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2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride

    • Product Name 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride
    • Alias 2-Chloro-6-fluoro-3-methylbenzoic acid chloride
    • Einecs 401-330-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    617228

    Cas Number 864781-89-1
    Molecular Formula C8H5Cl2FO
    Molecular Weight 207.03 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Chemical Name 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride
    Smiles CC1=C(C(=CC=C1Cl)C(=O)Cl)F
    Inchi Key FWJHLFNUCODWGP-UHFFFAOYSA-N
    Solubility Reacts with water; soluble in most organic solvents
    Synonyms 2-Chloro-6-fluoro-3-methylbenzoyl chloride
    Storage Temperature Store at 2-8°C

    As an accredited 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 250 grams of 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride, sealed with a screw cap; hazard labels included.
    Shipping 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride must be shipped as a hazardous chemical. It should be securely packed in tightly sealed, chemical-resistant containers, with proper labeling according to UN/ADR/IATA regulations. Transport must comply with local and international safety guidelines, including documentation of hazards, emergency procedures, and use of secondary containment to prevent leaks.
    Storage **Storage Description for 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride:** Store in a tightly sealed container under an inert atmosphere, such as nitrogen, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from moisture and incompatible materials like water, alcohols, and strong bases. Use corrosion-resistant shelving, and store separately from acids, oxidizers, and foodstuffs. Recommended storage temperature: 2-8°C.
    Application of 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride

    Applications of 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride in Industrial Manufacturing

    As a direct manufacturer, we supply 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride to specialized sectors requiring advanced intermediate compounds. The following sections detail the primary industrial applications, with specific compliance standards, formulation practices, integration stages, and finished product outcomes.

    1. Pharmaceutical Intermediate for Fluoroquinolone Antibiotics

    Major antibiotic producers incorporate this raw material as a key acylating agent in custom synthesis of advanced pharmaceutical intermediates for fluoroquinolone APIs, including moxifloxacin derivatives. The precise halogenated and methylated structure is critical for introducing selectivity in multi-step organic synthesis routes, ensuring reliable downstream yield and purity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current editions of EU Pharmacopoeia (Ph. Eur.) and US Pharmacopoeia (USP), specificity to API intermediates
    • China Drug Master File (DMF) registration where applicable
    • FDA 21 CFR Part 210/211 for drug-related synthesis

    Typical usage ratio

    • Mol ratio: 1.00–1.10 equivalent per amine or alcohol reactant
    • Variations depend on targeted intermediate structure, process yield, and impurity control specifications

    Downstream process integration

    • Used in early to mid-stage acylation step within multi-stage API synthesis, typically after protection group introduction, prior to final cyclization
    • Strict reaction monitoring for trace halide and byproduct residuals
    • Added as neat liquid or diluted in inert solvents under inert atmosphere

    Final product types

    • Moxifloxacin process intermediates
    • Halogenated piperazine derivatives for injectable and oral quinolone formulations
    • Refined bulk APIs for contract manufacturing

    2. Agrochemical Intermediate for Novel Aryloxyphenoxy Herbicides

    Leading crop protection manufacturers employ this material as a benzoyl chloride building block in the synthesis of aryloxyphenoxy herbicides. The selective substitution pattern helps fine-tune bioactivity against target weed species in rice and wheat fields by integrating unique fluoro and chloro functionalities into the final molecule.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 certified agrochemical production protocols
    • REACH registration and hazard communication as per EU Regulation (EC) No 1907/2006
    • Chinese National Standard GB 2763 for maximum residue limits

    Typical usage ratio

    • 0.8–1.2 mole equivalents relative to coupling phenol/amine substrates
    • Adjusted per batch based on anticipated conversion yields and residual chloride limits

    Downstream process integration

    • Introduced during core coupling step to form ester or amide linkages, typically before sulfurylation or methylation
    • Reaction conditions optimized to prevent hydrolysis and preserve positional halogen integrity
    • Batch and continuous synthesis practices depending on annual output

    Final product types

    • Fluorinated aryloxyphenoxypropionate herbicides (EC, SC formulations)
    • Granular and water-dispersible granule (WDG) pesticide products
    • Custom pre-mix herbicide intermediates for OEM and contract blends

    3. Synthesis of Advanced Liquid Crystal Alignment Materials

    Manufacturers of liquid crystal display (LCD) materials use this benzoyl chloride derivative to modify aromatic monomers, generating high-purity precursors for aligning agents on thin-film substrates. Its specific positioning of methyl, fluoro, and chloro groups enhances thermal and UV resistance in final orientational coatings on high-end display panels.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances in electronics
    • IEC 61249-2-21 flame resistance and halogen-free screening
    • ISO 9001:2015 and ISO/TS 16949 for electronic chemical QC
    • Japanese JIS C 6109 LCD chemical standards where applicable

    Typical usage ratio

    • 0.5–0.8 molar equivalent per target functionalized monomer batch
    • Adjusted for viscosity and end-group control in each batch

    Downstream process integration

    • Acylation step in specialty monomer synthesis used for subsequent alignment layer polymerization
    • Integration at pre-polymerization or copolymer modification point
    • Strict trace impurity removal via downstream chromatographic purification

    Final product types

    • Polyimide-based liquid crystal alignment coatings
    • Optically functionalized orientation layers for TFT-LCD and OLED display panels
    • Specialty acrylic or cinnamate monomers for next-generation electronic substrates

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Producers in the specialty dyes and pigments sector utilize this halogenated benzoyl chloride to introduce structural rigidity and electronic effects in new colorant molecules for textile, inkjet, and digital printing applications. The unique substitution pattern facilitates formation of specialty anthraquinone and azo compounds with controlled colorfastness and solubility characteristics.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for environmental safety in textile auxiliaries
    • REACH Annex XVII restrictions for hazardous aromatic amines
    • ISO 9001:2015 for batch traceability in colorant manufacturing
    • SDS and GHS-driven chemical safety documentation

    Typical usage ratio

    • 0.9–1.5 molar equivalents per coupling substrate, determined by dye nucleophile reactivity and shade requirements
    • Usage optimized based on chromophore intensity and waste elimination needs

    Downstream process integration

    • Key acylation/coupling step with aromatic amines or phenols during synthesis of intermediate dye structures
    • Process monitored for byproduct minimization and shade reproducibility
    • Acts as an input just before final azo or anthraquinone cyclization steps

    Final product types

    • Halogenated anthraquinone dyes for polyester fibers
    • Azo pigment intermediates with enhanced fastness for industrial coatings and inkjet formulations
    • Specialty functional and reactive dyes for technical textile segments
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    Certification & Compliance
    More Introduction

    2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride: The Chemistry Behind Purpose-Driven Molecules

    Direct from Our Reactors: Why Sourcing Matters

    In our plant, every batch of 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride is shaped by hands and minds that understand how small changes at the molecular level drive big differences in end products. We’ve relied on grounded techniques, thorough process monitoring, and hard-learned lessons from decades of scaling up to produce specialty benzoyl chlorides. What comes out of our reactor isn’t just a line item on a catalog—it’s the result of repeated refinement, daily process checks, and a team that fully grasps what’s at stake when custom molecules don’t live up to their promise.

    What Sets 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride Apart

    Most benzoyl chlorides serve in bulk chemical transformations. With 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride, reactivity and selectivity meet a tighter standard. Its pattern of substitution—chlorine and fluorine atoms positioned on the aromatic ring, with a methyl group at the 3-position—tunes reactivity in nuanced ways. In practice, this means that our product often finds its utility in workflows where simpler acyl chlorides fall short or produce too many side products.

    Researchers and process chemists often approach us with project plans that call for predictable acylation, less unwanted halogen exchange, or clean conversion into specialty amides, esters, or intermediates. Our team’s involvement doesn’t start or end with the reaction itself. It’s shaped by feedback from these chemists, their analysis of side-product profiles, and the hands-on, batch-to-batch experience we collect through direct supply relationships.

    Purity Matters—Not Just as a Number

    Years of on-site analytics have shown us that purity isn’t just about passing QC by tenths of a percent. High-performance liquid chromatography (HPLC) and gas chromatography (GC) can agree on 99% purity, but that last fraction often carries the ghosts of unwanted reactivity. Impurities in chlorinated or fluorinated benzoyl chlorides, no matter how minor, risk the formation of colored byproducts, loss of product yield, or even unstable intermediates during pharmaceutical or agrochemical synthesis.

    We take every practical step to avoid contamination with over-chlorinated, under-fluorinated, or trace oxygenated species. Vacuum distillation, not just filtration, plays a regular role in final purification, maintaining the delicate balance required for high-consequence end uses. As suppliers to pharmaceutical R&D, we see firsthand the downstream costs caused by ignoring these “final decimal” impurities—batch failures, regulatory headaches, and even delays in time-to-market.

    Applications Rooted in Real Need

    Producers of active pharmaceutical ingredients and crop protection products require intermediates that aren’t just “available”—they must function as precise tools in a tight sequence of steps. 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride fills a gap that broader-spectrum acyl chlorides can’t touch. Its unique structure makes it a key starting material for fluorinated benzamides, which often bring improved metabolic stability to API candidates.

    Throughout custom manufacturing, the real-world demands land far from textbook chemistry. A methyl group at the 3-position reduces steric hindrance just enough to favor certain acylation pathways. Meanwhile, the combined influence of the chloro and fluoro groups at the 2 and 6 positions modifies electron density, preventing over-acylation and suppressing formation of undesired regioisomers. These characteristics determine yields, purity, and scalability—factors we track not only on paper, but daily across production runs and in conversations with customers troubleshooting scale-up or formulation bottlenecks.

    Living with the Chemistry—Day to Day

    Our production operators don’t just “run the recipe.” Every batch, from weighing starting chlorotoluene to final bottling under moisture-controlled conditions, reflects practical challenges. Halogenated acyl chlorides, including this one, can hydrolyze in the presence of atmospheric moisture. A rushed or improperly sealed drum can lead to HCl evolution within hours, not days. We invest in double-sealed containers, moisture scrubbing in the fill lines, and tight controls on transfer and sampling—habits that grew out of hard lessons, including a handful of nonconformant lots and years of customer feedback.

    Wiping down surfaces, verifying gasket integrity, and teaching new staff the distinct “sharp” aroma of this compound short-circuits small problems before they grow. This isn’t about meeting a specification; it’s about keeping the days predictable for everyone down the line, from synthesis lab to QA inspection.

    Comparing This Product to Other Benzoyl Chlorides

    Some customers expect all aromatic acyl chlorides to behave similarly. In practice, each change in substitution creates a new set of quirks and pitfalls. Unsubstituted benzoyl chloride reacts rapidly but creates persistent byproducts in certain aromatic substitutions. The addition of a methyl group, as in 3-methylbenzoyl chloride, enhances solubility slightly and shaves some reactivity from the carbonyl center.

    Introducing both a chloro and fluoro returns another layer of reactivity control, as electron-withdrawing and steric effects stack up. With 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride, the pattern of reactivity suits protocols that demand minimal rearrangement or regioselectivity issues—a major concern for fine chemical and pharmaceutical synthesis. Our partners see fewer surprises in side-product screening, which pays dividends across downstream purification.

    Other halogenated benzoyl chlorides may seem superficially interchangeable. Direct experience tells us the cost of switching: new solvent choices, altered reaction times, and sometimes blocked or incomplete conversions. Standard benzoyl chloride may be less expensive, but time rescued from post-reaction troubleshooting or expensive column chromatography means a lot, especially at scale.

    Learning from Downstream Chemistry

    We didn’t settle on our purification and handling methods after reading a few papers. Our role as a direct manufacturer means we hear about every unexpected NMR peak, every yield dip, and every question about thermal stability. Early batches that left our plant in the 2000s almost always returned extra questions from R&D chemists: “Did you see carbonyl-containing impurities?”, “Any ortho-chlorination byproducts on your GC?”

    Stepwise, and through constant communication, we adapted. Advanced GC-MS and HPLC with photodiode array detection came off the capex wish list and into our day-to-day QC. Chromatograms that once looked acceptable got picked apart, and we learned to flag trace-level contaminants that had outsized effects on later-stage reactions. This iterative improvement loop rarely shows up in data sheets, but it weighs heavily for chemists building or scaling a new process.

    It’s not rare for process engineers to call and request slight modifications—a tighter cut on distillation, or a tweak to solvent carryover targets. Our plant’s focus on flexibility means we don’t hide behind “standard product” lines. Customization became our default mode, as supply partners with new project demands push us to refine every aspect of our production and purification for this specific molecule.

    Balancing Hazards with Practical Solutions

    Any benzoyl chloride stirs concerns about workplace exposure and reaction-scale handling. With halogenated derivatives, especially this one, the safety stakes rise. You find that moisture triggers release of corrosive gases. Here, safety gear, detailed procedural checklists, and practical transfer methods matter. We make key investments in drum pumps, powered local exhaust, and operator training, reinforced by real-world experience—because leaks, accidental spills, or poor ventilation don’t just disrupt the plant, they bring hazards everyone feels directly.

    Our experience says safety improvements rarely stay theoretical. After investing in self-sealing couplers and air filtration upgrades, we see workplace exposure readings drop. On review after each season, we harvest small lessons: which transfer technique leaves drums sealed longer, or which gasket materials hold up best. These granular changes don’t always reach spec sheets, but they protect both our crew and customers who open a new drum expecting stability and reliability.

    Environmental Responsibility Where it Counts

    Aromatic halogenated compounds draw regulatory and community scrutiny. We make the choice every month to recycle solvents, neutralize off-gas, and invest in closed-loop vent recovery, not just because regulations demand it, but because chlorine- and fluorine-containing offgassing can harm air and water quality fast. Waste from this molecule doesn’t get a free pass. We use in-house scrubbers and partner with permitted incinerators to ensure byproducts don’t slip off-site.

    On the manufacturing floor, controls range from spill containment to batchwise waste tracking and digital recordkeeping. Frequent agency audits, stack monitoring, and community reporting drive us to hold the line on compliance, but they also push process innovation. When we learn that a waste reduction tweak keeps more chlorinated intermediates off the outgoing load, we adopt it—not out of necessity, but because our experience shows real environmental wins add up over time.

    Insight into Consistency and Traceability

    At this project scale, traceability isn’t abstract. Every bottle carries a lot number linked to batch logs, retention samples, and raw material origins. When a scientist phones with a question about reaction behavior, we answer with details: GC-MS results from that run, temperature logs, purity checks at each stage, and even comments from QC staff flagging anything unusual. A supply partner’s trust hinges on knowing our process data is real, not recycled from old paperwork.

    Even after dispatch, we preserve split retention samples and digital chromatograms, ready to troubleshoot or cross-check. It’s not rare for a client to backtrack yield loss to a subtle change in impurity profile. With our archives in order, we don’t scramble or speculate; we provide concrete data so process chemists can make informed decisions, fast.

    From Pilot Batches to Multi-Ton Runs

    Scalability doesn’t equal predictability. Chemists tuning a reaction at 20 grams sometimes face scale-up failures at 20 kilos. We’ve learned that mixing, local temperature gradients, and solvent evaporation behave differently batch-to-batch and plant-to-plant. Early on, we reserved a line of glass reactors for pilot runs of new derivatives like 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride. We track each transition—from pilot to intermediate scale to continuous production—by mapping not only yields and impurity patterns but also small operational hiccups that threaten “process-fit.”

    Project teams rely on these observations. Often, reproduction of purity, color, and reactivity in every drum makes as much difference as price per kilo. Our direct feedback allows us to spot subtle shifts—from a new supplier’s change in raw material grade to a batch where the downstream product’s color drifts by a fraction. There’s no substitute for plant-level knowledge in preventing surprises at scale.

    Sustaining Supply Reliability in a Changing Landscape

    COVID-era supply shocks revealed the fragility in global chemical logistics. Rather than wait for crisis-driven panic, we started investing in local capacity, backup critical raw material sources, and on-site inventory buffers. The result: committed supply timelines, even when upstream chlorinated or fluorinated feedstocks grow scarce or logistics face bottlenecks. Our long-term partners benefit from this resilience, experiencing smooth project timelines while other suppliers scramble for material or accept QA lapses.

    Production rhythm is everything. Our team tracks not only procurement and processing, but the finer points—staff rotations, predictive maintenance on distillation equipment, and the impacts of even minor seasonal humidity shifts on storage stability. Years of production have taught us that consistency pays downstream, in both reaction yields and the trust of partners who build their process risks on our product reliability.

    The Human Factor in Chemical Manufacturing

    Nobody working the filling line or monitoring the distillation towers sees 2-Chloro-6-Fluoro-3-Methylbenzoyl Chloride as just another item to be boxed and shipped. We hire and train colleagues who understand that a misstep upstream can ripple into thousands of lost research hours or regulatory delays. The daily focus from shift leaders to QC staff revolves around small wins: cleaner filtrate, well-calibrated instruments, hands that move fast but not carelessly.

    Trainees learn to recognize not only equipment sounds, but also subtle changes in product appearance or smell. This peer knowledge, passed down in the plant, acts as the first line of defense against process drift that spreadsheets or lab results may miss for hours. We endure the night shifts, scrub down after leaks, track regulatory shifts, and keep lines open to our partners, because there’s no shortcut to building and sustaining trust in chemical supply.

    Looking Ahead with Customer-Driven Innovation

    Our technology and process improvements almost always start with direct requests from partners in research, custom synthesis, or manufacturing. Every season, someone brings us a frustration—a purification hang-up, a recurring impurity at scale, a bottleneck adapting to new regulatory demands. We respond with practical tweaks: new in-line filters, improved drying protocols, or shifts in process time-temperature cycles. Each solution comes bench-tested, not just hypothesized, before entering regular production.

    Clients directly influence our ongoing process evolution. What starts as a specialized run sometimes spins off process improvements that lift our entire range of benzoyl chlorides. Our team’s commitment never stops at the lab notebook stage; we carry these insights into each drum, every batch, and every phone call. The collective wisdom of plant staff, QC operators, and R&D contacts becomes embedded in the product, ensuring each shipment brings not only chemical value, but also years of practical, hard-won experience behind it.