[1,2,4]triazolo[1,5-a]pyridine, 6-iodo-

    • Product Name: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo-
    • Chemical Name (IUPAC): 6-iodo-[1,2,4]triazolo[1,5-a]pyridine
    • CAS No.: 272123-47-4
    • Chemical Formula: C6H4IN3
    • Form/Physical State: Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    499043

    Iupac Name 6-iodo-[1,2,4]triazolo[1,5-a]pyridine
    Molecular Formula C6H4IN3
    Molecular Weight 245.02 g/mol
    Cas Number 709679-32-1
    Smiles C1=CN2C=NC=N2C=C1I
    Inchi InChI=1S/C6H4IN3/c7-5-1-2-10-3-4-8-9-6(5)10/h1-4H
    Appearance Solid
    Pubchem Cid 11693638

    As an accredited [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 50-gram amber glass bottle with secure screw cap, labeled with chemical name "[1,2,4]triazolo[1,5-a]pyridine, 6-iodo-", and hazard symbols.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- involves secure, compliant packing for safe international chemical transport.
    Shipping **Shipping Description:** [1,2,4]Triazolo[1,5-a]pyridine, 6-iodo- is shipped in tightly sealed, chemically resistant containers to prevent moisture and light exposure. Packaging complies with hazardous material regulations. The chemical is dispatched with safety documentation, typically using express or regulated ground services, to ensure timely and secure delivery while maintaining product integrity.
    Storage [1,2,4]Triazolo[1,5-a]pyridine, 6-iodo- should be stored in a tightly sealed container, away from light, moisture, and sources of ignition. It should be kept in a cool, dry, well-ventilated area, ideally within a dedicated chemical storage cabinet. Ensure proper labeling, and avoid contact with incompatible substances. Only trained personnel should handle and store this chemical.
    Shelf Life The shelf life of 6-iodo-[1,2,4]triazolo[1,5-a]pyridine is typically 2–3 years under cool, dry, and tightly sealed storage conditions.
    Application of [1,2,4]triazolo[1,5-a]pyridine, 6-iodo-

    Purity 98%: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- with 98% purity is used in pharmaceutical synthesis, where enhanced reaction yield is observed.

    Melting Point 160°C: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- with a melting point of 160°C is used in medicinal chemistry research, where thermal stability supports high-temperature reactions.

    Particle Size 20 µm: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- with 20 µm particle size is used in solid-phase combinatorial synthesis, where uniform dispersion results in reproducible compound libraries.

    Stability Temperature 80°C: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- with stability up to 80°C is used in chemical storage applications, where prolonged shelf-life under moderate heat conditions is achieved.

    Molecular Weight 259.04 g/mol: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- with a molecular weight of 259.04 g/mol is used in lead compound optimization, where precise mass contributes to accurate analytical characterization.

    Assay ≥98%: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- with assay value of ≥98% is used in high-throughput screening, where compound purity ensures reliable biological activity results.

    Solubility in DMSO 50 mg/mL: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- soluble at 50 mg/mL in DMSO is used in bioassay development, where high solubility allows for concentrated stock solutions.

    Flash Point 128°C: [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- with a flash point of 128°C is used in laboratory reagent preparation, where reduced fire hazard increases operational safety.

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    Competitive [1,2,4]triazolo[1,5-a]pyridine, 6-iodo- prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine: Crafting New Possibilities in Heterocyclic Chemistry

    Direct from Our Labs: A Manufacturer’s Perspective

    Stepping onto our production floor on any given day, the dedicated team works with precision and care to ensure every batch of 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine meets the benchmarks chemists expect. This compound has played a recurring role in the evolution of heterocyclic pharmaceutical research, particularly as an intermediate in the pursuit of new therapeutic agents and advanced materials. The journey from raw starting materials to well-characterized, analytically verified product is not a simple one, and every stage holds its own challenges and opportunities.

    Unwrapping the Identity of 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine

    In our line of work, chemists have learned to recognize the nuance each atomic substitution brings. The introduction of an iodine atom at the 6th position of the [1,2,4]triazolo[1,5-a]pyridine scaffold unlocks a broader range of synthetic transformations, especially for those actively exploring cross-coupling and halogen exchange reactions. The compound stands out for its reliable reactivity—something experienced scientists value when mapping pathways toward new drug candidates, agricultural agents, or advanced electronic materials.

    Our model for this compound follows the stringent protocols honed through years of pilot production. Each lot passes rigorous crystallinity and purity benchmarks, confirmed by HPLC and NMR. We target impurity profiles based on practical lab experience: end users find residue organic solvents and trace heavy metals interfere most with downstream steps. Thus, we push every batch through multi-stage purification with real-time monitoring, favoring techniques that minimize residual contaminants without impacting the sensitive triazolopyridine skeleton.

    Specifications Shaped by Real-World Demands

    Producing 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine at scale means paying attention to the practical details that make life easier in both research and manufacturing environments. Our batches reflect a synthesis scale honed for both bench and pilot plant requirements, yielding crystalline solid with minimal dusting and consistent lot-to-lot reproducibility. We've seen chemists choose this compound over 6-bromo or 6-chloro analogs because the carbon–iodine bond in our product responds more rapidly in palladium-catalyzed couplings, enabling researchers to introduce wide-ranging substituents under milder conditions.

    Moisture and oxygen sensitivity remain controlled during both packaging and shipping, using protective inner liners and inert gas purging—lessons learned by watching the inevitable degradation in poorly handled material. Our team prioritizes storage in well-sealed containers to keep the compound in top form, guided by routine room-temperature and refrigerated stability trials that inform our recommended storage practices. Batch records include this empirical data, not just for lab compliance, but to reflect what genuinely works outside reference texts.

    How End Users Benefit in Synthesis

    Synthetic chemists frequently search for heterocycles with reliable halogenation patterns. Having 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine in hand gives them access to selective and high-yielding Suzuki and Sonogashira cross-couplings, which often outperform their chloro- and bromo-based cousins in the same scaffold series. In our own pilot labs, we've demonstrated that switching to the iodo derivative can cut reaction temperatures by up to 20°C, while reaction times get trimmed by several hours in many standard protocols.

    Academic collaborators have highlighted another practical win: the increased mass of the iodine atom makes ^13C and ^1H NMR spectral assignments easier, often helping to clarify ambiguous positions during rapid structure–activity relationship studies. Working directly with synthetic teams worldwide has shown us which purity ranges and lot sizes get consumed fastest, reinforcing our focus on both kilo-lab and gram-scale production, with documented batch records for precise traceability.

    Why Source Direct from a Manufacturer?

    The calls and emails we field weekly tell us a lot about the real concerns researchers face. Immediate technical support, traceable supply chains, and reliable batch consistency top the list. By manufacturing in-house, we exercise full control over key parameters—a critical advantage not just for process repeatability, but for building the direct technical relationships that convert a purchase order into lasting collaboration.

    Several colleagues in pharmaceutical development have reported problems with lower-purity imports, especially those sourced through extended distribution networks. Our ability to intersect analytical data with feedback from client scientists lets us adjust synthesis and purification in ways third-party suppliers rarely manage. If a downstream project requires additional characterization, custom particle size distribution, or documentation packs beyond the usual Certificate of Analysis, our technical staff stands ready to help. This real-world customer engagement shapes every decision, from packaging sizes to choice of analytical reference standards.

    Measured Differences from Close Analogs

    In practice, not every triazolopyridine behaves the same. Loading side-by-side samples of our 6-chloro, 6-bromo, and 6-iodo analogs onto the reactor shows clear distinctions: the iodo variant generally displays higher solubility in a range of polar aprotic solvents, and undergoes catalyst insertion under milder conditions. We have documented dozens of case studies where customers improved yield or shortened route development cycles by making the shift from bromide to iodide.

    The downstream purification also tells a story. Users regularly report that the iodine derivative’s byproducts form less persistent contaminant residues, simplifying post-reaction workups, and cutting down waste solvent volumes. Over multiple campaigns, some process chemists have estimated time and cost savings in the double-digit percentages simply from the cleaner reaction output and easier purification. These incremental improvements often tip the balance during process optimization runs.

    Purity, Analytical Backing, and What We’ve Learned

    Analytical results only become meaningful when they have direct bearing on downstream results. We track both HPLC and GC profiles for each shipment, supported by routine LC-MS to identify trace impurities below standard detection limits. Our in-house philosophy prioritizes full transparency: if a batch sits outside the tightest specifications, we isolate it and run supplementary purification cycles before release, or hold it for internal use. Users find value not only in the published analytical numbers, but in our willingness to discuss borderline cases openly—more than a few times, quick interventions on our end kept grams or even kilos of research progress on track.

    We seldom encounter requests for lower-purity technical grades, despite offering them by special arrangement. Most end users prefer the peace of mind that comes with analytical-grade material, particularly for sensitive catalytic transformations. Our long-term clients rely on the consistency of melting point, solubility, and spectral characteristics batch after batch. In crowded labs, time lost troubleshooting unexpected impurities quickly outweighs small savings on raw material. This real-world detail underpins our core business focus on high-purity stock.

    Addressing Environmental and Safety Aspects

    Handling halogenated heterocycles brings environmental and safety obligations under local and global regulations. Our experience with 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine reflects decades of pragmatic risk management. Production lines incorporate robust local exhaust ventilation, with continuous monitoring for airborne iodine traces. We document waste solvent profiles and treat them on-site prior to disposal, reflecting both regulatory requirements and the preferences of clients who, like us, want assurance that ethical sourcing extends to environmental stewardship.

    Our staff receive hands-on training in both operational and emergency protocols, reinforced by annual drills and practical refreshers. Over time, this approach has reduced the incidence of near-misses and recordable safety events to well below sector averages. Customer guidance sheets focus on actionable steps chemists can take to minimize inhalation and skin exposure during weighing and solution preparation.

    Choosing packaging also involves weighing both purity protection and sustainability. We favor recyclable containers and actively work with suppliers to trial more eco-friendly alternatives, including bioplastic liners and solvent-leachable paper drums. A handful of innovators in our customer base provide feedback on these packaging trials, often guiding further improvements from a front-line user’s perspective.

    Collaboration and Technical Support

    Working directly with research and process chemists keeps us sharp. Every batch order brings new conversations—troubleshooting scale-up routes, helping clients swap from parallel synthesis in medicinal chemistry programs to larger pilot plant campaigns, or discussing custom analytical verification for regulatory submissions. We regularly host video calls to review batch records in detail, or provide live support during initial method transfers.

    Peer-to-peer technical exchange holds the real key to unlocking value from complex heterocycles. Our internal team of PhD-level chemists—not “customer service” staff—refers back to process data, published case studies, and years of hands-on analytical work. This expertise becomes especially valuable for customers developing new applications, fine-tuning reaction conditions, or trouble shooting crystallization issues that fall outside published literature. Fields such as oncology, CNS research, and crop protection routinely drive our own development work, so we stay current on both the latest academic findings and real-world scale-up challenges.

    Continual Improvement: Lessons from Day-to-Day Operations

    A compound’s pathway from bench to pilot to commercial scale reveals more than you’ll find in any catalog. Each production run brings new knowledge about process robustness, yield optimization, and practical impurity control. Over the years, we’ve streamlined our workflow to squeeze out batch-to-batch variation—cleaning reactors with high-purity solvents after each run, screening starting materials for trace halides, and shifting to continuous-monitoring NMR where possible. These real improvements don’t look flashy on a spec sheet, but customers notice the results: cleaner end products, tighter analytical confirmation, and fewer surprises at the critical next stage of synthesis.

    Legacy decision-making doesn’t survive long here. Process changes flow both ways: feedback from clients feeds rapid updates to purification protocols or storage specs, sometimes resulting in overnight adjustments to packaging, documentation, or handling practices. Our support team keeps a running log of procedural “pain points” reported by customers, and we invest in training and equipment upgrades wherever those trends persist.

    Outlook for Future Research and Application

    The next wave of triazolopyridine research will test chemists’ resourcefulness even further. Applications in medicinal chemistry now focus on more challenging substitution patterns and faster iteration cycles. Crop science groups are pushing the boundaries of what heterocyclic scaffolds can do for pest resistance and selective activity. We keep pace by adapting both our scale and process to support those shifts—adding new purification steps, rethinking reaction conditions, and collaborating with customers both in the lab and in the field.

    Digital tracking of process data, raw material provenance, and analytical certification continues to expand. Sharing this technical depth with partners—rather than keeping it locked away—represents a real culture shift. Supported by lessons learned from daily production and feedback from end users, this open approach raises confidence both in the material itself and in the teams behind its manufacture. As new questions and research pressures arise, our collective experience anchors troubleshooting and fast adaptation, giving genuine flexibility in a perpetually changing environment.

    Choosing More Than a Catalog Number

    Purchasing 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine goes beyond checking purity and batch size specs. Customers demand partnership, not just supply. Those investing time, money, and reputation into complex syntheses need material that arrives as described, with complete data to support smooth downstream paths. Our team holds itself to that standard, recognizing the long-term value in reliability and direct communication over simple transactional fulfillment.

    Experience has taught us the difference between nominal purity and true utility in downstream chemistry. Every request—from custom drying procedures to alternative particle sizing or pre-weighed, solution-ready packaging—reflects the evolving needs of active research groups. We listen, adapt, and marshal our resources to deliver what actually matters to scientists whose own work depends on trustworthy starting points. The field’s demands shift every season, but the value of honest engagement never goes out of style.

    Final Thoughts: Experience Drives Excellence

    Years of hands-on manufacturing, countless technical conversations, and the pressure of real research timelines honed our approach to producing 6-Iodo-[1,2,4]triazolo[1,5-a]pyridine. Trusted relationships and direct feedback from front-line users build accountability and lead to genuine improvements batch after batch. Scientists relying on this key heterocycle to power discovery projects understand these lessons best—materials made right, shipped reliably, and supported by open technical dialogue, shape success long before a new molecule earns a place in the literature or on the market.

    We stand behind the value of experience, transparent process control, and a service mentality rooted in a shared commitment to progress. Manufacturing this compound means much more than scaling up a synthesis. It means growing with the field, supporting innovation, and never standing still in the pursuit of better chemistry and deeper technical partnership.