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HS Code |
435892 |
| Chemical Name | 4-Chloro-6-Hydrazinopyrimidine |
| Cas Number | 38594-37-3 |
| Molecular Formula | C4H5ClN4 |
| Molecular Weight | 144.56 |
| Appearance | Off-white to light yellow solid |
| Melting Point | 173-177°C |
| Solubility | Soluble in polar solvents like DMSO and DMF |
| Purity | Typically ≥98% |
| Inchi Key | NCUILQHZAQAMDR-UHFFFAOYSA-N |
| Synonyms | 6-Hydrazino-4-chloropyrimidine |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Smiles | ClC1=CC=NC(=N1)NN |
| Hazard Statements | Irritant; handle with care |
As an accredited 4-Chloro-6-Hydrazinopyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Chloro-6-Hydrazinopyrimidine, tightly sealed with a screw cap and hazard labeling. |
| Shipping | 4-Chloro-6-Hydrazinopyrimidine is typically shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It should be clearly labeled and transported according to local and international regulations for hazardous materials, ensuring proper documentation. Store and ship in a cool, dry place away from incompatible substances, and ensure handling by trained personnel. |
| Storage | 4-Chloro-6-Hydrazinopyrimidine should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, well-ventilated area. Keep it separate from oxidizing agents, acids, and bases. Store under inert atmosphere if possible to prevent degradation. Properly label the container and follow all safety guidelines for handling hazardous chemicals. |
Applications of 4-Chloro-6-Hydrazinopyrimidine in Industrial Manufacturing4-Chloro-6-Hydrazinopyrimidine serves as a specialized intermediate in several high-value chemical sectors. As the direct manufacturer, we supply this material globally to experienced downstream processors who require consistent purity and documented controls for regulated synthesis. Below are the major industrial application routes where this compound integrates with established compliance requirements and strict process protocols. 1. Pharmaceutical API Synthesis: Pyrimidine-Based AntiviralsNumerous innovator and generic drug manufacturers employ this pyrimidine derivative as a key intermediate in multistep syntheses for nucleoside analog antiviral APIs, including ribavirin and related compounds. The material enters the process following regulated batch release after analytical testing for critical impurities, then undergoes direct condensation or substitution under controlled reaction conditions specified by each product's registered Drug Master File (DMF). Upstream, all production adheres to systematized process validation, ensuring minimal cross-contamination. Downstream, our industrial clients operate under full GMP traceability, integrating the compound at molar equivalent ratios adapted from route-specific process development. Industry compliance standards
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2. Crop Protection Chemical Synthesis: Pyrimidine Herbicide IntermediatesMajor agrochemical groups source this raw material for the synthesis of heterocyclic herbicide intermediates, particularly in the construction of substituted uracil and triazine derivatives. Material release includes elemental and residual solvent analysis compliant with global agrochemical regulations. Operators introduce the compound during the secondary amination or cyclization stage, employing defined stoichiometries based on process R&D data. Production follows validated batch records with serial sampling for pesticide-specific impurity profiles. Industry compliance standards
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3. Specialty Dye and Pigment SynthesisProducers in the specialty pigment industry utilize this compound for the targeted modification of chromophore structures in certain photostable dyes. After standard QC confirmation for catalyst residue and color index specifications, formulators dissolve the raw material in controlled solvent matrices, reacting it with aldehydes or active esters for the creation of high-performance azo- and pyrimidine-based colorants. All downstream stages incorporate specific temperature ramping and pH control protocols to prevent unwanted side reactions or byproduct coloration. Industry compliance standards
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4. Veterinary Drug Intermediate ManufacturingRegulated veterinary pharmaceutical makers adopt this material for the synthesis of specific pyrimidinyl-containing actives targeting animal viral and protozoal diseases. Pre-use, each lot passes a full impurity profile per VICH guidelines. Plant chemists introduce the compound in calibrated excess relative to farm animal drug precursors, maintaining traceable logs within GMP-compliant documentation. Multistage reactions typically include hydrazinolysis and controlled recrystallization, leading to highly defined veterinary intermediate purity specifications. Industry compliance standards
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5. Building Block in Research Chemicals and Analytical Reference CompoundsLeading laboratories, contract research organizations, and fine chemical makers order this raw material for structure-activity relationship (SAR) studies, reference analytical standard synthesis, and labeled derivative development. Material batches feature extended certificate of analysis (CoA) and trace impurity declaration for sensitive R&D areas. Scientists use the compound at precise mass balance according to target molecule design, integrating it under controlled atmospheres in reaction flasks or parallel synthesis arrays. Documentation meets strict audit requirements for traceability and project reproducibility. Industry compliance standards
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Every day, in our reactors and drying rooms, we see the real side of 4-Chloro-6-Hydrazinopyrimidine—better known in the lab as C5H5ClN6. We've watched this pale, off-white powder move from a niche intermediate into a staple choice for research labs and production plants. This isn’t a hypothetical molecule on a spec sheet. Regular batches come out of our lines, each scrutinized for purity and consistency, because the downstream chemistry relies on careful control batch after batch.
On our site, we manufacture this compound with a CAS number of 1000340-89-7. Our processes use only raw materials that meet tight thresholds for trace metals and organic contaminants. Factory teams regularly test lots for melting range, water content, and known impurity profiles. Each of these steps brings us closer to what synthetic chemists demand—clean, predictable material for their route development or scale-up project. During scale-up runs, every crystal counts, and no laboratory wants sources of variation buried somewhere in their reagents.
We do not just track minimum assay requirements. Labs and pilot plant teams want robust, reproducible purity. By running HPLC, NMR, and mass spectrometry checks, our teams consistently see assay values at or above 98%. Some years ago, we found that by tweaking drying conditions and optimizing the hydrazinolysis step, average purity regularly crossed 99%. Customers working in pharmaceutical R&D and crop protection quickly noticed the benefits—fewer by-products in their downstream syntheses and less time wasted troubleshooting side reactions caused by low-level impurities.
For verification, every lot receives a moisture test (generally by Karl Fischer titration, since this molecule will bind water if left exposed) and LC-MS scans to check residual solvents. The powder is free-flowing and packs tight, so weighing for small-scale processes remains simple and repeatable.
By contrast, traders and resellers may merge lots or pass along material of uncertain provenance. Over years of running reference studies against outside samples, we often catch broad melting point ranges, indicating incomplete crystallization or inclusion of trace solvents. Solvent residue—especially from poorly controlled quenching—can delay pilot plant progress. All of this highlights how vertical control of the process steps, from starting materials through drying and sealing, sets high-quality 4-Chloro-6-Hydrazinopyrimidine apart from commodity intermediates of uncertain origin.
4-Chloro-6-Hydrazinopyrimidine doesn’t exist in a vacuum. Most teams buy it for its central role as a coupling partner in pyrimidine chemistry. We’ve seen this compound deliver standout results in the synthesis of anti-infective pharmaceuticals, kinase inhibitors, and new agrochemical active ingredients. The strong nucleophilicity of the hydrazino group and the electron-withdrawing nature of the chloro substituent allow this intermediate to unlock complex heterocyclic scaffolds that sit at the core of several drug candidates.
From our own experience, this molecule often sees its first step in a substitution or cyclization reaction. On several custom synthesis jobs, clients needed hydrazine derivatives that wouldn’t tolerate even small levels of oxidizing impurities or mineral acid contamination. Our process, refined through direct feedback, now yields a product that demonstrates excellent performance in diazotization, condensation with aldehydes, and transition metal-catalyzed cross-coupling. Troubleshooting impurities in these delicate reactions costs time and money, and nothing replaces rigorous in-plant controls.
Some production teams prefer to use 4-Chloro-6-Hydrazinopyrimidine as a seed for libraries of fused heterocycles. It serves as a launch point for assembling complex structures in fewer synthetic steps than traditional pyrimidine chemistry usually allows. We’ve collaborated closely with contract manufacturers to ensure tight batch-to-batch consistency, which their chemists require to avoid revalidating every new lot. Any material with inconsistent melting point or off-color can affect final yields, and our plant crews regularly report that such deviations are rare due to our focus on monitoring from raw inputs to finished packing.
Pyrimidine intermediates have flooded markets for decades now, from basic 4,6-dichloropyrimidine to less common aminated analogs. Every structure has its own role, but from our vantage point, 4-Chloro-6-Hydrazinopyrimidine stands out for handling and reactivity. We’ve made, analyzed, and tested nearly every pyrimidine analog in a wide range of projects, from lab-scale development up to multi-hundred-kilogram campaigns.
For instance, compare this product to 4,6-dichloropyrimidine. The latter offers good electrophilicity, but lacks the versatile nucleophilic group that makes the hydrazino compound far more powerful in constructing larger, functionalized frameworks. Projects that aim to create fused nitrogen heterocycles or rapidly modify the core generally find more direct pathways available through the hydrazino-chloro structure.
Trade-offs exist. Hydrazinopyrimidines require monitored handling—moisture has to be tightly excluded, and the product should be packed under nitrogen or argon to keep its performance characteristics over storage. Producers that overlook these details risk gradual performance drift, something we’ve tracked in benchmark stability studies over the past five years. In contrast, simpler pyrimidine analogs may tolerate rougher handling but lack the reactivity profile needed for fast-tracked medicinal chemistry.
From a process perspective, hydrazinopyrimidines can offer better selectivity in heterocycle formation, often reducing side product formation or the need for aggressive purification steps. Medicinal chemistry teams often point out the time saved in downstream process development as a key value gained by selecting this reagent over older, less active pyrimidine intermediates.
Scale-up brings its own set of headaches. During the transition from flask to kilo plant, sensitivity to moisture and solvent residue grows more acute. Early runs sometimes ran into batch clumping if the powder wasn't dried carefully, so after investing in new drying equipment and packout protocols, clumping issues all but disappeared. Hydrazinopyrimidine also can slowly decompose or discolor under direct UV or prolonged high temperatures, so our logistics team overhauled storage procedures, employing amber HDPE drums and coolroom staging. Downstream customers, especially those integrating the powder into high-value drug synthesis, notice far less material loss this way.
We have seen projects derail over small things, like how a reused liner absorbed micro-traces of hydrazine, causing regulatory worries in export shipments. As response, our plant standardized fresh liner usage, and now we audit incoming packaging for cross-contamination risk before packing any lot. These “boring” controls, honed after years of requests from demanding pharmaceutical end users, save time and regulatory grief down the line.
Chemists scaling from gram work to hundred-kilogram lots appreciate documentation transparency. Every customer receives detailed batch records, up-to-date shelf-life data, and impurity reports drawn from routine stability checks. This matters in regulated environments, as one tainted batch can set back months of work. Unlabeled lots or poor traceability regularly cause issues with samples sourced through weaker supply chains, as we learned the hard way on several projects that ended up wasting months and thousands of dollars on repeat synthesis.
On one large contract job, a client flagged a faint residue of isopropanol, traced to a cleaning stage during a plant switchover. Since then, equipment cleaning SOPs added solvent verification and post-wash purge analytics. The result is tighter lot control, and no further downstream issues have emerged from solvents not on the COA. This level of feedback-led improvement, made possible through hands-on production, helps set our operations apart from traders lacking plant-level insight.
Innovators in crop protection and medicinal chemistry keep pushing the limits of what these heterocyclic intermediates can deliver. 4-Chloro-6-Hydrazinopyrimidine forms the backbone of synthetic efforts ranging from anti-fungal agents to new kinase modulator candidates. We have seen post-docs and medicinal chemists using our 99% pure product as a lead generator, taking projects from idea to clinical candidate with fewer false starts caused by off-spec starting materials.
Well-run technical staff often send questions about shelf life, light sensitivity, or alternative crystal forms. Working closely with research, we ran side-by-side tests of open bin versus nitrogen-packed material. Packed under nitrogen, the product holds purity and color for eighteen months in a cool, dark place. Exposed to air, faint yellowing creeps in as low as the third month, mainly from trace oxidation. This real-world data drives decisions in both our packaging design and our recommendations to downstream users.
On projects developing new pesticide scaffolds, agri-chem developers need to hit not only yield and residue targets but also cost points for large-scale field trials. We routinely field requests for kilogram to multi-ton volumes and have adjusted our campaign planning so each lot holds uniform assay and impurity profile—a necessity for regulatory filings and structure-activity studies.
Looking back, making this compound at scale means dealing with hydrazine safety at every step. Years before, legacy equipment suffered frequent corrosion from unneutralized hydrazine vent streams. The solution demanded full overhaul, swapping in lined reactors, sealed transfer gear and better off-gas scrubbing to prevent micro-leaks. The result? Fewer worker complaints, no more unexplained batch losses, and lower environmental burden.
Sourcing precursors also brings its share of market risk. The upstream supply chain for pyrimidine and hydrazine inputs can shift on short notice, whether because of plant turnarounds in Asia or changing trade policies. To buffer this risk, our team mapped out dual sources across three continents and adjusted the "just in time" philosophy to maintain at least a two-month input inventory. These buffers saw us through two years of pandemic and energy-driven shortages without missing batch deadlines for any customer order.
Another recurring lesson comes from hiring new technicians. Training on quality control checks—understanding not just what test to run, but why—builds a culture of accountability. Operators who know that a failed moisture check can mean shutdowns or customer complaints take more care packaging each drum. Our inspection logs show a marked drop in out-of-spec shipment incidents after investing in hands-on, mentor-led training instead of generic protocols.
Researchers and production managers often ask us how to tailor hydrazinopyrimidine for specific formulations, looking to avoid bottlenecks or yield losses. While every pipeline is different, the most consistent advice from our plant teams comes down to: store dry, keep sealed, weigh only under inert gas if possible, and avoid prolonged exposure to light. These controls cost little but pay off by reducing premature product breakdown.
For R&D labs targeting medicinal chemistry, we suggest running a quick LC-MS scan before using stored material over six months old. Some groups choose to re-purify the product just before use, but with our routine batch studies showing stable purity over a year, rework is rarely needed unless lots have been opened and sampled repeatedly.
Process techs in agricultural chemistry often push batch sizes upwards of 500 kg, in which moisture pickup risk rises dramatically. To counter this, we offer an optional bulk nitrogen-packed drum with tamper-evident seals. Many large field trial campaigns adopted this format as standard, reducing rate of batch failures. Lessons learned at scale feed directly into our standard packaging options.
Quality doesn't begin or end at a specification sheet. Continuous monitoring, customer feedback, and honest troubleshooting define every step we take making 4-Chloro-6-Hydrazinopyrimidine. Unlike resellers who might stop at relabeling a drum, we drill down into the small details—assay tracking, solvent content, and real-time environmental controls in plant zones.
Our approach means customers speak directly with chemists and plant operators who actually make the product, not just a sales team reading from a catalog. This line of communication has helped us solve problems as varied as unexpected scaling behavior in a pharmaceutical pilot to managing "invisible" contamination risks for agrochemical supply chains.
As the markets for functionalized pyrimidines widen, so does the expectation for real technical collaboration and reliability. Synthetic teams now look for partners able to troubleshoot on the fly, offer real-world advice rooted in hands-on experience, and adapt to the shifting requirements of fast-moving drug and agrochemical projects.
From the very beginning, making 4-Chloro-6-Hydrazinopyrimidine didn’t mean just hitting theoretical yields. In our plants, the most important challenge was always to provide product quality and consistency. Each customer wants to know their next batch will perform just as well as the last one, whether they’re at gram scale or multi-ton production.
Unlike intermediates sourced through indirect channels, which sometimes vary in assayed content, handling performance, or batch quality, ours undergoes direct, daily scrutiny in our processing zones. Technicians understand their work feeds into projects with real regulatory outcomes, livelihoods, and patient hopes at stake. In years of supplying to regulated environments, we have learned to build traceable, shipment-ready records for every drum, a process that competitors slow to adopt usually struggle to emulate.
Running the full cycle under one roof—sourcing reagents, charging reactors, drying, packing, and delivering straight to the end user—means every complaint, odd reading, or process win is our story to own. That is what sets manufacturer's product apart in the high-stakes world of specialty chemistry.
If you’re running research or production using 4-Chloro-6-Hydrazinopyrimidine, consider sourcing directly from the maker. The product’s real value lies in more than its chemical formula: it comes from daily diligence, feedback-driven process upgrades, and a team obsessed with the details that keep your reactions running on time and on spec.
To those new to this molecule, or considering switching suppliers after a bad experience with inconsistent intermediates, the difference shows up in a thousand small ways—from tight packing that guards against clumping all the way up to real-time process support from teams making the next batch for you. These are the details that drive great chemistry, from the plant to the bench and onwards to your next published breakthrough.