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HS Code |
550348 |
| Productname | 4-Chloro-6-Ethyl-5-Fluoropyrimidine |
| Molecularformula | C6H6ClFN2 |
| Molecularweight | 160.58 g/mol |
| Casnumber | 127852-29-1 |
| Appearance | White to off-white solid |
| Meltingpoint | 56-60 °C |
| Solubility | Soluble in organic solvents like DMSO and DMF |
| Purity | Typically ≥98% |
| Storagetemperature | Store at 2-8 °C |
| Smiles | CC1=NC(=C(N=C1Cl)F) |
| Inchi | InChI=1S/C6H6ClFN2/c1-2-4-9-5(7)3(8)10-6(2)4/h2H2,1H3 |
| Synonyms | 6-Ethyl-4-chloro-5-fluoropyrimidine |
As an accredited 4-Chloro-6-Ethyl-5-Fluoropyrimidine 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-Ethyl-5-Fluoropyrimidine, sealed with tamper-evident cap and labeled with hazard symbols. |
| Shipping | 4-Chloro-6-Ethyl-5-Fluoropyrimidine is shipped in sealed, chemically-resistant containers. The packaging complies with international regulations for hazardous chemicals, ensuring protection from moisture, light, and physical damage. The container is clearly labeled, and material safety data sheets are provided. Shipment is conducted by certified carriers, with appropriate documentation and tracking throughout transit. |
| Storage | 4-Chloro-6-ethyl-5-fluoropyrimidine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it away from heat, moisture, and direct sunlight. Store at room temperature and ensure proper labeling. Use secondary containment to prevent accidental spills, and follow all relevant chemical safety guidelines. |
Applications of 4-Chloro-6-Ethyl-5-Fluoropyrimidine in Industrial ManufacturingAs a direct manufacturer, we supply 4-Chloro-6-ethyl-5-fluoropyrimidine to downstream partners who harness its structural properties for precise roles in advanced synthesis. This intermediate finds specialized application across select sectors focused on crop protection active ingredients, pharmaceutical building blocks, specialty heterocyclic compounds, and veterinary drug intermediates, each governed by strict compliance protocols, controlled addition rates, and integrated processing stages. 1. Agrochemical Active Ingredient Synthesis – Selective Herbicide IntermediatesProducers in the crop protection industry use this pyrimidine derivative as a core intermediate for synthesizing fluorinated heterocyclic herbicides. The molecular scaffold enables the construction of specific pyrimidinyl phenyl ether compounds through nucleophilic substitution and condensation steps. Intermediates created with this raw material undergo further functionalization, becoming active ingredients in low-dose, post-emergent weed control formulations that meet strict residue and safety requirements. Industry compliance standards
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2. Pharmaceutical Intermediate – Synthesis of Antiviral and Anticancer PyrimidinesAPI manufacturers utilize this chemical as a key ring substrate in multi-step syntheses for clinical candidates and registered drugs within the antiviral and anticancer classes. By introducing chlorine, ethyl, and fluorine substituents at defined positions, it supports structure-activity optimization. The intermediate undergoes coupling and further substitution to yield advanced heterocyclic scaffolds, later functionalized in GMP-supervised environments for finished API production or clinical-scale intermediates. Industry compliance standards
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3. Specialty Heterocyclic Compound Manufacturing – Advanced Electronic ChemicalsProducers of specialty heterocycles for electronic and luminescent material industries employ this compound as a building block for synthesizing electron-deficient fused rings. Utilized in Suzuki coupling or Stille coupling protocols, it allows for introducing controlled halogenation and alkyl/fluoro modification at critical positions, enhancing functional characteristics required for high-purity electronic grade small molecules used in display and sensor devices. Industry compliance standards
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4. Veterinary Drug Intermediate – Synthesis of Antiparasitic Pyrimidinyl CompoundsVeterinary API integrators include this intermediate in the synthetic pathway for developing modern antiparasitic agents. By leveraging its specific substitution pattern, chemists construct highly targeted pyrimidinyl structures with increased metabolic stability. The raw material enters at key nucleophilic substitution and condensation steps under controlled cGMP environments to ensure traceability and batch homogeneity for veterinary formulation supply. Industry compliance standards
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On the shop floor and in research labs, 4-Chloro-6-Ethyl-5-Fluoropyrimidine finds recurring demand for one reason: it delivers reliable reactivity for custom synthesis work. Few intermediates carry the distinctive arrangement of chlorine, ethyl, and fluorine on the pyrimidine ring, which gives this compound its edge for selective coupling reactions. Over the years, clients developing new pharmaceutical actives or fine-tuning agricultural actives have come to favor this molecule because of that precision. Chemists searching for a halogenated pyrimidine that doesn’t crowd out further functionalization repeatedly settle on this molecule after trial and error with others. Experience making and shipping it in hundreds of kilogram batches has shown us that small changes in starting materials or process parameters create real variation in yield and purity—details users feel immediately in their synthesis outcomes.
Other pyrimidines exist. The 2,4-dichloro analogues, or those with methyl in place of ethyl, sometimes draw interest. What actually happens during use determines the preference. That 6-ethyl group changes the lipophilicity just enough to alter absorption profiles in finished drug candidates. The 5-fluoro adds a degree of metabolic stability, while maintaining adequate electron density for nucleophilic substitution at the chlorinated position. These seem like textbook details, but the impact matters on a commercial scale. What often surprises newcomers is that slight alterations in the substitution pattern can force whole synthetic routes to change. Our process routes for the 4-chloro-6-ethyl-5-fluoro derivative keep batch cost under control, and extensive process optimization means impurities rarely surprise our customers.
Laboratory-grade pyrimidines sometimes impress under NMR but stumble when scaled. We have scoped our specification to real-world requirements through close work with process chemists. Each production lot is controlled for low moisture content, minimal residual solvents, and tightly limited isomeric contaminants. Our typical assay for 4-Chloro-6-Ethyl-5-Fluoropyrimidine runs above 98.5 percent by HPLC, with trace impurities consistently under 0.5 percent. These numbers come not just from analytical methods, but from confirmed downstream performance in hundreds of external and in-house syntheses. Chemists rely on a dry, stable, free-flowing powder that doesn’t clump or degrade under standard storage, and our operation has spent years tuning crystallization and drying steps to deliver that. That makes scale-ups and multi-batch campaigns more predictable.
Drug discovery teams first request samples in the few gram range. Once a hit compound emerges, we see the requests climb to kilogram and then multi-kilogram lots. In that transition, we hear two main concerns: consistency in appearance and absence of trace byproducts that could derail regulatory filing or cause side reactions. Our role as manufacturer gave us front-row insight into subtle issues like particle size influencing filtration, or certain residues affecting hydrogenation yields. When a batch-by-batch connection forms between source and user, feedback from scale-up trials allows us to tighten and adjust even further. 4-Chloro-6-Ethyl-5-Fluoropyrimidine still attracts attention not just for its unique substitution pattern, but for the confidence process chemists feel loading it into reactors at scale, knowing what result to expect.
No matter how clever the chemistry, practical handling sets the success of a project. In real plant conditions, 4-Chloro-6-Ethyl-5-Fluoropyrimidine stores well in standard packaging away from moisture—packing lines can move it without special training or awkward containment. Unlike some related halogenated compounds, it does not emit objectionable odors or fume aggressively at room temperature. Technicians accustomed to typical nitrile gloves and goggles report no unusual incidents, and crystal habit remains uniform through normal shipping vibration and warehouse conditions. Shelf-life studies over many seasons confirm the material arrives at customer sites performing as expected.
Downstream partners increasingly demand full analytical disclosure. We’ve invested in set procedures for batch testing: NMR, GC-MS, and HPLC profiles for every lot, shared proactively. Regulatory documentation remains strong—full traceability on starting materials, and impurity profiles developed in anticipation of ICH guidelines. Several projects using our 4-Chloro-6-Ethyl-5-Fluoropyrimidine as a starting block have advanced through early toxicity screens and into pilot manufacture, confirming for our R&D partners that the supply chain meets the reliability required for regulated industries. Our team remains available to share prior case experiences, offering a candid view into how this molecule’s identity and impurity spectrum affect synthesis at every stage.
It’s easy for fine chemicals to look identical on spec sheets. Actual outcomes diverge in subtle but meaningful ways: solubility in common solvents, ease of filtering after reactions, absence of haze or particulate in finished products. Bench chemists report that our 4-Chloro-6-Ethyl-5-Fluoropyrimidine dissolves rapidly in standard polar and slightly nonpolar solvents, like acetonitrile or ethyl acetate, without forming persistent residue. Process engineers cite low batch-to-batch variation as a relief, especially where process validation and QA auditing come into play during late-stage development. Some clients have tried to swap in structurally similar pyrimidines—after months of troubleshooting, many revert to the 4-chloro-6-ethyl-5-fluoro for its predictability and minimum downstream surprises.
Clients have compared this product with simpler fluoropyrimidines or ones using only chlorine substituents. Difference emerges at the coupling stage. The specific placement of fluorine at the 5-position in combination with chlorine at the 4-position and ethyl at the 6-position produces a reactivity balance unavailable in single-halogen analogues. Some alternative building blocks force end-users to tack on extra purification steps, driving up cost and labor. With our material, yield losses to unwanted byproducts in Suzuki or Buchwald reactions consistently stay low. The well-known alternatives often push upfront pricing down, only to raise total process costs through added work or inconsistent supply quality. After years of collaborative process support, our customers often cite the knock-on savings—and reduced regulatory headaches—as key, not just the per-kilogram price.
Over many product cycles, we have listened to project chemists, analysts, and operations staff working in pharma, crop-protection, and specialty chemicals. Their requests have shaped how we package, test, and refine 4-Chloro-6-Ethyl-5-Fluoropyrimidine. More than once, a client’s challenge with a reaction impurity or storage issue has led to tweaks in crystallization, switching to a different grade of anti-caking agent, or even changes in drum lining. Such iterative improvements add invisible value—often showing up in faster downstream processing or a reduced batch failure rate. Over time, we’ve built technical notes sharing best practices, and regularly share these insights during consultation, helping users get the best performance out of every order.
Shipment records stretching over a decade demonstrate a pattern of reliability. Each batch receives a unique identifier and full analytical archive, kept available for customer audits. We have established backward traceability to all input lots and process data. Our team reviews every lot with trained QA specialists using calibration control samples that match current pharma and agro standards—a practice honed not out of abstract compliance, but after multiple customer site visits and regulatory inspections. Consistency and transparency outweigh sales claims, and we share records freely in support of our client’s filing or validation needs.
Industry requirements continuously shift. Over recent years, global supply issues have tested every chemical manufacturer’s inventories and logistics. By holding critical raw materials in buffer stock and securing multiple secondary suppliers, we deliver stable supply for 4-Chloro-6-Ethyl-5-Fluoropyrimidine across project timelines. Even in high-demand stretches, backorders remain rare. Packaging takes into account international shipping guidelines, using tamper-proof, moisture-resistant drums and pails that pass leak and impact tests.
Shelf life of halogenated pyrimidines can worry users, but practical experience with our product—stored under ambient, dry warehouse settings—shows no detectable loss in potency or purity over 24 months from date of manufacture. Technical data is backed by real accelerated aging studies. For clients working towards green chemistry benchmarks or wishing to minimize their waste streams, we supply detailed reports of all process solvents and byproducts, enabling easier compliance with regional waste-management standards. Our production teams prioritize high-yield, low-waste steps wherever feasible, since plant operatives benefit from cleaner workspaces and simplified waste handling as much as management values regulatory compliance.
Project risks can spike when scale changes. In the early pilot stage, staff need clear, unambiguous batch records and responsive tech support. As demand grows, so do stakes—any process hiccup leads to delays down the line. Our in-house scale-up teams have spent years refining each synthesis, isolation, and packaging step for 4-Chloro-6-Ethyl-5-Fluoropyrimidine, catching bottlenecks before they hit our clients. Whether dispatching one kilo or many pallets, we realize that quality failures in a single drum can add days or weeks of delay to a project. By maintaining rigorous in-process controls and working closely with freight partners, we assure timelines stay intact.
Modern drug and agricultural developers ask for more than just “meets spec” chemicals. They expect well-documented, reproducible analyte profiles—sometimes even secondary testing or custom certificate formats. Since regulatory environments keep tightening, our analytical lab keeps calibration with traceable standard references, and all method validations are performed against independent control lots. We do not rely on a single analyst or piece of equipment; cross-training and cross-validation are part of normal operation. This brings peace of mind to regulatory affairs teams during submission, especially as expectations around traceability and sustainability expand each year.
Problems will occur—no production process stays perfect. What counts is response and fix. In the occasional instance where a shipment arrived below customer expectation, our technical support worked directly with end users to trace root causes, review storage and handling, and submit replacement materials within defined timelines. Lessons learned made their way back to raw materials procurement and plant engineering, either through bulk container upgrades, or change controls on incoming solvent lots. Responding to real issues with transparency and accurate investigation keeps relationships working, and helps all parties clear QC audits down the line.
Across many years and varied industries, a few needs persist: accurate specifications, consistent supply, responsive support. Our journey with 4-Chloro-6-Ethyl-5-Fluoropyrimidine started from a chemistry challenge, but it continues through countless project cycles, technical queries, and client feedback. Keeping synthesis routes as robust as possible, and incorporating quality in every step, makes this compound more than another entry in a catalog—it becomes a reliable partner in innovation. Our own technical staff help guide chemists through best work-up procedures, solvent screenings, and regulatory file readiness, not theoretically, but from having solved those same problems side-by-side with industry users over many years.
Manufacturing isn’t static. Minor tweaks in a raw material or warehouse condition can show up downstream. That’s why collaboration with customer technical teams becomes essential; honest dialogue about performance in real syntheses feeds back into incremental plant or QC upgrades. Every feedback cycle—positive or corrective—sits at the root of improvements made to how we make, test, and deliver 4-Chloro-6-Ethyl-5-Fluoropyrimidine. Practices like regular in-person audits, detailed Certificate of Analysis archiving, and regular process review meetings have become normal over time.
Suppliers farther from the manufacturing floor might overlook such details. As actual makers, our responsibility—and our pride—comes in upholding direct accountability, and making sure what’s in the drum or bottle matches exactly what our partners expect for their own critical work. This approach has built not just orders, but ongoing trust and mutual success.
Lessons learned running manufacturing at significant scale matter more than buzzwords. Processes that reduce waste, safeguard consistency, and stay aligned with regulatory demands don’t just look good on paper, they actually hold projects together under the pressure of commercial reality. We carry those principles in every lot of 4-Chloro-6-Ethyl-5-Fluoropyrimidine that moves through our packing hall to our partners’ facilities. Knowing every project’s integrity and end results often begin with the building blocks, we make it our business to ensure each batch delivers not abstract compliance, but real, measurable reliability, born from years in the field—not the catalog.