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5-Formyluracil

    • Product Name 5-Formyluracil
    • Alias 5-Formyl-2,4(1H,3H)-pyrimidinedione
    • Einecs 207-912-2
    • 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

    955572

    Chemical Name 5-Formyluracil
    Cas Number 612-62-4
    Molecular Formula C5H4N2O3
    Molecular Weight 140.10 g/mol
    Appearance White to off-white solid
    Melting Point 291-293°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Iupac Name 5-formyl-2,4(1H,3H)-pyrimidinedione
    Smiles C1=C(C=O)NC(=O)NC1=O
    Inchi InChI=1S/C5H4N2O3/c8-2-3-1-6-5(10)7-4(3)9/h1-2H,(H2,6,7,8,9,10)
    Storage Temperature 2-8°C (refrigerated)
    Synonyms 5-Formyl-2,4(1H,3H)-pyrimidinedione
    Pka Approx. 9.5 (for NH group)

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

    Packing & Storage
    Packing 5-Formyluracil, 1 gram, is packaged in a sealed amber glass vial with a tamper-evident cap and clear labeling.
    Shipping 5-Formyluracil is shipped in tightly sealed containers under ambient conditions, protected from moisture and light. It complies with standard chemical transport regulations and is labeled for laboratory use only. Packaging ensures minimal exposure to air and potential contaminants during transit. Handling and shipping follow all applicable safety and hazard protocols.
    Storage 5-Formyluracil should be stored in a tightly sealed container, away from light and moisture, at 2–8°C (refrigerated) to maintain stability. Store in a well-ventilated, cool, and dry place, separate from incompatible substances. Avoid exposure to heat, oxidizing agents, and sources of ignition. Proper labeling and secondary containment are recommended to prevent contamination and accidental release.
    Application of 5-Formyluracil

    Applications of 5-Formyluracil in Industrial Manufacturing

    5-Formyluracil serves as a functional intermediate in several advanced industrial manufacturing processes, particularly in sectors with stringent quality demands and regulatory oversight. The applications outlined below highlight real-world scenarios where this specialty chemical enables unique performance attributes and formulation advantages in downstream production.

    1. Nucleoside Pharmaceutical Synthesis

    5-Formyluracil plays a critical role in the targeted modification of pyrimidine bases for the production of nucleoside and nucleotide analogs. As a protected or functionalized uracil derivative, it enters the synthesis at key steps to enable the construction of therapeutic agents for antiviral and anticancer medications. Manufacturing operations routinely incorporate this intermediate during chemical transformations under controlled environments to ensure yield and purity meet regulatory requirements for active pharmaceutical ingredients (APIs).

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary) specifications for nucleoside APIs
    • European Pharmacopoeia (Ph. Eur.) quality monographs
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, US FDA)

    Typical usage ratio

    • 0.5–3.0 molar equivalents relative to core nucleoside starting material; the precise dosage depends on the degree of functionalization and the stepwise reaction sequence in multi-step synthesis.

    Downstream process integration

    • Dosed during selective formylation or condensation reactions, followed by isolation and further conversion into protected nucleoside intermediates or final actives.

    Final product types

    • Antiviral nucleoside drugs (e.g., anti-HIV, anti-hepatitis agents)
    • Cytostatic nucleotide analogs for cancer therapy
    • DNA/RNA synthesis building blocks for pharmaceutical research

    2. Biochemical Reagent Production

    5-Formyluracil is a valued reagent in the large-scale manufacture of biochemical assay kits and specialty oligonucleotide probes used in advanced life science laboratories. Its aldehyde function contributes to the chemical modification of DNA and RNA probes, permitting site-specific labeling or crosslinking for high-sensitivity diagnostics. Manufacturers must rigorously control formulation concentrations and reaction times to deliver products meeting analytical and clinical laboratory standards.

    Industry compliance standards

    • ISO 13485:2016 (Quality Management for Medical Devices and Diagnostics)
    • ISO 9001:2015 (Quality Management Systems for laboratories)
    • OECD Principles of Good Laboratory Practice (GLP)
    • CLSI (Clinical and Laboratory Standards Institute) guidelines for in vitro diagnostics

    Typical usage ratio

    • 0.1–1.2% by weight in oligonucleotide modification mixtures; adjusted in proportion to the number of labeling sites and probe design.

    Downstream process integration

    • Introduced during the post-synthetic modification step of oligonucleotides or nucleic acid probes; often treated with labeling or detection tags via reductive amination or hydrazine conjugation.

    Final product types

    • Fluorescently labeled DNA/RNA probes for molecular diagnostics
    • Enzyme-modified oligos for PCR and qPCR detection kits
    • High-specificity gene mutation assay kits

    3. Specialty Dye and Photoinitiator Synthesis

    As an intermediate, 5-Formyluracil participates in the preparation of specialty pyrimidine-derived dyes and photoinitiators, which are essential in high-value printing and imaging sectors. Its unique reactivity profile allows chemists to introduce specific structural motifs that impact light absorption and initiating properties. Formulators must optimize input ratios and maintain traceability throughout reaction monitoring to ensure batch-to-batch consistency aligned with end-user performance criteria.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • ISO 14001:2015 (Environmental Management in chemical manufacturing)
    • EN 71-3:2019 Safety of toys – migration of certain elements (for printing inks)
    • CQC (China Quality Certification) for industrial specialty chemicals

    Typical usage ratio

    • 1–8% by weight in initial dye or photoinitiator reaction formulations, with fine tuning based on desired chromophore density and photoinitiator efficiency.

    Downstream process integration

    • Charged during the heterocycle-functionalization stage, followed by condensation or alkylation to generate target dye structures or light-sensitive intermediates.

    Final product types

    • Photoresist components for circuit board imaging
    • UV-curable ink initiators
    • Fluorescent tracers and chromatographic markers

    4. Advanced Polymer and Material Modification

    The compound finds application in the surface modification and chemical functionalization of specialized polymers, allowing producers to embed aldehyde functions or reactive handles onto backbone structures. These modified polymers support use in biomedical devices, controlled release matrices, or as supports in solid-phase synthesis. Downstream manufacturers must validate process reproducibility, cross-reactivity, and long-term stability of the resulting composite materials.

    Industry compliance standards

    • ISO 10993-1:2020 (Biological evaluation of medical devices)
    • USP Class VI plastics certification for biomedical use
    • FDA 21 CFR 177.2600 (Indirect food additives: polymers)
    • ISO 14644 Cleanroom production guidelines (where required)

    Typical usage ratio

    • 0.2–2.5% by mass in polymer modification batches, depending on degree of surface functionalization and targeted polymer properties.

    Downstream process integration

    • Added via solution-phase or melt-phase blending during polymer extrusion or bead synthesis, immediately followed by crosslinking or covalent attachment with bioactive agents.

    Final product types

    • Biomedical device coatings with reactive aldehyde groups
    • Drug delivery matrix polymers
    • Solid-phase supports for automated synthesis platforms
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    Certification & Compliance
    More Introduction

    Introducing 5-Formyluracil: The Builder’s Pyrimidine for Modern Research and Industry

    5-Formyluracil stands out in our production schedule not just because of its chemical profile, but because laboratories, research teams, and even specialty syntheses keep turning to it when other analogs hit roadblocks. Our facility produces this compound at reliable scales, using streamlined crystallization that ensures product purity and reliability for demanding downstream tasks. The compound, visually distinct by its off-white crystalline look, carries CAS number 675-97-8 and serves as an important tool for multiple research sectors.

    Why 5-Formyluracil Draws Continued Attention in the Field

    Through years of working with uracil derivatives, we have observed the unique versatility of 5-Formyluracil as both a sensitive marker and a functional group carrier. Our internal tests on site show that this molecule’s aldehyde function at the 5-position allows chemists and biologists to introduce controlled modifications with much greater selectivity compared to plain uracil or its methyl- or hydroxymethyl- counterparts. This small structural shift gives it a much higher reactivity profile for conjugation reactions—something that synthetic chemists and nucleic acid chemistry labs value every week.

    During its development and scale-up in our synthesis labs, we noticed how clean the reaction profile could be when optimizing solvent composition and temperature. Such process control pays off for our customers who need not only a clean batch, but material that performs without sidetracks in HPLC assays, enzyme reactions, or as a reference standard.

    Model, Specifications, and Why Consistency Matters

    We manufacture 5-Formyluracil with a focus on reproducibility from batch to batch. Through our proprietary isolation steps, we routinely meet the target purity above 98% (HPLC), and we document moisture and trace metal content because downstream DNA work and diagnostic assay development depend on these quality parameters. Each batch passes full spectroscopic validation (NMR, MS), giving chemists the necessary confidence, especially in scale-sensitive or regulatory environments.

    A significant proportion of our partners work in medicinal and nucleic acid chemistry. For them, reliable results start with a material whose melting point, impurity profile, and particle characteristics don’t drift. Our model production approach prioritizes this need through in-line QC at each stage. As a result, our clients spend less time troubleshooting raw material issues and more time getting work done. We see this reflected in the feedback we receive from teams working on next-generation sequencing controls, chemical biology probes, and more.

    What Sets 5-Formyluracil Apart from Other Uracil Derivatives

    Uracil derivatives often seem interchangeable at first glance. Working as the actual manufacturer, we see nearly every variant run through our process lines—5-Methyluracil, 5-Hydroxymethyluracil, 5-Bromouracil, and of course, regular uracil. 5-Formyluracil offers specific benefits that stem directly from the presence of the reactive formyl group. This functional handle enables a series of reactions, especially for forming Schiff bases and linking with amines.

    Our partners in DNA damage studies request 5-Formyluracil because it serves as a key oxidative lesion and is more structurally relevant than the more widely known 8-oxo-guanine for pyrimidine studies. Our hands-on experience shows that synthesis involving 5-Formyluracil as a building block often leads to higher yield and specificity in bio-conjugation, compared to similar modifications at the 5-position. In diagnostic kit manufacturing, the formyl group presents almost uniquely for sensitive labeling without the synthetic complexity or background signal some other groups provoke.

    No two labs want exactly the same thing. Some groups need analytical reference material to quantify DNA modifications in clinical samples. Others value its role in probe construction, or as a pathway intermediate toward custom bases and nucleotides. From a manufacturing point, every downstream demand comes back to product reliability, ease of handling, and the way it stays stable under real lab conditions—refrigerated, freeze-dried, or ready for immediate coupling. Our team spends time re-evaluating formyl group retention across storage trials, solubility studies, and even transport simulations, because every misstep in these areas multiplies issues in sensitive nucleotide applications.

    Applications: From DNA Damage Research to Innovative Synthesis

    Our experience working side-by-side with research teams has shown that 5-Formyluracil underpins a surprising range of activity. Academic groups use it as a standard for mapping genomic DNA damage—an area gaining traction as research into oxidative stress and tumor biology grows. Synthetic chemistry labs value the formyl group’s reactivity for producing modified nucleoside phosphoramidites or as a stepping-stone toward biotinylated, fluorescent, or radiolabeled nucleotides. The compound behaves reliably in both organic and aqueous reactors due in large part to its crystal form and tight impurity control.

    During pilot studies with oligonucleotide synthesis partners, we have monitored how 5-Formyluracil modifications behave during solid-phase synthesis, as well as how the formyl group holds up after deprotection and purification. Our technical team also tracks its uptake in the rising field of aptamer research, where formyl-labeled libraries open doors to new forms of target recognition—especially for biosensor technology. These kinds of cooperative trials give our staff feedback loops that inform ongoing tweaks in manufacture and packaging.

    Beyond DNA sciences, we routinely see demand from chemical biology labs developing protein-nucleic acid crosslinkers, as well as medicinal chemistry groups exploring novel base-pair analogs for therapeutic design. Such projects use 5-Formyluracil in coupling reactions, enzyme assays, or direct incorporation into siRNA synthesis. These practical uses shape our internal production priorities and are the main reason we continue refining our process each season.

    Handling and Storage Insights from Long-Term Supply

    Unlike more labile pyrimidines, 5-Formyluracil handles storage well under inert atmosphere and low moisture. Our production managers follow these same guidelines in our own facilities, as a spike in moisture or oxygen can push unwanted side reactions, affecting the formyl group or ring stability. Each new drum or bottle leaves us with freshly checked loss on drying, and our packaging lines specifically select barrier materials to keep storage straightforward for end users.

    Clients often call about solubility. Based on our cumulative data, aqueous or buffered solutions perform best when prepared fresh, due to the aldehyde moiety’s mild reactivity. For longer-term stability in stock solutions, we have regularly found that freezing solutions after preparation extends usability in demanding applications. For solid material, simple desiccation and cold storage prevents the most common issues we’ve seen among early-stage researchers.

    Quality and Analytical Track Record

    We have invested years into both scale-up and quality control, building out an extended analytical capacity to cover each outgoing shipment. Each manufactured lot receives complete spectral traces, and staff record both process deviations and outcomes for ongoing process improvement. Out of hundreds of supplied kilograms, feedback pointing to unexpected impurities or physical artifacts remains well below industry averages. We attribute this mainly to origin control and continuous staff training on the unique parts of 5-Formyluracil synthesis.

    From our experience, researchers working in regulated sectors or publishing in critical journals cannot afford ambiguity about their starting materials. During audits, our clients rely on access to archived QC documentation, lot-specific impurity analysis, and retention samples for verification. We have seen a steady reduction in repeat inquiries and troubleshooting since moving to our current process configuration, which blends operator oversight with in-line analytical instrumentation.

    Current Challenges in Sourcing and What We’re Doing

    Supply of specialty pyrimidines often fluctuates since few producers dedicate a single unit solely to this class. We've watched disruptions in precursor streams drive up lead times, especially as demand for nucleic acid modifications intensifies across research sectors. We address this issue by maintaining redundant upstream sources and buffer stocks of core starting materials. This approach—relying on multiple vetted supply partners—means our production rarely pauses because of a bottleneck elsewhere.

    Since 5-Formyluracil synthesis relies on regioselective formylation, we've spent years developing new catalyst systems and purification steps that reduce side product formation at scale. R&D staff regularly re-examine the process using real-world feedback from our user community, leading to stepwise upgrades that keep both output and quality high. Each process change runs through a full validation cycle before release, so researchers receive the same expected results from each lot, even as process chemistry evolves.

    How Our Approach Differs from Intermediaries

    Many of our long-term clients communicate frustration with inconsistent quality, ambiguous documentation, or unclear traceability when working through dealers or resellers. Our direct engagement as a manufacturer minimizes information loss, improves accountability, and speeds up feedback resolution. By shipping directly from our own warehouse, every batch draws on fresh QC and known storage times; clients can trace every step from synthesis to shipment.

    Not all batches are perfect, and our philosophy—born out of daily lab work—accepts this reality. Still, being the actual source, we have the flexibility to adjust process parameters or packaging within weeks, not months. Collaboration with end users also allows us to develop special grades or custom pack sizes, drawing on our in-house analytical and applications teams. Instead of relaying messages between third parties, we see issues firsthand, which builds real-world trust over time.

    Regulatory and Safety Considerations from Our Manufacturing Team

    5-Formyluracil does not fall under most controlled substance frameworks, but research groups must use suitable lab safeguards and handle all pyrimidines with proper respect for their reactivity and biological activity. Based on over a decade shipping this compound worldwide, we support our customers with transport documentation, procurement certificates, and avenues for technical support when needed.

    Our on-site EHS managers update materials and training protocols as new data emerges. Teams review incident logs from our own process work each quarter, informing the handling and shipping advice we provide to clients. In some jurisdictions, importing nucleic acid building blocks requires additional documentation, which we support on request, based on our regulatory experience base.

    Looking Ahead: Opportunities and Continued Development

    The use landscape for 5-Formyluracil continues to expand. Novel sequencing methods incorporate formyl modifications to probe DNA repair pathways, and medicinal chemistry platforms take advantage of the unique reactivity for site-selective ligation. Synthetic biologists look to the compound as a bridge to even more exotic pyrimidine analogs and crosslinkable oligonucleotide libraries. In the last year alone, we have partnered with two new research centers exploring ambient-temperature ligation chemistry—requiring ever-tighter control of aldehyde retention and downstream coupling efficiency.

    From a manufacturer's perspective, the challenge comes down to two interconnected demands: maintaining batch-to-batch consistency, and keeping a direct line open to research teams for continual feedback. Our role centers on adapting the nuts and bolts of synthesis—fine-tuning catalysts, batch times, and packing methods—so the compound users receive remains fit for increasingly demanding protocols. Doing this well means we build on years of data, application stories, and ongoing communication.

    Final Thoughts from the Production Floor

    Producing 5-Formyluracil goes beyond managing reactors and lab notebooks. It means listening to project leaders, troubleshooting the last-mile challenges of reconstitution and storage, and sharing insight into what has worked across thousands of customer protocols. Everything we know about this compound grew from hands-on experience with clients and with the quirks of scale-up and troubleshooting.

    Researchers rely on our consistency not because of name recognition, but because over time we invested in process stability, traceable documentation, and a no-shortcuts culture in our facility. In practice, that equates to product arriving ready for experimentation, with all the key data in hand and staff able to address new technical questions.

    By focusing on what scientists and developers need most in their daily work—reproducible chemistry, complete records, and direct support—we see why the request list for 5-Formyluracil keeps growing. It remains an essential ingredient across molecular biology, chemical biology, diagnostics, and beyond, thanks to tight process control and an ongoing focus on researcher needs. Generation after generation of synthesis and application, we keep shaping both the molecule and its journey from production facility to laboratory bench.