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HS Code |
353918 |
| Product Name | 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride |
| Cas Number | 886372-37-6 |
| Molecular Formula | C8H2Cl2F4O |
| Molecular Weight | 261.00 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥ 98% |
| Solubility | Reacts with water, soluble in organic solvents |
| Synonyms | 2-Fluoro-3-chloro-6-(trifluoromethyl)benzoyl chloride |
| Smiles | C1=CC(=C(C(=C1C(F)(F)F)F)Cl)C(=O)Cl |
| Storage Conditions | Store under inert atmosphere, cool and dry place |
| Hazard Classification | Corrosive, causes burns |
As an accredited 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 g, tightly sealed with a PTFE-lined cap, labeled with hazard warnings and chemical identifier, packed in cushioning material. |
| Shipping | 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material and must be transported in compliance with relevant regulations (UN codes), with appropriate labeling, documentation, and secondary containment to prevent leaks and ensure the safety of handlers and the environment. |
| Storage | **Storage for 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride:** Store in a cool, dry, and well-ventilated area, tightly sealed in a corrosive-resistant container. Keep away from moisture, heat sources, and incompatible materials such as water, alcohols, bases, and strong oxidizers. Protect from light and avoid prolonged exposure to air. Only trained personnel with suitable protective equipment should handle the chemical. |
Applications of 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride in Industrial ManufacturingAs a manufacturer of advanced fluorinated benzoyl chloride intermediates, we supply 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride to clients in key segments of the fine chemicals industry. Below, we outline application scenarios where our material plays a direct, technical role in downstream synthesis, with detailed information on compliance, formulation, integration, and final manufactured product types. 1. Agrochemical Active Ingredient SynthesisAgrochemical manufacturers use this compound as a strategic coupling unit in the synthesis of selective herbicide and fungicide active ingredients, particularly those based on trifluoromethylated benzoyl groups. The molecule provides stability and reactivity during acylation steps for key structural motifs found in modern crop protection products. Downstream partners optimize its inclusion depending on the reactivity of other intermediates and final target bioactivity. Industry compliance standards
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2. Pharmaceutical Intermediate ManufacturingPharmaceutical CDMOs and API manufacturers employ this material for the synthesis of complex fluorinated benzamide and benzoxazole building blocks. Its reactivity with nitrogen-containing nucleophiles allows production of high-purity intermediates used in small molecule drug discovery and generics. Quality control of this stage impacts final drug substance impurity profiles and regulatory dossiers. Industry compliance standards
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3. Polymer Additive and Specialty Polymer SynthesisProducers of high-performance fluorinated polymers integrate this material as a functional chain capping or linking agent. It supports the synthesis of specialty copolymers with targeted hydrophobicity and thermal resistance, common in electronics encapsulants and engineered surface coatings. Its inclusion addresses demands for chemical resistance and processability. Industry compliance standards
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4. Fine Chemical Intermediate for Electronic Chemical SynthesisManufacturers of electronic-grade fine chemicals adopt this building block in the construction of advanced liquid crystal and OLED material precursors. The introduction of both chloro and fluoro substituents via this reagent is critical for specific electro-optical properties in precision displays and photonic devices. Industry compliance standards
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At our chemical plant, we don’t just run reactors and pack barrels. Every single batch of 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride is a product of deliberate engineering choices and consistent attention to detail. We have years of hands-on experience handling the subtleties of halogenated benzoyl chlorides. Watching the demand for precision chemicals grow over the past decade, it’s become clear that nuanced building blocks like this one are no longer niche compounds, but anchors for next-generation molecule design.
Our 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride — model code 326-TFMBC — is not just another halogenated benzoyl chloride off an anonymous catalog. Our team started with requests from pharmaceutical developers who needed a reagent offering both reactivity and selectivity for targeted acylation, in parallel with stability through storage and shipping. We collaborate directly with R&D teams who face the same challenges daily: unexpected side-reactions, temperature shifts, impurity build-up, and scaling unpredictability when moving from flask to ton-scale.
Over the years, we’ve dialed in a process that delivers sharp lot-to-lot consistency and purity benchmarks. Every tank is sampled and analyzed by GC, NMR, and HPLC, keeping residual solvents, trace metals, and related impurities to a bare minimum. The chemical arrives as a clear, colorless to pale yellow liquid, with a boiling point comfortably above ambient and a narrow impurity profile. Customers working in both bench and industrial settings appreciate handling stability across temperature changes, and a shelf-life that stands up to real storage conditions — including occasional shipping delays.
We produce this compound with the understanding that every functional group on the aromatic ring impacts downstream chemistry. The trifluoromethyl group provides electron-withdrawing strength that boosts acylation selectivity and manages reactivity patterns. The presence of both chlorine and fluorine at ortho and meta positions introduces steric effects, which many medicinal chemists rely on to nudge selectivity in late-stage functionalization. Unlike more common benzoyl chlorides, this model enables the design of molecules where electron density and substitution pattern are mission-critical to activity or binding.
Medchem teams often discuss the challenge of installing uniquely substituted benzoyl groups without sacrificing yield or triggering back-reactions. In our experience consulting with these teams, they’ve confirmed that 326-TFMBC leads to cleaner conversions where both reactivity and byproduct profiles are mapped out ahead of time. Analytical feedback on our batches repeatedly shows lower than standard hydrolysis rates compared to analogous products, which proves valuable during scale-up or extended reaction holds.
Agrochemical development brings its own requirements — specifically, the need for robust reagents that handle environmental exposure and resist breakdown during formulation steps. Over the course of industrial collaborations, QC managers have highlighted that minor differences in benzoyl chloride purity or impurity drift can cause significant downstream issues, whether it’s catalyst poisoning or trace byproducts in the final product. We regularly advise technical teams to consider reagent origin and process integrity, because the wrong impurity at the wrong time has ripple effects across multi-ton output.
Some in the market treat this as a commodity. At our plant, the operators running each batch have the experience to notice a coloration shift, a subtle viscosity change, or a faint odor. That level of attention is the difference between a batch that meets our release threshold and one that goes back for rework. We source starting aromatic compounds with traceability to the original manufacturer. We’re not interested in shortcuts or just-in-time shopping for raw materials. Instead, we’ve kept direct supplier relationships with people who share our standards, because that’s what avoids later surprises.
Temperature profiling sits at the heart of our process — precise reagent addition under nitrogen, pressure checks at every stage, batch cooling rates monitored and controlled. Our automation tracks every variable, but nothing replaces an operator’s eye. If a pressure rise looks out of range, or a reaction stalls, we expect a seasoned pair of hands to step in and problem-solve before downtime builds. This is where manufacturing knowledge comes through: not from an office, but from a plant floor that’s seen its share of repairs, reworks, and learning curves.
Quality assessment doesn’t leave anything to chance. We run cross-platform verification — GC and NMR analyses, water content checks, and certificate-of-analysis recordkeeping. On request, we supply extended impurity breakdowns for custom customers who face regulatory hurdles or challenging synthetic targets. We’ve encountered regulatory reviews that demand not just purity data, but rational process maps and impurity formation theories. Each review gives us the opportunity to rethink and strengthen our own internal controls.
Benzoyl chlorides populate the catalogs of countless suppliers, but each substitution pattern opens new routes to distinct molecular scaffolds. Ours stands out because we consistently achieve tight impurity specifications and reactant performance, batch after batch. The structure — combining trifluoromethyl, chlorine, and fluorine substituents — delivers unique steric and electronic effects that unlock synthetic pathways not possible with generic alternatives. Direct feedback from regular users confirms that expected conversions and selectivities align closely with theoretical models.
In comparison to 4-chlorobenzoyl chloride or the more commonly available benzoyl chlorides, our product enables installations where both reactivity and physical stability matter. Several of our clients, particularly those focused on fluorinated intermediates, report that the introduction of multiple electron-withdrawing groups makes possible some otherwise challenging couplings and acylations, especially under moderate conditions. These subtle changes carry weight during scale-up, where control and repeatability bear directly on project timelines and regulatory submissions.
Discussions with pharmaceutical process teams repeatedly return to the issue of reproducibility. Our experience shows that off-spec benzoyl chloride — whether due to peroxide content, UV degradation, or metal contaminants — has the potential to cause batch rejection or stalled development. We have taken pains to knock out typical sources of process drift: using fully inerted storage tanks, vessel cleaning routines documented per lot, and operator cross-training that teaches each team member not just how a reaction should work, but why each parameter matters.
Supporting chemists with transparent, practical advice always beats waving around a generic safety data sheet. We have noticed handling questions come up again and again: “How well does this store after opening?” “Does long-term storage affect reactivity?” “Is this suitable for dropwise addition, or does it fume too quickly at ambient?” — all feedback driven from years supplying plants and kilo-labs under real-world stress.
3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride responds best to cool, dry storage with tight seals. Outgassing is controlled through a process that leaves no residual acidic gases, which directly impacts odor and operator safety when the container first opens. Customers with limited indoor storage have remarked on our product’s resistance to yellowing or polymerizing, an outcome that owes a lot to high-purity starting materials and careful control of post-reaction work-up. We maintain packaging standards attuned to both drum and bottle users — lined containers for larger orders and sealed ampoules for high-value research customers.
We have watched trends shift: larger users request bulk deliveries for integrated manufacturing, while research clients may need only a few hundred grams for a pilot or a hit validation project. We offer both, knowing that the needs of a synthetic route do not always line up with bulk process planning. We’ve seen projects go from discovery to plant trials in less than a quarter, and we know it’s usually the small bottlenecks — like unforeseen solvent incompatibility or reagent shelf-life — that slow progress. That’s why we are realists about lead times and inventory, keeping some cushion built in to buffer against the unpredictable.
Our engineering team spends just as much time talking chemistry as running plant utilities. We frequently enter conversations with end users to dig into synthetic roadblocks; if a certain impurity shows up repeatedly, we’ll pull archived QC records, retrace process steps, and help untangle whether the root cause points back to our product or an unexpected process drift in downstream chemistry. It’s not unusual for us to pull in synthetic chemists or plant engineers for conference calls that last into the evening, trading process details, literature searches, and practical troubleshooting tips.
This kind of direct collaboration with customers sets the tone for how we think about product development. For contract manufacturers who must submit robust filings to health authorities or agricultural regulators, even very minor inconsistencies count. We always encourage technical due diligence, real-world trialing, and batch-matching. If an end-user process stalls or fails, we’re ready to review all records, check batch reserve samples, and step through each analytic record — because we know it’s not about metrics on a spec sheet, but delivering concrete results at scale.
No manufacturing run is perfect, and anyone who claims otherwise hasn’t spent enough time on a plant floor. Over the years, we’ve encountered unexpected filter clogging, trace solvent breakthrough, and oddball color changes. These occurrences taught us to never settle for “good enough.” We’ve updated SOPs, taught the new crew members how to spot early warning signs, and invested in improved in-line analytics to pick up drift before it becomes scrap. That vigilance finds its way into every customer’s bottle.
Risk is not just about process hazards or regulatory flags. We see it every time a client faces a sudden order spike or a regulatory headwind that suspends field applications. To manage these realities, we keep reserve stock on hand and issue honest lead time estimates. Waiting for a critical reagent due to overconfidence in just-in-time delivery can derail entire projects; underestimating the need for transparent communication with QC teams causes friction that nobody wants. We see ourselves not just as suppliers but as partners in reducing downtime and problem-solving in the real world.
Environmental compliance means more than logging a checklist. After a few regulatory audits, we learned what effective compliance looks like, beyond paperwork. We invested in closed capture systems for acid gases and optimized waste handling routines so that solvents are recycled rather than dumped. These efforts earn approval from downstream clients whose own compliance audits cover the supply chain. It’s clear from experience that sustainable handling and transparency about manufacturing practices ease both regulatory and customer trust concerns.
We work actively to minimize energy and material consumption, not because it’s trendy, but because energy waste or sloppy solvent loss hits the bottom line and the environment at the same time. Where possible, we reclaim and reprocess side-products that once would have counted as hazardous waste. Over time, we have built long-term relationships with downstream recyclers, keeping our footprint smaller and meeting both ethical and regulatory standards. This is not about marketing — it’s about running a reliable system where everyone, from plant to field, benefits.
Some procurement teams fixate on minor price differences between suppliers, thinking of halogenated benzoyl chlorides as interchangeable commodities. Our experience shows otherwise. The true value of 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride comes not just from molecule specs, but from the proven track record of manufacturing integrity, analytic transparency, and repeat customer support. Chemists building high-value molecules rely on reagents that do exactly what they’re supposed to, in process settings where small deviations can throw off entire batch releases.
During customer audits, we have walked plant managers through our batch records and impurity breakdown logs. We invite questions because we trust our process. Every decision — from sourcing to delivery — is open for review because we’re confident that extra scrutiny only strengthens confidence. We encourage chemists and process developers to look beyond any one-off best price. Think instead about the real cost of failed runs, wasted labor, out-of-spec batches, and last-minute cleanups. Our commitment is to help you reach your end goal without hidden trade-offs.
Innovation in fine chemical synthesis turns increasingly on access to well-characterized, high-performing building blocks. 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride fits this new landscape. It opens doors for synthetic routes that demand precise control over functional groups and push boundaries in agrochemistry, pharmaceuticals, and advanced materials. By keeping the focus on robust manufacturing, careful handling, and open technical dialogue, we help keep development on track and support researchers and production teams facing evolving challenges.
We’re continually learning, not just from our own operations but from every conversation with clients and partners. Our facility grows as the market grows. As new projects emerge — where selectivity, scale, and cost converge — we remain committed to supporting teams that turn chemical building blocks into new products. Our experience, both on the reactor floor and with end-users, drives an approach to supply that’s rooted in reliability, transparency, and real-world problem-solving.
3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoyl Chloride isn’t just another name in the catalog. For those of us who make it, every bottle and drum tells a story — of process improvements hard-won, of customer outcomes achieved, and of a manufacturing team committed to delivering on the promise of advanced synthetic chemistry.