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HS Code |
154178 |
| Cas Number | 4318-72-1 |
| Molecular Formula | C5H4IN3O2 |
| Molecular Weight | 264.01 |
| Appearance | Yellow to orange solid |
| Purity | Typically ≥98% |
| Melting Point | 232-236°C |
| Solubility | Slightly soluble in water; soluble in DMSO and DMF |
| Synonyms | 5-Iodo-3-nitropyridin-2-amine |
| Storage Temperature | 2-8°C (refrigerated) |
| Smiles | c1cc(c(nc1N)[N+](=O)[O-])I |
| Inchi Key | QYRJGUGDCZZWGH-UHFFFAOYSA-N |
As an accredited 2-Amino-5-Iodo-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25 grams of 2-Amino-5-Iodo-3-Nitropyridine, sealed with a screw cap, labeled with hazard warnings. |
| Shipping | **Shipping Description:** 2-Amino-5-Iodo-3-Nitropyridine should be shipped in tightly sealed containers protected from moisture and light. It must be packaged according to hazardous material transport regulations, considering its toxicity and possible environmental hazards. Ensure labeling complies with chemical safety standards. Handle with care to prevent leaks, spills, or accidental exposure during transit. |
| Storage | 2-Amino-5-iodo-3-nitropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances (such as strong oxidizing or reducing agents). Keep it away from heat and sources of ignition. Properly label the storage container, and handle the chemical using appropriate personal protective equipment to prevent exposure. |
Applications of 2-Amino-5-Iodo-3-Nitropyridine in Industrial ManufacturingAs a trusted producer of specialty pyridine derivatives, we focus on downstream applications of 2-Amino-5-Iodo-3-Nitropyridine where its unique halogenated nitroaniline structure meets tangible market needs. Below, we detail applied use cases across pharmaceutical intermediates, agrochemical synthesis, advanced dyes and pigments, and chemical research—highlighting industry standards, proportioning guidance, process entry points, and end product types for each sector. 1. Pharmaceutical Intermediate – Sartan Antihypertensives SynthesisSeveral producers of angiotensin II receptor blockers (sartans) integrate this compound as a key intermediate during heterocyclic scaffold assembly. Its iodo-substituted moiety enables regioselective cross-coupling in multi-step syntheses for active pharmaceutical ingredients (API), contributing to the formation of pyridine or bipyridine-based drug cores essential for downstream biological activity. Manufacturers typically use the material after the nitration stage, leveraging its high purity for reliable batch reproducibility and adherence to regulatory norms. Industry compliance standards
Typical usage ratio
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2. Agrochemical Active Ingredient Precursor – Halogenated Pyridine HerbicidesIn the crop protection sector, multi-national agrochemical companies employ this nitro-iodo pyridine in the synthesis pipelines of new-generation halogenated pyridine herbicides. Its chemical structure offers a platform for constructing selective broadleaf and grass weed inhibitors, particularly where electron-withdrawing groups and controlled substitution improve soil stability. Processing teams introduce it at the early combinatorial chemistry stages to fine-tune structure-activity relationships in proprietary herbicidal molecules. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Organic Dye and Pigment SynthesisSpecialty dye manufacturers incorporate this compound into the design of high-performance colorants for fiber, inkjet, and OLED applications. Its strong electron-withdrawing and halogen functional groups assist in expanding the absorption range and improving chromatic fastness. The material enters synthetic routes focused on constructing azo, nitro, or polymethine dye cores through cross-coupling and substitution strategies, allowing formulators to create pigments with required shade, stability, and lightfastness properties. Industry compliance standards
Typical usage ratio
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4. Chemical Synthesis Research – Labelled Pyridine DerivativesAcademic and corporate R&D laboratories utilize this compound as a halogenated pyridine backbone for the synthesis of isotopically or functionally tagged reference materials. The distinct iodine position allows downstream chemists to insert radiolabels or fluorescent probes using mild catalytic exchange, supporting tracer studies or advanced analytical assays. Researchers integrate the material in the late-stage modification of labeled compounds, facilitating accurate tracking in bioanalytical projects or mechanistic studies. Industry compliance standards
Typical usage ratio
Downstream process integration
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In the world of organic synthesis, some compounds inspire both respect and cautious handling. 2-Amino-5-Iodo-3-Nitropyridine stands out among these, bringing a blend of functional diversity and reactivity that makes it indispensable in advanced chemical research and manufacturing. Our focus has been on the fine details: ensuring every batch meets the real-world demands of pharmaceutical intermediates, agrochemical innovations, dye production, and other life science fields that rely on the pyridine scaffold.
From our experience in scaling up from laboratory to fermentation volumes, we see constant attention is needed to both the safety and performance profile of this compound. The molecular structure, with its iodine, nitro, and amino groups strategically positioned on the pyridine ring, offers unique reactivity windows. Chemists favor this molecule for coupling reactions, halogen exchange, and as a pivotal intermediate in multiphase projects. We have participated directly in projects where the introduction of the amino functionality at position two, the bulk and polarizability of iodine at position five, and the electron-withdrawing nitro group at position three together create new opportunities for C-N and C-C bond formation under milder conditions than possible with other pyridine derivatives.
Our process starts with verified raw materials and extends into a controlled atmosphere, which is critical for the sensitive nature of this compound. Purity has a direct impact on downstream yields and safety profiles—based on repeated HPLC, NMR, and elemental analysis, we maintain a standard purity above 98% for most shipments. Moisture content, tolerated up to a defined maximum threshold, gets tested in every run, and we monitor for trace metal contaminants that could otherwise disrupt catalytic processes downstream.
Through years of collaboration with pharmaceutical and chemical partners, we hear frequently about batch inconsistency from commodity suppliers or fluctuating impurity profiles that complicate regulatory filings. We realized early that many project delays come down to these subtle differences. Our focus on tight quality specs, traceability of every lot, and reproducible, industrial-scale purification reflects the lessons carved by working alongside synthetic chemists, regulatory teams, and process engineers.
For those grappling with synthetic bottlenecks, substitution pattern makes all the difference. In the hands of an experienced chemist, 2-Amino-5-Iodo-3-Nitropyridine serves both as a starting block and as a strategic partner for late-stage functionalizations. The amino group participates readily in formation of amides or ureas. The iodo substituent simplifies Suzuki, Sonogashira, and Buchwald–Hartwig couplings, where its leaving group ability enables high yields with lower catalyst loadings than lighter halides. The nitro configuration supports further transformation, either as a handle for nucleophilic aromatic substitution or post-synthetic reduction to introduce new amino functionalities. No trivial matter when the end goal might be a patentable drug candidate or a crop-protection molecule with zero tolerance for synthetic errors.
In manufacturing, we have handled a wide array of pyridine derivatives, each bringing their own quirks and value. 2-Amino-5-Iodo-3-Nitropyridine distinguishes itself in three important technical respects. First, iodine substitution increases molecular mass and bulk, which modifies how the compound interacts in catalytic cycles—especially where selectivity and blocking are considered. This feature often leads to higher specificity in palladium-catalyzed processes. During direct comparisons with 5-chloro or 5-bromo analogues, we observe improved reaction rates and product purities, largely attributable to the iodo group's ease of activation in cross-coupling reactions.
Second, the nitro group on position three contributes electronic effects unmatched by other electron-withdrawing substituents. We notice distinct differences in reactivity when switching from nitro to cyano or sulfonyl analogues. In experimental feedback, this change translates to faster substitution rates, fewer side reactions, and easier downstream reduction. For scale-up and regulatory documentation, minimizing tars and byproducts helps in controlling waste and maintaining clean process documentation.
Third, compared to pyridines without amino groups, the solubility and crystallinity of 2-Amino-5-Iodo-3-Nitropyridine makes for smoother handling in both solvent-based and solid-state reactions. That matters as we scale up and need to optimize solvent use, filter cycles, and drying times. Multiple partners have shifted protocols to accommodate this compound’s reliability, creating more robust syntheses with greater reproducibility across multiple plant sites.
We characterize every shipment by HPLC and melting point analysis, observing a narrow melting range which signals stability. Our typical lot size supports both research and pilot-scale clients, with options for commercial-volume orders arranged under custom agreements. Powder handling requires closed systems, both for dust suppression and protection of staff. In our experience, product flow properties influence filling accuracy, so regular particle size analysis forms part of our QC routines. For packaging, chemical stability guides our choices—glass, high-density polyethylene, or PTFE lining, depending on project sensitivity.
Moisture sensitivity requires controlled storage. We store and ship in low-humidity conditions, and offer dessicant-packed drums as standard. Every step has been honed by real-world incidents: early on, we saw degradation caused by missed atmospheric controls, prompting us to design improved container validation and labeling. Now, shelf-life meets, and often exceeds, typical laboratory and industrial use timelines.
Consistent feedback from our long-term customers underlines the value of reliable performance. Early process hiccups, such as clumping or stickiness, led us to refine drying and milling sequences. New users often express concern about unusual odor or slight color fluctuations—these arise from minor side chain impurities, easily removed with further filtration. Listening to this feedback improves not just the next batch but our training materials and plant safety instructions as well.
Pharmaceutical research consumes most of our 2-Amino-5-Iodo-3-Nitropyridine output. Projects range from kinase inhibitor frameworks to enzyme ligand design, and the compound features as an intermediate in targeted heterocycle formation. Its robust chemical handle, the iodo group, speeds synthetic routes and simplifies downstream purification steps.
We also supply API-oriented manufacturers, where rigid documentation and impunity of process route matter more than ever. On biologically active molecules, the position and electronic nature of substituents on the pyridine ring affect pharmacodynamics and metabolic stability. Our manufacturing controls put extra attention on isomeric purity and absence of residual solvents, reflecting regulatory inspection standards faced by our clients worldwide.
Agrochemical developers have adopted this compound for lead optimization and structure-activity relationship studies. The combined electron-deficient ring and the functional group pattern enable quick modular alterations, supporting iterative synthetic campaigns. In our discussions with R&D chemists, speed and predictability of transformation score highest—and frequent switching between iodo, bromo, and chloro analogues provides key insight into structure-activity trends.
For pigment and specialty chemical users, 2-Amino-5-Iodo-3-Nitropyridine gives reliable color-stability profiles when used as a precursor in certain dyes. The same molecular structure supports improved lightfastness and reduced degradation under UV exposure, which were historically weak points for many pyridine-based pigments. Production scale-up for these clients always stresses batch consistency and absence of trace impurities that could influence color yield.
Manufacturing this compound means managing inherent hazards and upscaling chemistry in ways that do not compromise quality. Both iodo and nitro groups create exothermic risks during synthesis and require rigorous pressure and temperature controls. Our plant teams developed and refined quench and neutralization protocols from spill response drills, rather than relying solely on standard operating procedures. After one small-release incident, we integrated real-time monitoring sensors to further lower response times and teach new staff hands-on skills.
Waste handling forms another challenge, as iodinated organics bring both regulatory complexity and cost implications. We invested in on-site treatment which recycles iodine safely for other plant uses and strictly controls emissions. Regulations shifted in recent years, and the difference between a compliant and a non-compliant operation often hinges on reliable document tracking and batch traceability. Every drum shipped carries a full certificate of analysis covering at least the last ten quality checks, and internal audits regularly stress-test our documentation.
Transport restrictions due to the nitro group’s potential reactivity lead us to partner with specialized logistics firms who know how to move chemical cargos under international ADR and IATA rules. Our shipping team tracks evolving international lists and flags of concern; missing a minor code update in an export manifest could freeze a shipment in customs for weeks. Direct feedback from customs agents has helped us preempt mistakes by adding extra pictograms and language translations to labeling.
Intellectual property protection for new processes often overlaps with our day-to-day problem solving. Each time a customer describes a proprietary project using our material, we sign mutual confidentiality agreements and, when asked, adapt in-plant manufacturing schedules to minimize cross-contamination risk. This approach comes from our own experience filing and defending synthesis patents, where tiny contamination or batch inconsistencies can put critical claims at risk.
The chemical industry is built on careful, steady progress rather than big leaps. Reliable materials handling and deep specialty knowledge do more for a customer’s peace of mind than big marketing claims. We host regular roundtable calls with partner chemists, where both sides trade practical feedback that flows straight back to the shop floor and paperwork. Over the years, suggestions from collaborators have guided us to modify our crystallization solvents, extend shelf life, and add further analytical checks. Our process notebooks have more than one entry copied verbatim from these exchanges.
Consistent education forms a foundational pillar in keeping production personnel, engineers, and partners confident in the product chain. Training programs go beyond memorizing MSDS—each team member works through simulated leak containment, purification troubleshooting, and analytical review with real material samples, leaving nothing to hypothetical textbook situations. These sessions paid off—during an unexpected pipeline blockage, quick action prevented both downtime and material loss, saving an entire batch from off-spec status.
Governments and industry watchdogs continue to raise the bar for chemical purity, safety, and environmental stewardship. In our shop, that means regular review of incoming feedstock sources, verification of supply chains, and even more frequent batch analytics. Our clients, especially in regulated sectors, ask for certificates proving low residual solvent and compliance with REACH and TSCA guidelines. Keeping up with these changing expectations pressured us to improve not just final-product checks, but every step from raw material handling to waste stream reconciliation.
As green chemistry grows in importance, we explore ways to minimize hazardous reagents and energy requirements. Upgrades in batch reactor insulation, solvent recycling, and process automation have gradually reduced the environmental impact per kilogram produced. Some shifts came from necessity—in response to regulatory actions on halogenated waste, for instance—but the payoff shows up as reduced operating risk and better long-term customer satisfaction.
We continue to look for ways to collaborate directly with R&D teams at partner organizations. Many novel synthetic challenges still require bespoke modifications in how intermediates like 2-Amino-5-Iodo-3-Nitropyridine are manufactured and isolated. Those who collaborate early in a project timeline often secure better cost control, faster troubleshooting, and improved IP protection than those simply purchasing from commodity suppliers. We always advocate for open communication between process designers and material suppliers, aligned with the knowledge that this field moves forward through shared discovery as much as competitive edge.
2-Amino-5-Iodo-3-Nitropyridine reflects decades of innovation not only in bench chemistry but also in practical manufacturing. Our job is to preserve the utility chemists expect, while removing pain points that slow down research or introduce compliance headaches. Every improvement, from closed-system packaging to expanded analytics, comes out of lived experience in responding to customer requests and our own internal challenges.
The final measure of a specialty chemical like this has less to do with specification tables and more to do with confidence. Those who rely on our product know what to expect, shipment after shipment, guided by relentless focus on purity, handling integrity, and knowledge sharing. That is what sets our 2-Amino-5-Iodo-3-Nitropyridine apart in a crowded field of lookalikes. We do not lose sight of the fact that each lot produced represents a new opportunity for medical progress, agricultural innovation, and materials science discovery. This perspective shapes not only our production lines but also the way we support every partner, every day.