Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,3,6-Trifluorobenzoyl Chloride

    • Product Name 2,3,6-Trifluorobenzoyl Chloride
    • Alias TFBC
    • Einecs 211-002-9
    • 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

    120688

    Cas Number 367-22-6
    Molecular Formula C7H2ClF3O
    Molecular Weight 194.54 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.44 g/mL at 25°C
    Boiling Point 62-64°C at 14 mmHg
    Purity Typically ≥98%
    Solubility Reacts with water, soluble in organic solvents such as dichloromethane and benzene
    Refractive Index n20/D 1.499
    Synonyms 2,3,6-Trifluorobenzoyl chloride; Benzoyl chloride, 2,3,6-trifluoro-

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

    Packing & Storage
    Packing A 250-gram amber glass bottle, tightly sealed with a Teflon-lined cap, labeled “2,3,6-Trifluorobenzoyl Chloride, ≥98%, corrosive.”
    Shipping 2,3,6-Trifluorobenzoyl Chloride is shipped in tightly sealed containers, protected from moisture and light, and kept cool and dry. It must be labeled as a corrosive and irritant chemical, complying with relevant hazardous materials regulations. Proper documentation and handling procedures are strictly followed to ensure safe and legal transportation.
    Storage 2,3,6-Trifluorobenzoyl chloride should be stored in a tightly closed container, away from moisture, base, and incompatible substances such as strong oxidizers. Store in a cool, dry, well-ventilated area, protected from light. Use chemical-resistant shelves and secondary containment. Avoid storing near areas where water can be present, as it reacts with moisture releasing corrosive hydrogen chloride fumes.
    Application of 2,3,6-Trifluorobenzoyl Chloride

    Applications of 2,3,6-Trifluorobenzoyl Chloride in Industrial Manufacturing

    2,3,6-Trifluorobenzoyl Chloride is an advanced acylating agent widely used in the synthesis of specialty molecules requiring high purity and selective reactivity. Our facility supplies this material directly to industrial customers engaged in demanding downstream applications that require rigorous control of synthesis parameters and adherence to sector-specific standards.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use 2,3,6-Trifluorobenzoyl Chloride as a key reagent to introduce trifluorobenzoyl groups into advanced drug intermediates. The compound enters multistep active pharmaceutical ingredient (API) syntheses, especially in fluoroquinolone derivatives and specialty antivirals. QC measures are tightly controlled during the acylation steps to ensure low residual starting material and absence of unreacted acid chlorides, as required by cGMP protocols. The reaction yield and purity directly impact the downstream crystallization and isolation processes, thus affecting the overall batch quality.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP and Ph. Eur. guidelines for impurity profiles
    • FDA 21 CFR Part 211
    • Chinese Pharmacopoeia (ChP) API synthesis standards

    Typical usage ratio

    • 0.95–1.10 molar equivalents per nucleophilic substrate
    • Adjusted according to specific intermediate reactivity and yield optimization requirements

    Downstream process integration

    • Introduced during the benzoylation or acylation step after base substrate preparation
    • Purification sequence follows using column chromatography or crystallization
    • Strict in-process controls for residual chloride and trace solvents
    • Final API crystallization and drying with full batch traceability

    Final product types

    • Pharmaceutical intermediates for anticancer and antiviral drugs
    • API building blocks for CNS and cardiovascular therapies
    • Custom intermediates for clinical trial material supply
    • Specialty fluoroaromatic reference standards

    2. Agrochemical Active Ingredient Production

    Manufacturers in crop protection utilize this material to synthesize fluorinated benzoyl derivatives incorporated into modern herbicides and fungicides. Its electron-withdrawing capacity increases biological stability and improves selectivity in enzyme inhibition. The reaction process requires tight environmental and occupational controls due to reactivity. Certified cleanroom environments and advanced fume extraction are often necessary to meet regional regulations, while final actives undergo detailed residue and stability testing before formulation into commercial products.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing
    • European Regulation (EC) No 1107/2009 for plant protection products
    • US EPA Pesticide Registration standards
    • GB 4839-2016 for chemical pesticide raw material quality in China

    Typical usage ratio

    • 85–120% stoichiometric ratio based on target substrate
    • Adjusted for side reaction minimization and waste reduction

    Downstream process integration

    • Reacted with amines or heterocycles to form fluorinated active centers
    • Followed by hydrolysis, neutralization, or solvent extraction steps
    • Subsequent granulation or suspension concentrate formulation
    • QC sampling for residual acid chloride and purity confirmation

    Final product types

    • Active ingredients for broad-spectrum herbicides
    • Intermediate compounds for contact and systemic fungicides
    • Seed treatment formulations
    • Custom fluorinated pesticide candidates for field trials

    3. Specialty Polymer Synthesis for Electronics

    Electronics materials firms integrate this compound as a functionalizing reagent for fluorinated polyimides and advanced engineering plastics. Its use promotes thermal stability, low dielectric loss, and enhanced chemical resistance in polymers targeting semiconductor and high-frequency electronic substrates. Polymerization reactors are designed to handle acid chloride reactivity, and all exhaust gases are treated according to strict emission protocols. Product batches undergo dielectric constant and purity testing before scaling to commercial film or resin production.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free base materials in printed wiring boards
    • RoHS Directive 2011/65/EU for hazardous substance management
    • ISO 9001:2015 for polymer and resin production
    • REACH Regulation EC/1907/2006 for chemical registration in the EU

    Typical usage ratio

    • 5–20 wt% incorporation into polymer backbone depending on final application requirements
    • Optimized by molecular weight targets and end-use property specifications

    Downstream process integration

    • Introduced during polyimide or polyester backbone modification steps
    • Controlled addition in solvent-rich environments to limit local overheating
    • Post-processing includes film casting, drying, and thermal imidization
    • Dielectric and thermal stability testing prior to shipment

    Final product types

    • Flexible circuit board base films
    • High-performance insulating resins
    • Fluorinated adhesives for microelectronics
    • Low-k dielectric films for IC fabrication

    4. Analytical Reagents and Derivatization Agents

    Analytical laboratories and commercial diagnostic kit manufacturers employ this reagent to derivatize amines, alcohols, and phenolic compounds for highly specific detection in chromatography and mass spectrometry. The reagent’s strong acylating properties yield fluorinated derivatives that improve detection sensitivity and analytical resolution. Laboratory batch records document precise reaction times and purification methods to comply with GLP standards, and reagent blank testing confirms the absence of interfering impurities.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Accreditation
    • GLP (OECD Principles of Good Laboratory Practice)
    • European Pharmacopoeia, Reagents Section
    • US Pharmacopeia Analytical Reagent specifications

    Typical usage ratio

    • 1.05–1.20 molar equivalents per analytical sample, depending on analyte concentration
    • Ratios adjusted to prevent unreacted baseline interference in instrument analysis

    Downstream process integration

    • Added directly to sample prior to chromatographic or spectrometric analysis
    • Followed by extraction or solid phase purification as per analytical protocol
    • Integration with automated derivatization platforms for high-throughput applications
    • Batches tracked under laboratory quality management system

    Final product types

    • Chromatography derivatization kits
    • Mass spectrometry calibration standards
    • Certified laboratory analytical reagents
    • Custom fluorinated labeling compounds for biomolecular research

    5. Fine Chemical Synthesis for Performance Materials

    Performance materials producers apply 2,3,6-Trifluorobenzoyl Chloride in the functionalization of aromatic and heterocyclic compounds used in coatings, fragrance intermediates, and high-stability dyes. The precise introduction of trifluoromethyl functional groups improves the material’s solubility, volatility, and UV stability. Process controls monitor side reactions to ensure consistent functionality, and effluent is treated to comply with local and export-oriented chemical safety rules.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical plant operation
    • National Chemical Inventory requirements (e.g., US TSCA, EU REACH, Korea K-REACH)
    • EN 71-3 (Chemical Safety of Toys – certain dye applications)
    • GB/T 23992-2009 Quality specification for dyestuff intermediates (China specific)

    Typical usage ratio

    • 0.8–1.2 equivalents relative to aromatic substrate in batch or semi-continuous production
    • Ratio changed based on target molecule reactivity and desired end-group density

    Downstream process integration

    • Added during functionalization or coupling reactions in reactor vessels
    • Post-reaction washing, drying, and purity adjustment by distillation or extraction
    • Downstream blending for coatings or formulation for fragrance intermediates
    • Batch and traceability procedures in line with export documentation

    Final product types

    • Photo-stable dyes for textile and plastic coloration
    • Advanced UV-resistant coating intermediates
    • Fine chemical intermediates for fragrance and aroma industries
    • Custom functionalized benzoic acid derivatives for niche applications
    Free Quote

    Competitive 2,3,6-Trifluorobenzoyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2,3,6-Trifluorobenzoyl Chloride: Experience from the Manufacturing Floor

    Every batch of 2,3,6-Trifluorobenzoyl Chloride tells a story. In the manufacturing plant, nothing stays theoretical for long. Workers move between reactors, and the unmistakable aroma of acyl chloride production gives a strong reminder: this compound carries serious potential. Its molecular structure, marked by three fluorine atoms on the benzene ring and an acyl chloride group, gives it a place among high-value fluorinated intermediates. We see the impact of these structural tweaks unfolding daily, from the unique reaction kinetics during synthesis to the sharp reactivity in downstream applications.

    Crafting for Today’s Specialty Chemicals

    The raw material sourcing phase for 2,3,6-Trifluorobenzoyl Chloride often causes some debate in our team. Purity standards run tight for reagents and solvents. Even a mild gap in raw feedstock quality steers us off course, risking downstream reactivity. We avoid recycled or suboptimal stocks; the performance drop speaks for itself, especially in demanding pharmaceutical or agrochemical transformations. Our output consistently hits high purity benchmarks—G.C. purity generally above 99%—which supports both research and full-scale production work. Such consistency doesn’t come from leaving things to chance. It requires routine maintenance on distillation lines and an experienced workforce that can troubleshoot subtle shifts in reactor temperature or solvent moisture.

    Differentiating from Other Fluorobenzoyl Chlorides

    It matters which trifluoro-substituted benzoyl chloride comes into the plant. Some buyers without direct experience believe these compounds only differ in the numbers on a safety data sheet. Research labs learn quickly: swap 2,3,6 for something like 2,4,5, and downstream selectivity changes. The placement of the fluorine atoms adjusts electron density on the aromatic ring, which in turn alters reactivity with nucleophiles. Our technical team finds the 2,3,6 isomer brings a predictable reaction profile to coupling reactions and nucleophilic substitutions. This sets it apart from isomers prone to generating more regioisomeric by-products or unstable intermediates during acylation, and helps chemists reduce purification steps in process development.

    Cost-conscious engineers in industrial settings have noted this practical benefit. It can affect catalyst life and boost yields in optimization campaigns for active pharmaceutical intermediates, crop protection chemicals, or functionalized polymers. These aren’t margin trivialities. We see production lines run more smoothly, documentation efforts shrink, and hazardous waste output go down compared to older halogenated acyl chlorides. Several long-standing customers rely on the consistent quality and chemical behavior for patented process routes, knowing that a single fluctuation can cascade through complex multi-step syntheses. No one excuses a glitch caused by inconsistent starting material, least of all the plant operators who have to remediate the mess.

    Production Practices That Drive Reliability

    We learned the hard way that environmental moisture is the stealth enemy for acyl chlorides. Even tiny leaks in storage or transfer lines trigger hydrolysis, pulling free hydrochloric acid and lowering the assay. To combat this issue, we operate under rigorously dried conditions, use inert gas blanketing, and train crews to monitor vessel integrity as habit, not afterthought. This diligence supports extended shelf life and reactivity retention, so users experience reliable performance during storage and transportation.

    Throughout scale-up phases, we mapped every process quirk. Uncertain temperature gradients in early large reactors once led to partial decomposition. Our engineers responded by tightening thermal controls, increasing agitation rates, and installing real-time in-line analytics for rapid process monitoring. These investments added upfront cost but trimmed far more from later reprocessing, waste generation, and lost man-hours. The tradition around here is to share operational feedback directly with our analytical group, looping back lessons from plant trials into process tweaks until the product leaves the warehouse on spec.

    In the packaging hall, every drum and jerry can passes through rigorous QA. Routine analytical screens for residual solvent, acid content, and trace impurities have grown to include mass spectrometric methods and isotopic testing for select applications. Custom labeling marks not just a batch code, but also links every container to a detailed batch record, supporting traceability back to every critical variable during synthesis.

    Applications Built on Reactivity and Reliability

    For years, our customers have driven innovation using 2,3,6-Trifluorobenzoyl Chloride as an acylating agent, especially where traditional benzoyl chlorides would stall or introduce side-products. Medicinal chemists focus on it for crafting specialized amide bonds—those tough, electron-poor targets in drug scaffolds where weaker acyl donors can’t deliver. In agricultural chemistry, its fluorinated character provides the molecular stability needed for certain herbicide and fungicide backbones. It’s a mainstay for materials science teams seeking durable fluorinated polymers or high-performance specialty coatings.

    As a manufacturer, we hear about the tough syntheses from the field. A pharma partner described an esterification step so moisture-sensitive, past acyl chlorides kept failing. With our product—kept scrupulously dry at every point—yields held steady over a multi-week campaign, shaving off hundreds of thousands in possible rework costs. Another story came from a materials science group. They explained how alternative fluorobenzoyl chlorides contaminated their cross-linked networks with excess by-products, but the 2,3,6 substitution created a much cleaner backbone, allowing predictable physical properties and stability under heat. These aren’t just theoretical talking points; they reflect real-world risk when the chemical doesn’t perform.

    Safety and Handling: Grounded in Daily Practice

    On the shop floor, few underestimate the hazards of acyl chlorides. Hydrolysis forms hydrogen chloride, which attacks mucous membranes without warning. Personal protective equipment rules—especially for respiratory and dermal exposure—get drilled into new hires before they ever see a drum. Operators know the spillage drill, vent line design, and scrubbing systems far better than any outsider reading a label. We invest in closed handling systems not just for compliance, but after witnessing what uncontrolled releases can do. Even the most experienced team member respects the containment protocols and the steady attention that this compound demands at all stages, from transfer to packaging.

    Our safety performance depends on consistent training, air quality monitoring, and a culture of looking out for co-workers. These practical steps build workplace trust, and underline the point that chemical manufacturing doesn’t tolerate shortcuts. Any fluctuation in material quality or handling reflects on both the operators and the downstream chemists who craft high-value products under unforgiving conditions.

    Environmental Responsibility: Reducing Waste and Emissions

    Every unit operation produces waste, but process improvements make a difference. Over the years, we managed to cut organic solvent waste by improving reaction selectivity and optimizing distillation setups. We route vented hydrochloric acid through scrubbers, mitigate spot emissions, and regularly invest in solvent recovery. Crews actively maintain filters and traps, which ensures that fugitive emissions rarely escape. We see continuous improvement as routine, not as a corporate slogan. Most progress came from feedback at the plant level, where operators suggested tweaks that engineering later formalized—making for safer, less wasteful production long after the initial design phase closed.

    Ongoing dialogue with customers shapes our approach to waste returns and recycling programs. In collaboration with key players in research and manufacturing, we recycle unused material and focus on returnable containers. The results speak for themselves: not only do costs go down, but customers see their own efficiency go up. This practical benefit gets more mileage than any feel-good slogan.

    Regulatory and Market Demands: Staying Ahead

    Regulation continues to move faster than many plants can adapt, especially across borders. From REACH compliance in the EU to EPA oversight in the US, documentation for materials like 2,3,6-Trifluorobenzoyl Chloride grows more complex every year. Our compliance group, rooted in real production knowledge, leads by combing through the details. They cut through red tape, address queries from international partners, and keep technical files up to date. Only those who try to ship a regulated chemical overseas know how even a minor record-keeping slip can halt containers at customs, with knock-on costs for everyone downstream.

    Feedback from procurement teams and regulatory officers at customer companies has shaped our documentation approach. We build SDSs and technical dossiers that include not just regulatory checkboxes but explanations of manufacturing steps, impurity profiles, and long-term stability. Some customers have told us that the clarity of documentation saves them countless hours in their own submissions and risk assessments. This mutual transparency fosters trust and cuts through the usual friction between suppliers and end users. Each time regulatory agencies raise the standard, we already have protocols in place, shaped by direct manufacturing experience, not just theoretical compliance.

    Collaborative Improvement with Industrial Partners

    Long-term relationships form the backbone of our manufacturing philosophy. Large customers bring challenging requests—higher purity demands, custom impurity profiling, unusual packaging sizes. Having these conversations on equal footing builds practical know-how. No single customer shapes the whole business, but their feedback brings fresh focus to process bottlenecks, revealing next steps for line upgrades or analytical refinements.

    In a recent project, a customer approached us with a need for accelerated delivery to keep up with a new product launch. Our team overhauled logistics and temporarily shifted production schedules, shaving lead times by nearly 30%. While the change put pressure on the plant, the shared urgency forged a sense of joint accomplishment. This spirit of open dialogue means we stay ahead of market shifts and technical hurdles, because any gain in reliability or performance for the user circles back to our own production standards.

    Expertise Rooted in Daily Engagement

    Our technical experts have watched 2,3,6-Trifluorobenzoyl Chloride applications expand over the last decade. Production line managers give hands-on feedback about unexpected crystal morphology, color shifts, or trace impurity spikes, all of which get relayed to both R&D and quality groups in real time. When a research group inquires about suitability for an exotic heterocycle, we dig into archived production records, historical QC data, and, when necessary, conduct short-batch trial runs. We share what we’ve learned about stability, solvent compatibility, and handling distinctions—all based on direct, recent processing data, not guesswork or recycled sales talk.

    This “boots on the ground” commitment means our guidance comes from a working knowledge of chemical behavior, not just literature citations. Our aim is to ensure partners not only order a drum or kilogram, but leave with a working understanding of how the compound behaves in their context, supporting scale-up and risk management with frankness that only comes from direct handling and real accountability.

    Looking Forward: Progress through Practicality

    Innovation rarely arrives as a grand reveal. More often, it takes shape through incremental improvement—new filter presses here, a solvent distillation tweak there. With 2,3,6-Trifluorobenzoyl Chloride, the incremental wins add up. Stability gets better, drums arrive cleaner, customer complaints fall to nearly zero. Downstream syntheses run longer and smoother. The everyday success comes from people who live with the process daily—chemists, operators, engineers, and inspectors—each pushing toward something a little better than the day before.

    By listening carefully, investing steadily, and sharing experience freely, we ensure this compound supports the ambitions of demanding research teams and non-stop industrial plants alike. Users know that a stable, high-purity supply chain matters when development budgets and production timelines hinge on a dependable result, not an experiment. The lessons gathered on our production floor become the guidance we offer—firm, grounded, and practical. That’s how we see 2,3,6-Trifluorobenzoyl Chloride: not just a formula, but a commitment forged by all those who make, test, and apply it, every single day.