4(3H)-pyrimidinone, 6-amino-2-mercapto-

    • Product Name: 4(3H)-pyrimidinone, 6-amino-2-mercapto-
    • Chemical Name (IUPAC): 6-amino-2-sulfanylidene-3,4-dihydropyrimidin-4-one
    • CAS No.: 14191-95-8
    • Chemical Formula: C4H5N3OS
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    341890

    Iupac Name 6-amino-2-mercapto-3H-pyrimidin-4-one
    Molecular Formula C4H5N3OS
    Molecular Weight 143.17 g/mol
    Cas Number 13410-45-2
    Appearance White to off-white crystalline powder
    Melting Point Above 300°C (decomposes)
    Solubility In Water Slightly soluble
    Smiles C1=C(NC(=O)NC1=S)N
    Inchi 1S/C4H5N3OS/c5-2-1-6-4(9)7-3(2)8/h1H,(H3,5,6,7,8,9)
    Pubchem Cid 51302

    As an accredited 4(3H)-pyrimidinone, 6-amino-2-mercapto- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle, tightly sealed, labeled with chemical name “6-amino-2-mercapto-4(3H)-pyrimidinone,” hazard symbols, and lot number.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 4(3H)-pyrimidinone, 6-amino-2-mercapto- involves secure, bulk chemical packaging with safety labeling and documentation.
    Shipping 4(3H)-Pyrimidinone, 6-amino-2-mercapto- is typically shipped in tightly sealed containers, protected from moisture and light. It should be packed according to standard regulations for chemicals, with appropriate hazard labeling. Transportation requires documentation of its classification and handling precautions to ensure safe and compliant delivery.
    Storage 4(3H)-Pyrimidinone, 6-amino-2-mercapto- should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it at room temperature in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Label storage clearly, and avoid exposure to excessive heat or humidity to ensure stability and prevent degradation.
    Shelf Life The shelf life of 4(3H)-pyrimidinone, 6-amino-2-mercapto- is typically 2-3 years when stored in a cool, dry, sealed container.
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    Certification & Compliance
    More Introduction

    Introducing 4(3H)-Pyrimidinone, 6-Amino-2-Mercapto-: Direct Insights from the Manufacturer

    Our Perspective on 4(3H)-Pyrimidinone, 6-Amino-2-Mercapto-

    On the factory floor, the story of every batch of 4(3H)-pyrimidinone, 6-amino-2-mercapto- starts with raw materials and steady hands. Each reaction, each filtration step, and every careful drying stage unfolds inside reactors we've optimized over years of work. This pyrimidine derivative lives in a unique niche in research and production settings worldwide. Unlike more basic heterocyclic compounds, it brings a combination of reactive sites and stability that makes it a standout for chemists seeking both performance and predictability in their syntheses.

    Understanding Its Composition and Model

    This compound, often referred to as 6-amino-2-mercapto-4(3H)-pyrimidinone, is a highly functionalized heterocycle. We know it by its molecular structure: a pyrimidinone ring with both amino and mercapto groups. Each production run, whether in gram or kilogram scale, receives the same attention: moisture level checks, purity testing using HPLC and NMR, and confirmation that it stays true to its theoretical melting point and color. In the manufacturing environment, small variances signal possible issues with process conditions or with raw material purity—both get swiftly handled to preserve batch consistency.

    Production Focus: Consistency Before Complexity

    Over years at the reactor controls, we have found that seemingly small details—like the temperature rate during addition, or the solvent’s water content—make far more difference than product datasheets ever reveal. In comparison to other similar pyrimidine-based chemicals, 4(3H)-pyrimidinone, 6-amino-2-mercapto- exhibits cleaner crystallization patterns and less tendency toward side reactions under common coupling or alkylation conditions. This matters a lot to those planning downstream modifications. In addition to people handling routine research, even pharmaceutical development teams value not just well-documented purity, but clear records showing the compound’s heritage from start to finish.

    Distinct Properties from a Manufacturer’s View

    Our batches typically display white to off-white crystalline appearance, reflecting both a well-controlled reaction and careful post-processing work. Moisture-sensitive groups in this molecule demand close attention to climate control and packaging. During one particularly humid summer, storage improvements had to be made to prevent subtle degradation. From personal observation, these steps give researchers greater confidence—less time re-running reactions, more time moving forward with new ideas. In the lab, a slight yellowish hue or unusual texture means backtracking through the process logs until the cause reveals itself. Such vigilance separates robust products from those plagued by impurity drift, and this difference carries straight through to our end users.

    Why 4(3H)-Pyrimidinone, 6-Amino-2-Mercapto- Stands Out Among Heterocyclic Building Blocks

    Within the workshop, there’s often discussion about how this compound’s dual functionalization—amino at the six-position, mercapto at the two—expands its reach compared to simpler heterocycles. The amino group enables straightforward acylation or diazotization flows, while the mercapto group serves as a site for thioether formation or sulfur crosslinking. As a manufacturer, I’ve seen firsthand how researchers gravitate to a compound that gives options: reduce reaction steps, simplify purification, focus on intellectual property development with less concern about unexpected isomer formation. Several jobs for agricultural compound developers leveraged the mercapto function, while medicinal teams set their sights on the amino group for further diversification. Chemical versatility like this often plays out more inside the process room and the fume hood than in the sales brochure.

    Our Experience with End Applications

    Through collaboration with academic and industrial partners, we've noted recurring trends in application. Medicinal chemists gravitate to this intermediate when building anti-viral and anti-cancer scaffolds. Its structural core finds its way into kinase inhibitor research and as a foundational block for modified nucleosides. Laboratory teams appreciate the clean reactivity with standard coupling agents—fewer failed reactions, lower by-product formation, and milder purification protocols. In one iterative drug-development project, researchers shared feedback about consistent high-yield intermediate formation, which pointed back to the batch controls we maintain and the fine particulate filtering stages implemented several years ago.

    Crop protection specialists value the mercapto group for sulfur incorporation, often using the base structure to explore fungicidal or insecticidal activity. The stable handling profile stands in contrast to similar sulfur-based heterocycles which often present odor issues or rapid oxidative breakdown. During a scale-up project, the clean separation of finished material from impurities meant downstream formulation required no special isolation procedures. This speaks directly to the careful solvent management and phase separations practiced daily in production.

    What Goes Into a High-Quality Batch

    Not all 4(3H)-pyrimidinone, 6-amino-2-mercapto- on the market comes off the line with equal care. As a manufacturer, every batch number carries our reputation. Operators recalibrate analytical equipment regularly. One lesson learned over the years—never rely solely on a supplier’s input certificate. Every delivery of raw amidines and thiourea undergoes full identity and purity checks, regardless of past history with that supplier. In some instances, off-spec batches highlight hidden issues—residual process solvents, microcrystalline contaminants, or even unknown side products from slightly off reagent ratios.

    Attention to purity remains the key factor in keeping color, melting point, and reactivity profiles exactly where the customer expects them. In our experience, it’s the “minor” by-products that cause major headaches downstream: isothiourea fragments, ring-opened variants, or mistakenly formed urea derivatives. These are not easily spotted by basic assays, so we leverage both HPLC and NMR alongside classical techniques. The difference becomes clear every time customers report smooth scale-up from milligram to multi-kilogram without additional optimization.

    Adapting to New Demands and Industry Trends

    Ten years ago, this compound held modest demand in custom synthesis labs. Now, demand has surged from both the pharmaceutical and agrochemical sectors, driven by a wave of new targets in bioactive molecule research. As a result, manufacturing practices adapted—narrower process windows, improved exhaust handling, better operator training on endpoint detection. Across batch records, we see how variations in reaction temperature or solvent swap protocols can impact shelf life and yield strength. The factory team works closely with customers, learning about their use-cases and adapting processes in response to practical bottlenecks reported from working chemists.

    Continuous improvement became more than a buzzword. A few years back, researchers complained about inconsistent moisture levels causing reaction quenching issues. The feedback prompted investment in dehumidification equipment and tighter packaging protocols. Since then, reports of compromised activity and unexpected product drift declined. This direct feedback loop with users keeps process improvements focused and relevant.

    Specifications Backed by Practice, Not Just Paper

    As one of the most trusted sources among synthetic chemists, we prioritize documentary transparency and hands-on batch control. Typical manufacturing lots present assay purities above 98 percent, narrowly controlled moisture levels, and fine crystalline form. We avoid compaction to preserve surface area, critical in downstream processes where rapid dissolution or surface reaction kinetics tip the balance between success and redo.

    Each new production run begins with reactor cleaning validated by swab checks, careful calibration, and a test synthesis run at small scale before full volume commences. By following this discipline, missteps get caught before they multiply—less waste, fewer recalls, and high re-order rates from repeat customers. Tolerance for deviation remains low; a shipment outside of the expected IR fingerprint spectrum triggers a full review from raw material receipt to final isolation.

    Why Direct Manufacture Benefits End Users

    As a chemical manufacturer, our involvement does not end once the product leaves the loading dock. Post-shipment support matters, and experienced chemists value quick, evidence-based responses to their technical queries. In one documented case, a pharmaceutical team encountered a solubility issue during a scale-up trial. Cross-referencing our retain samples and production logs made it possible to isolate a subtle batch variation linked to a raw material change. This open exchange led to corrections in both our input specifications and their formulation process, tightening consistency for future projects.

    The difference between supplier and manufacturer often comes down to understanding the impact of day-to-day production challenges on research outcomes. Direct communication between production engineers and laboratory users uncovers the kinds of problems that never appear in sales literature—like the way particle size subtly alters filtering speed or how repeated cycles of transfer affect final appearance. Without intermediate layers, answers come faster, and practical workarounds emerge naturally.

    Comparing With Other Pyrimidine Derivatives

    Within the pyrimidine family, 4(3H)-pyrimidinone, 6-amino-2-mercapto- stands out for its gentle handling characteristics and versatile reactivity. Unlike cytosine analogs, it resists hydrolysis under ambient moisture. When compared against 2-thiouracil or other simple mercaptoprimidines, our product exhibits less odor and remains more photostable—a point many QC teams mention after their first trials. The unique combination of amino and mercapto groups also opens routes for one-pot syntheses that reduce solvent usage and processing time. This matters for busy teams plugging into high-throughput arrays or scaling up for pilot runs where stability and reliability translate to cost savings.

    Comparisons with similar heterocycles produced using less controlled processes highlight fragility: unexpected side reactions, higher residual solvent content, and unpredictable color drifting. Our emphasis on tight environmental and process controls gives peace of mind to those weighing cost versus consistency. This approach also allows for batch customization without loss of core performance—a trait repeatedly requested by advanced research teams working on time-sensitive targets.

    Our Approach to Supporting Specific User Needs

    Each research project comes with unique challenges, and as a manufacturer, we respond with flexible lot scheduling, technical support, and willingness to provide technical disclosure. Some academic groups request finely milled product for rapid dissolution; others in pharmaceutical development want larger crystals to minimize dust and facilitate solid dosing. We deploy targeted process changes when needed. Our plant operators maintain open communication lines with technical managers so small but vital modifications—like extra sieving, high-vacuum drying, or modified packaging—can be implemented without introducing new risks.

    In the area of regulatory documentation and traceability, we’ve adapted robust internal logging with batch-level analytic records. It’s common to get audit requests from pharmaceutical partners who need verification of every handling step. See it from our side: auditors walk the floor, check calibration schedules, re-run certain QC checks, and ask for residue testing from past production lots. We welcome this scrutiny—it sharpens our methods and gives users a verified line from raw input to finished flask.

    Meeting Challenges Head-On—From Scale-Up to Shipment

    Unexpected issues pop up on even the best-run manufacturing lines. In high-humidity conditions, moisture pickup in drum packaging led to complaints about caking. Rather than deflect, we invested in improved barrier liners and doubled up on silica gels during the most humid quarters. Periodic review meetings ensure these improvements stick over time. None of these changes happen in isolation—they stem from direct conversations with researchers struggling in their own labs with challenges connected to physical form or storage.

    The rise in customized research protocols has shifted demand patterns. Some customers request alternative solvents to match their reaction conditions. Others bring up requests for tighter control on particle size or trace impurity thresholds. As engineers and chemists on the ground, we recognize that flexibility and reliability must exist together. Flexibility without discipline leads to unpredictability—a lesson learned after a few hard experiences with so-called “special” runs that lost consistency. Our focus, again and again, returns to robust, well-understood processes and honest communication about what each batch can deliver.

    Eyes on the Future: Sustainable Methods and Ongoing Partnerships

    Sustainability goals grow more urgent each year. As manufacturing leaders, we push to reduce solvent waste, cut process water use, and capture by-products for recycling. Our investments in vapor recovery and LED-based monitoring systems reflect a broad industry shift but also stem from practical experience—solvent costs, regulatory compliance, and plant safety all improve. Recent reviews of alternative purification flows highlighted possible pathways to further reduce our footprint. These are not theoretical projects; teams in our plant test new conditions, run kinetic models, and scale up promising ideas when the data proves out. The focus remains on maintaining high-quality output while trimming waste.

    Partnering closely with research organizations ensures not just supply, but insight. By following customer requests for analytical data, impurity breakdowns, and long-term storage stability, we build understanding that shapes future offerings. Our internal knowledge base continues to grow with every collaborative audit and every unique research protocol shared by our customers. In this way, 4(3H)-pyrimidinone, 6-amino-2-mercapto- becomes not just a product, but a reflection of user-driven advances in pharmaceutical and crop protection science.

    Conclusion: Manufacturer’s Commitment to Scientific Progress

    For every kilo we produce, each analytic run performed, and every technical conversation with end-users, the goal is straightforward: deliver reliable, high-purity 4(3H)-pyrimidinone, 6-amino-2-mercapto- to laboratories where innovation happens. This journey, shaped by years of experience and a hands-on approach to continual improvement, distinguishes our approach. The insights shared here draw from challenges faced and overcome—batch-to-batch consistency, process adaptability, and a culture of open technical support. With every shipment, we recognize the impact of our work on scientific discoveries, regulatory milestones, and new product development. By keeping our sights set on both rigorous control and honest dialogue, we help drive progress in the demanding sectors that rely on this unique chemical building block.