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HS Code |
156324 |
| Product Name | 2-Chloro-6-Fluoro-3-Methylbenzaldehyde |
| Cas Number | 863870-57-3 |
| Molecular Formula | C8H6ClFO |
| Molecular Weight | 172.59 g/mol |
| Appearance | Pale yellow to light brown solid |
| Purity | Typically ≥ 98% |
| Melting Point | 43-47°C |
| Boiling Point | No data available |
| Density | No data available |
| Solubility | Soluble in organic solvents like DMSO and ethanol |
| Storage Conditions | Store in cool, dry place; keep container tightly closed |
| Smiles | CC1=C(C=CC(=C1Cl)F)C=O |
| Refractive Index | No data available |
| Flash Point | No data available |
| Synonyms | 2-Chloro-6-fluoro-3-methylbenzaldehyde |
As an accredited 2-Chloro-6-Fluoro-3-Methylbenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2-Chloro-6-Fluoro-3-Methylbenzaldehyde, 25g, CAS 862129-56-4," with hazard pictograms and safety instructions. |
| Shipping | 2-Chloro-6-Fluoro-3-Methylbenzaldehyde is shipped in tightly sealed containers, compliant with chemical safety regulations. Transport is typically via ground or air, using packaging that prevents leaks and minimizes exposure. Proper labeling and documentation, including hazard information, accompany each shipment to ensure safe handling and regulatory compliance during transit. |
| Storage | 2-Chloro-6-fluoro-3-methylbenzaldehyde should be stored in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as oxidizing agents. Keep the container tightly closed and properly labelled. Store at room temperature or below, in a corrosion-resistant container, to prevent moisture or air exposure. Ensure access is restricted to trained personnel using appropriate personal protective equipment (PPE). |
Applications of 2-Chloro-6-Fluoro-3-Methylbenzaldehyde in Industrial Manufacturing2-Chloro-6-Fluoro-3-Methylbenzaldehyde serves as a key intermediate for advanced organic synthesis in critical chemical manufacturing sectors. The following application scenarios highlight practical downstream use cases, detailing compliance, formulation ratios, integration into production lines, and final goods delivered by international industrial clients. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers rely on 2-Chloro-6-Fluoro-3-Methylbenzaldehyde in the controlled multistep synthesis of specific APIs, particularly those targeting central nervous system disorders and anti-infective therapies. The aromatic substitution pattern is vital for the regioselective formation of complex heterocyclic APIs, allowing scalable batch or continuous processes. Stringent regulatory and traceability requirements govern each phase, from raw material intake through in-process intermediate control, supporting global drug master filing and regulatory submissions. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Fungicide Active Components)Major agrochemical producers adopt this compound as a custom intermediate to achieve highly substituted benzaldehyde cores required for constructing next-generation herbicides and fungicides. Due to its unique electronegative pattern, it facilitates downstream reactions yielding active ingredients well-documented for weed and fungal control, while ensuring residue compliance for crop use and environmental safety. Manufacturers invest in robust supply qualification supporting global agrochemical registration. Industry compliance standards
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3. Specialty Dye and Pigment Intermediate ManufacturingIndustrial dye and pigment companies use the compound in niches requiring heat- and solvent-resistant colorants for plastics and polymers. The electron-deficient ring structure is preferred in the condensation and coupling reactions forming high-value azo, anthraquinone, or heterocyclic dyes. Downstream processors require reliable impurity control and batch-to-batch traceable supply due to end-market quality and regulatory expectations in automotive and industrial plastics sectors. Industry compliance standards
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4. Fine Chemical & Electronic Material PrecursorProducers of fine chemical intermediates and advanced electronic materials apply the compound for constructing fluoroaryl and chlorinated benzene motifs used in advanced OLED emitters and specialty resins. Its halogen and methyl groups allow precise synthetic modification for electron transport layers or UV-cure resins in display and optical device fabrication, where contaminant thresholds and batch reproducibility are crucial for downstream client validation and regulatory reporting. Industry compliance standards
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Our team has devoted significant resources to the development and scale-up production of 2-Chloro-6-Fluoro-3-Methylbenzaldehyde, also known as 3-Methyl-2-chloro-6-fluorobenzaldehyde. Experienced chemists understand its value as a versatile intermediate, especially in pharmaceuticals and agrochemical research. In our plant, purity, reliability, and reproducibility remain our top priorities. During each campaign, our analytical staff confirms lot consistency with GC and NMR, carefully tracking subtle impurities, down to trace isomers and overchlorinated side products, so that users obtain starting material with minimal interference in downstream steps.
The chemical structure introduces careful selectivity into a benzaldehyde core. By attaching a chlorine at position 2, a fluorine at position 6, and a methyl at position 3, we create a molecule with tuned reactivity. That positioning isn’t random—it reflects hundreds of hours of process feedback. Med-chem teams count on these electron-withdrawing and donating groups to control properties in target molecules: modulating activity, metabolic fate, and process selectivity. The benzaldehyde motif isn’t new, but substituents like chlorine, fluorine, and methyl in these precise spots enable synthetic routes unavailable with standard ortho- or meta-benzaldehydes.
Our chemists implement a multi-step synthesis starting from pre-qualified halotoluenes, prioritizing safety in handling chlorinating agents and fluorination steps. Consistent crystallization and careful distillation ensure the targeted isomer profile. Each batch gets checked for traces of dihalogenated byproducts, plus verification of mass spec fragmentation patterns for full traceability. Unlike similar aromatic aldehydes, the presence of this specific pattern of substituents affects reactivity toward Grignard additions and oxidation routines, and stabilizes the compound during prolonged storage.
Conventional benzaldehydes often display high reactivity, sometimes too high for selective functional group transformation. Methyl and halogen substituents provide not just steric hindrance but also electronic tuning. For scale-up, unwanted side reactions (like over-oxidation or uncontrolled halogenation) can wreck yields and introduce expensive purification headaches. Standard grades of this aldehyde precursor, once supplied by general traders, frequently didn’t meet our analytical benchmarks, so we designed a process using robust in-line monitoring to suppress isomerically impure cuts. Each tank sample undergoes thermal stability testing, especially vital for long-haul shipments in non-climate-controlled environments.
We supply this product at a minimum purity level above 99% by GC, with residual solvents and water content stringently capped. Users have come to us after facing issues with sticky or semi-solid impurity-laden lots from third parties. By optimizing pressure and crystallization sequences, we crystallize product in a form that retains stability even during extended storage in drum or tote. These refinements come not from arbitrary spec sheets but from ongoing dialogue with process chemists actually running kilo-scale synthesis.
Because this aldehyde participates in multi-step campaigns—particularly in NCE (new chemical entity) work—chromatographic homogeneity carries major weight. We guarantee isomeric integrity by deploying multidimensional chromatography at each batch release. There’s a practical impact: downstream transformations, like reductive aminations or Wittig reactions, proceed with high conversion yields and fewer labor-intensive purifications. Our product flows readily for both manual bench work and automated dosing, a detail surfaced originally from feedback in our contract development labs. This seems minor until you’ve fought with congealed crystalline mass during a critical synthesis overnight.
Selecting the right intermediate for a target molecule design comes down to more than just functional groups on a drawing. Compared to similar compounds—like 2-chloro-3-methylbenzaldehyde or 2-fluoro-3-methylbenzaldehyde—our 2-chloro-6-fluoro-3-methylbenzaldehyde offers a unique blend of chemical stability and predictable reactivity. Chlorine at position 2 slows down certain oxidation steps, while fluorine at position 6 slightly suppresses undesired side aromatics. Methyl at position 3 increases lipophilicity, a value for med-chem optimization where classical benzaldehydes just can’t deliver the same SAR performance.
Common suppliers have long overlooked such nuances, treating benzaldehydes as undifferentiated. Over time, researchers recognized the benefit in using our controlled grades: improved batch homogeneity, reproducibility across campaigns, greater success transitioning discoveries from glassware to kilo scale, and easier regulatory filings, since our in-plant traceability delivers documentation for every single drum. Instead of just filling an order, we work with partners to anticipate which critical impurities could throw off their syntheses, using forensic-level NMR and mass spec so each release carries real peace of mind.
Work on heterocyclic building blocks often calls for benzaldehyde components functionalized for cross-coupling or ring-closing operations. Our product's particular combination of ortho-chlorine, para-fluorine, and meta-methyl lets it serve as a foothold for Suzuki and Sonogashira couplings, as well as for building advanced intermediates for kinase inhibitor projects. One pharma partner found their Buchwald–Hartwig amination skip unwanted debromination steps by moving to our aldehyde—errors that cost months of lost man-hours using poor-quality inputs.
Agrochemical innovators report improved yields in the final step of triazole and phenoxyacetic acid synthesis, thanks to the tailored electronic profile of our compound. We’ve seen multinational teams transition from random small-batch aldehydes to a locked-in supply from us, specifically to avoid stoppages after process optimization. Each custom lot arrives with documentation covering not only standard COA but also cycle records for each process stage, reinforcing traceability for inspections.
Scale-up brings serious health and safety questions, especially with chlorinated and fluorinated aromatics. Our production trains are fitted with closed-loop vapor capture and neutralization systems, greatly reducing risk of fugitive emissions. By keeping critical raw materials under continuous monitoring, we protect workers from unexpected pressure excursions or exotherms. Side products are recovered and recycled into secondary streams, so waste generation stays low and authorities get transparency via quarterly reporting. Environmental reviews from regulatory agencies support our approach; by integrating green chemistry principles into our design phase, we gain operational resilience and can maintain consistent output during audits and production peaks.
Compared to traders who consolidate drums from unknown sources, our operation controls every input and output. This translates into more than just lab stats—our tank farm and loading bays pass regular third-party inspections and our finished product always ships in UN-certified packaging. Clients no longer worry about off-spec aldehydes that risk contamination in reactors, nor do they find surprises from unreported stabilizers or anti-caking agents. By grinding through all the in-plant headaches from years of real-world usage, we preempt failure points instead of troubleshooting after the fact.
Synthesizing this benzaldehyde isn’t trivial. The halogenation steps carry risk of over-chlorination or double-fluorination if conditions drift, and byproduct phenols or acids can complicate crystallization. Poorly controlled processes in the wider market often result in yellowed, oily, or malodorous product—outcomes we can’t accept. It took over a dozen process optimization cycles to fine-tune our reaction times, temperatures, and quench stages. By embedding in-process sampling, we catch off-target runs in real-time, before a batch progresses down the line. Finished product that doesn’t meet spec gets recycled automatically; waste here isn’t landfilled but reprocessed, a decision reflecting our dedication both to cost control and environmental stewardship.
Shipping internationally demands additional vigilance, especially with materials sensitive to oxidation or photodegradation. We developed stable crystalline forms by optimizing solvent selection and cooling rates, in close collaboration with partner labs. There’s no secret stash of process tricks—just perseverance and learning from every failed attempt. Some of our most consistent product results stemmed from batch records dissected with external process engineers, where a stubborn impurity pointed to a minor valve leak or an undetected hot spot in the reactor jacket. Our plant culture prizes solving these problems over making excuses or passing them upstream.
We have listened directly to the frustrations and goals of researchers and process chemists who once settled for inconsistent inputs. Some reported sudden drops in reaction yield or unpredictable crystal forms, traced back to minor impurities like polyhalogenated residues. Others reached a crisis at crucial project milestones from batch-to-batch variability. Each story sharpened our focus on consistency. It’s not enough to fill a COA checkbox. We strive for continuous improvement, gathering annual customer feedback and integrating it into process changes, right down to how drums are sealed or how paperwork describes trace metal content.
Customers working in fast-paced R&D struggle most with supply interruptions or lot-to-lot shifts in performance. We’ve added reserve inventory and grown our logistics support, so surge orders or last-minute schedule flips don’t leave researchers stranded. Our lines stay running with contingency feedstock, and we test stability data under real-world conditions, not just theoretical shelf-life predictions. Every improvement follows not from market surveys or academic trends, but from researchers showing us first-hand the bottlenecks holding them back. Our response is practical: expanded batch sizes, better segregation of allergen sources, more transparent disclosure of auxiliary chemicals—and agile shifts in cleaning procedures between campaigns.
Over decades, trust grows less from marketing claims and more from shared project experience. Critical industries—such as pharmaceutical discovery, agrochemical launches, and specialty materials development—lean heavily on transparent access to technical data, clear communication for troubleshooting, and a willingness to tackle edge-case challenges. A new client value transparency and communication: they shared full synthesis routes with our staff, and our chemists flagged points of concern that might cause downstream blockages. Our history of detailed problem-solving, plant visits, and interdisciplinary feedback rounds out every transaction. We don’t rely on abstract promises, but on forthright technical review, method validation, and fast, thorough answers to every question received.
By keeping research staff informed about potential pitfalls in handling, stability, and compatibility, we reduce the risk of surprises. Our experience shows that even trivial parameters—such as pH in shipping lines, or the vibration frequency of filter presses—sometimes dictate product outcome far more than generic benchmarks. We share practical advice through regular bulletins and project meetings, looking beyond spec sheets so that researchers can focus on synthesis, not procurement drama.
The chemistry landscape shifts quickly. New targets, regulatory tightening, and advanced manufacturing—these trends all put pressure on raw material producers to stay ahead. We reinvest in not only people but also equipment: automating batch monitoring, expanding analytical lab capabilities, and participating in collaborative problem-solving networks with research partners. Every year we challenge our own process teams to lower impurity profiles, cut cycle times, and expand capacity—goals that align far more with real-world R&D than with standard logistics chains.
We never lose sight of the responsibility that comes with supplying critical intermediates. Advanced process monitoring, forward planning on job scheduling, and deep technical engagement with users all define how we approach the business of chemical manufacturing. For clients building the next frontline therapy or agricultural breakthrough, they deserve absolute confidence in each drum—confidence built on our willingness to learn, improve, and back each commitment with technical depth.
2-Chloro-6-Fluoro-3-Methylbenzaldehyde isn’t just another item on a chemicals list. With decades of combined experience, our team continues to deliver refined, analytically-validated product that supports the innovation goals of researchers in small labs and multinationals alike. Through hands-on process control, technical transparency, and a relentless focus on customer process pain points, we help teams bring ideas to life, not just on paper but in every successful campaign and every gram of final product. As the demands of advanced synthesis intensify, our commitment stays fixed: consistent chemistry, practical partnership, and the deep technical roots earned by running our own reactors—not by trading drum labels from afar.