|
HS Code |
232690 |
| Productname | 2-Amino-6-Chloro-3-Nitropyridine |
| Casnumber | 27329-19-7 |
| Molecularformula | C5H4ClN3O2 |
| Molecularweight | 173.56 |
| Appearance | Yellow to brown crystalline powder |
| Meltingpoint | 176-179°C |
| Purity | ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.59 g/cm³ (approximate) |
| Storagecondition | Store in a cool, dry place, tightly closed |
| Synonyms | 6-Chloro-2-amino-3-nitropyridine |
| Smiles | Nc1nc(ccc1Cl)[N+](=O)[O-] |
| Inchikey | YXNYKUZSPAFBML-UHFFFAOYSA-N |
As an accredited 2-Amino-6-Chloro-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Amino-6-Chloro-3-Nitropyridine is packaged in a 25g amber glass bottle with a secure screw cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2-Amino-6-Chloro-3-Nitropyridine packed securely in 25 kg fiber drums, totaling approximately 8-10 metric tons. |
| Shipping | 2-Amino-6-Chloro-3-Nitropyridine is shipped in tightly sealed containers compliant with chemical safety regulations. It should be protected from light, moisture, and physical damage. Transport must adhere to local and international regulations for hazardous materials, ensuring proper labeling and documentation. Store in a cool, dry place upon arrival to maintain stability and safety. |
| Storage | Store **2-Amino-6-Chloro-3-Nitropyridine** in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers or bases. Keep in a cool, dry, and well-ventilated area designated for hazardous chemicals. Clearly label the container, and ensure proper personal protective equipment is used when handling. Avoid sources of ignition and static discharge. |
| Shelf Life | 2-Amino-6-Chloro-3-Nitropyridine should be stored in a cool, dry place; shelf life is typically 2–3 years if unopened. |
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Purity 98%: 2-Amino-6-Chloro-3-Nitropyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and selective target compound formation. Melting Point 176°C: 2-Amino-6-Chloro-3-Nitropyridine with a melting point of 176°C is used in organic synthesis procedures, where it provides thermal stability during multi-step reactions. Molecular Weight 176.56 g/mol: 2-Amino-6-Chloro-3-Nitropyridine with a molecular weight of 176.56 g/mol is used in agrochemical formulations, where it enables precise stoichiometric calculations for active ingredient development. Particle Size <50 μm: 2-Amino-6-Chloro-3-Nitropyridine of particle size less than 50 μm is used in catalyst preparation, where it allows enhanced dispersion and improved catalytic surface area. Stability Temperature 120°C: 2-Amino-6-Chloro-3-Nitropyridine with stability up to 120°C is used in dye manufacturing processes, where it maintains chemical integrity under process conditions. Water Content ≤0.5%: 2-Amino-6-Chloro-3-Nitropyridine with a water content of ≤0.5% is used in electronics material synthesis, where low moisture prevents unwanted side reactions and enhances product reliability. Assay ≥99%: 2-Amino-6-Chloro-3-Nitropyridine with assay ≥99% is used in fine chemical production, where high analytical purity maximizes batch-to-batch consistency and performance. Sulphated Ash <0.1%: 2-Amino-6-Chloro-3-Nitropyridine with sulphated ash below 0.1% is used in laboratory reagent preparation, where minimal inorganic residue reduces contamination risks. |
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Chemistry offers some unsung heroes that quietly shape the backbone of many modern products. 2-Amino-6-Chloro-3-Nitropyridine stands as a good example. Its name alone draws a picture of a molecule built for versatility. The presence of an amino group, a nitro group, and a chlorine atom on a pyridine ring might not mean much to someone outside the lab, but for chemists and manufacturers, this trio opens up doors to creative synthesis pathways. On a practical note, this compound often enters the stage as a precursor — a starting point for crafting more complex structures that end up in fields as varied as pharmaceuticals, agrochemicals, and specialty materials.
The specific model under discussion, 2-Amino-6-Chloro-3-Nitropyridine, offers a combination of properties that are tough to match. It occupies that spot between raw reactivity and selectivity, making it a go-to choice when precision counts. The crystalline powder, yellow in color, signals a stable intermediate. Its melting point and moisture-sensitivity demand care during handling, which seasoned chemists appreciate. The molecule’s configuration lends itself to a surprising array of modification routes, letting users tailor downstream products with less process waste. That advantage may reduce the number of synthetic steps required, saving time and minimizing unwanted byproducts.
One feature that often gets attention among those who use specialty chemicals is consistency. Labs that depend on reliable reactivity can hit a wall when their starting materials vary too much between batches. The manufacturing process for 2-Amino-6-Chloro-3-Nitropyridine — when done right — aims for narrow specification windows, meaning less risk for those surprises that throw off a big synthesis. In work where a single impurity can derail weeks of effort, this kind of reliability matters more than a glossy brochure ever could. Many manufacturers run their own purity tests and require certificates of analysis, reflecting a shared understanding that mistakes at the starting stage can echo all the way through to the finished product.
In my experience, the true significance of this compound comes into focus once you start counting the cost of time and quality in multi-stage syntheses. I’ve been on both sides — as someone running routine reactions, and as a team member troubleshooting why a product batch missed its target. Getting the starting materials right sets the tone for everything that follows.
In pharmaceutical work, for example, 2-Amino-6-Chloro-3-Nitropyridine can act as a key intermediate in the development of kinase inhibitors or anti-infective agents. The electron-withdrawing nature of both the nitro and chloro groups on the aromatic ring adds a layer of predictability in nucleophilic substitution and reduction reactions. Instead of wasting hours trying to coax a reaction to finish, chemists benefit from a more straightforward path to the end compound. Out in the real world, this results in fewer failed batches, more reliable timelines, and less wasted effort.
Beyond pharma, the agricultural industry finds value too. Herbicides and fungicides sometimes rely on pyridine derivatives, with structural tweaks designed to hit specific targets in weeds or pests, yet stay safe for crops. Modifying the position of functional groups on a pyridine ring, especially with sturdy groups like chlorine and nitro, lets companies fine-tune activity with impressive precision. This creates more effective and less harmful crop protection options.
Research teams in materials science aren’t left out either. By using the reactivity balance of the compound, they can construct new polymers, dyes, or specialty coatings. These end uses benefit from starting materials that offer both the right chemistry and the level of documentation that makes scaling up to pilot or commercial volumes less stressful.
Stacking this chemical up against similar options reveals the differences that matter in practice. Think about 2-Amino-3-Nitropyridine, which lacks the chlorine atom at the six position. The absence of chlorine changes how certain substitution reactions proceed, limiting the range of modifications possible in the downstream product. That single atom can define which route a synthesis team takes — or if they can reach their target at all.
Related molecules without the nitro or amino group may be easier to handle, but they offer less flexibility in further synthesis. The nitro’s strong electron-withdrawing properties make selective reductions and ring transformations possible in ways that less functionalized versions can’t match. For chemists building libraries of novel candidates, or process engineers aiming for a scalable route from gram to kilo scale, starting with a more highly functionalized base can cut development timelines significantly.
I remember projects where the wrong starting material forced awkward detours. Choosing a less reactive analog meant adding steps to plug in the missing functionality — driving up costs and lengthening timelines. Since this compound combines several enabling groups into one package, many teams see its value as a time-saver and risk reducer.
It’s easy for specialty chemicals to end up as line items on spreadsheets, but every order tells a story about balancing real-world demands. I’ve seen procurement managers stress over suppliers who promise much but deliver little, or who can’t back their claims with analytical reports. Here’s where documented specifications and clear quality control shift from paperwork to necessity.
The right product batch brings with it a sense of security — melting within the expected temperature range, arriving in moisture-protective packaging, and matching the spectroscopic fingerprints that the synthetic route demands. Customers in regulated sectors like pharmaceuticals may require trace-level impurity quantification, not just purity above 98 percent. Those details turn into lower regulatory headaches and smoother scale-up to manufacturing.
One practical example is the use of liquid chromatography to verify that 2-Amino-6-Chloro-3-Nitropyridine doesn’t carry over halogenated or nitrated impurities that complicate downstream purification. High-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) both serve not only as analytical tools, but as peace of mind. Laboratories that take advantage of suppliers providing detailed spectra save time — and, sometimes, their reputations.
Logistics matter too. This compound needs dry, cool storage and careful packaging to ward off hydrolysis and decomposition. Shippers work best with partners who understand UN hazardous goods guidelines, since compliance with regulations is not just about ticking a box but keeping real people and assets safe. Every shipment links several teams — quality control, operations, safety — and smooth collaboration depends on predictability at every link.
Even with all these strengths, users see problems pop up from time to time. I’ve walked into storerooms where a leaking bag or container cost us a whole month’s worth of starting material. The point of fail-safe packaging and clear labeling never feels like overkill in those moments. For many teams, it’s as simple as verifying batch numbers and look for any signs of caking or clumping before accepting delivery.
Price also shapes the decision to stick with or switch away from this compound. Shortages or supply interruptions cause headaches all the way down to the lab bench. Some buyers keep backup suppliers or even multiple product grades on hand. The extra cost of higher purity grades can sometimes be justified by ease of downstream filtration or fewer side reactions on scale-up.
Sustainability now enters every procurement conversation, not out of obligation but as a natural extension of running a responsible operation. Suppliers who show clear disposal options for off-spec or expired material, and who minimize solvent waste in their manufacturing process, win points — not just from compliance departments but from scientists who care about their own exposure and the broader environmental picture.
Nobody expects a perfect world where every consignment always matches the COA down to the last decimal, but open dialogue between buyers and suppliers makes life easier. In conversations with colleagues across the industry, transparency stands out as a shared value. Asking about batch-to-batch variation, requesting datasets from multiple runs, or requesting updates on any post-synthesis filtration or drying steps keeps surprises to a minimum. In regulated markets, requesting certification to standards like ISO 9001 or Good Manufacturing Practice (GMP) brings a practical layer of protection.
It also pays to keep an eye on advances in synthetic methodology. One trend that has direct impact on products like 2-Amino-6-Chloro-3-Nitropyridine is flow chemistry. With continuous production lines replacing traditional batch reactors, many manufacturers now offer better purity and reduced impurity profiles. Adopting or sourcing from companies who modernize their approach often pays off in terms of both cost and consistency.
Scale-up work, in particular, shows where small changes matter. Adjusting solvent systems or order of addition changes impurity formation as well as product recovery. Labs that share these details with their suppliers — instead of treating them as top-secret — often see collaborative improvements, resulting in a product better tailored to actual usage, not just a generic lab recipe from years past.
Anyone working with aromatic nitro compounds pays close attention to safety, both in terms of environmental risk and personal protection. Toolkits stocked with gloves and ventilation systems become everyday companions. It’s not enough to rely on routine — every new lot can bring subtle changes, and the most experienced chemists join safety teams in reviewing each incoming batch’s documentation and, more importantly, how it behaves in real time.
The nitro group in 2-Amino-6-Chloro-3-Nitropyridine offers reactivity that enables a range of reductions, substitutions, and ring transformations, but it also heightens the need for care during handling and waste treatment. Disposal rightfully draws scrutiny from local regulators and community safety advocates. Having reliable destruction or neutralization protocols matters just as much as yields or reagent costs.
Product stewardship extends to every stage. From safe storage to responsible shipping and on to thoughtful disposal, each link in the chain helps maintain trust among the teams who depend on these molecules. Sharing best practices isn’t just about compliance; it means everyone — from the shipping dock to the research lab — goes home safe and with work they can be proud of.
The competitive edge of 2-Amino-6-Chloro-3-Nitropyridine stems from both its chemical profile and that layer of practical, real-world support offered by knowledgeable suppliers. The old adage, “trust but verify”, applies at every level, as teams strive to maintain high standards while navigating supply chain unpredictability. The science marches forward, and companies who lean into process improvement, transparent testing, and open-ended problem-solving do best in the long run.
Open channels of communication across the user base also foster smarter practices. I have seen the impact when bench chemists share unexpected results with technical support contacts at their suppliers. In one instance, that simple feedback on an outlier batch led to an adjustment in recrystallization protocols, cutting out a persistent impurity. Making it routine to collect and report product performance not only improves overall quality, but democratizes innovation at every level.
Tools from digital tracking to blockchain traceability are helping some organizations lock in the chain of custody from factory to end user, avoiding counterfeiting risks and strengthening recall systems should problems emerge. For a compound as important as this one, transparency doesn’t just smooth procurement — it builds confidence throughout the market.
In the changing landscape of specialty chemicals, smaller-batch, high-value intermediates like 2-Amino-6-Chloro-3-Nitropyridine gain ground. Pharmaceutical innovation, global food supply, and high-tech material design all depend on these workhorses: compounds that quietly do their job in the background. Real advances depend as much on the supply chain as on the textbook chemistry.
Increasing regulatory oversight, especially in the pharmaceutical sector, means that documentation practices grow ever more rigorous – and with good reason. Patient safety, environmental stewardship, and company reputations ride on every kilo of product that leaves the warehouse. Digital product tracking, robust analytical documentation, and quality certifications now serve as much more than bureaucratic requirements; they add value at every stage.
Companies who understand the importance of supporting information, not just the product itself, stand out. Analytical summaries, impurity profiles, and clear storage recommendations build trust among buyers who lean on these chemicals as dependable building blocks. As the industry moves forward, the expectation for transparency and shared responsibility will only increase.
What I see in the evolution of products like this is a steady broadening of applications. At first, many thought of pyridine derivatives as niche players, good mainly for dense medicinal chemistry or crop science. Needs have shifted. Novel polymers, high-performance dyes, and new branches of analytical chemistry now take advantage of these enabling intermediates. This pattern keeps repeating: every few years, as new fields push the boundaries, they reach back for starting points that allow creative synthesis, efficient modification, and clear documentation.
The point isn’t just about a single molecule but about how researchers and companies adapt old tools to suit new challenges. I have seen new areas emerge, like battery technology, where new ionic liquids or catalysts build on structures derived from pyridine systems. Product developers in these sectors select intermediates for both their chemical reactivity and their documentation, understanding that traceability helps meet both regulatory and performance needs.
This feedback between end user and supplier – from bench chemist to sales manager to production operator – holds the real secret behind the success of intermediates like 2-Amino-6-Chloro-3-Nitropyridine. Teams who keep lines of communication open, ask for better data, and support new applications find ways to save money, reduce waste, and speed up discovery.
Success with any specialized intermediate comes down to a few simple factors. Quality, reliability, safety, and transparency shape every transaction, every scale-up campaign, every package delivered or returned. People who use these products recognize the value not just in the chemistry, but in the relationships and routines built around each shipment and project.
I’ve watched seasoned chemists check product certifications with the care born of experience, knowing that the smallest oversight can upend an entire research program. They appreciate suppliers who welcome direct feedback and provide clear records and quick answers. Detailed documentation, ready at hand, beats any promise or sales pitch.
Demand for safety, consistent documentation, and clear support only grows with each new regulation and every new field that draws on these versatile compounds. Choosing products based on both technical merit and the support system behind them makes sense for any team looking to balance innovation, compliance, and safety.
The story of 2-Amino-6-Chloro-3-Nitropyridine runs deeper than just a chemical formula or a list of use cases. It highlights what works when technical performance meets practical support: purity, reliability, shared data, and honest conversations among all those who take responsibility for moving science forward. Its blend of key functional groups makes complex synthesis routes shorter and more manageable, and its documented history in exacting industries gives teams the confidence needed to push boundaries.
Choosing the right intermediate makes a big difference, not just in one project but across the life of a facility, a drug, or a material. When suppliers, scientists, and support staff keep their standards high and their communication clear, progress becomes not just possible, but steady and sustainable.