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HS Code |
442763 |
| Cas Number | 13298-41-6 |
| Molecular Formula | C5H4Cl2N2 |
| Molecular Weight | 163.01 g/mol |
| Appearance | Light yellow to brown solid |
| Melting Point | 90-93°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Synonyms | 5-Amino-2,3-dichloropyridine; 2,3-Dichloro-5-aminopyridine |
| Smiles | c1c(N)cc(Cl)nc1Cl |
| Inchi | InChI=1S/C5H4Cl2N2/c6-3-1-4(8)2-9-5(3)7 |
As an accredited 5-Amino-2,3-dichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-Amino-2,3-dichloropyridine, 25g, is packaged in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | 20′ FCL loads 12 MT of 5-Amino-2,3-dichloropyridine, packed in 25 kg fiber drums, safely secured for transit. |
| Shipping | 5-Amino-2,3-dichloropyridine should be shipped in tightly sealed containers, labeled properly, and protected from light and moisture. Transport must comply with relevant chemical safety regulations, ensuring avoidance of incompatible substances. Handle with protective gear, and ship at ambient temperature unless otherwise specified by the supplier or regulatory guidelines for hazardous chemicals. |
| Storage | **5-Amino-2,3-dichloropyridine** should be stored in a cool, dry, and well-ventilated area, tightly sealed in its original container, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Ensure the storage area is clearly labeled and equipped with appropriate safety equipment. Follow all relevant safety and regulatory guidelines for handling and storage. |
| Shelf Life | 5-Amino-2,3-dichloropyridine generally has a shelf life of 2-3 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 5-Amino-2,3-dichloropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting Point 122°C: 5-Amino-2,3-dichloropyridine with melting point 122°C is used in agrochemical formulation processes, where it offers thermal stability during compound processing. Low Water Content: 5-Amino-2,3-dichloropyridine with low water content is used in fine chemical production, where it maintains reactivity and prevents hydrolysis. Stability Temperature 150°C: 5-Amino-2,3-dichloropyridine with stability temperature 150°C is used in heterocycle ring closure reactions, where it enables reliable high-temperature operations. Particle Size <50 μm: 5-Amino-2,3-dichloropyridine with particle size less than 50 μm is used in solid-state pharmaceutical applications, where it enhances blending uniformity. High Assay 99%: 5-Amino-2,3-dichloropyridine with high assay 99% is used in specialty material modification, where it ensures minimal impurities for optimal end-product quality. Chromatographic Purity >98%: 5-Amino-2,3-dichloropyridine with chromatographic purity greater than 98% is used in molecular research labs, where it supports reproducible analytical results. Bulk Density 0.85 g/cm³: 5-Amino-2,3-dichloropyridine with bulk density 0.85 g/cm³ is used in automated dispensing systems, where it promotes precise volumetric dosing. |
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Chemistry often shapes industries in ways few people stop to consider. In laboratories across the world, scientists pore over the details of new compounds, hoping a fresh molecule can solve practical problems—make a medicine more effective, a material more resilient, or a process less costly. Amidst this ongoing pursuit, 5-Amino-2,3-dichloropyridine stands out as one compound that drives real progress in both pharmaceutical and chemical research.
For anyone working in drug discovery, 5-Amino-2,3-dichloropyridine feels like a friend you can count on. Its core structure, the pyridine ring, sits at the foundation of countless pharmaceutical agents. With two chlorine atoms sitting at the 2- and 3-positions, and an amino group at position 5, this compound delivers a unique handle for synthetic chemists. That arrangement opens doors to targeted modifications. By working with this compound, researchers build molecules with very specific activity profiles, increasing the odds of landing a drug candidate that’s highly selective. In my experience, fine-tuning these sorts of molecular details frequently determines whether a project inches forward or stalls out entirely.
The unique substitution pattern found in 5-Amino-2,3-dichloropyridine carves out new possibilities for diversification. Pharmaceutical teams look for intermediates that don’t just provide versatility, but also consistency and purity. Small impurities may completely derail efforts to push a compound forward in the development pipeline. Chemists lean on intermediates like this because it allows for the preparation of rare or challenging derivatives—pyridine-based drugs often show strong activity against neurological or infectious disease targets, but compound availability consistently sets the upper limit on what’s possible in a laboratory setting.
For those of us who have ever spent hours troubleshooting a stubborn reaction, talking about “specifications” starts to feel like more than just paperwork—meeting quality standards can mean the difference between a publishable synthesis and a round of wasted efforts. Typically, 5-Amino-2,3-dichloropyridine is supplied as a pale to yellowish crystalline powder, with a molecular formula of C5H4Cl2N2 and a molecular weight of about 179.01 g/mol. The melting point often falls between 150 and 155 degrees Celsius, a range that allows convenient handling in most labs without the need for extra cooling equipment.
Purity plays a crucial role. Reputable sources routinely provide material with chemical purity exceeding 98%, often tested through techniques such as high-performance liquid chromatography and nuclear magnetic resonance. These are not just arbitrary numbers on certificates—the absence of unwanted isomers or residual solvents means onward chemistry can progress without surprises.
With so many pyridine derivatives available, it may seem easy to opt for any similar intermediate. In practice, substituting another compound for 5-Amino-2,3-dichloropyridine usually means reworking entire reaction schemes. The precise positioning of the chloro groups impacts both the reactivity and selectivity during downstream synthesis. Not all dichloropyridine isomers are equal; moving a chlorine atom from the 3- to the 4-position, or from the 2- to the 6-position, shifts electronic effects and introduces steric factors that cause reactions to grind to a halt or veer off course.
Where some similar compounds see limited use because they introduce byproducts or fail to provide the required nucleophilicity at the amino site, 5-Amino-2,3-dichloropyridine stands out as both reliable and versatile. When modifications on the pyridine nucleus need to be selective, this intermediate supplies enough functionalization options without the headaches tied to overreactivity or uncontrollable side reactions. Medicinal chemists who have run into problems with less refined isomers can appreciate the clarity this specific substitution pattern brings.
The uses of 5-Amino-2,3-dichloropyridine spread beyond just forming the backbone of active pharmaceutical ingredients. This compound helps build advanced materials that rely on stable, well-defined molecular frameworks. In the agrochemical sector, derivatives serve as building blocks for crop protection agents or growth regulators. Functional groups on the molecule provide access to further modifications: it has been used as an anchor for preparing more elaborate heterocyclic scaffolds destined for antimicrobials or enzyme inhibitors.
I have seen this compound appear in multi-step syntheses where traditional amino-substituted pyridines faltered. Reactions that require precision—like Suzuki coupling or Buchwald-Hartwig amination—fit more easily within standard protocols when the starting material offers predictable reactivity. In the hands of an experienced process chemist, each controllable functional group means fewer surprises downstream.
Working with chemicals brings environmental and personal safety concerns that can’t be ignored. 5-Amino-2,3-dichloropyridine usually comes with manageable risk: it presents as a stable, non-volatile solid under normal conditions. Nonetheless, good laboratory practice always prevails. Avoid inhalation, use gloves, and keep the material in well-ventilated spaces—all common-sense measures for anyone with time spent at the bench.
Disposal deserves careful attention, especially with halogenated aromatic compounds. Analytical labs typically collect waste for controlled incineration and remind team members to segregate halogenated waste from general laboratory refuse. Those small steps keep hazardous chemicals out of waterways and off landfill sites, reinforcing the larger theme of safer, greener chemistry.
Consistent results set strong intermediates apart from nearly-there chemicals. I remember a project that hit repeated roadblocks using a less pure pyridine derivative from a low-cost source. The difference wasn’t subtle: poor yields, tricky purifications, and frequent failures that cost time and budget. Switching back to a trusted batch of 5-Amino-2,3-dichloropyridine resolved those issues. It may sound dull, but routine success underpins any push toward innovation. The smallest impurity may mask a real breakthrough.
Colleagues in scale-up chemistry echo this point: a material that works in the academic lab may stumble on the kilogram scale unless its reproducibility holds up. Reliable intermediates mean fewer failed batches, lower solvent use for purification, and reduced downtime. At an industrial site, these factors don’t just save money—they make R&D timelines more realistic and support a climate of creativity instead of chronic troubleshooting.
Responsible sourcing goes beyond paperwork. Well-documented batches of 5-Amino-2,3-dichloropyridine usually include assays for heavy metals, moisture, and chemical identity, not because regulators enjoy red tape, but because the downstream risk is real. In pharmaceuticals, tiny contaminants cascade through the workflow, sowing unpredictability and potential risk for patients further down the line. Even outside of drug synthesis, impurities in an intermediate can seed defects in plastics, electronic materials, or dyes. Over time, I have realized that robust quality management doesn't slow progress; it makes it sustainable and credible, meeting the ever-growing scrutiny from both regulators and end users.
Look up regulatory status, and you'll see this compound referenced in registration dossiers, export documentation, and inspection reports. It’s reassuring to work with something familiar to customs and compliance teams—a practical advantage for companies exporting finished goods or raw materials. Documentation brings transparency, and consistency here means more than just meeting a requirement—it ensures the product ends up in the right place, every time.
Chasing after the lowest-cost supplier for a specialized intermediate often backfires. Memories of failed experiments and shipping delays are hard to forget. Over the years, building strong relationships with suppliers has clear benefits—clear lines of communication, consistent documentation, and ready answers to questions about shelf life or stability. Reliable suppliers flag changes in synthesis methods or packaging long before an unexpected result shows up at the lab bench.
For teams tackling complex, multi-step syntheses, dependable sourcing does more than move a molecule from A to B. It shields R&D schedules from disruption and keeps projects pointed toward final goals. For smaller startups or academic groups, these relationships can mean the difference between a smooth campaign and a disappointing dead end.
High-value intermediates rarely come cheap, and 5-Amino-2,3-dichloropyridine is no exception. Cost per gram may deter those working under tight budget constraints. On the other hand, a modest investment upfront almost always pays off down the line through higher yields or more robust data. I’ve learned the hard way that using a cheaper, less characterized substitute can cost more in wasted effort than the perceived savings at the point of purchase.
Supply chain disruptions have become a new normal in recent years. Global events sometimes create shortages of basic chemicals, including seemingly mundane heterocyclic intermediates. When a reliable supplier delivers on schedule, with full certificates and matching specifications, research runs smoother and confidence grows. Budgets and timelines benefit from a little predictability, a rare commodity in a rapidly shifting global landscape.
Academic researchers searching for breakthrough discoveries make choices about intermediates with care. Availability in the right purity, and, importantly, in suitable pack sizes, removes unnecessary obstacles from early-stage projects. A graduate student can only make progress if each building block performs as promised. In my own research, the most productive weeks have happened when I could focus on solving genuinely new problems instead of troubleshooting routine chemistry—getting the right intermediate helps make that a reality.
5-Amino-2,3-dichloropyridine serves as an enabler, not because it transforms the field, but because it smooths over many of the common headaches that stall creative synthesis. Its unique balance between stability and reactivity doesn’t make headlines, but it earns respect from those who rely on producing actionable results. Robust intermediates give talented researchers the breathing space needed to focus on what really matters: discovery, analysis, and refinement.
Scientific progress depends on open access to reliable tools. Increasing availability of research intermediates like 5-Amino-2,3-dichloropyridine, including small-scale packs and rapid delivery, levels the playing field for innovators everywhere. More transparent batch documentation helps catch and resolve problems earlier. Improved communication between suppliers and end users ensures what arrives matches both stated needs and regulatory expectations.
Industries benefit when suppliers bundle support and technical know-how, not just a bottle in a box. Experienced synthesis partners can advise on tricky reaction points, suggest storage tips, and share updates on longer-term supply trends. Building these kinds of collaborations not only speeds up problem-solving but strengthens the network of trust underpinning research, both academic and industrial.
In a field defined by precision and progress, the quest for better intermediates never really ends. 5-Amino-2,3-dichloropyridine demonstrates how specialized building blocks can quietly underpin larger breakthroughs. By rewarding reliability, purity, and thoughtful supply chain practices, researchers create the conditions necessary for bigger advances—whether in medicine, agriculture, or materials science. Each time a chemist reaches for a trusted intermediate and it delivers as expected, it frees up time, energy, and creativity for the work that really matters.
Products like 5-Amino-2,3-dichloropyridine won’t grab headlines on their own, but anyone who’s ever tried to troubleshoot a stubborn synthesis or rescue a failing project knows the true value of quality intermediates: they keep innovation moving forward—one well-characterized compound at a time.