and reliability.
As a manufacturer, we see less call for direct competitive comparison than most might expect. Our clients care more about reliability—absence of tarring, breakdown on storage, or solubility surprise during scale-up. Through hundreds of batches, we’ve found the bromo analog as robust as any in our heterocyclic toolbox, with predictable behavior across reaction conditions.
People who have spent years in bench chemistry or production learn that lab-scale performance is only half the story. Minor impurity carryover, subtle phase behaviors, and storage stability make the difference in kilogram work. For the 3-bromo pyrazolopyridine, we refined our process steps from direct customer input—one pharmaceutical customer had placed multiple repeat orders, and after tracking a minor yield loss in late-stage coupling, we re-ran NMR, finding less than 0.1% residual dibromopyridine in a single batch. That sparked an internal review, which led to enhanced QA checkpoints that now apply to every lot.
We have hosted many site visits from clients’ QC and purchasing representatives. It’s clear that experience in the real-world production of heterocycles like this pulls us apart from import traders or resellers who depend on third-party factories. We see the look on chemists' faces when they handle a drum with clear labeling, packaging built for both short and medium-term storage, and with COAs that reflect genuine batch data instead of boilerplate printouts. We hear appreciation for end-to-end process transparency. All these operational choices help bridge the gap between molecule and results for real R&D units.
Not every year brings the same order volumes. We’ve seen spikes in demand whenever a popular research article drops or a new patent claims this scaffold. For less agile operations, the lag between run scheduling and delivery can stretch from weeks into months. We invested in modular production lines some years back; this makes it easier to adjust runs based on leading indicators from our top ten clients.
Stock management takes up more resources than most appreciate. On-site warehousing enables us to ship out promptly. Once, a sudden surge in orders forced a run on our supplies, which nearly left customers facing project delays. From that experience, we doubled our routine batch size and improved our forecast modeling by partnering with clients on multi-quarter planning. Safe delivery grows from working relationships, not last-minute rushes.
Most batches that leave our plant head for pharmaceutical R&D and high-throughput screening labs. One medicinal chemistry team shared insight on how rapid introduction of aryl, heteroaryl, or alkynyl elements onto the scaffold shortened their iteration cycles. The bromo group provides a more tractable exit vector than, say, a triflate or a chloride, particularly where selective activation is needed. Teams designing kinase inhibitors, CNS agents, or antineoplastic candidates routinely select this scaffold as a springboard.
In agricultural research, this compound’s scaffold gets tested as a core in new herbicide and fungicide prototypes. Researchers from the agrochemical sector favor the bromo derivative for ease of late-stage derivatization, yielding lead candidates with less synthetic overhead than starting with unsubstituted or other halogenated variants.
We maintain a long-term commitment to refining our process and upgrading our offerings. This means not just regular audit of raw materials and solvent recovery but staying in step with downstream regulations and product safety expectations. Years of cumulative production teach that reliability and responsiveness count most. That’s why our entire team—from procurement to QA to shipping—shares regular updates on analytical trends and synthesis outcomes.
Close partnership with advanced R&D teams brings regular requests for custom quantities or variations in specification. We take that as a sign of trust—one that drives our ongoing investments in both facility and talent. On several occasions, a complex multi-step synthesis used our 3-bromo analog as an early intermediate; the R&D leads sent us spectral data and feedback from their process, helping us tighten process parameters to hit their requirements on reaction recurrence and downstream yield.
Large-scale chemistry brings its own set of problems, from heat management in bromination reactions to risk of cross-contamination in multi-product plants. As the demand for this product has grown, we introduced dedicated production lines, giving us direct oversight into cleaning, batch segregation, and calibration. Each scale-up batch draws from lessons recorded in pilot runs; we debrief after each large delivery to check what went well and what can improve next time.
Distribution logistics play a bigger role than most realize. Some of our key customers operate on razor-thin timelines; they rely on direct-from-factory supply chains and clear channel visibility. Our approach includes proactive communication, tracking, and resolver teams ready to expedite or adjust based on customer input or shifting market conditions.
Working with halogenated heterocycles comes with safety obligations. We invest not just in internal staff training but in clear, end-user-facing documentation. All batches ship with full traceability to the originating synthesis lot and QC records. From storage conditions to recommended disposal routes, all operational instructions pull from direct manufacturing experience—this goes beyond minimum requirements and charts a course for product stewardship.
A lot of organizations that buy from global distributors miss out on this continuity. Unexpected product behavior, obscure histories, or mismatched labels create confusion and risk. Pulling from decades of plant data and daily production oversight, we aim to remove those worries at the source.
The market for advanced intermediates like 1H-Pyrazolo[3,4-b]pyridine, 3-Bromo-, will continue to expand as research volumes climb in pharmaceuticals and agrisciences. Synthetic routes will keep evolving, bringing additional pressure on yield improvement and sustainable process design. We’re committed to meeting these challenges head on, drawing on our ground-level manufacturing experience and direct client interactions to set benchmarks in reliability, performance, and environmental stewardship.
As more researchers look for trusted, transparent sources of complex scaffolds, those of us on the manufacturing side see opportunity and obligation in equal measure. From method development to customer follow-up, every step gets shaped by real production insights. These lessons drive both innovation and quality—qualities that stand behind every shipment of 1H-Pyrazolo[3,4-b]pyridine, 3-Bromo- leaving our facility.