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2-Chloro-4-Nitrobenzonitrile

    • Product Name 2-Chloro-4-Nitrobenzonitrile
    • Alias 2-Chloro-4-nitrobenzenecarbonitrile
    • Einecs 221-847-2
    • 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
    VTB
    Specifications

    HS Code

    465949

    Chemical Name 2-Chloro-4-Nitrobenzonitrile
    Cas Number 2140-00-9
    Molecular Formula C7H3ClN2O2
    Molecular Weight 182.57
    Appearance Yellow crystalline solid
    Melting Point 144-146°C
    Boiling Point 359°C at 760 mmHg
    Density 1.48 g/cm3
    Solubility Insoluble in water, soluble in organic solvents
    Refractive Index 1.624
    Smiles C1=CC(=C(C=C1Cl)[N+](=O)[O-])C#N
    Pubchem Cid 222779

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

    Packing & Storage
    Packing The packaging for 2-Chloro-4-Nitrobenzonitrile, 100 grams, features an amber glass bottle with a secure screw cap and hazard labeling.
    Shipping **Shipping Description:** 2-Chloro-4-Nitrobenzonitrile should be shipped in accordance with all applicable local, national, and international regulations for hazardous chemicals. Use sturdy, sealed containers, properly labeled. Store and transport away from incompatible materials. Handle with protective gear to prevent skin or eye contact. Ensure compliance with UN/IMDG/IATA guidelines for hazardous substances.
    Storage **2-Chloro-4-Nitrobenzonitrile** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong acids, bases, and oxidizing agents. Protect from moisture and direct sunlight. Ensure proper labeling, and store in accordance with all relevant safety regulations and guidelines for hazardous chemicals.
    Application of 2-Chloro-4-Nitrobenzonitrile

    Applications of 2-Chloro-4-Nitrobenzonitrile in Industrial Manufacturing

    2-Chloro-4-Nitrobenzonitrile serves as a pivotal intermediate in multiple high-value industrial synthesis tracks. Our factory supplies this material for defined downstream applications, each demanding stringent formulation controls, traceable regulatory compliance, and a direct integration into established end-product manufacturing processes.

    1. Agrochemical Active Ingredient Synthesis

    Leading agrochemical manufacturers incorporate this compound primarily in the preparation of selective herbicide intermediates and certain insecticide building blocks. The molecule’s halonitrile structure allows for controlled introduction during nucleophilic aromatic substitution, making it critical in complex multi-step active ingredient synthesis. Producers adjust input proportion based on targeted yield, toxicity regulation, and end-use purity requirements for different agricultural climates.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agrochemical Production
    • REACH Regulation (EC 1907/2006)
    • National Registration evaluation under US EPA (FIFRA) and China ICAMA

    Typical usage ratio

    • 5%–15% by weight relative to total active intermediate batch, adjusted to optimize yield versus side-reaction control and environmental discharge management

    Downstream process integration

    • Charged at the nucleophilic displacement step after initial feedstock activation, often before reduction or amide coupling phases

    Final product types

    • Selective pre-emergent and post-emergent herbicides (e.g., acetanilide derivatives)
    • Nitrile-based insecticide actives
    • Field-ready formulation concentrates

    2. Pharmaceutical Intermediate Production

    Pharmaceutical synthesis teams leverage this raw material mostly for its role as a precursor in the manufacture of specific aniline and aminobenzonitrile derivatives, which become core fragments in APIs for antifungal, antihypertensive, and anti-inflammatory drugs. Material purity and residual solvent profile undergo batch-specific QC targeting ICH and local pharmacopeia standards.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidelines
    • EU GMP Part II (API Manufacturing)
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)

    Typical usage ratio

    • 2%–7% molar equivalent relative to total starting substrate in stepwise synthesis; variations depend on targeted ring system and specific API

    Downstream process integration

    • Introduced in initial condensation or amidation steps, followed by sequential reduction and acylation as dictated by compound pathway

    Final product types

    • Benzimidazole-derived antivirals
    • Aminonitrile-based hypertension therapies
    • Finished pharmaceutical actives (pre-formulation stage)

    3. Dyes and Pigments Intermediate

    Major dye manufacturers utilize this chemical as an electrophilic coupling partner for synthesizing azo and disperse dye intermediates, where the chloro and nitro functionality allows for tuning electrophilicity and color fastness properties. Input proportion changes in response to target chromophore structure and downstream stability parameters for textiles and plastics.

    Industry compliance standards

    • Oeko-Tex Standard 100 (for Yarn and Fabric-Grade Pigments)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 14001:2015 Environmental Management
    • GHS labeling regulations for intermediate handling

    Typical usage ratio

    • 8%–18% by weight per colorant batch formulation, adjusted by desired molar coupling efficiency and color intensity

    Downstream process integration

    • Added during diazotization–coupling reaction sequence; subsequent integration into sulfonation or condensation processes for pigment finishing

    Final product types

    • Azo pigments for synthetic fiber blends
    • Disperse dyes for polyester and acetate textiles
    • Intermediate blends for technical plastic colorants

    4. Specialty Chemical Synthesis: Photographic and Electronic Materials

    Electronic and imaging material producers depend on this nitrile for its reactivity in forming key intermediates used in photographic chemicals and specialty polyimide film production. Specific process design ensures minimal trace impurities affecting dielectric properties and image resolution. The quantity varies based on batch size and functional group conversion efficiency, with all operations within traceable cleanroom or iso-class production.

    Industry compliance standards

    • IEC 60417 for Component Manufacturing
    • ISO 14644 Cleanroom Standards
    • RoHS Directive 2011/65/EU
    • Japanese Industrial Standards (JIS) for photographic chemicals

    Typical usage ratio

    • 3%–10% by weight in intermediate solution, higher ratios for polyimide precursor routes, optimized for dielectric loss and image clarity

    Downstream process integration

    • Introduced during aromatic nitrile condensation in photosensitive salt or polyimide resin synthesis, followed by controlled cyclization and refining

    Final product types

    • Photoresist chemicals for semiconductor lithography
    • High-performance polyimide film coatings
    • Silver halide image formation additives

    5. Fine Chemical Manufacturing for Aromatic Building Blocks

    Producers in the fine chemical sector rely on this raw material for downstream customization into specialty aromatic components via reduction, hydrolysis, or metal-catalyzed coupling. These building blocks subsequently enter performance additive and modifier lines for industrial resins and lubricants where tight property control is required.

    Industry compliance standards

    • ISO 9001:2015 (Fine Chemical Manufacturing)
    • Chemical Facility Anti-Terrorism Standards (CFATS, US DHS)
    • REACH Registration for Specialty Intermediates
    • Responsible Care® Global Charter

    Typical usage ratio

    • 6%–12% by formulation batch, based on process route (reduction/coupling) and desired final component loading

    Downstream process integration

    • Fed into reaction vessels prior to catalytic hydrogenation, or sequenced in Suzuki/Miyaura cross-coupling protocols for advanced aromatic assembly

    Final product types

    • Halogenated benzene intermediates for specialty resins
    • Aromatic amines for lubricant antioxidative additives
    • Functionalized aromatic acids for epoxy modifier production
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    Certification & Compliance
    More Introduction

    2-Chloro-4-Nitrobenzonitrile: The Backbone of Fine Chemical Synthesis

    Our Practical Experience with 2-Chloro-4-Nitrobenzonitrile

    In the world of industrial chemistry, few aromatic nitrile compounds offer both the reactivity and stability required for dependable synthesis routes. Our work with 2-Chloro-4-Nitrobenzonitrile (CAS 873-32-5) stretches back over a decade. We’ve pushed its synthesis efficiency and purity to meet the strict standards requested by clients who focus on pharmaceuticals, agrochemicals, and dye intermediates. Each batch we produce begins with a focus on contaminant minimization, providing a crystalline powder with purity over 99% by HPLC, light to dark yellow, and a melting point consistently in the 139—142°C range. By holding onto these production principles, we reduce offcut formation in downstream reactions, saving customers solvent costs and troubleshooting hours.

    Our team deals in scale: over the years, we have achieved multi-ton outputs per month, adjusting the chlorination and nitration steps for higher yield and better waste management. The model designation C4NB series identifies grades best suited for demanding synthesis environments. It reflects our adjustment of particle size and moisture content, which we customize for specific process requirements, whether the needs involve solid-phase, slurry, or solution-phase reactions.

    How 2-Chloro-4-Nitrobenzonitrile Behaves in Synthesis

    What sets 2-Chloro-4-Nitrobenzonitrile apart from other benzonitriles is the unique positioning of substituents. The para-nitro and ortho-chloro placements on the benzene ring create a highly activated aromatic system. Electrophilic aromatic substitution becomes less likely, making nucleophilic aromatic substitution the clear path for further derivatization. This facilitates the controlled introduction of amines, thiols, or alkoxides. Many customers, especially in pharmaceutical R&D, have seen their reaction timelines shrink by switching to this compound, reducing temperature and eliminating side reactions that typically plague less substituted isomers. We’ve found that nucleophilic substitution on this nitrile offers higher selectivity for “hard” nucleophiles compared to other halogenated nitrobenzonitriles.

    Pharmaceutical manufacturers often need to develop process routes for key intermediates like anilines, amides, or diaryl ethers. This compound’s reactivity streamlines multistep synthesis, as its nitrile group permits subsequent transformation to acids or amides without extra protection and deprotection steps. The combination of nitro and chloro functionalities also serves as an excellent entry point for building heterocyclic cores. Agrochemical teams develop defoliants, herbicides, and plant hormone analogs from frameworks built on this backbone.

    Applications and Role in Industry

    Years of working with specialty chemical clients have shown us that this molecule doesn’t just sit on a shelf — it's engineered for end-use. Its application starts in intermediate synthesis for both bulk and fine chemical sectors. In dye manufacturing, it assists in the formation of phthalonitrile-based pigments, giving vibrant colors with strong light fastness. In the pharmaceutical industry, we’ve seen customers use it to synthesize molecules active against cancer, diabetes, and infections. The compound’s robust nitrile group survives even under strong acid or base, while the nitro and chloro groups add multiple chemical handles for elaborating complexity.

    In our facilities, the safety and mechanical durability of the material matter just as much as the chemistry. We test each batch for thermal stability and dust formation to help large reactors run safely. During pilot plant trials with pharmaceutical clients, batches blended straight into high-pressure reactors, avoiding the clumping and inconsistent mixing problems often caused by off-specification particle sizes. These tiny details, overlooked by traders and casual resellers, illustrate the assurance that comes from working with a real manufacturer who has seen pilot plants and full-scale facilities grind to a halt on technicalities that could have been avoided at the source.

    The Value of Controlled Synthesis and Purity

    From our operations, we learned that the repeatability of reactions directly depends on raw material quality. The difference between a reliable, reproducible process and a week filled with failed runs rests on purity, particle size uniformity, and moisture content in 2-Chloro-4-Nitrobenzonitrile. Pharmaceutical chemists have passed along headlines about regulatory authorities barring shipments for a 0.2% unknown impurity or for 1% water picked up in a humid warehouse. We’ve designed drying, milling, and packaging protocols to address those pain points before they reach our customer’s line.

    What sets our product apart is the integrated approach: molecular sieves in the bulk storage areas, sealed double-layer drum packaging, and on-site cold chain facilities for sensitive orders. These measures don’t come from specifications alone; they grew out of feedback from customers whose pilot or commercial runs hit snags due to overlooked operational weaknesses further upstream.

    Direct Comparison With Other Benzonitrile Derivatives

    Chemically, 2-Chloro-4-Nitrobenzonitrile isn’t interchangeable with other benzonitriles. Take 4-chlorobenzonitrile or 2-nitrobenzonitrile, both of which have different ortho/para substitution and thus react differently with nucleophiles. The activating nitro group on the para position in our molecule increases the electron withdrawal synergistically with the ortho-chloro, making the aromatic ring much more susceptible to nucleophilic substitution — think of faster and cleaner reactions for forming C-N or C-O bonds.

    Some customers tried to substitute with 2-chloro-5-nitrobenzonitrile, thinking the close chemical resemblance would translate to equivalent outcomes. The difference in byproduct formation and lower selectivity became clear after a few pilot runs, often causing methylation or hydrogenation steps to produce more side products and decrease overall yield. Instead of saving costs, the switch created more spending on separation and purification, with additional solvent recovery steps. We routinely see customers returning to the 2-Chloro-4-Nitrobenzonitrile scaffold for reliability and speed, particularly for late-stage intermediate synthesis.

    The safety profile also changes with minor shifts in substitution pattern. Many ortho-nitrobenzonitriles have a higher tendency for exothermic decomposition under high concentration, which can trigger runaway reactions. 2-Chloro-4-Nitrobenzonitrile’s stability up to 180°C makes it much friendlier for manufacturing settings that require scale, heat, and long residence times. These qualities allow greater process window flexibility for production teams.

    Meeting Regulatory and Quality Demands

    Stringent regulatory requirements from both domestic and export markets keep raising the bar for traceability and impurity control. Long before these guidelines became popular, we tracked production lots with in-plant barcoding and sample archiving. We keep years of batch documentation, letting our clients retrieve retention samples and certificates at short notice — especially useful for pharmaceutical audits or recalling processing history in case of downstream changes.

    Analytical methods such as HPLC and GC-MS are used in-process, not just on outgoing quality control. This close monitoring lets us detect problem batches before they reach our client’s facility, avoiding production gaps. We take seriously our responsibility to support downstream regulatory submissions with robust data, knowing that a small change at our step could mean weeks of delay at registration or plant approval phases.

    Challenges and Solutions in 2-Chloro-4-Nitrobenzonitrile Manufacturing

    Achieving high yield in nitration and chlorination steps requires precise reaction control. Too aggressive a nitration leads to dinitro byproducts, while poor temperature control in the chlorination stage results in over-chlorinated or hydrolyzed materials. Years of tinkering and process audits led us to fine-tune batch protocols, understanding the subtle interaction between solvent moisture, reaction agitation, and feedstock quality.

    On the environmental front, minimizing chlorinated and nitro byproducts demands a focus on waste stream separation. We invested in scrubbers and recycling for process gases, using catalytic incinerators to break down hazardous exhaust. Before these systems, we frequently struggled with compliance documentation and waste disposal challenges, which risked fines and reputational harm.

    Clients sometimes share concerns about supply continuity. In the past, unexpected facility outages in China or India led to global shortages, with clients scrambling for spot purchases from traders who couldn’t guarantee traceability. To ensure reliability, we built buffer inventory and sourced raw materials from several audited suppliers. Our in-house engineering team designed modular reactors, letting us ramp up or down depending on seasonal and market demand swings.

    Customer Stories Speak Louder Than Claims

    We’ve partnered with global pharma houses that moved from pilot to market-phase scale on the back of our consistent supply. Once, a project targeting a difficult phenol ether used our benzonitrile to streamline both amination and O-alkylation without intermediate protection steps. The effort shaved months off their development time, helping their new drug reach clinical trials before competitors. The client attributed success to a single change: choosing a manufacturer over intermediaries, ensuring access to technical troubleshooting and process transparency.

    In the pigments business, a longstanding customer builds organic dyes for plastics. Their focus is on deep hues, and light and thermal stability in the final products. Competing nitriles failed by introducing unwanted tints and short shelf life due to byproducts. Since switching to our 2-Chloro-4-Nitrobenzonitrile, batch failures dropped below statistically relevant levels, letting them lock in global contracts with automakers demanding color-fast performance. Over time, selling the same dye at higher volumes justified upgrading to larger reactors, which our plant supplied with no lag in production rate.

    Another story comes from the agrochemical sector, where a new herbicide’s synthesis depended on clean nucleophilic substitution step. Trials with lower-purity material sourced from traders created trace impurities, stalling approval at a government regulatory lab. Once the client moved to our high-purity, low-residue product, testing passed, and registration completed in half the time projected when delays first emerged.

    Continuous Improvement in Our Manufacturing Process

    Improving yield and cutting emissions are non-stop efforts in our workshops. Every year, we take feedback from clients as well as our own staff. Many times, a technician on the packaging line or a plant engineer pointed out small changes that cut material losses or hazards. For example, tightening the drying process in the final step increased shelf life by reducing marginal moisture content. Adding positive-pressure rooms stopped dust migration, a win for both product containment and worker safety.

    Research and development teams periodically test new catalysts for both nitration and chlorination phases, seeking processes that cut both time and waste. Some years back, a trial of alternative chlorination reagents gave a 3% boost in yield and halved side-product formation. Incremental improvements like this build over time, compounding into better cost structures for both us and our partners. By lowering energy and solvent requirements, we keep operating expenses in check while reducing overall environmental burden.

    On the analytical front, in-line monitoring now forms part of our continuous process feedback. Troubleshooting and optimization cycles have shortened because we identify impurities before the product ever leaves the reactor. All of this translates into less downtime and higher confidence for customers locking in long-term supply agreements.

    Why Direct Manufacturer Access Makes the Difference

    In our two decades producing 2-Chloro-4-Nitrobenzonitrile, direct communication with end-users remains the biggest factor in our mutual success. Process questions, scale-up support, or analytical fingerprinting—these conversations close the gap between lab research and commercial operations. Intermediate traders rarely possess the manufacturing knowledge to answer root-cause queries about reactivity, residual solvents, or handling best practices.

    End-users come to value technical support offered by those who make the product, not just those who sell it. When hiccups arise in a reaction step, we provide troubleshooting pulled from hundreds of real-world runs, not just textbook numbers. The ability to adjust particle size, supply pre-dried material, or provide rapid batch documentation only comes from an integrated producer who controls the process from raw materials to finished drum.

    Knowledge sharing, site visits, and data transparency have proven essential over the years. Rigorous quality and safety don’t happen overnight—they are rooted in operational discipline, investment, and staff expertise. Our site tours often surprise prospective partners—metal detectors and magnet bars pick up tramp material before blending; each filling line is pressure-checked for leaks and contamination before every run. Customers’ regulatory teams have pointed to these protocols as reasons for approving our material in their filings.

    Conclusion: A Solid Foundation for Chemical Manufacture

    The years have taught us that the quality and reliability of 2-Chloro-4-Nitrobenzonitrile define the difference between smooth processing and headaches at every step of synthesis. From first samples through to tonnage quantities, steadfast process control and genuine expertise determine whether customers achieve their targets in pharmaceuticals, dyes, or agrochemicals. By staying close to our production line and our customers, we support not only consistent supply, but innovation, trust, and safety in every shipment. Real experience—built on years invested in perfecting every part of the process—makes the difference, and that’s the story we bring to every drum of 2-Chloro-4-Nitrobenzonitrile that leaves our gates.