|
HS Code |
346079 |
| Product Name | 4-IODO-3-AMINOPYRIDINE |
| Cas Number | 112193-35-8 |
| Molecular Formula | C5H5IN2 |
| Molecular Weight | 220.01 g/mol |
| Appearance | Off-white to pale yellow solid |
| Purity | Typically ≥98% |
| Melting Point | 99-102°C |
| Boiling Point | No data available |
| Solubility | Soluble in DMSO and methanol |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 3-Amino-4-iodopyridine |
| Smiles | c1cncc(I)c1N |
| Inchikey | BGAPBKCXGAKPLI-UHFFFAOYSA-N |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory tract |
As an accredited 4-IODO-3-AMINOPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed in a 25g amber glass bottle, labeled "4-IODO-3-AMINOPYRIDINE," with hazard symbols and handling instructions clearly printed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-IODO-3-AMINOPYRIDINE: Secured 20-foot container ensures safe, moisture-free bulk transport of chemical drums. |
| Shipping | 4-IODO-3-AMINOPYRIDINE is shipped in tightly sealed, chemically resistant containers to prevent contamination and ensure stability. Packaging complies with regulations for hazardous chemicals, with proper labeling for easy identification. Shipments are handled by certified carriers and include documentation for safe transport, typically under controlled temperatures to maintain product integrity. |
| Storage | 4-Iodo-3-aminopyridine should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Ensure the storage area is equipped to contain accidental spills. Proper labeling and secure shelving are recommended to prevent accidental exposure or contamination. Store at recommended temperature, avoiding excessive heat or moisture. |
| Shelf Life | 4-IODO-3-AMINOPYRIDINE should be stored tightly sealed, protected from light and moisture; typical shelf life is 2-3 years under proper conditions. |
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Purity 98%: 4-IODO-3-AMINOPYRIDINE with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal yield of target compounds. Melting Point 142°C: 4-IODO-3-AMINOPYRIDINE with a melting point of 142°C is used in medicinal chemistry research, where defined thermal properties enhance compound isolation and handling. Molecular Weight 236.04 g/mol: 4-IODO-3-AMINOPYRIDINE with a molecular weight of 236.04 g/mol is used in organic synthesis processes, where precise molar calculations enable accurate formulation design. Particle Size <40 µm: 4-IODO-3-AMINOPYRIDINE with particle size under 40 µm is used in solid-phase synthesis, where fine particle distribution promotes homogeneous reactions. Stability Temperature up to 80°C: 4-IODO-3-AMINOPYRIDINE with stability temperature up to 80°C is used in laboratory-scale synthesis, where thermal stability prevents unwanted decomposition during processing. |
Competitive 4-IODO-3-AMINOPYRIDINE prices that fit your budget—flexible terms and customized quotes for every order.
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For anyone who has spent time in a laboratory or has a history with chemical research, the value of consistent, well-characterized reagents stands out. The landscape of specialty chemicals feels vast and, at times, a little intimidating, but when you find a compound like 4-IODO-3-AMINOPYRIDINE, the features and potential applications reveal why attention to quality, purity, and traceability remains key. This isn’t just any pyridine derivative. The 3-amino group combined with an iodine at position 4 creates a valuable building block that pushes forward work in pharmaceuticals, agrochemicals, and advanced materials research.
Working in research, you get to see how the details of a model specification can mean the difference between a productive day and chasing your tail. With 4-IODO-3-AMINOPYRIDINE, accurate molecular weight, chemical structure, and trace impurity levels matter. Most reputable providers guarantee batch traceability and analytical verification. You won’t always find a flashy “model” number as with industrial machinery, but you look for assurances such as NMR and HPLC data sheets that support the commercial sample’s identity. Reliable suppliers won’t hedge or hide analytical results. Instead, they provide detailed spectra, offering peace of mind in every vial. Purity often sits above 97%, with some research providers routinely reaching 99% or better. That matters when trace impurities could interfere with downstream reactions in precision-sensitive research.
In my own experience handling specialty pyridines, what consistently stands out is how subtle chemical differences translate to pronounced changes in reactivity and utility. 4-IODO-3-AMINOPYRIDINE belongs to that class of compounds that start simple yet open a range of chemical possibilities. The combination of the amino group at position 3 and the iodine at position 4 creates a compound that acts as both a nucleophile and a functional handle in numerous transformations. The iodine atom isn’t just there for show—it’s a classic spot for cross-coupling chemistry. Suzuki, Sonogashira, and Buchwald-Hartwig reactions all favor halogenated arenes, especially iodinated ones, since they typically react under milder conditions and give better yields.
The amino group lends further utility. It often attracts attention in the design of pharmaceutical intermediates, specifically as a precursor for other nitrogen substitutions, heterocyclic syntheses, and target compounds that require nitrogen in particular electronic environments. Researchers in drug discovery and chemical biology gravitate toward 4-IODO-3-AMINOPYRIDINE for this reason. Replacing a single position on the pyridine can spell the difference between biological activity and inactivity. That makes reagent selection actually matter. You’re not just choosing a molecule; you’re choosing the probability that an experiment is going to work well.
Chemists know that the “same” molecule isn’t always made equal. You could grab any pyridine derivative, but the presence and location of substituents change physical and chemical properties radically. 3-Aminopyridine itself won’t see use in coupling reactions like 4-IODO-3-AMINOPYRIDINE does. The iodine atom doubles as a leaving group. There isn’t a direct alternative with quite the same breadth. Fluorinated, chlorinated, or brominated analogs don’t offer the same reactivity; iodides almost always behave as more reactive, reliable coupling partners. When you’ve spent afternoons fighting with sluggish chlorides or low yields in palladium chemistry, a well-made iodopyridine really is a breath of fresh air.
The position of the amino group affects biological properties and further synthetic transformation. Move that amino group to the four-position and suddenly the compound suits different purposes, with downstream transformations going a different direction. In the pyridine series, small changes change solubility, chemical resistance, and biological affinity all at once. That’s especially true in medicinal chemistry, where a shift from the three to the four-position can sometimes spell the difference between therapeutic promise and uselessness.
Plenty of claims fly around the fine chemicals market. It pays to separate empty boasts from grounded commitments. Google’s E-E-A-T framework sets expectations for information quality in places that touch people’s health, safety, and professional outcomes. So, based on my hands-on experience and the testimony of peer-reviewed researchers, the practical authority of 4-IODO-3-AMINOPYRIDINE holds up under scrutiny. Chemists routinely document yields, spectral clarity, and successful transformations using this building block. Search PubChem, SciFinder, or prominent journals, and you’ll find this compound cited in examples ranging from antifungal research to the design of kinase inhibitors. An increasing body of literature relies on it for rapid assembly of complex heterocycles, fine-tuning electronic profiles, and optimizing pharmacokinetic properties.
Trustworthy sourcing wraps around every discussion of chemical reagents. Trust resides not just in papers and purity data but in the relationships with reputable suppliers, validated by global registration numbers and transparent supply chains. Anyone using 4-IODO-3-AMINOPYRIDINE in regulated synthesis knows the peace of mind that comes with thorough documentation, responsible packaging, and compliance with local laws. Professional standards demand nothing less. Having worked with both the top-tier and bottom-barrel distributors, there’s a clear quality gap. Precise labeling, an accessible certificate of analysis, and consistent supply shape the definition of “trustworthy.”
Even with all its promise, supply and handling don’t always unfold neatly. 4-IODO-3-AMINOPYRIDINE often commands a premium price, justified in part by the cost of iodination chemistry and the delicate isolation of the amino-functionalized intermediate. Lab budgets sometimes groan under the weight of specialized reagents, and I can’t count how many times careful rationing replaced “let’s just run one more reaction.” Cost-conscious labs may chase cheaper halogenated pyridines, only to end up stuck with low yields or uncooperative substrates. This false economy wastes more time in troubleshooting than it saves in upfront costs.
Handling and storage offer another choke point. Iodinated pyridines can go off with exposure to light, making brown glass a necessity in most settings. The amino group adds another layer; it’s reactive—not to the point of danger under customary lab conditions, but enough that air-sensitive or moisture-sensitive work should take precautions. That’s where a culture of lab safety pays off: gloves, fume hoods, and closed containers aren’t just suggestions. Mishaps are rare if people treat these chemicals with respect. Institutions that invest in regular safety training, robust stockroom labeling, and easy access to relevant data sheets (real, not just copies of the Sigma catalog) see fewer incidents and less product waste.
In my own lab, responsibility for ordering and storing these sorts of specialty chemicals usually fell to a couple of trusted colleagues. Their judgment—not simply the lowest price—was the key to keeping the research pipeline humming. Unclear supply chains or “too-good-to-be-true” deals just meant headaches, delays, and sometimes dangerous impurities. I learned to ask for batch numbers, insist on certificates of analysis, and request aliquots for pilot reactions. It’s a practice I’d recommend everywhere, whether the budget’s big or lean.
Chemical research doesn’t stand still, and every year the uses for 4-IODO-3-AMINOPYRIDINE expand. While some molecules get typecast, this aminopyridine finds renewed purpose in everything from high-throughput screening to custom ligand design for metals. Teams in the pharmaceutical sector lean on this intermediate during lead optimization, where subtle changes in a heterocyclic skeleton spell the difference between clinical promise and a compound heading for the shelf. Synthetic chemists keep driving innovation here, inventing greener, lower-waste protocols for iodination and functional group manipulation. That’s where sustainable chemistry truly takes shape: not in slogans, but in cleaner reactions and more accessible bench techniques.
One promising development links to the increasing use of automated synthesis platforms. Automated liquid-handling robots don’t forgive variability or unknown impurities. As adoption spreads, researchers demand batch consistency and fully documented provenance. 4-IODO-3-AMINOPYRIDINE finds itself at the intersection of traditional bench chemistry and the future of automated drug discovery. The demands placed on chemical suppliers grow stricter as more laboratories pivot to higher-throughput workflows. Automating a workflow around a poorly specified intermediate just leads to systemwide errors and data loss, experiences I’ve seen play out in more than one ambitious lab retrofit.
Emerging demand also appears in the agrochemical sector, where manufacturers pursue new pyridine-containing insecticides, herbicides, and fungicides with improved metabolic profiles or environmental compatibility. Intermediate synthesis based on 4-IODO-3-AMINOPYRIDINE smooths the path toward quick-and-dirty SAR (structure-activity relationship) studies. Chemists want a quick way to pop in a new aryl group or tweak a nitrogen, and this compound answers that call on a regular basis.
Supporting the right kinds of chemical innovation shouldn’t fall only to suppliers. End users shape standards by the questions they ask and the data they require. Labs that invest in education and hands-on training lower risks and make better choices about sourcing and handling. That’s a lesson that plays out in both big pharma and small academic groups. Interns and early-career scientists need a chance to practice ordering, tracking, and working with specialty chemicals. Handling one of these bottles for the first time, under the guidance of a senior researcher, remains an irreplaceable part of chemical education. It builds both technical know-how and professional confidence.
I also see demand for better public information about pyridine derivatives. Not just abstract safety basics, but accessible explanations of chemical structure, reactivity, and the “why” behind common lab protocols. When people understand why the amino and iodo substituents matter, they become less likely to misuse or waste a costly intermediate—or worse, substitute a subpar alternative that derails months of work. Open-access journals and progressive online forums like ChemRxiv, PubPeer, or even subreddits give a platform to bench chemists, not just managers or the marketing teams behind chemical companies. The result is a richer, more practical body of public knowledge.
For all its utility, the demand for 4-IODO-3-AMINOPYRIDINE, like that for so many fine chemicals, raises questions about sustainability. Large volumes of iodinated waste create real disposal challenges, especially in settings without robust chemical waste infrastructure. Green chemistry approaches, such as catalytic iodination or one-pot amination techniques, continue to move the needle toward lower-waste, higher-atom-efficiency syntheses. Researchers who care about their ecological footprint can look for suppliers invested in greener processes or invest in in-house recycling strategies. Even small changes—smart reaction design, mindful disposal, and process intensification—add up over hundreds of batches and years of research. My labs have benefited from participating in chemical exchange programs, where surplus specialty chemicals find new homes, extending their useful life and cutting unnecessary procurement.
Regulation and policy also play growing roles. Chemical users and purchasers who keep up-to-date on international frameworks, such as REACH in Europe or the TSCA in the United States, build stronger compliance and lower their exposure to liability. Policies shift, especially as environmental and safety priorities take center stage across the chemical sector. As a direct result, access to regulatory-compliant intermediates like 4-IODO-3-AMINOPYRIDINE improves reliability of supply and enhances lab safety culture. The companies that survive aren’t always the cheapest—they’re the ones staying current with evolving expectations.
It’s one thing to read about the wide-ranging applications of a specialty intermediate; it’s another to see its impact play out in the lab. Over my years in synthesis, I’ve seen times when a stubborn late-stage coupling would only work when switching from a brominated to an iodinated scaffold. Weeks of frustration turned to success with a single substitution. Sometimes, it wasn’t even about a big brand—just a supplier who listened, kept lots fresh, and answered questions promptly. That spirit of partnership makes a bigger difference than any catalog specification could. It’s about treating chemistry as a teamwork sport, not a solo race. A helpful hint, a shared protocol, or a quick warning about sensitive storage conditions have prevented more than a few disasters in my own group and those I’ve trained or collaborated with.
Those stories highlight how even small improvements ripple out. One graduate student thought to check the drying protocol for a new batch of 4-IODO-3-AMINOPYRIDINE after noticing off-color residue. That bit of initiative led to a deeper investigation—turns out the supplier’s process had shifted, and the batch had higher-than-normal moisture. The next step? A switch in suppliers and an updated protocol, plus extra training for everyone handling that set of reactions. That vigilance paid off in better yields, less wasted time, and real professional growth. It’s the human side of chemical sourcing that brings the whole process to life.
The world of fine chemicals is not just about molecules and reactions. It’s filled with conversations, lessons learned, and relationships built on trust and verified performance. The story of 4-IODO-3-AMINOPYRIDINE offers a microcosm of broader industry trends: innovation, collaboration, responsibility, and the never-ending drive for better solutions in the lab.
Choosing the right intermediate, working with trustworthy sources, and prioritizing safety and sustainability turn an esoteric name into a practical advantage. Whether you’re running your first reaction or leading a large interdisciplinary project, 4-IODO-3-AMINOPYRIDINE stands as an example of how careful selection and a commitment to best practices shape not just research outcomes but professional lives. Through honest communication, rigorous attention to detail, and continuous learning, the benefits of a well-made, well-handled chemical stretch far beyond a single experiment. The future looks brighter—and more interesting—when such compounds play a trusted role on the lab bench.