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2'-Deoxyuridine

    • Product Name 2'-Deoxyuridine
    • Alias 2′-Deoxyuridine
    • Einecs 208-831-0
    • 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
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    Specifications

    HS Code

    748430

    Product Name 2'-Deoxyuridine
    Cas Number 951-78-0
    Molecular Formula C9H12N2O5
    Molecular Weight 228.20 g/mol
    Appearance White crystalline powder
    Melting Point 162-164°C
    Solubility In Water Soluble
    Purity Typically ≥98%
    Synonyms 2'-Deoxy-β-D-uridine
    Storage Temperature 2-8°C
    Iupac Name 1-β-D-2-deoxyribofuranosyluracil
    Unii 4842JWS2F9

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

    Packing & Storage
    Packing 2'-Deoxyuridine is supplied in a sealed amber glass vial containing 1 gram, clearly labeled with product details and safety information.
    Shipping 2'-Deoxyuridine is shipped in tightly sealed containers under dry, cool conditions to protect it from moisture and light. The product is typically packed with desiccants and sent via priority courier, complying with all relevant regulations for safe transport of laboratory chemicals. Temperature-sensitive shipping options are available upon request.
    Storage 2'-Deoxyuridine should be stored in a tightly closed container, protected from light and moisture. Keep at a temperature of 2-8°C (refrigerator) unless otherwise specified by the manufacturer. Ensure the storage area is well-ventilated and away from incompatible substances. Proper labeling and secure shelving help prevent contamination and degradation. Avoid repeated freeze-thaw cycles to maintain chemical stability.
    Application of 2'-Deoxyuridine

    Applications of 2'-Deoxyuridine in Industrial Manufacturing

    2'-Deoxyuridine is a nucleoside compound with established roles across DNA synthesis and biotechnology sectors. As a manufacturer, we supply this raw material for key industrial applications where strict adherence to industry standards, precise formulation, defined process steps, and specific final product requirements dictate successful downstream performance.

    1. Oligonucleotide Synthesis for PCR and Genetic Testing

    Oligonucleotide manufacturers incorporate 2'-Deoxyuridine during the solid-phase phosphoramidite method to introduce uracil residues in synthetic DNA sequences. This enables downstream PCR-mediated site-directed mutagenesis or creation of uracil-containing probes for molecular diagnostics. The material enters during the automated coupling step in DNA synthesizers, requiring tight batch-to-batch consistency and purity to meet the quality demands of clinical and research laboratories.

    Industry compliance standards

    • ISO 13485: Medical Devices–Quality Management Systems
    • USP-NF (United States Pharmacopeia–National Formulary) for nucleic acid raw materials
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 820: FDA Quality System Regulation for Diagnostics

    Typical usage ratio

    • 1–15% of total nucleoside input, adjusted depending on sequence design and the required number of uracil bases per probe/oligo

    Downstream process integration

    • Integrated at the phosphoramidite addition step in automated DNA/RNA synthesizer cycles to replace thymidine at targeted positions

    Final product types

    • PCR primers and probes with site-specific uracil
    • Synthetic oligonucleotides for gene editing
    • DNA standards for diagnostic kits
    • Research-grade control oligos

    2. Antisense Therapeutic Research and Preclinical Manufacturing

    Research and early preclinical manufacturing groups in the pharmaceutical sector utilize 2'-Deoxyuridine to introduce single or multiple uracil residues into antisense oligonucleotide backbones. This modification can enhance nucleic acid drugs' target recognition or enable enzymatic degradation strategies, crucial for mechanistic research and preclinical proof-of-concept studies.

    Industry compliance standards

    • ICH Q11: Development and Manufacture of Drug Substances (Chemical Entities and Biotechnological/Biological Entities)
    • Good Laboratory Practice (GLP) guidelines
    • USP General Chapters <1045> (Biotechnology-Derived Products)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 2–10% w/w in oligonucleotide batches; optimized for target sequence and mechanism, adjusted through analytical validation

    Downstream process integration

    • Added during custom antisense strand synthesis, typically using solid-phase synthesis amidite chemistry in controlled environments

    Final product types

    • Antisense oligonucleotide candidates for cell culture validation
    • siRNA and modified DNA for gene silencing assays
    • Enzyme-cleavable oligonucleotide constructs
    • Lead compound seed libraries for early-stage drug discovery

    3. Isotopically Labeled Uracil Precursors for Clinical Tracing and Research

    Specialty chemical and isotope labeling facilities employ 2'-Deoxyuridine as a substrate to produce uracil derivatives with isotopic labels (such as 13C or 15N) used as tracers in metabolic pathway studies and in vivo pharmacokinetics testing. Consistent isotopic purity and chemical quality are required for reproducible data in downstream biomedical investigations.

    Industry compliance standards

    • ISO 17034: General Requirements for the Competence of Reference Material Producers
    • ISO/IEC 17025: Testing and Calibration Laboratories
    • Good Manufacturing Practice (GMP) where compounds are used in clinical research
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals–EU, if exported)

    Typical usage ratio

    • Variable, often 100% feedstock for isotope labeling; precursor solution concentrations between 10–50 mM as required by downstream synthesis yields

    Downstream process integration

    • Introduced as a pure substrate in enzymatic or chemical isotope labeling processes, followed by chromatographic purification to recover labeled nucleosides

    Final product types

    • Isotopically labeled deoxyuridine for pharmacokinetic tracing
    • 13C-/ 15N-labeled uracil for metabolic flux studies
    • Calibration standards for mass spectrometry in clinical labs
    • Reference materials for drug metabolism investigations

    4. Cell Culture Media Supplementation for Nucleotide Metabolism Studies

    Biotechnology companies and cell biology laboratories supplement cell culture media with 2'-Deoxyuridine to study nucleotide salvage pathways, DNA repair mechanisms, or as a selection agent in gene-editing protocols. Reliable dissolution and biological grade purity are necessary for reproducible results and controlled experimental outcomes in academic, pharmaceutical, and industrial research settings.

    Industry compliance standards

    • ISO 13408-1: Aseptic Processing of Healthcare Products
    • USP General Chapter <1043> on Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • GLP requirements for research laboratories
    • FBS/animal-free certifications for xeno-free cell culture applications

    Typical usage ratio

    • 0.1–1 mM in final cell culture medium; optimized based on cell type, experimental protocol, and culture period

    Downstream process integration

    • Dissolved in sterile buffer then sterile-filtered into basal or custom media formulations prior to cell seeding

    Final product types

    • DNA repair assay-ready cell culture kits
    • Custom-formulated media for gene-editing selection
    • Experimental metabolic labeling blends
    • Nucleotide metabolism research reagents
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    Certification & Compliance
    More Introduction

    2'-Deoxyuridine: A Manufacturer’s Perspective on Value and Application

    Our Approach to 2'-Deoxyuridine Production and Quality

    Making nucleoside derivatives year after year, our team has seen how a single building block can shape the future of medicine, diagnostics, and research. 2'-Deoxyuridine stands out in this field. Every batch we produce reflects the experience built from direct handling of raw materials and fine-tuning of reaction conditions. No two production runs are exactly the same, and each brings new insight into what this molecule can achieve in the right hands.

    The moment we put 2'-Deoxyuridine into production, we committed to clear chromatographic purity and reliable yield. Typical lots reach above 99% HPLC purity, and residual solvent is tightly monitored. Our technical staff conduct identity verification using NMR and mass spectrometry. These standards stem not only from regulatory expectations, but also from decades of customer feedback and our own project collaborations with research partners. Unwanted impurities risk more than a spoiled reaction; they can hold back entire research timelines.

    We source our uracil and protectant reagents from trusted chemical producers, and every lot is traceable back through full documentation. With the growing focus on data transparency and reproducibility in the life sciences, we take extra care to provide supporting analytical results. Customers working on oligonucleotide synthesis or metabolic studies benefit from clear reference spectra and testing data. By sticking to these practices, we see research outcomes improve year after year.

    What Sets 2'-Deoxyuridine Apart?

    Ask any bench scientist to pick between the available nucleosides, and decisions often hinge on small changes. Unlike its ribose cousin, uridine, 2'-Deoxyuridine replaces the 2'-hydroxyl group with a hydrogen. This subtle adjustment transforms not only the compound’s reactivity but also its role in DNA replication and labeling studies. Enzymes that act on DNA, such as polymerases or nucleases, respond differently to this deoxy structure versus ribonucleosides. Such details are not academic— omitting the 2'-hydroxyl ends up being essential for precise experiments.

    Many researchers come to us confused by the choices in the nucleoside family. Ribosides, deoxyribosides, and their substituted variants line up in catalogues, often promising similar functions. What truly distinguishes 2'-Deoxyuridine is its compatibility with enzymatic synthesis protocols. DNA polymerases generally incorporate 2'-deoxynucleosides, not ribonucleosides, so selecting the right starting material avoids reaction failures and wasted time. In DNA labeling, substituting uridine for deoxyuridine cuts down on background and improves detection limits.

    Storage and stability also shape real-world usage. 2'-Deoxyuridine, with its protected sugar moiety, displays greater shelf stability in dry, cool conditions than corresponding ribonucleosides. In our facility, this allows us to prepare and deliver larger orders without risking loss due to rapid degradation. Chemists working on solid-phase nucleic acid synthesis see real productivity gains when their stocks remain reliable from month to month.

    We offer the product as a crystalline powder, white to off-white in appearance, often with minimal odor and low moisture content. It dissolves readily in water and the common buffers used in molecular biology. Each batch includes full analytical documentation, drawn from our own runs. Customers supporting pharmaceutical projects and academic research both rely on timely shipment in secure, sealed containers—so integrity and accurate labeling rank above all else.

    Why 2'-Deoxyuridine Matters in Research and Industry

    Pharmaceutical development never stands still, and nucleoside analogs play a major part in shaping current and future therapies. 2'-Deoxyuridine has earned a reputation as a key intermediate. DNA synthesis by both biological and chemical means depends on reliable access to its derivatives. In our experience, the demand for this product rises most steeply during project ramp-ups for clinical candidate development and diagnostic tool improvement. Teams working on PCR probes, FISH labeling, and DNA fragmentation analysis put our batches to the test week after week.

    Radiolabeling studies benefit from deoxyuridine’s willingness to form stable DNA adducts. Incorporating isotopic versions offers sensitive tracking of nucleotide incorporation. Many colleagues working on in vivo imaging for cancer research or pharmacokinetics signal the usefulness of having clean, high-purity deoxyuridine free of interfering nucleosides or degradation products.

    Beyond direct DNA synthesis, metabolic tracing depends on uniform and accurate supplies of nucleosides. Cell culture specialists routinely reach out for gram or multi-gram orders, seeking support for their pulse-chase experiments using 2'-Deoxyuridine to halt cell proliferation or stress cellular pathways. Past experience shows that contaminants or slight formulation changes can throw off interpretations, leading to false conclusions in cell cycle research.

    In microbiology, we partner with groups using 2'-Deoxyuridine to probe microbial pathways, especially for understanding thymidylate synthase inhibitors and other metabolic flux studies. It emerges as a strategic tool, not just a raw material, because it can discriminate among nucleoside processing pathways. The feedback from these laboratories continually shapes how we handle and deliver our product.

    Production Expertise and Challenges in Sourcing Raw Materials

    Day-to-day, our chemists spend almost as much time following supply chains as they do in the lab. Reliable uracil starting material often comes down to building trust with a handful of raw material suppliers. Disruptions, from transport delays to policy changes for chemical precursors, have the capacity to reshape our pricing and delivery timelines. For 2'-Deoxyuridine, this challenge is manageable, but not trivial. We choose partners who consistently provide verified source documentation and whose purity claims stand up to our incoming quality checks.

    The production itself involves multi-step synthesis and purification. Efficient dehydration and careful deprotection steps prevent formation of undesired byproducts. Unlike simpler chemicals, nucleosides resist large-scale synthesis. Even with automation, quality rests on the hands and eyes of each chemist handling glassware, chromatographic columns, and lyophilization processes. Our analytical lab spends hours running HPLC, NMR, and mass spectrometry for each lot—not just to meet regulatory expectations, but to catch outliers and avoid recalls or project setbacks.

    Waste handling and solvent management also take up sizeable resources. The drive for sustainability has encouraged us to recycle solvents and adopt greener approaches. At the same time, these practices can never compromise analytical quality. Every refinement in our production line—whether a new purification resin, filtering method, or solvent switch—brings feedback from batch testing and customer trials.

    No production process in this market stands alone. Respecting confidentiality, sometimes we work with pharmaceutical project managers or lead process engineers to address specialized requirements. These might include scaling up for larger clinical runs, or dialling down impurities that would affect a customer’s downstream modification reactions. In all these cases, adaptability arises not from planned documentation, but from lived experience with chemical synthesis at the gram-to-kilogram scale.

    Differences Between 2'-Deoxyuridine and Other Related Nucleosides

    Within the nucleoside landscape, minor alterations translate to significant functional differences. We regularly explain the distinctions between 2'-Deoxyuridine, standard uridine, and other deoxy analogs such as deoxycytidine or thymidine. The switch from the ribose to deoxyribose backbone, for instance, directly influences which enzymes incorporate the nucleoside, how easily it degrades under heat or pH extremes, and its role in template-directed DNA synthesis.

    The most frequently asked question centers on the difference between 2'-Deoxyuridine and thymidine. Though both share a deoxyribose sugar, thymidine carries a methyl group at the 5-position instead of a hydrogen. This methyl substitution affects both enzymatic recognition and base pairing properties. In DNA, deoxyuridine substitutes for thymidine only under specific circumstances, often for labeling or artificial modification purposes. Overuse risks misinterpretation of sequencing or labeling outcomes.

    Compared to deoxycytidine, deoxyuridine exposes research systems to uracil DNA glycosylase (UDG) activity, making it suitable in systems where controlled degradation or removal of labeled bases is crucial. By contrast, standard uridine or cytidine feature a ribose sugar, restricting their usefulness to RNA-related studies or enzymatic reactions involving ribonucleases.

    Some customers ask about using related nucleoside products sourced from competitors selling "ultra-pure" grades or "enhanced" DNA building blocks. Our view relies on direct lab comparisons. Differences in crystallinity, solubility, or impurity profiles emerge quickly, especially during oligonucleotide solid-phase synthesis or enzymatic reactions. Only hands-on use distinguishes whether a product performs at scale, and we regularly run in-house control experiments to ensure our output exceeds commercial alternatives.

    Considerations for Storage, Handling, and Safety

    In our warehouses and customer operations, conditions for storage and handling directly affect the longevity and performance of 2'-Deoxyuridine. Experience shows that desiccated environments, dark storage, and sealed containers minimize decomposition. Moisture ingress results in slow hydrolysis or aggregation, manifested as changes in powder texture and eventual purity drift.

    Chemists storing 2'-Deoxyuridine for repeated use within large or multi-shift labs gain peace of mind from accurate labeling and full traceability. We use tamper-evident seals and detailed batch information, including the date of production and recommended best-by intervals. The decision to re-test or move stock to a dedicated cold room can swing on minor variations in lab humidity or staff workload.

    Practical safety handling guidance beats generic documentation in the real world. While 2'-Deoxyuridine itself lacks the acute toxicity of many analogs, repeated exposure to powders increases the risk of inhalation. Our manufacturing team uses protective gear, localized exhaust, and closed transfer systems for all weighing and packing steps. Personal stories from the floor—avoiding eye contact, careful cleaning of balances—have shaped our in-house protocols as much as any printed guideline.

    Transport remains a consideration both locally and for export customers. Customs documentation and temperature control during delivery can spell the difference between a seamless experience and costly project delays. Shipping partners with experience handling fine chemicals, and familiarity with customs documentation, foster smoother end-to-end supply chains. We invest significant time training logistics teams to pack, track, and communicate about every shipment, especially where multiple batches travel together for on-site validation.

    Supporting Scientists, Engineers, and Product Developers

    Our engagement with customers starts the moment questions arise about consistency from lot to lot, documentation detail, and application support. Over two decades, we’ve watched research trends shift from bulk DNA production to targeted genomic labeling and personalized diagnostics. Modern developers push our product into machineries we never imagined in our early days as a manufacturer. Collaboration often leads us to customize handling advice, provide sample reference spectra, or discuss analytical approaches.

    Most of our feedback revolves around performance in critical protocols. Does the batch generate clean oligonucleotide synthesis with minimal capping or truncation? Are research teams able to track metabolic fluxes without surprising background? By running our own control reactions in parallel with customers, we piece together solutions to project-specific problems. Sometimes it means a last-minute resupply for an urgent clinical batch; sometimes it means finding a workaround for a new contaminant Signal detected in high-sensitivity mass spectrometry.

    We advocate for ongoing education around nucleoside selection, contamination risks, and batch-specific properties. The world of nucleic acid chemistry keeps moving, and what worked yesterday may not fit the latest analytical platform or automated synthesis system. We document key parameters for each batch but encourage customers to carry out pilot studies, especially for large or regulatory-heavy projects. Experience proves that pre-qualification prevents more lost time than any late-stage remedy.

    Anticipating Future Needs and Challenges

    Looking forward, the demand for clear, reproducible nucleoside products such as 2'-Deoxyuridine only grows. Novel DNA synthesis protocols and therapeutic delivery methods expand usage scenarios. The pressure for even tighter analytical tolerances, greener chemistry, and faster turnaround continues. We keep investing in staff training, equipment upgrades, and streamlined documentation to meet these evolving standards.

    Global research priorities shift quickly, often accelerated by changes in funding, regulatory frameworks, or healthcare demands. Pandemic disruptions demonstrated the need for reliable access to nucleosides. We adapted by expanding storage, forging partnerships for overland and air freight, and working closely with regulatory bodies to keep product flowing. These lessons filter down into daily operations and shape the resilience of our supply chain.

    Research outcomes remain our greatest motivation. Each batch of 2'-Deoxyuridine leaves our facility with more than a product label. It reflects years of refining synthesis, building trust with sourcing partners, and learning from the detailed questions of bench scientists. We see new uses emerge every quarter, from advanced diagnostic platforms to breakthroughs in DNA repair studies. The next chapter for this product will bring challenges, but manufacturers grounded in real-world use and continuous improvement remain best positioned to support discovery and innovation.