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4-Amino-2,6-Dichloropyrimidine

    • Product Name 4-Amino-2,6-Dichloropyrimidine
    • Alias 2,6-Dichloro-4-aminopyrimidine
    • Einecs 219-353-2
    • 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
    VTB
    Specifications

    HS Code

    851502

    Product Name 4-Amino-2,6-Dichloropyrimidine
    Cas Number 56-06-4
    Molecular Formula C4H3Cl2N3
    Molecular Weight 180.00
    Appearance White to off-white crystalline powder
    Melting Point 220-224°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Density 1.63 g/cm³
    Synonyms 2,6-Dichloro-4-aminopyrimidine
    Smiles C1=NC(=NC(=C1Cl)N)Cl
    Inchi InChI=1S/C4H3Cl2N3/c5-2-1-8-4(7)9-3(2)6/h1H,(H2,7,8,9)

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

    Packing & Storage
    Packing The 25g amber glass bottle features a white screw cap and hazard labeling for 4-Amino-2,6-Dichloropyrimidine, ensuring safe chemical storage.
    Shipping 4-Amino-2,6-Dichloropyrimidine is shipped in tightly sealed containers, protected from moisture and light. It should be packaged according to chemical safety regulations, labeled as a hazardous material, and accompanied by Safety Data Sheets (SDS). Handle with care, avoiding exposure and complying with all local, national, and international shipping requirements.
    Storage 4-Amino-2,6-Dichloropyrimidine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. It should be kept at room temperature and handled in accordance with standard laboratory safety procedures. Ensure proper labelling and restrict access to trained personnel only.
    Application of 4-Amino-2,6-Dichloropyrimidine

    Applications of 4-Amino-2,6-Dichloropyrimidine in Industrial Manufacturing

    4-Amino-2,6-Dichloropyrimidine serves as a crucial intermediate in several specialized industrial sectors. The following sections outline its principal downstream applications with precise industrial compliance, formulation details, integration points, and typical end products.

    1. Pharmaceutical Intermediates ― Antiviral Drug Synthesis

    This material acts as a core building block during multi-step synthesis routes for pyrimidine-based antivirals. Our clients employ it in condensation and substitution reactions to create key molecular scaffolds, especially for nucleoside analog development. Critical batch consistency and impurity control govern all manufacturing stages.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) standards for APIs
    • US FDA 21 CFR Part 211 regulations (where final APIs are for US market)
    • Chinese Pharmacopoeia for domestic pharma supply

    Typical usage ratio

    • Mol ratios from 0.8:1 to 1.2:1 relative to nucleoside precursor substrate; adjusted based on required substitution degrees and reaction route

    Downstream process integration

    • Material charged in initial pyrimidine scaffold assembly; enters during the primary coupling or halogen-exchange step before functional group derivatization and crystal purification

    Final product types

    • API intermediates for antivirals (e.g., acyclovir derivatives, other nucleoside analogs)
    • Active antiviral pharmaceutical ingredients after further downstream modifications

    2. Agrochemical Synthesis – Herbicide Intermediate

    Agrochemical manufacturers use this compound to construct chlorinated pyrimidine rings found in selective herbicides. The unique dichloroamino structure boosts substitution reactivity, allowing precise introduction of functional groups in later steps. Product purity and batch tracking remain closely monitored throughout the synthesis.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO Specifications for Pesticide Products
    • China GB 2763 standards for agrochemical residues
    • REACH registration (if exported to Europe)

    Typical usage ratio

    • Typically 20-35% w/w of total pyrimidine-containing step reagent batch, depending on target molecular structure and conversion efficiency

    Downstream process integration

    • Material enters during early-stage condensation or cyclization stages of pyrimidine herbicide core production, preceding oxidative chlorination or etherification.

    Final product types

    • Pyrimidine-based selective pre-emergent and post-emergent herbicides
    • Chlorinated pesticide intermediates

    3. Dye and Pigment Manufacturing – Reactive Dye Intermediate

    Producers of specialty dyes use this raw material in crafting pyrimidine-based chromophores for fiber-reactive colorants. Its dichloro groups support subsequent nucleophilic substitutions, generating highly dye-fast molecules. Control of trace amines and halides is critical for color consistency and textile compatibility.

    Industry compliance standards

    • OEKO-TEX Standard 100 for hazardous substance limits
    • REACH Annex XVII restrictions on aromatic amines in dyes
    • ZDHC MRSL compliance for export textile dyes
    • ISO 9001-certified production flow monitoring

    Typical usage ratio

    • Usually 15-25% by molar input per batch, defined by degree of chromatophore assembly and dye anchor group requirements

    Downstream process integration

    • Integrated during second or third-step substitutions in dye chromophore assembly; feed solution added prior to sulfonation or functional group finalization

    Final product types

    • Fiber-reactive dyes for cotton and cellulose textiles
    • Specialty pigment intermediates for inks and coatings

    4. Veterinary Drug Manufacturing – Antiparasitic Compound Precursor

    Veterinary medicine formulators employ this substance in multi-stage syntheses leading to chlorine-substituted pyrimidine active agents against parasite infections. Close batch documentation, intermediate assay, and solvent residue assessment support regulatory compliance for animal health supply chains.

    Industry compliance standards

    • VICH GL2 GMP for active veterinary pharmaceutical ingredients
    • Directive 2001/82/EC for veterinary medicinal products in the EU
    • US FDA 21 CFR Part 226 cGMP for animal drugs
    • WHO Guidelines for Veterinary Drug Quality Control

    Typical usage ratio

    • Ranges from 0.5 mol to 1 mol per mol of acid chlorides or relevant nucleophiles, with adjustments based on specific antiparasitic agent architecture

    Downstream process integration

    • Material is introduced after ring activation, combining with nucleophilic amines or thioethers prior to final salt formation and formulation phases

    Final product types

    • Synthetic intermediates for pyrimidine-based antiparasitic veterinary drugs
    • Precursor materials for topical and systemic antiparasitic formulations

    5. Fine Chemical Synthesis – Electronic Material Precursor

    Manufacturers in the electronics and specialty materials sector utilize this compound in the synthesis of heterocyclic intermediates for optoelectronic and semiconducting polymers. Consistency in particle size, trace impurity profiling, and thermal profile testing are tightly controlled during production and downstream delivery.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for restricted substances
    • ISO 14001:2015 Environmental Management System
    • IEC 62474 Material Declaration for electrical/electronic products
    • UL Recognized Component Mark (if part of the composite system for N. America)

    Typical usage ratio

    • Usually 10-18% by mass in polymer precursor feedstock; precise dosage adjusted to required intermediate chain length and target electronic properties

    Downstream process integration

    • Charged at the heterocyclic ring substitution phase; reacts prior to condensation with conducting polymer backbones or during halide-amine exchange

    Final product types

    • Pyrimidine-functionalized optoelectronic materials
    • Intermediate blocks for organic semiconductors and high-performance printed electronics
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    Certification & Compliance
    More Introduction

    Introducing 4-Amino-2,6-Dichloropyrimidine: Insights from the Manufacturer's Bench

    The Workhorse Behind Modern Syntheses

    Our daily operations revolve around seeing raw chemical ideas take on shape and substance. Over the years, few compounds have shaped our production lines and project conversations quite like 4-Amino-2,6-Dichloropyrimidine. In this fast-changing field, it finds a particular place—both for its adaptability and for how it has challenged us to refine our own understanding of process chemistry on a practical level.

    Getting to Know Its Structure and Specifications

    Many people glance at the molecular formula—C4H3Cl2N3—and see just another substituted pyrimidine. On the floor, though, every detail counts. The two chlorine atoms, each bonded at the 2- and 6-positions, plus the primary amino group at the 4-position, give this molecule a profile different from most other pyrimidine derivatives we've encountered. The white to off-white crystalline nature signals purity to a seasoned eye; any coloration flags potential byproducts or shelf-life factors we need to control.

    Production aims for a purity above 99% by HPLC. Moisture content, checked regularly by Karl Fischer titration, remains below 0.5%. We’ve worked with various particle sizes, often sieving product to pass an 80-mesh screen. Storage in tightly sealed containers prevents hydrolysis and preserves material moving from line to line. Every batch receives a methodical workup—in our case, that means repeated recrystallization from ethanol or other alcohols, guided by the twin goals of batch-to-batch consistency and a clean analytical profile.

    How It Took Its Place in the Industry

    Back at the start, 4-Amino-2,6-Dichloropyrimidine didn’t seem destined to anchor so many syntheses. Industry demand for specialty pyrimidines grew steadily. In pharmaceuticals, this compound serves as a key building block for antibiotics, antiviral agents, and kinase inhibitors. Some years back, our partners in agrochemicals reached out as their research teams tracked new classes of herbicides and fungicides—many shared a backbone built on this dichloroamino framework. We have since witnessed custom projects for pigment manufacture, too, where its electron-poor skeleton steers ring functionalization in ways few other pyrimidines can replicate.

    Beyond these end products, the compound excels at accepting further substitution, especially at the open 5-position, and its reactivity enables efficient steps in multi-stage procedures. In real-world projects, timelines can hinge on a reliable source. That urgency motivates us more than anything you’ll read in technical literature.

    Why Purity and Handling Methods Matter

    Having seen countless batches run—from kilo-labs all the way up through full-plant semi-continuous lines—we’ve learned where things can go off-rail. For this compound, even a sliver over the moisture specification can set off slow degradation, or affect final yield in downstream transformations. We’ve established protocols to assure a dry and controlled atmosphere from weighing through filling. Amino pyrimidines sometimes attract trace acid contamination; we keep close tabs by regularly calibrating our pH measurements and refining our cleaning routines between runs. Each improvement adds value, not by raising theoretical yield but by keeping product uniform across campaigns, which matters most to our customers who scale up their own chemistry.

    The Science Behind the Differences

    Plenty of pyrimidines come through this plant—some with methyl, ethyl, or nitro groups, some tri-substituted, others halogen-free. What sets 4-Amino-2,6-Dichloropyrimidine apart, in our experience, is the specific push-pull of electron effects from two chlorines and an amino group in precise configuration. We’ve run side-by-side experiments or reacted different pyrimidines under identical conditions. The dichloro substitution boosts resistance to nucleophilic attack at the 2- and 6-positions. Meanwhile, the exposed 4-amino site maintains sufficient nucleophilicity, opening possibilities for coupling, alkylation, acylation, or diazotization steps.

    Chemists in the field report that similar pyrimidines carrying only mono-chloro or other halogen groups fail to match the selectivity or final yields we have charted with the dichloro version. This is more than a structural curiosity—each difference means tangible benefits or drawbacks in scale-up, work-up, and environmental profiles for downstream processes.

    Direct Feedback: What End Users Tell Us

    We make this compound, but the way we see its value inflates every time we interact with clients running high-pressure reactors or continuous flow equipment. Many users express gratitude less for the certificate of analysis and more for our willingness to tweak parameters: a finer cut on particle size to help them dissolve material quickly, or a specially dried batch for glove-box transfer.

    One recurring story comes from process developers in pharmaceutical labs. With other pyrimidines, they hit snags during nucleophilic substitution reactions—solubility or work-up headaches block progress. 4-Amino-2,6-Dichloropyrimidine, by contrast, dissolves readily in common polar solvents, opens up broad coupling options, and survives conditions that would often degrade comparable molecules with less electron-withdrawing substitution. This feedback loops directly into our production approach, as we see the impact of every micro-improvement we deliver.

    Manufacturing Realities: Solvents, Scale, and Safety

    Some chemical manufacturers describe their products in the abstract. In our case, “manufacture” means workers in PPE at stainless steel reactors, vacuum dryers running overnight, and hours spent on batch endpoint checks. Our standard route involves chlorination of a pyrimidine core under anhydrous conditions, followed by controlled amination using ammonia or appropriate amines. Each step delivers opportunities for waste minimization, yield enhancement, and energy reduction.

    Efforts to drive sustainability saw us replace older chlorinating agents with greener alternatives wherever possible. Managing gas-phase reactants demands experienced hands—we’ve built a culture where operators know their equipment inside and out, because each run yields insights the next shift stands to gain from. Batch records stretching back years guide us as much as the latest analytical readouts.

    Our process minimizes hazardous byproducts, and all liquid and solid waste streams receive treatment according to locally enforced regulations. Any attempt to cut corners on solvent purity, drying cycles, or worker training shows up in the next batch sheets—learning this taught us the kind of discipline you don’t see in textbooks.

    Key Chemical Transformations: What Sets It Apart

    Our chemists have pushed 4-Amino-2,6-Dichloropyrimidine into dozens of applications. What fascinates us, year after year, is its role in Suzuki and Buchwald-Hartwig couplings, in direct aminations, or even as a precursor for fused-ring heterocycles. While simple chloropyrimidines struggle with incomplete conversion, the dichloroamino setup offers reliable activation.

    We’ve fielded requests to prepare small, custom analogs—swapping substituents, tuning reactivity, and rerunning standard reactions to validate ideas from synthetic teams at customer sites. Each time, the base compound holds up under conditions that stress-test more labile pyrimidines. It has even served as a testbed for new catalysis protocols. In-house, our best results use a mix of carefully dried DMF, base-promoted aminations, and strict nitrogen blanketing, especially when the risk of hydrolysis looms.

    Handling and Storage: Lessons We Learned the Hard Way

    Many a batch in this business owes success, or failure, to how well storage and transfer get managed. Humidity in the environment and temperature cycling wreak subtle but cumulative damage. Once, in the early days, a few drums stored in an improperly sealed warehouse revealed trace degradation by the following quarter. Our revised protocol keeps stock in moisture-barrier drums, stored out of direct sunlight and away from oxidizing agents.

    We share these practices not because they make for dramatic headlines, but because familiarity with them lets us prevent setbacks before they snowball. Shipments leave our site ready for container-to-plant transfer, and documentation follows each lot so our customers get predictable behavior from the raw material all the way through their finished products.

    Comparing to Other Pyrimidines: Practical Points

    There’s theory, and then there’s what actually happens on the shop floor. Colleagues sometimes ask about switching to more available or supposedly easier-to-handle pyrimidines—2,4-dichloro-6-aminopyrimidine, or mono-chlorinated variants. We’ve tested many of these, in direct side-by-side manufacture and in customers’ pilot plants. They often bring solubility differences, leading to extra filtration or slower conversion. Residual acidity or reactivity at the unsubstituted sites gives inconsistent color and raises byproduct burdens. The distinct layout of 4-Amino-2,6-Dichloropyrimidine turns these liabilities into assets, making the workflow smoother, even if the raw material cost looks higher up front.

    We report fewer HPLC peaks from byproducts, and our NMR tracking of finished products affirms this pattern. In a world where yield, purity, and predictable performance guide production schedules, these differences affect downstream profits and delivery schedules alike.

    The Learning Curve: Training, Troubleshooting, and In-House Knowhow

    Every new operator we train on this process goes through a cycle we know well: theory, then practice. On paper, safety or handling looks like a checklist. In the trenches, unusual temperatures or batch-to-batch moisture trends require split-second judgement. During a scheduled audit a few years ago, unexpected side reactions showed up in the reactor—trace water from a reused solvent drum. We responded by reinforcing solvent control training and swapping in real-time moisture probes.

    Troubleshooting batch anomalies grew our problem-solving muscle. When product quality dips, we dig down—cleaning protocols, raw material logs, or even updating our SOPs to respond to subtle supply chain shifts. Customers benefit, but so do our own future teams. The body of in-house knowhow around this product now forms an asset as tangible as any capital equipment.

    Connecting with Research Teams: Direct Feedback Loops

    A handful of new research collaborations changed the landscape. Chemists building active pharmaceutical ingredients wanted to probe limits—extra-high purity, micronized lots, lots certified for absence of specific trace metals. Their questions became our R&D roadmap. In one case, a project demanded product free from trace solvents, down to detection limits below 10 ppm by GC-MS. We built out a stepwise distillation and purging protocol just for them.

    This experience brought home a truth we repeat often: the real value of any chemical intermediate depends on a clear feedback loop between the shop floor, the analytical chemist, and the end-user. Not all chemistry can be “one size fits all.” With every new formulation or purification method, the set of potential applications broadens, and every tweak pays off in future efficiency or new markets opened.

    Continuous Improvement: Our Evolving Process

    No manufacturing process stays static—not in this era. We have experimented with alternative chlorination methods, greener solvents, and reduced-waste separation techniques. Each experiment runs through pilot-scale validation and routine analysis before making the leap to production. Small reductions in wash water or waste halide content may sound trivial. In total, though, these changes yield measurable cuts in energy, labor, and disposal costs.

    A recent series of kaizen workshops—born directly from shop floor feedback—helped us optimize batch turnaround time. Those lessons ripple through each subsequent batch, so that newer workers inherit not just formal procedures, but an ethos of constant improvement. We see our investments returned with each smoother run, each fewer hours of equipment downtime.

    User Experience: Problems and Real Solutions

    We know, better than most, that the story doesn’t end with a successful reaction. Real-world feedback often points to pain points downstream: product caking, inconsistent solubility, or packaging challenges. After shipping lots for a long-haul export, we noticed clumping in certain drums—moisture ingress along the shipping route. Packing in double-layered liners and using desiccants cut this limp in its tracks.

    Solubility problems sometimes crop up on scale-up as well, especially in colder climates or poorly mixed reactors. Sharing best practices—heating protocols, solvent blends, agitation rates—helps resolve these practical issues long before they threaten batch rejection. This feedback builds strong relationships: we see fewer customers calling with last-minute headaches, and more inviting us into their process improvement conversations.

    Regulatory and Quality: Standards We Live By

    Modern chemical manufacturing requires more than compliance. We work to exceed the regulations set for purity, batch traceability, and environmental controls. Our quality management system maintains comprehensive documentation—batch records, analytic reports, change logs—so every lot stays traceable through manufacture to end use. We routinely audit both supply chain and in-house protocols, guided as much by hard experience as by outside rules.

    Certifications and independent lab verifications keep us accountable and lift barriers for partners in regulated industries. Pharmaceutical and agricultural customers in particular audit our systems to ensure every shipment aligns with their stringent in-house acceptance criteria. Meeting these standards takes more than paperwork; it comes from building a culture where anyone on the team will sound the alarm if they notice anything out of line.

    Final Thoughts: Meeting Tomorrow’s Needs Today

    The story of 4-Amino-2,6-Dichloropyrimidine in our plant stretches over two decades. It is not just a line item in a catalog, but the culmination of teamwork, technical learning, and direct attention to end-user needs. Its place in modern pharmaceutical, agricultural, and specialty chemical landscapes reflects both the strengths and the constant improvement mindsets within our shop.

    We look forward to meeting new challenges for this trusted compound, sharing what we’ve learned, and growing a network of informed users who measure success not only by specs but by how reliably raw materials drive their own innovations and productivity. In this business, nothing replaces hands-on experience and honest feedback—the heart of why we continue producing, refining, and standing behind every shipment of 4-Amino-2,6-Dichloropyrimidine.