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6-Amino-1-Methyluracil

    • Product Name 6-Amino-1-Methyluracil
    • Alias 6-AMU
    • Einecs 205-424-4
    • 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

    148434

    Chemical Name 6-Amino-1-Methyluracil
    Molecular Formula C5H7N3O2
    Molecular Weight 141.13 g/mol
    Cas Number 1123-34-4
    Appearance White to off-white crystalline powder
    Melting Point 303-305 °C
    Solubility In Water Slightly soluble
    Pubchem Cid 98117
    Iupac Name 6-amino-1-methylpyrimidine-2,4(1H,3H)-dione

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

    Packing & Storage
    Packing The 100g 6-Amino-1-Methyluracil is securely packaged in a sealed amber glass bottle with a clearly labeled, tamper-evident cap.
    Shipping 6-Amino-1-Methyluracil is shipped in tightly sealed containers to prevent contamination and moisture absorption. The packaging complies with chemical safety regulations, using cushioning materials for protection during transit. It is transported via appropriate carriers, clearly labeled with hazard information, and the shipment is accompanied by a safety data sheet (SDS) for handling guidance.
    Storage 6-Amino-1-Methyluracil should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Ensure compatibility with surrounding chemicals and avoid sources of ignition. Label the container clearly, and restrict access to trained personnel to ensure safe handling and storage.
    Application of 6-Amino-1-Methyluracil

    Applications of 6-Amino-1-Methyluracil in Industrial Manufacturing

    6-Amino-1-Methyluracil serves as a highly specialized raw material in the synthesis of active pharmaceutical ingredients and fine chemicals, recognized for its consistent performance in complex, regulated production environments. As an original manufacturer, we supply this material to downstream sectors that demand strict quality, compliance, and manufacturing precision for advanced chemical and life science products.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers rely on 6-Amino-1-Methyluracil primarily as a heterocyclic building block during the multi-step synthesis of pyrimidine-based drug molecules. It introduces an amino group and a methyl-substituted uracil framework in targeted reactions, contributing to the pharmacophore of several antiviral, anticancer, and cardiovascular therapeutics. Our material supports controlled nucleophilic substitution and ring transformation under GMP-compliant production lines, ensuring batch reproducibility for bulk API preparation.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • Ph. Eur., USP monographs for API synthetic processes
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 10–25% w/w of stepwise intermediate mass; adjusted based on yield optimization and residual impurity control during multi-stage synthesis

    Downstream process integration

    • Charged in the initial condensation or ring opening stage, often under temperature-controlled environments, enabling direct integration into existing synthetic reaction trains

    Final product types

    • Antiviral APIs (e.g., nucleoside analogs)
    • Anticancer compounds
    • Active ingredient intermediates for cardiovascular medicines
    • Pharmaceutical research compounds

    2. Veterinary Drug Synthesis

    In the veterinary pharmaceutical sector, 6-Amino-1-Methyluracil functions as a nucleobase precursor for the formulation of small molecule veterinary medicines, including agents targeting livestock viral infections and metabolic disorders. Downstream processors implement this material for route-specific analog synthesis, supporting compliance with animal health and feed additive safety standards during batch processing for veterinary medicines.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) for Veterinary Drugs (Chinese GMP for Veterinary Drugs)
    • VICH GL20 (Stability Testing for New Veterinary Drug Substances)
    • European Pharmacopeia monographs for veterinary actives
    • ISO 17025 Laboratory Quality Assurance

    Typical usage ratio

    • 5–18% w/w in active ingredient precursor blend; determined by desired final conversion rate and residual solvent limits post-synthesis

    Downstream process integration

    • Added during the heterocycle assembly or selective methylation phase to produce veterinary pharmaceutical bases before formulation and granulation

    Final product types

    • Livestock antiviral agents
    • Small molecule veterinary pharmaceuticals for primary care
    • Diagnostic reagents for veterinary use
    • Animal feed medical additives

    3. Pharmaceutical Impurity Reference and Analytical Standards

    Analytical chemistry and regulatory laboratories use 6-Amino-1-Methyluracil as a certified impurity reference for the identification and quantitation of process impurities, related substances, and degradation products in finished drug formulations. It acts as a benchmarking standard for validating HPLC, LC-MS, and GC-MS methods, ensuring compliance with global impurity profiling regulations and supporting reliable release testing workflows for pharmaceutical quality control.

    Industry compliance standards

    • ICH Q3A & Q3B (Impurities in New Drug Substances/Products)
    • USP General Chapter <1225> Validation of Compendial Methods
    • Ph. Eur. 5.10 Control of Impurities
    • ISO/IEC 17025:2017 Lab Accreditation

    Typical usage ratio

    • 0.01–0.10% as a spike-in or dilution control in calibrator or reference mixtures; tailored to instrument detection limits and target assay quantitation

    Downstream process integration

    • Used in QC labs as part of certified reference material preparation or in analytical sample panels accompanying pharmaceutical batch release testing

    Final product types

    • Certified analytical reference standards
    • Pharmaceutical impurity marker sets
    • Calibration mixtures for regulated testing laboratories
    • Product registration submission dossiers

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Producers in the dye and pigment sector introduce 6-Amino-1-Methyluracil as a tailor-made intermediate when developing specialty pyrimidine-based chromophores for textile, inkjet, or technical pigment applications. The amino and methyl substituents support subsequent diazotization or condensation reactions, unlocking new chromophore design routes while meeting sector-specific environmental safety and purity standards for end-use colorants.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006) for chemical safety and registration
    • OEKO-TEX Standard 100 for textile-chemical safety
    • ISO 9001:2015 Quality Management Systems for dye and pigment production
    • EN 71-3:2019 (Safety of Toys – migration of certain elements) for pigment user sectors

    Typical usage ratio

    • 12–30% of theoretical molecular input for downstream chromophore assembly; adjusted according to color density targets and byproduct formation rate

    Downstream process integration

    • Introduced during the chromophore core formation or functional group modification phase, frequently as part of high-purity reaction controls for specialized pigment synthesis

    Final product types

    • Technical grade azo and anthraquinone dyes
    • Specialty inks for digital printing
    • Pyrimidine-based fluorescent pigments
    • Color additives for plastics and rubber applications
    Free Quote

    Competitive 6-Amino-1-Methyluracil 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.

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    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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    Certification & Compliance
    More Introduction

    6-Amino-1-Methyluracil: Reliable Chemistry for Evolving Needs

    Understanding What Sets 6-Amino-1-Methyluracil Apart

    Decades in chemical production teach you a lot about molecules. Every batch starts with a story from the shop floor: the hum of reactors, the scent of reaction mass, beads of condensation on steel. 6-Amino-1-Methyluracil stands out in that environment as an old colleague—dependable, familiar, versatile, and effective in both research and manufacturing pipelines. Born out of barbituric acid chemistry, this compound occupies a unique spot in nucleic acid analog synthesis, pyrimidine chemistry, and certain pharmaceutical formulations. Our production uses a refined route, steering through multiple filtration and purification steps to keep impurity profiles consistent and predictable. People ask about synthetic shortcuts or new “green” approaches, but harsh truth sits in the reactivity and heat-sensitivity of its precursor intermediates. Precision and patience trump innovation when batch consistency matters—no side reactions, no color formation, no off-smells.

    From the synthesis line, batches of 6-Amino-1-Methyluracil step into their own in crystallization tanks. White, fine-powdered needles, not a whiff of odd odor—this speaks to a solid process and fresh material. Analytical staff confirm purity via HPLC, matched against known spectra. Moisture content stays sane, because trace water triggers clumping and degradation. Our quality crew spends hours dialing in the dry room conditions—45% humidity, strict temperature windows, no shortcuts. Every kilogram gets inspected for uniformity and filtered through a sieve mill, a physical check our team swears by. Years ago a run went slightly off, losing downstream solubility, and not one of us has forgotten those lessons.

    Some chemists chase after uracil analogs for research, building blocks, or pharmaceuticals. Methyl substitutions at the N1 position alter properties: change in hydrogen bonding, improved lipophilicity, and a fresh set of interactions inside biological systems. The addition of an amino group at position 6 turns this uracil family member into something with both donor and acceptor sites, a little more reactive, slightly more polar. The result—6-Amino-1-Methyluracil—slots itself into research as an intermediate, but pulls its weight as a reference material. Biochemists often comment on its clear spectra and easy derivatization. Unlike unsubstituted uracils, the 6-amino moiety opens doors for further functionalization or ring-cleavage reactions, enabling access to a broader scaffold library.

    From Making to Using: The Story of an Ingredient

    Inside our plant, making 6-Amino-1-Methyluracil demands tough attention to time, reagent quality, and technical detail. Recrystallization, purification, and careful drying define the downstream process. Our reactors tire out before the staff, but every engineer here knows: an overcooked batch means a wasted day and unreliable yield. Each process tweak comes from live experience—not from a textbook—and most operators build intuition batch after batch, feeling for a certain viscosity and learning to recognize a “clean” batch visually. We hand over this product to formulators and R&D chemists who appreciate that attention to detail: no sticking, no caking, no lingering moisture. Packaging counts too, as sensitive pyrimidines require resistant liners and tight packing. We’ve tested everything from double-layer bags to foil-sealed tubs.

    Formulators come calling with questions about stability, solubility, and handling. 6-Amino-1-Methyluracil dissolves somewhat better in water than straight uracil, and the methyl group adds just a touch of organosolubility. Hydrogen bonding gives it a predictable, low-odor profile—less “fishy” than related aminopyrimidines. In complex systems, that stability translates to longer shelf-life and less decomposition, saving time and reducing costs on the customer end. QC labs get steady melting points near 316–318°C and consistent NMR spectra, batch after batch. Analysts note that the compound resists photolytic breakdown, and shelf tests under both ambient and low-light conditions support a two-year storage window in appropriate containers.

    What’s in a Specification: Beyond the Data Sheet

    Lots of people treat data sheets as gospel, but in manufacturing, real specifications stem from the needs of downstream processes. We’ve worked with researchers who want critical impurities below 0.05%, so we calibrate purification accordingly. Chemistry for nucleoside analogs cares less about trace sodium, more about organic carryover. In our process, that means checking for condensation byproducts, urea traces, and incomplete methylation. These checks grew from batches in the mid-2000s where rare off-colors signaled unseen impurities—no substitute for direct vigilance.

    Contrast 6-Amino-1-Methyluracil with the parent 6-Aminouracil or simple uracil: the methylation at position 1 brings a difference in reactivity. Because the methyl group occupies a key nitrogen site, it blocks hydrogen bonding, suppresses certain side reactions, and opens up alternative mechanisms. For synthetic chemists chasing rare analogs or prodrugs, methylation removes unwanted reactivity, streamlining downstream transformations. The extra methyl atom also influences solubility, giving a slightly better fit for organic solvent systems and certain formulation needs. Compared to 5-methyl or 5,6-dimethyl analogs, our product avoids steric congestion that frustrates some substitution chemistry, so chemists find it easier to append substituents or craft new heterocycles.

    We’ve helped customers troubleshoot stubborn re-crystallizations and have supplied custom micronized lots, since particle size influences suspension stability. High surface area, fine mesh grades work much better in some microfluidic and coating processes. In pharma and diagnostics, our tight batch reproducibility pays back in regulatory submissions, where every variance can cost months.

    Supporting Scientists and Formulators: Because Consistency Builds Trust

    Every customer who returns with a success story reminds us what manufacturing is really about: reliability. One research team once ran out mid-campaign and called for an urgent resupply. We fired up the smaller reactor, ran overnight, and shipped the next evening. That experience shapes how we think about planning and inventory. We hold safety stocks bigger than most competitors in the region for this very reason—no academic or commercial project deserves a hold because of supply chain delays. Every year, supply chain interruptions hit someone, but our plant crews know that backup capacity and trained staff are the best insurance against the unexpected. Box by box, ton by ton, we’ve seen projects ranging from oncology research to agricultural formulations draw on our batches for reproducible performance.

    Our own processing history also informs outreach. We spend time translating lab-scale tricks into bulletproof plant-scale steps, which cuts down on troubleshooting for customers. Transparent technical support—real chemists answering questions, not call center scripts—keeps relationships alive. Someone calls about pH drift in a reaction, another about borderline melting behavior—the answers come not from manuals but from that muscle memory you only get from years in a plant.

    Knowledge from Experience: Handling, Storage, and Future Directions

    Handling 6-Amino-1-Methyluracil presents fewer headaches than many, but no chemical forgives neglect. Fine powders react to static and poor air flows, so our team learned early to standardize grounding and local extraction. Twice we saw minor dust issues trigger unnecessary alarms. We run a tight ship—sealed containers, desiccant packs, clear labeling, and robust MSDS training. We’ve learned to avoid storing the material near acids or oxidizers; keeping batches cool, dry, and protected from light ensures longevity. One batch, stored poorly, clumped and degraded well before its shelf life. Failures like that pushed us to invest in high-grade warehouse environments with filtered air and climate controls.

    Some groups ask about long-term environmental impact and sustainability. Over years, we’ve swapped out harsher reagents for milder options where possible. Waste management improved after partnering with certified incinerators and recyclers. We log and monitor our effluent—ammonia, organics, and trace byproducts—down to the part-per-million. Our local regulatory office visits every other year and inspects everything: logbooks, waste tanks, and air scrubbers. The last audit noted no detectable stack emissions and praised our closed-loop solvent recycling features. Getting there took years, training, and investment, but it gives our customers—especially multinationals—confidence that our material supports both their ethics and regulatory due diligence.

    Looking ahead, continuous improvement remains the mindset in our plant. Few molecules offer 6-Amino-1-Methyluracil’s balance of synthetic tractability and versatility, but customers keep stretching its uses into enzyme substrates, detection kits, and new prodrug scaffolds. Each new application teaches us more about required specifications, purity needs, and processing hacks. We field requests for lower residual solvent grades, non-GMO sourcing, and even isotope-labeled versions for mechanistic work. Sometimes, suggestions from a single customer trigger internal process reviews and improvements.

    6-Amino-1-Methyluracil in Context: Demand, Applications, and the Shifting Market

    Global demand cycles have thrown us curveballs throughout the past two decades. During biotech booms, our inventories pour into startup labs; during regulatory slowdowns, inquiries dry up for a while. Pharmaceutical interest remains strongest, where 6-Amino-1-Methyluracil appears in active studies on antitumor and antiviral compounds. Intriguingly, certain agricultural R&D projects use our compound in mutation breeding programs and metabolic pathway clarifications, since the analogue interferes selectively in cellular pathways. We’ve signed confidential supplier agreements for customers pushing into personalized medicine, biosensor development, and textile dyes—each with unique requirements for purity, handling, or analytical documentation.

    As a manufacturer, keeping up with governing bodies worldwide adds to our workload. Stringent declarations on residual solvents, trace heavy metals, and allergen status originated in the EU, but North American and Asian regulators aren’t far behind. GMP and ISO certifications matter for customers upstream of human trial submissions. We maintain dossiers detailing every process change and batch history, so a customer up against a regulatory query gets detailed support. When regulators shift requirements on permissible impurities or handling precautions, our adjustments work their way through SOPs, batch records, and plant practices—real costs, but the industry has no patience for shortcuts or dropped standards.

    A common thread among successful applications emerges: every user benefits from reproducibility. Product evaluation often becomes clearer at scale; what succeeds in a microgram pilot sometimes stumbles at multi-kilogram production. We’ve sat with pharma partners untangling a scaleup issue caused by something as subtle as changes in the water used for crystallization. No catalogue or external consultant captures those little process gremlins. Internal knowledge, logged observations, and plain experience build the best defense.

    Why Differences Matter: A Manufacturer’s View on Competing Chemistries

    Not all 6-Amino-1-Methyluracil products act alike. Some producers push for high-throughput at the expense of through washing and fine drying. Others focus on niche grades for specific synthetic goals. Our own methodology anchors on validated, mid-scale production that balances thoroughness with flexibility. The smallest variations in precursor source, methylation technique, or ambient humidity during drying can shift performance. We hate hearing about inhomogeneous performance between lots or vendors, which is why every outgoing batch wears the same analytical fingerprint: tight melting range, HPLC trace without creeping baselines, and mass spec confirmation of mother ion. This trust takes seasons to build and minutes to lose. We’ve talked to buyers burned by inconsistent quality from elsewhere, and every time, root cause traces back to corner-cutting during scaleup or missed cleaning cycles.

    Market competition drives technical improvements, but it also breeds confusion in technical claims. We’ve seen datasheets tout “enhanced solubility” without disclosing tradeoffs in byproduct profiles or altered shelf life. Some products shipped under the same label turn sticky, clump on opening, or fail final purity tests in customer labs. Our sales team never promises virtues our QC labs can’t guarantee. We put technical sheets behind every shipment, showing actual test data batch-by-batch, and invite audits on short notice. Experienced chemists, whether in small startups or industrial giants, notice those fine differences. In high-value applications, a ten-cent-per-gram saving on a suspect lot quickly evaporates if it costs an unplanned halt or regulatory question.

    In the end, the biggest difference between 6-Amino-1-Methyluracil suppliers often comes down to two things: process integrity and customer collaboration. Any plant can run a line, mill a powder, or slap a label on a drum, but it’s the years spent refining parameters, training staff, and listening to user feedback that sets high-performing product apart. No process stays perfect forever. We monitor, adjust, and test new tweaks, always holding ourselves to a higher standard than the strictest inspector who ever walked our floor.

    Serving Diverse Industries While Staying True to Craft

    Variety in use keeps us honest. From research chemistry, to scaleup for fine chemical suppliers, to the regulated worlds of diagnostics and pharmaceuticals, each sector values 6-Amino-1-Methyluracil for a slightly different reason. Synthetic chemists love the ease of functionalization, and analytical teams appreciate transparent documentation for every delivery. Plant operators on a pilot line look for particle-size options, consistent flows, and predictable dissolution. On every order, our operations team matches those needs without losing sight of upstream integrity—starting material traceability, in-process tracking, and finished goods checks meet the highest bar we can set. Our policy discourages dropshipping, re-labeling, or blending; what leaves our gates carries our name and our commitment.

    We also see shifting trends: sustainable chemistry, more robust documentation, and inquiries from emerging fields. Biotech customers want certified non-animal sourcing; green chemistry initiatives push us to trim waste and energy. We listen because long-term growth lies in anticipating those demands and meeting them before standards force the issue. Constructing better tracking systems, improving waste recovery, and investing in cleaner energy sources carry both reputational and operational benefits. No batch is anonymous: if a customer finds an oddity, response time and traceability mean fewer headaches and faster answers for all involved.

    Conclusion: A Product Shaped by Experience, Commitment, and Practical Chemistry

    Making and supplying 6-Amino-1-Methyluracil involves more than mixing reagents or following a recipe. Each kilo packs in accumulated knowledge—problem-solving under pressure, learning from process deviations, teamwork in addressing customer needs. We treat every challenge as a chance to improve, from small tweaks in crystallization to big steps in waste reduction. The stories that matter come not from lab benches or datasheets, but from teams who trust their suppliers and suppliers who see themselves not as mere makers of product, but as partners in innovation. Our 6-Amino-1-Methyluracil stands on the foundation of decades of manufacturing integrity, chemistry know-how, and transparent collaboration across industries. Any new application or user becomes part of that ongoing story, and each batch shipped carries a piece of that shared journey towards better science.