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2,3,4,5-Tetrachlorobenzoyl Chloride

    • Product Name 2,3,4,5-Tetrachlorobenzoyl Chloride
    • Alias TCBC
    • Einecs 221-645-3
    • 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

    749796

    Chemical Name 2,3,4,5-Tetrachlorobenzoyl Chloride
    Molecular Formula C7HCl5O
    Molecular Weight 278.3 g/mol
    Cas Number 6334-32-1
    Appearance White to off-white solid
    Melting Point 110-112°C
    Boiling Point 315°C
    Density 1.71 g/cm³
    Solubility Decomposes in water
    Purity Typically >98%
    Storage Conditions Store in a cool, dry place and tightly closed container
    Synonyms Tetrachlorobenzoyl chloride, TCBCl

    As an accredited 2,3,4,5-Tetrachlorobenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle, sealed with a Teflon-lined cap, labeled “2,3,4,5-Tetrachlorobenzoyl Chloride, for laboratory use.”
    Shipping 2,3,4,5-Tetrachlorobenzoyl Chloride is shipped as a hazardous material due to its corrosive nature. It should be packed in sealed, compatible containers, protected from moisture, and labeled according to regulations. The shipping process must comply with international and domestic transport guidelines for dangerous goods, ensuring proper documentation and handling.
    Storage 2,3,4,5-Tetrachlorobenzoyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture. It should be kept away from incompatible substances such as strong bases, alcohols, and amines. Storage conditions must protect from light and humidity to prevent hydrolysis and decomposition, and appropriate chemical safety protocols should be followed.
    Application of 2,3,4,5-Tetrachlorobenzoyl Chloride

    Applications of 2,3,4,5-Tetrachlorobenzoyl Chloride in Industrial Manufacturing

    As the direct manufacturer, we supply 2,3,4,5-Tetrachlorobenzoyl Chloride (TCBC) to specialized sectors serving advanced chemical synthesis, including pharmaceuticals, agrochemicals, polymer additives, and liquid crystal materials. Each application deploys TCBC in high-precision workflows, meeting rigorous process and regulatory benchmarks set by global industries.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies employ TCBC to introduce tetrachlorobenzoyl functional groups during the synthesis of active pharmaceutical ingredients (APIs), especially in the preparation of select anti-inflammatory and oncological agents. This material serves as a key acylating agent, enabling formation of highly substituted aromatic carboxamides or esters through stepwise condensation reactions. The high purity requirement and specific reactivity profile support strict GMP workflows.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • USP/NF specifications for starting materials
    • EMA guideline on limits of genotoxic impurities
    • 21 CFR Part 211 (US FDA GMP for finished pharmaceuticals)

    Typical usage ratio

    • 0.8–1.2 mol equivalents per target substrate, adjusted for reaction conversion rates and impurity control

    Downstream process integration

    • Acylation step in heterocycle or aromatic API precursor synthesis
    • Followed by isolation, purification, and crystallization
    • Used under controlled temperature and inert atmosphere handling to protect against unwanted hydrolysis and side reactions

    Final product types

    • Intermediate compounds for anti-tumor APIs
    • Precursors for non-steroidal anti-inflammatory drugs (NSAIDs)
    • Complex benzamide drugs in clinical trials
    • Substituted intermediates for custom research molecules

    2. Agrochemical Active Ingredient Manufacturing

    Producers of selective herbicides and insecticides utilize TCBC in the multi-step synthesis of chlorinated aromatic intermediates. Its high chlorination level and reactive benzoyl chloride function facilitate coupling and further derivatization, critical in creating final molecules with desired pest control properties. Stringent process controls and environmental compliance are required during large-scale batching.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • FAO/WHO Specifications for Pesticide Technical Material
    • REACH regulation (EC 1907/2006) for manufacturing and downstream use
    • China GB 2763 maximum residue limits when applicable to domestic agrochemicals

    Typical usage ratio

    • 0.95–1.1 equivalents relative to core phenolic or amino substrates in the presence of acid scavengers

    Downstream process integration

    • Integrated in acylation steps for pesticide intermediate assembly
    • Combined with nucleophilic aromatic substitution for later stage functionality
    • Process employs scrubbing systems for HCl byproduct containment

    Final product types

    • Chlorinated phenoxy herbicide precursors
    • Intermediate compounds for pyrazole or triazine systems
    • Active ingredients for systemic and contact insecticides
    • Building blocks in fungicide pipeline R&D

    3. High-Performance Polymer Additives

    Specialty polymer manufacturers integrate TCBC into advanced polymer formulations for enhanced flame-resistance and thermal stability. Used as a modifying reagent to introduce polar and halogenated aromatic groups onto polymer backbones, TCBC enables functionalization of polyesters and specialty resins. Rigorous batch testing ensures uniformity and end-use compliance for electronic and construction industries.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • ISO 9001 production management systems
    • RoHS Directive 2011/65/EU for hazardous substances
    • ISO 14001 (Environmental Management)

    Typical usage ratio

    • 0.5–3% by weight of the total polymer blend, dosed based on desired flame-retardant grading and material compatibility

    Downstream process integration

    • Added during reactive extrusion or pre-polymer modification
    • Activated under controlled temperature and catalysis
    • Integrated before pelletizing for compounding into masterbatches

    Final product types

    • Flame-retardant unsaturated polyester moldings
    • Modified epoxy resins for coatings
    • Engineered thermoplastics for electrical device enclosures
    • Construction-grade polymer panels

    4. Liquid Crystal Material Precursors

    Manufacturers producing intermediate and advanced materials for display technologies use TCBC in the fine synthesis of chlorinated aromatic cores destined for liquid crystal compounds. High product specification and controlled impurity profiles support stringent quality required by display panel OEMs. The compound’s properties allow for selective introduction onto biphenyl and related scaffolds, ensuring precise thermal and optical properties in the final mixtures.

    Industry compliance standards

    • ISO 9001:2015 for process and batch traceability
    • RoHS 2 (Restriction of Hazardous Substances)
    • IEC 61249 for materials in printed circuit technology
    • Customer-specific QC protocols for LC purity and clarity

    Typical usage ratio

    • 1.0–1.05 equivalents per aromatic core, optimized for molecular weight and transition temperature control

    Downstream process integration

    • Acyl chloride is introduced in early-stage electrophilic aromatic substitution reactions
    • Followed by selective hydrolysis and subsequent coupling
    • Material passes through multiple purification and fractionation steps

    Final product types

    • Liquid crystal monomers for TFT-LCD panels
    • Mixes for high-resolution display fluids
    • Specialty intermediates for OLED application research
    • Aromatic core structures for optoelectronic displays
    Free Quote

    Competitive 2,3,4,5-Tetrachlorobenzoyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,3,4,5-Tetrachlorobenzoyl Chloride: The Chemist’s Perspective

    Understanding the Product

    Our team has spent years working with 2,3,4,5-Tetrachlorobenzoyl Chloride, often simply called TCBC in the lab. This compound goes beyond basic applications; it brings specific reactivity and a profile of performance not found in every acid chloride. The model TCBC that leaves our site appears as a pale yellow to off-white crystalline solid, its purity voluntarily subjected to strict quality controls to meet the requirements found in demanding synthesis routes. In our experience, this keeps operations stable, reduces batch variability, and cuts down on the chance of unwanted byproducts making their way into downstream chemistry.

    Specifications That Matter to the End User

    Chemists appreciate materials that deliver the same performance across production runs. Having handled bulk manufacturing and scale-up for years, we focus our controls on those parameters that actually matter: chlorine content, melting point, hydrolyzable chloride, and residue after ignition. Our standard lots of TCBC demonstrate a purity above 98 percent, supported by gas chromatography and HPLC checks. The melting range, usually in the 78 to 81 degrees Celsius corridor, tells us it’s clean and ready for coupling reactions. Moisture content gets checked using Karl Fischer titration, since humidity can ruin entire batches by hydrolyzing the acid chloride group prematurely. Fine particles are screened to avoid dust issues during loading, especially for workers handling open vessels.

    Roles in Modern Chemical Processes

    Most who reach out for TCBC rely on its unique four-chlorine substitution pattern. This characteristic makes it an especially strong acyl chloride, ready to participate in Friedel-Crafts acylation, peptide and ester synthesis, or as an intermediate for agricultural and pharmaceutical molecules. Over the past decade, our product has landed in the toolkits of those designing new organochlorine herbicides, for those needing reliable building blocks in API development, and even for specialty materials like liquid crystals. We’ve seen research chemists use it to activate carboxylic acids, bringing higher yields and cleaner profiles in the resulting esters.

    Unlike simpler benzoyl chlorides, this one stands out for its electron-withdrawing character. Four chlorine atoms on the ring draw electron density away from the carbonyl, making this molecule more reactive than monochloro or dichlorinated cousins. This higher reactivity opens up reaction possibilities where sluggish benzoylation agents would stall or require aggressive conditions.

    Why TCBC Differs From Other Benzoyl Chlorides

    During daily production, we directly observe how substituents on the aromatic ring swing the outcome of a synthetic route. Standard benzoyl chloride, with no ring substitution, appears stable but much less electrophilic than TCBC. If you drop in the two, three, or four chlorine atoms, you see deeper color changes, differences in volatility, and a noticeably sharper reaction behavior during acylation steps.

    From a reactivity standpoint, TCBC acts fast and often allows milder reaction conditions where unchlorinated or monochlorinated versions can’t. Some customers making specialty polyesters point out the difference in product color and performance after using our high-purity TCBC compared to less chlorinated mixtures. We get fewer reports of tar formation or sticky residues in their reactors—a concern when you push less reactive acid chlorides and start pulling in side products.

    Environmental and Safety Context

    As a manufacturer, we interact regularly with safety officers and process teams about how TCBC handles during storage, transit, and use. It reacts violently with water, liberating hydrochloric acid and risking corrosion or occupational exposure. Because we ship this solid in moisture-barrier drums with real-time humidity sensors inside, users know each delivery lands in prime form, not half-hydrolyzed or caked together. Our experience shows that granular handling—not just sealed drums—reduces airborne dust and keeps workers safer during loading. Staff on our lines wear acid-resistant gloves and use exhaust ventilation. These real lessons translate to practical safety advice we share with formulators and pilot plant engineers, so operations move forward without costly stoppages due to leaks or exposure incidents.

    We take lessons from the regulatory front as well. While TCBC is not classed as a universal hazardous substance like some reactive halides, national and international transport standards classify it as a corrosive solid, requiring labels and emergency response procedures. Our own incident records remain clear thanks to aggressive staff training and constant review of how the material moves through our warehouse and transport systems. On the environmental side, downstream users sometimes worry about byproducts from hydrolysis, especially in wastewater. We supply extensive documentation on neutralization techniques, storage tank cleaning, and ventilation system compatibility—advice drawn from real plant failures and fixes, not just from the literature.

    Supply Chain Considerations

    Sourcing reliable TCBC comes down to transparent manufacturing and clear documentation. Shortcuts at the production stage will show up downstream as clogging, off-odors, or failing HPLC specs on intermediates. Raw materials start with carefully vetted monochlorobenzene and thionyl chloride. We don’t tolerate recycled solvents that could introduce sulfur contamination or embed trace metal ions. Our teams screen every incoming lot of precursor chemicals because a bad day sourcing means a week lost reworking or dumping production runs.

    Consistency influences cost and risk. Off-spec batches cause rework or, worse, contaminated goods shipped to a high-value customer. We test for trace chlorinated biphenyls and assure levels remain far below detection. Packing dates and run numbers permanently anchor each drum, paving the way for smooth recall documentation or product performance tracking if an analytical anomaly ever flags in partnership labs. This way, users get the peace of mind that comes from dealing with the actual maker of the product, not just someone passing along a drum sourced from unknown origins.

    Usage Feedback and Continuous Improvement

    Our users span research chemists at small labs to technical teams in multinational agrochemical operations. Early feedback often centers on reactivity—initial trial runs sometimes push the reaction harder than optimal, expecting more sluggish performance based on experience with less-chlorinated analogs. Realizing the higher reactivity lets them cut back on promoter acids or reduce heating, saving energy and reducing fouling in reactors. We encourage process teams to run pilot assays and document yield, purity, and exotherm profiles.

    In one notable scale-up, a client reported unexpected crystallization in feed lines. By reviewing our own handling records, we noticed a slight drop in ambient temperature at their plant during early spring. We adjusted shipping advice—insulated drums, short transfer times, and pre-warming lines—which eliminated the issue in the next batch. Direct manufacturer-customer contact, not relayed through middlemen, allows these kinds of quick, tailored solutions.

    Feedback mechanisms run both ways. Synthetic methodologies evolve as our customers attempt greener, safer protocols. We have responded by tightening release specs on low-boiling organochlorines, not waiting for regulations to force our hand. Customer drives for lower batch-to-batch variability spark us to invest in online analytics and tighter process control, so every drum leaving our facility displays the same spectral fingerprint.

    Comparing TCBC With Other Acyl Chlorides

    A question we often answer is why a chemist would opt for a tetrachlorinated product over simpler acyl chlorides. There’s a visible trend in pharmaceutical discovery away from broad-spectrum reagents toward finely tuned building blocks. TCBC fills that spot when molecular precision trumps cost. It delivers sharper reactivity, reduced side reactions, and fewer purification headaches in target product synthesis.

    Beyond benzoyl chlorides, we see interest in acyl bromides and mixed halides. These compounds often out-power unchlorinated benzoyl chloride, but TCBC carves its own niche with predictable behavior, lower volatility, and more manageable toxicology profiles. In our operations, the presence of four chlorines yields improvements in shelf life compared to fresher, more hydrolysis-prone acyl bromides that need constant refrigeration and handling under anhydrous conditions. Our facility’s material loss rates, traced over years, appear lowest for TCBC among our specialty acyl chloride offerings.

    Practical Tips Gained From Manufacturing

    Our days rarely pass without hands-on experience with the product. Heating and loading drums during winter triggers effects not evident in summer, so batch setup guidelines change seasonally. We rotate storage drums to avoid compaction, check for seal integrity, and run regular moisture checks on stored product. Drums never sit directly on concrete floors to prevent condensation, and secondary containment remains a non-negotiable even though we rarely see leaks.

    From a synthetic standpoint, we recommend process engineers dose TCBC in well-ventilated environments, preferably under dry nitrogen. For scale-up runs exceeding several hundred kilograms, staged addition keeps thermal runaway in check and reduces vapor-related stress on the reactor. Digital process control valves and jacketed reactors keep the system stable and allow tight control as the exotherm rises during addition. Scrubbing systems run on continuous monitoring, and trained operators never leave a line unattended during charge. These strict protocols don’t just protect operators—they ensure every gram of feedstock enters the reaction at optimum reactivity, improving conversion and reducing batch corrections.

    Challenges in Today’s Marketplace

    We see volatility in global supply lines for critical inputs, along with shifts in end-market regulation. Customers expect full traceability—sourcing a drum of TCBC from our plant means getting full upstream documentation, not just a single page of analytical data stapled to the outside. Tightening environmental controls shift the types of auxiliary chemicals users request. More often, we see requests for detailed emissions data, spent acid management advice, and lifecycle analysis. Our answer has been to embed these data and solutions into product rollouts, both at the point of sale and in post-sales technical support.

    The regulatory picture keeps changing. In the past, some regions overlooked organochlorine intermediates in their national inventories, but now careful document review and declarations of use appear as regular features. This prompts us to keep product profiles updated and notify customers of any raw material or compliance changes long before they would face an audit or government notice at their site.

    Shaping the Road Ahead

    Access to high-purity 2,3,4,5-Tetrachlorobenzoyl Chloride remains critical for innovation in sectors pushing the boundaries of organic and materials chemistry. Those willing to share data and feedback—be it through pilot plant observations or full process analytics—help us refine every ton leaving our site. Some of our longest-standing customers have built entire product lines on the reliability and reactivity profile of this compound, adapting core synthesis steps together with our technical teams to deal with everything from changing local solvent regulations to emerging classification schemes for chlorinated aromatics.

    The improved reproducibility we achieve at manufacturing scale reduces end-user headaches, lets bench chemists focus on design, and spares procurement staff endless qualification paperwork. Shipping product that works straight from the drum, without hours of fiddling or rework, counts as the real separator between a full-cycle manufacturer and a generic repackager. We take pride in the fact that, time and again, the properties of our TCBC hold up to both the expectations of demanding synthetic chemistry and the scrutiny of compliance-driven procurement.

    A Manufacturer’s Commitment

    As the team hands-on involved from synthesis all the way to the last seal on every drum, we see our role extending beyond the sale. We adapt not because a regulation dictated a response, but because real operators and process managers tell us how their requirements change—from new downstream chemistry to shifts in packaging and delivery timelines. The real-world challenges we solve shape a more robust, predictable, and technically sound supply of 2,3,4,5-Tetrachlorobenzoyl Chloride, and we look forward to continuing this dialog with those on the frontlines of chemical innovation.