|
HS Code |
584679 |
| Iupac Name | 3-chloro-4-bromobenzonitrile |
| Molecular Formula | C7H3BrClN |
| Cas Number | 17201-42-4 |
| Appearance | White to off-white solid |
| Melting Point | 84-88°C |
| Density | 1.71 g/cm³ (estimated) |
| Solubility In Water | Insoluble |
| Purity | Typically ≥98% |
| Smiles | N#Cc1ccc(Cl)c(Br)c1 |
| Flash Point | >110°C (estimated) |
| Storage Conditions | Store in a cool, dry, well-ventilated place |
| Ec Number | 695-060-8 |
As an accredited 3-Chloro-4-Bromobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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| Shipping | |
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Every manufacturing floor has its workhorse materials, and 3-Chloro-4-Bromobenzonitrile keeps showing up where serious synthesis happens. With its molecular formula of C7H3BrClN and a CAS number recognized in labs worldwide, this compound draws attention for more than just its formula. Chemists have trusted it for building aromatic rings, tackling pharmaceutical research, and making robust investigations possible in the agrochemical sector. I remember my early days in the lab, hesitating to handle halogenated benzonitriles—until repeated, reliable outcomes with this molecule dissolved any doubt.
You can spot 3-Chloro-4-Bromobenzonitrile as an off-white to almost light-tan solid at room temperature. The melting point generally falls just under 80 degrees Celsius. This isn’t the sort of powder that clumps up or creates confusion at the scale-up phase. It dissolves readily in most polar aprotic solvents, including DMSO and DMF, which earns it points among process engineers. Compared with standard benzonitriles, it resists hydrolysis better, making cleanup and downstream filtering easier. That sort of reliability is what lets production chemists stick with this ingredient when margins are tight and deadlines approach.
What keeps 3-Chloro-4-Bromobenzonitrile in demand is the functional group pairing. Chlorine and bromine substituents line up ortho- and meta- to the nitrile, which means you can jump right into cross-coupling reactions knowing you’ve got flexibility on the aryl halides. I’ve watched teams use this molecule to anchor Suzuki and Buchwald-Hartwig couplings, creating complex heterocycles in shorter steps. In pharmaceutical discovery, custom analogues often get their core structure from scaffolds like this, allowing project leads to iterate on promising leads without redrawing their process map every time.
Agrochemical companies turn to 3-Chloro-4-Bromobenzonitrile when screening for new herbicide backbones. It handles elevated temperatures in reactors without shifting or forming stubborn byproducts. When your tech transfer team spends less time debugging workups, there’s room for additional screening cycles and exploratory chemistry. That's how advances in crop protection chemicals have become more rapid, and why this compound rarely sits on warehouse shelves for long.
For companies deciding between halogenated benzonitriles, it’s easy to ask whether this variant actually changes things. Experience shows it matters, especially when you demand selectivity in metal-catalyzed substitution. The difference between 3-Chloro-4-Bromobenzonitrile and a plain bromobenzonitrile may seem small on a data sheet, but anyone who’s been through a failed coupling underlines it. Even subtle shifts on the aromatic ring can make or break scale-up. Double halogenation as seen here allows options at both ortho- and para- positions, opening up routes to specialty products that single-substituted nitriles cannot provide.
Economics plays a role too. Even as raw material prices fluctuate, the synthetic route using this intermediate often proves more cost-efficient because you skip lengthy protecting group strategies. Several of my colleagues have cut step counts in pilot projects by switching over to it instead of piecing together less reactive, single-halide aromatics. Fewer steps don't just mean cost savings—they mean less environmental load, lower energy use, and safer working conditions. That’s become more important as regulations tighten on solvent use and hazardous waste.
Labs that run comparative NMR and GC-MS on incoming batches tend to note high purity levels when sourcing from established suppliers. Most analytical spec sheets show purity upwards of 98 percent, which limits troubleshooting and keeps R&D teams from chasing phantom impurities. Stability on the shelf gains extra points, too. In practical terms, the compound rarely shows discoloration or aggregation over reasonable storage intervals. That predictability directly benefits flow chemistry applications, which demand feedstocks with minimal batch-to-batch drift.
I remember a scaled-up run for an exploratory pharmaceutical program where we switched to this compound halfway through the lead series campaign. The change saved hours—and plenty of frustration—when we didn’t see variable breakdown products after weeks of storage or rigorous downstream handling. Those kinds of process improvements stick with you, especially in industries where speed and reproducibility drive profits.
Plenty of university labs feature 3-Chloro-4-Bromobenzonitrile on their order forms for undergraduate and graduate experiments. In my experience, students pick up basic skills in functional group transformation while also being exposed to modern cross-coupling techniques. Instructors prefer it for advanced coursework because the compound behaves in line with published literature and provides clear pathways to verification. Lab managers appreciate the compound’s manageable environmental profile. While no material is hazard-free, clear labeling and robust supplier documentation help maintain high safety standards within academic settings.
In the world of dyes and material science, the compound supports the build-out of new pigments with fine-tuned optical properties. Research teams looking to design organic light-emitting diodes or investigate thin-film semiconductors turn to such nitriles for core building blocks. That’s an example of industry technology pulling from the same toolkit as pharmaceutical researchers. As the push for more sustainable, efficient electronic materials grows, the need for aromatic frameworks that tolerate both heat and moisture becomes sharper.
Almost every project manager I’ve dealt with over the years asks about compliance: what about REACH, what about inventory limits, what about downstream product registration? In the case of 3-Chloro-4-Bromobenzonitrile, chemical safety and regulatory records are well documented by most recognized suppliers. Having reliable analytical documentation—like certificates of analysis with batch-level transparency and documentation on residual solvents—can make or break a multinational supply agreement. Such transparency stems not from regulations alone, but from supplier experience in international markets where the cost of a recall or resynthesis quickly outweighs up-front diligence.
Smaller companies also benefit. With rising pressure to trace and limit toxic or persistent organic pollutants, showcasing responsible sourcing and lifecycle documentation wins points during audits. Suppliers offering this compound at tight specification tolerances can open new doors for collaborations, especially in the European and Asian chemical markets where traceability has become non-negotiable.
Whether a team is working in a small custom batch facility or ramping up for large-scale commercial production, the role of intermediates like 3-Chloro-4-Bromobenzonitrile continues to expand. Startups in the green chemistry space have explored direct functionalization routes using this compound, where avoiding extra purification steps lines up with their mission to lower waste. Some have reported stepwise reductions in overall process time after moving away from labor-intensive, multi-reagent procedures. Those anecdotes resonate with any chemist who’s watched a night-shift operator get bogged down in unnecessary processing.
The real innovation appears when project timelines shrink as synthesis gets more streamlined and flexible. Holding inventory of a flexible intermediate makes exploratory research less risky. Teams can change course or chase promising new targets without waiting on a custom precursor run. This isn’t just a convenience; fast pivots in R&D can mean the difference between winning a patent race and playing catch-up with competitors.
Despite the clear benefits, there are issues not to brush aside. Halogenated aromatics—while useful—raise concerns about environmental impact and worker exposure. Waste disposal, effluent cleanup, and long-term persistence need careful management, especially at scale. While many facilities now use closed-system handling, older facilities or resource-limited startups might struggle to match those safety protocols. Responsible suppliers outline both risks and best practices, and ongoing hazard communications remain a priority for any manager who wants to avoid downtime or incidents.
Pricing pressure sometimes nudges companies toward less rigorously characterized intermediates, tempting buyers to accept the risk of variable impurity profiles. I’ve seen projects stall due to impurities carried over from substandard batches, forcing a return to better-documented sources. The lesson rings clear: for critical steps, you can’t shortcut transparency or quality control. Emerging green chemistry regulations are motivating the industry to phase in less hazardous or more recyclable intermediates, so this landscape will shift with time—but right now, tight process control remains king.
For those ordering 3-Chloro-4-Bromobenzonitrile for the first time, or looking to switch suppliers, the checklist begins with purity data but goes much further. Look closely at supplier track records for on-time deliveries, batch consistency, and technical support. Is documentation easily available? Will the supplier walk through analytical data, or do they brush off questions with assurances alone? Genuine partners engage openly, helping customers interpret complex issues like minor impurity spikes or supply chain disruptions.
For smaller buyers, group purchasing through established procurement networks can mean bulk rates without sacrificing traceability. I’ve seen contract manufacturers cut their inventory carrying costs in half by pooling orders and locking in fixed-term contracts. Large buyers benefit most from supplier alignment in EHS (environment, health, safety) practices, where shared responsibility for worker safety and emissions control builds trust on both sides of the table.
From a manufacturing angle, every batch counts. Top management in chemical production recognizes the push toward sustainability, but operational teams know that a stable, easy-to-purify intermediate drives productivity and profits. Fewer steps mean shorter downtimes, fewer storage tanks tied up, and more consistent output. Reliable melting point and solubility data mean predictable phase behavior in reactors, and engineers can run at higher throughput without risking plugged filters or contaminated side streams.
Blending new production technologies—including flow chemistry and real-time monitoring—into older processes runs more smoothly with intermediates like this, which do not introduce unexpected handling issues. A robust intermediate supports both batch and continuous processes, improving plant flexibility and hedging against unexpected swings in customer demand. The move toward digital process monitoring amplifies these benefits, since tighter process windows and automated alerts hinge on consistent product quality.
Future directions will focus more sharply on the sustainability profile of 3-Chloro-4-Bromobenzonitrile. Industry groups are encouraging greener halogen sources and investigating waste minimization across the supply chain. Smart sourcing now means not just price checks, but close collaboration with suppliers offering lifecycle analysis or lower-carbon-footprint production plants.
This echoes where chemical intermediates must go—toward less resource-intensive manufacturing. Labs and companies leading with sustainability often share best practices and press for supplier innovation, using their purchasing power to demand more transparency and continual improvement. By supporting such suppliers and sharing lessons learned in waste minimization, the sector can reduce the environmental load without compromising research or production flexibility.
3-Chloro-4-Bromobenzonitrile stands as a reliable, versatile intermediate for those who know how much downstream work depends on a handful of rock-solid inputs. From pharmaceutical research to material science, its unique pairing of halogens combined with the nitrile group shapes countless synthetic platforms. As environmental, safety, and regulatory standards rise, it’s reassuring for buyers and R&D leads to count on suppliers committed to quality, transparency, and continual improvement. Drawing on both lab and industry experience, it’s clear that the right intermediate isn’t just another stock item—it’s the cornerstone of innovative chemistry with an eye toward a safer, more sustainable future.