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HS Code |
186454 |
| Iupac Name | 2-amino-5-iodo-4-methylpyridine-3-carbonitrile |
| Molecular Formula | C7H6IN3 |
| Molecular Weight | 259.05 g/mol |
| Appearance | Solid (presumed, dependent on purity and form) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | Cc1c(nc(c=c1I)C#N)N |
| Inchi | InChI=1S/C7H6IN3/c1-4-5(3-9)6(10)11-7(8)2-12-4/h2,10H,1H3 |
As an accredited 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle, labeled with chemical name and hazard warnings, containing 25 grams of 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl-. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- involves secure packaging, labeling, and safe stowage for export. |
| Shipping | 3-Pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- should be shipped in tightly sealed, chemical-resistant containers, protected from light, moisture, and extreme temperatures. Applicable hazardous material regulations must be followed, with appropriate labeling and documentation. Transport should comply with international and local guidelines for handling hazardous chemicals. Avoid exposure to heat, flames, or incompatible substances. |
| Storage | 3-Pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizers. Store at room temperature and clearly label containers. Ensure appropriate chemical spill containment and access to safety equipment such as eyewash stations and emergency showers. |
| Shelf Life | The shelf life of 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- is typically 2–3 years when stored in a cool, dry place. |
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Purity 98%: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 172°C: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with melting point 172°C is used in heterocyclic compound development, where it provides optimal process handling during recrystallization steps. Particle Size <10 µm: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with particle size less than 10 µm is used in fine chemical manufacturing, where it enables enhanced dissolution rates and homogeneous blending. Stability Temperature 25°C: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with stability temperature 25°C is used in research laboratories, where it maintains compound integrity during extended storage. Assay ≥99%: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with assay ≥99% is used in custom chemical synthesis, where it ensures reliable analytical results and reproducible product quality. Moisture Content <0.5%: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with moisture content below 0.5% is used in organic synthesis routes, where it prevents unwanted side reactions and protects sensitive reagents. Molecular Weight 259.04 g/mol: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with molecular weight 259.04 g/mol is used in drug discovery projects, where it facilitates accurate formulation and dosage calculation. Solubility in DMSO: 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- with high solubility in DMSO is used in chemical screening assays, where it allows for efficient compound delivery and uniform test results. |
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Working within the core of chemical manufacturing isn’t a matter of pushing products through assembly lines. Each compound carries its own challenges, quirks, and occasionally pleasant surprises. Over the past decade, the hands-on experience shaping and refining the synthesis of 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- has guided us toward a better process and closer connection with our clients’ needs. This product isn’t simply a bottle of chemicals dispatched to the pharmaceutical or fine-chemical industries, but the result of countless hours ensuring confidence and consistent performance for downstream synthesis.
Colleagues in our laboratory often reflect that manufacturing isn’t just about yield and purity—it’s about control. 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- reminds us of this fact. Those who have prepared halogenated pyridines at scale understand that minor shifts in reaction temperature or atmosphere can quickly influence the profile of impurities. Our process design depends on diligent monitoring, as well as experience interpreting subtle chemical cues—a slight color change, a difference in solubility, or the behavior of a side product. Such knowledge rarely appears in textbooks.
Meeting a specification may appear as numbers and ranges on a paper, but to our customers, those numbers translate to actual performance during multi-step synthesis. While 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- falls under the family of substituted pyridines, its highly reactive iodo group and the presence of both an amino and a methyl substituent set it apart.
We produce the compound to achieve purity of >98% by HPLC. Residual starting materials and halide impurities can sabotage a downstream reaction or poison a catalyst, so in-process controls prevent such issues from reaching our clients’ reactors. The moisture content, typically controlled below 0.5%, presents another daily challenge. Water can attack the nitrile or interfere with functional group conversions, so every batch undergoes Karl Fischer testing. Packaging in inert atmosphere pouches or amber glass bottles is standard, not for show but from direct experience with light and air degrading the sensitive iodo group over time.
Physical appearance shouldn’t be reduced to a trivial property. While the material’s fine crystalline texture—usually a yellowish to light brown tone—sounds mundane, it ensures not just aesthetic satisfaction but consistent dosing and dispersibility in organic solvents. Our team recalls the learning curve before we achieved reproducible batch-to-batch particle size that balances processability with the tendency of iodoaromatics to clump.
Many seasoned synthetic chemists regard this compound as a workhorse intermediate. It finds a niche where a highly functionalized pyridine skeleton can serve as a core for heterocycle construction and target molecule modification. The amino group allows for straightforward derivatization, especially amidation and condensation reactions. The iodo substituent opens doors to efficient C–C coupling chemistry—mainly through Suzuki, Sonogashira, and Stille routes.
The methyl group at the 4-position shifts reactivity, sometimes in subtle but crucial ways. It shields the ring, mediates electronic properties, and offers another vector for downstream functionalization. Looking beyond standard applications, our clients have disclosed projects incorporating this compound into kinase inhibitors, agrochemical actives, and advanced polymer systems where precision matter in building blocks can determine the property of the final product.
On the surface, many aromatic nitriles appear similar—yet, chemists with in-depth experience recognize key distinctions between various halogen, alkyl, and amino substitution patterns. One reaction where these characteristics become apparent is during transition metal-catalyzed cross-coupling. The iodo group on our product enables much milder conditions compared to chloro or bromo analogs, which often necessitate higher temperatures, longer reaction times, or less-selective catalysts.
Our focus on 2-amino versus 3- or 4-amino substitution further tailors reactivity and selectivity in subsequent transformations. The position and presence of the methyl group influence not only solubility but also crystallization behavior and downstream purification. Anecdotally, several pharmaceutical partners have remarked that switching from a para-methylated derivative to our compound simplified chromatography and improved product isolation in their pilot-scale runs.
With experience in manufacturing both the bromo and iodo compounds, the differences in their reactivity aren’t just theoretical—they’re observed daily in yield, side reaction suppression, and batch stability. We track shelf life over months under real-world warehouse and laboratory conditions, sharing those insights openly with our partners instead of merely referencing data sheets. Transparency regarding what to expect over time helps downstream planners avoid production surprises.
Producing halogenated aromatic nitriles involves responsible sourcing of reagents, especially iodine. We maintain relationships with suppliers who value sustainable extraction and waste minimization. Process improvements over the years have focused not only on yield but waste reduction: Our current route reduces side stream halogenated waste by nearly 30%, compared to earlier iterations. By carefully choosing reaction vessels and inert gas handling, we keep emissions and operator exposure within strict safety boundaries.
Wastewater from our plant undergoes on-site treatment before leaving our facility, using specialized protocols for organohalide removal. Previously, we partnered with an outside laboratory for validation, but now we rely on in-house GC-MS and ion chromatography monitoring. A lesson learned early remains fresh: a single missed batch of contaminated solvent can snowball into regulatory headaches and damaged trust with clients and regulators.
One aspect that distinguishes a manufacturer’s approach is the willingness to adapt production to customer-specific requests. Several years ago, a research client requested a lot with extremely low trace-metal content for catalytic studies in sensitive drug development. Our standard grade already meets stringent limits (<10 ppm transition metals), but the client needed these levels even lower.
Implementing additional purification and replacing all contact surfaces with PTFE-lined hardware, the plant team delivered a material below 1 ppm of total transition metals, as verified by outside laboratories. Not every company persists through iterative process tweaks or takes the financial hit in modifying processes for customer efficacy data, but we’ve always favored long-term partnerships and scientific integrity.
Technical support after delivery extends far beyond basic compliance. We field calls and emails about solubility, spectral assignments, unusual reactivity, or even troubleshooting strange outcomes at our customers’ sites. Many customers’ success stories—obtaining target molecules or scaling up a new intermediate—trace back to day-to-day collaboration beyond paperwork. From shipping on custom pallets to adapting labeling for secure documentation at controlled labs, our involvement spans beyond chemical synthesis. Those personal connections and shared knowledge rarely make a headline, yet foster trust in the product and team behind it.
Handling nitrogenous and halogenated organics presents safety questions from the first gram up to drum scale. Over the years, repeated small incidents—unexpected spills, over-pressurized vessels, sudden off-gassing—have led to a set of protocols based on hands-on experience, more so than regulatory mandates. Access to proper venting and a commitment to protective gear stem not just from compliance, but firsthand appreciation for how readily these compounds can irritate the skin or emit noxious fumes.
For new users of 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl-, we recommend working in well-ventilated hoods, relying on inert atmosphere transfers, and storing away from sources of light and air. The chemical’s reactivity with certain bases or nucleophiles creates challenges, so each operator receives comprehensive briefings tailored to the batch scale and operational context. Lessons learned on the production floor get translated directly to customer guidance, not as vague caution but as lived experience.
Transitioning from laboratory to full-plant production reveals differences that theory often understates. At tens or hundreds of kilograms, agitation and phase transfer behave differently. Solids can cake and settle, or tiny amounts of moisture can propagate through a large vessel far more quickly than expected. Our engineers and chemists spend as much time observing real reactions as they spend reviewing paperwork.
Years ago, a scale-up batch unexpectedly stalled. Closer examination revealed tiny oxygen leaks at a joint that was sealed just tightly enough to satisfy standard checks, but not enough to completely exclude oxygen. Such minor lapses at scale could produce highly colored impurities, leading to expensive purification or outright failure to meet client timelines. Since then, our maintenance routines have doubled in frequency, and review of seal integrity is routine, not just an initial check box. Such changes feel costly in the moment but pale in comparison to sending out inconsistent chemical.
Clients often consult us before scaling their own processes. We advise them not merely based on literature, but on repeated, real-life stumbling blocks about solvent compatibility, order of addition, reaction quenching, and product isolation. Powder flowability, a topic that might seem minor, often determines how smoothly a kilo-lab process can transition to pilot or commercial scale. Superficially similar compounds sometimes require entirely different handling and storage regimes. This is where many distributors and speculators fail their customers—by focusing on price over process understanding.
Shifts in scientific understanding and market requirements mean our work never sits idle. Regulatory landscapes evolve, and chemists developing biologically active heterocycles demand ever purer, more consistent starting materials. Some years, we adjust to heightened expectations of residual solvent content. Others, attention shifts to specific halide traces, chirality, or trace-level inorganics.
Research teams push us for information on trace byproduct formation, reaction kinetics, and physical properties. We maintain a close partnership with those customers, providing data gleaned not just from a sample vial but from parallel plant runs at successive scales. Iterative feedback results in both process improvements and empowering end users to make informed decisions—pragmatic rather than theoretical.
The decision to invest in better analytical instrumentation, from LC-MS to advanced solid-state NMR and XRF, doesn’t occur in a vacuum. Our team spent long evenings debating which upgrades would translate most directly to batch confidence and customer trust. Since integrating these tools and providing the option of tailored certificates of analysis, we’ve seen a shift in the nature of questions coming from clients—from “what’s wrong?” to “how can we push our reactions further with your material?”
Chemical manufacturing asks for adaptation and openness rather than the pursuit of uniformity at any cost. Our most successful collaborations involve back-and-forth learning between our manufacturing team and the chemists in research or process development. Application-focused feedback has spurred changes in solvent drying and packaging, batch labelling for improved traceability, and batch-to-batch synthetic route documentation. Quality control isn’t a box-ticking exercise but a real commitment to scientific trust.
Supporting new discoveries sometimes means accepting unprofitable customization on a short run, in the interest of partnership. We’ve run extra analytics, held back release on borderline lots, and split finished goods by batch for side-by-side comparison at customer sites. Sometimes, these requests pull our planned timelines apart, but the benefits always accrue in the form of stronger, more resilient client relationships, and—on occasion—scientific breakthroughs in our clients’ labs, for which our product played a crucial role.
Every bottle and drum of 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- carries more than a part number. Hands-on experience and a focus on scientific partnership drive our work. Every synthesis, every lot, and every customer query form part of a larger story—where quality doesn’t rest on a single analytic result, but on proven consistency, open communication, and relentless pursuit of improvement. For those seeking a source for this compound, connection with a proven manufacturer often spells the difference between project continuity and unforeseen interruption.
The satisfaction of seeing a customer’s research paper, patent, or commercial product citing our material offers a reminder that each incremental improvement, each careful tweak, adds up over years. In short, 3-pyridinecarbonitrile, 2-amino-5-iodo-4-methyl- serves not merely as another chemical, but as a link in a chain that connects real people doing real science from bench to full-scale manufacture. In this way, expertise, reliability, and scientific curiosity don’t just support a product—they keep progress alive.