|
HS Code |
303229 |
| Product Name | 4-Chloropyridine HCL |
| Chemical Formula | C5H4ClN·HCl |
| Molecular Weight | 164.00 g/mol |
| Appearance | White to off-white crystalline powder |
| Cas Number | 6289-13-4 |
| Melting Point | 209-213°C |
| Solubility | Soluble in water |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, in a tightly closed container |
| Synonyms | 4-Chloropyridinium chloride |
| Odor | No significant odor |
| Ph | Acidic (in aqueous solution) |
| Stability | Stable under recommended storage conditions |
| Hazard Classification | Irritant |
As an accredited 4-Chloropyridine HCL factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Chloropyridine HCl is supplied in a 25g amber glass bottle, securely sealed, with hazard and product identification labels. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-Chloropyridine HCL ensures secure, efficient packing of bulk chemical drums for safe international transport. |
| Shipping | 4-Chloropyridine HCl is shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. Packaging complies with international regulations for hazardous materials, ensuring safe transport. The compound is shipped under ambient conditions with proper labeling, safety documentation, and handling instructions to ensure compliance and safe delivery. |
| Storage | 4-Chloropyridine HCl should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area. Protect the chemical from moisture and direct sunlight. Store away from incompatible substances such as strong oxidizers and acids. Always ensure proper labeling and limit exposure to air to prevent degradation. Follow all relevant safety protocols and local regulations when storing. |
| Shelf Life | 4-Chloropyridine HCl typically has a shelf life of 2–3 years if stored in a cool, dry, tightly sealed container. |
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Purity 99%: 4-Chloropyridine HCL with purity 99% is used in pharmaceutical intermediate synthesis, where high-purity ensures minimal impurity propagation. Melting Point 235°C: 4-Chloropyridine HCL with a melting point of 235°C is used in high-temperature organic transformations, where it demonstrates superior thermal stability during processing. Particle Size <10 µm: 4-Chloropyridine HCL with particle size less than 10 µm is used in catalyst preparation, where fine particle distribution promotes enhanced surface reactivity. Moisture Content <0.5%: 4-Chloropyridine HCL with moisture content below 0.5% is used in agrochemical manufacturing, where low moisture prevents unwanted hydrolysis and increases yield. Stability at 60°C: 4-Chloropyridine HCL with stability at 60°C is used in long-term reagent storage, where sustained chemical integrity is maintained under elevated conditions. Assay 98% (HPLC): 4-Chloropyridine HCL with 98% assay by HPLC is used in specialty dye synthesis, where accurate concentration ensures reproducible colorimetric properties. Residual Solvent <0.2%: 4-Chloropyridine HCL with residual solvent content less than 0.2% is used in active pharmaceutical ingredient production, where low solvent residues comply with regulatory safety standards. pH 3.5 (1% Solution): 4-Chloropyridine HCL with a pH of 3.5 in 1% solution is used in laboratory titration processes, where controlled acidity enables precise analytical measurements. |
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In almost every chemical laboratory, researchers look for compounds that offer reliability and flexibility. 4-Chloropyridine HCl earns its place on the shelf because of its steady performance in a range of synthesis pathways. This compound, which presents as a solid hydrochloride of 4-chloropyridine, allows chemists to tap into the reactive pyridine core while harnessing the stabilizing benefits of the hydrochloride form.
The typical model for 4-Chloropyridine HCl available in the market is the crystalline, white to off-white powder. You can see its purity on the label, usually over 98%, which means little wasted effort on purification. Chemists who specialize in the design of new pharmaceuticals or specialty materials rely on purity, since stray contaminants can disrupt downstream reactions, waste reagents, and confound results. Experience in a university research group has shown me how even small lapses in reagent quality translate to hours of extra troubleshooting, so sticking to high-assay products ends up saving both sanity and money.
4-Chloropyridine HCl distinguishes itself with straightforward physical specs that lab technicians value: a firm melting point, easy handling, and solubility that works well with both water and organic solvents. The boiling point doesn’t usually come into the routine discussion, because most users are interested in reactivity, stability, and storage rather than distillation. The compound’s solid, granular texture keeps spills rare and allows precise measurement — vital in environments where scaling up means managing hundreds of grams at a time.
One factor overlooked is stability, especially in labs without ideal storage. 4-Chloropyridine HCl resists atmospheric moisture and doesn’t cake up as quickly as freebase variants. In settings where humidity runs high or storage rooms heat up in summer, this durability ensures consistent dosing. A former colleague in process chemistry once said, “Any product that can survive Michigan summer is all right by me,” noting fewer headaches from batch-to-batch inconsistencies.
Modern synthetic chemistry leans on 4-Chloropyridine HCl for its versatility. This compound finds widespread use as an intermediate. Pharmaceutical scientists see it as a key building block for creating small, arylated or heterocyclic molecules. It often shows up in projects aiming to introduce halogenated pyridine structures into drug candidates, agricultural chemicals, or advanced materials.
My own encounters with this product came during a project building new antimalarial scaffolds. We valued 4-Chloropyridine HCl for the straightforward way it allowed us to insert a 4-chloropyridyl unit with minimal side reactions, especially when compared to analogs that caused competitive substitution. Pyridines challenge many synthetic chemists because their nitrogen can act in unpredictable ways during metal-catalyzed processes, but the hydrochloride salt keeps impurities in check and behaves with more predictability under palladium catalysis.
Outside pharmaceuticals, materials scientists working on advanced polymers use the same compound as a precursor for specialty ligands, coordination complexes, and tuning optoelectronic properties. The hydrochloride salt helps maintain reproducibility — the difference between a functioning device and wasted trial runs can rest on reagent consistency.
The synthetic landscape bursts with pyridine derivatives, each tailored for specific tasks. What sets 4-Chloropyridine HCl apart is its balance of reactivity and manageability. Freebase 4-chloropyridine, often available as a liquid or semi-crystalline solid, comes with a sharp odor, higher volatility, and increased handling risks. Hydrochloride salts do away with some volatility, offering a lower hazard rating for day-to-day work, which makes a real difference for crowded benchtops in academic labs or production facilities.
Take, for comparison, 2-chloropyridine derivatives. While they offer certain unique coupling opportunities for biaryls and heterocycles, their positional isomerism tends to complicate downstream reactions due to electronic and steric factors. The 4-chloro isomer sits right for para-substitution and delivers more straightforward patterns in cross-coupling, nucleophilic aromatic substitution, or directed ortho-lithiation. Years of trial-and-error in medicinal chemistry have reinforced the reliability of the para-chloro-pyridine motif, especially when the goal is to maintain a clear, single pathway in multistep synthesis.
Pyridine hydrochloride, the parent salt, lacks the halogen’s distinct electronic signature and is less useful for structures seeking increased lipophilicity or specific electronic effects. Chlorinated derivatives, like 4-Chloropyridine HCl, strike a valuable middle ground: they permit clean functional group interconversion while preserving the rings’ core reactivity.
Purchasing department decisions often skate past the human consequences of low-quality intermediates. Early in my career, we learned the hard way that a 95% purity sample cost us weeks. Unexpected side-products gummed up our chromatography, and repeat syntheses wasted thousands. With 4-Chloropyridine HCl, consistent high-purity batches dry and stable in routine conditions free teams to focus on the real work: innovation and discovery.
Producers who prioritize stringent manufacturing — including careful crystallization, rigorous quality control, and batch testing for residual solvents — turn out a better lot. Trust forms around suppliers who invest in process transparency and consistent outputs, not just the lowest sticker price.
Regulations in pharmaceutical and specialty chemical manufacturing set strict requirements for trace contaminants, especially for scale-up and late-stage candidates. 4-Chloropyridine HCl, thanks to its stable hydrochloride form, meets or exceeds many common regulatory thresholds for heavy metals, solvent residues, and known precursors to mutagenic impurities. Researchers who worry about audit trails or regulatory filings find reassurance knowing their intermediates already comply with core international guidelines, such as ICH Q3C for residual solvents and Q3D for elemental impurities.
Working with 4-Chloropyridine HCl feels safer compared to some more volatile pyridine derivatives. Its crystalline form reduces airborne particulates and vapor risk. Still, experienced chemists wear appropriate PPE, manage spills promptly, and maintain clear labeling. Early mentorship impressed upon me the value of safety culture, especially around pyridine-related compounds, due to their potential toxicity through dermal or respiratory exposure.
Labs that integrate regular safety training, clear written procedures, and a sense of shared responsibility tend to report fewer incidents. Compared with other chlorinated heterocycles, 4-Chloropyridine HCl rarely triggers acute incidents, and storage stability means fewer unexpected surprises lurking in old reagent bottles.
On the sustainability front, waste disposal presents a challenge. Heterocyclic compounds, particularly those bearing halogens, demand careful neutralization and incineration, a lesson reinforced by interactions with environmental managers in larger chemical companies. The industry trend moves toward reduced-waste syntheses, encouraging catalysis that limits byproducts and developing processes that recover or destroy chlorine-containing fragments safely.
Beyond pharmaceutical and material science roles, the value proposition of 4-Chloropyridine HCl extends to fine chemicals and new frontiers in agrochemical research. Scientists optimizing next-generation pesticides or fungicides have adopted halogenated pyridines for their metabolic stability and predictable environmental fate.
As industries increase their focus on green chemistry, the choice of intermediates like 4-Chloropyridine HCl becomes strategic. Halogenated heterocycles, once maligned for their persistence, now see revived interest where their structure can confer selectivity or degradation profiles less likely to harm non-target organisms. Teams adopting greener synthetic protocols often look for derivatives that perform well under milder reaction conditions or support biocatalytic transformations, both of which align with the solid-performance profile of this compound.
During collaboration between regulatory specialists and product developers, input from toxicological studies shapes product selection. 4-Chloropyridine HCl’s mutagenicity and acute toxicity have been reviewed in published studies, and a thorough risk assessment results in smart, evidence-based approaches to its integration into larger synthetic pipelines. Creating well-documented safety data supplements scientific creativity with practical risk management.
Supply chain disruptions have always shaped chemical availability, and the years since global pandemics and logistical delays have sharpened the focus on reliability of access. 4-Chloropyridine HCl, though made by established producers worldwide, saw price swings as ports shut down and shipping routes snarled. Labs rolling out new drug candidates or materials projects count on suppliers who can back up their contracts with inventory and responsiveness. Long lead times or stockouts can delay crucial research stages or product launches by months.
Collaborative supplier relationships now dominate procurement: companies value regular communication, transparent batch histories, and timely technical support. This isn’t a luxury; it’s risk management. During a critical stage of a multi-year pharmaceutical campaign, dependable access to reagent inventory averted a funding crisis, maintaining momentum and trust from grant agencies. These practical stories shape the reputation of intermediates like 4-Chloropyridine HCl more than a glossy catalog ever could.
Every compound comes with quirks, and 4-Chloropyridine HCl is no exception. Its hydrochloride salt form, while less volatile, attracts small amounts of atmospheric moisture if left open for long, potentially leading to minor clumping. My advice, learned through cautionary reminders at lab meetings, is simple: keep containers tightly sealed and store them in moisture-controlled cabinets. Failing to do this can create headaches later, as clumped material dissolves more slowly and may skew measurements if dosed directly as a solid.
Chemists dealing with grams to kilograms know the importance of accurate weighing, so a little effort on storage saves a lot of recalibration. Some teams adopt single-use vials or aliquots, especially for high-throughput screening operations, reducing contamination and exposure.
Stories circulate about product loss to careless handling. One production run suffered a costly delay when an open container sat beneath an air vent, absorbing water and altering the batch outcome. Care in storage and weighing, combined with clear training, keeps these issues at bay.
Manufacturing novel molecules relies not just on clever design but on robust intermediates that behave predictably, time after time. 4-Chloropyridine HCl supports innovation because it delivers this reliability. Scientists drawn into development cycles that last months or years treasure a product that distinguishes itself by not causing trouble.
Familiarity counts too. Chemists who move between academic labs, startups, and established firms know that some intermediates work in theory but cause endless problems in practice. The hydrochloride salt’s blend of stability, solubility, and low vapor pressure keeps the focus on chemistry, not cleanup. In feedback sessions and postmortems, research teams often note how access to solid, reproducible intermediates keeps timelines on track and morale high. Facing setbacks in late-stage synthesis is hard enough without losing hours to mysterious product behavior.
As research priorities shift toward faster design cycles, predictive modeling, and scaling to manufacture, the role of simple, sturdy intermediates like 4-Chloropyridine HCl grows more important. The explosion of artificial intelligence in reaction planning relies on curated databases, and consistent input helps train these systems to generate more reliable predictions. Blips in reagent quality can throw off entire retrosynthetic routes, leading to false negatives or wasted optimization runs. Feedback from process chemists in large pharma has made the case for greater investment in upstream intermediate consistency, calling 4-Chloropyridine HCl a linchpin in rapid prototyping cycles.
Automation and robotics in chemical synthesis are another rising trend. Robotics can execute parallel reactions, staggering hundreds of trials using only milligram quantities per test. Each run depends on uniform reagents, and solid, non-volatile 4-Chloropyridine HCl fits these systems well, feeding the algorithms the dependable starting point they require. It stands out from other chloropyridine variants that might not dispense as smoothly or require labor-intensive handling.
4-Chloropyridine HCl owes its popularity to a mix of qualities: manageable properties, broad reactivity, and the steady reliability researchers crave. It doesn’t dominate headlines, but for those in the trenches of discovery and scale-up, its role stays central. Labs everywhere — from small startups crafting one-off drugs to major manufacturers optimizing supply chains — recognize its value not by glossy promotions, but by the work it enables. In a crowded field of chemical intermediates, this compound carries the kind of reputation built on consistent results, thoughtful industrial stewardship, and a long track record of supporting genuine scientific progress.