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HS Code |
271895 |
| Chemical Name | 2-Iodoadenosine |
| Molecular Formula | C10H12IN5O4 |
| Molecular Weight | 389.14 g/mol |
| Cas Number | 37356-21-3 |
| Appearance | White to off-white powder |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Purity | Typically ≥98% |
| Storage Temperature | -20°C (desiccated) |
| Synonyms | 2-Iodo-9-β-D-arabinofuranosyladenine, 2-Iodo-adenosine |
| Smiles | C1=NC2=C(N1C3C(C(C(O3)CO)O)O)N=CN=C2I |
As an accredited 2-Iodoadenosine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Iodoadenosine is supplied in a 100 mg amber glass vial, securely sealed with a screw cap, and labeled for laboratory use. |
| Shipping | 2-Iodoadenosine is shipped in accordance with applicable chemical safety regulations. It is securely packaged in sealed containers to prevent contamination and degradation. Typically, it is shipped with cooling elements or on dry ice to preserve stability. All shipments include proper labeling and documentation for safe transport and regulatory compliance. |
| Storage | 2-Iodoadenosine should be stored in a tightly sealed container, protected from light and moisture. Keep it at -20°C (freezer) to maintain stability and prevent decomposition. Store in a dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Handle under an inert atmosphere if possible to avoid hydrolysis or degradation. |
Applications of 2-Iodoadenosine in Industrial Manufacturing2-Iodoadenosine plays a specialized role in advanced bioscience manufacturing, nucleoside analog synthesis, and diagnostic product formulation. As a manufacturer, we supply this material for specified applications where precise compliance, accurate formulation control, and robust integration into industrial-scale processes support reliable production of sensitive biological, pharmaceutical, and analytical end goods. Below, we outline its application in verified downstream settings, detailing integration points, regulation references, and typical formulation guidance. 1. Nucleoside Analog API Intermediate SynthesisDownstream nucleoside pharmaceutical manufacturers use 2-Iodoadenosine as a substantive building block in the semi-synthetic preparation of modified adenosine-based active pharmaceutical ingredients (APIs), especially for antiviral and anticancer medicines. The compound enters stepwise coupling reactions, facilitating selective halogenation and subsequent derivatization crucial for target specificity in final APIs. Compliance with stringent pharmacopoeial and quality statutes remains mandatory throughout all processing stages. Industry compliance standards
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2. Biochemical Assay Reagent ManufacturingSpecialty biochemical reagent producers integrate 2-Iodoadenosine as a selective chemical probe in enzyme kinetic assays, particularly for adenosine deaminases and nucleoside transferase characterization. This usage depends on precise reagent quality, clear traceability of batch documentation, and supply chain oversight to ensure downstream laboratories and diagnostics companies can reliably use produced kits in regulated biomedical applications. Industry compliance standards
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3. Radiopharmaceutical Precursor PreparationRadiochemical synthesis units use 2-Iodoadenosine as a precursor for radioiodination in the development of PET/SPECT imaging tracers. The stable iodine atom provides an anchor point for subsequent isotopic exchange or labeling with isotopes such as 123I, 125I, and 131I. Producers of radionuclide-labeled biomolecules must meet rigorous radiochemical purity and safety criteria, as medical imaging standards dictate the permitted isotope load, specific activity, and chemical stability. Industry compliance standards
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4. Synthetic Biology Oligonucleotide ProductionProducers of modified oligonucleotide strands employ 2-Iodoadenosine for the site-specific incorporation of halogenated bases into DNA and RNA oligos, advancing the design of bio-orthogonal probes and nucleic acid drug candidates. This application demands tightly controlled anhydrous conditions, automated oligo synthesizer compatibility, and validation against custom sequence specifications in accordance with international quality documentation for genetic materials. Industry compliance standards
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2-Iodoadenosine stands out as a fascinating nucleoside, with its iodinated purine core bridging a vital gap between selective biochemistry and advanced organic synthesis. This product enters the lab not as a generic building block but as a working tool for researchers seeking specificity and control in modifying adenosine frameworks. As a chemical manufacturer, we navigate the entire process—right from sourcing reagents with traceable purity, through reaction optimization, and extending to monitoring shelf stability batch after batch. This perspective gives a unique position to describe not just the composition, but the genuine ways in which 2-Iodoadenosine impacts research and development.
Each lot of 2-Iodoadenosine produced reflects real-time monitoring of crystallinity, impurity thresholds, and yield assessment. The most challenging aspect usually lies in the iodination step itself. We meet issues such as incomplete substitution and the possibility of over-iodination by fine-tuning reagent ratios and time, rarely relying on a “one protocol fits all.” For every reaction, solvents are tested for aggressiveness and side-reaction profile, and product isolation is tailored to avoid co-elution of close analogs. Not every synthesis run checks all boxes on the first attempt. Real troubleshooting means addressing seed crystal formation or tackling difficult-to-remove byproducts through different purification methods—preparative HPLC, repeated recrystallization, or even repeated column runs. Gathering this experience directly influences lot-to-lot quality and confidence in what leaves the production floor.
Our standard model for 2-Iodoadenosine features remarkable purity, which we measure and document through HPLC and NMR. Frequently, demand arises from molecular biology groups seeking lots with specified water content, free from residual solvents, and a guaranteed minimum chromatographic purity. Beyond the white powder’s look, we routinely provide samples to collaborating labs for method validation and feedback. This continuous dialogue shapes operational practices as well as batch documentation.
Practitioners in synthetic biology, analytical chemistry, and medical research all find themselves reaching for 2-Iodoadenosine for similar but distinct reasons. In enzymology, teams aiming to probe nucleoside binding profiles prefer this compound for its ability to mimic adenosine while enabling selective modification. Structurally, the iodine atom at the 2-position offers a clear handle for further synthetic elaboration. Cross-coupling experiments benefit especially, as the carbon-iodine bond shows optimal reactivity under palladium and copper-mediated transformations. Medicinal chemists who explore nucleoside analogs for antiviral and anticancer testing rely on the specificity and predictable reactivity profile this molecule brings.
We’ve worked alongside groups designing radiolabels where the 2-iodo functionality gets exchanged with radioactive isotopes, something not possible with standard adenosine. The larger atomic radius and increased electron density of the iodine atom play a subtle role in receptor binding assays, giving pharmacologists an avenue to study structure-activity relationships more rigorously. Bulk purchases typically come from biotech firms developing modified oligonucleotides, as the 2-iodo adduct helps sidestep unwanted cross-reactivity during automated DNA synthesis protocols.
The chemistry of nucleosides is crowded—thymidine, guanosine, and cytidine derivatives each fill unique needs. Among those, 2-Iodoadenosine carries a versatility that distinguishes it not only from plain adenosine but from halogenated variants like 8-bromo-adenosine as well. The 2-iodo substitution offers the best blend of reactivity and site-selectivity; bromo- and chloro- analogs react less readily, increasing reaction temperatures and frequently reducing tolerance to delicate functional groups. Fluorinated adenosine analogs fail to provide the same cross-coupling utility or radiolabeling compatibility.
Synthesizing this compound internally as a manufacturer, we see clear evidence for its tighter melting point, greater hydrophobicity, and lower solubility in water when compared with parent adenosine. These physical property shifts influence everything from solvent choice in reactions to the stability of formulated products. In projects demanding controlled release or bio-orthogonal tagging, researchers use the 2-iodo form instead of the simple adenosine scaffold precisely because of these differences. Custom requests often involve batch-matching particle size for solid-phase chemistry, or pre-dissolving to a specified concentration in DMF for direct use in coupling reactions in high-throughput settings.
Turning to real-world use and storage, the challenges of maintaining 2-Iodoadenosine’s integrity are not theoretical. Sensitive to both light and humidity, this material remains viable longest when stored in amber glass, capped under dry inert atmosphere. We see firsthand the impact of less-than-ideal storage—a slight yellowing or clumping signals hydrolysis or iodide migration. Regular shelf testing for active iodine content and impurity spikes becomes vital, as small changes can alter how well the product fits into downstream work.
If requested, we tailor packaging formats to project needs, whether that means larger, single-use aliquots for high-throughput screening or microgram vials for exploratory medicinal chemistry routes. Feedback loops back to our warehouse and drying teams; when clients struggle with hygroscopicity in humid climates, we redesign packs or increase the use of desiccant sachets inside secondary containers. Longevity in downstream experiments depends heavily on diligence at every point—from synthesis through shipping.
Navigating regulatory demands for 2-Iodoadenosine, especially as more projects reach clinical or diagnostic use, involves detailed documentation. As manufacturers, we do not simply reference outside analysis; every Certificate of Analysis reflects direct in-house characterization, retention samples, and traceable instrument records. Standard procedures require validation for not only identity and purity, but also residual solvent testing by GC, heavy metal screening, and biological contaminant checks. Feedback from major life science firms often highlights the need for flexible documentation; some request extended impurity profiles, others demand batch-specific spectral libraries.
International shipment presents its own hurdles—customs authorities frequently request documentation verifying the non-pharmaceutical, non-controlled status of 2-Iodoadenosine. First-hand experience shows that a comprehensive dossier preempts shipment delays, as do clear markings on transport containers indicating light- and moisture-sensitivity. For those operating in regulated markets—be it research-use-only, or precursor supply for GMP manufacture—our teams collaborate directly with compliance officers to smooth user audits.
Batch-to-batch consistency rarely plays out on paper the way it does at scale. Initial gram-scale runs may show clean conversions and strong isolated yields. Scaling up exposes bottlenecks: exothermic reaction profiles intensify, local overheating can cause partial decomposition, and the solubility profile may change. Pumps, not stir bars, introduce atmospheric oxygen unless sealed carefully, threatening the stability of the reactive iodine group.
Adaptation means hands-on adjustments—modifying agitation speeds, controlling addition rates, or switching out glassware for jacketed reactors to ensure even heat distribution. Analytical workup shifts from NMR of neat samples to in-line HPLC with impurity tracking. Downstream washing and drying steps expand, running longer filtration times or introducing nitrogen purging in drying cabinets. These manufacturing tweaks mark the line between small-scale availability and reliable, reproducible shipments for industrial clients.
Direct conversations with scientists lay bare the emerging opportunities for 2-Iodoadenosine. Peptide chemists use its iodinated nucleoside to assemble site-directed conjugates, attaching fluorescent reporters or cleavable linkers, impossible with unmodified adenosines. DNA-protein interaction explorers rely on the iodine handle’s bulk and polarizability to probe binding site specificity. Each new demand translates into a challenge for manufacturing—consistently hitting ultrapure thresholds for use in cell assays, or engineering process routes that deliver sufficient quantity for high-throughput screening projects.
Custom orders frequently arise: High-volume nucleic acid manufacturers request validations at the preparative scale, timing delivery to the launch of new oligo products. Smaller synthetic groups commonly need sub-gram quantities, each with bespoke documentation to match internal SOPs. Every batch goes out with chain-of-custody and manufacturing traceability. We remain in the feedback loop—results from initial test reactions guide the next round of raw material adjustment or purification protocol upgrades.
Responsible manufacturing underpins all stages of our process. Handling iodine and adenosine derivatives involves inherent hazard management. Personnel training addresses not only spill handling and storage protocols but also the broader push toward waste minimization. Internal systems collect and neutralize iodinated byproducts, diverting contaminated solvents through recovery and incineration. As more of the scientific community drives sustainable chemistry forward, we’ve invested in greener solvent options and in recycling wherever acceptable without sacrificing product consistency.
Occasional process changes bring surprises—switching to lower-volume iodination, for instance, can reduce waste but may require more concentrated conditions and tighter control of exothermic risk. Each adjustment finds scrutiny through batch records, and we track not only manufacturing yield, but also volume of hazardous waste generated. In-house toxicologists and safety professionals oversee any updates to chemical risk assessments, ensuring that employee safety and client product safety go hand-in-hand, whether shipping kilogram drums or research vials.
Collaboration stands out as a driving force behind improved product performance and evolving formulations. International academic partners share early results on applications for 2-Iodoadenosine in sensor technology or single-molecule studies, which in turn shape new internal R&D. Technology transfer involves open protocols, pilot studies, and supply of analytical samples for cross-validation. Real problems—such as batch-specific background in mass spectrometry assays—move from anonymous troubleshooting to joint resolution, with input flowing back into the next pilot run.
Our technical support and application teams field questions not only about product use, but about long-term storage, co-solvent compatibility, or even alternatives when project pivots occur. This open communication helps bridge the knowledge gap between what gets produced at scale and what proves reliable in the field. Multi-year partnerships build trust, with many long-term users feeding back directly on purity tolerances or documentation needs that could otherwise escape notice during routine batch release.
As a manufacturer, every batch tells a story. We see raw material lots impacted by small changes in global supply, and we adjust to incoming variations in reagent purity or source. This hands-on vigilance translates to finished 2-Iodoadenosine that consistently meets trace impurity and moisture content benchmarks for demanding applications. We constantly tweak the process—not just the synthesis, but drying regimens, filtration steps, and even shipping protocols. Doing so allows anticipation of problems that surface only at scale or under real world transport and storage conditions.
We don't merely turn out a product; we stand behind every shipment—with technical documentation, shelf-life testing, and interactive support, especially as projects move from discovery toward development and application. This dedication to responsive manufacturing pays off for users, who rely on transparency and consistency when working on the cutting edge of biological and chemical research.
Producing 2-Iodoadenosine is more than tasking a reactor with raw ingredients and expecting a finished product to emerge. Each advancement or hiccup in the lab tweaks the process and elevates standards. Long-term relationships reveal that high-performance research depends on going beyond the basics in quality, analytical support, logistics, and candid communication. The lessons drawn from each campaign on the manufacturing line inform not only our current approach but help shape the future paths of nucleoside chemistry—in support of those pushing the boundaries in diagnostics, drug discovery, and the broader world of molecular science.