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4-Hydroxypyrimidine

    • Product Name 4-Hydroxypyrimidine
    • Alias 4-Pyrimidinol
    • Einecs 207-993-8
    • 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

    248551

    Cas Number 519-74-4
    Molecular Formula C4H4N2O
    Molecular Weight 96.09 g/mol
    Iupac Name 4-hydroxypyrimidine
    Appearance White to off-white solid
    Melting Point 220-223 °C
    Solubility In Water Slightly soluble
    Pka 8.73 (for the N1 hydrogen)
    Smiles C1=CN=CC(=O)N1
    Inchi InChI=1S/C4H4N2O/c7-4-1-2-5-3-6-4/h1-3H,(H,5,6,7)
    Pubchem Cid 98561

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

    Packing & Storage
    Packing 4-Hydroxypyrimidine, 25g is supplied in a sealed amber glass bottle with a tamper-evident cap and detailed label.
    Shipping 4-Hydroxypyrimidine is shipped in securely sealed containers to prevent contamination and moisture exposure. It is packed according to standard chemical transportation regulations, ensuring safe handling and delivery. Proper labeling, documentation, and hazard information accompany each shipment, with temperature controls applied if necessary to maintain product integrity during transit.
    Storage 4-Hydroxypyrimidine should be stored in a tightly sealed container, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Ensure proper labeling and restrict access to authorized personnel. Regularly check the container for leaks or signs of degradation.
    Application of 4-Hydroxypyrimidine

    Applications of 4-Hydroxypyrimidine in Industrial Manufacturing

    4-Hydroxypyrimidine provides chemical functionality and versatility required in several specialized industrial flows as a core intermediate. We support downstream partners in pharmaceuticals and advanced fine chemical sectors with material that meets stringent quality and performance criteria for scalable production environments.

    1. Pharmaceutical Intermediate for Antiviral API Synthesis

    Our material serves as a direct building block in the synthesis of various pyrimidine-based antiviral active pharmaceutical ingredients (APIs), including those targeting RNA viruses. Customers rely on its precise reactivity in nucleophilic substitution and ring modification steps, where its purity significantly impacts yield and final API impurity profiles. Production environments use analytical HPLC methods for tight quality release, with documentation provided to support regulatory filings for both EU and US markets.

    Industry compliance standards

    • ICH Q7 GMP for API manufacturing environments
    • 21 CFR Part 210/211 for US market supply
    • Ph. Eur. and USP monograph conformance for critical intermediates
    • ISO 9001:2015 quality management system oversight

    Typical usage ratio

    • 5–20% of reaction mass by moles, ratio adjusted per API target and route
    • Molar ratio tuned per structure-activity relationship (SAR) requirements in lead optimization processes

    Downstream process integration

    • Introduced in the first or second step of heterocyclic API backbone assembly
    • Used during amidation, acylation, or nucleophilic aromatic substitution stages
    • QC ensures <0.5% high-purity side product formation prior to further condensation reactions

    Final product types

    • Nucleoside analog antiviral tablets and capsules
    • Ready-to-formulate pyrimidine-derivative API bulk crystals
    • Pharmaceutical intermediates for custom synthesis to regulatory standards

    2. Agrochemical Active Ingredient Precursor

    Agricultural chemical manufacturers employ 4-Hydroxypyrimidine as a coupling component in the manufacture of broad-spectrum fungicide and herbicide actives. The compound supports the formation of triazole and pyrimidinyl derivatives via selective alkylation or halogenation. Reliable input quality and particle size profile permit seamless scaling for pilot and commercial batch production under established safe process parameters.

    Industry compliance standards

    • FAO and WHO pesticide specification guidelines
    • REACH regulation for import and downstream processing in the EU
    • ISO 17025 analytical lab validation for residue and purity tracking

    Typical usage ratio

    • 10–30% by moles within intermediate coupling reactions
    • Adjustment based on desired crop protection spectrum and final product stability requirements

    Downstream process integration

    • Charged in early-stage active synthesis as a nucleophilic core
    • Subjected to chlorination or methylation, forming protected derivatives before further functionalization
    • Maintained in inert gas blanketing for thermal safety during exothermic steps

    Final product types

    • Pyrimidinyl fungicide actives (e.g., triazole-based protective agents)
    • Pre-mixed wettable powder and suspension concentrate formulations
    • Custom intermediates for downstream combination products with adjuvants

    3. Dye and Pigment Synthesis for Specialty Inks

    Manufacturers of electronic and security inks utilize the pyrimidine structure as a precursor in the synthesis of specialty organic pigments. Controlled reactivity enables the formation of highly substituted derivatives with tailored chromatic properties and stability under UV and chemical exposure. Batch traceability supports compliance with electronic component marking safety standards and end-user documentation requirements.

    Industry compliance standards

    • RoHS Directive for electronic marking inks
    • EN 71-3 for toy and packaging ink safety
    • ISO 2846 color reproducibility standards
    • SVHC restrictions under REACH

    Typical usage ratio

    • 2–10% by mass of pigment precursor batch, tailored to pigment intensity targets
    • Modified based on the number of ring substitutions in target dye molecules

    Downstream process integration

    • Input for heterocycle assembly via condensation reactions
    • Intermediate step before azo or quinone coupling for hue adjustment
    • HPLC and GC-MS monitoring for impurity and lot-to-lot performance control

    Final product types

    • Fluorescent and anti-counterfeit ink formulations
    • Semi-conductive pigment dispersions for industrial inkjet systems
    • UV-stable organic colorants used in microchip and PCB marking

    4. Active Material for Analytical Reagent Production

    Producers of reference reagents and buffer solutions incorporate this raw material as a functional group donor in high-purity indicator and diagnostic preparations. Strict trace metal and organic impurity control enable the finished goods to meet trace analysis demands found in pharma QC and research sectors. Documentation supports full batch certification and downstream compliance in regulated labs.

    Industry compliance standards

    • ISO 17034 reference material production
    • ISO/IEC 17025 accreditation for analytical reagent production labs
    • Analytical reagent (AR) and HPLC grade purity benchmarks

    Typical usage ratio

    • 1–5% by volume or mass, depending on required buffer capacity or chromophore intensity
    • Calculated per application for each lot number and regulatory submission

    Downstream process integration

    • Dissolved or solubilized during controlled pH adjustment or colorimetry preparation steps
    • Filtered under validated conditions to minimize particulate or trace metal entry
    • Final product validated by UV-VIS or HPLC trace analysis

    Final product types

    • Certified analytical standards for spectroscopy and HPLC
    • Buffer solutions for laboratory and pharmaceutical QC
    • Diagnostic indicator solutions for biotech and chemical labs

    5. Building Block for Custom Heterocyclic Fine Chemicals

    Specialty fine chemical manufacturers rely on this intermediate for constructing advanced heterocyclic scaffolds used in R&D, material science, and pilot-scale specialty chemical production. Control over particle size, residual solvent content, and reactivity enables smooth scaling of downstream synthetic procedures involving alkylation, acylation, or ring expansion. Our production supports cGMP or non-GMP inquiries, with full CoA and accompanying technical data for regulatory and investigational flows.

    Industry compliance standards

    • ISO 9001:2015 certified custom chemical production
    • GLP guidelines for investigational chemical supply
    • REACH notification for EU downstream users

    Typical usage ratio

    • Ranging 5–25% by mass per batch, formulated according to reaction scaling and structure complexity
    • Adjusted by stoichiometry for sequential functionalization and derivatization steps

    Downstream process integration

    • Charged during early ring assembly or as a modular functional handle later in multi-step synthesis
    • Subjected to hydrolysis, N-acylation, or halogenation as required by project specification
    • Fractional crystallization or preparative chromatography for impurity control before delivery

    Final product types

    • Tailored heterocyclic intermediates for pharmaceutical or biotech research
    • Specialty fine chemical stocks for advanced materials or OLED research
    • Precursor molecules for patented or pipeline API candidates
    Free Quote

    Competitive 4-Hydroxypyrimidine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Hydroxypyrimidine: A Straightforward Introduction From an Experienced Manufacturer

    The Chemistry Behind 4-Hydroxypyrimidine

    On the production floor, few compounds pull as much attention as 4-hydroxypyrimidine. Its structure counts in both laboratory and industrial applications and shapes the way fine chemicals interact in a range of synthetic processes. Chemically, it features a pyrimidine ring with a single hydroxyl substitution. Each batch tells a clear story of careful handling, purity checks, and well-validated crystallization steps that mark serious chemical manufacturing.

    Our standard material comes as a white to off-white solid, with purity regularly exceeding 99.0%. Purity targets are strictly verified, not out of formality but because downstream reactions can trip up on residual byproducts, including impurities left behind in insufficiently controlled batches. We have learned the importance of meticulous process parameters for maintaining a product that holds up to HPLC scrutiny and meets established benchmarks for physical consistency.

    Specification Driven by Real-World Application

    We provide 4-hydroxypyrimidine in a model that supports most research, pilot, and large-scale needs: 25 kg fiber drums serve heavy users, while smaller quantities reach academic labs, biotech start-ups, and custom synthesis houses. We focus on low moisture and tight particle size distribution, not simply for shelf stability, but because caking or degradation can throw off process yields or even sabotage spectral analysis in the hands of our customers.

    After years of observing customer workflows, it has become clear that vendors who cut corners around drying steps or skip re-crystallization see more complaints on purity drift. We run our drying cycles until moisture content falls well below 0.5%, routinely reporting LOI figures so users are never left guessing. Such attention pays off, as inconsistent batches cost both time and money during validation.

    Making Sense of Usage: Where Skill Meets Practice

    Chemists using 4-hydroxypyrimidine routinely seek a viable platform for heterocyclic synthesis. This compound enables access to a spread of pharmaceuticals, crop protection agents, and advanced materials. Its functional group—hydroxyl at the fourth position—offers a versatile anchor for further derivatization, which is the gateway to pyrimidine-based drugs like allopurinol, and intermediates in CNS-active compounds. Over the past decade, our analytical team has supported projects ranging from small batch intermediates for preclinical R&D to ongoing supply streams for catalog fine chemicals.

    No laboratory enjoys tackling a reaction that suffers from erratic starting material quality. Even seldom-seen trace contaminants risk introducing unpredictable side reactions. Our standard for elemental and chromatographic purity exceeds commonly published values. Over hundreds of campaigns, feedback points to the same truth: solid fundamentals in compound preparation produce reliable reactions. Our 4-hydroxypyrimidine supports Suzuki cross-couplings, nucleophilic substitutions, and metalation steps without introducing noise during scale-up.

    Compared to Other Building Blocks: Where Function and Form Split Paths

    Most chemistries revolving around the pyrimidine scaffold reach for the classic unsubstituted pyrimidine, or perhaps its methylated or aminated cousins. These serve in heterocycle libraries, but each offers a different set of handles for modification. 4-hydroxypyrimidine stands apart by presenting a distinct polarity and tautomeric character. In the lab, this translates into unique hydrogen bonding, easier ring closure under certain conditions, and pathways for regioselective functionalization. Formulators and medicinal chemists both benefit by having access to the hydroxyl group, since it can redirect the course of electrophilic attacks or serve as a direct anchor in target syntheses.

    We have prepared countless variants and analogs—such as 2-hydroxypyrimidine and dimethylpyrimidines—and each exhibits its own quirks. Take the example of 2-hydroxypyrimidine: due to its tautomeric equilibrium, you often see unpredictability in reactivity. 4-hydroxypyrimidine keeps things streamlined, thanks to a better-defined electron density and more predictable chemical behavior in the ring.

    Compared to its more hydrophobic relatives, 4-hydroxypyrimidine also grants solubility advantages. Seeing it in action, analysts can work up solutions in polar and semi-polar systems with greater ease, and chromatographers comment on gentler elution profiles. Its neat crystalline form helps avoid the headaches associated with sticky, deliquescent bases that show up in related heterocycles.

    Lessons from the Field: What Actually Matters Upstream

    We have stood beside process chemists who run multi-kilogram syntheses, and the conversations always cycle back to two things: trust in the starting material and flexibility for modification. Over time, we have adopted process controls specifically to minimize batch-to-batch variation. Routine infrared, NMR, and mass spectrometry analysis set the baseline, but only through careful scale monitoring and solvent handling have we tamed hydroxy-substituted pyrimidine’s tendency to form colored impurities during dry-down.

    Feedback loops built into our quality system catch out-of-trend patterns early. Our staff holds long experience resolving off-specification events, whether it is an uptick in particulates during filtration or a glycolic note creeping into GC profiles. These direct interventions shape why our 4-hydroxypyrimidine sits on high shelves at large pharma, biotech, and catalogue houses.

    End-Use Considerations: Beyond Labels and Grades

    Applications drive the real tests of performance. In our shipments to medicinal chemistry labs, ease of measurement stands out as a daily concern. Crystals that slide easily into micro-spatulas save precious minutes. In formulation chemistries, the need for consistent pH and low buffering behavior can make the difference between success and days lost troubleshooting HPLC peaks.

    One manufacturer’s idea of “fine chemical grade” often misses the nuances required by downstream handlers. We have long since chosen to calibrate our analytical routines not by regulatory minimums, but by the functional limits seen in our end-users’ applications, including mass balance during scale-up and reaction tracking over seasonal changes. This direct exposure to bench chemistry has motivated improvements in packaging, lot numbering, and even re-seal design so that the product meets real usage needs, not just the paperwork.

    Meeting Environmental and Safety Expectations

    Manufacturing isn’t only about product output; environmental responsibility matters just as much. The synthesis and purification of 4-hydroxypyrimidine produce waste streams that call for dedicated handling. Our plant integrates modern capture and neutralization units, so both effluent and solid byproducts end up within legal discharge limits. Routine audits track metrics more closely than regulatory agencies require, reflecting our belief that chemical makers shape community standards from inside the fence line.

    Worker safety gets equal attention. The process chemistry behind hydroxylated pyrimidines does involve common solvent hazards and high-temperature stages. Our long-tenured staff benefit from repetitive in-person training and loud, simple signage in every relevant bay. Keeping accident rates low sits high on our list, knowing that even a trivial slip costs more than a few minutes out of production—it risks career health and puts team trust under strain.

    Real Industry Experience Puts Product Claims to the Test

    A typical synthesist wants more than assumptions about a chemical’s merit. They scan certificates of analysis for batch history, scan for weird spikes in IR traces, and ask for residual solvent levels lower than most published monographs. Over the years, we’ve shifted away from assumptions and spent time under real scale-up constraints—hearing from engineers about solvent recoveries, seeing the knock-on effect of an accidental pH drift on recovery yields, or tracing a single bad lot back to minor temperature excursions in a midnight shift.

    These experiences leave little room for “acceptable” compromise. Customers appreciate stability, and seeing the same test results over dozens of shipments puts their minds at ease. We’ve fielded requests for low-odor variants, special particle-cut forms, and ultra-dried grades. Each new request pushes us to examine process bottlenecks and make small, meaningful adjustments to reactor protocols or drying times.

    Supporting Research and Development With Consistency

    R&D labs building new molecular targets turn to 4-hydroxypyrimidine as a springboard. Access to a high-purity, well-characterized sample removes hurdles and gives teams a better shot at hitting project milestones. Our material arrives fully documented, with stability data when needed, easing tech transfer from discovery to process scale. Chemists often notice batch notes; small changes matter, and details catch the eye of anyone running synthetic routes with high downstream value.

    Thanks to many partnerships, we see our compound help construct kinase inhibitors, anti-viral chemotypes, and ligands for organometallic screens. Each year brings more demand for screw-capped jars small enough for glovebox transfer, or bags suited to automated dispensing, so we stay agile and expand packaging variations without disrupting baseline performance. This kind of collaboration with users forms the backbone of the chemical industry—feedback loops directly connect bench work to plant operations, not just this year but across decades.

    Regulatory and Analytical Value: Trust That Sticks

    Compliance isn’t just an obligation, it's about giving researchers a reliable foundation. Each batch ships with full HPLC, NMR, and MS documentation, plus residual solvent and trace impurity analysis using established compendia methods. From time to time, we see the audit teams of customers scrutinize our location, check logs on solvent management, and follow product all the way through order picking and shipment labeling.

    By investing in proper traceability, we prevent confusion and enable users to compare results year to year without recalibrating instruments after each delivery. Analytical transparency saves time and builds the sort of trust that outlasts mere contracts.

    Supporting Complex Synthesis: Looking at the Bigger Picture

    Complexity in organic synthesis often scales up unpredictably. As process chemists move from milligram to kilogram runs, small variances in 4-hydroxypyrimidine can magnify. Whether it’s sticking on silica columns or showing tailing in LC methods, these subtle issues show up more if the incoming product drifts outside tight specification windows.

    We have stood alongside pilot plant engineers reviewing failed crystallizations and traced problems back to just one poorly resolved impurity. Moments like these drive home the value of manufacturing discipline to avoid downtime. Upgrading driers and resourcing extra QC staff slots deliver results that pay for themselves in shorter project times for our loyal users.

    Adapting Supply Chains for Special Needs

    Logistics remains one of the biggest hidden factors in delivering high-quality organics. Poor packing or transit damage undoes careful laboratory work in a single mishap. Our shipping warehouse relies on tamper-evident drums and reinforced cartons for smaller batches, since moisture intrusion saps stability and leaves researchers cleaning up needless mess.

    Recently, the move to more distributed research centers worldwide calls for extra vigilance. Weather shifts, customs delays, and supply shocks all put pressure on stability and consistency. By carrying stocks in multiple hub regions and rotating inventory more frequently, we’ve kept disruption to a minimum even when outside pressures bite.

    Final Thoughts: Why Experience Counts

    After years in chemical manufacturing, shortcuts tend to show up sooner or later. Any compound—especially a reactive one like 4-hydroxypyrimidine—can trip up newcomers to production. Our approach hinges on tight in-process monitoring, clear connection with users, and an openness to dig deep into customer experience reports.

    Innovation in chemistry means nothing if the basic building blocks can’t be trusted. As research pushes boundaries, only properly made, consistently supplied materials enable the breakthroughs our customers aim for. Whether in a discovery lab or a pilot plant, the value of quality—woven throughout every process—makes all the difference between creative frustration and scientific achievement.