4,6-Dichloropyrimidine

    • Product Name: 4,6-Dichloropyrimidine
    • Chemical Name (IUPAC): 4,6-dichloropyrimidine
    • CAS No.: 1193-21-1
    • Chemical Formula: C4H2Cl2N2
    • Form/Physical State: Powder/Solid
    • Factroy Site: No.15, Daqing Road Qinglong Chemical Industry Yard, Haimen, Jiangsu Province, P.R. China
    • Price Inquiry: sales9@alchemist-chem.com
    • Manufacturer: Nantong Changhai Food Additive Co., Ltd
    • CONTACT NOW
    Specifications

    HS Code

    703776

    Chemicalname 4,6-Dichloropyrimidine
    Casnumber 1193-21-1
    Molecularformula C4H2Cl2N2
    Molecularweight 164.98
    Appearance White to off-white crystalline powder
    Meltingpoint 60-63°C
    Boilingpoint 232°C
    Density 1.46 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles Clc1cc(Cl)nc[nH]1
    Inchi InChI=1S/C4H2Cl2N2/c5-2-1-3(6)8-4(7)9
    Refractiveindex 1.606
    Storage Store in a cool, dry place away from light
    Hazardclass Irritant

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

    Application of 4,6-Dichloropyrimidine

    Purity 99%: 4,6-Dichloropyrimidine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting Point 110°C: 4,6-Dichloropyrimidine with a melting point of 110°C is used in heterocyclic compound formulation, where it facilitates efficient thermal processing.

    Stability Temperature 60°C: 4,6-Dichloropyrimidine stable up to 60°C is used in agrochemical manufacturing, where it maintains molecular integrity during storage.

    Particle Size <100 μm: 4,6-Dichloropyrimidine with particle size less than 100 μm is used in fine chemical reactions, where it achieves improved dissolution rate.

    Moisture Content <0.2%: 4,6-Dichloropyrimidine with moisture content below 0.2% is used in active pharmaceutical ingredient development, where it prevents hydrolytic degradation.

    Assay ≥98%: 4,6-Dichloropyrimidine with assay greater than or equal to 98% is used in analytical reference standards, where it provides accurate quantification in quality control.

    Residual Solvent <500 ppm: 4,6-Dichloropyrimidine with residual solvent below 500 ppm is used in medicinal chemistry research, where it reduces impurity interference in synthesis.

    Chromatographic Purity ≥99%: 4,6-Dichloropyrimidine with chromatographic purity of at least 99% is used in high-throughput screening, where it increases data reliability.

    Molecular Weight 148.98 g/mol: 4,6-Dichloropyrimidine with molecular weight of 148.98 g/mol is used in structure-activity relationship studies, where it aids precise molecular modeling.

    Storage Condition ≤25°C: 4,6-Dichloropyrimidine stored below 25°C is used in chemical stock management, where it preserves product quality over extended periods.

    Packing & Storage
    Packing 4,6-Dichloropyrimidine, 100 grams, is packaged in an amber glass bottle with a secure screw cap and clear hazard labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 4,6-Dichloropyrimidine: 12 metric tons packed in 25 kg fiber drums or bags, securely palletized.
    Shipping 4,6-Dichloropyrimidine is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified as a hazardous chemical and handled according to local and international transport regulations. Appropriate labeling and documentation are provided to ensure safe transit. Store and transport in a cool, well-ventilated area away from incompatible substances.
    Storage 4,6-Dichloropyrimidine should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Ensure proper labeling and store under conditions recommended by the manufacturer. Always use appropriate personal protective equipment when handling or transferring this chemical.
    Shelf Life 4,6-Dichloropyrimidine is stable under recommended storage conditions; typically, its shelf life exceeds two years when kept cool, dry, and sealed.
    Free Quote

    Competitive 4,6-Dichloropyrimidine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615651039172 or mail to sales9@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615651039172

    Email: sales9@alchemist-chem.com

    Get Free Quote of Nantong Changhai Food Additive Co., Ltd

    Flexible payment, competitive price, premium service - Inquire now!

    More Introduction

    4,6-Dichloropyrimidine: A Fine Chemical for Advanced Synthesis

    Direct Insight from the Chemical Manufacturer’s Bench

    4,6-Dichloropyrimidine is a pyrimidine derivative with two chlorine atoms uniquely positioned at the 4 and 6 locations on the ring. In high-purity solid form, this compound serves as a backbone for many pharmaceutical, agrochemical, and material science projects. From decades of hands-on production experience, the role this molecule plays in modern synthesis goes far beyond just being a reactive intermediate. Our chemists have synthesized and handled tons of this compound, troubleshooting process upsets and making continual improvements to the reliability of each batch. What separates real manufacturing from trading is knowledge of every step—from distillation to final quality control. We see exactly what goes right, and what goes wrong, and our perspective on this molecule comes straight from that daily, practical engagement.

    Technical Context and Observable Characteristics

    In crystalline form, 4,6-Dichloropyrimidine exhibits off-white to pale yellow coloration, with a characteristic mild odor. The melting point sits around 67–70°C, and it demonstrates notable stability under controlled, dry storage. Chemically, the chlorines at the 4 and 6 positions drive this molecule’s hyper-reactivity in nucleophilic aromatic substitution reactions, making it indispensable for introducing nitrogen, oxygen, or sulfur functional groups. This reactivity profile dramatically sets 4,6-Dichloropyrimidine apart from analogs like 2,4-dichloropyrimidine or 2,6-dichloropyrimidine, where the electron distribution and steric influences shift the outcome of coupling reactions. As one of the central intermediates, it stands out from more generic dichloro aromatics because it not only delivers regioselectivity but also balances speed and controllability in scale-up settings.

    Pioneering Synthesis: The Imperative of Purity and Consistency

    Among chemists and formulators, process purity always surfaces as a pressing need. Trace contaminants, retained solvents, and residual acids erode reaction yields in downstream steps. On our manufacturing floor, routine gas chromatography and liquid chromatography analyses verify each lot exceeds 99% purity, limiting unknown impurities to far below typical international benchmarks. Many processors—especially those working under stringent cGMP or customized performance requirements—benefit when starting materials are defined with this level of clarity.

    The consistency we cultivate comes from persistent control over raw material sources, precise temperature management in chlorination and cyclization, and batch records tracked down to each vessel and valve. Analytics teams here continually push to lower batch-to-batch variability, because we’ve seen first-hand how just a few tenths of a percent impurity can cause headaches in process development at the customer site. Repeat inquiries from major global pharma firms align with this view: they want unwavering regularity in the feedstock, because their own process optimization depends on it.

    Applied Uses: Building Complex Molecules, Supporting Real Discoveries

    4,6-Dichloropyrimidine appears in the blueprint stage for drug discovery groups screening kinase inhibitors, antiviral agents, and materials scientists building functional polymers. Medicinal chemists favor this particular dichloro isomer because the electron-deficient ring system, with its activated chlorines, speeds up nucleophilic aromatic substitutions—most notably displacement with amines, alcohols, and thiols—without requiring harsh conditions that would decompose more delicate molecular fragments.

    Year after year, we witness customers requesting ton-scale shipments destined for multi-step syntheses of active pharmaceutical ingredients. The ease of functionalizing this platform accelerates timelines in both custom synthesis and high-throughput medicinal chemistry. At the same time, in fields like crop protection research, analogs bearing functional groups introduced via 4,6-Dichloropyrimidine enable more selective, less persistent formulations with favorable environmental profiles.

    Why Distinguish 4,6-Dichloropyrimidine from Other Chlorinated Pyrimidines?

    While structurally similar to its 2,4- or 2,6-dichloro cousins, the 4,6 variant offers a distinct activation of the aromatic ring. Empirical studies and real-world process feedback confirm it reacts faster and cleaner, especially in the presence of weak nucleophiles. With 2,4-dichloropyrimidine, positional isomerism causes substitution to prefer the 4-site, reducing synthetic versatility. Using the 4,6 isomer guarantees both reaction direction and product distribution, supporting designers of complex drug candidates who need each synthetic step to be predictable.

    On the factory floor, this difference becomes clear when scaling up: 4,6-Dichloropyrimidine endures challenging conditions—high temperatures, various solvents—without decomposing or producing unwanted byproducts. Analytical work often uncovers subtle differences in impurity patterns, vital for companies that must maintain strict regulatory filings over years. No chemist wants to re-validate a whole process because of a small change in a base intermediate, so the degree of assurance with the 4,6 isomer can cut huge costs over the lifetime of a project.

    Solubility and Formulation: Process-Friendly Characteristics

    In terms of solubility, 4,6-Dichloropyrimidine works well in polar aprotic solvents—DMF, DMSO, acetonitrile, and dioxane. Chemists handling scale-up have noticed its manageable handling properties: it dissolves quickly and separates efficiently during extraction and workup. While other halogenated pyrimidines sometimes linger in solutions or produce gelatinous residues, the 4,6 isomer filters and purifies with noticeably fewer steps, especially with pressure filtration and rotary evaporation. This difference delivers time savings on processing lines that already run near their capacity limits.

    When designing processes or introducing automation to reaction steps, the predictable performance of this compound reduces the risk of bottlenecks. Our in-process control teams dedicated years to refining solvent recovery and waste minimization, learning what works best in real-world batch production—critical insights for colleagues in cost-sensitive industries.

    Scaling Up: Sharing Lessons from Real-Life Batch Operations

    Experience shapes manufacturing more than any academic spec sheet. Whether a project needs kilograms or metric tons, production reality starts with raw material provenance and moves through dozens of hands and eyes on the floor. Reliability means more than just purity on a certificate—it demands transparency about scale-dependent challenges. Over the years, we responded to customer scale-ups that highlighted everything from subtle crystallization issues to off-spec color developed by micro-impurities in heat-exchange loops.

    Bringing 4,6-Dichloropyrimidine from pilot to full-scale meant navigating shifts in particle size, filterability, and solvent association—a knowledge base built line by line from practical oversight. Teams here maintain direct logs of every deviation, sharing learning globally so the standard improves over time. We capture real lessons, not just bullet points: by working hand-in-hand with end users, we spot root causes and build out protocols that customers can rely on, project after project.

    Risk Mitigation and Regulatory Considerations

    Markets demand transparency on regulatory status and toxicological information. Over the past decade, regulatory landscapes shifted with new REACH and global GHS requirements. We adapted each production stage—raw material screening, emissions controls, even worker PPE requirements—before these reached customer specification sheets.

    From firsthand experience, documentation gaps emerge most often when supply chains fragment through brokers or traders with no visibility on factory controls. We retain direct batch data, chain-of-custody logs, and continuous monitoring of trace contaminants, providing full narratives on production lots destined for regulated applications. When end users ask for technical packages, impurity profiling, or historical manufacturing data, our response draws on direct plant records, not purchased paper certificates.

    Real Solutions to Industry Pain Points

    Plant operators and synthetic chemists frequently wrestle with process reproducibility. Mystery impurities, inconsistent supply, or undetected micro-incompatability with solvents all cause headaches for technical teams striving to hit launch targets. The best results stem from manufacturer-to-user communication—across years, not just shipments. With 4,6-Dichloropyrimidine, direct, recurring feedback from manufacturers drives incremental improvements: particle size uniformity, moisture exclusion in packaging, solvent residue studies using up-to-date analytical methods.

    We address these process frustrations by prioritizing direct technical support, periodic site visits (virtual or otherwise), and data sharing. Chemists on both sides learn how particle morphology fits their downstream steps, how minor tuning of the drying stage affects crystallinity, and how adjusting the packing line prevents static charge build-up—a surprising cause of lot-to-lot handling issues for automated filling setups.

    Partnering for the Long Term: Our Commitment and Industry Voice

    Leaving out intermediaries means we control the conversation and the factory process. This commitment doesn’t end at a signed contract. On every order, teams from QC, safety, production, and logistics review performance so new methods or market requirements trigger internal updates. Over dozens of audit cycles, tightening controls and listening to technical specialists builds endurance and mutual success. No team has all the right answers on day one, but the approach changes when feedback cycles span years and both parties invest in preventing issues well before scale-up hits.

    Choosing 4,6-Dichloropyrimidine for Your Process Innovation

    Across fields from small-molecule pharmaceuticals through agricultural research, those who use 4,6-Dichloropyrimidine gain strategic advantages—better chemical reactivity, trusted sourcing, and support designed from shopfloor realities. Experience with actual scale-up, not just laboratory gram-scale work, infuses every improvement and protocol. As regulatory frameworks tighten and technical standards become more challenging, our model is to keep transparency at the center, sharing both strengths and found limitations.

    The applications for this molecule expand year on year. New uses appear in electroactive materials, advanced diagnostics, and as building blocks in complex heterocycle assembly. The depth of know-how in continuous production, backed by direct troubleshooting, can’t be replicated by traders, middlemen, or algorithmic resellers. Our team’s confidence comes from long-term repetition, open dialogue with users, and a desire to solve problems before they become obstacles. Each batch produced, each process refined, shapes tomorrow’s standards—and keeps 4,6-Dichloropyrimidine at the front of genuine chemical innovation.