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HS Code |
324702 |
| Productname | 3-Chloro-2,6-Difluorobenzoyl Chloride |
| Casnumber | 85118-39-8 |
| Molecularformula | C7H2Cl2F2O |
| Molecularweight | 210.99 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥ 97% |
| Boilingpoint | 83-85°C at 13 mmHg |
| Density | 1.54 g/cm³ (approximate) |
| Refractiveindex | 1.525 (approximate) |
| Solubility | Reacts with water, soluble in organic solvents |
| Storageconditions | Store at 2-8°C, tightly closed |
| Hazardclass | Corrosive, causes burns |
| Smiles | C1=C(C=C(C(=C1F)Cl)C(=O)Cl)F |
| Inchi | InChI=1S/C7H2Cl2F2O/c8-4-1-3(7(10)12)2-5(11)6(4)9/h1-2H |
As an accredited 3-Chloro-2,6-Difluorobenzoyl Chloride 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, tightly sealed with a PTFE-lined cap, labeled: “3-Chloro-2,6-Difluorobenzoyl Chloride, hazardous, keep dry.” |
| Shipping | **Shipping Description:** 3-Chloro-2,6-Difluorobenzoyl Chloride should be shipped in tightly sealed containers, protected from moisture, and stored in a cool, well-ventilated area. It is classified as a corrosive and potentially hazardous substance, requiring proper labeling and adherence to all relevant transportation regulations, including UN packing and hazardous material protocols. |
| Storage | Store 3-Chloro-2,6-difluorobenzoyl chloride in a tightly sealed container, away from moisture, air, and incompatible materials such as water, alcohols, and strong bases. Keep it in a cool, dry, and well-ventilated area, preferably inside a chemical fume hood. Protect from light and store at room temperature or below. Ensure clear labeling and restrict access to authorized personnel only. |
Applications of 3-Chloro-2,6-Difluorobenzoyl Chloride in Industrial Manufacturing3-Chloro-2,6-Difluorobenzoyl Chloride is a specialized intermediate used by downstream manufacturers in multiple regulated chemical production sectors. This section details real industrial scenarios, each with practical application parameters, relevant standards, and integration points in manufacturing lines. 1. Synthesis of Agrochemical Active IngredientsPlant protection manufacturers employ 3-Chloro-2,6-Difluorobenzoyl Chloride for the acylation step in selective herbicide and pesticide API production, especially for difluorinated benzoyl-based actives used in cereal crops. Precise molar ratios and reaction conditions ensure legal residue compliance and targeted biological activity. QC teams monitor impurity profiles as required by government regulators for export and domestic sales. Industry compliance standards
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2. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug SynthesisAPI manufacturers integrate 3-Chloro-2,6-Difluorobenzoyl Chloride as an advanced intermediate to construct fluorinated aromatic ring components in selected non-steroidal anti-inflammatory drug (NSAID) molecules. GMP environments use validated technical protocols to govern synthesis and control potential genotoxic impurities, matching pharmacopeial quality requirements for finished APIs. Industry compliance standards
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3. Advanced Intermediate in Liquid Crystal Display (LCD) Material ProductionManufacturers supplying the electronics industry use 3-Chloro-2,6-Difluorobenzoyl Chloride to construct fluorinated aromatic structures for high dielectric constant and low birefringence LC mixtures. Accurate dosing in precursor synthesis ensures the consistency of optical properties critical for smartphone and television panels. Electronic-grade standards require strict environmental and impurity controls. Industry compliance standards
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4. Fluoroaromatic Monomer Production for Performance PolymersSpecialty polymer producers rely on 3-Chloro-2,6-Difluorobenzoyl Chloride to manufacture monomer building blocks for engineered plastics and high-performance polyamides. The acyl chloride’s introduction at controlled stages in multi-functional monomer synthesis provides chemical stability and tailored mechanical or dielectric properties in end-use polymers used for automotive or cable insulation applications. Industry compliance standards
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For the past two decades, we’ve crafted aromatic acid chlorides for pharmaceutical and agrochemical syntheses, and 3-Chloro-2,6-Difluorobenzoyl Chloride holds a central spot in our catalog. Our work with this compound comes from a deep need for reliable, high-purity intermediates in complex synthetic pathways. Over the years, chemists in top labs and manufacturing sites have relied on this specialty chloride to build new molecular connections—each time, quality and consistency determine the success of the entire project. If a single batch of such a reactive intermediate falls below spec, it never just affects the immediate lot; it throws off everything downstream.
We produce this compound under controlled conditions to keep impurities—like unreacted acid or mixed isomers—at bay. A good many research teams mention that switching suppliers often renders inconsistent yields or impurity spikes, highlighting the importance of rooted experience. Dealing with such a sensitive acid chloride means everything from drum storage to gas scrubbing needs routine inspection and adjustment.
3-Chloro-2,6-Difluorobenzoyl Chloride wears the identifier 446254-76-6. This is more than just a catalog item; it’s a finely tuned synthesis target. Its structure features three distinct reactive points on the aromatic ring. The chlorine atom sits at the 3-position, nudging the molecule’s reactivity, while the two fluorine atoms at positions 2 and 6 tighten the electron density, affecting both its handling and its downstream chemistry. Occasionally, a client requests a discussion with our technical team to better understand whether this specific substitution pattern or another might best fit their route; it’s never just about what molecule you have, but how it moves under your process conditions.
Day-to-day, our crew synthesizes this acid chloride using clean, dry reagents and maintains an atmosphere free of moisture. As veteran operators know, trace water means hydrolysis, leading to lower product—and more acid in the drum. During reaction, our monitoring process crosschecks GC and NMR results to confirm positional purity, rather than only relying on melting point or IR tests that can miss minor isomeric byproducts. In the most recent quarter, we tightened our chlorinating agent additions to control for temperature spikes, learning from feedback about occasional batch exotherms.
We send each batch through a thorough filtration and distillation setup. Glass-lined reactors keep the acid from eroding metal surfaces. When packaging, we avoid PVC containers due to compatibility issues; high-density polyethylene lined with PTFE works best, as it holds up against both the product and transit shocks. Final containers seal tightly to guard against airborne water. Our staff tracks lot histories with dates and production conditions, something contract manufacturers rarely share. If a client identifies an anomaly, we can retrace every step of synthesis and storage for that batch.
Standard commercial lots run at a minimum of 99 percent GC purity. For those pursuing fine electronic materials or advanced intermediates, we can push the number even higher with custom distillation—though yield drops somewhat in these runs. Color is rarely just aesthetic; light yellow often flags subtle oxidation, so strict visual inspection complements analytical checks. Moisture content also matters. Karl Fischer tests keep water beneath 0.05 percent, since even minor hydrolysis changes yield in the next synthetic step. For every outgoing drum, we record these measurements alongside batch records, so a returning customer always gets the same product profile.
We measure acidity and identify halide contaminants to verify starting material consumption. Chloroform-extractable impurities receive particular scrutiny. Our analytics department invests daily in keeping these results sharp because, beyond regulatory mandates, they reflect the feedback loop from downstream performance. If a pesticide formulation turns sluggish or an API synthesis runs off course, the problem sometimes traces to a hidden impurity. Experience has taught us that an ignored decimal point costs everyone money and confidence.
The real meat of choosing 3-Chloro-2,6-Difluorobenzoyl Chloride is found in its track record as a coupling partner and building block. Pharmaceutical manufacturers count on it during amide bond formation, especially for introducing fluorinated/chlorinated motifs that can affect metabolic stability and target selectivity. In crop sciences, it adds weight to new-generation herbicides where halogen substitution narrows biological spectrum and helps tune persistence in soil. Electronic material manufacturers have probed its reactivity as a precursor for certain liquid crystals or functional coatings, favoring the unique mix of halogens for dielectric control.
We engage with research teams and production lines who need more than just the chemical—they need insights about downstream compatibility, gas release, or how the molecule handles in scaled reactors. Many share feedback on filtration requirements or note where a milder co-solvent might serve better. Through these exchanges, we learn and adapt our own operating procedures to fix bottlenecks before they reach the client’s plant.
A lot of newcomers think swapping a 3-chloro for a 4-chloro, or grabbing a different fluorination pattern, makes little difference in reactivity or physical properties. In practice, every substitution changes something—from reactivity with nucleophiles, to volatility, to environmental fate. Compared to 3,4-dichlorobenzoyl chloride or difluorobenzoyl chloride, our product delivers a unique balance of steric and electronic effects. Chemistry teams tell us they see cleaner reaction profiles and less byproduct formation when the 2,6-difluoro and 3-chloro setup is built into the scaffold. There’s also feedback from formulation chemists who need reliable solubility or specific physical behavior in solution. Given the high reactivity of the acid chloride group, handling demands strict moisture exclusion, much more so than its less halogenated cousins.
Some customers run direct comparisons between our 3-Chloro-2,6-Difluorobenzoyl Chloride and other aromatic acid chlorides. Those with more ortho or para chloro might hydrolyze slower, but typically show less clean coupling and lower yields. Increased fluorination, particularly at certain positions, shifts electron density, demanding changes in catalyst or solvent choice mid-process. In our daily technical calls, most questions hinge less on price and more on consistency, reactivity, and aftersales troubleshooting. Years of supporting reaction optimization have built trust which can’t be matched by commodity traders or bulk importers.
A topic that rarely gets enough daylight is operator safety. Anyone who’s spent a shift decanting acid chlorides knows the risks: fumes, corrosivity, and the ever-present threat of hydrolysis. Our shopfloor protocols specify low-temperature transfers, real-time ventilation, and fully enclosed pump setups. Emergency trips to the eyewash station are rare, because daily training keeps staff ahead of hazards. For outgoing shipments, certified sealed drums eliminate most in-transit vapor leaks. Every new lot gets a review not only of its composition but of feedback from warehouse staff who physically move the drums.
Working as the actual manufacturer means problems show up on your own doorstep—not just as phone calls from end users, but as practical problems in your own facility. In colder months, we adjust drum warming schedules to ensure fluid flow and avoid crystallization on lines. Humidity spikes shift how quickly open containers need to be resealed, and even what time of day it makes sense to move product between processing stations. Anyone promising worry-free acid chloride handling is missing the sweat of daily plant work.
Decades in chemical manufacturing teach the value of scrutinizing not only specifications, but the way each material behaves in real-world processes. We field routine questions about scale-up, reagent order of addition, and clean-up procedures. Many users discover that even small changes in equipment can affect reaction trajectory. The difference between a smooth scale up and a stalled batch sometimes depends on how the initial acid chloride was synthesized, dried, and stored before it leaves our floor. We’ve helped develop dedicated filtration protocols or drum-warming schedules when odd cold-flow effects popped up in a client’s plant. These services and learnings grow out of long supplier relationships—not short-term procurement cycles.
Year by year, we’ve improved our own methods because we keep hearing what’s working or broken in customer plants. For those new to working with this compound, we share stability and compatibility details from the actual batches—not simply quoting from a generic data sheet. By staying in dialogue with users defining new reactions, we learn where minor impurities or changes in acidity may influence results. One development chemist brought us insight into how dissolved metal ions affect coupling with electron-poor amines, pushing us to invest in stricter trace metal controls.
Environmental stewardship can’t be just a box checked on paperwork. Benzoyl chlorides like this one demand responsible emissions control. Our facility captures HCl and other off-gases using dedicated scrubbers—upgraded after audits showed areas for better airflow and neutralization capacity. Our operations include neutralizing washwaters and careful recordkeeping of byproducts, helping us track and cut down waste over time. We inform downstream partners about the environmental load of using this chlorinated, fluorinated intermediate and recommend process tweaks where they help reduce overall emissions.
Regulatory standards always ratchet upward, and we treat every design change as a chance to lead, not just comply. By shifting to more efficient transfer systems and investing in containment, our team has slashed accidental spills and fugitive releases over the last three years. The environmental team shares quarterly impact data with both management and the shopfloor, so issues don’t get buried.
Long-term partnerships shape how we improve both the product and the process of supplying it. Many returning customers come with new projects that push the limits of what the standard specification delivers. In collaboration, we regularly undertake stability profiling, reaction optimization, and custom packaging requests to ensure the product works for next-generation techniques, not just legacy processes. Some R&D groups return each year to discuss unique application challenges—how an unplanned interaction in pilot plants could cause unexpected residue or purity swings. We troubleshoot these issues together, always treating field data as vital feedback, not as post-sale problem dumping.
As technology advances and regulations tighten, expectations for chemical intermediates rise. Unlike many products sourced through distributors or distant brokers, our offering reflects the lessons only direct manufacturing brings—tightened process controls, real-world handling adjustments, and an open ear for field challenges. In all these, the relationship between manufacturer and user is never transactional but grows deeper as both sides share practical fixes and past mistakes.
Producing and supplying 3-Chloro-2,6-Difluorobenzoyl Chloride isn’t only about ticking off chemical names on a catalog. Every batch tells the story of staff training, careful equipment maintenance, and fixed lessons from field failures and triumphs. The work links deep chemistry knowledge, tough operator routines, and practical relationships with real researchers and plant supervisors. Our own confidence comes not from raw output, but from the repeat calls for advice, custom tweaks, and feedback on chemical performance.
Whether destined for a key step in a billion-dollar synthesis or for a bench-scale experiment, each shipment begins with known building blocks and finishes with the real substance behind precise, honest manufacturing. This perspective, shaped by daily practice and heaps of feedback from teams using the product across the world, stands at the core of our work. Each lot is not just a package, but a continuation of years-long partnerships dedicated to solving practical problems and advancing both science and reliable industrial supply.