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2,4,6-Trichloro-5-Methylpyrimidine

    • Product Name 2,4,6-Trichloro-5-Methylpyrimidine
    • Alias 2,4,6-Trichloro-5-methylpyrimidine
    • Einecs 211-522-7
    • 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

    789197

    Cas Number 1780-35-4
    Molecular Formula C5H2Cl3N2
    Molecular Weight 213.45 g/mol
    Appearance White to off-white solid
    Melting Point 68-70°C
    Boiling Point 282°C
    Density 1.59 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms 2,4,6-Trichloro-5-methylpyrimidine

    As an accredited 2,4,6-Trichloro-5-Methylpyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a tight-seal cap, labeled "2,4,6-Trichloro-5-Methylpyrimidine," includes hazard and handling information.
    Shipping 2,4,6-Trichloro-5-Methylpyrimidine is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled as a hazardous chemical, following all applicable regulations. Shipping must comply with local, national, and international guidelines for hazardous materials to ensure safe transport and prevent accidental exposure or environmental contamination.
    Storage 2,4,6-Trichloro-5-Methylpyrimidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure storage area is equipped for handling hazardous chemicals and labeled appropriately. Avoid contact with skin and eyes, and store in accordance with all local regulations and guidelines.
    Application of 2,4,6-Trichloro-5-Methylpyrimidine

    Applications of 2,4,6-Trichloro-5-Methylpyrimidine in Industrial Manufacturing

    2,4,6-Trichloro-5-Methylpyrimidine serves as a key intermediate in specialized chemical manufacturing streams. Our production focus supports leading sectors through stringent process control, ensuring safety, compliance, and consistent supply. Our global customers in life science, advanced materials, and specialty synthesis integrate this compound under controlled conditions to drive their product development pipelines.

    1. Agrochemical Active Ingredient Synthesis

    Major pesticide and herbicide manufacturers select this intermediate for chlorinated pyrimidine-based molecules. During multi-step synthesis, our material supports the assembly of selective herbicides and crop protection agents targeting specific weed resistance. Quality control emphasizes isomer purity and batch traceability to ensure downstream product consistency.

    Industry compliance standards

    • ISO 9001-certified quality management systems
    • REACH registration compliance (EC 1907/2006)
    • U.S. EPA regulations for pesticide actives (FIFRA)
    • FAO/WHO specifications for technical materials

    Typical usage ratio

    • Normally 0.3–1.2 molar equivalent in stepwise condensation or cyclization reactions
    • Exact ratio determined by the targeted agrochemical structure and impurity profile of starting materials

    Downstream process integration

    • Initial chlorination/coupling in API block synthesis
    • Reagent in nucleophilic substitution for structure modification
    • Precursor blend in batch or continuous flow synthesis units

    Final product types

    • Selective herbicides, especially for cereals and rice
    • Insect growth regulators
    • Fungicidal actives for seed treatment
    • Weed control premixes

    2. Pharmaceutical Intermediate for Antiviral and Antineoplastic Agents

    The pharmaceutical sector applies this material in pyrimidine core modifications when synthesizing nucleotide analogues and kinase inhibitors. Strict process analytical techniques monitor impurity carryover to meet international API standards. Our engineers focus on specification controls that reflect the criticality of this raw material at early synthesis stages.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • USP/Ph. Eur. standards for intermediate traceability
    • DMF submission standards (US FDA/CFDA)
    • ISO 13485 where used for medical-grade compounds

    Typical usage ratio

    • 0.5–1.0 molar equivalent during nucleophilic aromatic substitution
    • Adjusted based on target molecule and desired conversion, considering potential side product formation

    Downstream process integration

    • Stepwise halogen exchange for side-chain installation
    • Direct coupling in heterocycle extension
    • Recrystallization and purification before final API assembly

    Final product types

    • Antiviral drug intermediates (e.g., for HIV and HCV compounds)
    • Oncology small-molecule drug scaffolds
    • Pyrimidine-based enzyme inhibitors
    • Proprietary drug candidates in clinical development

    3. Dye and Pigment Intermediate Synthesis

    Colorant producers employ this pyrimidine derivative to introduce chlorinated aromatic features in specialty dyes. The controlled addition enables tunable shade and stability for high-performance colorants. Purity and lot homogeneity remain essential for ensuring reproducible product color and fastness.

    Industry compliance standards

    • Oeko-Tex Standard 100 (where applicable for textile dyes)
    • ISO 9001 QMS for pigment manufacturing
    • EU REACH Annex XVII for dye safety
    • EN 71-3 safety for pigments in toy coatings

    Typical usage ratio

    • 2–8% by mass in the primary dye coupling reaction
    • Range varies with final chromophore complexity and application (ink, fabric, plastic resin)

    Downstream process integration

    • Chlorinated building block for azo or anthraquinone dyes
    • Monomer coupling for pigment backbone assembly
    • Co-feeding with aniline or phenol derivatives during batch processing

    Final product types

    • Specialty textile dyes
    • High-lightfast pigments for plastics and inks
    • Color masterbatches for synthetic fibers
    • Industrial coatings for automotive and consumer goods

    4. Specialty Coating and Polymer Modifier Synthesis

    Advanced materials producers incorporate this compound for creating crosslinked or halogenated resin modifiers. Its chlorinated heterocycle integrates into pre-polymer streams to adjust thermal and chemical resistance in specialty coatings and engineered plastics. Formulation parameters account for stability, reactivity, and end-user performance standards.

    Industry compliance standards

    • ISO 14001 for environmental management in production
    • US EPA TSCA (Toxic Substances Control Act) inventory listing
    • EN 13501-1 flame retardancy standards (coating applications)
    • RoHS directive (for electronic and electrical components)

    Typical usage ratio

    • 0.2–2.0% by weight of total monomer/polymer batch depending on target property enhancement
    • Ratio tailored to desired degree of crosslinking or chlorination

    Downstream process integration

    • Chain-extension in resin prepolymer stage
    • Halogen donor in reactive extrusion or batch curing
    • Blending in solvent-based coating formulations

    Final product types

    • Halogen-modified epoxy and polyester resins
    • High-durability industrial floor coatings
    • Electronics encapsulation compounds
    • Fire-resistant thermoplastic finishes

    5. Veterinary Active Intermediate Manufacture

    Veterinary pharmaceutical producers use this pyrimidine in the synthesis of animal health actives, especially for compounded antiparasitic agents. This raw material enters multi-step active ingredient routes, where batch traceability and regulatory documentation are integral to supply chain compliance and regional market access.

    Industry compliance standards

    • VICH GL Technical Guidelines (Good Manufacturing Practice for APIs in veterinary use)
    • EMEA/CVMP Active Substance Master File procedures
    • US FDA 21 CFR 514.1(b) (veterinary drug ingredients)
    • GMP+ for feed additive supply (where applicable)

    Typical usage ratio

    • 0.4–1.1 molar equivalent in the key cyclization or halogenation step
    • Adjustment governed by impurity target and yield optimization for animal drug actives

    Downstream process integration

    • Initial ring closure for heterocyclic actives
    • Functionalization step for prodrug derivatives
    • Incorporation in final amide or ester linkage stage

    Final product types

    • Anthelmintic and antiparasitic veterinary actives
    • Compounded animal feed medicaments
    • External lice and mite control solutions
    • Veterinary suspension concentrates
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    Certification & Compliance
    More Introduction

    2,4,6-Trichloro-5-Methylpyrimidine: A Reliable Choice for Modern Synthesis

    At our plant, 2,4,6-Trichloro-5-Methylpyrimidine represents the culmination of years of experience in heterocyclic compound production. Our staff understands the pivotal position this compound holds in the fine chemical sector, particularly for pharmaceutical intermediates and advanced agrochemical applications. Every batch we deliver attests to careful control, stringent testing, and a deep respect for the process from raw material selection right down to final packaging.

    Product Profile

    The chemical structure of 2,4,6-Trichloro-5-Methylpyrimidine leads to an array of reactivity options. Three chlorine atoms at the 2, 4, and 6 positions on the pyrimidine ring, paired with a methyl group at position 5, offer unique versatility. Our production adheres to strict quality benchmarks. By overseeing every step from chlorination to purification, we deliver a product that supports pharmaceutical and crop-protection chemistry with consistent chlorine substitution patterns and minimal impurity levels.

    Material is presented as a white to off-white crystalline solid, sometimes slightly beige, depending on lot size and analytical finish. Nothing escapes our eye during inspection. Our technical teams check for moisture, residual solvents, and unwanted chlorinated byproducts so that our 2,4,6-Trichloro-5-Methylpyrimidine meets typical assay standards of >98.0% purity. We regularly field requests to dial in particle size for specific end-use scenarios and carry out supplementary drying for moisture-sensitive synthesis. These touches may seem small, but they reflect our steady, methodical approach.

    Model and Specifications

    We manufacture for both standard and custom volumes, supplying from kilograms to development-scale lots for multinational partners tackling new active ingredient discovery. Common lots run in the 25 kg fiber drum, with smaller pack sizes available for those in method development or pilot landscapes. Our own control lab checks each lot for melting point, content by HPLC, and acid-base titration, and we log every data point for full traceability.

    Handling a material like this demands close attention to shelf-life. Even with the best storage practices, hydrolysis can occur if residual water isn’t managed at every stage. For that reason, we seal our packages in moisture-barrier liners, tracking each lot’s storage conditions right from production to transit. Fine chemical users see fewer losses and greater confidence in their results with this step. We don't shy away from tough questions about shelf-life, solubility in varied media, or compatibility with downstream reactants. Over the years, customer feedback allowed us to reduce typical trace impurity levels that can interfere with downstream conversions, especially when constructing more complex molecules.

    Expertise in Usage and Application

    In practice, chemists rely on 2,4,6-Trichloro-5-Methylpyrimidine for nucleophilic aromatic substitution reactions, targeting agrochemical intermediates, pharmaceutical scaffolds, and high-value dyes. Our experience covers process-scale preparation of aryl ether, amine, and thioether derivatives, each requiring a clean source of pyrimidine. The multiple chloro groups mean customers can selectively substitute positions under controlled conditions, enabling stepwise functionalization strategies in heterocyclic drug design.

    Another aspect stems from our knowledge of process safety. This compound, being reactive, puts special pressure on batch operators during handling and charging. We have fine-tuned our containment and ventilation protocols so that both the product and the people involved receive proper protection. Our own operators use full-face shields and advanced ventilated enclosures, and we offer customers the results of our hazard analyses to inform their own SOPs. This covers everything from dust control to first-aid provisions. Our goal remains unchanged: keep people safe, keep the product stable, and honor the chemistry.

    In crop science, users prize 2,4,6-Trichloro-5-Methylpyrimidine for constructing new herbicide candidates. The presence of both electron-withdrawing chloro and electron-donating methyl groups leads to a scaffold primed for further selective modification. In our experience, formulating precursors to active substances works best with controlled reactivity, and we built redundancy into our QC to catch any unpredictable contaminants.

    What Makes This Product Distinct

    We often discuss why chemists move toward 2,4,6-Trichloro-5-Methylpyrimidine despite the existence of related pyrimidines. The answer sits in the unique substitution pattern, which creates a platform for synthesis where stepwise nucleophilic attacks achieve high selectivity. Compounds such as 2,6-Dichloropyrimidine lack that third chlorine, which closes off transformation at position 4, reducing the number of substitution options. With the methyl group added, the molecule exhibits improved properties for downstream reactions, especially in designing physiologically active ingredients.

    Technical staff in our plant compared process runs between 2,4,6-Trichloropyrimidine without the methyl group and our flagship 2,4,6-Trichloro-5-Methylpyrimidine. They saw greater control over regioselectivity and easier purification of final target molecules with the methyl derivative. Customers working in late-stage API discovery confirm that this compound provides unmatched versatility, especially during milligram-to-ton scale up.

    In areas such as pharmaceutical development, minute changes in precursor structure can shift the biological profile of a finished product. We work closely with R&D scientists who need assurance on both purity and structural correctness. Our in-house NMR and mass spectrometry teams confirm the integrity of each batch. By cutting down on byproducts, we save our clients time on chromatographic purification, translating to faster pilot runs and less solvent lost downstream.

    From Factory Floor to R&D Pipeline

    Our operators value regular hands-on training. We don’t rely solely on technical bulletins; direct experience running multiple high-precision tasks is what delivers reproducible batches. From prepping glass-lined reactors to staged feed addition during chlorination, every check and recheck underpins a final product that chemists can trust. Our engineers reinforce protocols with root-cause analyses after every deviation or unusual result, always tracing issues back to specific process points. This pursuit of incremental process improvement matches well with the demands on our customers, many of whom operate in highly regulated environments.

    For new entrants into heterocycle chemistry, handling 2,4,6-Trichloro-5-Methylpyrimidine introduces them to the delicate balance between reactivity and stability. We receive frequent inquiries about re-crystallization solvents, safe heating conditions, and optimal base selection for substitution steps. We answer every one by sharing case studies and intervention logs from our own work, not just textbook guidance. This practical advice closes the gap between theory and application.

    Meeting Today's Industry Challenges

    Many downstream users now face pressure to reduce waste, eliminate persistent contaminants, and ensure fully documented provenance of all source materials. Over the past decade, we have invested in cleaner reaction technologies and moved away from less-efficient chlorination reagents. We now deploy closed-loop systems that recycle solvents and reduce off-gassing, with scrubbers built in at every vent. Customers seeking certifications or compliance documentation receive detailed breakdowns of batch history, and our approach has drawn positive remarks from third-party auditors.

    Sustainability targets in the fine chemical sector dovetail with regulatory trends worldwide. Our site maintains a robust environmental monitoring system. We log all inputs and waste outputs, working to lower chlorinated waste streams below commonly accepted benchmarks. This aligns our in-house targets with the growing demands for transparency and responsible sourcing in the chemical industry.

    The need to demonstrate traceability has never been higher. Our digital recordkeeping provides a transparent chain of custody for every production batch of 2,4,6-Trichloro-5-Methylpyrimidine. As new regulations appear in lead markets, we adjust procedures to account for batch notification, so our partners stay compliant. With every lot, clients see a full batch history and certificate list, along with impurity profiles, all directly accessible for audits.

    Challenges and Solutions in Quality Assurance

    Delivering material that meets rising standards means we must stay ahead of potential contamination sources. One common issue centers on maintaining batch-to-batch consistency, especially with complex heterocyclic systems. Our plant upgraded analytical instruments for real-time monitoring, allowing earlier intervention in the event of process drift. If a lot falls outside control limits during the synthesis of 2,4,6-Trichloro-5-Methylpyrimidine, we investigate root causes and halt production long before dispatch.

    Another challenge surrounds storage stability. Over time and under less-than-ideal transport conditions, the fine crystals of this compound can absorb moisture leading to hydrolysis. We combat this by implementing advanced desiccant liners, using only inert gas for shipment, and keeping everything in climate-controlled storage. Years of experience show us that keeping close tabs on residual moisture keeps downstream users from running into surprises during scale-up.

    Impurity control remains top priority. Many users require ultra-pure starting materials to avoid adverse effects in synthesis, especially during high-throughput screening or regulatory dossier assembly. Our staff carries out methodical impurity tracking, going beyond standard chlorinated contaminants to search for unknowns by high-resolution mass spec. When we spot a new peak, we report, investigate, and share findings with our most demanding clients, helping guide their own risk assessments.

    Industry Dialogue and Knowledge Sharing

    Our history in pyrimidine chemistry means we have picked up a few lessons about what makes a difference for customers. Not just the technical identity of the product, but the lived reality of consistent supply, clear answers to technical queries, and readiness to collaborate in process trouble-shooting. In the world of process chemistry, surprises and bottlenecks happen. Our teams stay available to talk through modification steps, address purification snags, and advise on waste disposal options for spent pyrimidines. Customers frequently ask about optimal substitutions and reagent compatibility; our chemists enjoy the chance to get into the details, always building on their direct lab experience rather than generic answers.

    The value of human expertise cannot be overstated. Our technical support stretches beyond paperwork. Chemists call in to reach people who know the quirks of 2,4,6-Trichloro-5-Methylpyrimidine: its behavior under different nucleophilic conditions, safe routes for upscaling, best solvents for dissolution, and pitfalls to avoid in downstream use. We gather these experiences into training modules for both our staff and interested partners, keeping expertise alive and available.

    An Eye Toward the Future

    Driving toward higher-quality synthetic intermediates, the industry sees consistent demand for ever-better technical support, more transparent supply chains, and innovation in process control. We respond with continuous investment in plant upgrades, analytics, and staff training. Tomorrow’s 2,4,6-Trichloro-5-Methylpyrimidine will still come from the same chemical backbone, but cleaner, purer, and backed by an even deeper understanding of end-user needs.

    From our earliest days working with small molecule intermediates, we recognized that a good reputation grows out of many small commitments: listening to those who use the compound every day, responding rapidly when things go wrong, and always looking for ways to push the quality bar higher. Our approach is rooted in decades of cumulative lessons learned—always focused on delivering what matters most to those at the bench and on the factory floor. 2,4,6-Trichloro-5-Methylpyrimidine isn’t just another entry in a catalog. It stands as a testament to meticulous manufacturing, transparent partnership, and a shared pursuit of better science.