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HS Code |
561917 |
| Iupac Name | 5-bromo-3-iodo-1H-pyrazolo[3,4-b]pyridine |
| Molecular Formula | C6H3BrIN3 |
| Molecular Weight | 323.92 g/mol |
| Cas Number | 1020263-48-8 |
| Appearance | Solid |
| Solubility | Slightly soluble in DMSO and methanol |
| Smiles | C1=NC2=C(C(=NN2)I)C=C1Br |
| Inchi | InChI=1S/C6H3BrIN3/c7-3-1-4-5(2-9-3)10-11-6(4)8/h1-2H,(H,10,11) |
As an accredited 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo-, sealed with a tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- involves safe, secure packing in sealed drums or bags. |
| Shipping | The chemical **1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo-** is typically shipped in tightly sealed containers, protected from light and moisture. It is handled in compliance with hazardous materials regulations, often requiring specialized packaging and labeling. Shipping is conducted by certified carriers, with necessary safety documentation and protocols to ensure safe transport. |
| Storage | 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, well-ventilated area. Store at room temperature or lower, away from incompatible substances such as strong oxidizing agents. Use appropriate safety measures, including gloves and eye protection, when handling the chemical to avoid contact. |
| Shelf Life | Shelf life of 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo-: Typically stable for 2-3 years when stored cool, dry, and protected from light. |
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Purity 98%: 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimizes byproduct formation. Melting Point 210-213°C: 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with a melting point of 210-213°C is used in solid-phase organic synthesis, where it provides thermal stability during reagent coupling steps. Molecular Weight 324.92 g/mol: 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with a molecular weight of 324.92 g/mol is used in medicinal chemistry research applications, where it allows precise mass balance calculations for structure-activity relationship studies. Stability Temperature ≤ 60°C: 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with a stability temperature of ≤ 60°C is used in reagent storage protocols, where it maintains compound integrity and minimizes degradation during long-term storage. Particle Size < 100 μm: 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with particle size < 100 μm is used in combinatorial library preparation, where it enhances mixing homogeneity and increases reaction reproducibility. Assay ≥ 97% (HPLC): 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with assay ≥ 97% (HPLC) is used in custom chemical synthesis, where it contributes to accurate stoichiometry and consistent product quality. Solubility in DMSO 10 mg/mL: 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with solubility in DMSO at 10 mg/mL is used in high-throughput screening assays, where it enables efficient sample preparation and reliable bioactivity testing. Light Sensitivity: 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- with light sensitivity is used in protected-environment storage, where it prevents photodegradation and preserves compound potency. |
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Working the reactors, seeing tanks fill with 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo-, and running the controls day in and out has taught our team hard lessons about what matters in manufacturing specialty heterocycles. This molecule lays a crucial foundation in fine chemistry, especially when the job calls for highly functionalized intermediates with both halogen and nitrogen-rich architectures. Chemists rely on this compound for more than the numbers in a catalog; they count on its consistency, reactivity, and traceability.
Our production lines turn out this advanced intermediate at varying scales. Day-to-day batches can shift from a few kilograms for research and pilot, up to several hundred for downstream API and agrochemical development. The actual bridge from the planning desk to a running reactor takes grit – it’s more than tweaking spreadsheets. Solvents evaporate, pressure bumps, and operators need engineering controls to keep halogenation safe, especially with reactive iodine and bromine agents. In our rooms, every “standard” model number carries the thumbprint of actual hands who’ve spent days troubleshooting exotherms and cleaning glassware.
The backbone of 1H-pyrazolo[3,4-b]pyridine has long attracted medicinal chemists hunting for new kinase inhibitors, antiviral scaffolds, or advanced materials. Our 5-bromo-3-iodo derivative sharpens this platform even further. The dual halogen substitution at ring positions 3 and 5 isn’t just theory on a reaction scheme; it carries real consequences in coupling chemistry, ADME optimization, and final crystallization steps.
Compared with unsubstituted analogues, this molecule hands extra leverage to synthetic chemists. More than once, we’ve watched researchers build combinatorial libraries with it, slotting in their desired groups through Suzuki or Sonogashira couplings. Catalysts respond differently to bromine than to iodine. Scale-down test runs reveal those differences in yield, selectivity, and cost. Time on our process development reactors has shown that 5-bromo-3-iodo substitution boosts the flexibility for downstream transformation, allowing for selective activation of either functional group in sequential cross-coupling. This translates into less wasted material, fewer protection steps, and tighter control on impurity profiles.
It’s tempting to think that technical grade and high-purity forms differ only by the number on the label, but batch chemists learn soon enough that analytical details shape production realities. The most common models we produce meet demanding specs: HPLC purity typically exceeds 98%, and we document moisture content and single-impurity profiles by LC-MS and NMR. Consistency across batches starts with our raw material qualification: both pyrazolopyridine core and the halide sources pass QC long before they touch a kettle.
Production lots differ from those turned out by contract partners or importers. From cleaning validation to solvent recovery, we track and record every step. Like any fine chemical, handling 5-bromo-3-iodo pyrazolopyridine takes specialized containment. Some compounds can get by with open flasks or shared gear. Halogenated heterocycles like this tear through seals unless reactors and piping use the right linings. That’s why long-term investment in glass-lined reactors and on-site testing equipment remains non-negotiable in real-world manufacturing.
We listen to chemists further down the chain. One year, users needed enhanced solubility for certain bioconjugation sequences. The next, regulatory scrutiny forced adoption of green solvent alternatives during isolation. We don’t just supply material; our process team and QC lab share spectra, impurity tracking, and sometimes even advice on workup and storage.
Feedback cycles reveal which synthetic routes generate more byproducts or call for complex purification. Reproducibility concerns steer us to more robust methods, even at the expense of higher raw material or equipment costs. The decision to use direct halogen exchange over stepwise NBS or iodination routes wasn’t made in a vacuum. Our analytical crew tracked the results through the full process and helped us retain the right balance between output, cost, and ecological compliance.
Manufacturing specialty halogenated intermediates challenges everyone on the crew to keep people and environment at the forefront. Both brominating and iodinating reagents demand ventilation upgrades, spill control, and extensive PPE. After a close call with a runaway batch several years ago, we updated our protocols with automated temperature interlocks and expanded team drills.
Waste management never drops off our radar. Some team members have decades of experience with solvent recycling and effluent treatment. We minimize open transfers and maximize wash solution recovery. Nothing replaces a skilled operator with a well-trained eye for unusual color shifts or gas release. Regular investment in environmental monitoring lets us back up every claim with data, which auditors and customers now expect.
Across the last ten years, we've synthesized a portfolio of pyrazolopyridines with various halogen substitutions. Each variant finds its own audience: some researchers favor di-bromo or di-chloro motifs, but the 5-bromo-3-iodo arrangement stands apart for its dual-site reactivity. Iodine’s high leaving group ability opens aryl coupling channels closed to pure bromides. The slightly higher cost of iodine pays back in fewer synthetic steps later.
Other suppliers offer mixed-halide intermediates from stock, but consistency wobbles across shipments. More than once, reports from customers highlighted darkening during storage or stubborn side-products from poorly controlled halogenation. Our process controls – refined by countless small adjustments and structured troubleshooting – keep light and oxygen exposure tightly monitored. Results show up as lighter powder color, cleaner chromatograms, and longer shelf stability even after months in inventory.
Collaboration with pharmaceutical R&D centers puts this intermediate into kinase inhibitor discovery, anti-inflammatory candidate screening, and even select pesticide design. At the milligram-to-gram research stage, users want small, high-purity lots for rapid testing. Once something shows promise, teams reach out for batch-scale material, and that’s where our plant delivers. Working close to end users, our technical team fields questions about stability, appearance, and process impurities. Rarely do weeks go by without requests for additional documentation supporting IND or patent filings.
Our own records trace back how 5-bromo-3-iodo pyrazolopyridine formed the backbone for more than one proprietary API intermediate. Publication records and patent literature confirm its value in providing privileged molecular space for late-stage diversification. Straightforward Suzuki couplings on the bromo and further functionalization from the iodo unlocks rapid SAR exploration. The structure’s versatility, shaped by the skills and processes honed on our shop floor, continues to unlock new bioactive and industrial candidates.
Quality in fine chemicals often reads like a checklist, but actual manufacturing brings a different reality. NMR confirmation and chromatographic purity mean little unless process parameters eliminate as much batch-to-batch drift as possible. Every process transfer, from lab scale to pilot, and then plant, can bring surprise side-products and separation issues. Our team invests in site-wide training and cross-checks, from raw material testing to end-product packaging, because experience shows shortcuts create future headaches.
Collaboration across departments, from process engineering to maintenance and safety, roots out weak points. Crystallization trials to lock in polymorph control, moisture monitoring for better packaging, and strict documentation provide the backbone our customers trust. Surprises still appear: an unexpected polymorph or higher-than-expected moisture holding due to shifts in raw material suppliers. Rapid in-house testing capacity keeps schedules on track, preventing hold-ups in customer projects.
No product escapes global logistical and cost swings, and specialty chemicals track their own set of risks. Fluctuating supplies of iodine, pressure on bromo reagents, and transportation headaches for controlled substances each shape raw cost curves. We’ve weathered sourcing crises by building long-term relationships with key material producers and maintain contingency plans that give us redundancy on critical inputs.
Margins matter, but so does delivering a molecule that does its job in labs an ocean away. Cost-saving measures through process intensification, yield improvements, and recovery optimization run as ongoing projects. Team members pass down “lessons learned” about process tweaks that cut time without risking product quality or environmental footprint. Today’s new solvent recovery skid, tomorrow’s minor requalification, and regular process audits provide the flexibility to absorb unexpected demand spikes or delayed shipments of scarce halogens.
No batch process stands still. Evolution in the 1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- category mirrors shifts in global research and regulatory demands. Soon, greener reagents promise to reduce both our effluent and air emissions. We test new continuous-flow modules for smaller, safer halogenations and keep an eye on renewable solvents and next-generation crystallization approaches. Working chemists drive real-world change, and our operations department follows their cue.
Being a manufacturer makes clear that every small improvement in process safety or product quality builds trust. The long, collaborative relationships with technical users and regulatory bodies turn raw chemical expertise into working, reliable product. Knowing every process technician, analytical chemist, and logistics planner by name matters more than sliding a PDF across a desk. That is what creates reliability where it counts.
1H-pyrazolo[3,4-b]pyridine, 5-bromo-3-iodo- doesn’t arrive in a bottle by magic; it’s the end point of years of process tinkering, real troubleshooting, and investment in people and equipment. Its value lives not just in a reaction scheme but in decades of craft and continual improvement. Each kilogram produced at our site stands as proof that specialty chemicals deserve real expertise and grounded commitment at every step. This makes the difference for researchers seeking reliability and performance at the lab bench or on the production line downstream.