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2-Methyl-5-Pyrimidinemethanol

    • Product Name 2-Methyl-5-Pyrimidinemethanol
    • Alias 2-methyl-pyrimidin-5-yl)methanol
    • Einecs 624-919-2
    • 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

    854260

    Chemical Name 2-Methyl-5-pyrimidinemethanol
    Cas Number 828-57-3
    Molecular Formula C6H8N2O
    Molecular Weight 124.14
    Appearance White to off-white solid
    Melting Point 107-110°C
    Boiling Point 330.8°C at 760 mmHg
    Density 1.202 g/cm3
    Solubility In Water Soluble
    Purity Typically ≥98%
    Synonyms 5-(Hydroxymethyl)-2-methylpyrimidine
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 2-Methyl-5-Pyrimidinemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Methyl-5-Pyrimidinemethanol, 25g: Supplied in a sealed amber glass bottle with tamper-evident cap, labeled with safety and handling instructions.
    Shipping 2-Methyl-5-Pyrimidinemethanol is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be packaged according to relevant chemical safety regulations, labeled clearly, and transported under ambient conditions. Ensure handling by trained personnel and compliance with local, national, and international hazardous material shipping guidelines when applicable.
    Storage 2-Methyl-5-pyrimidinemethanol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from light, moisture, and excessive heat. Clearly label the storage vessel, and handle it using appropriate personal protective equipment to avoid inhalation or skin contact. Store according to relevant chemical safety guidelines.
    Application of 2-Methyl-5-Pyrimidinemethanol

    Applications of 2-Methyl-5-Pyrimidinemethanol in Industrial Manufacturing

    As an established chemical raw material producer, we supply 2-Methyl-5-Pyrimidinemethanol to critical sectors focused on synthesis and innovation. Below are specialized industrial application scenarios, elaborated according to actual manufacturing practices and compliance requirements.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ 2-Methyl-5-Pyrimidinemethanol as a core intermediate in the synthesis of targeted pyrimidine-based APIs. It serves as a precursor in stepwise production of specific antiviral, antitumor, and central nervous system active pharmaceuticals, where its structure supports selective substitutions. Chemical engineers optimize process parameters based on the desired final molecule, ensuring high conversion yield, controlled impurity profiles, and traceability. Downstream, downstream synthesis stages utilize this intermediate in acylation, alkylation, or cyclization steps, leading to APIs intended for regulated markets including the US, EU, and Japan.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP)
    • EU Directive 2011/62/EU on Falsified Medicines
    • USP, EP, and JP pharmacopoeial requirements (where applicable to the product class)

    Typical usage ratio

    • 0.5-5.0 molar equivalents per batch, adjusted based on stoichiometric requirements and side reaction minimization strategies

    Downstream process integration

    • Loaded directly into the reaction vessel at the intermediate stage, following initial base structure assembly
    • Often introduced with an alkylating or acylating agent under controlled temperature and inert atmosphere
    • Purified through crystallization or preparative chromatography before proceeding to subsequent API synthesis stages

    Final product types

    • Cytostatic drugs (e.g., select nucleoside analogs)
    • Antiviral medications targeting RNA/DNA polymerase
    • Intermediate compounds supplied for secondary synthesis routes

    2. Agrochemical R&D and Formulation

    Leading agrochemical producers integrate 2-Methyl-5-Pyrimidinemethanol in the development of new active ingredients and optimized lead compounds for herbicides and fungicides. The functionalized pyrimidine ring facilitates custom derivatization by the R&D lab, enabling modulation of molecular activity and environmental stability. This raw material appears in early lead generation workflows, later in pilot plant trials, and in some approved products as part of multistep scale-up. Process teams closely monitor residue profiles and metabolite pathways as required by agricultural regulatory bodies, assuring field application safety and compliance.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • Regulation (EC) No 1107/2009 on Plant Protection Products (EU)
    • EPA 40 CFR Parts 150–189 (US pesticide regulations)
    • ISO 9001:2015 Quality Management System for production records

    Typical usage ratio

    • 5–20% w/w relative to the total input material in active compound synthesis, depending on targeted yield and substitution efficiency

    Downstream process integration

    • Initiated at the lead optimization or derivatization stage in the laboratory
    • Used in multistep synthesis before final molecular coupling or esterification
    • Isolated through phase separation or solvent extraction, then assayed for purity and reaction byproducts

    Final product types

    • Pyrimidine-based herbicide actives
    • Fungicide intermediate stock solutions
    • Lead compounds submitted for regulatory field trial approval

    3. Fine Chemicals & Specialty Synthesis

    Chemical manufacturers in the fine and specialty segment utilize 2-Methyl-5-Pyrimidinemethanol to create advanced intermediates for dyes, optical brighteners, and analytical reagents. Its reactive positions enable selective functional group attachments critical to brightness tuning, chromophore modification, or analytical specificity. Analytical chemists frequently demand high-purity lots with traceable batch history, particularly when the resultant products enter regulated or high-precision applications. The substance plays a key role in both pilot and multi-ton scale batches, where conversion and byproduct management remain central to plant throughput strategies.

    Industry compliance standards

    • ISO 9001:2015 Quality Management (traceability, documentation)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • Specialty industry customers may request certification to ISO 14001 Environmental Management System

    Typical usage ratio

    • 2.0–8.0% by weight of batch formula, fine-tuned according to target molecule’s chain length and final molecular mass

    Downstream process integration

    • Processed through condensation or alkylation reactions within jacketed vessels, temperature- and atmosphere-controlled
    • Often subjected to post-reaction distillation to recover unreacted starting material and limit contamination
    • Final intermediates isolated by liquid-liquid extraction or membrane filtration

    Final product types

    • Optical brighteners for specialty plastics and paper
    • Analytical standards for chromatography or spectroscopic validation
    • Advanced dye components for textile and imaging sectors

    4. Custom Key Starting Material (KSM) Manufacturing

    Producers in the contract synthesis and custom API markets use 2-Methyl-5-Pyrimidinemethanol as a Key Starting Material (KSM) for exclusive syntheses. These projects typically require strict process documentation, change control, and analytical method validation per client submission. The substance supports controlled multi-step transformations in the custom synthesis pipeline, allowing for site-specific functionalization and the preparation of rare or proprietary intermediates. These operations focus on reproducible reaction profiles, minimal impurity co-elution, and traceable supply chain records as required by end-pharmaceutical or biotechnology clients.

    Industry compliance standards

    • GMP requirements per ICH Q7 for KSMs used in API synthesis
    • US DMF (Drug Master File) registration as required by end-customers
    • Full cGMP traceability (batch production records, chain of custody, impurity tracking)

    Typical usage ratio

    • 0.8–3.0 molar equivalents per reaction stage, adjusted to provide excess only where justified by downstream conversion rates

    Downstream process integration

    • Charged at early or midpoint in proprietary synthesis route, via in-cell addition or automated dosing
    • Intermediates subjected to column purification or preparative HPLC depending on final client specification
    • Batch output segregated and documented to align with client regulatory submissions

    Final product types

    • Pharma-registered intermediates for custom APIs
    • Proprietary building blocks for advanced research compounds
    • High-purity intermediates for biotechnology pilot and scale-up projects
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    Certification & Compliance
    More Introduction

    Introducing 2-Methyl-5-Pyrimidinemethanol: Practical Applications and Insights from a Manufacturer’s View

    Understanding 2-Methyl-5-Pyrimidinemethanol

    Direct chemistry starts on our production floors, not in a textbook. Every batch of 2-Methyl-5-Pyrimidinemethanol (2M5PMOH) that leaves our reactor reflects hard-earned lessons, practical experience, and ongoing investment in reliable processes. Over the years, we have improved our methods to bring consistent high-purity material to customers who work in fields ranging from API synthesis to diagnostics research. As manufacturers who shoulder these daily challenges, we see our job as more than producing a finished product: we drive performance, manage emissions, and innovate safety. The specs are important, but the story of every kilogram synthesized says even more about a chemical’s actual place in industry.

    Physical and Chemical Characteristics

    Let’s dig into the product itself. 2-Methyl-5-Pyrimidinemethanol doesn’t just sit on a warehouse shelf; it exists as a fine, off-white solid with reliable solubility in various polar solvents—this means easy incorporation into typical lab or production-scale protocols. Our standard batches maintain a purity level above 99.0% by HPLC, and we regularly validate this through trusted third-party analytic methods. Ensuring low water content (measured by Karl Fischer titration) and tight control of trace metals stems directly from how our reactors operate and how we condition the raw materials. These details matter because even minor impurities can throw off downstream reactions, particularly those that build upon the pyrimidine ring.

    To put it plainly: 2M5PMOH’s structure (the methyl group at the 2 position, the methanol chain at the 5 position) makes it reactive in ways that are simply unavailable with related pyrimidine alcohols or simple pyrimidine derivatives. Our operators work on these differences every day, managing temperature ramps, reaction kinetics, and purification columns to keep impurities at bay. This hands-on vigilance ensures reproducibility for customers who can’t tolerate variation between lots.

    How 2-Methyl-5-Pyrimidinemethanol Finds Value in Real Application

    There’s a reason major pharmaceutical and research labs ask for this compound by name. The methyl and hydroxymethyl substitutions allow users to introduce the pyrimidine core into a variety of chemical frameworks, especially where classic 5-methylpyrimidine or unsubstituted pyrimidine won’t perform. As manufacturers, we’ve seen repeat orders for projects developing kinase inhibitors, viral RNA analogs, and custom oligonucleotide intermediates. Synthesis teams want precise control over functional group placement and use the methyl/hydroxymethyl pattern to open new reaction sites, particularly where mild conditions or selective alkylations are desired. The compound’s clear path for downstream modification saves time, cuts unnecessary protection/deprotection steps, and sidesteps bottlenecks that frequently slow drug development.

    In laboratory-scale work, chemists make use of 2M5PMOH's reliable crystallinity for easy purification by recrystallization or chromatography, and the material handles storage well under inert atmosphere at ambient temperature. We sometimes get questions about stability, and from practical experience, the batches we store properly have shown little degradation over a year’s time, as long as they are protected from moisture and direct sunlight. Our own procedures reflect this knowledge, favoring glass containers and sealed packs to prevent cross-contamination during storage and shipping.

    What Sets Our Manufacturing Approach Apart

    We get routine samples from producers around the world for competitive benchmarking, and too often, glaring differences in purity, color, and metal content turn up. The source of these problems rarely shows up in a data sheet. We trace it to things like poor pH control in the key methylation stage, lack of attention during the methanol functionalization, or outdated drying procedures. Our approach prioritizes reactor cleanliness, continuous monitoring, and using qualified staff with enough training to notice small anomalies during processing.

    It’s not about “meeting customer requirements” as an abstract goal, but about knowing that poorly controlled residual solvents or mismanaged oxidation steps can ruin downstream productivity for scientists counting on each delivery. From experience, we’ve learned that regular batch consistency brings more repeat customers than beating generic price targets. Tighter impurity profiles also translate into more reliable analytical results and less troubleshooting for our customers.

    We have found that many buyers compare 2M5PMOH to alternatives like 4-methylpyrimidine or unsubstituted 5-pyrimidinemethanol, but the presence of both methyl and methanol side chains brings unique reactivity. For example, during C–N coupling reactions, that methyl group at C2 often blocks unwanted side reactions that otherwise complicate purification in more symmetrical pyrimidine derivatives. These small differences guide experienced chemists toward reliable scale-up and cleaner final products, explained not by a number from a catalog but from first-hand accounts in their own process notes.

    Practical Knowledge from the Floor

    Our technicians understand more than just the recipe. For example, we modified our quench procedure several years back after a run produced unexpected color impurities and low yield from a moisture-laden batch of starting material. The fix came from listening to seasoned operators who noticed a characteristic odor and viscosity change in the solution, signaling unwanted byproducts. We later confirmed through analysis that improved inert gas flow and a gentler quenching protocol not only boosted yield but reduced formation of colored tars detectable on TLC and LC-MS.

    This attention to detail doesn’t make it to glossy catalogs. It results from real-time troubleshooting and knowing the impact of each parameter from practical experience. Keeping water content below 0.1% has proven critical to avoiding side reactions, particularly for customers pursuing nucleoside synthesis. It’s these technical nuances that reinforce trust in a manufacturer with actual production track records rather than a trading interface.

    Applications: Going Beyond the Data Sheet

    As a real-world input, 2M5PMOH enables synthesis of building blocks for nucleic acid analogs and advanced heterocycles. Its two functional handles (methyl at C2, methanol at C5) give it value for researchers tailoring new chemotypes aimed at antivirals, CNS drugs, and other biologically active molecules. We’ve seen requests from teams developing new prodrugs, fluorinated analogs, and molecules for fluorescence-labeled research agents. The combination of electronic properties from the pyrimidine core with steric modulation at the reactive sites means this material remains relevant across evolving drug discovery platforms.

    In addition, we’ve heard from polymer chemists exploring pyrimidine-based scaffolds for advanced materials, crediting 2M5PMOH's ready derivatization. One recent example included multi-step alkylation work, initiated at the methanolic function, followed by chain elongation and further substitution. These reactions would become tedious or even impossible with more heavily substituted or oxidized pyrimidines.

    Analytical scientists working on GMP processes have highlighted our product’s lot-to-lot consistency as cutting down on unnecessary requalification steps. They prefer material with trace metals below 10 ppm and low residual solvent levels, achievable through vigilant vacuum stripping and rigorous solvent change procedures repeated with every batch. This is not abstract talk; it comes from responding to feedback tied directly to analytical failures and project timeline delays caused by inconsistent raw inputs.

    Safety and Environmental Commitment from a Manufacturer’s Perspective

    Daily production brings practical challenges beyond purity. Safe handling of 2M5PMOH takes precedence at every stage—paying close attention to dust formation during charging and sampling limits cross-contamination, and protected storage under inert conditions preserves product quality. Our production line operates with closed-system transfers and proper air filtration, not only protecting operators but ensuring minimal environmental release.

    From a regulatory standpoint, we never shortcut waste management. Residual solvent recovery, in-line scrubbers for exhaust streams, and correctly segregated aqueous washes all play a part in lowering our production footprint. Because customers increasingly ask for traceability and assurance regarding sustainable practices, we have gone the extra mile by recovering mother liquors when feasible, training each operator fully, and validating cleaning of glassware and equipment with robust analytical checks. These actions are more than compliance—they form the fabric of daily chemical production.

    Continuous Improvement and Feedback Loops

    Feedback from long-term users has shaped ongoing tweaks in our process. A few years ago, customer complaints about isolated crystal color led us to reevaluate not only solvent purity but also the washing protocols and drying temperatures. We found that a slightly lower final drying temperature, combined with a higher flush of dry nitrogen, sharpened the final color and reduced trace decomposition products, even in bulk batches exceeding 50 kg.

    Our team believes that honest, two-way technical dialogue with users gives clearer answers than long lists of untested claims in a product catalog. Many solutions to customer headaches—such as increasing impurity control during extended storage, making available custom batch sizes, or providing technical documentation about stability—come straight from these real-world conversations, not from a marketing playbook. The same applies to how we handle complaints or rush orders: recognizing that researchers face volatile project timelines, we keep buffer inventory of pure material, and communicate clearly about batch availability without hedging.

    Comparisons to Other Pyrimidine-Based Intermediates

    Markets offer a wide selection of pyrimidine derivatives, but close inspection quickly splits solid performers from the run-of-the-mill. For instance, simple pyrimidinemethanol lacks the blocking power at the 2-position, leaving it more susceptible to nonselective substitution. Others try to modify 5-methylpyrimidine with post-synthetic oxidation, but the resulting mixtures and harsher conditions usually complicate purification, raising overall project costs.

    Reactive sites positioned just one atom apart, as seen in 2M5PMOH, can be a blessing or a curse—depending on who produces the chemical. In skilled hands, its two-pronged reactivity shortens synthesis routes and adds options for building up more elaborate heterocyclic systems. Factory mistakes, such as uncontrolled reaction exotherms or impure water usage, often show up in colored, off-odor batches that create headaches for users. Our experience with such quality disparities motivates us to invest not only in better analytical control, but also in real-time monitoring and smarter scheduling to avoid carrying over equipment residues between runs.

    Batch Traceability and What It Means for Users

    Traceability may sound plain, but on the factory floor, it spells relief for customers during regulatory inspections or whenever troubleshooting becomes necessary. For 2M5PMOH, we keep every batch logged by date, operator, and raw material lot. If a user ever finds an anomaly, pulling detailed records gives faster answers. Overlooked details—like minor changes in solvent grade or subtle shifts in temperature profiles—get picked up because we systematically cross-check process charts before product release. This way, customers never face delays due to lack of documentation.

    Feedback regularly mentions how much time and stress this kind of accountability saves for laboratories working on GMP-regulated projects or sensitive process development where paperwork matters as much as pure material. This real commitment to product stewardship—both documentation and human expertise—beats automation-driven, price-slashing operations that never see their chemical in action on the bench or in scaling up a pilot reactor.

    A Manufacturer’s Relationship with Customers: Building Trust, Not Just Filling Orders

    Chemical manufacturing teaches humility and attention to detail. Technical teams who talk with customers about synthetic challenges or batch-specific hurdles develop genuine trust. We’ve seen development chemists share project details—in strict confidence—to get advice on modifying late-stage functionalization strategies. These relationships mean we sometimes adjust granularity or supply solvent-free material to serve each unique downstream application.

    Real dialogue solves more problems than one-way order fulfillment. Clients tackling troublesome reactions or tight development windows come back to us, not because they read a fancy brochure, but because batches from our lines have proven themselves under stress. The best reputation doesn’t come from claims—it comes from being able to provide samples, answer detailed technical questions, and adjust our process to deliver the specific impurity profile or particle format a client needs to unlock their chemistry.

    Forward Outlook: Anticipating Technical Needs in a Dynamic Marketplace

    Trends in pharmaceutical research push demand for cleaner, more tailored intermediates. We see requests for 2M5PMOH with narrower impurity cut-offs, sometimes with a focus on specific stereo- or regioisomers in a series. Our R&D team has begun piloting micro-flow reactor upgrades to allow for better heat management, continuous processing, and easier containment of any exotherms that risk product quality. These investments stem from measured evaluation of both problems and feedback from experts who need quicker ramp-up to pilot scale.

    Customers with specialty demands have inspired modular packaging strategies, improved inert gas blanketing, and tighter batch size control. None of these practices come from a one-size-fits-all approach; they represent lessons collected over years of listening, adapting, and observing where value is truly delivered in practice—not in theory. Every kilogram of 2M5PMOH shipped integrates not just chemical know-how but a real partnership with those who transform raw materials into life-changing products.

    Conclusion: The Real Value in Real Experience

    As a manufacturer, our perspective on 2-Methyl-5-Pyrimidinemethanol comes from lived experience, not marketing scripts. Every challenge—be it a scale-up safety review, receipt of a confusing customer complaint, or the refinement of an aging reactor protocol—teaches us how to refine and improve both product and process. Through close engagement with researchers, process developers, and procurement specialists, we’ve learned what matters most: reliability, openness, and practical advice. Beyond paperwork and numbers, the true worth of a manufacturer’s chemical lies in how it performs in end-users’ hands, project after project. Our track record with 2M5PMOH bears out these lessons, and we look forward to expanding them in partnership with those who value quality informed by real manufacturing experience.