|
HS Code |
598715 |
| Product Name | 3-fluoro-4-chloropyridineHCl |
| Molecular Formula | C5H3ClFN·HCl |
| Appearance | White to off-white solid |
| Cas Number | 252916-29-3 |
| Purity | ≥98% |
| Melting Point | 163-167°C |
| Solubility | Soluble in water and DMSO |
| Storage Temperature | 2-8°C |
| Synonyms | 3-fluoro-4-chloropyridine hydrochloride |
| Inchi Key | FAIXPCOKCZJVKN-UHFFFAOYSA-N |
| Smiles | C1=CN=CC(=C1Cl)F.Cl |
As an accredited 3-fluoro-4-chloropyridineHCl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 3-fluoro-4-chloropyridineHCl, sealed with a screw cap and labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-fluoro-4-chloropyridine HCl ensures safe, moisture-free bulk packing with secure palletization for efficient shipping. |
| Shipping | 3-Fluoro-4-chloropyridine hydrochloride is shipped in tightly sealed containers, protected from moisture, light, and incompatible substances. It is packaged according to regulatory guidelines for hazardous chemicals, typically using robust, leak-proof bottles with clear labeling. Transportation complies with relevant safety regulations to minimize risk during handling and transit. |
| Storage | **3-Fluoro-4-chloropyridine HCl** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers and bases. Protect from direct sunlight and sources of heat. Ensure proper labeling and restrict access to authorized personnel only, following standard chemical storage guidelines for hazardous substances. |
| Shelf Life | 3-Fluoro-4-chloropyridine HCl is stable for at least 2 years when stored tightly sealed at room temperature, away from moisture. |
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Purity 98%: 3-fluoro-4-chloropyridineHCl with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures reproducible yield and product consistency. Melting Point 195°C: 3-fluoro-4-chloropyridineHCl featuring a melting point of 195°C is used in organic synthesis, where superior thermal stability prevents decomposition during high-temperature reactions. Particle Size <10 μm: 3-fluoro-4-chloropyridineHCl with particle size less than 10 μm is used in fine chemical production, where smaller particle size enables rapid dissolution and homogeneous reaction kinetics. Moisture Content <0.2%: 3-fluoro-4-chloropyridineHCl with moisture content below 0.2% is used in catalyst precursor formulation, where low moisture reduces unwanted hydrolysis and side products. Stability Temperature 70°C: 3-fluoro-4-chloropyridineHCl stable up to 70°C is used in agrochemical intermediate manufacturing, where temperature stability maintains molecular integrity under processing conditions. |
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In a world where chemical advances shape not only science but daily life, compounds like 3-fluoro-4-chloropyridineHCl quietly support innovation across medicine, agriculture, and materials research. Working hands-on in a research lab, I’ve seen how the choice of an intermediate shapes everything that comes after. Each decision in that process, from purity to functional groups, drives both success rates and the reliability of downstream products. 3-fluoro-4-chloropyridineHCl, by offering a well-balanced combination of reactivity and stability, helps chemists sidestep common bottlenecks seen with less reliable analogs.
3-fluoro-4-chloropyridineHCl stands apart through the distinctive pairing of fluorine and chlorine on the pyridine ring—a structure familiar to anyone working with nitrogen heterocycles. This compound, whose molecular formula is C5H3ClFN·HCl, presents a sharp tool for those fine-tuning selectivity or seeking new pharmacophores in medicinal chemistry. Its hydrochloride form increases water solubility and simplifies handling when compared to the free base, attributes that become crucial during scale-up and synthesis steps.
In practical experiments, I’ve noticed that the hydrochloride salt prevents the formation of airborne dust, which can be a real issue with light, crystalline substances. That kind of detail doesn’t end up in flashy brochures but matters a great deal for safe working habits over years in the lab.
Specifications for this compound build confidence for researchers counting on reproducibility. Purity often reaches above 98 percent, which reduces concerns about side-products interfering during synthetic reactions. Melting point and solubility data aren’t just technical trivia—they mean less troubleshooting, more predictable purification, and faster results during testing.
Few things frustrate researchers like unknown impurities throwing off bioassay outcomes or chromatography results. I’ve run TLCs and HPLCs on batches from different suppliers and found a marked variance in peak clarity. High-purity batches of 3-fluoro-4-chloropyridineHCl hold their own in both academic and industrial settings where reliability wins out over untested bargain options.
Outside the pages of chemistry textbooks, 3-fluoro-4-chloropyridineHCl plays a hands-on role in drug discovery and fine chemical production. Medicinal chemists often look at the pyridine scaffold as a backbone for bioactive molecules. By swapping in fluorine and chlorine, they alter electronic properties and metabolic pathways—a crucial step in developing new therapeutics. In my own experience, building selective kinase inhibitors starts with smart intermediates like this one.
Beyond pharmaceuticals, this compound gets picked up in agrochemical research, where modifying the substitution pattern on the ring aids in finding pesticides with safer profiles and less environmental persistence. Material scientists push its limits when engineering polymers or specialty additives, exploiting the combination of halogens to adjust thermal and electrochemical properties.
Pyridine rings get a lot of attention due to their versatility, but not all substitutions yield the same results. When I first began screening for building blocks, I learned fast that changing the positioning and nature of substituents provides chemists with more than just incremental options. With 3-fluoro-4-chloropyridineHCl, the combined effects of fluorine’s electron-withdrawing strength and chlorine’s unique sterics deliver nuanced reactivity.
Contrasting this compound with unsubstituted pyridine or even 3-chloro-4-fluoropyridine, you get not just shifts in how fast reactions proceed but different outcomes altogether. Fluorine’s influence can make oxidative steps more controlled, while chlorine offers an anchor for palladium- or copper-catalyzed couplings. Some alternate derivatives lack this flexibility, leading to lengthy detours or undesired side chains. Consistency matters: using the hydrochloride form means moisture uptake is better managed than with hydrophobic analogs, streamlining both storage and formulation.
Pharmaceutical patents stand on the shoulders of small molecular changes that often begin with compounds like this. In an industry governed by regulatory expectations, starting clean and consistent protects timelines and ultimately patients. One of my colleagues recently recounted a batch rejection traced to an intermediate with trace solvent residues—problems that might be overlooked early but can shut down a product launch if caught later. By choosing a product with transparent specifications like melting point, purity limits, and analytical traceability, researchers avoid costly missteps.
Analytical chemists appreciate the clarity that a well-characterized starting material brings to their workflows. During method development, traceable impurities can confound interpretations in NMR, LC-MS, or IR readings. Having worked through numerous troubleshooting sessions, I’ve learned that investing in high-quality reagents saves more resources than it costs.
Young scientists sometimes underestimate the impact of starting materials on the reproducibility of their results. In my own work, early efforts using off-brand pyridine derivatives led to inconsistent yields and rare, unexplained byproducts. These headaches led to delays and even dead-ends in promising research. 3-fluoro-4-chloropyridineHCl, when purchased from suppliers with strong QC programs, delivers batch-to-batch consistency that supports reliable method development—a must for researchers preparing data for publication or submission to regulatory bodies.
In industry, development pipelines routinely see setbacks from subtle differences in intermediate quality. Observing the success rates of teams who focused on refining their material sources compared to those taking shortcuts, it becomes clear that better reagents shape better projects. Large-scale workflows often incorporate feedback from hands-on chemists who know the stakes of trace contamination or minor process drifts.
I’ve spoken with research pharmacologists who point to 3-fluoro-4-chloropyridineHCl as a reliable partner in heterocyclic syntheses. Small-molecule library construction, a foundation for bioactivity screening, relies on a short list of robust intermediates. By using this compound, researchers sidestep complications like inconsistent coupling efficiency or excessive side product formation, which often plague less-refined analogs.
In academic labs, the compound sees steady use in building blocks for cross-coupling reactions, enabling the insertion of new functional groups with minimal unwanted interactions. The combination of the hydrochloride salt’s ease of handling and its reactivity under Suzuki, Buchwald-Hartwig, and Ullmann conditions makes it especially popular among synthetic chemists starting new exploratory work.
Agrochemists highlight this molecule’s role in developing next-generation crop protection agents. As global challenges shift toward sustainability, finding intermediates that balance efficacy with rapid biodegradation becomes a worthy pursuit. The unique halogen pattern on this pyridine ring can promote faster degradation in soil, depending on downstream modifications—a trend worth watching as the regulatory landscape tightens around persistence.
With chemical progress comes responsibility. The use of halogenated aromatics attracts scrutiny from both environmental agencies and internal safety committees. Disposal and recycling processes must evolve as usage expands. Facilities adopting 3-fluoro-4-chloropyridineHCl on a large scale invest in improved ventilation and waste treatment, making sure that worker exposure and environmental release are contained.
Some newer labs implement green chemistry protocols by integrating reagent recovery and recycling into their daily routines. When buying or using halogenated intermediates, organizations now factor in lifecycle cost and impact, not just the up-front order price. Safety trainers often remind younger colleagues to respect not only local regulations, but also best practices that protect shared workspaces. Transparent sourcing, clear labeling, and regular audits go hand-in-hand with sustainable chemical progress.
In conversations with colleagues in regulatory affairs, I’ve seen documentation and audit trails become growing priorities. As the importance of safety data sheets grows and regulators require more transparency, knowing exactly how each batch matches specifications is a baseline expectation. Trusted suppliers incorporate independent lab verification or ISO certification, anchoring the whole supply chain in proven best practice.
Chemical research isn’t merely about speed; it’s shaped by foresight, judgment, and adaptation. Looking at the role of 3-fluoro-4-chloropyridineHCl in developing novel therapeutics, crop protection solutions, or new specialty materials, you realize the link between high-quality reagents and discovery itself. I’ve worked with teams who make reagent selection a priority. Their reliability rates, measured in publication acceptances and successful grant renewals, show the payoff of such diligence.
Peer-reviewed studies frequently highlight the subtle but crucial effects that halogenated pyridines exert on biological pathways. Differences in logP, pKa, and metabolic stability become the foundation for completely new lines of inquiry. Students working on their first syntheses often learn this lesson quickly—the wrong intermediate can tie up resources and result in negative data, while the right choice opens doors.
As chemical supply chains grow more sophisticated, the differences between off-the-shelf and customized production shrink. Organizations willing to invest in batch-specific documentation or impurity profiling end up with greater leverage, cutting risk and shortening timelines. Researchers who use verified, fully characterized intermediates position themselves as more reliable partners for collaborations or funding.
While the standard for reagents has grown, there’s always room for improvement. Suppliers looking to set themselves apart provide extra details beyond minimum specs—traceability, comprehensive impurity profiles, and stability data. Forward-thinking organizations encourage open reporting of unexpected findings, be they crystal anomalies or solubility shifts, creating feedback that strengthens products at every level.
Teams can lobby for greater transparency from their procurement offices. I’ve worked in environments where side-by-side bench testing of two suppliers uncovered not just purity differences but ease-of-use features, such as packaging that resists humidity or spills. Those kinds of discoveries trickle upward, shaping policy and, ultimately, end-user satisfaction.
Researchers play a proactive role as well—documenting and publishing not only their synthetic successes but the challenges and failures linked to reagent quality. As open-access chemical data grows, broader communities benefit, building collective knowledge that helps everyone avoid hidden pitfalls or leverage new opportunities.
Some innovators are now working with green chemistry organizations to develop new, less hazardous pyridine intermediates. Their progress could someday lessen the reliance on halogenated compounds altogether. Until then, opting for more thoroughly documented and higher-quality products like 3-fluoro-4-chloropyridineHCl can serve as one turning point—one that paves the way for responsible, state-of-the-art research and safer, more reliable chemical production.
3-fluoro-4-chloropyridineHCl doesn’t carry the flash of brand-name drugs or market-ready agrochemicals. Instead, it sits quietly in the background, making breakthroughs possible by serving as a dependable stepping stone. Its blend of chemical stability, clean reactivity, and reliable supply positions it not just as a commodity, but as a real asset to forward-looking research organizations and businesses. Through careful sourcing and attention to every detail, scientists and industry professionals can shape better outcomes—for themselves, for the people counting on their products, and for the environment.