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HS Code |
111387 |
| Cas Number | 1120-95-2 |
| Molecular Formula | C4H3IN2 |
| Molecular Weight | 218.99 g/mol |
| Iupac Name | 2-iodopyrazine |
| Appearance | Light yellow to brown solid |
| Melting Point | 41-45 °C |
| Boiling Point | 249 °C |
| Density | 2.13 g/cm³ |
| Solubility In Water | Slightly soluble |
| Synonyms | Pyrazine, 2-iodo- |
| Pubchem Cid | 136025 |
| Smiles | C1=CN=CC(=N1)I |
As an accredited Iodopyrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Iodopyrazine is supplied in a 25g amber glass bottle with a secure screw cap, labeled with hazard warnings and product details. |
| Shipping | Iodopyrazine should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled as a hazardous chemical and transported according to local, national, and international regulations for dangerous goods. Typically, it is shipped in small quantities via certified carriers specialized in handling chemicals. |
| Storage | Iodopyrazine 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 substances such as strong oxidizers and acids. Store at room temperature and avoid excessive heat. Ensure the storage area has appropriate chemical spill containment and that proper labeling and safety measures are in place. |
Applications of Iodopyrazine in Industrial ManufacturingIodopyrazine plays a key role as a specialized intermediate in several industrial sectors. Its molecular structure enables targeted halogenation, introducing functional groups critical to complex synthesis workflows. Our production supports B2B partners advancing high-performance goods for regulated application areas. 1. Pharmaceutical Active Ingredient SynthesisAPI manufacturers select iodopyrazine for targeted iodination during heterocyclic compound synthesis. Its electron-withdrawing iodine moiety allows regioselective functionalization in the key assembly of kinase inhibitors and anti-infective drug scaffolds. Custom processes leverage iodopyrazine during late-stage Suzuki or Sonogashira coupling, supporting compliance with validated GMP route steps. End-use validation covers impurity profiling and residual halogen characterization as mandated by regulatory agencies. Industry compliance standards
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2. Agrochemical Intermediate for Crop ProtectionLeading agrochemical formulators use iodopyrazine to introduce high-precision heterocyclic building blocks in fungicide and herbicide synthesis. Its iodine substituent enhances reactivity in follow-up nucleophilic or metallation substitutions, streamlining the production of pyrazine-based bioactive ingredients. Formulation QC requires batch traceability and monitored halogen content before downstream etherification or amination. Industry compliance standards
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3. Electronic Materials and Specialty PolymersElectronics-grade manufacturers deploy iodopyrazine inside design chains for performance polymer fabrication and liquid crystal material development. The aromatic iodine group acts as a site-selective initiator for C–C coupling, essential for constructing conductive and emissive polymeric networks. Process managers integrate this intermediate in microelectronics coating synthesis, prioritizing particle-free transfer and batch reproducibility per SEMI and JEDEC guidelines. Industry compliance standards
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4. Specialty Flavors for Food and Beverage ApplicationsProducers of food-grade savory flavorants deploy iodopyrazine as a target precursor during controlled Maillard reaction simulation. It participates in forming highly aroma-active pyrazine derivatives with roasted, nutty, and meaty profiles. Every manufacturing sequence logs batch compliance with food additive frameworks and restricts residual halide levels by enforced purification. Industry compliance standards
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5. Research and Fine Chemical SynthesisChemical R&D institutions and pilot plant operators rely on iodopyrazine as a foundation for structural diversification during advanced heterocycle development. Its defined halogen position allows precision control in target-oriented synthesis for pharmaceutical probes, agrochemical standards, and luminescent dye design. Researchers favor its reproducibility and minimal side products in reaction scalability campaigns. Industry compliance standards
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Standing in the shoes of a chemical manufacturer, it’s easy to appreciate the journey a molecule like iodopyrazine takes from concept to bulk production. Our plant’s daily operations include monitoring precise reactions, managing supply chains, and fielding requests from researchers seeking unique building blocks. Iodopyrazine emerges as a pivotal compound in this landscape, thanks to its niche in medicinal research and organic synthesis.
We produce iodopyrazine at a scale meant for labs and industrial partners aiming at novel molecule development. The product consistently reaches purity levels above 98%, which is critical for downstream reactions. Batch-to-batch reproducibility forms the backbone of our quality program. Every consignment gets a certificate verifying not just purity, but also moisture content and residual solvent levels using validated techniques such as HPLC and GC. Our customers can order 2-iodopyrazine as a fine white crystalline powder, easily handled and engineered for optimal solubility in key organic solvents.
Every batch leaves our facility because a chemist on the other side plans to use it in the synthesis of new entities—often anything from antiviral candidates to agrochemical intermediates. The halogen functionality attached to the pyrazine ring acts as a handle for cross-coupling chemistry, especially palladium-catalyzed Suzuki and Sonogashira reactions. This gives researchers flexibility to introduce a range of substituents on the aromatic scaffold. The product’s role extends far beyond just lab-scale curiosity; it appears in life science projects involving kinase inhibitors, diagnostic reagents, and complex ligands.
As direct manufacturers, we’ve fielded requests for custom-scale and specification tweaks: some synthetic schemes only succeed when water is under 0.2%, or residual iodine byproducts stay below limits detectable by ICP-MS. Our controls start at the source chemicals and finish at each drum sealed, and we respond quickly to specification shifts. These operational details go unnoticed in spec sheets but matter every week as our process chemists and QC staff connect directly with research teams worldwide.
Customers often debate whether to deploy iodinated compounds or other halogenated counterparts like bromopyrazine or chloropyrazine. From our production lines, the chemistry behind iodopyrazine offers clear advantages. The iodine atom, being larger and more polarizable, enables milder and higher-yielding metal-catalyzed cross-coupling reactions than its bromo or chloro cousins. It’s easier to achieve selective arylation or alkynylation when working from the iodo derivative, which catalyzes reliable extension into multi-functional frameworks.
Bromopyrazine costs less but usually requires more aggressive conditions or extended reaction times, often dropping isolated yields below what some pharmaceutical R&D operations accept. Chloropyrazine is even less reactive, and typically only suits limited transformations or must be converted up to the iodo or bromo form first. We see iodopyrazine as a premium building block, saving time at the bench and unlocking chemistry that can stall with less reactive partners. As an in-house manufacturer, we’re familiar with the push and pull behind these decisions, and frequently collaborate with process development teams to weigh the total project cost—not just the per-kilo price.
Turning out high-purity iodopyrazine requires more than knowledge of bench-scale synthesis. Our plant team manages process safety risks, precise temperature control, and reagent stability that challenge every scale-up. We carry experience working through the quirks of halogen exchange and high-boiling media. The actual iodination typically involves a two-step methodology. Preparing the pyrazine precursor, which calls for scrutiny of catalyst quality and oxygen exposure, ensures downstream steps stay on target.
Once the core intermediate is in hand, our process team must handle iodine and activating reagents under controlled airflow and PPE. Although the chemistry appears textbook, it can turn erratic if the exotherm runs away or solvents carry over too much water. Continuous in-process monitoring (TLC, NMR, GC) has cut our fail rate dramatically over the last several production cycles. Years ago, batches ran hot and showed color traces. Iterative process improvement—involving not just operations managers but chemists from our R&D lab—dropped impurities to a fraction of previous runs. Each improvement comes from listening to repeat clients, who share how even trace impurities hinder a trial or scale-up.
Once synthesized, iodopyrazine travels through several purification and packaging steps designed by team members who have handled these products day-in, day-out. Crystallization and vacuum drying get timed carefully, avoiding co-crystallization with side-products. Our QC chemists analyze every finished lot for residual iodine, which if left unchecked, can sabotage the next catalytic bond-formation step. Our shipping and logistics arm ensures product reaches global markets under proper temperature and humidity controls, and our technical support follows up with researchers doing late-stage synthesis on clinical candidates or specialty chemicals.
Batch segregation supports pharmaceutical GMP, but clients in the agrochemical sector often use larger, less sensitive lots, which lets us reduce bottling and handling steps. Still, every gram leaves our plant after extensive screening for trace metals and environmental contaminants, reflecting the real-world demands of research and market launch timelines. Being a manufacturer rather than a distributor lets us act instantly on feedback—if customers report filtration problems, our teams run follow-up analyses and tweak the drying cycle or filtration schedule to restore ease of use in their workflow.
Industry partnerships often go beyond just bulk chemical sales. We get calls from team leaders involved with multi-step syntheses for pharmaceutical APIs. They ask about tweaking crystal habits or granularity, or controlling for trace contaminants that might not even register on standard purity assays. Our plant team shares firsthand insight on modifying the reaction environment—offering collaborative, on-the-ground troubleshooting that lets clients maintain their project momentum.
One memorable client, working with kinase inhibitor analogs, found a conversion bottleneck when switching from commercial-grade to our lab-pure iodopyrazine. Because we control every stage in-house, we reproduced their workup, ran trial reactions, and discovered the culprit: a subtle but consistent trace of metallic contaminant in a competitor’s supply. Small actions like washing glassware in process and ramping up vacuum drying transformed their yields. We drew from months of records on reactor maintenance and solvent analysis, showcasing how, in manufacturing, recursive feedback sharpens both quality and trust.
From the standpoint of both chemistry and practical use, iodopyrazine stands apart from other halogen-pyrazines. The heavier iodine substituent on the aromatic base increases selectivity and efficiency in coupling reactions. Reaction partners show improved yields and reduced by-product formation. Chemists who value reactivity consistently vote for the iodo over bromo or chloro versions, despite slightly higher costs. In many synthetic schemes, the bromo group can sometimes be sufficient, but certain metal-catalyzed reactions display a marked improvement in both turnover and selectivity with the iodo derivative.
It’s a product we advise for high-value research and challenging scale-up projects where time, purity, and yield all hold sway. Cost-conscious decisions often sit better with bromopyrazine, and for simple substitution, some users may opt for chloro derivatives. Still, iodopyrazine becomes essential once complexity rises and predictable reaction profiles matter. We don’t preach exclusivity, but share real-world insight from our own process optimization runs, and stories from partner firms in both pharmaceuticals and crop protection.
Manufacturing chemicals like iodopyrazine brings relationships into play on every shipment. The market includes labs ordering sub-gram quantities for exploratory medicinal chemistry, and operations purchasing drums for pilot plant development. Each group brings a different set of requirements: some request a specific lot documented for every stage; others value quick lead times over deep characterization. Our team keeps communication lines open, working with procurement, R&D, and production managers around the world. We keep pricing transparent and respond quickly to changing demand or new regulatory guidelines.
In the past year, several global regulatory agencies tightened scrutiny on trace byproducts in heterocycles used in drug synthesis. Our QC and regulatory group responded by modifying analytical runs, implementing additional screening, and instituting customer-specific batch release plans. While we don’t dictate a single standard for every client, we adapt our own plant’s output to meet each team’s needs—often within a single production cycle. Our facility flexibility comes from years of taking feedback directly from industry leaders and small labs alike.
Facility improvements rely on experience at every level. Years of process work highlighted where small tweaks, such as switching to new reactors or adjusting decoction cycles, yielded major advances in final product isolation. On some lots, controlling for trace residual water avoided batch failures for partners using sensitive organometallic reagents. As a manufacturer, we keep meticulous logs and regular review meetings to incorporate every learning into future runs.
Sustainability has grown in importance, both to our operations and those of our customers. Many downstream users in pharma and agrochemicals request reduced solvent loads, waste minimization, and green chemistry practices. We’ve invested in solvent recycling units, alternate iodination methods with fewer hazardous intermediates, and novel crystallization protocols that reduce energy use. These changes create tangible differences beyond marketing claims—lower volume disposal, improved worker safety, and a smaller environmental footprint. All these benefits feed back into downstream products, improving their sustainability score from bench to launch.
Manufacturers face continual supply chain bottlenecks—whether with raw pyrazine, iodine sourcing, or transportation logistics for regulated chemicals. Our operations team diversifies suppliers, stocks key inputs, and maintains close partnerships with freight firms experienced in hazardous material transport. Recently, global disruptions impacted several precursors; by balancing multiple inputs and investing in on-site storage, we buffered output and protected our end clients’ timelines. Our firsthand experience means that instead of pausing production until a shipment clears customs, we hold stock with traceable provenance, updating end users ahead of time.
Technical support plays a major role in real-world adoption of iodopyrazine. Some clients report unpredictable solubility profiles or incompatibility with specific coupling agents. In those cases, technical staff run side-by-side experiments, pairing our product with common co-reactants and troubleshooting any process hiccups. These partnerships build trust and ensure end-users reach project milestones faster.
Beyond chemistry, handling and environmental compliance stand as central priorities. We reduced halogenated solvent use by retrofitting our workup platforms and moving toward water-based quenching where feasible. These improvements reduce the overall environmental burden and cut down emissions—matters regulators increasingly scrutinize.
Every kilogram of iodopyrazine leaving our plant comes from a process blending chemical understanding, operational safety, and customer-driven innovation. Years of dialogue with academic and industry partners shaped batch sizes, handling features, and analytical protocols. As regulatory standards tighten and downstream synthetic pathways become more intricate, we rely on direct feedback loops to guide product evolution. It’s an ongoing process: every new requirement, every unique synthesis design, becomes a blueprint for better manufacturing and support.
Experience in direct manufacturing brings a different perspective than trading or redistribution. We see molecule production from the ground up, with hands-on awareness of what shifts production metrics or lends competitive advantage to a client’s R&D cycle. Rather than stacking abstract benefits or neutral claims, we share results from our labs, insights from production runs, and lessons from decades of collaborative work. That approach grounds our commitment to serving chemists who choose iodopyrazine as a key part of their research and innovation.