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HS Code |
493881 |
| Productname | 6-Bromoindazole |
| Casnumber | 1833-57-8 |
| Molecularformula | C7H5BrN2 |
| Molecularweight | 197.04 |
| Appearance | Off-white to light brown powder |
| Meltingpoint | 80-84 °C |
| Purity | ≥98% |
| Boilingpoint | Unknown |
| Synonyms | 1H-Indazole, 6-bromo- |
| Smiles | Brc1ccc2[nH]ncc2c1 |
| Storagetemperature | Store at room temperature |
| Solubility | Slightly soluble in water, soluble in organic solvents |
As an accredited 6-Bromoindazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 6-Bromoindazole (25 grams) is a sealed, labeled amber glass bottle with chemical hazard and handling information. |
| Shipping | 6-Bromoindazole is shipped in secure, airtight containers to prevent contamination and degradation. Packaging meets international regulations for hazardous materials. The chemical is labeled clearly, and accompanying documentation includes safety data sheets. Shipping is handled by certified carriers, ensuring prompt and safe delivery, typically at controlled room temperature unless otherwise specified. |
| Storage | 6-Bromoindazole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. It should be kept at room temperature and protected from moisture and incompatible substances such as strong oxidizing agents. Proper labeling and adherence to chemical safety guidelines are essential to ensure safe storage. |
Applications of 6-Bromoindazole in Industrial Manufacturing6-Bromoindazole serves as a highly specialized intermediate for fine chemical synthesis in several industrial segments. Its molecular structure enables efficient and selective modifications, offering process consistency and controlled end product purity in regulated manufacturing environments. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical companies routinely apply 6-Bromoindazole as an advanced heterocyclic building block during the synthesis of kinase inhibitors, anticonvulsants, and other indazole-based active pharmaceutical ingredients. Its stable bromo functionality provides a reliable handle for robust Suzuki and Buchwald–Hartwig coupling reactions, supporting scalable route design for regulatory submission. Controlled lot consistency and impurity profiles are essential for downstream solid oral dosage forms and injectable APIs produced under strict current Good Manufacturing Practice conditions. Industry compliance standards
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2. Agricultural Chemical Intermediate Production6-Bromoindazole plays a significant role in the synthesis of advanced intermediates for select agrochemicals including herbicides and fungicides. Its bromo-indazole motif supports functionalization for constructing indazole-triazole hybrids, which are evaluated for soil and foliar activity. Manufacturers require accurate traceability, residual purity analysis, and management of regulated waste during high-volume batch production for agricultural applications. Industry compliance standards
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3. Dye and Specialty Pigment ManufacturingThe high reactivity of 6-Bromoindazole’s aromatic moiety enables dye manufacturers to construct colorant backbones for use in specialty printing, textile pigment, and inkjet ink segments. Its introduction into azo and diazo coupling pathways allows controlled substitution for chromophore finetuning, where resistance to light and chemicals is critical for product qualification. Manufacturers focus on batch traceability and compatibility with solvent systems while meeting environmental and export regulations for pigments. Industry compliance standards
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4. Advanced Materials and Functional Polymer Additives6-Bromoindazole enables synthesis of high-value indazole-functionalized monomers used in electronic materials, optoelectronic polymers, and specialty resins. Its use supports development of heterocyclic crosslinkers, charge transporting layers, and UV-absorbing additives in multilayer film and device fabrication. Manufacturers require strict in-process controls, impurity tracking, and solvent recovery to support component qualification for use in electronics assembly and functional coatings. Industry compliance standards
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For the past twenty years in specialty synthesis, some molecules draw steady demand from research and industry. 6-Bromoindazole has kept our reactors and purification systems busy every month without the product ever becoming just another catalog item. Each batch offers a lesson in raw material sourcing, solvent control, process optimization, and, above all, consistently delivering to chemists who expect straightforward quality and honest dialogue about what is actually in their bottle.
The backbone of our 6-Bromoindazole process stays constant: a cyclization route using selective halogenation to target the 6-position of indazole. Decades ago, we ran small flasks by hand, cataloging small shifts in product appearance and analytical profile when using slightly different grades of starting indazole and brominating agent. With confidence in one robust method, scale-up moved to kilo lots, and our TLC sheets gave way to fully integrated HPLC and NMR profiles on every batch. We’ve kept our synthesis deliberately simple in terms of work-up and isolation, as this means we can do away with excess washing, recrystallizing, or distillation that only wastes solvents. At this point, most output leaves our facility as a fine, off-white to cream-colored crystalline solid, a sign of low impurity carryover and precise control of halogenation conditions.
Commercial customers commonly request 6-Bromoindazole in 25kg drums, with research groups favoring sealed foil packs around one kilogram. The model number internally tracks the route, solvent ratio, and quenching conditions—this helps both our QC team and returning buyers who need their material consistent from lot to lot. During years of working with this molecule, we found a broad range of pharma and materials groups depend on the batch-to-batch uniformity of both purity and minor impurity profile. Anyone working on bioactive indazole frameworks knows that even a fraction of unreacted indazole or dibromo byproduct can disrupt a synthetic sequence or biological assay.
Running an indazole halogenation plant doesn’t just mean strict adherence to SOP or typical reagent lists. Indazole itself can vary in trace content by vendor and batch. Brominating agents come with their own stability quirks, with some turning sluggish in monsoon humidity or storage. Over years, we have implemented sealed reactors and in-line drying steps specifically to prevent trace moisture from activating unwanted side reactions or color formation. We don’t aim for the highest theoretical yield; past certain limits, incremental yield gains only risk escalating impurity carryover or introducing tricky-to-remove side products.
Process design boils down to one rule for us: reliable selectivity. We calibrate reaction stoichiometry to minimize double bromination, tuning temperature ramps and quench timing rather than just adding more bromine. This choice cuts down on difficult purification steps. Final isolation optimizes product crystallinity, making downstream handling more manageable for chemists loading columns, weighing solid for further reactions, or setting up scale-dependent pilot studies.
Each kilogram of 6-Bromoindazole passes through a set battery of analysis: proton and carbon NMR, HPLC for quantitative purity assessment, GC when residue volatiles can crop up, and mass spectrometry to spot trace levels of by-products. NMR verifies critical regioselectivity at the 6-position, ruling out isomeric bromination at positions 4 or 5. HPLC profiles set the threshold for allowable unknowns, with every change in raw materials or process shift prompting a full impurity mapping. By the time a batch clears QC, it has passed through both automated analytics and physical inspection for uniform solid content and absence of discolored inclusions. We often invite customers to review the full analytical data with our technical staff, building trust and open dialogue that helps resolve any downstream issues quickly.
Downstream, 6-Bromoindazole becomes a versatile handle for further reactions, from Suzuki couplings to other cross-coupling strategies. Indazole frameworks have shown recurring bioactivity in kinase inhibitors, oncology trials, and agrochemical candidates. Having the bromine positioned at 6 gives researchers a concise entry point into highly decorated or fused ring systems, with broad compatibility across dozens of metal-mediated coupling chemistries. Recently, the push for new indazole derivatives in optoelectronic materials required kilograms of reagent-grade brominated scaffolds, and we’ve adapted our washing and drying to suit the ultra-low-metal specifications of electronics developers. By talking directly with customer formulation teams, our plant can flag even low-level silica or washing residue that wouldn’t trouble pharma buyers but might derail a precision polymerization run. Back-and-forth like this has allowed us to tune our process to stretch across unlikely industries, rather than chasing only the biggest or flashiest application.
Many indazole products sold on the market today come from brokers or blending centers, drawing from different small-batch producers over years. The appearance on a certificate may read the same, but side-by-side, practical differences show up fast. Color changes, odor, and the tendency to cake with time point to different solvent residues or minor impurities. After feedback from a pharmaceutical client regarding trace acetic acid formation in some blends, we retooled our isolation procedure to use higher-purity water and switched our glassware cleaning protocol. Direct traceability back to each raw material lot underpins our specification system, preventing the slip-in of unintended source changes. Being both the process designer and manufacturer means we catch lot variability before it ever reaches the customer’s bench.
Many customers ask about particle size and behavior. Our 6-Bromoindazole typically holds to a fine crystalline morphology—suitable for dispensing and weighing in open air without excessive static cling or dusting. This contrasts with milled or granulated versions that some traders provide, which can lose mass during transfer or perform inconsistently in liquid-phase couplings. We process to minimize trapped solvent, target moisture below 0.3%, and keep residual organics low enough that no functional impact shows up in scale-up studies from grams to multi-kilo lots. The final product gives a clean melt and sharp NMR, offering technical teams confidence in their downstream transformations.
For the majority of laboratory supplies, subpar batches only create small frustrations—a lower-yielding reaction or extra purification step. In the case of building blocks like 6-Bromoindazole, unpredictability blocks entire research programs or clinical supply chains. We know stories from customers who ran long exploratory syntheses only to hit a wall due to an isomeric impurity or chain-halogenated byproduct that was missed in less diligent analysis. Our plant runs analytical checks after drying, after interim purification, and again before packaging to make sure not a single lot has an unknown impurity above the limits set by our most demanding customers. During audits, clients have walked the floor, reviewing our chromatograms and storage protocols, and this level of access is part of keeping both sides honest.
Comparisons with other halogenated indazoles, like 4- or 5-bromoindazole, demonstrate why positional isomerism matters so heavily in structure-activity studies. Reagents supplied as ‘mixed bromoindazole’ from unaccredited brokers have left more than one pharma chemist repeating steps or discarding entire runs. We only proceed with lots for shipment after side-by-side NMR and coupling profiling match our reference standards for 6-regioselectivity. There is no shortcut for this verification, and experience has taught us audit trails and rigorous documentation head off problems for everyone involved.
Despite all the careful systems, occasional problems do surface—the worst scenario from a manufacturer’s viewpoint. Shipping during high-winter months can lead to product clumping or slight color shifts that the lab never observed during warm-season trials. We’re always reachable for photos and side-by-side analytical reassessment, and have, on occasion, replaced lots at our own expense rather than let a customer delay development. Transparency here helps not only the end-user but keeps our own teams honest in process review. We treat each issue as a wedge for process improvement, not a failed checkpoint.
This approach has put us on the preferred supplier shortlist for several pharma and contract research customers who need both specification adherence and day-to-day technical troubleshooting. It’s not only a matter of meeting a purity cutoff or an HPLC trace—questions about residual ions, stability in long-term storage, or performance in coupling reactions lead to real process changes. Just this year, new collaborations with electronics developers led to tighter residual metal checks, with product now passing stricter impurity screening before approval for final application. Our QC data expands every year as industries diversify their performance expectations, and the willingness to adapt is part of what keeps our jobs interesting.
From a manufacturer’s perspective, ethical sourcing and environmental safeguards evolve from buzzwords into working policies. We source our indazole and brominating agent from accredited chemical producers who offer full batch traceability, reducing the risk of problematic impurities. Solvents are reclaimed through in-house distillation to minimize both cost and waste. We track every kilogram of spent solvent and reaction byproduct for regulatory compliance well above regional requirements. As brominating chemistry raises legitimate safety questions, we built a closed-loop ventilation and neutralization system years ago, cutting worker exposure and environmental release substantially. These choices may never feature on a spec sheet, but customers notice the difference in batch regularity and shipment reliability over time. This transparency has led several clients to ask about our standards and, in some cases, push their other suppliers to follow suit.
Direct manufacturing means full oversight from first material check-in to final product pack-off. Traders and third-party bottlers rely on descriptions or random sampling, unable to verify every kilogram’s provenance or minor process variations. As chemists ourselves, we’ve learned that even well-meaning brokers struggle to match the diligence required for demanding projects. Our batches only leave the plant after analytical signoff, and our raw materials are never shared with other chemistry streams that could introduce contamination. This vertical control sits at the heart of every reliable relationship we’ve built over the years, replacing transaction-based supply with partnerships based on open data exchange and direct accountability.
A few years ago, global supply chain disruptions squeezed both brominating agents and indazole intermediates. Some producers rationed material or diverted stockpiled inventory from less visible lots to urgent high-profile pharmaceutical contracts. We handled the shortage by communicating openly with customers, scaling production shifts around core groups willing to sign updated offtake agreements rather than stockpiling at the first hint of shortage. Small customers, not only majors, received consistent supply—a choice that cost us some short-term volume but enabled continued R&D for those teams relying on us for their work. This period reinforced the value of steering closer to our customers and focusing on process stability even when raw material markets are unpredictable. With the global market now stabilizing, our experience through that squeeze has strengthened not only our sourcing strategy but the way we communicate with both long-time buyers and new contacts entering the field.
For many, 6-Bromoindazole is simply a line in a synthetic route or a shelf-stable bottle destined for the next transformation. We see it instead as part of the ongoing relationship between manufacturer and researcher, a product embedding decades of process evolution, technical exchange, and shared responsibility for results and safety. Each production run continues to reflect what we, as a chemical plant, learn from our customers: move fast, communicate openly, and always challenge the details until every batch ships with both quality and confidence built in. As new fields open up, from sophisticated drug candidates to advanced sensors and displays, the role of trustworthy chemical building blocks only increases. We’re committed to keeping our standards high, our dialogue honest, and our operations accountable, ensuring 6-Bromoindazole continues earning its reputation as a foundation for progress, not just a commodity.