|
HS Code |
516353 |
| Chemical Name | 4-Bromopyridine Hydrochloride |
| Cas Number | 641-68-9 |
| Molecular Formula | C5H5BrN·HCl |
| Molecular Weight | 210.47 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 200-204°C (decomposes) |
| Solubility | Soluble in water |
| Purity | Typically ≥98% |
| Storage Temperature | Room temperature, protected from moisture |
| Synonyms | 4-Bromopyridinium chloride |
As an accredited 4-Bromopyridine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of 4-Bromopyridine Hydrochloride is securely sealed in an amber glass bottle with a tamper-evident screw cap. |
| Shipping | 4-Bromopyridine Hydrochloride is shipped in tightly sealed containers to prevent moisture exposure and contamination. It is packaged according to relevant safety regulations, labeled with hazard information, and transported under cool, dry conditions. Appropriate documentation accompanies the shipment, ensuring compliance with chemical transportation guidelines and regulations for hazardous materials. |
| Storage | 4-Bromopyridine Hydrochloride should be stored in a tightly sealed container, away from moisture and incompatible substances. Keep it in a cool, dry, and well-ventilated area, preferably at room temperature (15–25°C). Protect the chemical from light to prevent degradation, and ensure proper labeling to avoid accidental misuse. Follow standard laboratory protocols for handling hazardous chemicals. |
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Purity 98%: 4-Bromopyridine Hydrochloride with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Molecular weight 192.47 g/mol: 4-Bromopyridine Hydrochloride with molecular weight 192.47 g/mol is used in heterocyclic compound development, where it provides predictable reaction stoichiometry. Melting point 230°C: 4-Bromopyridine Hydrochloride with a melting point of 230°C is used in solid-phase peptide synthesis, where it contributes to precise temperature control and product stability. Particle size <50 microns: 4-Bromopyridine Hydrochloride with particle size below 50 microns is used in fine chemical manufacturing, where it enables uniform dispersion and enhanced reactivity. Stability temperature up to 120°C: 4-Bromopyridine Hydrochloride with stability up to 120°C is used in catalyst preparation, where it maintains chemical integrity during processing conditions. Moisture content <0.5%: 4-Bromopyridine Hydrochloride with moisture content below 0.5% is used in analytical calibration standards, where it minimizes hygroscopic interference and improves measurement accuracy. Assay (HPLC) ≥99%: 4-Bromopyridine Hydrochloride with assay by HPLC not less than 99% is used in API precursor production, where it guarantees batch-to-batch consistency and regulatory compliance. |
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Each year, research teams and chemical manufacturers face the same puzzle: how to push the limits of molecules, make compounds safer, and build platforms that can handle the growing demands of modern applications. Somewhere along the synthesis chain, 4-Bromopyridine Hydrochloride comes into play. This crystalline white or off-white compound, known for its chemical stability and relatively straightforward handling, offers a starting point for many reactions in both industrial and academic labs. At its core, this chemical stands out by combining the structural benefits of pyridine with the selective reactivity introduced by the bromine atom at the four-position.
There’s a good chance anyone spending time in a bench lab or coordinating batch reactions has come across this compound, sometimes by name, sometimes by structure. What grabs the attention isn’t only the formula—C5H5BrN·HCl—but also the doors it opens for complex synthesis. Whenever chemists seek a practical and efficient route toward more elaborate nitrogen and halide-functionalized molecules, they tend to keep a close eye on compounds like this.
4-Bromopyridine Hydrochloride commonly appears as a white to off-white crystalline powder, with a purity that can climb above 98%, often taken for granted as a benchmark for fine chemical reagents. The melting point hovers around 178–182°C, providing reassurance that it can be handled in typical lab conditions without surprises. Its solubility in water broadens its scope. Many pyridine derivatives trip up in solubility or create headaches for extraction—this one behaves well in both organic and aqueous settings, simplifying post-reaction clean-up and downstream processing.
Experience in the field has shown that small details, like stable melting points and clean color profiles, can indicate higher batch-to-batch consistency. This lets chemists focus on the transformations at hand instead of troubleshooting unexpected byproducts or batch variability. Students often discover early on that working with pure, well-characterized reagents saves time, energy, and resources in the long run.
4-Bromopyridine Hydrochloride regularly features in medicinal chemistry, crop science, and advanced material synthesis. During cross-coupling reactions, especially Suzuki or Buchwald-Hartwig couplings, this compound performs as an effective electrophilic partner. The positioning of the bromine atom makes it easier for metal-catalyzed processes to insert new groups, especially aryl or alkyl fragments.
While students in an undergraduate synthetic lab might encounter it in small-scale experiments, most of the industry demand comes from pharmaceutical development and agrochemical innovation. In these settings, subtle shifts in the pyridine ring can unlock an array of pharmacologically active molecules, enzyme inhibitors, or advanced ligands for organometallic applications. Having spent years troubleshooting reactions in a real-world drug discovery environment, the choices surrounding which halopyridine to use directly impact cost, scalability, and purity of final targets.
In practice, downstream derivatization processes often require selective reactivity. Here this compound’s balance of reactivity and stability stands out. The hydrochloride salt not only improves handling—minimizing unpleasant odors and workplace exposure—but also mitigates dustiness and static charging. Many older bromopyridines in free base form either sublimed away, worsened exposure, or increased the risk of product loss. With this hydrochloride, there’s greater peace of mind in both bench-top work and pilot-scale runs.
Other halogenated pyridines, such as 2-bromopyridine or 3-chloropyridine, serve overlapping but distinct functions. Their pattern of reactivity changes as the halogen moves around the pyridine ring. For example, 2-bromopyridine tends to behave differently in cross-coupling since the adjacent nitrogen can strongly influence metal activation and positional selectivity. By moving the bromine to the four-position, this compound strikes a more controlled reactivity, which translates into cleaner, higher-yielding reactions in many settings.
In stories from the lab, the function of the hydrochloride salt again comes up. Free bases sometimes absorb water from the air and turn oily or degrade, muddying up workups and product purifications. As the hydrochloride, 4-Bromopyridine holds its form, which matters a lot during storage and during long experiments in humid environments. Even minor process improvements can have large effects across hundreds of kilos of material.
Anyone who has spent time in regulatory-driven spaces, such as pharmaceutical quality control, will recognize how difference in reagent lots can disrupt entire project timelines. Many pyridine derivatives, including this one, find their way into active ingredient synthesis or intermediates for regulated industries. Each batch needs to deliver on purity, documented traceability, and predictable impurity profiles to clear quality audits and ensure consumer safety. Here, the proven track record of 4-Bromopyridine Hydrochloride from reputable suppliers becomes a form of risk mitigation, cutting down surprises in analytical results or scaling hiccups.
Even on the academic side, research reproducibility stands or falls on the back of functional and reliable starting materials. Projects that try to build new ligand scaffolds, medical imaging agents, or agrochemical active ingredients need to know what’s in the bottle and what will actually react. Specifications like exact weight, water content, and residual solvents need to be trusted, or the chemistry can easily go off-course. Mistakes or surprises mean time and money lost, sometimes for weeks or months. The corrosive experience of re-running failed syntheses leaves lasting lessons in the value of well-characterized, certified reagents.
While some reagents demand glove box handling or specialty ventilation, this hydrochloride version of 4-Bromopyridine allows for routine use in fume hoods or standard lab setups. The risk profile is less intense compared to free pyridine derivatives, in part because the hydrochloride makes the compound less volatile and easier to scoop or weigh. For many years, this simple property has saved headaches and preserved lab safety, especially in teaching environments or process labs moving larger quantities.
The material can be weighed, dissolved, and transferred like any ordinary laboratory salt. Water solubility makes it straightforward to use in both polar and mixed solvent systems. In my own experience running student labs, switching to this salt has cut down on odor complaints and accidental spills, which can become real workflow problems with bulkier or smellier alternatives.
Beyond its textbook cross-coupling reactivity, 4-Bromopyridine Hydrochloride sees steady action in nucleophilic substitution and palladium-catalyzed transformations. This utility feeds directly into the creation of novel heterocyclic scaffolds that underpin pharmaceutical and material innovations. Chemists often prefer halogenated pyridines because selective functionalization allows tuning of molecular properties: electron density, binding pocket fit, water solubility, or lipophilicity.
In academic research, the same compound sees use in synthesizing ligands for catalysis, chiral auxiliaries, and even advanced dyes or imaging labels. The practical aspects, such as ease of workup and compatibility with standard glassware and solvents, let bench scientists focus on pushing the science forward. Students get a leg up in learning reproducible, scalable reaction techniques by engaging with stable and reliable sources of such reagents.
Decades of industrial experience have shown that regulatory scrutiny around pyridine derivatives calls for clear documentation and safety metrics at every stage. 4-Bromopyridine Hydrochloride tends to present fewer transportation and storage challenges than some other less stable pyridines. The stability as a hydrochloride salt means fewer surprises with packaging or shipment, especially for firms sending materials globally.
Material Safety Data Sheets underline the usual precautions: avoid ingestion, minimize direct contact, use standard personal protective gear. With the proper protocols, risks are manageable and well-understood in the community. This practical reality encourages broader use not just in cutting-edge pharma, but also in agricultural chemistry and university teaching.
The global chemical industry faces rising pressure to minimize environmental impact. Pyridine chemistry, especially older processes, sometimes left behind toxic byproducts or involved hazardous intermediates. 4-Bromopyridine Hydrochloride offers a better-balanced profile. Many cross-coupling reactions now use greener solvents, optimized catalyst loading, and reduce hazardous waste, leaning on predictable salts and halides for efficiency.
From personal observation, the move towards more stable, less volatile intermediates like this hydrochloride has already contributed to lower fume emissions, reduced handling incidents, and a cleaner bench culture. Industrial players and academic research alike share a stronger focus on recycling solvents, reusing side streams, and pushing for green chemistry approaches—often enabled by more forgiving, robust reagents like 4-Bromopyridine Hydrochloride.
Global events have a way of disrupting chemical supply chains, sometimes stranding dozens of research projects or pharmaceutical campaigns. The standardized, well-documented production of 4-Bromopyridine Hydrochloride helps reduce that fragility. Reliable specification sheets, well-calibrated logistics, and a network of trusted suppliers mean this compound often remains available where others stumble during shortages or transportation bottlenecks.
Experienced research managers understand the difference between a robust supply of key building blocks and an unpredictable pipeline. The stress from material disruptions can echo across a project, impacting development timelines years down the road. In tough times, access to a high-purity, stable intermediate like this one lets innovation continue, avoids expensive project resets, and empowers both routine and high-stakes chemistry.
Lab teams frequently debate the right reagents for scaling up syntheses or troubleshooting roadblocks in complex routes. A compound like 4-Bromopyridine Hydrochloride demonstrates its value when batch size increases or process impurities threaten product quality. Because the hydrochloride salt format is less hydroscopic and possesses a tightly controlled impurity profile, process development chemists breathe easier during regulatory or customer audits.
It helps, too, that this compound does not bring surprise safety or compatibility issues with standard glass, plastics, or solvent systems. Even subtle changes—from switching free base to hydrochloride salt—can save countless hours of purification and validation work. For those developing new catalyst systems or optimizing yields in high-throughput environments, the reproducibility of 4-Bromopyridine Hydrochloride remains a competitive advantage.
Years of hands-on synthesis have highlighted how modest improvements in material consistency, handling safety, and documentation shorten the learning curve for new staff while preserving quality on established projects. This saves both money and frustration, as well-articulated handling and analytical protocols become part of institutional knowledge across chemistry teams.
While much of the buzz around 4-Bromopyridine Hydrochloride centers on pharmaceutical research, its reach has quietly expanded. Agrochemical companies and advanced materials firms increasingly rely on well-characterized intermediates to meet regulatory standards and market demands. Improvements in crop protection or plant growth additives often trace back to innovations in heterocyclic chemistry. Switching to more reliable halopyridines like the hydrochloride has tangibly improved development cycles, reduced rework, and enhanced products aimed at a rapidly evolving agricultural market.
Meanwhile, research in electronics and battery technology pushes the envelope on new conductive polymers, ligands, and redox-active cores. Pyridine derivatives, and especially well-behaved brominated options, show up in early-stage material screening and process development. The combination of purity, solubility, and manageable disposal sets a new standard for intermediates tailored to emerging industries.
Sustainable progress in chemistry rarely boils down to one new discovery or trick reagent. Rather, it reflects a thousand small decisions: choosing robust, safe intermediates; insisting on full documentation; making careful process optimizations at each stage. 4-Bromopyridine Hydrochloride isn’t flashy, but its reliability, consistency, and compatibility build the foundation for meaningful advances both in labs and on production lines.
Those new to synthetic chemistry often find swift success with this reagent because predictable behavior underpins skill development and process troubleshooting. In large organizations and lean startup labs alike, the same basic truth remains: high-quality inputs return dividends in both scientific achievement and business outcomes. Fewer failed batches translate to faster commercial launches, while improved occupational health profiles keep teams motivated and engaged. As cross-disciplinary projects stretch from medicine to agriculture to electronics, simple choices like reaching for well-characterized, stable intermediates keep chemists ready to meet new challenges.
From leading-edge pharmaceutical research to practical teaching labs, 4-Bromopyridine Hydrochloride has secured its place as a quiet enabler of chemical progress. Its mix of chemical flexibility, handling safety, and proven quality control standards supports a culture of excellence. Having spent considerable time in both hands-on synthesis and managerial oversight, it’s clear that success often unfolds from such reliable tools. As the global demand for innovative, sustainable chemicals grows, the significance of proven intermediates—delivering on quality, safety, and traceability—only grows.