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HS Code |
501626 |
| Name | 3-Iodo-4-Aminopyridine |
| Synonyms | 4-Amino-3-iodopyridine |
| Cas Number | 6298-57-9 |
| Molecular Formula | C5H5IN2 |
| Molecular Weight | 220.01 |
| Appearance | Off-white to light yellow solid |
| Melting Point | 158-162°C |
| Solubility | Soluble in DMSO and methanol |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8°C |
| Smiles | c1cncc(N)c1I |
| Inchi | InChI=1S/C5H5IN2/c6-4-1-2-7-3-5(4)8/h1-3H,(H2,7,8) |
| Pubchem Cid | 114680 |
As an accredited 3-Iodo-4-Aminopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 3-Iodo-4-Aminopyridine is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 3-Iodo-4-Aminopyridine is shipped in tightly sealed containers, protected from light and moisture. It is packed according to chemical safety regulations, including appropriate hazard labeling. The chemical is typically transported by certified carriers, with documentation for safe handling, and may require temperature control or specific storage conditions during transit to ensure stability. |
| Storage | 3-Iodo-4-Aminopyridine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ideally, storage should be at room temperature or lower, and in accordance with local chemical safety regulations. Always refer to the manufacturer’s safety data sheet (SDS) for specific instructions. |
Applications of 3-Iodo-4-Aminopyridine in Industrial Manufacturing3-Iodo-4-Aminopyridine serves as a critical intermediate in several specialized industrial fields. Our direct manufacturing expertise supports advanced downstream applications across pharmaceutical synthesis, agrochemical production, and specialty chemical development. Below, we detail authentic manufacturing scenarios, compliance benchmarks, process roles, and the types of finished products produced using this key raw material. 1. API Intermediate for Ion Channel Modulator PharmaceuticalsPharmaceutical companies use 3-Iodo-4-Aminopyridine as an essential intermediate when synthesizing advanced ion channel modulators for neurological disorder treatments. This material enters multi-step syntheses to introduce iodopyridine motifs crucial for target molecule activity. Handling and tracing require strict adherence to cGMP standards for active pharmaceutical ingredient (API) manufacture due to its potency and reactivity. Industry compliance standards
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2. Agrochemical Active Ingredient Manufacturing3-Iodo-4-Aminopyridine is used as an advanced intermediate in the manufacture of selective insecticides and seed treatment actives. Agrochemical formulators utilize its aminopyridine core for further modifications, introducing functionality vital to pest control molecules. All processing and formulation comply with global agrochemical registration guidelines, ensuring environmental and occupational safety. Industry compliance standards
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3. Synthesis of Diagnostics and Fine Chemical ReagentsAnalytical and life science reagent manufacturers rely on 3-Iodo-4-Aminopyridine to synthesize specialty labeling reagents and diagnostic markers. This material allows for the construction of nitrogen-heterocycle tags, used in enzyme immunoassays or as fluorescent scaffolds. Each manufacturing step conforms with purity and contaminant controls required for sensitive analytical use. Industry compliance standards
Typical usage ratio
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4. Advanced Material and Polymer ResearchIn advanced polymer and functional material research, development teams incorporate 3-Iodo-4-Aminopyridine for synthesizing modified pyridine-based monomers. These monomers enable the formation of conductive polymers and functionalized materials, primarily for electronics and sensor applications. Academic, pilot, and pre-commercial operations adhere to rigorous chemical management and safety protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
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Working in the specialty chemicals sector, experience has shown how certain molecules become essential, not just for chemists but for entire industries. 3-Iodo-4-Aminopyridine, with the CAS number 63108-40-3, is one such compound. Here, manufacturing doesn’t just mean following recipes—it means understanding why each property of this material counts for researchers and production teams down the line.
Our typical batches include 3-Iodo-4-Aminopyridine with purity that consistently exceeds 98 percent by HPLC testing. This standard supports work where trace impurities could alter catalytic activity or skew pharmacological investigations. The solid form, collected as light tan to off-white crystalline powder, allows consistent weighing and transfer for those in both bench-top and pilot-scale setups. We control moisture under 0.5 percent and residual solvents to less than 100ppm where feasible, because we have seen firsthand how persistent traces of DMF or DCM can disrupt product development further downstream.
The melting range sits reliably between 179°C and 182°C. Each lot runs through a controlled crystallization and filtration process to ensure consistency between shipments. Color and bulk density may vary slightly batch to batch; that’s the nature of organic synthesis on an industrial scale. Instead of aiming for unattainable visual uniformity, focus stays on function and reproducibility. Analytical data, verified by our own QC chemists, supports what the material can actually do in real-world labs, not just how it looks on paper.
The value of 3-Iodo-4-Aminopyridine shows up most clearly in the hands of experienced chemists. Its structure, featuring both an iodine and an amino group on the pyridine ring, makes it a versatile intermediate. In pharmaceutical research, this dual reactivity opens pathways for palladium-catalyzed coupling reactions and selective substitutions. Our customers in medicinal chemistry design and build novel scaffolds for neurological or immunological drug candidates, often leveraging this core as a modular building block.
In crop-science and agricultural chemical synthesis, the aminopyridine motif has proven essential for designing compounds with specific herbicidal or insecticidal properties. From experience working with these industries, we understand how tight timelines and regulatory deadlines demand a reliable supply chain, backed by production that avoids lot-to-lot surprises. Engineers using 3-Iodo-4-Aminopyridine for scale-up appreciate tight particle size control and minimal fines that hamper powder handling or filtration. We have adjusted crystallization parameters through years of batch analysis to improve flow and reduce static, which translates directly into safer and cleaner processing in our clients’ facilities.
In developing the manufacturing route, we selected iodination strategies that minimize iodide and nitrate waste. The old lab-scale methods using excess oxidants resulted in safety headaches and low yield when scaled. By investing in multi-stage purification and strictly defined reactant ratios, we’ve managed to cut byproduct formation and ease the post-reaction workup. These reductions don’t just offer environmental benefits—they protect workers on our lines from unnecessary exposure and reduce the amount of hazardous waste requiring downstream treatment.
Batch reproducibility counts for more than just QA paperwork. Our operators note even subtle shifts in reaction color or exotherm profiles, and we have process logs filled with notes on the impact of ambient humidity, agitation rates, and raw material lots. These records led us to implement extra drying steps and switch to higher grade starting pyridines after seeing sporadic yield losses over time. Labs requesting reference samples often confirm matching retention times and impurity profiles over several years’ worth of product, proof that thoughtful manufacturing trumps automation without oversight.
Laboratories buying intermediates for regulated synthesis rely on traceable purity and contamination data. We offer full HPLC, NMR, LC-MS, and GC reports with each batch, retaining reserve samples for two years after dispatch. In one case, a repeat customer identified a potential cross-contamination from a supplier of another aminopyridine. Our ability to provide archive samples for root cause analysis helped that customer avoid a production recall and maintain audit compliance.
Our internal cross-checks frequently highlight issues invisible to basic spot tests. Early batches faced sporadic colored impurities after prolonged storage, usually due to trace metal residues introduced during iodination. We addressed this by refining the filtration protocol and running additional EDTA treatments before final drying, based on side-by-side customer lab feedback. The result: batches today perform more predictably in Suzuki-Miyaura and Heck reactions than those from smaller-scale or contract labs relying on generic purification.
Some clients have asked about the real difference between our product and samples coming out of contract labs or bulk trading houses. The main point is not simply about price per kilo. Once, a pharmaceutical client sourced material from a generic supplier, only to find incomplete conversion during derivatization steps and unanticipated side reactions. Later investigation traced these setbacks to batch impurities missed by less rigorous process controls. In another case, a kilogram of “equivalent” 3-Iodo-4-Aminopyridine from a third-party vendor forced cleanup by additional silica gel filtration, wasting two full days of development time and spiking operational costs.
Direct manufacturing control means we never lose sight of which solvents touch the product, which processing equipment runs each lot, and how batch records capture operator interventions. That’s more than a compliance checkbox—it’s a core driver for process safety and reliability, particularly with scale-sensitive molecules like iodinated pyridines that can be highly reactive with trace acids or bases.
Every chemical has handling guidelines drawn from direct experience as much as from regulatory templates. 3-Iodo-4-Aminopyridine generates dust readily, and prolonged skin contact should be avoided due to moderate irritancy. Our packaging lines now use anti-static liners and stitched polyethylene bags, based on multiple incidents of material bridging in family-press drums during humid weather. By switching from standard PE jars to moisture-proof barrier containers, customer complaints about clumping and caking dropped by half over a single year.
Interactive safety training, not just formal SDS sheets, forms part of onboarding for all plant workers. We have learned to train operators to recognize the distinct sharp odor that signals vapor phase contamination, especially during long rotary evaporation steps. Prompt cleanup with inert absorbents prevents minor spills from upscaling into broader contamination events. Plant managers report that investment in localized extraction—not a universal fix but a focused improvement—cut powder inhalation complaints in the charging area to near zero, based on a running two-year health record.
As the only producer with in-house route development, we field queries that go beyond generic FAQs. One persistent challenge: balancing purity with yield as batch sizes rise. Typical side products, such as 3-hydroxy-4-aminopyridine, require careful monitoring since their presence can skew biological screening and confuse downstream analytics. While percentage losses per kilo might seem small, even trace carryover can escalate out-of-specification results in regulated settings.
Suppliers often downplay these risks, but as manufacturers, tracking yield losses and controlling impurities is our direct responsibility. We continue to trial new purification media, including pilot runs of mixed-bed resin columns and newer semi-preparative chromatography setups, all aimed at minimizing byproducts. By sharing failed runs and impurity profiles candidly with R&D users, we help our partners calibrate their analytical thresholds for complex syntheses. This open feedback loop works both ways: users’ performance data often highlights flaws invisible in our own batch testing, prompting us to re-examine process steps that would otherwise pass unnoticed.
3-Iodo-4-Aminopyridine finds routes into small academic pilot projects as well as into metric ton lots for industrial R&D programs. Smaller research groups value our willingness to ship lower-MOQ lots without compromising on the analytical support or batch data quality. We have established job histories with custom synthesis houses designing CNS-active compounds, where every milligram shipped comes with a pedigree of traceability for later regulatory filings.
Large-scale projects in the pharmaceutical and agrochemical sectors benefit from our ability to ramp up batch sizes with stable performance. With every scale increase, potential for batch segregation or subtle process drift rises. Having operated glass-lined and stainless reactors side by side, we know how even trace differences in thermal cycling or agitation can show up downstream as unexplained analytical peaks. By keeping process records granular and maintaining a dialogue with process users, we cut surprises and help clients avoid costly troubleshooting later.
Environmental responsibility grows more pressing each year—not just as a regulatory checkmark, but as part of daily operations. Iodinated and aminated organic compounds present special waste and effluent challenges. Over the past five years, we redesigned the workup process to better capture waste iodine and reduce total nitrogen discharge. Switching over to closed-system aqueous extraction cut fugitive emissions and limited volatilized organic waste, streamlining permitting and reducing incident response costs.
Energy consumption persists as a bottleneck during crystallization and drying. By investing in more efficient jacketed dryers and heat exchange systems, batch turnaround now cuts resource load by nearly 20 percent per kilo produced. These process changes build on plant-floor observations—valve leaks, slow heat-up rates, uneven agitation—fed back from experienced operators who know how theoretical yields translate into utility bills and real-time factory performance.
Manufacturers don’t operate in a vacuum. End-users face procurement pressures, unexpected run-ins with customs, and timeline crunches that traders and brokers rarely factor in. Managing our own inventory, we keep rolling stock on hand rather than producing only to order. This buffers clients against raw material disruptions and allows emergency shipments if a customer’s previous supplier drops out of compliance or misses a batch release.
Direct factory-to-lab contact means real answers from technical staff with intimate process knowledge. Clients are not routed through layers of sales. Questions on lot history, packing adjustments, or unexpected analytical anomalies go straight to someone who handled that batch, not a distant distributor skimming paperwork. We have seen productivity gains for both sides in reducing lag—one pharmaceutical client re-launched a halted synthesis trial in under a week after a competitor failed to deliver, simply by accessing our ready inventory.
Chemicals serve as tools, not just commodities. End users regularly bring specific needs to the table: particle size for high-throughput reactors, alternative package sizing for automated dosing machines, impurity spectrum for ultra-sensitive bioassay thresholds. By customizing crystallization conditions or packaging formats, we have enabled faster adoption in distinct research applications, both for pioneering pharmaceutical leads and specialty agrochemical development.
Recently, one biologics customer faced scale-up trouble during a hybrid peptide conjugation and needed ultra-low halogen background. Routine supply chains balked at special requests, but by switching our isolation method, we supplied material that hit their target without need for additional repurification. In another project, an academic group pioneering kinase inhibitors required frequent analytical support to trace a previously undetected byproduct. Our lab collaborated directly, running side-by-side NMR comparisons and HPLC method development, eventually fine-tuning the synthesis route to their satisfaction.
These interactions go deeper than standard order fulfillment. They inform how we invest in plant upgrades, analytical instrumentation, and in developing new approaches to process challenges that previous generations just accepted as inevitable.
Third-party trading houses or less-specialized suppliers often treat material like 3-Iodo-4-Aminopyridine as bulk commodity. In reality, reliability comes from tight in-process control, iterative feedback from experienced users, and willingness to innovate batch after batch. Our manufacturing experience spans every stage, from initial route selection to scale tweaks and after-sale support. This means that every shipment leaves with a process history directly traceable to plant staff with ownership of its outcome.
Instead of chasing lowest cost by cutting process corners, we focus on keeping impurity, moisture, and residual solvent levels under strict thresholds. That is what enables researchers and production chemists to trust downstream reactivity, biological compatibility, and regulatory traceability. Laboratories never face guesswork about what they’ll receive; even the packaging choices reflect years of feedback from high-throughput facilities and solo academic investigators alike.
For those who count on uninterrupted R&D timelines, predictable reactivity, and less rework or troubleshooting, the difference becomes clear: not every supplier is the actual maker of what they sell, but every batch of 3-Iodo-4-Aminopyridine that leaves our line brings with it the assurance of genuine manufacturer oversight, responsiveness, and continued investment in chemical quality and process consistency.