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2-Chloro-6-Nitrobenzonitrile

    • Product Name 2-Chloro-6-Nitrobenzonitrile
    • Alias 2-Chloro-6-nitrobenzonitrile
    • Einecs 221-724-2
    • 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
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    Specifications

    HS Code

    560929

    Chemical Name 2-Chloro-6-Nitrobenzonitrile
    Cas Number 350-03-8
    Molecular Formula C7H3ClN2O2
    Molecular Weight 182.57
    Appearance Yellow crystalline solid
    Melting Point 77-80°C
    Boiling Point 330°C
    Density 1.53 g/cm3
    Solubility In Water Insoluble
    Smiles C1=CC(=C(C(=C1Cl)N#C)[N+](=O)[O-])
    Inchi InChI=1S/C7H3ClN2O2/c8-6-2-1-5(10(11)12)3-7(6)4-9
    Refractive Index 1.600 (estimated)

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, sealed with tamper-evident cap. Label includes chemical name, formula, hazard symbols, and handling instructions.
    Shipping **Shipping Description:** 2-Chloro-6-Nitrobenzonitrile should be shipped in tightly sealed containers, protected from physical damage and moisture. It must be labeled as harmful/irritant according to chemical regulations. During transport, it should be kept away from oxidizers and acids. Appropriate hazard documentation and safety data sheets must accompany all shipments.
    Storage **2-Chloro-6-Nitrobenzonitrile** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and clearly labeled. Store separately from incompatible substances such as strong acids, strong bases, and oxidizing agents. Use appropriate chemical-resistant containers and avoid contact with moisture to maintain substance stability.
    Application of 2-Chloro-6-Nitrobenzonitrile

    Applications of 2-Chloro-6-Nitrobenzonitrile in Industrial Manufacturing

    2-Chloro-6-Nitrobenzonitrile serves as a critical intermediate in several advanced chemical synthesis pathways. As a direct manufacturer, we enable precise integration into targeted downstream industrial sectors, supporting stringent compliance and high-value end-product output through controlled process parameters and consistent quality.

    1. Agrochemical Active Ingredient Synthesis

    Manufacturers in the agrochemical sector utilize 2-Chloro-6-Nitrobenzonitrile as a core building block during the stepwise synthesis of selective herbicides and insecticides. The nitrile group’s reactivity enables formation of target molecular scaffolds via nucleophilic aromatic substitution reactions, necessary for advanced herbicide families such as substituted phenylureas and pyridines. Chlorination and nitration patterns determine subsequent coupling yields and purity profiles, making the starting material’s specification essential for reliable agricultural product registration. Integrated production lines often require close adjustment of temperature, pressure, and solvent coordination to limit side-product formation and maximize yield.

    Industry compliance standards

    • GB 20810-2006 (China National Standard for Pesticide Technical Material)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006 for Registration, Evaluation, Authorisation and Restriction of Chemicals

    Typical usage ratio

    • 15–25% by mass in precursor coupling reactions—final concentration depends on the specific synthetic route and performance target of the herbicide formulation

    Downstream process integration

    • Introduced during initial condensation stage with secondary amines or alkoxy reactants to form urea or ether-linked intermediates for downstream chlorination or sulfonation steps

    Final product types

    • Triazine and pyridine herbicide actives
    • Phenoxy acid growth regulators
    • Systemic insecticides with nitrile functional groups
    • Non-selective pre-emergence weed control agents

    2. Pharmaceutical Intermediate for Anti-Hypertensive and CNS Actives

    In fine chemical synthesis for active pharmaceutical ingredient (API) production, 2-Chloro-6-Nitrobenzonitrile acts as a key step intermediate, particularly in the manufacture of antihypertensive medications and select CNS agents. Its electron-withdrawing substituents influence regioselectivity during amination and reduction, which establishes high-purity core intermediates for further heterocycle construction. Strict process analytics ensure the intermediate meets pharmaceutical GMP standards, preventing cross-contamination or residual impurity carryover to the final API. Scale-up requires comprehensive material balance and residue assessment to satisfy regulatory batch documentation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients (API)
    • European Pharmacopoeia (EP), USP standards for intermediate documentation
    • China GMP for Pharmaceutical Raw Materials (2020 Revision)
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 18–22% of overall batch weight as a core intermediate. Adjusted per process yield requirements and downstream hydrogenation/reduction efficiency.

    Downstream process integration

    • Input in the nitro group reduction stage preceding ring closure and amide/amine coupling, typically under controlled hydrogen or palladium-catalyzed flow reactors

    Final product types

    • Angiotensin receptor blockers (ARBs)
    • Central nervous system (CNS) active compounds, including certain antipsychotics
    • Antiarrhythmic agents based on benzene or indole scaffolds
    • Intermediates for patented bulk pharmaceutical chemicals

    3. Dye and Pigment Manufacturing

    The specialty dye industry uses 2-Chloro-6-Nitrobenzonitrile for synthesizing advanced azo and anthraquinone dyes, essential for high-value applications in technical textiles and industrial coatings. The material’s reactivity supports efficient nucleophilic aromatic substitution with hydrazine or amine dye components, yielding chromophores with controlled absorption spectra and lightfastness. Batch consistency and narrow impurity profile are critical, as downstream diazotization or coupling steps are highly sensitive to starting material purity. Large-scale dye production lines often employ continuous flow reactors for precise material feed-in during dye precursor assembly.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile chemicals safety)
    • GHS/CLP Regulation (EC) No 1272/2008 for classification and labeling of chemicals
    • Zero Discharge of Hazardous Chemicals (ZDHC) Programme requirements for dyes
    • ISO 9001:2015 for Quality Management in industrial pigment manufacturing

    Typical usage ratio

    • 12–19% of dye precursor mass, fine-tuned per color depth, targeted substrate adhesion, or intended solubility grading

    Downstream process integration

    • Employed at the substitution stage with resorcinol or phenylenediamine under controlled temperature, ensuring optimal chromophore assembly and minimized byproduct levels

    Final product types

    • Reactive textile dyes for cellulose fibers
    • Industrial organic pigments for automotive coatings
    • Solvent dyes for plastics and resins
    • Azo pigment precursors for printing inks

    4. Advanced Material Polymerization and Resins

    Chemical producers incorporate 2-Chloro-6-Nitrobenzonitrile into specialty polymer synthesis, notably for the construction of high-performance engineering resins and specialty aramid fibers. Its unique functionalization pattern supports chemical cross-linking and thermal stability during copolymerization with diamines or dihydroxybenzenes. Controlled reaction environments are necessary to manage exotherms and ensure consistent molecular weight distribution, both critical to downstream mechanical and thermal specifications of finished engineering polymers. Material purity directly impacts polymer color grade and dielectric property consistency.

    Industry compliance standards

    • ISO 10993-18 (chemical characterization of polymeric materials)
    • ASTM D5630 (Loss-On-Ignition of polymer resins)
    • REACH Regulation (EC) No 1907/2006 for polymer raw material registration
    • UL 94 (Flammability testing of polymeric materials)

    Typical usage ratio

    • 10–16% of the monomer input. Adjusted based on target thermoset versus thermoplastic resin characteristics, and desired mechanical property endpoints.

    Downstream process integration

    • Included as starting monomer in condensation polymerization, reacting with diamines under elevated pressure and temperature for prepolymer formation

    Final product types

    • Heat-resistant aramid fibers
    • High-gloss epoxy resins for electronics
    • Advanced composite matrix polymers
    • Flame-retardant molding compounds

    5. Specialty Chemical Catalysts and Ligands

    In advanced fine chemical production, companies use 2-Chloro-6-Nitrobenzonitrile as a starting entity for the construction of specific organometallic ligands and catalyst supports. Its electron-deficient aromatic ring facilitates selective functionalization in ligand assembly, creating highly tailored chelating systems for transition metal catalysis. Downstream usage in palladium or platinum-catalyzed cross-coupling reactions enables efficient fine chemical synthesis with minimized catalyst load and improved process economy. Strict impurity and moisture controls during precursor formulation ensure catalyst performance and prevent reaction inhibition.

    Industry compliance standards

    • ISO 17025 (Laboratory testing for chemical synthesis intermediates)
    • REACH Regulation compliance for specialty chemicals
    • GHS (Globally Harmonized System) for transport and labeling
    • GMP for fine chemical and catalyst intermediates when supporting pharmaceutical synthesis

    Typical usage ratio

    • 5–12% of ligand total mass, depending on target chelating structure and strength/donating property requirements in the catalyst system

    Downstream process integration

    • Acts as a substituted aromatic precursor in the initial ligand assembly, typically under strictly anhydrous conditions for transition metal incorporation

    Final product types

    • Palladium-based cross-coupling catalysts
    • Coordination ligands for chiral catalysis
    • Supported phase-transfer catalytic systems
    • Specialty redox-active complexes for high-purity synthesis applications
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    Certification & Compliance
    More Introduction

    Understanding 2-Chloro-6-Nitrobenzonitrile: From Production to Application

    Introduction to 2-Chloro-6-Nitrobenzonitrile

    Over the years in chemical manufacturing, the drive to support innovation in fine chemicals and pharmaceuticals has led to the growth of specialties like 2-Chloro-6-Nitrobenzonitrile. This compound, often referenced in-house by its CAS number 3277-43-2, takes a central role in the formation of several complex molecules found in multiple high-performance sectors. Its molecular formula, C7H3ClN2O2, signals potential for diverse chemical transformations—a quality that’s seen steady demand in recent years.

    Our involvement in producing 2-Chloro-6-Nitrobenzonitrile extends over a decade. Investments in dedicated synthesis lines, closed-loop quality analytics, and rigorous batch tracking reinforce our ability to meet shifting requirements from downstream users. Every drum or bag that leaves our plant reflects chemistry that’s been honed through countless production cycles, with a commitment to both purity and process efficiency.

    The Realities of Production: Methods and Control

    Manufacturing 2-Chloro-6-Nitrobenzonitrile isn’t a single-step affair. Our main process typically starts with 2-Chlorobenzonitrile, followed by nitration with mixed acids under closely monitored temperature and stirring regimes. The byproduct profile can fluctuate with even slight temperature deviations; as a producer, that’s a constant challenge. Nitration reactions tend to generate tars or unwanted isomers if batch controls slip, so we have adopted inline spectroscopic monitoring backed by real-time flow chemistry trials. Process control teams remain hands-on, often running close-knit shifts to catch outliers.

    On the plant floor, attention falls not only on core chemistry but on cleaning protocols and line changeovers. Leftover residues from prior runs can lower yields or introduce amorphous impurities. Using high-purity acids and implementing scheduled downtime for thorough reactor washes keeps process repeatability high. Logistics specialists need to synchronize sharply with R&D—keen to prevent cross-contamination at every transfer point.

    From a manufacturer’s perspective, the most reliable batches crystallize quickly, forming yellow to light brown crystals with consistent particulate size. Morphology and free-flowing behavior matter, as both downstream nylon filtration and charging of reaction vessels often depend on powder handling traits honed during drying and milling. This sort of insight usually comes with long-term plant experience and tight collaboration across departments.

    Purity and Quality Standards: Variations That Matter

    There’s no one-size-fits-all target for 2-Chloro-6-Nitrobenzonitrile purity. Large-volume agrochemical makers sometimes accept slightly relaxed NMR profiles, provided major impurities remain below visual or spectral detection thresholds. Pharmaceutical intermediates demand tighter content—often greater than 99% by HPLC, plus trace metal and residual solvent checks per ICH guidelines.

    Our facility uses dual-mode analytics. Rapid GC or HPLC screens give overnight feedback, but lab-scale sample retesting supports ongoing statistical process control. Each lot’s data traces back to original raw material shipments and batch reactant profiles. Technical teams run parallel checks for moisture and particle sizing, since hygroscopicity and caking can dent downstream reaction yields. It’s not just about major component content—end use sometimes hinges on how smoothly powders flow or dissolve. Learning officers routinely work with customers to interpret results—not simply report numbers.

    Requests for higher assay grades create operational ripple effects. Some users specify micro-trace monitoring for aromatic amines, dioxane, or halide levels. This calls for periodic investment in new calibration standards and internal reference compounds. Even so, too much filtration or overzealous purification steps can sometimes drag down effective recovery rates. We’ve learned it pays to seek the minimum effective purification for each intended application, rather than overshooting in pursuit of idealized benchmarks.

    Applications: Putting Chemistry to Work

    The role of 2-Chloro-6-Nitrobenzonitrile rarely ends with itself. In most cases, the value lies in what users build from it. Agrochemical researchers rely on its nitrile and nitro functionalities as foundational blocks in herbicide and fungicide synthesis. Nucleophilic aromatic substitutions—enabled by the electron-withdrawing nitro and chloro groups—let them create diverse scaffolds quickly.

    Pharmaceutical scientists count on 2-Chloro-6-Nitrobenzonitrile for generating substituted anilines and heterocycles. These intermediates often wind up feeding pipelines for antihypertensive, antimicrobial, or CNS-active molecules. Its halide positioning simplifies transformations using palladium-catalyzed coupling reactions. Analytical chemists occasionally deploy it as a labeling agent, thanks to its distinct UV and chromophore characteristics. Process development chemists value its predictable reactivity profile; whether crafting pilot-scale batches or setting up multi-tonne campaigns, consistency cuts risk.

    Beyond human health and agriculture, electronic materials manufacturers seek tight control of every functional group. Polymers and specialty dye precursors demand nitroaromatic inputs that resist premature side reactions under process heat and solvent pressure. Chemical engineers in this field turn to the reliability and narrow impurity window of a tightly monitored 2-Chloro-6-Nitrobenzonitrile stream. The lessons learned in our own R&D collaboration feed directly into these sectors, where the cost of process failure can dwarf raw material outlay.

    Comparing 2-Chloro-6-Nitrobenzonitrile to Similar Intermediates

    Within the knit of aromatic nitriles, each substitution pattern offers its own chemical character. The ortho arrangement of chlorine and nitro groups on the benzonitrile ring sets 2-Chloro-6-Nitrobenzonitrile apart. For chemists seeking regiochemical control—whether entering nucleophilic aromatic substitution or planning reductions—these substituent positions matter. Compare this with 4-chloro or 3-nitro versions, which react at different ring sites and under different milder or harsher conditions.

    Direct substitution and electron distribution shape practical handling as well. Chlorine at the ortho position relative to nitrile tightens the melting point and sometimes increases the compound's volatility under process heat. This property creates both advantages and headaches for plant operators—reliable melting aids certain reactions, but excess volatility can waste product or demand specialized condensers on reflux lines.

    In contrast, isomeric compounds or analogs with only a single chloro or nitro group tend to lack the same catalytic versatility. For users developing multi-step chemical transformations, this limits flexibility down the line. Pairing nitro and chloro substituents enables more streamlined process modifications compared to compounds lacking such symmetry.

    Safety regimes also vary depending on the compound’s substitution pattern. Experience shows that 2-Chloro-6-Nitrobenzonitrile generally resists direct oxidation or reduction better than counterparts where the nitro group is para to the nitrile, reducing undesired runaway reactions. Thermal stability in the storage tank or during transit, a constant concern for large-scale shippers, benefits from the specific arrangement here.

    Logistics and Handling in a Manufacturing Setting

    Transporting and handling 2-Chloro-6-Nitrobenzonitrile draws as much attention within our operation as the synthesis itself. Moisture and airborne particulates threaten both purity and long-term storage life. Drum filling operations run in climate-controlled bays, with desiccant packs enclosed if extended warehouse times look likely. Custom flake or granular forms can reduce dusting, improving both yield and worker safety.

    Experience has shaped how we manage accidental exposure risks. Dust control protocols rely on local exhaust ventilation and point-source vacuuming. Though toxicity sits under common aromatic nitro standards, company medics and safety officers keep routine screening and PPE audits in rotation. Waste water from floor washes or production cleanup routes through onsite treatment stations; it’s never simply sent to municipal drains. These practicalities mark the difference between actual producers and remote traders—manufacturers coordinate across technical, environmental, and packaging teams daily.

    Shipping hazards spark regular review of documentation, emergency plans, and on-call logistics staff. Local regulations covering net weights, overpack labeling, and secondary containment have become tighter, driving more direct investment in training and tracking systems. On our busiest days, as many as a dozen dedicated team members focus purely on keeping each load secure and shipment records audit-proof. Real lessons come not from protocols but from adapting to near-misses and sharing those stories across shift handovers.

    Environmental Responsibility and Manufacturing Innovation

    Manufacturing fine chemicals can place stress on the environment if not caught early in process design. We have taken repeated steps to lower the footprint of our 2-Chloro-6-Nitrobenzonitrile lines. These include closed-loop water cooling, solvent recovery systems, and periodic audits of nontarget effluents from both acid and organic waste streams. High-efficiency condensers and improved distillation sequences push the bulk of used solvents back into waiting tanks, with only trace purges heading for secure incineration.

    Technicians have piloted new approaches as well, like phase-transfer catalysts and greener nitrating agent systems. These projects don’t always yield immediate results, but longer-term, the reductions in both energy consumption and hazardous waste create measurable savings. Early engagement with raw material vendors has also lowered the starting point for upstream impurities—helping deliver a safer and more sustainable product to end users.

    Communication up and down supply chains forms the core of environmental improvement. Our site’s regular engagement with downstream buyers and regulators has identified points where even small modifications—like adopting multilayer barrier liners in packaging—can lower spoilage and handling risk. This cooperative feedback often drives greater change than sporadic certification audits alone.

    Quality Assurance: Learning Across Batches and Customers

    Long-term manufacturing success rides on real-world feedback. None of our operating procedures stand still for long. Each time a customer flags a pressure point—be it a marginal batch or a new specification target—the investigation runs through both the technical leads and shop floor crews. Our best yield boosts haven’t come from theoretical optimization, but from blending operator insight with returned sample analysis.

    Every site batch links to digital production records, down to source lot and operator code. This traceability underpins not just the audit trail but the deep learning necessary to continually tune plant settings. Out-of-spec results prompt clear process reviews, not blame. Return rates have dropped over time, in part because teams act openly with each concern and share solutions across shifts. Over the years, our process chemists and analytical staff move quickly to retire obsolete procedures, keeping only those steps that truly chisel away inconsistency.

    End users sometimes require custom particle sizing or alternate solvent rinsing; accommodating these rarely means starting over. Plant teams use modular drying and milling equipment and schedule trial runs by working closely with customer labs. That flexibility, backed by years of experience running both high-throughput and multi-kilogram bespoke requests, brings real value to both sides. Our emphasis on real dialogue means little gets lost in translation—performance data and real use cases always stand at the core.

    Meeting Future Demands: Investment, Training, and Flexibility

    The future continues to bring both challenge and opportunity for manufacturers of targeted intermediates like 2-Chloro-6-Nitrobenzonitrile. New lead candidates from drug discovery labs or regulatory shifts in the agrochemicals space can jumpstart demand or change specification requirements overnight. We’ve learned to invest ahead of the curve—upgrading analytical capacity before it’s squeezed, increasing closed-system automation to limit both manual error and exposure risk, and designing training that doesn’t assume a static plant or workforce.

    Engineers, operators, and chemists take part in upskilling programs focused both on cutting-edge chemistry and practical shop-floor troubleshooting. Visiting customer R&D teams—whether from pharmaceuticals or advanced materials—often highlight new requirements for next-generation downstream processes. Staying plugged into those conversations lets us anticipate changes, not simply react.

    Infrastructure also gets rotating upgrades. Nine out of ten process hiccups get resolved in plant maintenance before they ever reach a customer. Newer bulk pneumatic and robotic handling systems—piloted across our main lines—reduce handling error and streamline material movement. Investment never stands on vanity; it always starts with what makes shipment and usage safer, smoother, and more predictable for core users.

    Bringing It Together: Why Manufacture, Not Trade

    What separates chemical manufacturing from simple trading is the depth of knowledge in product, process, and application. Each kilogram of 2-Chloro-6-Nitrobenzonitrile that moves through our lines carries the imprint of many hands—plant operators measuring reagents, QA analysts qualifying samples, and logistics crews tracking shipment compliance. The certainty we offer users stems from this lived experience, the kind that refines process parameters, responds quickly to changing demand, and keeps lines running even as specifications shift.

    Customers feel the difference not just in the numbers reported on a certificate of analysis, but in every conversation with technical support, every documentation package shipped alongside product, and every post-use review meeting. As the market for specialized aromatics tightens—pressured by supply chain disruptions or escalating regulatory targets—real production expertise proves its worth.

    The chemical industry never stands still. At our manufacturing core, we face down challenges boldly, using the lessons passed across generations of chemists and engineers, meeting each new order for 2-Chloro-6-Nitrobenzonitrile not as a transaction, but as an ongoing partnership with discovery itself.