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2,3-Dichlorobenzonitrile

    • Product Name 2,3-Dichlorobenzonitrile
    • Alias Dicryl
    • Einecs 221-069-9
    • 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

    234836

    Cas Number 612-20-2
    Molecular Formula C7H3Cl2N
    Molecular Weight 172.01 g/mol
    Iupac Name 2,3-dichlorobenzonitrile
    Appearance White to off-white crystalline powder
    Melting Point 50-54°C
    Boiling Point 277-279°C
    Density 1.39 g/cm³
    Solubility In Water Poorly soluble
    Flash Point 122°C
    Synonyms Dichlobenil, 2,3-DCBN
    Odor Characteristic aromatic odor

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

    Packing & Storage
    Packing The 250g bottle of 2,3-Dichlorobenzonitrile features a white screw cap, hazard labels, and clear chemical identification on the label.
    Shipping 2,3-Dichlorobenzonitrile should be shipped in tightly sealed, properly labeled containers and protected from physical damage. It must comply with relevant hazardous material regulations, typically classified under UN 3276. Avoid exposure to moisture and incompatible substances during transit. Shipping should adhere to all local, national, and international safety guidelines.
    Storage 2,3-Dichlorobenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep it away from direct sunlight, heat sources, and moisture. Clearly label the container and ensure it is stored in a chemical storage cabinet designed for hazardous materials.
    Application of 2,3-Dichlorobenzonitrile

    Applications of 2,3-Dichlorobenzonitrile in Industrial Manufacturing

    2,3-Dichlorobenzonitrile serves as a crucial intermediate in multiple industrial sectors, enabling the synthesis of advanced specialty chemicals by facilitating specific reaction pathways. As an original chemical raw material manufacturer, we focus on its verified end-use applications, supporting our B2B partners with precise grade control and formulation guidance for compliant, large-scale production environments.

    1. Synthesis of Agrochemical Active Ingredients

    In the agrochemical sector, producers rely on this intermediate to construct chlorinated aromatic scaffolds for high-demand herbicidal active molecules. The material functions as a key building block, covalently bonded during multi-step organic synthesis, directly impacting downstream batch yields and impurity profiles. Process engineers precisely dose the intermediate based on target substrate capacity and maintain strict monitoring at the nitrile-to-amide conversion stage to ensure regulatory compliance and finished crop protection quality.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System for Chemical Synthesis)
    • REACH (EC 1907/2006) Registration and SVHC Assessment
    • FAO/WHO Specifications for Pesticide Technical Materials
    • China GB/T 1600-2001 Agrochemical Product Standards

    Typical usage ratio

    • 0.2–0.6 molar equivalents per mole of target herbicidal compound; dosage adjusted in accord with process yield optimization and conversion efficiency.

    Downstream process integration

    • Introduction at Stage 2 of the synthetic reaction, following initial chlorination but prior to condensation with amines; tight control of anhydrous and temperature conditions enables selective nitrile reactivity without byproduct formation.

    Final product types

    • Herbicidal actives (e.g., dichlobenil derivatives, pre-emergent weed control agents)
    • Aromatic pesticide intermediates supplied to formulation plants

    2. Manufacturing of Specialty Aromatic Polymers

    Within polymer and material sciences, 2,3-dichlorobenzonitrile plays a technical role as a co-monomer for the synthesis of heat-resistant specialty polymers. Manufacturers employ this building block to introduce electron-withdrawing groups on the aromatic ring, which elevates the thermal stability and chemical resistance of engineering plastics. Quality assurance teams validate the input dosage to maintain chain uniformity and avoid cross-contamination during batch-scale polymerization.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management for Chemical Plants)
    • RoHS Directive 2011/65/EU (Heavy Metals Content for Plastics Applications)
    • EN ISO 1043-1 (Polymer Identification and Nomenclature)
    • UL 94 (Polymer Flammability Classifications)

    Typical usage ratio

    • 3–8 wt% relative to total monomer mass; lower end for flexible resins, higher for rigid grades with improved insulating properties.

    Downstream process integration

    • Chemical introduction during pre-polymer resin blending stage, prior to free-radical or step-growth polymerization; agitation and solvent selection ensure even distribution and co-polymer incorporation.

    Final product types

    • High-performance engineering plastics for automotive and electronics
    • Crosslinked specialty polymer films and sheets

    3. Fine Chemical Intermediate for Pharmaceutical Synthesis

    In advanced pharmaceutical manufacturing, this intermediate delivers precise aromatic substitution necessary for constructing pharmaceutical precursors in the central nervous system, anti-inflammatory, or cardio-protective drug classes. Custom API facilities integrate the raw material under GMP oversight, tracking every step from incoming quality control to active ingredient isolation. The nitrile undergoes controlled transformation in catalytic hydrogenation or nucleophilic aromatic substitution steps, after which process analytics verify purity and conversion.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP and EP Monograph Compliance (Active Ingredients Traceability)
    • Chinese Pharmacopoeia (Part II: Chemical Drugs)
    • FDA 21 CFR Part 211 for Finished Pharmaceutical Manufacturing

    Typical usage ratio

    • 0.15–0.35 molar equivalents per mole of pharmaceutical precursor; actual quantity determined based on expected conversion percentage and impurity profile.

    Downstream process integration

    • Charged at the aromatic substitution stage, prior to amide or amine group formation; pharmaceutical process chemists conduct in-process controls for critical intermediate generation and downstream purification efficiency.

    Final product types

    • Pharmaceutical intermediates for APIs (e.g., benzamide and substituted aniline derivatives)
    • Custom fine chemicals for contract manufacturing organizations (CMOs)

    4. UV-Curable Coating and Adhesive Synthesis

    In the coatings industry, formulators use dichlorobenzonitrile derivatives as functional additives to enhance UV-curable resin systems, imparting increased adhesion, scratch resistance, and chemical durability through ring chlorination. Manufacturing teams batch-dose the intermediate during prepolymerization, tuning the incorporation level to achieve performance targets for high-value electronics and industrial finishes. Downstream operations must control viscosity and photoreactivity, monitoring for residue and crosslink uniformity.

    Industry compliance standards

    • ISO 9001:2015 (Quality Control in Coating Manufacturing)
    • EU REACH Annex XVII (Restrictions for Coating Chemicals)
    • GB/T 23986-2009 (Industrial UV-Curable Coating Standards)
    • ASTM D7767 (UV-Cure Coatings Performance Testing)

    Typical usage ratio

    • 0.5–2.5 wt% in resin pre-mix; dosage corresponds to layer thickness, curing speed, and application substrate (metal, glass, polymer).

    Downstream process integration

    • Direct blending with prepolymer and photoinitiator mixtures prior to UV curing; production lines set exposure parameters using spectrophotometry to validate complete crosslinking.

    Final product types

    • UV-cured industrial and electronic adhesives
    • Protective surface coatings for electronics, automotive interiors, and optical lenses
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    Certification & Compliance
    More Introduction

    Introducing 2,3-Dichlorobenzonitrile: A Practical Perspective from the Manufacturing Floor

    Real-World Experience with 2,3-Dichlorobenzonitrile

    Standing at the intersection of synthetic chemistry and practical application, 2,3-dichlorobenzonitrile has found its role in the chemical world through years of precise formulation and rigorous control. Developing this compound calls for clear attention to detail, as even small differences in structure or impurity profile can have broad effects, especially in industries where every downstream process counts.

    Regular feedback from both lab chemists and process engineers guides our manufacturing process. Handling 2,3-dichlorobenzonitrile isn't about just ticking boxes and hitting broad specs. It’s about managing raw material quality, maintaining the fine line between yield and purity, and staying alert to shifts in international standards. This isn’t theory; every change in temperature or solvent quality can nudge the product in a different direction.

    Model and Specifications: What Matters in Daily Production

    Our 2,3-dichlorobenzonitrile consistently runs to high-purity thresholds. Over repeated batches, we ensure the typical minimal purity exceeds 98.5% as measured by advanced GC techniques. Small shifts here have prompted direct process adjustments—real-world issues, like minor increases in ortho-chloro or para-chloro impurity, lead not only to equipment cleanouts but to updates in incoming raw material screening.

    Moisture content remains a day-to-day challenge, especially in climates with high ambient humidity. Left unchecked, even trace water in the product can complicate storage or subsequent chemical reactions. We utilize both vacuum drying and in-process analytics to keep this problem in check, seeing every batch through to a completion profile that matches the actual needs of subsequent steps.

    Physical form isn’t a throwaway detail. The fine crystalline solid tends toward light yellow when impurities climb; that tells any skilled eye something changed upstream. We monitor color, particle size, and flow characteristics for every lot. Even if it might look trivial, improper particle size can clog feeders or slow reactions downstream.

    Beyond the Formula: What Sets 2,3-Dichlorobenzonitrile Apart

    Many people in chemistry know benzonitrile derivatives—from the basic benzonitrile to poly-substituted forms—but the 2,3-dichloro pattern stands out for its reliable reactivity and stability. Modifications in either the 2- or 3- position lead to clear performance changes once you move to actual process chemistry. The disubstitution tightens its molecular behavior, granting chemists or engineers more predictability than with single-chloro or 3,4-dichlorinated variants.

    Manufacturing experience shows that 2,3-dichlorobenzonitrile handles process stress better than its isomers. Less side-product formation and lower volatility at comparable temperatures support safer industrial work. Our teams have measured solvent losses and component stability head-to-head, with this product standing out in terms of both ease of handling and shelf stability.

    In our direct synthesis lines, small shifts in the purity or isomeric content of 2,3-dichlorobenzonitrile reliably show up downstream. We’ve witnessed this when customers attempted to substitute with 2,4- or 3,4-isomers—reaction yields dipped, and purification steps stretched out beyond planned schedules. The 2,3-pattern cuts these headaches short, reinforcing why it commands a respected place in tightly channeled synthesis.

    Main Uses and Value to Industry

    Looking beyond the textbook, the largest use for 2,3-dichlorobenzonitrile within our experience falls into the pesticide sector, especially in the production of precursors for selective herbicides. Our ongoing collaborations with formulators have shown that slight impurities in this compound can translate directly to unwanted side-reactions, increased byproducts, or less reliable herbicide performance. Several plant trials have reinforced that even non-toxic impurities can impact catalyst longevity or formulation stability.

    Another important use lies in specialty chemicals, where this compound serves as a starting building block for more complex molecules. Medicinal research teams reach for 2,3-dichlorobenzonitrile when other, less substituted nitriles can’t provide the rigidity or selectivity needed for discovery-phase syntheses. We've worked closely with researchers who require consistently high-purity material—any deviation led directly to lost project time and an uptick in troubleshooting.

    Within colorant and dye work, our materials science partners rely on the specific electron distribution of the 2,3-dichloro structure to drive coupling reactions cleanly. Their success stories, as well as their batch failures, underline the real-world importance of avoiding both isomeric cross-contamination and trace metal impurities—details which only plant-level process control can guarantee.

    Some specialty plastics producers have experimented with this material as a chain stopper or modifier. Outcomes vary widely, but again, the story returns to consistency. Inconsistent batches led to polymerization problems, foaming, or off-colors. We maintain lot-by-lot records tracing every tank and filter cycle so that end-users can talk to us about specific batches with confidence grounded in objective detail.

    Manufacturing Process: Challenges and Solutions Gained Over Years

    Many might not realize how nuanced the synthesis of 2,3-dichlorobenzonitrile can become at scale. On paper, direct chlorination or route selection seems straightforward. Real work tells a different story: reaction kinetics must match up precisely to avoid over-chlorination or undesirable side products. Reactor design also plays a role, as batch-to-batch thermal variations can favor rival isomer formation.

    Early on, we failed a few crucial lots until tighter control over temperature ramping and agitation speeds made the difference. Sampling during reaction—sometimes as frequently as every 30 minutes—helped us dial in the process to favor the right isomer consistently. These lessons now inform every control system upgrade, every calibration of analytic equipment, and every new technician’s training.

    Waste management adds another layer of complexity. Our team developed solvent recovery and side-product scrubbing units after seeing both cost spikes and downstream environmental issues crop up from ignored purification fractions. Each improvement draws directly from operator suggestions and chemist observations. Direct communication between operators, QA experts, and engineers gives us the agility to address quality issues before they reach a warehouse or client site.

    Shipping and handling protocols have changed over time. Requests from partners on different continents mean our storage methods must resist moisture ingress and oxidative degradation across a wide temperature range. We introduced nitrogen blanketing and triple-seal containers after learning from atmospheric tests in real transport settings. Shift supervisors continue to monitor feedback on packaging so the material arrives ready for immediate use.

    Quality Assurance and Traceability: More Than Just Paperwork

    Merely quoting “specification sheets” never paints the full picture of working with 2,3-dichlorobenzonitrile. Traceability at our plant starts with the raw materials. We record every shipment’s source, impurity content, and handling notes. This approach proved itself when a trace contaminant in an upstream chlorinating agent caused a temporary product discoloration; our records allowed rapid identification, correction, and communication with partners.

    Plant personnel review analytical data on every batch—not just the pass/fail certificates. Trends over time prompt real changes: a run of slightly elevated residual solvent readings might push us to slow down certain steps or bake the product for longer, rather than trust the average as “good enough.” Certification is backed by ongoing discussion, from the morning shift change to daily report summaries distributed in the control lab.

    Traceability speaks directly to customer confidence. Technical directors frequently ask for batch histories or want to know about minor procedural deviations. We share this information candidly. Not only does it build trust, it also reveals patterns we might have overlooked ourselves—coaching us to invest in equipment upgrades or procedural changes that pay off cycle after cycle.

    Comparing 2,3-Dichlorobenzonitrile with Other Compounds in Its Class

    2,3-dichlorobenzonitrile doesn’t simply fill a spot left by more common single-chlorinated nitriles. With two chlorine atoms on the ring, it offers distinct reactivity patterns. Take 3,4-dichlorobenzonitrile—chemically close, but outcomes differ sharply in catalyzed coupling or reduction reactions. Process teams have documented higher yields and less byproduct when they stick with the 2,3- pattern instead of the 3,4- comparator.

    This difference boils down to substitution pattern, impacting steric hindrance, resonance stabilization, and the ease with which downstream reagents interact with the molecule. At a lab level, this material allows for sharper selectivity. On the plant floor, its reliable melting point and crystallization behavior support easier material transfers and more streamlined filtration.

    Some teams working in specialty pharma have even tried substituting with simple benzonitrile or 2-chlorobenzonitrile, only to find complex reaction mixtures and poor final purity. These setbacks always circle back to the basic structural features; with the 2,3-dichloro structure, chlorines on adjacent positions create an electron-withdrawing environment ideal for controlled downstream substitution or coupling reactions.

    Working with enough lots, differences in storage stability between isomers become obvious. Where single-chloro versions may degrade or release trace volatiles, the 2,3-dichlorinated material stays consistent, as shown by our stability studies across multiple climate zones. Notably, this reliability feeds directly into production planning, reducing unexpected outages or re-test burdens.

    The People Behind the Product: Putting Experience into Action

    It’s unfair to imagine 2,3-dichlorobenzonitrile as simply another fine chemical—every successful batch relies on a blend of machine precision and human judgment. Many of our team members have worked with this molecule for years; their insights during routine check-ins have driven many of our key process improvements. Even the smallest change in the texture of a finished batch can prompt an impromptu team meeting—discussing, not theorizing, how best to adjust the system.

    This experience translates into practical customer support. We’ve hosted visitors in our control room, showing them our real-time monitoring systems and the subtle tweaks we’ve adopted after years of fine-tuning. If a shipment ever fails to meet expectations, our team jumps in on live calls—ready to walk through purification steps, logistical chains, and the actual data behind the results.

    On-the-ground experience informs more than internal technical culture. We shape our standards not just by what’s “allowed,” but by listening closely to complaints, compliments, and recurring questions from partners. If a lab encounters stubborn dissolution slowdowns or unexpected chromatographic peaks, our process records help pinpoint exactly what needs to change—before it slows down a critical research or production timeline.

    Challenges Faced and Overcome: Learning Through Adjustment

    Few chemicals transition from lab curiosity to industrial workhorse without learning some tough lessons along the way. We faced scale-up hurdles firsthand—unexpected exotherms, sticky residues in reactors, filter blinding, intermittent trace metallics, and shifts in drying times as plant conditions change. These cases forced us to rethink not only batch size, but the actual basis for every temperature range, feed rate, or agitation setting we apply.

    Moisture ingress once caused an entire campaign to develop off-spec crystals. An operator’s suggestion of improved drum purging led us to rework drum handling practices. In another instance, high-purity solvent bottlenecks temporarily threatened on-time deliveries; close supplier relationships and solvent loop upgrades gave us steadier control and reduced future cycle time.

    We document every failure and response. These case histories train each new engineer and line lead, helping us pass along wisdom that saves time and prevents repeat problems on future runs. Building this kind of robust process memory happens only with active collaboration across synthesis, QA, and logistics.

    Environmental and Regulatory Considerations

    As chemical manufacturers, staying on top of environmental compliance is more than a checkmark. Regulatory requirements shape our waste treatment, packaging, air emissions, and reporting structures. Regulations change; community expectations change. This means each improvement—whether in process controls, waste neutralization, or solvent recycling—not only helps the bottom line, but reduces the potential impact on local environments.

    We recall shifts in permitted emissions that forced quick investments in improved scrubbing and storage. Management didn’t just pass the costs down the line—they pulled engineers and operators together, asked for practical solutions, and implemented those. The end result gave us cleaner air discharges, satisfied inspections, and lessons we now extend to new formulation lines.

    Handling 2,3-dichlorobenzonitrile at scale, we commit to regular third-party audits, transparent data sharing, and ongoing communication with both local authorities and customers needing documentation for their own compliance frameworks. Our own learning proves that the best strategy is understandable, evidence-based practice—helped by the kind of real transparency that makes both customers and neighbors more comfortable about what goes on behind the factory fence.

    Ongoing Improvements and Future Opportunities

    Manufacturing never stands still. Process upgrades, equipment retrofits, and analytic advances offer new benchmarks year after year. Recently, investments in high-throughput GC and LC instrumentation gave us earlier warning on potential impurity formation and allowed us to adapt more quickly to minor upstream surprises. Operator feedback prompted several controls upgrades, making routine cycles shorter and safer.

    We continue to test new filtration media, solvent blends, and thermal control systems. Every time global regulations shift or a customer develops a novel use, those changes ripple back into process design. Conversations with university partners and downstream users remind us there’s still more to learn about how our product fits into tomorrow’s innovations—rather than just today’s established segments.

    Green chemistry and sustainability also figure into ongoing planning. Whether by reducing waste, recovering solvents, or investing in energy management, these steps benefit both our process economics and our relationships with environmentally conscious partners. Each improvement cycle looks beyond just next quarter, aiming for reliability that supports not only production, but broader community trust.

    Why Direct Manufacturing Experience Makes the Difference

    There’s more to producing 2,3-dichlorobenzonitrile than what a sales brochure would ever show. The difference comes from direct experience: adjusting conditions, responding to issues mid-batch, learning what makes a difference for real-world applications. Years in the field have drilled in how each decision—batch size, drying profile, filtration method—can ripple all the way to a customer’s plant or research bench.

    By staying grounded in process reality, not just compliance or standardization, we continuously improve what our chemical can accomplish for users—backed by traceable records, customer input, and a hard-earned understanding of what quality means batch after batch. Our work never really ends. There's always another challenge, another process tweak, or another application waiting for informed, responsive manufacturing to make the most of what 2,3-dichlorobenzonitrile can do.