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6-Amino-5-Bromo-1-Methyluracil Monohydrate

    • Product Name 6-Amino-5-Bromo-1-Methyluracil Monohydrate
    • Alias BRM
    • Einecs 630-484-7
    • 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

    805671

    Productname 6-Amino-5-Bromo-1-Methyluracil Monohydrate
    Casnumber 2998-71-4
    Molecularformula C5H7BrN4O2·H2O
    Molecularweight 253.07 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Slightly soluble in water
    Meltingpoint No data available (decomposes)
    Storagetemperature 2-8°C (refrigerated)
    Synonyms 1-Methyl-5-bromo-6-aminouracil monohydrate
    Iupacname 5-bromo-6-amino-1-methyl-2,4(1H,3H)-pyrimidinedione monohydrate

    As an accredited 6-Amino-5-Bromo-1-Methyluracil Monohydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25g amber glass bottle, sealed with a screw cap, and labeled with hazard and identification details.
    Shipping **Shipping Description:** 6-Amino-5-Bromo-1-Methyluracil Monohydrate is shipped in tightly sealed containers to protect from moisture and light. The packaging complies with chemical safety regulations and includes appropriate labeling and documentation for safe transportation. All shipments are handled by certified carriers, ensuring compliance with local and international chemical transport standards.
    Storage Store **6-Amino-5-Bromo-1-Methyluracil Monohydrate** in a tightly sealed container, protected from light and moisture. Keep at room temperature or as specified by the manufacturer, away from sources of heat and incompatible substances. Ensure the storage area is well-ventilated, dry, and appropriately labeled. Avoid inhalation, ingestion, and contact with skin or eyes when handling the compound.
    Application of 6-Amino-5-Bromo-1-Methyluracil Monohydrate

    Applications of 6-Amino-5-Bromo-1-Methyluracil Monohydrate in Industrial Manufacturing

    As a specialized manufacturer of 6-Amino-5-Bromo-1-Methyluracil Monohydrate, we supply this nucleobase analogue to downstream producers operating in tightly regulated pharmaceutical and biotechnology sectors. Below, we outline key industrial applications where our material supports advanced synthesis, providing critical function in targeted manufacturing environments.

    1. Antiviral Drug Intermediate Synthesis

    Producers of nucleoside analogue antivirals utilize this compound as a critical building block in the multi-step synthesis of modified uracil-based agents. Its specific bromine and amino functionalization enables controlled derivatization during the formation of pharmaceutical actives for treatments targeting viral DNA or RNA replication pathways. Regulatory and formulation requirements drive precise integration into the active pharmaceutical ingredient (API) core, ensuring batch traceability and impurity control throughout all process steps leading to sterile finished dosage forms.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, Ph. Eur., JP monograph alignment for nucleoside APIs
    • FDA and EMA guidelines for starting materials
    • ISO 9001:2015 certified quality management system

    Typical usage ratio

    • Applied at 1–3 molar equivalents relative to core nucleoside framework; specific equivalents adjusted based on downstream protection group strategy and yield optimization

    Downstream process integration

    • Introduced in the earliest nucleobase modification steps; participates in alkylation, amination, and condensation reactions prior to sugar attachment and subsequent API purification

    Final product types

    • Solid oral antiviral tablets and capsules (e.g., hepatitis B/C, herpesvirus therapies)
    • Powder or solution for injection vials

    2. Cytotoxic Anticancer Agent Synthesis

    Manufacturers of specialty chemotherapeutic agents incorporate this molecule during the construction of uracil-derived cytostatic compounds. Its distinct halogen and amine substitution supports targeted functionalization for the production of pyrimidine analogues designed to disrupt tumor cell nucleic acid synthesis. The raw material directly feeds into multi-stage organic synthesis routes under strict cleanroom and traceability oversight, supporting regulatory submissions both for generic and proprietary cytostatic APIs.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP)
    • 44th or current USP-NF for anticancer APIs
    • EudraLex Volume 4—EU Guidelines for GMP
    • REACH registration for intermediate use

    Typical usage ratio

    • Ranges from 0.8–1.2 parts per part of final API formed, depending on modification path and scalability assessment; higher loadings required for multi-substituted product lines

    Downstream process integration

    • Fed into early-stage nucleobase assembly, subjected to sequential halogenation and substitution, followed by purification prior to coupling with cytostatic vectors

    Final product types

    • Injectable cytotoxic formulations (e.g., oncology IV drips)
    • Oral anticancer drugs

    3. Diagnostic Bioprobe Manufacture

    Producers of nucleic acid-based diagnostic reagents select this compound as a modified base for oligonucleotide synthesis, serving as a precursor for site-specific labeling or as an artificial base in probe design. The monohydrate form integrates directly into DNA/RNA synthesizer feedstocks for use in molecular hybridization and real-time PCR kits, providing functionality critical to enhanced binding specificity or signal generation. Supplier-batch documentation and high-purity profiles support regulatory and commercial diagnostics workflows.

    Industry compliance standards

    • ISO 13485 for in vitro diagnostic (IVD) medical devices
    • FDA 21 CFR Part 820 (Quality System Regulation)
    • CLSI requirements for probe chemistry
    • CE/IVD marking for European market

    Typical usage ratio

    • Introduced at 1:20 to 1:50 molar insertion with standard nucleotides; ratio refined based on intended probe length and application sensitivity

    Downstream process integration

    • Incorporated in phosphoramidite synthesis cycles; post-synthetically modified or tagged for hybridization or signal generation in finished oligonucleotides

    Final product types

    • PCR/qPCR kits with specialty probes
    • Fluorescent or chemiluminescent oligonucleotide arrays
    • Custom gene detection cartridges

    4. Research-Grade Nucleoside Analogue Libraries

    Academic and industrial research facilities assemble nucleoside analogue libraries for drug discovery and biochemical analysis by starting with our material. Its unique amino-bromo-methyl functionalization allows scientists to synthesize modified bases for studies in enzyme inhibition, nucleic acid interaction, and high-throughput screening. We support this segment by ensuring precise documentation, batch consistency, and the ability to trace all critical process parameters for RC and GLP studies, including certificate of analysis aligned with research purity standards.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for research reagents
    • Analytical grade specifications (ACS Reagent Grade, Ph. Eur. research)
    • Material Safety Data Sheet (MSDS) according to GHS and REACH Annex II
    • Ethical review and biosafety protocols for chemical libraries

    Typical usage ratio

    • Applied at 0.5–2 mmol per synthesis batch within combinatorial library production; volume adjusted by target compound diversity and screening requirements

    Downstream process integration

    • Employed in first-round solution-phase or solid-phase base modifications; proceeds through iterative combinatorial reactions for lead compound optimization

    Final product types

    • High-diversity nucleoside analogue libraries
    • Reference standards for enzyme assay development
    • Screening sets for pharmaceutical and academic research
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    Certification & Compliance
    More Introduction

    6-Amino-5-Bromo-1-Methyluracil Monohydrate: An Insider’s Perspective from the Lab Floor

    Understanding What Sets This Compound Apart

    At our plant, we handle a wide array of pyrimidine derivatives, each with its challenges during synthesis and each showing different faces in actual use. 6-Amino-5-Bromo-1-Methyluracil Monohydrate stands out in this family for several reasons. People who see chemicals as just a string of letters and numbers often miss the story behind each product. But in our experience, small changes in a molecule like adding a bromine or methyl group completely shift how a compound performs in the real world.

    Product Profile: What We See in the Drum

    You can spot 6-Amino-5-Bromo-1-Methyluracil Monohydrate by its pale color and consistent particle structure. When preparing a batch, our team pays close attention to the crystallization stage. Getting the right particle distribution directly impacts both solubility and how easy it is to work with further down the line, especially if the compound is moving into the pharmaceutical sector or advanced materials development.

    The structure, C5H5BrN4O2·H2O, means it brings together both hydrophobic and hydrophilic qualities—somewhat unusual for a nucleobase analog. That presents both challenges and opportunities. For our in-house analytical chemists, verification is more than a checkbox; the subtle hydration state calls for careful drying and environmental control all the way from synthesis through to packaging.

    Working With Water: The Monohydrate Influence

    Monohydrate forms like this one behave differently from their anhydrous counterparts. Water molecules integrated within the lattice improve the stability of the product during storage. Over years in manufacturing, we’ve seen monohydrate products hold up better in conditions where humidity would cause caking or degradation in similar, drier formulas. We see fewer returns and complaints related to flow properties or shelf-life as a result.

    This particular hydration also improves dissolution rates. In process development, our pharmaceutical partners have found the monohydrate enters solution more smoothly, saving time and reducing the need for additional solvents or heat. That gains momentum in formulation—especially when you’re manufacturing at scale. The difference appears subtle on paper, but anyone who’s had a major batch clog up a reactor during addition knows the cost and safety risks of overlooked details.

    Applications in Synthesis and Beyond

    Researchers approach us for 6-Amino-5-Bromo-1-Methyluracil Monohydrate as an intermediate for more complex heterocyclic synthesis. The preference for this version comes down to consistent availability of the amino and bromine functionalities. Bromine at the 5-position makes the compound a convenient launching point for palladium-catalyzed coupling or functionalization, letting chemists build purines, modified nucleobases, or advanced materials more directly.

    From experience, we have seen our product migrate from academic benches to pilot manufacturing with surprisingly little drama. Other analogs sometimes bring unexpected lumps or present purification headaches, but the monohydrate's behavior under scale-up conditions gets high marks from both their technical and procurement teams.

    Comparisons with Other Pyrimidine Derivatives

    Years of production allow for a unique view on the quirks of similar chemicals. Compared to 5-Bromo-uracil derivatives without the amino or methyl group, the 6-Amino-5-Bromo-1-Methyluracil Monohydrate displays markedly better batch-to-batch reproducibility. The amino group at position six gives access to amidation and peptide-coupling approaches, important for some rare APIs and newer materials.

    We often get asked why not simply use 5-Bromo-1-Methyluracil without the amino addition. The answer lies in the extra layer of functionality, as the amino group creates new binding opportunities during further transformations. The hydrophilic edge lent by the monohydrate means it sits better in water-heavy systems, and our partners have been able to avoid introducing more aggressive organic solvents, which are subject to regulatory limitations.

    Manufacturing Insights: From Reaction to Packaging

    Running a plant that handles products like this means walking a tightrope between product purity and operational efficiency. Brominated intermediates need careful environmental and waste controls. We've dedicated equipment to ensure that our solution doesn't contaminate other product lines, with in-line sensors programmed to catch any deviation before it becomes a problem.

    Maintaining the monohydrate form of this uracil derivative proved tricky at first. Early batches occasionally lost their water under summer heat or absorbed excess moisture during long transit periods. After some tough lessons, we retooled our storage areas for climate control and switched up our drying protocols. Today, stable hydration is no longer a guessing game.

    Granularity also factors in because our customers run everything from 5 g research vials to 100 kg blenders. Consistency gives them what they need for reliable results, not just a spec sheet with numbers designed to impress on paper. We now work closely with several formulation teams, blending QA feedback directly into process tweaks.

    Quality Control: Beyond Compliance

    Quality sits at the core of manufacturing, not just for keeping certificates up to date, but to guard real progress in downstream research. HPLC and NMR are routine, but we’ve added live in-process assessments any time a batch veers out of expected range. Every operator gets trained in both equipment handling and the actual reasoning behind the steps—people learn not just to follow instructions, but to recognize oddities a computer will miss.

    One downside of close engagement: when a batch fails, you hear about it straight from people we’ve worked with for years. Delays cost companies, but they also slow real scientific discoveries. As a team on the manufacturing side, we’re challenged every day to get things right the first time. Trust doesn’t come from meeting a formal spec; it’s built over years by shipping drums of a clean, stable, and thoroughly checked product. For this compound, we never shortchange time in QA or sign off without double checks—even if it means slower turnarounds sometimes.

    Safety, Handling, and the Supplier’s Role

    Most intermediates are less hazardous than finished APIs or technical-grade solvents, but brominated uracils still need careful handling. We’ve trained our shipping team to recognize proper labeling, and we only use containers that block UV and moisture. From pharma startups to global chemical majors, feedback on packaging has led to minor but telling adjustments—like reinforced lids and re-sealable internal liners to maintain hydration during long voyages.

    Certain users requested more data on long-term storage. In response, our R&D crew spent months tracking product stability across temperature and humidity ranges. That data let us refine our handling advice, but it also convinced several partners to trust monohydrate material over powders that frequently get swapped for dryer analogs in similar work.

    Environmental Treatments and Responsible Manufacturing

    As scrutiny over brominated organics has grown, we set up in-house scrubbers and recovery tanks to capture off-gassing or trace leaks. Waste is tracked batch by batch, with full accountability at every step. That investment paid off: we weathered local and international audits without trouble, avoiding shutdowns that hurt both us and our partners. Careful sourcing of raw materials is essential, avoiding brokers with unknown origins or questionable handling records.

    We sometimes get asked about greener synthesis methods. Though the classic bromination steps remain robust, we’ve explored alternatives using photocatalysis or milder reagents. So far, no replacement has matched current purity or yield, but we keep running pilots and monitor advances in the academic literature. Our equipment team regularly visits conferences and suppliers, scouting options that might eventually slot in without disrupting a reliable supply chain.

    Feedback Loops: Real Benefits from Real Users

    Some improvements only start when partners encounter snags in their workflow. If a powder is clumping or granulation turns erratic, we don’t blame the customer for handling error. Instead, field teams visit or connect by call, gathering feedback on mixing, dissolution profiles, and how the monohydrate form compares to other options. That knowledge cycles straight to QA, where specs get tightened or relaxation points are debated and, where change benefits the majority, swiftly revised.

    In an industry where changes can ripple widely, we keep records of feedback, failed batches, and successful improvisations. Over the years, these conversations have directly shaped our current process for this uracil monohydrate—from drying times and particle cut points to drum lining choices.

    Why Choose 6-Amino-5-Bromo-1-Methyluracil Monohydrate: A Manufacturer’s Take

    Some products earn their keep by being replaceable; they’re cheap, abundant, and interchangeable. With this compound, more buyers report that substitutes cause more trouble—ranging from solubility issues to unwanted impurities—not business as usual when you must run exacting research or regulatory work.

    Attempts to switch in cheaper, unhydrated or less pure versions have led to more downtime, failed target synthesis, and even lost funding in development jobs. The monohydrate, by contrast, presents reproducible physical form, good stability, and offers enough reactivity to suit both routine and innovative syntheses. As a result, we see demand not just from legacy pharma customers, but also from new players looking for dependable starting points in custom synthesis.

    Customer Partnerships: Building Knowledge, Sharing Improvements

    The process doesn’t stop after a shipment leaves our facility. Technical support teams field calls about scale-up, batch records, or unexpected solubility behavior. That information helps us trace root causes and offers customers not just a solution, but an education. We run workshops for customers new to brominated pyrimidines, teaching best handling practices, storage tips, and the practical difference between monohydrate and anhydrous forms.

    On a few occasions, we’ve joined early-phase process teams in a client’s lab to troubleshoot reactors or advise on product transition. These collaborations spark small but meaningful process tweaks—changing addition temperatures, adjusting agitation speeds, or upgrading filtration steps—to fit the unique character of 6-Amino-5-Bromo-1-Methyluracil Monohydrate.

    Continuous Improvement: Listening, Learning, Adapting

    Markets and expectations change quickly, but the underlying chemistry remains steady. We maintain a focus on thorough, open communication, and transparency with customers, always looking for the next leap in safety, process reliability, and product quality. That means investing in analytical capabilities, recruiting people who care about details, and never assuming that current results set a ceiling for future improvement.

    On the manufacturing floor, quality is about far more than passing an audit. It’s about knowing that what leaves our site backs the work of scientists, process engineers, and innovators along the chain. 6-Amino-5-Bromo-1-Methyluracil Monohydrate hasn’t carved out its place by luck. Reliable hydration, clean production, and robust feedback have let us support a broad range of R&D and commercial goals. We don’t claim perfection, but we do offer openness, a willingness to adapt, and a demonstrated record of learning from both successes and setbacks to keep raising the standard for this important class of compounds.