|
HS Code |
833345 |
| Chemical Name | 4,7-Dibromo-1H-Indole |
| Cas Number | 16722-46-0 |
| Molecular Formula | C8H5Br2N |
| Molecular Weight | 286.94 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | around 180-183°C |
| Solubility | Slightly soluble in organic solvents such as DMSO and DMF |
| Smiles | Brc1ccc2[nH]ccc2c1Br |
| Inchi | InChI=1S/C8H5Br2N/c9-5-1-2-8-6(3-5)7(10)4-11-8/h1-4,11H |
| Synonyms | 4,7-Dibromoindole |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at room temperature, away from light and moisture |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 4,7-Dibromo-1H-Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Anyone who’s spent enough years elbow-deep in organic synthesis labs knows that some molecules just stand out. 4,7-Dibromo-1H-Indole belongs to that group. Reactions move quicker, outcomes get cleaner, and possibilities open wider when a compound hits the sweet spot of stability and versatility. This isn’t just another intermediate — it pushes projects forward in pharmaceutical research, agrochemical formulation, and material science.
4,7-Dibromo-1H-Indole takes its shape around the classic indole ring, but those twin bromine atoms, settled at the 4 and 7 positions, transform its profile in real-world applications. Chemical intuition tells you that these substitutions shift reactivity patterns, unlocking selectivity where a basic indole falls short. Toss this molecule into a Suzuki coupling, and you’ll see how easily you can add new functional groups—no complicated protecting group strategies, no endless troubleshooting. In a busy workflow, reliable reactivity lets you skip the mental gymnastics and focus on results.
Purity levels often make or break a project. In my experience, jumping from an 86% purity off-the-shelf compound to a refined 98% batch saves hours in column chromatography and takes a load off your mind when the analytical reports come in. I’ve run into compounds that look fine at first glance but drag trouble along with them—trace metals from crude syntheses, moisture hiding in cheap packaging, or ambiguous melting points. With 4,7-Dibromo-1H-Indole, top-tier suppliers deliver a crisp, white to off-white powder with transparent documentation and batch-specific COAs. The melting range for this indole clocks in consistently between 146–148°C, so you don’t chase wild goose indicators or wonder what’s lurking inside.
Anyone screening for kinase inhibitors, antimicrobial leads, or small-molecule drugs has probably encountered projects that dead-end due to inflexible starting materials. Substituting the usual unsubstituted indole with 4,7-dibromo analogs can save development teams weeks. The extra bromine atoms make cross-coupling reactions more reliable, and their presence supports structure-activity relationship studies. This lets you make meaningful changes to your scaffolds instead of incremental tweaks that rarely justify another round of funding.
Take one example from my past work with early-stage kinase inhibitor libraries. The plain indole often meant dead yields in late-stage derivatization. The dibromo version flipped the script: more derivatives in fewer steps, with better chemical yields. Medicinal chemists can build out libraries faster without a spike in failure rates. Target selectivity can be explored with more confidence, and hit-to-lead timelines tighten up. That’s real progress you feel in weekly project meetings, not abstract progress on a whiteboard.
4,7-Dibromo-1H-Indole doesn’t settle for one industry. The rise of organic electronics—OLEDs, photovoltaic cells, and next-gen sensors—puts unique demands on intermediates. The brominated indole’s robust structure helps it serve as a building block for complex polymers and optoelectronic materials. Having spent months on trial syntheses of organic semiconductors, I can’t overstate the relief in finding a halogenated indole that won’t decompose in the midst of a reaction or poison your catalyst. If you need monomers with strong electronic properties or well-defined conjugation, this compound offers a predictable route without crippling side-product headaches.
Once you’ve worked with different indole derivatives, the differences turning up in the lab get hard to ignore. Unsubstituted indoles offer flexibility, but they can lack selective reactivity for modern cross-coupling or substitution reactions. Monobromo indoles, on the other hand, often limit your options—one reaction, one site, then you’re out of moves. The dibromo version shifts that paradigm. Having two distinct positions ready for functionalization doubles the ways to tweak your molecule, opening up entirely new synthetic pathways.
I remember one project aiming to synthesize a biotech dye sensitive across the visible spectrum. Monobromo-indole gave limited access to the range of structural variants we needed. With 4,7-dibromo, new colors and properties emerged from straightforward synthesis. That subtle change—adding one more bromine—expanded the palette and shaved weeks from the development cycle.
No synthetic chemist wants their results to suffer because of avoidable impurities. Sulfate or chloride traces, even in tiny amounts, have a way of derailing scale-ups or gumming up analytical runs. Reliable sources of 4,7-Dibromo-1H-Indole provide products that ship with detailed impurity profiles and batch data. Having gone through several rounds of failed reactions thanks to off-brand, “cost-effective” reagents, I’ve reached the point where I’d rather pay a little more upfront for the peace of mind that comes with authenticated purity and long-term storage stability.
This compound holds up well on the shelf, provided it gets stored away from light and heat—a standard approach, but critical. Early on, we learned that even a hint of photodegradation saps nucleophilicity and makes downstream reactions unpredictable. Small amber vials, tight seals, and low humidity go a long way with brominated aromatics. It’s a minor step with outsized benefits if you care about reproducibility.
Cost and safety might dominate most sourcing decisions, but environmental accountability has started to play a larger role in our industry. Brominated compounds carry persistent concerns, from waste disposal to worker exposure. Regulatory guidelines in North America, Europe, and Asia highlight acceptable limits, but everyday handling builds best practices into a routine. Responsible suppliers benchmark their packaging standards, ship in compliance with all major transit regulations, and openly document their approach to minimizing hazardous waste. Any lab manager worth their salt will demand those assurances before signing off on a big order. My own team has pressed suppliers for certificates of analysis, shipping documentation, and clear safety data, and have benefited in both lab safety scores and reduced time lost to compliance paperwork.
Given all its benefits, 4,7-Dibromo-1H-Indole still requires attentive handling. The key here lies in methodical approach, not overengineering. Dispense with nonreactive gloves, and always weigh out small quantities in a draft-free, low-humidity area. The powder can cling to glassware and utensils, so anti-static measures aren’t just nice to have—they prevent wastage during transfer. If you’re scaling up, invest time in vacuum drying right before use, especially if a reaction shows sluggish yields or you smell even a hint of decomposition.
Storage at room temperature is feasible for weeks, but medium- to long-term retention calls for refrigeration, out of direct light. I’ve lost valuable reagents to overstuffed chemical cabinets where heat cycles led to slow, silent degradation. Avoid storing near sources of acid fumes or open containers of bases—the brominated positions make these molecules more susceptible to side reactions than you might expect at a glance.
Moving from milligram batches in an academic lab to multi-kilo production at an industrial site introduces a new set of hurdles. When I helped transition a discovery-stage synthesis into routine pilot runs, the most overlooked barrier was batch-to-batch consistency. That challenge gets solved more readily when the starting block—like 4,7-Dibromo-1H-Indole—shows little variance from order to order. Quality control at this stage involves not just basic chemical assays, but also particle size analysis and moisture content studies. If you’ve ever spent a month chasing down a batch-effect anomaly, you know how crucial this kind of consistency becomes.
On the regulatory side, import and export can get sticky thanks to both the bromines and the indole core itself. Some countries classify certain intermediates as controlled or precursor chemicals, or layer hefty documentation standards on shipments. My work with global R&D suggests that a proactive relationship with suppliers beats any after-the-fact scramble. Direct communication allows adaptation to shifting regulations and helps avoid a frustrating hold-up at customs—a real risk for rushed projects.
Research cycles move faster when chemists have more than one reliable option at their disposal. The addition of 4,7-Dibromo-1H-Indole to procurement lists supports broader medicinal chemistry campaigns, where new scaffolds or analogs mean new opportunities for patentable discoveries. In a patent landscape that grows more crowded each year, being able to diversify building blocks gives development teams a distinct edge.
I draw on years in a university lab where half-finished syntheses sat, orphaned, because another intermediate couldn’t unlock the route we envisioned. It’s not about replacing every classic indole; it’s about adding flexibility. The dibrominated analog opens up new coupling strategies, supports asymmetric transformations, and streamlines late-stage functionalization. In team science, where breakthroughs come as much from new ideas as from relentless execution, having access to robust starting materials like this one matters more each year.
Lab safety culture can seem like nothing but poster slogans and endless checklists until an accident wakes everyone up. The halogen atoms increase reactivity but may also raise toxicity and environmental persistence. I’ve personally seen cleanup headaches multiply from careless brominated compound spills—gloves and dust control help, but so does a culture of shared responsibility. From proper labeling to scheduled disposal, steps that might look tedious in the moment seriously pay off over time.
Any chemist working with 4,7-Dibromo-1H-Indole, whether at the benchtop or managing a larger reagent store, will benefit from built-in awareness of its hazards. Small investments—ventilated hoods, spill kits, clear MSDS files—add up to fewer near-misses and less disruption from preventable incidents. Many companies also run in-house refresher training on handling brominated materials. From personal experience, even seasoned professionals can pick up better habits in these sessions.
Research budgets never stretch as far as we’d like. Going cheap on staple intermediates might look appealing, but in practice it leads to more lost reactions, late nights re-purifying failed runs, and stress on project timelines. More than once, I’ve watched colleagues patch together a protocol with off-brand material, only to lose valuable weeks to troubleshooting. With quality 4,7-Dibromo-1H-Indole, the higher upfront investment translates to fewer headaches—and a clearer path to publication or product launch. The longer I’ve worked in this field, the more I see how strategic purchasing of quality intermediates saves more money than it costs.
Not every supplier stocks specialized dibromo-indoles with any regularity. Frequent supply shortages slow down progress and can derail otherwise viable research projects. Building relationships with reliable chemical distributors allows researchers to forecast needs, arrange standing orders, or negotiate for scheduled deliveries. Some labs also team up in consortia or shared purchasing pools to achieve better terms and steady access.
Transparency in delivery times and honest updates about availability help set realistic expectations. I’ve dealt with my share of last-minute supply chain hiccups, and I’ve learned that up-front communication with suppliers often saves more time than frantic calls weeks into an experiment. In my own group, we created a shared spreadsheet to track delivery times, quality issues, and price shifts—with that data, we have sidestepped outages and kept crucial projects moving.
Interest in indole derivatives continues to grow, especially as more academics and industry labs adopt DNA-encoded libraries, high-throughput screening, and artificial intelligence-driven molecule design. The flexibility of 4,7-Dibromo-1H-Indole translates well to these new approaches, where generating many analogs quickly becomes essential instead of optional. Data-driven design cycles grind to a halt if there isn’t a responsive supply chain ready to deliver high-quality building blocks.
Material science teams see new uses, too—innovative organic conductors, dye molecules, and polymers draw on the unique properties of brominated indole rings. Collaborations between academic chemists and engineering groups move faster when foundational materials are widely available, well-characterized, and supported with thorough documentation.
Anyone who’s worked through countless hours in the lab recognizes the value of reagents that don’t fail the moment after purchase. 4,7-Dibromo-1H-Indole’s combination of reactivity, stability, and documentation means more research time gets spent on discovery rather than on damage control. Colleagues working on everything from flavor chemistry to advanced diagnostics have found common ground in the reliability of this intermediate. It underpins better science and smarter process design, which pays off in publications, patents, and practical impact in fields as varied as new medicines and green energy.
From my vantage point, quality chemical intermediates amount to more than just a tick-box purchase. They reflect a deepening commitment to scientific rigor, safety, and collaboration. In the case of 4,7-Dibromo-1H-Indole, its growing adoption signals that the field values intermediates that align with both demanding research agendas and evolving regulatory standards. In every lab where I’ve encountered this compound, the result has always been the same: more options, fewer setbacks, and a growing sense of control in an unpredictable world of discovery.