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2-Hydroxypyrimidine

    • Product Name 2-Hydroxypyrimidine
    • Alias 2-Pyrimidinol
    • Einecs 206-425-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    616647

    Chemical Name 2-Hydroxypyrimidine
    Molecular Formula C4H4N2O
    Molar Mass 96.09 g/mol
    Cas Number 109-42-2
    Appearance White to light beige solid
    Melting Point 315-317 °C
    Solubility In Water Moderately soluble
    Pka 11.7 (of the hydroxyl group)
    Density 1.450 g/cm³
    Synonyms 2-Pyrimidinol, 2-Oxopyrimidine
    Iupac Name Pyrimidin-2-ol

    As an accredited 2-Hydroxypyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle labeled "2-Hydroxypyrimidine, CAS 7556-80-7" with hazard symbols and safety instructions prominently displayed.
    Shipping 2-Hydroxypyrimidine is shipped in secure, airtight containers to prevent contamination and moisture exposure. Proper labeling, including hazard identification, accompanies each package. During transit, it is protected from heat, sunlight, and incompatible substances, in accordance with relevant regulations to ensure safety and maintain chemical integrity throughout transportation.
    Storage 2-Hydroxypyrimidine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. It should be kept away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Store it at room temperature and protect it from direct sunlight. Proper chemical labeling and secure storage arrangements are essential to ensure safety and prevent contamination.
    Application of 2-Hydroxypyrimidine

    Applications of 2-Hydroxypyrimidine in Industrial Manufacturing

    As a direct manufacturer of 2-Hydroxypyrimidine, we supply this specialized heterocyclic compound to a defined set of advanced industrial sectors. Our material supports precise downstream applications where its unique chemical functionalities contribute to the formulation and process performance in areas such as active pharmaceutical ingredients, specialty agrochemicals, polymer synthesis, and advanced dye intermediates. Below are targeted industry scenarios that reflect established usage and regulatory compliance frameworks.

    1. Pharmaceutical Intermediates for Antiviral and Anticancer APIs

    Pharmaceutical companies incorporate 2-Hydroxypyrimidine in multi-step synthesis routes for nucleoside analogues and enzyme inhibitors. Its ring structure enables the targeted modification of pyrimidine moieties in active molecules, which are essential for antiviral and anticancer agents. The compound typically enters the process as a nucleophilic precursor during the core heterocycle construction or a protective group phase, influencing the final activity spectrum and purity profile of APIs.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. impurity limits for synthetic intermediates
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Local pharmacopoeias and regulatory submission dossiers

    Typical usage ratio

    • Ranges from 5–15% molar ratio within synthetic steps, depending on route yield and intermediate purity requirements; material excess often adjusted for reaction completion and downstream recovery efficiency.

    Downstream process integration

    • Charged during the heterocycle assembly or as a modifying agent in the amidation, chlorination, or alkylation steps relevant to nucleoside and pyrimidine analogue formation; residue monitored through analytical QC prior to API crystallization.

    Final product types

    • Brivudine, Zidovudine, and several patent-stage anticancer pyrimidine derivatives
    • Specific kinase inhibitors and DNA polymerase blockers
    • Pyrimidine-based immunosuppressants

    2. Agrochemical Synthesis: Herbicide and Fungicide Intermediates

    Major crop protection manufacturers employ 2-Hydroxypyrimidine in the synthesis of selective herbicides and fungicides, taking advantage of its ring activation and reactivity. The intermediate facilitates the formation of active heterocyclic scaffolds found in novel triazolopyrimidine and dihydropyrimidine agrochemicals, contributing to target selectivity and field stability of the final products.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Intermediates
    • ISO 9001-guided in-process quality assurance
    • REACH Regulation (EC) No. 1907/2006—registered intermediate status
    • Country-specific agrochemical authorization requirements (e.g., US EPA, EU PPP regulation EC 1107/2009)

    Typical usage ratio

    • Normal charge: 8–18% w/w relative to total batch input; precise level adjusted by the targeted chemical yield, with higher use in longer-chain or multi-ring product syntheses.

    Downstream process integration

    • Added at the heterocycle formation or ring closure stage in the manufacture of key active ingredients; removal and purity checked prior to formulation into concentrates or granules.

    Final product types

    • Pyrimidinylurea herbicides (e.g., Benzothiadiazole derivatives)
    • Triazolopyrimidine sulfonanilide fungicides
    • Precursor to plant growth regulators and safeners

    3. High-Performance Dye and Pigment Precursors

    Specialty dye makers use 2-Hydroxypyrimidine as a key building block for light-fast dyes and pigment molecules, particularly those requiring electron-rich, nitrogen-containing aromatic systems. Its role in azo and anthraquinone dye precursor synthesis supports the manufacture of colorants meeting technical requirements in textile, inkjet, and polymer coloration processes, where stability and chromatic properties depend on the heterocyclic core’s integrity.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textile dyes
    • ISO 105-X12:2016 (Textiles—Tests for Colour Fastness)
    • REACH Annex XVII compliance for azo compounds and colorants
    • Customer-accepted purity/control specifications (99%+ required for specialty dyes)

    Typical usage ratio

    • Normally 10–20% of batch input as precursor; the ratio varies by required dye shade depth and final chromophore structure.

    Downstream process integration

    • Introduced into ring substitution or coupling steps of pigment synthesis, prior to sulfonation or metallization for color enhancement; monitored for trace impurity carryover into finished dye lots.

    Final product types

    • Anthraquinone dyes for polyester and acetate fibers
    • Azoic dye intermediates and pigment dispersions
    • High-purity colorants for inkjet and specialty coatings

    4. Polymer Crosslinking Agents and Functional Resin Modifiers

    Manufacturers of advanced resins and specialty polymers utilize 2-Hydroxypyrimidine for its ring activation potential in crosslinking and functionalization steps. The compound supports the synthesis of thermosetting resins and specialty adhesives where it imparts improved curing profiles, chemical resistance, and end-use thermal stability, especially in electronic encapsulants and engineered composite matrices.

    Industry compliance standards

    • ISO 9001 and ISO 14001:2015 for production quality and environmental safety
    • UL 94 (Flammability of Plastic Materials for Parts)
    • Restriction of Hazardous Substances Directive (RoHS) for electrical/electronic applications
    • OEM-specific performance and durability testing standards

    Typical usage ratio

    • Low incorporation level of 0.5–2.5% by polymer weight; often adjusted by desired crosslink density, with higher levels for heat-resistant or structural grades.

    Downstream process integration

    • Added into prepolymer or resin mixtures at the curing agent addition stage or during copolymerization; ensures thorough dispersion by in situ mixing and monitored via rheological testing of final blend.

    Final product types

    • Epoxy and phenolic resins for high-reliability electronics
    • Specialty adhesives in structural laminates
    • Composite matrix materials for aerospace and automotive components
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    Certification & Compliance
    More Introduction

    2-Hydroxypyrimidine: Manufacturing Insights and Practical Applications

    Perspective from the Production Floor

    In chemical manufacturing, some compounds demand an extra level of care, precision, and experience from those who produce them. 2-Hydroxypyrimidine sits in that category. Over the years, repeated hands-on production cycles have shown that even a seemingly minor compound—at least by market volume—can present its own unique profile of challenges and rewards. In our plants, we don’t just synthesize materials; we learn their character, from the first feedstock delivery to the final drum leaving our warehouse.

    We have handled 2-Hydroxypyrimidine in tonnage batches as well as pilot-scale quantities meant for research and specialty use. Its appeal grows both in dedicated industrial processes and academic formulations. It sees demand spikes not simply because it’s a raw material, but because it plays a crucial part in catalytic reactions, bioactive molecule development, and several other specialties. Unlike trading companies who only see order numbers and paperwork, we connect the dots from raw chemistry to the final impact on a research outcome or a production line.

    Understanding the Chemistry and Its Importance

    2-Hydroxypyrimidine occupies a significant role in pyrimidine chemistry. With the CAS number 109-42-2, it features a six-membered aromatic heterocycle, a pyrimidine ring, with a hydroxyl group at the second position. Its molecular formula—C4H4N2O—may look simple on paper, but the presence of that hydroxyl at the 2-position changes reactivity substantially compared to unsubstituted pyrimidine or other isomers like 4- or 5-hydroxypyrimidine.

    In practice, this structure lends itself to distinctive hydrogen bonding patterns and nucleophilicity, and it provides a handle for downstream functionalization. I’ve seen firsthand the role that this unique behavior plays during work-up and purification steps: reactions can stall if the purity falls ever so slightly below required limits, especially when scaled up for pharmaceutical intermediate production or electronic material applications.

    Our Manufacturing Approach

    At scale, producing 2-Hydroxypyrimidine calls for a high level of process control. We run our syntheses under tightly regulated temperatures—too high, and side products soar, leading to decreased yield and a tough purification; too low, and conversion rates dip, fueling unwanted batch-to-batch variability. Reagent choices also matter: using overly aggressive bases or oxidants can cause ring cleavage or unwanted rearrangements.

    In our plant, we favor reliable, stepwise reaction sequences with real-time monitoring at crucial points. We’ve dialed in solid-phase extraction and short-path distillation steps to minimize exposure to air and moisture, both of which can drive degradation or introduce colored impurities. Over time, this hands-on experience leads to process tweaks. Sometimes it means changing a stirring speed; other times, it’s the decision to swap a glass vessel for stainless to mitigate corrosion.

    We store the finished product in lined containers that guard against atmospheric water pick-up, keeping the powder free-flowing and minimizing caking. Because 2-Hydroxypyrimidine can absorb moisture, we keep humidity in the final packing room below a strict upper limit, checked hourly. Every plant will face slight differences—local water purity, seasonal temperature swings, or equipment legacy—but direct experience teaches what a specification sheet never reveals.

    Typical Specifications from the Source

    Our 2-Hydroxypyrimidine typically presents as a white to pale yellow powder, thanks to high-grade purification systems and careful attention during handling. We keep assay values above 99 percent for pharma and electronics grade, with special lots available for users who require even tighter qualification. Residual solvent levels remain below regulatory thresholds, routinely verified through GC/MS.

    Particle size influences handling and solubility in applications such as catalyst synthesis, so we customize drying and grinding to deliver either a fine powder or a granulated material, depending on what works best for downstream blending or dissolution. Water and ash content seldom draw interest until a process behaves oddly; our data give customers confidence, often making the difference between a smooth run and a failed batch.

    We test every lot for pyrogens and heavy metals, particularly for users in biomedicine and fine electronics. While this may not seem essential for broader industrial uses, failing to control trace elements could compromise sensitive catalytic cycles or interfere with downstream analytical results. Even after years on the job, minor tweaks to washing and drying steps show up immediately in the certificate-of-analysis trends.

    Where 2-Hydroxypyrimidine Finds Use

    Some chemical products flow into commodity roles, but 2-Hydroxypyrimidine nearly always ends up in high-stakes projects. Its most talked-about function involves work as a building block or precursor in drug discovery. Medicinal chemists incorporate it into lead molecules for its hydrogen-bonding abilities, which reflect in improved biological activity or selectivity.

    In our experience supporting R&D and pilot campaigns, labs often rely on 2-Hydroxypyrimidine as a scaffold for kinase inhibitor synthesis or anti-infective candidates. The same nucleophilic oxygen that distinguishes it from unadorned pyrimidine makes a difference: coupling reactions that fail with analogs often succeed with the 2-hydroxy derivative, opening new chemical space for library design.

    Beyond pharmaceuticals, the compound appears in specialized catalysts and ligands for organometallic chemistry, where its planar structure and lone pairs enhance metal coordination. Synthetic chemists might reach for it when other heterocycles prove too inert or lack the same substitution pattern flexibility. A few electronics applications have emerged too, particularly in organic semiconductors, where its electronic structure can tune the charge transport properties.

    From time to time, it shows up as a corrosion inhibitor or in ink formulations, though these demands remain intermittent. Each end-use carries strict requirements—impurity profiles, residual solvent tolerances, polymorph control when the crystalline state matters. We track these performance drivers directly with customer process engineers and project leads, not just through procurement channels, which helps everyone knock out surprises before a new production scale-up.

    2-Hydroxypyrimidine Compared to Related Compounds

    In our work with 2-Hydroxypyrimidine, one recurring question comes up: How does it differ in practice from similar heterocycles, like 4-hydroxypyrimidine, 2-aminopyrimidine, or unmodified pyrimidine? The distinctions seem obvious on paper, but as production chemists, we see the evidence pile up in the plant and in customer feedback.

    Substituent position changes reactivity in ways that process engineers can’t ignore. 4-Hydroxypyrimidine, for instance, orients the hydroxyl group differently within the aromatic ring, altering how it forms hydrogen bonds or participates in coupling reactions. Processes tuned for 2-Hydroxypyrimidine simply don’t deliver the same conversions or product profiles with its positional isomers. Storage stability differs as well: the 2- position offers stronger intramolecular hydrogen bonds, sometimes delivering greater shelf stability, but it can also complicate crystallization.

    Compared with amine-substituted pyrimidines, the hydroxy-driven polarity enables better solubility in water and polar aprotic solvents, which can aid in extractions and process work-ups. Yet, that same solubility raises challenges for drying and final packaging, particularly in humid climates. In our experience, trace moisture can trigger caking or even deliquescence; practically, a plant operator with a hygrometer often does more to maintain product stability than the most sophisticated air dryer.

    Untouched pyrimidine acts as a weaker nucleophile and doesn’t show the same reactivity in Suzuki or Heck-type couplings. Our technical teams routinely hear from development chemists wanting to know why a pathway that works with 2-Hydroxypyrimidine fails with plain pyrimidine or 2-aminopyrimidine. Years in the field show it’s rarely about purity or vendor differences, but fundamentally about the electronic structure imparted by that specific 2-hydroxy group.

    Even in shelf life, 2-Hydroxypyrimidine distinguishes itself. Well-sealed batches hold up for years, while competitors working with less diligent moisture control tend to see degradation or off-odors develop in under a year. Our team monitors this rigorously, adding real value well beyond a bundled analytical report.

    Experience with End-User Needs and Challenges

    Large-scale users tend to demand more than just specification compliance—they expect assurance throughout the batch cycle and responsiveness to process upsets. Over time, our team has built up a toolkit of solutions for common hiccups. For instance, if a customer’s filtration step slows unexpectedly, it often traces back to subtle inhomogeneities in powder grain. We adjust milling protocols right away, not after a mountain of email chains.

    Some applications require exceptionally tight control over trace solvents, particularly for synthetic steps sensitive to ketone residues or halogenated solvent carryover. While routine batch handlers might miss these micro-contaminants, we catch shifts in the tail of a GC curve as part of daily operations. If the tail looks off, we investigate, rerun, and inform buyers before any product ships. Trust grows with these habits, serving both innovation-driven start-ups and established industry leaders.

    Sourcing managers sometimes question why 2-Hydroxypyrimidine from one supplier diverges so much in performance from another’s, when “specs” look identical. Our experience has revealed that slight variations in residual moisture, particle size, or even minor variances in trace metal content produce differences in catalytic efficiency, biological results, or downstream yield. We document these subtleties and share insights proactively. Being the genuine manufacturer, we maintain tight feedback loops: insights from customer complaints or abnormal application outcomes drive real-time process adjustments, not afterthought corrections.

    Pursuing Sustainability and Safety at Scale

    Over the last decade, we have faced rising expectations—not just for product consistency and technical service, but also for safer, greener production. 2-Hydroxypyrimidine poses its share of environmental and handling risks. Some precursor materials and by-products demand stringent containment. Every new campaign gets reviewed by our EH&S team, collaborating directly with operations to implement the safest routes. We’ve invested in closed-loop reactors with advanced scrubber systems to keep fugitive emissions close to negligible, rather than treating this as an afterthought.

    Waste minimization matters, too. Rather than disposing of spent solvents outright, we recover and distill them, feeding clean streams back into other production runs. The learning curve was steep, but solvent recovery now forms a profitable part of the plant—benefiting cost structure and environment alike. For us, treating each batch as a learning opportunity improves safety. Routine “toolbox talks” amongst operators turn near-misses into process improvements before problems can recur.

    Downstream users working in pharma and electronic industries ask for full traceability and compliance with local rules. Our internal tracking links every production lot with its origin batch, synthesis operator, and even the air and water quality that day. These safeguards protect not only supply chains, but the people who ultimately work with our product.

    Potential Solutions to Common Challenges

    Experience has shown that end-users sometimes run into problems that standard technical data fails to anticipate. Issues like unexpected reactivity, color changes, or even clumping in storage can derail otherwise seamless projects. Addressing these often means working hand-in-hand with customer technical teams, debriefing at the bench or plant floor, rather than just sending more paperwork.

    Adjusting storage conditions solves most issues with clumping or color change, but some situations need deeper intervention—such as switching packaging materials, doubling silicate dessicant, or introducing purging nitrogen before sealing. When process color blooms earlier than expected, we review drying curves, screen for iron or copper particulates, and audit glassware cleaning protocols. Quick correction, openness, and ongoing relationship matter more than the most robust “standard” QC program.

    On the application side, chemists frequently encounter hiccups in scale transitions, especially moving from analytic to multi-kilo batches. We host site visits, organize direct peer-to-peer conversations, and perform joint troubleshooting when their analytical tools spot unknown side-products. Practical support goes beyond the initial shipment; our technical team stays on call for guidance long after the purchase order is satisfied.

    Supply interruptions pose another risk that only a credible manufacturer can address credibly. Our redundancy in raw material sourcing, investment in plant reliability, and regular preventive maintenance cycles shrink the odds of delay. If market pressures or regulatory shifts do threaten timelines, long-term partners hear the news early, with genuine solutions, not belated excuses.

    Lessons Learned: Why True Manufacturing Experience Matters

    Although datasheets and brochures can make 2-Hydroxypyrimidine look simple, real-world production and application expose its quirks and strengths. Whether managing process safety, tweaking purification, or catching minute shifts in process performance, the difference between a manufacturing origin and just another supply chain step becomes clear with time. We have built our reputation not by hiding behind a curtain, but by dealing candidly with customers, listening to bench-scale feedback, and making process innovations a daily part of the job.

    The next generation of end uses for 2-Hydroxypyrimidine may arrive soon—likely driven by both regulatory demands and frontier applications in medicine and electronics. As those new frontier projects move forward, those companies who know the compound from the inside out, who have weathered its sticking points in both small and bulk production, will be best positioned to drive innovation and reliability.

    Our story with 2-Hydroxypyrimidine, handed down from operator to operator and debated in countless project meetings, demonstrates what real expertise looks like: a hands-on partnership with a molecule, a constant openness to improvement, and a willingness to share both challenges and victories with partners up and down the value chain. Every batch produced, every new insight learned from customers and our own teams, adds a layer to that understanding—and ultimately, it benefits every chemist, engineer, and team member who relies on our work.