Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

5-Iodo-2'-Deoxycytidine

    • Product Name 5-Iodo-2'-Deoxycytidine
    • Alias 5-Iododeoxycytidine
    • Einecs 259-758-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    834418

    Productname 5-Iodo-2'-Deoxycytidine
    Casnumber 13815-86-6
    Molecularformula C9H12IN3O4
    Molecularweight 369.12
    Appearance White to off-white powder
    Purity ≥98%
    Meltingpoint 177-180°C
    Solubility Soluble in DMSO and water
    Storagetemperature -20°C
    Synonyms 5-Iodo-2'-deoxycytosine nucleoside
    Smiles C1=CN(C(=O)NC1=N)C2C(C(C(O2)CO)O)I
    Inchikey NCYZAUMBIREFME-UHFFFAOYSA-N

    As an accredited 5-Iodo-2'-Deoxycytidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Iodo-2'-Deoxycytidine is supplied in a 100 mg amber glass vial, securely sealed, with a detailed product and hazard label.
    Shipping 5-Iodo-2'-Deoxycytidine is shipped in secure, chemical-resistant packaging to maintain stability and prevent contamination. The product is usually transported at controlled ambient or refrigerated temperatures, depending on supplier guidelines, and accompanied by appropriate documentation and labeling, in accordance with international and domestic regulations for the handling and transport of research chemicals.
    Storage 5-Iodo-2'-Deoxycytidine should be stored in a cool, dry place, protected from light and moisture. It is recommended to keep the chemical at -20°C in a tightly sealed container to prevent degradation. Avoid exposure to air and humidity. Proper labeling and safe handling practices are essential to maintain stability and ensure laboratory safety.
    Application of 5-Iodo-2'-Deoxycytidine

    Applications of 5-Iodo-2'-Deoxycytidine in Industrial Manufacturing

    As a high-purity nucleoside intermediate, 5-Iodo-2'-Deoxycytidine plays a critical role in advanced nucleotide chemistry and pharmaceutical synthesis. Below, we highlight its dedicated downstream industrial applications, focusing on technical requirements, integration in customer formulations, and direct links to compliant, large-scale manufacturing.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Anticancer Drugs

    Research-driven pharmaceutical manufacturers utilize 5-Iodo-2'-Deoxycytidine as a building block in the synthesis of cytidine analogues for oncology therapies. By leveraging iodinated nucleoside chemistry, process chemists selectively introduce this intermediate during the key nucleoside modification steps, particularly within GMP-compliant cytostatic agent development lines. Stringent global pharmaceutical regulations require precise raw material handling, traceable batch records, and stringent process validation at each step from nucleoside conversion to final active substance release. End uses include injectable cytidine derivative medications for clinical oncology protocols.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • FDA 21 CFR Part 211 (U.S. cGMP)
    • EU GMP Guidelines (EudraLex Volume 4)
    • Japanese Pharmacopoeia monographs for cytidine derivatives

    Typical usage ratio

    • 0.2%–2.5% (w/w, calculated on total nucleoside precursor mass); adjusted based on yield optimization and impurity profile requirements in batch or flow protocols.

    Downstream process integration

    • Introduced at the nucleoside precursor iodination stage; used in regioselective halogenation prior to glycosylation or phosphorylation; typically isolated before advanced protecting group manipulations for further enzymatic transformation.

    Final product types

    • Anticancer cytidine analogue APIs
    • Small-molecule drug substance intermediates for oncology pipelines

    2. Modified Oligonucleotide Probe Manufacturing

    Manufacturers of synthetic DNA probes for molecular diagnostics incorporate iodinated cytidine analogues at specific sequence locations to enable downstream labeling or structural stability enhancements. During automated solid-phase oligonucleotide synthesis, technicians incorporate the modified nucleoside via phosphoramidite chemistry. Integration must comply with high-throughput synthesis QC standards and raw material traceability, especially when manufacturing probes for use in regulated clinical or laboratory settings. The downstream application enables users to develop advanced PCR diagnostic kits and gene-editing control probes.

    Industry compliance standards

    • ISO 13485:2016 (Medical device QMS for diagnostic products)
    • FDA 21 CFR Part 820 (Quality System Regulation for IVD devices)
    • OECD Guidelines for Synthetic DNA Quality

    Typical usage ratio

    • Single or multiple residues per target sequence (typically 1–5 units per 20–100mer oligo, 0.1–0.5 µmol scale); incorporated via amidite loading adjusted per batch requirements and probe application.

    Downstream process integration

    • Added during the automated oligonucleotide chain assembly on a solid support; incorporated in-cycle at designated phosphoramidite coupling steps for post-synthetic labeling or target affinity modification.

    Final product types

    • Fluorescent or radiolabeled DNA/RNA probes for diagnostic assays
    • PCR and qPCR test kits
    • Gene-editing control oligos

    3. Radiolabeling Substrate Preparation for Biomedical Research

    Life science research and radiochemistry labs require high-purity, structurally defined iodinated cytidine intermediates as starting materials for further radioiodination. Researchers perform isotopic exchange or direct labeling with radioisotopes (e.g., I-125 or I-131) to track nucleoside incorporation in cell or animal models. Standard hygiene, safety, and labeling documentation apply due to radioactive handling. By using this material at defined steps, researchers ensure reproducibility in nucleic acid tracer studies and preclinical pharmacokinetic analyses.

    Industry compliance standards

    • IAEA Safety Standards for Radiopharmaceuticals
    • ISO 2919:2012 (Sealed Radioactive Sources)
    • GLP (Good Laboratory Practice, OECD Principles)

    Typical usage ratio

    • 100% substrate for the radioiodination reaction (stoichiometric amount, typically on 0.5–5 µmol scale per batch); molar equivalents adjusted according to labeling efficiency and purity targets.

    Downstream process integration

    • Acts as the sole nucleoside precursor in isotopic exchange reactions or direct aromatic iodination by radiochemistry teams following pre-activation and substrate drying stages.

    Final product types

    • Radioiodinated nucleoside tracers
    • Preclinical imaging agents
    • Cell uptake and metabolism assay reagents

    4. Reference Standard Production for Pharmaceutical Quality Control

    Pharmaceutical reference standard manufacturers employ high-purity iodinated cytidine as a calibration tool for HPLC, LC-MS, or related analytical platforms during impurity profiling and release testing of cytidine-based drug APIs. Production teams prepare and certify this material through validated purification, assignment of absolute structure, and traceable documentation under ISO/IEC 17025-accredited methods. Downstream customers rely on these standards to maintain method validation consistency across global manufacturing and regulatory inspections.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • USP General Chapter <1224> (Reference Standards)
    • Ph. Eur. reference standard production guidelines

    Typical usage ratio

    • Used as primary standard at 0.1–0.5 mg/mL for calibration solutions in analytical method validation; exact mass concentration prepared for batch-specific certificates of analysis.

    Downstream process integration

    • Employed as analytical reference in system suitability tests, peak identification, impurity determination, and stability studies during cGMP batch release and continuous process monitoring.

    Final product types

    • Certified reference materials (CRMs) for cytidine derivatives
    • Calibration kits for HPLC, LC-MS, and related analytical equipment
    Free Quote

    Competitive 5-Iodo-2'-Deoxycytidine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    5-Iodo-2'-Deoxycytidine: Direct from the Factory Floor

    A Making Story Built on Experience

    In the world of nucleoside analogues, 5-Iodo-2'-Deoxycytidine grabs attention partly because of its critical use in research and partly because of the technical know-how that goes into making it right. Years of being on the manufacturing line teach that even the tiniest deviation in production will ripple downstream. Consistency isn’t just a buzzword here; it shows up in how products like this influence cellular studies, DNA methylation work, or antiviral experimentation.

    Every batch of 5-Iodo-2'-Deoxycytidine, with its chemical name 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-5-iodocytosine, tells a story of careful process control. Producing this compound calls for a steady hand at every step. The molecular formula, C9H11IN3O4, and molecular weight, about 353.11 g/mol, make it a bit heavier and more halogen-laden than more common cytidine analogues. That slight difference plays a considerable role once it enters chemical or biological systems.

    One detail that can’t be ignored in practice: iodine at the 5-position. That halogen atom isn’t riding along for show — it switches up hydrogen bonding, electronic character, and overall reactivity. Years ago, changing the halogen would often create headaches in subsequent coupling reactions or stability testing. The 5-iodo group, though, brings a reliable handle for further derivatization or tagging in the lab. During synthesis and purification, keeping that iodine intact becomes a daily point of focus.

    Mindful Manufacturing Means Repeatable Results

    Walking through the actual synthesis, the level of detail often gets overlooked by end-users. People notice only if things don’t work as expected. Experience on the production team brings a different kind of respect for purity and uniform lot characteristics. The process rarely presents an easy path. Moisture, temperature swings, or trace contaminants sneak in easily and spoil a run. Getting the finished 5-Iodo-2'-Deoxycytidine to meet specification isn’t about ticking boxes but about the chemical doing its job inside a cellular assay or nucleic acid probe.

    For us, handling this molecule in-house, not through intermediaries, means real control over raw materials and each stage of the process. Sourcing high-grade 2'-deoxycytidine as a starting point becomes step one. Improvements in halogenation selectivity over the years have given better batch-to-batch consistency. By focusing on exact iodine placement, side reactions stay low, and the product profile remains as expected.

    Traditional silica gel chromatography hasn’t always been enough to meet the purity marks researchers demand. We moved to high-performance liquid chromatography (HPLC) as routine, monitoring by both UV-Vis detector and mass spectrometry. Most finished runs test for purity upwards of 98%, but the real proof surfaces when customers report clear, sharp results in their biological work. The moment impurity peaks begin to show up, internal investigations kick off—not because statistics say so but because down the road, downstream work risks uncertainty.

    Differences That Matter in Real-World Labs

    Stacking 5-Iodo-2'-Deoxycytidine against other cytidine analogues brings its uniqueness into focus. Standard deoxycytidine is critical in DNA synthesis but lacks functional handles for further modification. Once you bring in a halogen at the 5-position, you create both a point for downstream chemistry and an altered electronic profile. This isn’t just academic. In-probe labeling or radiolabeling, for example, the iodo group opens a door where a plain hydrogen would leave you locked out.

    Comparisons to 5-bromo or 5-fluoro analogues usually come up. Iodine carries higher molecular weight and gives different reactivity profiles than the smaller halides. In hands-on applications—such as Pd-catalyzed cross-couplings—the iodo variant often proves more reactive. There's a practical payoff for researchers chasing site-selective functionalizations. Iodine leaves less ambiguity about reaction completion and downstream purification. Over time and many runs, we’ve noticed that the iodo-compound stands up better to a wide range of ligation and substitution conditions. Stability in storage and ease of dissolution—key for solution prep—make it reliable for repeat work.

    Some customers ask about residue or trace metals from production. Years of fielding these questions motivated us to switch over to high-purity reagents and solvent systems. Mercury-free iodine sources and avoiding transition metal catalysts except where absolutely necessary have trimmed down sources of heavy metal contamination. Ion chromatography and ICP-MS readouts tell their own story, but our lineup of in-process controls keeps the batch well below the industry-accepted limits. These improvements, led by customers’ feedback and our own troubleshooting, have made a tangible dent in troubleshooting time on the customer side.

    From R&D to Scale-Up: A Manufacturer’s Eye View

    On the R&D side, 5-Iodo-2'-Deoxycytidine appears first as a gleam in a chemist’s eye, often envisioned as a taggable building block for oligonucleotide synthesis. That’s the theory. In practice, the daily grind of turning out high-quality product in kilogram lots means balancing reaction yield, byproduct cleanup, and reproducible handling. Each increase in scale brings its own surprises, from keeping reaction exotherms in check to streamlining aqueous work-up without losing material downstream.

    Customer questions sometimes land on the differences they notice between lots made in different years or from different facilities. In-house control gives us tighter oversight, reducing lot-to-lot drift. Years of tuning process conditions have taught that small changes—time of addition, reaction temperature, solvent grade—show up later as inconsistencies in the finished product. We shifted to closed-system reactors and dry-room protocols, shaving off moisture ingress and boosting reproducibility. Our spec sheets reflect real production history, not copied numbers from external references.

    Another part worth noting: handling and storage conditions impact more than shelf-life dates. We pack the finished compound under inert gas and test stability under various humidity and light exposures. Our operators physically inspect every bottle before it moves to the warehouse. Once in the hands of researchers, it tends to reconstitute smoothly in standard aqueous buffers, owing to attention paid during lyophilization and pre-packing drying.

    Supporting Research—Why Purity and Reliability Count

    Few places show the impact of product purity like research labs running sensitive assays. Any sight of an extra peak in the LC trace, a color shift during an enzymatic reaction, or dropout in PCR experiments means delays and extra troubleshooting cycles. Lab budgets and deadlines don’t stretch to cover sub-par reagents. Direct conversations with research end-users over the years have pressed home a basic fact: if the product acts up, project timelines slip.

    Chromatographic purity, clear NMR signatures, and absence of unexpected UV-absorbing contaminants lift some of that burden. Our QA/QC process spends as much time confirming residual solvent levels are below trace detection as it does tuning the synthetic route for yield. Several times in the past decade, as molecular biology protocols tightened their requirements, we invested in new purification skids and re-trained the QC chemists to spot subtle changes in impurity profiles. It’s not a cost-cutting exercise. The mindset stays rooted in keeping the science running.

    The impact stretches from the micro-level details to broader research aims. In epigenetics studies, for example, inaccurate methylation or improper blocking from trace contaminants can throw entire datasets into doubt. In diagnostic probe work, clarity around base modification and confidence in chemical integrity become non-negotiable. We learned the hard way that labeling product as "research grade" sets a minimum standard, but feedback-driven tweaks earned trust for more ambitious projects.

    Bridging the Production–Research Gap

    Bridging the gap between chemical production and laboratory users sometimes feels like walking a tightrope. Requests for custom batch sizes, tailored particle size distributions, or even alternative counter-ions pop up often. Direct feedback—from conversations at conferences, through customer questionnaires, or as troubleshooting requests—shapes the evolution of each product. We use these exchanges as direct input for process improvement.

    Occasionally, an application arises that puts the product under new scrutiny—like click chemistry modifications or radiolabeling for PET imaging research. Scaling for these applications requires more than following SOPs. Real-world use cases lay out unexpected requirements for solubility, freeze-thaw stability, or even the speed at which a bottle can be unsealed. We’ve pivoted production schedules to support pilot studies, coordinated real-time with logistics to ensure product integrity during longer transits, and ramped up technical support when researchers try new protocols. Every challenge brings a clearer view of what matters most to end-users.

    Advances in Analytical Rigor

    Looking back over product development, one clear trend stands out: Analytical demands rise every year. Once, a compound passing TLC and UV absorption tests satisfied most customers. Now, high-resolution mass spectrometry, HPLC/UPLC purity, and trace metal content matter more than ever. We responded by investing in better on-site capabilities and training chemists to recognize batch-specific quirks, such as subtle shifts in retention time or unexpected fragments in MS spectra.

    Satisfying these higher standards comes from investing in tools and cultivating a culture on the production floor that values precision. When issues arise—unexpected color changes, incomplete runs, or ambiguous QC signals—the response is hands-on troubleshooting. Our laboratory team, armed with years of accumulated experience, pulls problematic lots for repeat purification, retesting until the product clears all hurdles. Most researchers never see this backstage process, but each lot that ships owes its quality to that commitment.

    Continual Improvement and the Road Ahead

    Production never stands still. Regulatory trends, environmental considerations, or shifts in research focus push manufacturers to adapt. For compounds like 5-Iodo-2'-Deoxycytidine, ensuring reliable access means monitoring upstream supply chains, troubleshooting emerging analytical standards, and staying ready to modify processes in response to changing scientific needs.

    Environmental stewardship looks different in fine chemical manufacturing than in bulk commodity circles. Careful solvent recovery, reduced halogen waste, and safe handling of iodine residues eat up hours each month. From experience, placing these protocols isn't about checking compliance boxes but about keeping production sustainable for the long haul. The reality of chemical synthesis brings tradeoffs, and responding thoughtfully to those pressures builds a more resilient operation.

    Why Sourcing Direct Means More than a Label

    Whether researchers notice it or not, buying direct from a chemical manufacturer shapes the experience in the lab. Stories from conversations with customers who switched from brokered product to direct supply underline the differences: better lot transparency, swifter troubleshooting support, more predictable stock, and custom options when required. The feedback loop from users to production teams is short and immediate. Small requests—such as extra documentation, special bottle sizes, or even minor tweaks in spec—move quickly when there’s no buffer between the customer and the manufacturer.

    Researchers navigating the maze of nucleoside analogues need more than a catalog listing. They need reliable supply, transparent quality, and answers to their questions that reflect an understanding of their workbench realities. The relationship with each 5-Iodo-2'-Deoxycytidine customer builds on the practical experience of making, testing, and improving the compound—batch after batch, year after year. As manufacturing teams, we know that every gram carries the weight of countless experiments, and we take that responsibility seriously.

    Final Thoughts from the Manufacturing Line

    There’s real pride rooted in the process of making a compound like 5-Iodo-2'-Deoxycytidine. Producing it well means harnessing technical skill, attention to detail, and a commitment to the research community. Chemical manufacturing thrives on solving practical problems, not just hitting paperwork targets.

    Reflecting on years of work bringing this product from the reactor to the lab bench, the lessons feel both specific and universal. Handle the raw materials with care. Pay attention to every detail during synthesis, isolation, and testing. Listen to researchers working at the edge of what's possible, and bring their insights into each new production cycle. Only then does a product like 5-Iodo-2'-Deoxycytidine move beyond a name on a label and into the foundation of scientific discovery.