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2-Chloro-4,6-Dimethylpyrimidine

    • Product Name 2-Chloro-4,6-Dimethylpyrimidine
    • Alias 2-Chloro-4,6-dimethylpyrimidine
    • Einecs 217-946-3
    • 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
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    Specifications

    HS Code

    321787

    Chemicalname 2-Chloro-4,6-Dimethylpyrimidine
    Casnumber 24353-73-5
    Molecularformula C6H7ClN2
    Molecularweight 142.59
    Appearance White to light yellow crystalline powder
    Meltingpoint 46-50°C
    Boilingpoint 224°C
    Density 1.19 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Flashpoint 114°C
    Smiles CC1=NC(=NC(=C1)Cl)C
    Synonyms 2-Chloro-4,6-dimethyl-1,3-pyrimidine
    Refractiveindex 1.552

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

    Packing & Storage
    Packing 2-Chloro-4,6-Dimethylpyrimidine is supplied in a 100g amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 2-Chloro-4,6-Dimethylpyrimidine should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Handle in accordance with local, national, and international regulations for hazardous chemicals. Typically transported as a solid in a dry, cool environment. Proper hazard labeling and documentation are required for safe shipping.
    Storage 2-Chloro-4,6-Dimethylpyrimidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Always follow standard laboratory safety protocols, including the use of chemical-resistant gloves and goggles when handling or transferring this substance.
    Application of 2-Chloro-4,6-Dimethylpyrimidine

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

    2-Chloro-4,6-Dimethylpyrimidine features prominently as a key intermediate in several specialized chemical sectors. Our manufacturing expertise supports downstream industries with consistent quality, enabling customers to meet rigorous production and compliance standards. The following subsections outline main industrial applications based on actual market data and technical collaboration with leading enterprises.

    1. Pharmaceutical Intermediate for Antiviral Synthesis

    Major pharmaceutical companies use this compound as a critical building block in the multi-step synthesis of antiviral APIs, notably in pyrimidine-based nucleoside analogs. The reagent introduces selective chlorination at the pyrimidine core and enables subsequent nucleophilic substitution to access complex structures, particularly nitrogen-substituted intermediates required for next-generation antiviral formulation. Process integration depends on batch or continuous flow methods, with stringent impurity and residual solvent controls per regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Chinese Pharmacopoeia (ChP) for raw material sourcing and purity
    • USP General Chapters for Impurities and Residual Solvents
    • European Medicines Agency Guideline on Pharmaceutical Quality Systems (ICH Q10)

    Typical usage ratio

    • 5%–15% molar ratio as starting pyrimidine ring donor per API synthesis batch size
    • Adjustment based on required product yield and subsequent conversion rates
    • Typical excess of 1.05–1.10 equivalents to ensure complete chlorination reaction
    • Reaction optimized to minimize downstream purification steps

    Downstream process integration

    • Fed into Step 1–2 of multi-stage heterocyclic core construction
    • Solubilized in polar aprotic solvents for nucleophilic aromatic substitution
    • Integrated with charged base reagents under closed GMP-controlled reactors
    • Inline HPLC or GC to track residuals before API coupling sequence

    Final product types

    • Ribavirin intermediates
    • Sofosbuvir intermediates
    • Other synthetic pyrimidine antiviral agents
    • Pharmaceutical intermediates for clinical trial material

    2. Agrochemical Intermediate for Pyrimidine-based Herbicides

    Leading agrochemical plants use this material as a core intermediate in synthesizing selective herbicides featuring methyl, chloro, and nitrogen functionalities on a pyrimidine scaffold. The compound reacts under alkaline conditions to yield target aminopyrimidine structures for weed control. Downstream producers demand consistently narrow specification ranges for impurity levels due to environmental and crop safety regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 16140 Guidance for Analytical Quality Control
    • China Pesticide Registration Regulations (Ministry of Agriculture PRC)
    • REACH Registration, Evaluation, and Authorization of Chemicals (Europe)

    Typical usage ratio

    • 8%–20% by total mass in active synthesis step of aminopyrimidine herbicide intermediates
    • Ratio selected based on potency of the desired final product and batch yield optimization
    • Process engineers adjust chlorination agent proportion based on soil residue criteria
    • Quality control labs document and verify assay on delivery and consumption

    Downstream process integration

    • Loaded into stirred-tank reactors for nucleophilic substitution with primary amines
    • Operates under strictly monitored temperature and pH to ensure desired conversion
    • Subsequent downstream extraction and crystallization before formulation
    • End-to-end traceability from raw material receipt to final herbicide formulation

    Final product types

    • Pyrimidine-type selective pre-emergence herbicides
    • Chemical weed control solutions for cereals and legumes
    • Active intermediates for proprietary herbicide brands
    • Registered agrochemical formulation components

    3. Specialty Dye and Pigment Manufacturing

    Dye manufacturers utilize 2-Chloro-4,6-Dimethylpyrimidine as a reactive intermediate, particularly in the synthesis of heterocyclic azo and vat dyes. The compound acts as a nucleophile-activating group in chromophore construction, contributing to dye molecules with enhanced binding affinity to cellulose and synthetic fibers. Plants operating under major textile and industrial pigment brands require purity certifications and validated residue management.

    Industry compliance standards

    • Oeko-Tex Standard 100 for certified dyes
    • ECHA SVHC (Substances of Very High Concern) List
    • GB/T 22864-2009 Quality Standards for Textile Dyes
    • ISO 14001 Environmental Management in Dye Production

    Typical usage ratio

    • 1.5%–4.5% by weight in main dye reactor process
    • Variance by chromophore type, modulation of color fastness
    • Process engineers increase ratio for deep shade and vat dye series
    • Quality control monitors residual chlorine and methyl content in final dye

    Downstream process integration

    • Introduced at the coupling stage for ring substitution/reduction
    • Activated under acidic or alkaline aqueous conditions by diazotization
    • Post-reaction washing with deionized water for residual removal
    • Integration verified by HPLC color index and structural confirmation assays

    Final product types

    • Azo dyes for cotton and viscose textiles
    • Heterocyclic vat dyes
    • Colorants for industrial polymer and plastics processing
    • Custom pigment preparations for ink and paint

    4. Advanced Material Science – Electronic Chemical Synthesis

    Producers of OLED materials and photoresist coatings deploy this compound as a key precursor for electron-rich pyrimidine-containing ligands and functionalized heterocycles. The halogenated dimethyl substitution ensures precise electronic modulation, critical in tuning dielectric properties and charge transport for optoelectronic applications. Facilities operate under strict trace metal and halide monitoring due to downstream requirements in device fabrication.

    Industry compliance standards

    • IPC-4101B Electronic Interconnect Material Specifications
    • SEMATECH Guidelines for Organic Semiconductor Materials
    • GB/T 31444 Quality Requirements for Electronic Chemicals
    • ISO 9001:2015 Quality Management for Material Production

    Typical usage ratio

    • 0.2%–1.2% by weight in high-purity electronic chemical blends
    • Dosed according to target molar electronic bandgap adjustments
    • Batch-to-batch variation monitored by trace level comparative analysis
    • Excess minimized for end-use in photolithographic applications

    Downstream process integration

    • Metered addition to heterocycle-forming condensation reactions
    • Solubilized in specialty solvents with controlled particulate filtration
    • Admitted under inert gas, low-halide atmospheric enclosures
    • In-process QC by UV-Vis spectroscopy and electrical property assessment

    Final product types

    • OLED hole transport and emission layer ligands
    • Photoresist precursors for semiconductor lithography
    • Small molecule organic semiconductors
    • Materials for advanced display and sensor fabrication

    5. Intermediate for Veterinary API Manufacturing

    Animal health product producers adopt this material as an essential intermediate in synthesizing veterinary-grade pyrimidine drugs, such as new-generation antibacterials and coccidiostats. The raw material allows targeted halogenation and methylation during early-stage synthesis under GMP and VICH-compliant operations. U.S., E.U., and China market access requires full traceability regarding source and analytical verification.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practice for Veterinary Pharmaceuticals
    • USP Veterinary Drug Monographs
    • Chinese Veterinary Pharmacopoeia
    • ISO 22535 Veterinary Drug Production Quality Control

    Typical usage ratio

    • 5%–12% by molar input as a starting building block per synthetic batch
    • Ratio adjusted according to yield optimization in final step
    • Slight excess used to ensure full conversion at ring formation stage
    • Residual checks required before intermediate transfer

    Downstream process integration

    • Charged into high-shear reactors during heterocycle assembly
    • Controlled under VICH-GL18 environment for contamination risk
    • Batch sampling for interim impurity profiles and documentation
    • Release for further formulation only after QA clearance

    Final product types

    • Pyrimidine-based veterinary antimicrobials
    • Coccidiostats for livestock feed additives
    • Bulk actives for injectable and oral veterinary drugs
    • Specialty animal health intermediates
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    Certification & Compliance
    More Introduction

    2-Chloro-4,6-Dimethylpyrimidine: A Manufacturer’s Introduction

    Our Understanding and Commitment

    After decades producing intermediate chemicals for pharma and fine chemicals, we’ve seen how small changes in a molecule — a methyl group moved, a chlorine swapped — can lead to big changes in behavior. 2-Chloro-4,6-dimethylpyrimidine isn’t just another step in a long catalog, it’s a distilled result of steady customer demand and real-world testing. Whether we’re running batch synthesis or scaling up in continuous lines, we know this compound’s profile from the ground up: raw material to finished drum.

    How the Molecule Sets Itself Apart

    Chemists think of the pyrimidine ring as one of nature’s core building blocks, found everywhere from nucleic acids to corrosion inhibitors. By attaching two methyl groups at the 4 and 6 positions and adding a chlorine at the 2-position, we help tune both reactivity and solubility. In our operation, we keep close control over chlorination and methylation steps, seeing that the reactivity isn’t just theoretically “high” – it consistently makes the next transformation reliable for our downstream users. Customers in pharma and crop protection like this structure because the methyl groups make the ring a little more resistant to over-reaction, while the chlorine remains reactive enough for nucleophilic substitution. We don’t just chase extreme purity numbers; our batches meet a balance between cost, ease of handling, and reliable downstream chemistry.

    Clarity in Specifications

    Real-world synthesis deals with a lot more than what the theoretical pathway suggests. We manufacture our 2-chloro-4,6-dimethylpyrimidine to tight specifications, often above 98% purity by GC, and we routinely screen for related pyrimidine isomers and residual monochloro impurities. We’ve found that keeping residual water low — target below 0.5% — makes storage and subsequent reactions smoother, especially for large-scale acylation or amine substitution. While some users want custom granular sieving or unique packaging, our standard shipments come in sealed drums or jerry cans to keep stability in humid transit. Color is pale yellow, odor faintly aromatic, and the product flows easily — no clumping or caking in reasonable warehouse conditions.

    We don’t see a “secret formula” to better product; it boils down to unglamorous, daily process control. Our operators run regular HPLC, GC, and NMR checks, understanding that a little extra methyl at the 4- or 6-position can start to tilt reaction yields if left unchecked. Once, after rolling out a new catalyst batch, we caught a subtle extra isomer by careful headspace analysis. This attention helps downstream customers avoid hiccups with regulatory filings or product approval.

    Typical Uses in the Chemical World

    Demand fluctuates, but we ship the bulk of our output to major pharma and agchem makers. In pharma, the molecule serves as a core intermediate in the synthesis of advanced pyrimidine-based drugs: kinase inhibitors, anti-viral agents, cardiovascular drugs. Research teams have built libraries by swapping the chlorine for different amines, or by fusing the molecule onto complex bicyclic cores. Some of our agchem partners use this compound to anchor new herbicides and fungicides, leveraging the methyl groups to dial in both selectivity and bioavailability.

    We know the ins and outs because we watch where our product lands. Almost all of it eventually ends up transformed — the chlorine replaced by primary or secondary amines, then further modified or cyclized. The reactivity at the 2-position lets customers run reactions at moderate temperature, with high selectivity, keeping byproducts low. Compared to unsubstituted 2-chloropyrimidine, our dimethyl version often gives better crystallinity and better handling, especially in large-batch operations where every percent yield means thousands of dollars.

    We’ve helped customers move beyond traditional solvents in their synthesis — encouraging greener, less hazardous choices. Some report they’re able to cut reaction times and reduce their waste profile with our product. From our perspective, that means the compound punches above its weight for process safety and sustainability.

    Comparisons, Contrasts, and the Value of Practical Experience

    Other pyrimidine chlorides show up in the market: 2-chloropyrimidine, 2-chloro-4-methylpyrimidine, even 2-chloro-6-methylpyrimidine. Structurally, our 4,6-dimethyl product stands apart by offering extra bulk and electron richness, increasing resistance to hydrolysis and controlling the site of substitution. In production, we notice the difference most dramatically in shelf stability and less propensity to pick up atmospheric moisture.

    For those familiar with 2-chloropyrimidine, you’ll notice the handling improvements right away. Our dimethylated material avoids the brittleness and dustiness of the parent ring — fewer problems with inconsistent dosing or floating dust in automated feeders. It’s friendlier for continuous production lines, where operators want predictable flow rates and reliable solubility profiles in the usual range of polar aprotic and aromatic solvents.

    Yields and selectivity also differentiate the molecule. The methyls at 4 and 6 serve as “guards,” protecting those positions during further elaboration. By blocking access, they minimize side product formation and boost downstream yield. Over years of feedback, process engineers have told us the extra methyl isn’t just a novelty — it translates to higher output and less downtime troubleshooting overreacted byproducts.

    Handling safety won’t be overlooked, either. The added methyl groups dampen some of the irritant properties seen in unsubstituted chloropyrimidine derivatives. This doesn’t mean the material becomes benign — standard goggles, gloves, and fume hoods remain necessary. But operators report fewer nuisance exposures and easier cleanup after scale-up runs.

    Economics play a role. None of us make decisions on chemistry alone. While the starting materials for the dimethylated product cost a bit more than the base pyrimidine ring, the savings downstream — lower byproduct formation, less purification, less rework — often outweigh the extra upfront cost. We’ve run trial campaigns for some multinationals showing a 10%-15% improvement in isolated yields, compared to the next best alternative, with faster purification and fewer lost batches to byproduct contamination.

    Challenges and Solutions in Production

    Raw materials markets rarely sit still. Our approach demands flexibility with benzyl chloride, methylating agents, and the supporting catalyst systems. We built redundancy into our supply chain and invested in in-house methylation reactors to keep a stable output during market hiccups. We adjust temperatures and reaction stoichiometry, always verifying quality upfront, not just at the tail end. In a recent period of feedstock volatility, this let us maintain shipment schedules when competitors saw supply problems.

    On the technical side, making a pure 2-chloro-4,6-dimethylpyrimidine batch isn’t as simple as scaling a lab recipe. Impurities sneak in from side reactions — over-chlorination, ring closure mishaps, incomplete methylation. Experience teaches patience here. Early on, we dealt with sticky residues and color issues by optimizing temperature ramps and in-process purification, sometimes running extra passes on short-path distillation. Our QA team still keeps records on every adjustment, so we can trace outcomes batch by batch. Every time a new grad chemist walks into the plant, we remind them: The product specification is more than a number on paper. It’s the sum of dozens of small tweaks and human decisions.

    Industrial hygiene remains a day-to-day focus. Chlorinated pyrimidines demand respect — trace exposure can irritate skin and lungs, so we enforce regular air monitoring and run closed-system transfer for everything above the kilo scale. We hold semi-regular safety drills; no product is worth an accident. This also means that waste disposal and scrubber system design stays front of mind. Chlorine byproducts and spent acids pass through multiple neutralization and cleanup steps, and audits from both local regulators and customer teams keep us sharp.

    Customer-Driven Innovation

    Product development rarely follows a straight path. Years back, one of our European pharma customers ran into problems with their amine substitution step — their old supplier’s product gave erratic yields. They reached out because they’d heard we cared about impurity profiles, not just top-end purity. We ran side-by-side tests and traced the trouble back to a persistent trace compound that slipped by standard GC – something the larger players overlooked. Quick process change on our end eliminated the issue, and their new campaign shipped on time.

    Another time, a major agchem outfit wanted ultra-low chloride content for a sensitive downstream enzyme step. We couldn’t just add saline washes or throw it through a generic carbon column: we had to retrofit a segment of our plant to handle microfiltration and custom-grade drying. This constant cycle — listen, test, correct, repeat — drives us to keep refining both process and final product. Every oddball request or nonstandard assay uncovers ways to improve the final output for everyone.

    Logistics and Reliability

    You learn quickly in manufacturing: chemistry doesn’t matter if delivery fails. We never treat shipping as an afterthought. Our team coordinates closely with global and local freight services, auditing every pallet for sealing, drum quality, and shipment tracking. Odd-sized loads, temperature excursions at customs, storms at sea — we’ve seen them all. Having backup inventory and clear lines of communication means that our product shows up ready for use, with Certificates of Analysis and supporting documentation in line with regulatory filings. We don’t shortcut on documentation — batch traceability, MSDS, and compliance audits run as a standard part of each shipment.

    Smaller-batch customers often need something the multinationals don’t: flexibility. Shorter lead times, bespoke packaging, freezer storage, different drum sizes. We invested in temperature-monitored storerooms and flexible packaging lines so smaller research units get the same quality and consistency as industrial-scale buyers.

    Environmental Responsibility and Future Steps

    We bear responsibility for what comes out of our plant, not just for output but for its longer tail in the environment. We’ve moved toward more sustainable solvents, with a focus on closed-loop recovery of methylating and chlorinating agents. Our waste streams pass through evaporative concentration, neutralization, and multi-stage filtration before leaving the plant. We share regular audit and emissions data not just for regulatory requirements, but so our customers can see their supply chain’s compliance in real time.

    Some buyers want reduction in carbon footprint or greener credentials for their procurement teams. Our team is studying bio-based pyrimidines, better catalyst recycling, and less energy-intensive drying methods. While these aren’t always ready for full-scale commercial output, we publish our process improvements and audit them with third-party verification.

    The Manufacturer’s View: The Importance of Partnership

    End users often view 2-chloro-4,6-dimethylpyrimidine through the lens of a technical data sheet. From our side, it is the result of both process and partnership — people, machinery, and relationships all driving toward reliable output. The technical insights we gather from our production floor feed directly into the support we offer customers: real troubleshooting, structure-activity feedback, alternative scale-up options.

    Our goal isn’t to be the cheapest source or to claim perfection. Instead, we aim to be the supplier whose product helps R&D teams work faster, with fewer hiccups, and the confidence that every drum, every can, matches what you expect — or better. As applications continue to expand, from pharma and agchem to new specialty materials, our commitment stays the same: practical innovation, genuine support, and honest dialogue to keep chemistry — and business — moving forward.