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2,3,4,5-Tetrachlorobenzonitrile

    • Product Name 2,3,4,5-Tetrachlorobenzonitrile
    • Alias Tetrachlorophthalonitrile
    • Einecs 219-600-3
    • 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

    625082

    Product Name 2,3,4,5-Tetrachlorobenzonitrile
    Cas Number 117-18-0
    Molecular Formula C7HCl4N
    Molecular Weight 239.91
    Appearance White to off-white crystalline powder
    Melting Point 163-165°C
    Boiling Point 351.7°C at 760 mmHg
    Density 1.70 g/cm³
    Solubility Insoluble in water; soluble in organic solvents
    Flash Point 166°C
    Synonyms 2,3,4,5-Tetrachloro-benzonitrile
    Smiles C1=C(C(=C(C(=C1Cl)Cl)Cl)C#N)Cl

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

    Packing & Storage
    Packing Packaging: 100g of 2,3,4,5-Tetrachlorobenzonitrile supplied in a sealed amber glass bottle with tamper-evident cap and chemical hazard labeling.
    Shipping 2,3,4,5-Tetrachlorobenzonitrile should be shipped in tightly sealed, inert containers, protected from moisture and incompatible materials. Transport in accordance with applicable local, national, and international regulations for hazardous chemicals. Shipping documents must include relevant hazard identification information, ensuring compliance with safety protocols and environmental guidelines during transit.
    Storage 2,3,4,5-Tetrachlorobenzonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong oxidizers and acids. Appropriate chemical-resistant shelving or cabinets should be used, and clearly labeled for hazardous materials.
    Application of 2,3,4,5-Tetrachlorobenzonitrile

    Applications of 2,3,4,5-Tetrachlorobenzonitrile in Industrial Manufacturing

    2,3,4,5-Tetrachlorobenzonitrile is a key chlorinated aromatic nitrile leveraged by leading enterprise manufacturers as an essential intermediate across select sectors with high regulatory scrutiny and precise functional demands. As the original producer, we rigorously support downstream partners with technical guidance through every step of process formulation, batch integration, and industry compliance to enable reliable production of advanced chemical derivatives. Below, we outline the principal validated industrial applications, each presenting the necessary technical parameters for responsible, scaled use.

    1. Synthesis of Chlorfenapyr (Agrochemical Intermediates)

    This material serves as a critical intermediate for producing chlorfenapyr, a specialized insecticidal active widely used in crop protection formulations. Manufacturers introduce this nitrile during the phenylpyrrole synthesis phase, enabling chlorination under controlled conditions. Adherence to regulatory methodology for active substance precursors, as well as stringent contaminant controls throughout the catalytic hydrogenation steps, are essential in agrochemical synthesis facilities.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • European Union Regulation (EC) No 1107/2009 for Pesticide Approval
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) Registration for Intermediates
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 1.05–1.12 molar equivalents relative to product target; adjustments depend on impurity profile and reaction yield, commonly 120–135 g per batch (per 100 kg final active)

    Downstream process integration

    • Chlorinated aromatic nitrile added after initial base condensation as reactant in a staged nucleophilic substitution; integration temperature maintains 110–135°C to preserve core ring integrity

    Final product types

    • Chlorfenapyr technical concentrate (TK)
    • Wettable powder and water-dispersible granules
    • Suspension concentrates and pre-formulated insecticide blends

    2. Industrial Colorant and Pigment Precursors

    Downstream pigment producers utilize 2,3,4,5-tetrachlorobenzonitrile in multi-step reactions for synthesizing specific phthalocyanine pigments and quinacridone derivatives. During the pigmentary condensation, the compound acts as a halogen source, imparting color strength, weather-fastness, and dispersion properties tuned for high-performance plastics and coatings. Inclusion at this point determines heavy metal content and toxicological compliance for finished applications.

    Industry compliance standards

    • EN 71-3 Safety of Toys (Migration of Certain Elements)
    • RoHS Directive (2011/65/EU) for Electronic Equipment
    • ASTM D5398 Standard for Pigment Purity
    • REACH Annex XVII (Regulation of CMR Substances)

    Typical usage ratio

    • 0.5–2.3% weight/weight in pigment batches; based on desired color profile and matrix compatibility

    Downstream process integration

    • Introduced following ring closure and before final crystal modification; complete solvent removal and purification precede pigment grinding and dispersion

    Final product types

    • Phthalocyanine green and blue pigments for plastics and inks
    • Quinacridone magenta and violet pigments
    • High-grade dispersions for automotive and industrial coatings

    3. Fine Chemical Intermediates for Pharmaceutical Synthesis

    Active pharmaceutical ingredient manufacturers integrate 2,3,4,5-tetrachlorobenzonitrile into multi-stage syntheses of select heterocyclic intermediates. This step plays a role in introducing functionality compatible with later amide or imine transformations. Accurate dosage control and monitored conversion are enforced to comply with pharmacopeial impurity thresholds at each synthesis stage, especially for regulated APIs and registered intermediates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP <233> (Elemental Impurities) and <467> (Residual Solvents)
    • EU GMP for Chemical APIs (Directive 2003/94/EC)
    • Specific Drug Master File (DMF) submission guidelines

    Typical usage ratio

    • 0.8–1.3 molar equivalents relative to subsequent coupling step; usage tailored according to final batch purity and downstream analytical specification

    Downstream process integration

    • Charged into dedicated reactor sequence for aromatic ring functionalization following initial halogen exchange, with in-process HPLC monitoring; isolation precedes further transformation

    Final product types

    • Cyclic imide or amide drug intermediates
    • Chlorinated heterocycles for anti-infective and CNS therapeutic development

    4. Polymer Stabilizer and Additive Synthesis

    Polymer manufacturing operations incorporate this compound in the production of highly halogenated benzotriazole and benzoxazole additives, which function as light and thermal stabilizers for specialty polyolefins and engineering plastics. Process control during blending and condensation determines additive efficacy and compatibility and ensures emissions stay within safe handling thresholds for large-scale extrusion environments.

    Industry compliance standards

    • FDA 21 CFR 177.1520 for Polymers in Contact with Food
    • ISO 14001 Environmental Management (for emissions and handling)
    • GB/T 33356-2016 (Chinese standard for plastic additives)
    • REACH Regulation (Annex XV dossiers for monomers/additives)

    Typical usage ratio

    • 0.2–0.7% weight/weight depending on base polymer and targeted UV protection index; higher loading assessed under accelerated aging tests

    Downstream process integration

    • Introduced during polymer stabilization masterbatch preparation, immediately post-polymerization; high-shear blending ensures homogeneous additive dispersion before final pelletizing

    Final product types

    • UV-stabilized polypropylene and polyethylene compounds
    • Engineering thermoplastic masterbatches for outdoor use
    • Pre-compounded additive pellets for bottle and film extrusion lines
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    Certification & Compliance
    More Introduction

    2,3,4,5-Tetrachlorobenzonitrile: A Trusted Cornerstone in Chlorinated Aromatics

    Understanding 2,3,4,5-Tetrachlorobenzonitrile from the Manufacturer’s Viewpoint

    Every producer of specialty chemicals comes to know certain intermediates through thousands of batches, careful hands-on process improvements, and follow-up with real customers facing real production challenges. 2,3,4,5-Tetrachlorobenzonitrile, or TCBN for short, has long stood out in the family of chlorinated aromatic nitriles. From our factory floor, we don’t just see this product as a catalogue entry. Over years of scaling up, troubleshooting and fine-tuning, we’ve learned what makes a reliable TCBN, how users in crop sciences and fine chemicals depend on it, and which minor variations can have major downstream effects.

    The Essence of TCBN

    At its core, TCBN’s four chlorine atoms on the benzene ring, paired with a nitrile group, give it a set of chemical behaviors and handling needs quite distinct from isomers or lower-chlorinated analogues. The specific substitution pattern provides much of this material’s practical value—yielding a molecule that’s at once highly reactive for coupling or transformation, and stable enough to be shipped worldwide without loss of integrity. Over the years, we’ve fielded questions about why four chlorines, and why this precise arrangement. Users running plant protection syntheses or pharmaceutical intermediates know that even small changes in the pattern change yields in key reactions or create unwanted by-products.

    Typical Model and Reliable Specifications

    Long-term production has honed us to a tight model—pure, off-white to pale yellow crystalline powder, typically offered at industrial scale with purity above 98 percent by HPLC, with residual moisture and volatile matter checked for each shipment. Particle size does not just influence container packing but can affect dispersion in liquid-phase transformation reactions; we screen for consistent granularity as specified by our core customers in crop protection and specialty colorants. Trace impurities, particularly polychlorinated by-products, have a way of creeping in during chlorination stages. Projects in dye intermediates or advanced agricultural synthesis often demand extended impurity data—so our analytical methods include GC-MS and LC-MS profiles available on request, not just a base purity percentage on the certificate of analysis.

    Why Do Users Choose TCBN Over Similar Molecules?

    Chlorinated benzonitriles form an essential platform in organic chemistry, but jobs that call for TCBN are seldom solved by swapping in a tri- or pentachlorinated alternative. Throughout years serving customers at the bench and in the field, we’ve seen how the four-chlorine pattern here lines up with very specific reaction sites. Downstream products, from herbicides to specialty dyes to pharmaceutical intermediates, depend on the right ratio of electronic effects and steric hindrance. For instance, excessive chlorination can block key coupling sites or complicate waste treatment, while lower-chlorinated versions underperform on efficiency or purity in the final product step. The 2,3,4,5-substitution pattern produces a molecule both electron-withdrawing and reactive at defined positions—just right for follow-up cyanation, oxidation, or aromatic substitution reactions.

    We have seen engineers try to cut corners by trying TCBN analogues or blending different isomers. In nearly every case, results flounder due to off-pathway side reactions, solubility problems, or difficult-to-remove byproducts. Feedback directly from process chemists backs up lab talk with plant-scale data: TCBN behaves dependably batch to batch, helping downstream synthesis run smoothly, and tracing any variances usually leads back to process changes upstream.

    Practical Production Insights

    Manufacturing high-purity TCBN at relevant scale remains technically demanding. Chlorination reactions, if not tightly controlled, throw off a mix of isomers and over-chlorinated by-products, some of which closely mimic the target’s properties in crude state. We’ve invested heavily in continuous process monitoring—each reactor run is tracked for input stoichiometry, reaction temperature ramp, and extraction dynamics. It took dozens of small upgrades each year to get to a point where a campaign run delivers kilo after kilo at consistent quality, without need for extensive post-reaction rework. Solvent recovery, waste neutralization and air emission controls all demand attention, as chlorinated aromatics bring both profit and responsibility.

    Users have occasionally pressed for “just-in-time” shipments or customization to proprietary process requirements. From our side, fulfilling these needs takes forward planning to ensure consistent material is always on hand for timely shipment, and flexibility in drying or micronization setups to suit downstream feedstock needs without causing batch variability. Data from daily QC checks often fuels process tweaks—discovering a deviation in melting point or impurity level early lets us isolate, diagnose, and fix rather than pass along risks down the chain.

    Direct Uses and Field Experience

    In real-world application, 2,3,4,5-Tetrachlorobenzonitrile is rarely a strictly end-use product. It most commonly serves as an intermediate in the synthesis of herbicides, fungicides and pharmaceutical precursors. In the crop protection field, multiple well-known active ingredients depend on a high-purity source of this compound for key coupling reactions; the chlorine pattern here makes selective substitution and further transformation possible without tangling into adjustment of downstream synthetic steps. Customers have built entire formulation lines around the consistent supply of TCBN, using it as a backbone for oxygenation, halogen exchange, or further nitrile chemistry.

    In dyes and pigment manufacture, TCBN’s pattern brings the right reactivity and stability for certain specialty colorants, especially those requiring electron-withdrawing groups in orthogonal positions. Years of comparative work with dye manufacturers taught us where switching to an alternative starting material either reduces yield, alters colorfastness, or complicates waste treatment. Research labs exploring new pharmaceutical syntheses often choose our TCBN batches when mapping out lead discovery paths, as minor contamination or wrong isomer content at this stage quickly derails a multi-step program. The long run of production batches behind our material provides users not just a chemical, but a degree of predictability in how each lot will perform across years of R&D and plant trials.

    Regulatory Status and Safety Knowledge

    Chlorinated aromatic nitriles capture the attention of regulatory agencies, so plant operators and EHS teams expect transparent supply records and data. We operate under national and local frameworks, and much of our ongoing investment goes to documentation—full traceability on raw materials, emissions logs, and safe handling protocols. Having seen new requirements roll out, we stay ahead by keeping data and samples from earlier batches ready for spot checks or regulatory questions. Last-minute substitutions or unclear provenance do not have a place in this space; neither customers nor authorities take risks with materials that could slip into sensitive applications.

    In terms of safety, our line staff know that this isn’t a table salt operation. Eyes, hands, and lungs are always protected by real-world PPE, and air extraction systems run round the clock. Years of working with this chlorinated benzonitrile have built up a set of best practices on containment, spill response, and off-gas handling. We train our operators alongside each process upgrade, as the lessons learned from minor incidents—undetected line leaks, measured skin contacts, or filter failures—prevent larger problems down the road.

    Supply Chain and Customer Feedback Drives Evolution

    We’ve observed, from a manufacturer’s perspective, that the market for intermediates like TCBN is increasingly shaped by buyers’ own compliance pressures, production deadlines, and performance needs. Material shortages or low-quality imports can disrupt downstream processes for weeks or months—sometimes costing users entire batches of high-value products. Our response has always been straight: keep safety stocks, communicate openly about lead times, and support technical troubleshooting when conversions or batch variability raises red flags. Customers, particularly in global agricultural companies and specialty chemical providers, tell us how one weak link in this supply chain undermines entire business cycles. Being the manufacturer isn’t just about certification or meeting the numbers on a datasheet; it’s about partnering to prevent costly downtime and avoidable recalls.

    Some years ago, one major customer in the agrochemicals sector faced a string of losses attributed to minor impurities in one raw material component—root cause analysis traced the problem all the way upstream to the precise grade of TCBN being delivered. After recalibrating process controls and providing real sample archives for investigation, we rebuilt not just that relationship but an even sharper focus on trace-level impurity control throughout the process. These practical lessons guide how we maintain records, how we validate new process steps, and how closely we tie the production line to the feedback loop from end users.

    Differences Between TCBN and Other Chlorinated Benzonitriles

    Those looking for alternatives often ask: Why not use 2,4,6-trichlorobenzonitrile, or 2,3,5,6-tetrachlorobenzonitrile, or even pentachlorobenzonitrile? Over time, experience has taught the industry that changing the chlorine count or positions disrupts manufacturability, downstream reaction efficiency and product profile. In dye synthesis, for example, the specific electron density and steric map shaped by 2,3,4,5-substitution makes the difference between a compound that cleanly reacts and one that won’t follow the desired route, or yields unwanted side colors. In crop protection, major actives built off this scaffold fail to meet efficacy or regulatory thresholds when substitution patterns drift. Even the product’s physical characteristics—such as melting range, solubility in key solvents, or tendency for static clumping—shift with the position and number of chlorines.

    In our plant, we’ve developed thorough batch records, comparative pilot data, and customer-verified certificates pinning down distinctions between “same type” intermediates, which for years passed in some markets as interchangeable. Short-term savings from choosing the wrong isomer often get wiped out by greater reprocessing costs and persistent quality failures. The market does not treat these products as fungible, and for good reason.

    Complexities Beyond the Simple Molecule

    Though it’s easy to talk about chemical intermediates as commodities, the lived reality of making and using TCBN involves a tightly woven set of controls and relationships. Each run through our reactor is more than a file in a database; it reflects the sum of regulatory oversight, raw material trends, operator skill, customer specifications, and evolving technical best practices. Years in the business reveal how even seemingly small changes—temperature profiles, reagent source variability, washing protocol—impact the final product’s suitability for downstream synthesis. Mistakes at the molecular level cost hours and dollars at the plant scale, and our job as a manufacturer is to keep those mistakes off our customer’s desk.

    Communication with our supply chain partners flows both ways. We regularly incorporate lessons from users’ shop floors into our quality control steps and batch review meetings. Breakdowns—such as a lost truck, a customs snag, or a process bottleneck—translate to missed deadlines, excess holding costs, and sometimes the loss of entire specialty product campaigns. Over the years, sharing not just product but process know-how has paid dividends for customer relationships and our own production resilience.

    What Sets Our Approach Apart

    We have always tasked our teams to track not only every drum we ship, but every technical query we field—be it about solubility in a custom solvent system, limits on polychlorinated impurities, or the environmental fate of off-gassed residues. Our regular technical exchanges with crop science companies, pigment manufacturers and R&D labs identify new needs, whether for ever-lower impurity thresholds, alternatives to legacy solvents, or batch-to-batch consistency that allows faster plant validation. Our technical and operational specialists take pride in meeting these needs without the marketing fluff or distributor runaround. Reliability, from the viewpoint of those at the reactor and those receiving the shipment, depends more on daily vigilance than one-off investments.

    We don’t shy away from reporting production difficulties or market disruptions; customers face fewer surprises when they hear directly from the manufacturer about raw material hiccups, regulatory updates, or lead time pushes. The backbone of our business remains integrity in production, backed by current data, accessible archives, and personal accountability for every batch released.

    Charting a Way Forward in Chlorinated Intermediates

    Emerging requirements in global trade, environmental controls, and downstream process innovation keep pushing the demands placed on TCBN and similar molecules. Our ongoing investments focus on reducing waste generation in the chlorination step, automating sampling and analysis, and actively collaborating with academic groups and industrial partners to pilot greener process routes. Some customers now request lifecycle data or help with recycling solvent streams, aligning chemical production with broader sustainability goals. By engaging in technical and environmental working groups, we help shape best practices that set new standards in safety and product stewardship.

    Future tweaks to TCBN production—such as shifting to new chlorinating agents or deploying digital process controls—reflect both regulatory urgencies and the on-the-ground economics of chemical manufacture. Operators, engineers, and chemists here drive the transition with day-to-day attention to changing customer specs, updated industry norms and forward-looking environmental policies. Our strategy remains simple in purpose but complex in execution: maintain direct access to manufacturing data, keep human eyes on every lot, and partner with users to fit evolving production regimes.

    Direct Manufacturer Support: Experience Matters

    Over the years, plant managers, laboratory leaders and procurement officers have told us what matters most about their TCBN supplier: responsiveness, transparency, and an ingrained understanding of the realities behind every purchase order. Standing behind our product means more than just delivering to spec—it means sustaining the know-how, traceability, and predictability that keeps clients’ operations running tight. We recognize the weight that manufacturing carries—technical, regulatory, reputational—and we serve not just as a source of raw material, but as an industry partner shaped and seasoned by decades of direct production.

    In the landscape of chlorinated aromatic intermediates, 2,3,4,5-Tetrachlorobenzonitrile stands as a benchmark not for its novelty, but for the rigor it demands in manufacture and the trust it has earned from users worldwide. Our commitment is straightforward: keep standards high, anticipate user needs, and deliver genuine value from plant gate to end-user. The partnership between responsible manufacturer and smart user builds resilience in every molecule we produce—and in every business that depends on it.