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HS Code |
827810 |
| Chemical Name | 2-hydroxy-4-chloro-5-nitropyridine |
| Molecular Formula | C5H3ClN2O3 |
| Molecular Weight | 174.54 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | 174-177°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Cas Number | 39304-19-5 |
| Density | Approx. 1.6 g/cm³ (estimated) |
| Synonyms | 4-chloro-5-nitro-2-pyridinol |
| Chemical Structure | Pyridine ring with hydroxy at position 2, chloro at position 4, nitro at position 5 |
| Pubchem Cid | 3619089 |
As an accredited 2-hydroxy-4-chloro-5-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-hydroxy-4-chloro-5-nitropyridine, sealed with a screw cap and labeled with safety information. |
| Container Loading (20′ FCL) | 20′ FCL container typically holds 10–12 metric tons of 2-hydroxy-4-chloro-5-nitropyridine, packed in sealed fiber drums. |
| Shipping | 2-Hydroxy-4-chloro-5-nitropyridine should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must comply with regulations for hazardous chemicals, including appropriate labeling and documentation. Transport should be conducted by authorized carriers with necessary precautions to prevent leaks, spills, or environmental contamination during transit. |
| Storage | Store 2-hydroxy-4-chloro-5-nitropyridine in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Label the container clearly, and handle using appropriate personal protective equipment to minimize exposure. |
| Shelf Life | 2-hydroxy-4-chloro-5-nitropyridine typically has a shelf life of 2 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 2-hydroxy-4-chloro-5-nitropyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimizes by-product formation. Melting Point 175°C: 2-hydroxy-4-chloro-5-nitropyridine with a melting point of 175°C is used in agrochemical formulation, where it enables stable incorporation into solid delivery systems. Molecular Weight 176.54 g/mol: 2-hydroxy-4-chloro-5-nitropyridine with a molecular weight of 176.54 g/mol is used in heterocyclic compound design, where it improves molecular compatibility and reactivity. Particle Size ≤50 μm: 2-hydroxy-4-chloro-5-nitropyridine with a particle size of ≤50 μm is used in high-performance coatings, where it promotes uniform dispersion and surface coverage. Thermal Stability up to 120°C: 2-hydroxy-4-chloro-5-nitropyridine with thermal stability up to 120°C is used in catalyst manufacturing, where it maintains structural integrity during synthesis reactions. Water Solubility 0.5 g/L: 2-hydroxy-4-chloro-5-nitropyridine with water solubility of 0.5 g/L is used in dye intermediate processes, where it allows controlled solubilization and reaction efficiency. |
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In today’s world, the drive to innovate and advance materials often boils down to the fine details—those compounds that empower the creation of medicine, dyes, and specialty materials. 2-hydroxy-4-chloro-5-nitropyridine has steadily become an invaluable compound for chemists, researchers, and manufacturers. As someone familiar with academic research and industrial applications, I’ve watched how the precise performance of small molecules often shapes the success of much bigger projects.
At its core, this compound carries a unique arrangement of functional groups on the pyridine ring. The hydroxy, chloro, and nitro groups all bring their own properties. These affect reactivity, solubility, and compatibility with downstream chemical processes. The presence of these groups on the ring isn’t random—chemists consistently seek out this structure to guide syntheses that demand both stability and reactivity under controlled conditions.
The molecular formula of 2-hydroxy-4-chloro-5-nitropyridine is C5H3ClN2O3, giving it a balanced mix of functionalization and stability. In practical terms, its molecular weight and melting point allow for predictable behavior during storage and synthesis. Chemists learn to respect a compound’s purity early on, and in this case, purity often reaches above 98%. This level allows sensitive reactions—pharmaceutical intermediates cannot tolerate trace impurities that might lead to costly failures later on.
One difference that experienced users notice relates to color and consistency. A pale yellow crystalline powder, this compound resists caking and clumping unless handled in extreme conditions. Bread-and-butter chemicals like sodium chloride seem simple, but specialized materials require this level of care because batch consistency and purity affect not only lab experiments but also large-scale manufacturing. Even subtle color changes can signal problematic impurities—a lesson many process chemists learn firsthand.
As for solubility, 2-hydroxy-4-chloro-5-nitropyridine dissolves well in polar organic solvents like DMSO, DMF, and ethanol. It rarely dissolves in water, making it easier to separate from aqueous solutions or apply in non-aqueous synthesis. For those running extractions or purifications, this property saves time and reduces solvent waste.
Those working in pharmaceutical research appreciate how the structural features of 2-hydroxy-4-chloro-5-nitropyridine provide solid intermediate steps for complex active pharmaceutical ingredients. Medicinal chemists recognize patterns in molecules, searching for building blocks that open new synthesis strategies. This compound introduces both electron-withdrawing and electron-donating properties onto the pyridine ring, a foundation that helps engineer bioactive molecules.
In small molecule synthesis, predictability counts. Years ago, I watched a team struggle to find a reliable precursor for heterocyclic compounds, only for this chemical to offer a breakthrough in yield and purity. Chemists work hard to limit steps and remove toxic reagents, so when a compound brings reactivity without excessive side reactions, it earns trust in the lab.
For pigment and dye production, the electron-rich and electron-deficient parts of this molecule open routes to bright and stable colors. Organic electronics (an emerging field connecting chemistry to practical devices) sometimes call for highly substituted pyridines because their properties act as the backbone of new, conductive, or light-emitting materials. Academic labs also rely on this compound to demonstrate reaction mechanisms that show students the real-world side of organic transformations.
Not every lab uses it for high-stakes innovation—some rely on it as a teaching tool because it helps demonstrate the interplay between electron effects and regioselectivity. Watching students try to figure out which carbon atoms react next always brings forward the value of molecules built with purpose.
Some newcomers to synthesis may ask why not stick with simpler pyridine derivatives. After years in research, one quickly learns that subtle changes in molecular structure drive performance differences that cannot be ignored. Swap the nitro group for an amino group, and suddenly, the entire reaction pathway changes. Drop the chlorine, and a chemist forfeits an ideal opportunity for cross-coupling or halide-based transformations.
2-hydroxy-4-chloro-5-nitropyridine stands apart from related chemicals like 2-hydroxy-5-nitropyridine or 4-chloro-2-methylpyridine. The blend of hydroxy, chloro, and nitro substitutions covers a unique point in the spectrum of pyridine derivatives, letting researchers tune reactivity, solubility, and even environmental persistence. Not every compound can match this balance. Some alternative substances lose selectivity or produce higher levels of unwanted byproducts.
In industry, consistent supply of specialty chemicals like this one supports long-term planning. In my own experience communicating with suppliers, I have found that those who specialize in niche compounds often deliver more robust quality management and deeper technical knowledge. That feedback loop makes projects more predictable—a huge difference compared to generic precursor molecules that may vary widely from supplier to supplier.
The reputation of 2-hydroxy-4-chloro-5-nitropyridine among users rests on reliability. Quality goes beyond technical data on a label. Experienced users watch certificates of analysis, but they also rely on direct testing—taking a new batch, running a test reaction, and confirming outcomes before committing to a scale-up. I’ve seen production lines delayed because a batch from a lesser supplier gave unpredictable results. This experience shapes a strong preference for proven sources and tight quality documentation.
Some buyers focus on price, but researchers and manufacturers soon learn that cheap, inconsistent supply costs more in failure and rework. Reliable suppliers maintain rigorous checks for residual solvents, trace metals, and unwanted byproducts. Labs do not have time or budget for surprises. Product quality feeds into every stage—from raw material checks to final product validation in pharmaceuticals or fine chemicals. For those producing critical materials, a single quality lapse can reverberate all the way to end users.
Environmental considerations add to the conversation. Some pyridine derivatives persist in soil or water, upsetting regulatory review or causing downstream waste challenges. The structure of 2-hydroxy-4-chloro-5-nitropyridine, while engineered for reactivity, poses questions for disposal and safety practices. Responsible suppliers offer detailed safety documentation and guide customers in safe handling and waste minimization. That focus reflects a larger shift: manufacturers and procurers now study every step of a chemical’s life cycle, from procurement to final disposal.
Transparency along the supply chain builds confidence on both sides. It’s not just about a clear yellow powder in a drum—it’s about building relationships where information on purity, stability, and provenance flows easily between supplier and user. This is especially important as industries face stricter regulations and more public scrutiny.
Anyone familiar with chemical handling recognizes the importance of routine. 2-hydroxy-4-chloro-5-nitropyridine, while stable in typical environments, calls for the standard arsenal: gloves, eye protection, proper lab coats, well-ventilated spaces, and careful storage. Chemical dusts, even in minute amounts, can cause skin irritation or respiratory problems. Accidental exposure is rare among experienced handlers, but that is due to consistent safety protocols, not luck.
Waste disposal, though not glamorous, matters in the everyday routine. For many researchers, safe disposal of pyridine derivatives means collecting all residues and unwanted materials for professional processing in controlled facilities. Some are tempted to shortcut these practices, but years of audits and surprise inspections underscore why best practices persist—the potential for contamination, ecological damage, or regulatory violations cannot be ignored.
Manufacturers and users benefit by building safety into every transaction. Clear labeling, training for new staff, and regular reviews of technical literature keep safety incidents low. In my time working alongside both entry-level chemists and seasoned professionals, most incidents traced back to a moment’s distraction or a missing safety barrier. Tools like safety data sheets and regular training keep teams vigilant.
As regulatory pressures rise and customers demand greener solutions, those working with 2-hydroxy-4-chloro-5-nitropyridine look for ways to limit waste, reduce hazardous byproducts, and lower the energy footprint of production. Some invest in process intensification or switch to bio-based solvents, trying to cut down the impact of organic synthesis.
Collaborations between producers and academic partners have occasionally led to new insights. For instance, some syntheses now use milder oxidants or more selective catalysts to achieve the same results with fewer unwanted residues. Precedence from other pyridine derivatives suggests that green chemistry approaches work, given enough research and willingness to invest upfront.
Smarter design at the plant level counts as well. Recovering solvents, recycling wash streams, and limiting fugitive emissions go a long way towards making fine chemical production compatible with sustainability targets. It’s tempting to treat specialty chemicals as niche items outside the scope of sustainability, but more industries wake up to the reality that sustainability impacts cost, regulatory approvals, and global competitiveness.
Users play a part as well. Careful ordering, minimizing waste stock, and collaborating with suppliers to implement return programs or minimize single-use packaging are becoming more common. Some researchers join green chemistry consortia to advocate for higher standards across the board. For producers, it’s a good business decision—customers who see a strong sustainability stand are more loyal and less likely to switch for small price differences.
Even with the many strengths of 2-hydroxy-4-chloro-5-nitropyridine, ongoing challenges shape its use. Supply chain disruptions have shown how global dynamics—logistics bottlenecks, raw material shortages, or international regulations—can make sourcing even basic research chemicals unexpectedly difficult. Labs that once took stable supply for granted now keep closer tabs on stock levels and maintain backup sources.
Another concern often circles around intellectual property. Some pharmaceutical manufacturers rely on unique intermediates like this to secure patents or sidestep litigation. In these cases, controlling information on process routes and precursor molecules adds a layer of complexity to purchasing decisions. Trust between buyer and seller becomes crucial, especially for contract or custom synthesis.
Regulatory scrutiny isn’t likely to disappear. Authorities continue tightening controls on the use, transport, and disposal of pyridine derivatives. While these moves bring safety and environmental advantages, they also create compliance hurdles for researchers and producers. Detailed documentation, regular audits, and up-to-date training become daily routines.
Finally, the market for specialty chemicals always faces pressures from shifting technology trends. Digital chemistry tools—like predictive modeling for reaction outcomes—are gaining traction. These could influence demand for certain intermediates as synthetic pathways shift or become more efficient. Still, few compounds with the precise combination of hydroxy, chloro, and nitro functional groups rival the versatility found in 2-hydroxy-4-chloro-5-nitropyridine.
Experience teaches the value of building a personal knowledge base. Don’t just trust sales pitches or certificates—take time to study how this compound reacts under your specific lab or plant conditions. Determine the best storage practices based on temperature, humidity, and packaging material. Compare results batch by batch, and keep good records for traceability.
Building a good relationship with suppliers pays off. Reliable partners answer technical questions, flag potential changes, and provide support during troubleshooting. In my research work, I found that even a ten-minute call with a knowledgeable supplier could save days of trial and error. They may also offer insight into new process developments or regulatory changes that could affect your workflow.
Watching trends across the sector gives users an advantage. Trade publications, scientific journals, and regulatory updates contain signals about evolving expectations. Those who stay ahead of the curve adapt more smoothly, integrating improvements to quality management or sustainability before these are mandated.
Sharing experience with colleagues counts too. Younger chemists, new lab technicians, and even process engineers benefit from firsthand accounts—mistakes and successes alike. By treating knowledge as communal rather than proprietary, the quality and impact of research or production improves for all.
From small-scale academic research to large-scale chemical manufacturing, 2-hydroxy-4-chloro-5-nitropyridine remains a practical, trusted choice for those requiring both specificity and flexibility. Its structure equips chemists to design and optimize new synthetic routes while supporting innovation in pharmaceuticals, dyes, and material science. Reliability and strong supplier relationships support trust and performance at every step.
I’ve seen firsthand how the right specialty chemical can move a project from concept to success—or stall it in limbo. The track record of 2-hydroxy-4-chloro-5-nitropyridine continues to set it apart among fine chemical intermediates. Its performance, consistency, and adaptability highlight the best of what specialty chemicals offer: a solid foundation for innovation in ever-changing scientific landscapes.