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4-Thiouridine

    • Product Name 4-Thiouridine
    • Alias 4-Thio-U
    • Einecs 219-151-8
    • 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

    674219

    Name 4-Thiouridine
    Cas Number 145-98-0
    Molecular Formula C9H12N2O5S
    Molecular Weight 260.27 g/mol
    Purity typically ≥98%
    Appearance yellow powder
    Melting Point melts with decomposition
    Solubility soluble in water
    Storage Temperature -20°C
    Synonyms 4-Thio-uridine
    Iupac Name 1-β-D-ribofuranosyl-4-thiouracil
    Smiles C1=CN(C(=O)NC1=S)C2C(C(C(O2)CO)O)O
    Application RNA labeling and photo-crosslinking
    Stability light-sensitive
    Inchi Key AAQOGOQOBXSDME-LURJTMIESA-N

    As an accredited 4-Thiouridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Thiouridine, 1 gram, is supplied in a sealed amber glass vial with a screw cap, labeled with product and safety information.
    Shipping 4-Thiouridine is carefully packaged in tightly sealed containers to ensure stability during transit. It is shipped at ambient temperature, unless otherwise specified, and handled as a non-hazardous laboratory reagent. All shipments comply with relevant chemical transport regulations, ensuring secure and timely delivery to research or industrial destinations.
    Storage 4-Thiouridine should be stored in a tightly sealed container, protected from light and moisture. Keep at -20°C in a dry, well-ventilated area. Avoid exposure to air and oxidizing agents to maintain stability. Proper labeling and handling procedures must be followed to ensure chemical integrity and safety. Use personal protective equipment when handling to avoid contamination or degradation.
    Application of 4-Thiouridine

    Applications of 4-Thiouridine in Industrial Manufacturing

    4-Thiouridine is a specialized nucleoside analog widely adopted in advanced biotechnology, pharmaceutical synthesis, diagnostics, and academic research. Its unique structural modifications enable precise functionality in RNA labeling, antisense drug development, nucleic acid diagnostics, biochemical assay reagents, and molecular biology research tools. As a chemical raw material manufacturer, we support high-purity, consistent production of 4-Thiouridine for these critical industrial applications.

    1. RNA Metabolic Labeling for Molecular Biology Research

    4-Thiouridine is systematically incorporated during in vivo RNA synthesis for metabolic RNA labeling studies. Researchers use metabolic labeling to track RNA turnover, processing, and interactions at the cellular level. The integration of 4-Thiouridine into nascent RNA enables selective enrichment and precise identification of newly transcribed RNA when combined with biotinylation or photoactivatable crosslinking techniques, supporting transcriptomics and RNA-protein interactome mapping. This method is integral for cellular dynamic studies in academic and industrial research laboratories.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for research reagents manufacturing
    • Good Laboratory Practice (GLP) for research-use-only (RUO) reagents
    • REACH Regulation (EC) No 1907/2006—Substance Registration and Safety
    • Harmonized System Nomenclature for biochemical reagents export

    Typical usage ratio

    • Typically 100–500 μM in cell culture medium; concentration depends on cell type sensitivity and desired labeling window duration

    Downstream process integration

    • Dissolve in culture media as nucleoside supplement prior to cell seeding or experiment start
    • Cells exposed during transcriptional pulse period
    • Harvest and isolate total RNA; perform biotinylation or crosslinking step

    Final product types

    • Biotin-labeled RNA for high-throughput sequencing
    • Purified nascent RNA pools for transcriptomic profiling
    • RNA-protein crosslinking samples for proteomic analysis
    • Academic research data packages for publication or patenting

    2. Antisense Oligonucleotide and Therapeutic Nucleic Acid Synthesis

    Pharmaceutical companies utilize 4-Thiouridine for developing modified nucleic acid therapeutics, including antisense oligonucleotides, siRNA, and mRNA therapeutics. The sulfur modification at position 4 enhances nuclease resistance and hybridization properties, significantly improving stability and pharmacokinetics. The incorporation of 4-Thiouridine occurs during solid-phase synthesis of oligonucleotides, where precise stoichiometry and automated synthesis methods guarantee batch-to-batch consistency. Products undergo extensive purification and are manufactured under stringent regulatory guidelines for preclinical and clinical applications.

    Industry compliance standards

    • International Conference on Harmonisation ICH Q7 (GMP for pharmaceuticals)
    • US FDA 21 CFR Part 210/211 (cGMP Finished Pharmaceuticals)
    • European Pharmacopoeia monographs for nucleic acid-based medicines
    • USP General Chapter <1045> Biotechnology-Derived Articles

    Typical usage ratio

    • 0.5–20% of total nucleotide content for mixed-sequence oligonucleotides; full replacement in some modified siRNAs or antisense constructs

    Downstream process integration

    • Delivered as an activated nucleoside phosphoramidite for automated solid-phase synthesis
    • Assembly on controlled-pore glass (CPG) supports
    • Post-synthesis cleavage, deprotection, and high-performance liquid chromatography (HPLC) purification

    Final product types

    • Antisense oligonucleotide therapeutics
    • siRNA drug candidates
    • mRNA vaccines with site-specific nucleoside modification
    • Companion analytical reference standards

    3. Diagnostic Probe and Hybridization Assay Reagent Production

    Manufacturers in the molecular diagnostics sector apply 4-Thiouridine for the synthesis of thiolated probes and molecular beacons used in hybridization-based tests and real-time PCR assays. 4-Thiouridine facilitates covalent labeling and enables site-specific immobilization on sensor surfaces or microarrays. Its unique chemical reactivity supports the fabrication of oligo probes with increased stability and signal sensitivity for nucleic acid detection kits, genomic diagnostics, and multiplex in vitro diagnostics (IVD) systems.

    Industry compliance standards

    • ISO 13485:2016 (Medical devices, including IVD reagents)
    • EU In Vitro Diagnostic Regulation (IVDR 2017/746)
    • US FDA 21 CFR 820—Quality System Regulation (for IVDs)
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 1–5 equivalents per 20-mer oligonucleotide probe, adjusted for probe length and desired functionalization degree

    Downstream process integration

    • Incorporated at defined site(s) during chemical oligonucleotide synthesis
    • Post-synthetic labeling or solid support immobilization using thiol-reactive chemistries
    • QC with capillary electrophoresis and mass spectrometry

    Final product types

    • DNA/RNA microarray probes
    • Fluorescent molecular beacons
    • Custom hybridization detection kits for clinical diagnostics
    • Point-of-care nucleic acid detection cartridges

    4. Enzyme Substrate and Inhibitor Screening for Biochemical Assays

    Producers of enzyme assay kits and research tools use 4-Thiouridine as a defined substrate or inhibitor for uridine-modifying enzymes, including uridine phosphorylases and RNA methyltransferases. The compound enables high-specificity colorimetric, fluorometric, and radiometric assay development, supporting drug discovery screening, enzyme kinetic studies, and biochemical pathway elucidation. Controlled synthesis and high analytical purity ensure reliable results in high-throughput and reference laboratory settings.

    Industry compliance standards

    • ISO 9001:2015 for laboratory reagent manufacturing processes
    • OECD Good Laboratory Practice (GLP) for assay validation studies
    • REACH compliance for chemical safety in laboratory use
    • Material Safety Data Sheet (MSDS) requirements for end-user safety

    Typical usage ratio

    • Concentration typically 10–100 μM per assay, fine-tuned for enzyme source and detection sensitivity

    Downstream process integration

    • Added to assay buffer as substrate or inhibitor control
    • Combined with biological sample or recombinant enzyme solution
    • Detection via absorbance, fluorescence, or LC-MS/MS readouts

    Final product types

    • Enzyme assay kits for research and pharmaceutical QC
    • Reference standards for analytical instrumentation calibration
    • Biochemical screening panels for drug discovery
    • Academic research toolkits for enzyme mechanism studies

    5. Photoreactive Crosslinking Reagent for RNA-Protein Interaction Mapping

    In the proteomics and molecular interaction analysis field, research-grade 4-Thiouridine is an essential photoreactive probe for capturing RNA-protein interactions. Upon exposure to UV irradiation at 365 nm, incorporated 4-Thiouridine forms covalent crosslinks with proximal proteins in living cells or cell extracts. This unique feature allows for isolation of specific ribonucleoprotein (RNP) complexes and construction of protein-RNA interactome libraries, enabling high-sensitivity mapping of molecular networks in functional genomics studies.

    Industry compliance standards

    • ISO 17034:2016 (Reference material production and quality)
    • Good Laboratory Practice (GLP) for reagents and sample preparation
    • REACH Regulation (EC) No 1907/2006—Registration and material handling
    • Institutional Biosafety Committee (IBC) protocols at end-user sites

    Typical usage ratio

    • Typically 0.1–0.5 mM in cell culture or extract, optimized for protein interaction yield

    Downstream process integration

    • Added to transcription system or cell culture for in situ RNA labeling
    • Post-labeling, samples exposed to UV irradiation at 365 nm for crosslinking
    • Isolation of RNP complexes via immunoprecipitation, followed by RNA and protein analysis

    Final product types

    • RNA-protein crosslinked complexes for mass spectrometry
    • Interactome libraries for next-generation sequencing
    • Reference datasets for pharmaceutical research
    • Biotechnological R&D tools for structure-function studies
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    Certification & Compliance
    More Introduction

    4-Thiouridine: Bringing Purity and Reliability to Nucleic Acid Research

    An Introduction Based on Shop-Floor Experience

    Working in chemical synthesis, I see firsthand that minor structural changes in nucleosides turn into major leaps for life science research. 4-Thiouridine, or sometimes called 4SU, stands out as one of those rare modifications that really make a difference in both basic and applied bioscience. Out in the plant, we produce this specialized analog through a dedicated process stream, hitting purity levels demanded by biologists, molecular labs, and pharmaceutical developers. Our model of 4-Thiouridine leans on years of fine-tuning, eliminating batch-to-batch fuzziness and making the compound accessible for both consistent high-throughput and small experimental runs.

    The Unique Structure That Drives Its Usefulness

    Classic uridine has set the basic template for so many discoveries, but 4-Thiouridine introduces a sulfur atom onto the uracil ring at position four. This is no routine substitution. Swapping oxygen for sulfur makes the ribonucleoside a responsive probe for a range of biological reactions. In RNA, this thionucleoside incorporates naturally or synthetically, providing a handle for downstream labeling, crosslinking, and turnover studies.

    Lab after lab has found that the sulfur atom reacts differently from oxygen. This small change means much more than a theoretical difference—our quality control teams routinely see the shift in UV absorption and chemical behavior. The unique spectroscopic and photoreactivity aspects power sensitive detection and time-resolved monitoring in research applications.

    Quality Manufacturing: How We Approach It

    Every facility claims purity. We build it from the ground up—starting from honest raw materials, tightly controlled solvents, and rigorous checks at each synthetic and purification stage. Chromatography profiles cut no corners; the final analysis goes well past standard NMR and HPLC, so researchers don’t have to worry about trace contaminants or side-products creeping into sensitive experiments. Reliability, not just purity, sets our 4-Thiouridine apart.

    We manufacture at defined scales, but adapt to both gram and kilogram orders without shortcuts. Internal stability tests have shown our batch lots resist degradation through shipping and storage. For every scale, our test records are checked not just by automated systems but read by chemical technologists. Lab results prove product consistency, confirming precise melting points, spectral data, and solubility.

    Specifications: More Than a Number

    Our current product lines provide 4-Thiouridine at over 98% HPLC purity, verified by independent analysis beyond our own facilities. We see this not as a marketing point but as a requirement for scientists working with RNA-sensitive enzymes or demanding downstream synthesis. Each batch record links back to a full traceable log, and on occasion, clients send back feedback that helps us push even higher in purity or add additional checks if a new use case arises.

    Moisture, solubility, and particle size matter to chemists using solid-phase synthesis methods or biochemical applications. Our process engineers have optimized the drying and handling stages so the final material flows easily without caking or introducing static charges that cause headaches at the bench. Lyophilization steps ensure longevity, which is confirmed in shipments to humid or challenging climates.

    How 4-Thiouridine Is Used: Insights From Real-World Labs

    We ship thousands of grams to RNA biochemistry teams for metabolic labeling. 4-Thiouridine’s greatest value comes from its specific incorporation into newly transcribed RNA. Researchers can then selectively isolate and track recently synthesized RNA using thiol-specific probes or crosslinkers. This makes pulse-labeling experiments cleaner and more sensitive than alternative tags.

    In high-throughput sequencing and transcriptomics, the 4-thio handle lets groups map RNA life cycles and gene expression changes under almost any cellular condition. Our experience teaches us that any impurity—especially analogs that look like uridine or cytidine—can throw off quantification or interfere with selective binding. The pharmaceutical industry has also used our material for testing RNA-modified therapeutics, as 4-Thiouridine adds resistance against certain nucleases and alters immune responses.

    Chemical biologists lean on it for photo-crosslinking; the sulfur group reacts with selected wavelengths, letting proteins or other nucleic acids “lock” onto RNA at contact points for structural or interactome studies. In cellular biology, toxicity and off-target effects can complicate labeling, so our process aims to deliver pure, well-characterized 4-Thiouridine with no biological byproducts.

    Comparing 4-Thiouridine to Related Nucleosides

    Nucleoside analogs come in many flavors. Methylated uridines, pseudouridine, 5-bromouridine—all fill some specialty niche. The advantage of 4-Thiouridine stands out in its dual ability to both “label” and act as a chemical handle. While 5-fluorouridine unfolds new opportunities in RNA mutagenesis or cancer research, it can cause chain termination or confuse polymerases. Many analogs fail to insert reliably during in vitro transcription, or their downstream processing becomes cumbersome due to compromised solubility or elaborate purification needs.

    Through direct customer communication, we learn that some groups try inserting 2-thiouridine or s4U, but the positional isomer creates different reactive sites, which don’t work well for the same crosslinking or biochemical footprint. Our 4-Thiouridine avoids this confusion, offering a sharper “signature” in mass spectrometry and cleaner reaction profiles in crosslink experiments. The sulfur modification at this position gives reproducible photoreactivity not matched by other nucleoside thiosubstitutions.

    Natural uridine finds use in almost every RNA-related assay, but lacks the tagging efficiency and selective chemical reactivity. 4-Thiouridine offers a gateway to more advanced chemical and biological manipulation, making it central to many epitranscriptomics projects, which are growing rapidly every year. Many teams in academia and industry depend on the reproducibility and downstream compatibility our product provides—especially when results are going to appear in published papers or form a basis for clinical development.

    What Matters Most: Consistency and Reliable Supply

    Any chemist who’s spent a night wrestling with a failed labeling experiment appreciates the value of consistency—not just purity. Our operation keeps batch standards above regulatory requirements and tracks documentation, so researchers in Europe, Asia, or the Americas each pull from identical lots, with traceable logs, minimizing variance between experiments or sites. We’ve invested in redundant supply lines so a delay in one region doesn’t force a research team to compromise or switch suppliers mid-project.

    Feedback loops from end-users shape how we further develop our product. Sometimes a research lab working on a human disease model will send unexpected results tied to micro-contaminants or fine variations in particle size. We encourage these conversations, and adapt—not just updating a spreadsheet, but testing new drying cycles or extending post-synthesis hold times to give the product the stability customers need. If a quality control report spots an anomaly, we halt that batch and go back to root-cause, even if it means scrapping valuable product. Reliability counts more than volume for building lasting scientific trust.

    Supporting Innovation in Modification Chemistry

    We notice a steady growth in requests for 4-Thiouridine derivatives—phosphoramidites and triphosphates primarily. The modification serves as a building block for more sophisticated oligonucleotide synthesis. For every gram delivered, we get back insights from method development teams: how they push the molecule further in click chemistry, affinity enrichment, or new hybridization protocols.

    Having access to a clean, well-characterized 4-Thiouridine opens the door to more than routine labeling. It becomes a launchpad for site-specific modifications, hybrid structures, and proof-of-concept molecules aimed at antiviral or gene therapy applications. DNA and RNA assembly methods using sulfur-modified nucleotides show improved performance in duplex stability and selective reactivity. The innovation doesn’t end at shipping—we’re regularly expanding our offering in response to trends like single-molecule sequencing, super-resolution imaging, and emerging clinical requirements for molecular diagnostics using sulfur-rich handles.

    Addressing Technical and Supply Chain Challenges

    Running a nucleoside manufacturing operation means solving real-world problems, not just shipping product. Handling sulfur-containing intermediates demands specialized equipment and continuous air monitoring. We take extra precautions on waste streams and equipment cleaning to prevent cross-contamination with other high-demand nucleosides. Trace metal analysis and moisture monitoring keep our product free from leftover reactants that would spell trouble in enzyme-side reactions.

    At the same time, meeting the sharp demand spikes for 4-Thiouridine—often driven by new grant cycles, emergent pathogen research, or regulatory shifts—calls for both flexible scheduling and buffer inventory. Supply chain interruptions have hit the industry several times, especially in shipping regulated solvents or precursor chemicals across borders. By holding critical intermediates and negotiating longer-term supplier contracts, we keep our production timelines steady and shielded from abrupt global changes.

    Continual Investment in Quality and Sustainability

    Any experienced manufacturer recognizes that quality and sustainability go hand-in-hand, especially for specialty chemicals destined for live cell work or human therapeutic support. We’ve reduced solvent loads, improved water recycling, and introduced greener workups at each synthetic stage. Not every adjustment shows up in the bottom line, but it shows in customer feedback about fewer product recalls, longer shelf-life, and improved batch performance.

    We also commit to investing in analytical science, not just in infrastructure but in staff expertise. Several teams now handle routine as well as advanced NMR, mass spectrometry, and residual solvent analysis. New hires learn from seasoned operators who have run purification columns and troubleshooting batches through real seasons and real process upsets, building memory into the whole manufacturing chain.

    Future Pathways and Customer Collaboration

    Chemical manufacturing is not a stagnant trade, least of all in nucleosides. Collaborations with biotechnology companies drive us to develop not just 4-Thiouridine, but analogs and value-add products—phosphorylated versions, lyophilized kits, and custom-scale synthesis for pharmaceutical development. Each partnership forces us to rethink product specs, turnaround times, and logistics. Often, insights from one customer spark a product improvement relevant to the entire research community.

    Consistent communication with our clients, ranging from academic molecular biology labs to multinational pharma, lifts our whole team’s awareness about evolving standard practices. Integrated platforms now help track order trends and anticipate demand spikes, so we are ready to step up capacity without bottlenecks or the need for long customer waitlists. These insights also feed into longer-term planning around compliance, waste management, and process optimization.

    Practical Solutions to Common Issues

    Researchers frequently ask about storage conditions, reconstitution protocols, or best practices in experimental design using 4-Thiouridine. Our technical support team, built of synthetic chemists and analytical scientists, provides grounded advice. For example, we frequently suggest reconstituting in molecular biology grade water or buffer, aliquoting to limit freeze-thaw cycles, and validating the solution by UV or HPLC before use. Standardized advice, rooted in direct experience, gives labs higher confidence on results.

    We also help labs troubleshoot interference caused by similar nucleosides or impurities, especially in complex RNA-protein crosslinking studies. Close customer collaboration has led us to supply extended documentation—detailed chromatography traces, impurity breakdowns, and real shelf-life studies—getting users past the unknowns that can otherwise derail weeks or months of scientific work.

    Closing Thoughts on 4-Thiouridine’s Place in Scientific Progress

    4-Thiouridine continues to shape new generations of RNA research and gene expression studies. From manufacturing through to real-world application, its role in biological labeling, photoreactivity, and RNA engineering only grows. Direct experience with both technical hurdles and customer ingenuity has taught our team the importance of integrity in supply, reliability in quality, and openness to research-driven feedback.

    As labs expand their horizons and tackle ever more complex molecular challenges, we dedicate ourselves to supporting their insight and needs. Doing so with an open ear and a commitment to honest manufacturing, we see 4-Thiouridine becoming not just a specialized ingredient, but a dependable part of the modern scientific toolkit.