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4-Amino-5-Chloro-2,6-Dimethylpyrimidine

    • Product Name 4-Amino-5-Chloro-2,6-Dimethylpyrimidine
    • Alias 4-ACDP
    • Einecs 217-681-3
    • 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

    995899

    Product Name 4-Amino-5-Chloro-2,6-Dimethylpyrimidine
    Cas Number 35686-84-5
    Molecular Formula C6H8ClN3
    Molecular Weight 157.6 g/mol
    Appearance White to off-white solid
    Melting Point 163-167°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 5-Chloro-2,6-dimethyl-4-aminopyrimidine
    Chemical Structure C1C(=NC(=C(N1N)Cl)C)C

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

    Packing & Storage
    Packing Sealed 100g amber glass bottle with tamper-evident cap, labeled with chemical name, hazard symbols, batch number, and handling instructions.
    Shipping **Shipping Description:** 4-Amino-5-Chloro-2,6-Dimethylpyrimidine should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must comply with local, national, and international regulations for chemical transport. Appropriate labeling and documentation are required, and the package should be handled by trained personnel using suitable personal protective equipment (PPE).
    Storage Store 4-Amino-5-Chloro-2,6-Dimethylpyrimidine in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture, heat, and direct sunlight. Properly label the storage container, and avoid exposure to dust. Follow all relevant safety guidelines for handling and storing chemical substances.
    Application of 4-Amino-5-Chloro-2,6-Dimethylpyrimidine

    Applications of 4-Amino-5-Chloro-2,6-Dimethylpyrimidine in Industrial Manufacturing

    4-Amino-5-Chloro-2,6-Dimethylpyrimidine supports multiple downstream industries through its role as a core intermediate. As the direct manufacturer, we supply this compound for precise use in regulated industrial synthesis streams. Below are the main application scenarios with industry-specific process and compliance details.

    1. Pharmaceutical Intermediate for Antiviral API Synthesis

    This material functions as a critical intermediate in the multi-step process of producing select pyrimidine-based antiviral active pharmaceutical ingredients. In such applications, customer processes integrate the compound during nucleoside modification stages, where its aminated ring structure facilitates coupling reactions. Pharmaceutical customers monitor lot traceability and set high purity benchmarks to align with strict market authorization requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) standards for API intermediates
    • EU EudraLex Volume 4 GMP guidelines
    • China Pharmacopoeia (ChP) mandates for intermediate control

    Typical usage ratio

    • Usage ranges from 0.8 to 1.15 molar equivalents per reaction batch, with ratio adjusted based on downstream chain extension length and targeted impurity profile.

    Downstream process integration

    • Added during alkylation or amidation steps following initial pyrimidine scaffold formation, usually after solvent exchange and catalyst introduction under nitrogen protection.

    Final product types

    • Antiviral small molecule APIs such as acyclovir derivatives
    • Pharmaceutical grade pyrimidine nucleoside analog intermediates
    • Finished dosage antiviral formulations

    2. Agrochemical Active Ingredient Synthesis

    Several agrochemical companies use this compound in the manufacture of selective herbicides and fungicidal agents. It typically reacts during the penultimate stage in pyrimidine synthesis schemes, where the presence of the chloro substituent enables regioselective substitution, key for creating target-active structures. Process control emphasizes residue testing and adherence to agricultural input regulations for raw material sources.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agrochemical Production
    • REACH registration and safety documentation (Europe)
    • China Ministry of Agriculture GB standards for pesticide intermediates

    Typical usage ratio

    • Typically 1.0 to 1.3 equivalents per batch, varied depending on the desired substitution pattern in final compound and batch scale-up kinetics.

    Downstream process integration

    • Enters after halogenation and before final condensation or cyclization, often under mild acidic conditions and with in-process QC for unreacted amine content.

    Final product types

    • Selective herbicides (e.g., pyrimidine-based acetolactate synthase inhibitors)
    • Fungicide precursors
    • Formulated crop protection chemicals

    3. Dye and Pigment Synthesis

    Within the specialty dye sector, formulators include our pyrimidine derivative as a building block for synthesizing functionalized azo and heterocyclic dyes. Its electron-rich amine group increases reactivity during coupling, supporting high-performance pigments used in plastics and inks. Compliance with hazardous substance regulations is critical, as is confirmation of absence of forbidden aromatic amines in finished pigment batches.

    Industry compliance standards

    • EU REACH Annex XVII restriction on aromatic amines
    • EN 71-3 for safety of toys regarding migration of certain elements (for pigments in toy applications)
    • ISO 9001 for pigment and dye manufacturing processes
    • GHS labeling and documentation

    Typical usage ratio

    • Typically dosed at 0.5 to 1.0 parts per part of core chromophore, with precise ratio adjusted for desired dye bath reactivity and end-use color intensity.

    Downstream process integration

    • Introduced during either azo coupling or late-stage heterocyclic ring formation, often under aqueous or high-boiling solvent conditions with pH control.

    Final product types

    • High-performance plastic colorants
    • Industrial inks and coatings
    • Textile and fiber-reactive dyes

    4. Intermediate for Veterinary Drug Synthesis

    The compound sees routine use in animal health product manufacturing, particularly in the preparation of pyrimidine-based antiparasitic agents. Synthesis routes leverage the amine and chloro substituents for subsequent modification, typically inserting the compound after heterocycle formation but before side-chain closure. Regulatory checks for veterinary intermediates focus on traceability and purity at each step.

    Industry compliance standards

    • VICH GL10: Good Manufacturing Practice for Veterinary Products
    • Pharmacopoeia of the People's Republic of China (ChP) for veterinary APIs
    • ISO 22593 for quality of veterinary medicines
    • OECD Guidelines for the Testing of Chemicals (veterinary use)

    Typical usage ratio

    • Ratios from 0.95 to 1.05 equivalents, closely managed to limit formation of process impurities and assure consistent conversion yield.

    Downstream process integration

    • Charged during the intermediate stage following pyrimidine ring assembly, before introduction of pharmacophoric side-groups and final condensation.

    Final product types

    • Antiparasitic veterinary actives
    • Finished veterinary suspensions and tablets
    • Bulk intermediates for further formulation

    5. Fine Chemicals for Electronic Materials

    This pyrimidine derivative is used in the electronic chemicals sector. Manufacturers rely on its stable ring system for creating specialized functional monomers and intermediates utilized in liquid crystal display (LCD) alignment layers and photoresist formulations. Integration requires tight control of elemental impurities and batch-to-batch consistency, particularly when targeting optoelectronic grade final materials.

    Industry compliance standards

    • RoHS Directive (EU) for electronic substances
    • IEC 62474 declarable substance requirements
    • ISO 14001 Environmental Management for Electronic Chemicals
    • JIS Q 9100 for electronic device material suppliers

    Typical usage ratio

    • Ranges from 0.2 to 0.6 equivalents, with adjustment for monomer versus oligomer target and batch synthesis size for downstream polycondensation reactions.

    Downstream process integration

    • Used in nucleophilic aromatic substitution to functionalize aryl halides, often as part of a two-step synthesis for monomer preparation under controlled temperature protocols.

    Final product types

    • LCD alignment layer components
    • Photoresist intermediate chemicals
    • Functional monomers for conductive polymer systems

    6. Custom Synthesis for Research and Development Compounds

    Contract research and custom synthesis organizations incorporate this material in small-scale projects targeting new therapeutic or diagnostic entities. The nature of research compounds requires compliance with laboratory-scale handling standards and effective documentation of synthetic routes. Integration details follow sponsor specifications, but typically employ the compound for core scaffold diversification or site-directed functionalization.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025 for laboratory testing and calibration
    • Local R&D legal and safety regulations
    • Material Safety Data Sheet (MSDS) documentation

    Typical usage ratio

    • Ranges from sub-stoichiometric to slight excess (0.5–1.2 equivalents), set according to specific synthetic target, with adjustments for byproduct control and downstream purification requirements.

    Downstream process integration

    • Introduced into target synthesis as a core building block, often at the scaffold construction or ring-extension step; purification and analytical QC follow each major chemical transformation.

    Final product types

    • Experimental pharmaceutical leads
    • Diagnostic chemical entities
    • Synthetic reference standards
    Free Quote

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    Certification & Compliance
    More Introduction

    Exploring 4-Amino-5-Chloro-2,6-Dimethylpyrimidine: More Than Just a Building Block in Modern Chemistry

    At the Core of Synthetic Innovation

    As a manufacturer deeply rooted in the world of pyrimidine chemistry, we’ve worked hands-on with countless molecules. Through decades of research, pilot programs, and volume production, 4-Amino-5-Chloro-2,6-Dimethylpyrimidine has emerged as one of those compounds that keeps earning its place in the development pipeline. Our daily grind involves more than reaction yields or purity numbers—it’s about understanding how each chemical behaves, where subtle structural tweaks open doors, and what the practical needs of formulators really are.

    Molecular Blueprint That Dictates Function

    This compound draws attention for a reason: structurally, it unites a chlorinated pyrimidine core with an amine group sitting at the 4-position and methyl substitutions at the 2 and 6 positions. Such an arrangement matters. Each group influences electron density, reactivity, and solubility, which means the final product isn’t just “another pyrimidine.” The amine activates positions for nucleophilic reactions, while the chlorine offers a handhold for substitution chemistry, and the methyl groups improve lipophilicity—a key consideration for pharmaceutical intermediates.

    We synthesize this compound under controlled atmospheres, using a route that ensures reproducibility and removes by-products at each step. After years of scaling up, we’ve settled on a process that anticipates the questions chemists in drug discovery would ask: Has the product been recrystallized under clean, conditions? Is the batch free from unreacted halogenated by-products? Are the physical properties consistent from drum to drum? We monitor melting point, water content, and color with every lot, because we’ve seen what even trace impurities can do in the next stage of chemical synthesis.

    Where 4-Amino-5-Chloro-2,6-Dimethylpyrimidine Stands Apart

    In the crowded landscape of pyrimidine derivatives, differences often boil down to fine details. We’ve produced chlorinated and methylated pyrimidines with the same basic core but without the amine, and their behavior can be surprisingly different. For instance, without the para-amino group, the molecule loses a key touchpoint for hydrogen bonding, which can change both its solubility in solvents and its ability to serve as a coupling partner in pharmaceutical synthesis.

    We get questions about how this compound performs compared to 2,4,6-Trimethylpyrimidine or 4,6-Dichloro-2-Methylpyrimidine. My team has often seen how the extra methyl at the 6-position in our product isn’t just window dressing—it makes for a more hydrophobic intermediate and often affects crystal form (and, subsequently, filtration speed). Customers aiming to introduce substitutions specifically at the C-5 or C-4 positions have remarked that other substituted pyrimidines just don’t deliver the same result in heterocycle-forming reactions. The amine and chloro positions provide unique reactivity that you do not find in unsubstituted variants.

    Applications Where Precision is Not Optional

    4-Amino-5-Chloro-2,6-Dimethylpyrimidine shows up most often as an intermediate in pharmaceutical research and agrochemical development. We’ve collaborated with teams racing to produce second-generation fungicides, and there, the compound’s dual substitution pattern—chlorine and amine—offers more versatility for constructing complex scaffolds than monosubstituted or unsubstituted analogs. In practice, this means your library of potential actives grows when you start from here. Each functional group serves as a lever. Chlorine provides a reactive center for Suzuki or Buchwald-Hartwig cross-couplings, while the amine can engage in urea, sulfonamide, or amide formation. That dual-point reactivity reduces steps in synthetic routes.

    On the pharmaceutical side, we’ve worked with customers on nucleoside analogues and kinase inhibitors where a quick swap of the amino or chloro substituents tunes the target molecule’s activity profile. You won’t get the same flexibility or speed with 4,6-dichloropyrimidines—they simply don’t provide a direct amine that can enter those condensation reactions.

    There are other sectors where this molecule grows in importance. Material scientists and dye chemists looking for chemical handles that tolerate redox modifications and extreme pH sometimes seek a starting point that behaves reliably under demand. In those cases, 4-Amino-5-Chloro-2,6-Dimethylpyrimidine’s unique substitution pattern stands up to harsh conditions better than its less-protected relatives.

    Reliability and Consistency in Production

    Chemistry can surprise even the most experienced of us, but surprises have no place in commercial manufacturing. Our batches reflect a commitment to consistency. Before releasing a shipment, we run strict HPLC and GC analyses, examine solid-state purity by NMR, and determine water content through Karl Fischer titration. Small changes in crystallinity or residual solvent content might sound minor, but in downstream coupling or modification steps, even a fraction of a percent can derail a reaction or force rework—and no one wants that, whether in milligram, kilogram, or metric ton quantities.

    Batches receive batch-specific certificate of analysis, but the focus always returns to real-life process feedback. We have taken calls from partners stumped by failed scale-ups using material sourced elsewhere, only to find unrecognized by-products present. From our point of view, vigilance means catching batch differences in real time and investing in in-line purification, dry-box handling for the most sensitive requests, and explicit documentation. Reliability becomes more than a tagline; it’s a day-to-day struggle with solvents, glassware, and analytical lists, rooted in the knowledge that someone’s project hinges on these details.

    Supporting Responsible Chemistry

    Environmental and workplace safety considerations guide our methods at each step. We design processes around minimizing solvent waste and recovering starting materials, not just reducing disposal costs but also lessening environmental risk. We staff technicians fully trained in hazard recognition and response, recognizing that both human health and product purity trace back to a controlled shop floor. Chlorinated compounds require care in handling, but our long-term familiarity helps us reduce exposure potential and implement rigorous ventilation, filtration, and spill protocols.

    Nothing frustrates a chemist more than hearing about chlorinated pyrimidine contamination in plant effluent—or facing a regulatory audit over uncontrolled emissions. Even without strict mandates, we have internalized the need to monitor each tank, vent line, and filter waste stream for persistent organics. Our products pass into tough hands: companies conducting multi-ton extraction runs, government labs monitoring residues in water and soil, start-ups whose investors demand green credentials. We welcome collaboration in method development for further down-the-pipe destruction of by-products, always prioritizing safer routes and fully closed operational loops wherever we can.

    Navigating Supply Chain Challenges

    We don’t view ourselves as just another cog—our plant’s role as an original producer means we own both the rewards and headaches of sourcing every kilo of precursor. Markets for 2,6-dimethylpyrimidine and other chlorinated building blocks face periodic disruptions. Climate, regulatory restrictions, and market dynamics make pricing and lead times volatile, sometimes unexpectedly. For buyers relying on spot orders, this unpredictability can mean delays, but strategic partnerships and production forecasting help buffer against most shortages. We openly discuss forecasts with key partners, sharing the reality behind raw material access and turnaround timelines. Transparency in sourcing allows our customers to plan well in advance—and places us ahead of the curve when market shocks hit.

    Achieving steady supply means extending warehouse capacity, dual-sourcing precursors, and walking the fine line between on-hand inventory and cash flow. It’s not glamorous work—yet keeping reactors fed and orders fulfilled separates experienced producers from brokers running on uncertainty and hope. The value of “manufacturer-direct” is more apparent in tough markets—if there’s a failure or constraint, customers reach us without the intermediation or guesswork that comes from disconnected supply chains.

    Quality Versus the “Commodity” Mindset

    Competition from low-cost, high-volume suppliers will always tempt buyers to treat such pyrimidines as commoditized. Our years of producing high-purity 4-Amino-5-Chloro-2,6-Dimethylpyrimidine taught some hard lessons about why price-per-kilo often fails as the only selection basis. Downstream applications—particularly API development or regulated crop protection trials—amplify every upstream mistake, leading to out-of-spec results or audit concerns. We refine our crystallization and drying conditions, test a larger range of potential contaminants, and involve our application chemists in every run.

    Pragmatically, our product costs more than the lowest-cost alternatives, but our customers often report faster, more reliable reaction set-ups, fewer purification headaches, and less rework downstream. Each interaction with technical and procurement teams circles back to one question: will the material show up as ordered, every time, with batch records available and support a call or email away? We know the answer in advance, because we control the entire production lot history and respond directly to every concern.

    Customization Rooted in Daily Experience

    Standard purity levels typically exceed 98 percent by HPLC, but we do not shy away from requests: an extra purification step for a demanding route, custom micronization for a process that struggles with filtration, or unique solvent recrystallization to accommodate a novel formulation. In our view, flexibility arises naturally from intimately knowing the process, not simply tweaking specs on paper. We routinely analyze scale-up notes from customers, propose alternate crystallization solvents, and even invite chemists to observe a pilot batch so they gain real-world confidence.

    Our background in continuous improvement makes us quick to incorporate new analytical techniques, whether it’s handheld spectrometry, automated moisture testing, or more sensitive LC/MS screening. Shaving hours off drying time, trimming percent-impurity, or finding a more stable hydrate form translates to actual performance—less process fuss, higher final yield, and fewer unexpected hiccups. This direct technical support separates seasoned manufacturers from those unable to connect formulation issues to origin.

    Chemical Safety and Compliance—Learning from the Past

    We take compliance standards seriously—not as hurdles, but as lessons written by the hard experiences of the industry. Audits, waste logs, and operator training fill many days, but these practices create the difference between a reliable partner and “unknowns” who may cut corners. We know what it means to answer a regulator facing a cross-border shipment with a full documentation pack—every shipment contains not just the product, but its measured handling, chain of custody, and reporting certified by experts on-site.

    This compound, with its amine and chloro groups, does prompt careful hazard analysis. We maintain clear labeling, fully train material handlers, and run mock drills for spills and exposures. Over the years, prompt action and thorough documentation have headed off incidents that might have grown if left to chance. Echoes of past mishaps across the industry inform our discipline about test batch quarantine and final release only after all checks clear.

    Bringing Research Expertise to Practical Outcomes

    Some chemists prize 4-Amino-5-Chloro-2,6-Dimethylpyrimidine for a very specific hydrolysis mechanism or condensation pathway, citing journal articles and patent filings by the dozen. For them, theoretical reactivity ranks high. We balance those insights with the daily realities of solvent recycling, loading rates, and filtration bottlenecks—all part of the continuous process of transforming a promising intermediate into a ready-to-use building block. Our team’s development chemists regularly return to the reactors when a new customer’s reaction underperforms, reviewing solvent polarity, temperature ramps, and addition speeds, then proposing tweaks that actually work in a kilo or ton batch.

    This dialogue between theory and hands-on production infuses our process with rigor. We learn from setbacks—a crystal form that resists drying, a batch with unwelcome color, or a reaction sequence that yields too much by-product. Solutions come from directly confronting each issue and collaborating to fix it, not by ignoring problems or glossing over rough spots. We build every campaign on feedback loops between the lab and the plant floor, ensuring knowledge transfer happens in real time.

    The Role of 4-Amino-5-Chloro-2,6-Dimethylpyrimidine in Accelerating Innovation

    Synthetic chemistry is rarely just about moving atoms around. The choices in starting materials set projects on faster, more reliable footing—or force delay and troubleshooting. Over years of direct manufacturing, we’ve watched this compound enable customers to shave steps from multi-gram to multi-ton syntheses, launch pilot plant runs ahead of schedule, and troubleshoot unexplained side reactions. Our investment in refined analytical testing, process improvements, and genuine partnership delivers an intermediate that often serves as the cornerstone for critical research programs.

    Technological advances may reshape the industry, but the fundamentals of reliable, traceable, and pure starting materials do not change. By keeping the conversation open with formulators, analysts, and plant operators, we continue to adapt both process and product to fit evolving needs. The value of a compound like 4-Amino-5-Chloro-2,6-Dimethylpyrimidine lies in its proven performance that stands up to scrutiny and drives results at the bench, in the plant, and, in many cases, at the regulatory interface.

    Summary

    To anyone entering the field or searching for a proven intermediate with broad utility in pharmaceutical and agrochemical innovation, this compound represents years of learning, not just a formula in a catalog. Our responsibility is to ensure its delivery meets your standards today and stays ahead of expectations as science and market pressures evolve. Each batch leaves our site backed by process rigor, technical knowledge, and professional pride that only an original manufacturer can bring. We view every order as an extension of the continuous journey to produce chemicals that actually work, where it counts—in real reactions, with real people, solving tough problems every day.