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4-Chloro-3-Nitrobenzonitrile

    • Product Name 4-Chloro-3-Nitrobenzonitrile
    • Alias 4-Chloro-3-nitrobenzenecarbonitrile
    • Einecs 244-957-5
    • 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

    205212

    Chemical Name 4-Chloro-3-Nitrobenzonitrile
    Cas Number 619-64-7
    Molecular Formula C7H3ClN2O2
    Molar Mass 182.57 g/mol
    Appearance Yellow crystalline powder
    Melting Point 151-153 °C
    Density 1.54 g/cm³
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Synonyms 3-Nitro-4-chlorobenzonitrile
    Smiles C1=CC(=C(C=C1Cl)[N+](=O)[O-])C#N
    Inchi InChI=1S/C7H3ClN2O2/c8-6-2-1-5(4-9)7(3-6)10(11)12/h1-3H
    Storage Conditions Store in a cool, dry place, keep container tightly closed

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

    Packing & Storage
    Packing The 100-gram amber glass bottle features a yellow chemical hazard label stating "4-Chloro-3-Nitrobenzonitrile, C₇H₃ClN₂O₂, 100g."
    Shipping 4-Chloro-3-Nitrobenzonitrile is shipped in sealed containers, protected from moisture and direct sunlight. It is classified as a potentially hazardous material and must be handled according to local, national, and international regulations. Transport typically occurs via ground or air freight, with appropriate labeling and documentation ensuring safe and compliant delivery.
    Storage 4-Chloro-3-nitrobenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flame. Keep it separate from incompatible substances such as strong oxidizers and bases. Ensure storage is clearly labeled, and access is restricted to trained personnel. Use appropriate secondary containment to prevent leaks or spills.
    Application of 4-Chloro-3-Nitrobenzonitrile

    Applications of 4-Chloro-3-Nitrobenzonitrile in Industrial Manufacturing

    As a specialized manufacturer of 4-Chloro-3-Nitrobenzonitrile, we supply this intermediate to a focused range of chemical industries where its selective reactivity enables precise synthesis functions. This section details its real-world industrial deployment, with scenario-specific formulation guidance, compliance standards, integration points in batch and continuous production, and the exact types of downstream products manufactured using our material.

    1. Pharmaceutical Intermediate Production for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical companies incorporate this raw material as a building block in multi-step syntheses, most notably in the preparation of heterocyclic moieties for antihypertensive and antitumor APIs. Its electron-withdrawing group configuration ensures high site-selectivity during nucleophilic aromatic substitution, helping streamline purity assurance from early route scouting to large-scale reactor charging. Our technical service teams engage with API manufacturers to support validation batches targeting the synthesis of quinazoline, indole, and pyrido[2,3-d]pyrimidine derivatives, where minimal residual process impurities are critical for regulatory filings.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • EU GMP Annex 21 for starting materials
    • USP–NF and Ph. Eur. reference monographs for related substances
    • FDA 21 CFR Part 210/211 for process validation and impurity control

    Typical usage ratio

    • 0.8–2.5 molar equivalents, based on target molecular structure and required conversion rates; ratios adjusted according to step yield and impurity formation within the route's limiting synthetic step.

    Downstream process integration

    • Charged at Step 2–4 in multi-step organic synthesis sequences; introduced post initial aromatic ring activation and prior to cyclization or alkylation, under strictly controlled atmospheric and temperature conditions, often within hydrogenation or palladium-catalyzed segments.

    Final product types

    • Sartan-class antihypertensive active pharmaceutical ingredients (e.g., Losartan intermediates)
    • Indole-based kinase inhibitor intermediates
    • Quinazoline skeleton intermediates for anti-cancer drugs
    • Pyridopyrimidine fragments in CNS medication scaffolds

    2. Agrochemical Synthesis for Selective Herbicide Actives

    This raw material plays a crucial role in the synthesis of pre- and post-emergence herbicide actives, where its nitrile and nitro substituents underpin key reactivity for constructing pyridine and benzamide cores. Downstream users engage it during the early-stage coupling steps, allowing for high-purity crop protection molecules with selectivity toward broadleaf weeds in cereal and soy cultivation. Kinetic monitoring during scale-up ensures that the structure retains its functional groups critical for fast-track regulatory field trials and environmental risk assessments.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for Testing of Chemicals (Batch impurity profiling, 107 & 117)
    • REACH Regulation (EC) No. 1907/2006 for registration and evaluation
    • ISO 17025 for laboratory quality and traceability in batch analysis

    Typical usage ratio

    • 5–10% by weight in initial coupling reactions; optimized on a per-formulation basis to align with required precursor conversion rates and minimize waste generation in downstream purification.

    Downstream process integration

    • Added at the condensation reaction stage for benzamide or pyridine ring assembly, typically before halide exchange or amidation, and processed under inert atmosphere with real-time HPLC endpoint detection to ensure specified purity for agrochemical actives.

    Final product types

    • Triazine herbicide intermediates (used in crops such as maize and wheat)
    • Benzonitrile herbicide ingredients (auxins blockers for soybean fields)
    • Nicotinic acid-derived selective herbicides

    3. Specialty Dye and Pigment Manufacturing

    Producers of high-performance azo and disperse dyes use this chemical as a critical diazo coupling partner, where its controlled reactivity under acidic or basic conditions allows for synthesis of molecularly tuned pigments. Its presence governs lightfastness and solubility in formulated dye products, with addition rates and purification stringently monitored to meet downstream requirements for color strength and migration resistance in textile fiber and plastics coloration. All unit operations require closed process systems due to the reactive nitro group, and batch records reflect complete traceability under international dyestuff standards.

    Industry compliance standards

    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substance List)
    • Oeko-Tex Standard 100 (textile chemical inputs)
    • EN 71-3 (Safety of Toys – migration of certain elements, for pigment compliance)
    • REACH Annex XVII dye restrictions

    Typical usage ratio

    • 1.2–7% by weight of total dye molecule mass; exact percentage varies with chromophore target intensity and substrate type (polyester, nylon, cellulose).

    Downstream process integration

    • Utilized in diazotization or azo-coupling reaction stage, immediately following precursor amine chlorination or nitration; staged addition supports control over pigment particle size and target shade reproducibility for both batch and continuous dye syntheses.

    Final product types

    • Monoazo and disazo textile dyes (suitable for synthetic fiber dyeing)
    • Disperse pigments for plastics and polyester fibers
    • Specialty colorants for inkjet and digital printing applications

    4. Electronic Chemical Synthesis for OLED and Photoconductor Materials

    Advanced materials manufacturers who produce organic electronic components employ this intermediate in functionalizing aromatic scaffolds used within OLED emitters and photoconductor films. The controlled introduction of both nitro and cyano groups provides electron-accepting properties critical for hole-transport and emission balance in device architectures. Precise molar dosing during the assembly of polyaromatic compounds ensures batch-to-batch consistency required for display color reproducibility, with all material batches subject to electronic-grade quality screening tailored to semiconductor application routes.

    Industry compliance standards

    • IPC-6012 (Qualification and Performance for Rigid Printed Boards)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances in electrical equipment)
    • JEITA ED-7309 (Organic semiconductor material qualification for display use)
    • IEC 62474 (Material Data Exchange for Electronic Industry)

    Typical usage ratio

    • 0.5–2% by weight in precursor blends; adjusted for emission layer tuning or improved charge mobility depending on display or photoconductor matrix requirements.

    Downstream process integration

    • Reacted during Suzuki or Buchwald-Hartwig cross-coupling stages in aromatic core extension; integration points selected based on desired optoelectronic function (e.g., shift in emission wavelength or improved thermal stability).

    Final product types

    • OLED emitter precursors (green and blue emission materials)
    • Organic photoconductor layer monomers for imaging and sensor arrays
    • Tailored high-performance liquid crystalline display chemicals
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    Certification & Compliance
    More Introduction

    4-Chloro-3-Nitrobenzonitrile: Shaping Reliable Chemical Intermediates from the Manufacturer’s Perspective

    The Chemical at a Glance

    In this commentary, I am drawing directly from our daily production floor where 4-Chloro-3-Nitrobenzonitrile moves from raw material to finished product under strict process control. This compound, with its chemical formula C7H3ClN2O2 and CAS number 121-90-4, takes on a crucial role for manufacturers developing advanced pharmaceuticals, agrochemicals, and dyes. Unlike more pedestrian nitriles, the distinct substitution pattern—chlorine at the 4-position and nitro at the 3—hardwires selectivity into each batch, channeling reactivity along paths that suit targeted synthesis steps.

    How We Approach Model and Specification

    Each time we set up a run for 4-Chloro-3-Nitrobenzonitrile—internally referenced as model BNC3404—the climate-controlled space comes alive with careful weighing, filtration, and crystallization. That hands-on involvement ensures consistency batch after batch. The off-white to pale yellow crystalline solid signals correct synthesis. Our technicians check melting points, inspect particle size under magnification, and run 1H NMR, HPLC, and GC analysis. Most lots clock in with purity above 99.5%. Water content gets pushed well below the 0.2% mark through in-line drying. Chloride ion residue rarely tips the scales over the 0.01% mark on our analytical reports. Packing density, flow characteristics, and tablet press compatibility get measured and logged—practical yardsticks that matter more to us than abstract quality metrics.

    How We Got Here: Why This Niche Intermediary Matters

    Every manufacturer has watched downstream partners endure frustration from poor handling upgrades or missed reactivity. Before adopting rigorous controls, we sometimes dealt with complaints about off-odor or unwanted side-products. A single misplaced impurity in a batch can throw off an entire pharmaceutical synthesis, leading to regulatory headaches and financial loss. That’s why we adapted our production lines to run closed-loop sampling and purge any source of metallic contamination. For end-users, predictability comes from traceable inputs, not random sampling or vague specifications.

    Over a decade ago, few customers asked detailed questions about isomeric purity or particle morphology. Today, they press us for precise FT-IR patterns and surface area measurements, knowing that small variances can make or break cost efficiency in a pilot plant. Our lab responded with daily checks: polymorph screening, high-throughput stability aging, and careful record-keeping. We keep retention samples and share chromatograms, not just certificate of analysis forms. Every data point gets anchored by the judgement of an experienced chemist, not an algorithm.

    Practical Usage: A Direct Line to Industry Results

    In our own research and feedback cycles, three main areas of industrial usage keep surfacing for 4-Chloro-3-Nitrobenzonitrile. The primary demand comes from pharmaceutical manufacturers. Medicinal chemists build complex heterocycles using this compound as a precursor for benzamide derivatives, antihypertensive drugs, and oncology research compounds. Its electronic structure permits selective nucleophilic aromatic substitution, giving customers a springboard to synthesize molecules that aren’t achievable with unsubstituted benzonitriles. We see it employed in Suzuki–Miyaura coupling, direct reduction for amine analogs, and as a platform for cyanation reactions.

    Pesticide and fungicide formulators land at our doors looking for scalable sources of bench-tested intermediates. For these teams, 4-Chloro-3-Nitrobenzonitrile ensures consistency in the stepwise construction of triazole and pyridine active ingredients, helping to solidify active ingredient registration without supply-chain disruption. Demand spikes in months before planting seasons often stress the global market. We handle these cycles by maintaining stable raw inventory and monitoring predictive purchase data—not waiting for last-minute procurement requests.

    Next, dye and pigment producers use our material for their high-stakes product launches. Organic pigments require deep chromatic purity so textile, paint, and ink manufacturers meet clothing and packaging standards. Impurities cause color fading or binding failures at the textile mill, which explains why analytical certifications alone lose meaning unless backed by real industrial runs.

    Why Specifications Define More Than a Number

    Living with this compound through every stage of processing has taught us that not every “99% pure” label means similar performance. During one scale-up, a customer flagged differences between competitors' 4-Chloro-3-Nitrobenzonitrile grades showing identical purity by HPLC but diverging in process yields. Autoclave trials revealed that trace metals and subtle isomeric cross-contamination explained the drop in output. Our process engineers took this as a challenge, tightening the distillation profile and refining acid washes to prevent side-product formation. Flash chromatography, usually reserved for lab-scale refinement, became a routine check for pilot and commercial batches. We also reinforced nitrogen blanket procedures to shield product from airborne moisture and contaminants.

    We learned that small particulate variations affect the wet milling and blending stages at the end-use plant. Material shipped in summer can absorb moisture during transit, so we doubled up on desiccant layering inside polyethylene liners. Before dispatch, each drum passes a vibration and drop test, ensuring lumps don’t form in storage. These practical tweaks minimized customer downtime and increased repeat orders.

    Every certificate of analysis features lot-specific reading for heavy metals—arsenic, lead, mercury—well below international safety guidelines. Solvent residues from synthesis steps (acetone, dichloromethane, toluene, methanol) stay under strict regulatory thresholds. Our compliance officers keep our processes current with both European REACH and FDA guidelines. No report leaves the site unless verified in duplicate, and we field regular audits from long-term partners.

    Key Differences Between 4-Chloro-3-Nitrobenzonitrile and Other Benzonitrile Intermediates

    In practice, there’s a world of difference between 4-Chloro-3-Nitrobenzonitrile and other commonly traded benzonitriles like 3-chloro-4-nitrobenzonitrile or simple benzonitrile. The shift in chlorine and nitro positioning radically alters reactivity. With the 4-chloro at the para position, nucleophilic aromatic substitution — especially for amine and alkoxide groups — proceeds with greater selectivity. That controls side-reactions, saving weeks of purification downstream. The 3-nitro group amplifies electron withdrawal, boosting coupling efficiency in C–N and C–C bond-forming reactions. The net result is cleaner product formation and simpler purification.

    By contrast, other benzonitrile derivatives lack this fine-tuned selectivity, which can saddle chemists with higher byproduct levels or force use of more aggressive conditions. Not only do these alternatives complicate waste-stream management, but they sometimes limit suitability for tightly regulated finished goods. We’ve seen synthesis teams spend months reworking process economics and GMP filings due to poorly characterized intermediates. Customers who choose our 4-Chloro-3-Nitrobenzonitrile see higher yield and batch-to-batch homogeneity because the molecular structure dovetails with intended downstream chemistry.

    Cost structure also diverges. Lower-cost materials often hide processing shortcuts, leading to inconsistent performance. Instead of pricing based on theoretical content, we audit every run for mass balance and impurity mapping. If regulatory standards evolve, we change our process specification—never the other way around. Some alternative intermediates trade at a lower sticker price per kilo, but factor in labor, cleaning, and batch rejection, and the cost advantage disappears.

    Manufacturing Insights: Where Quality is Decided

    Shared experience has shown that every upstream shortcut telegraphs pain downstream. Operators who cut drying time to increase throughput end up forcing customers to troubleshoot clumpy, hard-to-dissolve product. The temptation to swap out fresh solvents for recycled blends creates savings on paper but triggers a spike in residual solvents—a persistent headache for compliance officers. Even subtle batch-to-batch variation in anti-caking agents and drum lining compounds can raise red flags for sharp-eyed end users.

    We hold weekly cross-team reviews—QC, production, logistics, and R&D—to analyze any deviation, even if it seems minor. During supply chain crunches—such as global shortages in chloro-nitro starting materials—ROA (root-cause analysis) disciplines help us get to the source, whether it’s a trace impurity from a new vendor or a delay in cold chain transit. By sticking with partners who commit to consistent inputs and documenting each load’s full legacy, we reduce chaos. That discipline grows out of hard-won lessons, not marketing slogans.

    Meeting Global and Local Demands: Scalability and Consistency

    International partners look for more than a product—reliability across continents and markets defines our reputation. Local pharmaceutical users depend on security of supply, especially under GMP demands. We build redundancy in both raw material vendors and finished product supply, holding buffer stocks in temperature-controlled warehouses. In summer heat or winter chill, containerized storage preserves crystal integrity and prevents caking.

    Handling export documentation, customs, and on-site regulatory inspections requires more than paperwork. Every lot comes with full origin tracing. Quality inspectors conduct live batch sampling at port prior to shipping. We maintain open communication with global compliance teams, regularly updating declarations on SVHC (Substances of Very High Concern) status and other risk registers. Customers in North America, Asia, and the EU receive the exact same performance profile—no stepping down for so-called “regional” standards.

    Challenges in Handling and Solutions Applied

    Real manufacturing means facing dust, heat, risk of static ignition, and operator safety. 4-Chloro-3-Nitrobenzonitrile, like most aromatic nitriles, requires dust containment. Our facilities run with HEPA filtration and explosion-proof equipment. Handlers wear full PPE, including nitrile gloves, goggles, and respirators during charging and drum filling. Regular air monitoring and dust control audits target all exposure points.

    We deploy automated drum fillers to reduce variation in fill levels, eliminate airborne particulates, and shrink operator exposure risk. Cleaning logs are reviewed daily, and scheduled equipment shut-downs upstream ensure cross-contamination never enters a lot. Only bulk drums with tamper-evident closures get approved for outbound shipment. We destroy all off-specification product in-house, no matter how small the deviation.

    To support long-term storage, we keep moisture levels below critical thresholds using double-foil liners and vacuum sealing. Any sign of off-odor or unknown surface residues triggers an immediate block and investigation. We share these quality incident reports with downstream partners as a demonstration of transparency, allowing joint troubleshooting where needed. The goal is simple: prevent contamination before a container ever leaves our gate, not after.

    Environmental Considerations and Regulatory Alignment

    Manufacturing responsibility today means addressing everything from solvent recovery to waste-stream neutralization. Chlorinated and nitroaromatic by-products must be treated on-site through multi-stage scrubbing and catalytic oxidation units. Our engineers track every kilo of hazardous waste, routing it into controlled neutralization streams. Real-time reporting to environmental oversight boards has replaced legacy batch logs.

    Our process innovations include solvent recapture at over 90% efficiency and zero liquid discharge policies in product work-up. New employee training emphasizes safe loading, correct PPE, strict record-keeping, and alarm response. We work with outside auditors each quarter to review environmental impact statements and implement new legal requirements from changing international frameworks. Every regulatory shift—from revision of the EU CLP Regulation to new REACH requirements—leaves its mark on our control protocols and engineering upgrades.

    We also revisit water usage and energy consumption during every corporate investment cycle. New heat exchangers and cooling towers have knocked our per-tonne energy usage down by over 13% in the last five years. These savings matter both for sustainability and cost competitiveness. Our partners want documentation on green manufacturing, not just an eco-label, and we keep a repository of ongoing environmental improvements accessible for customer audits.

    Supporting R&D and Collaborative Progress

    One of the more rewarding parts of manufacturing comes through partnerships with R&D teams tackling new challenges. Chemists from biotech startups and major pharma labs visit us to test pilot runs, aiming to optimize synthetic strategies with our 4-Chloro-3-Nitrobenzonitrile as a starting node. We run custom kilo-scale batches to support early-stage development, offering flexible lots and tailored delivery times.

    Data sharing stands out as a crucial value-add. We regularly issue anonymized process analytics so that innovators can predict reaction performance in larger production settings. By opening up our own yield tracking and process bottlenecks, we foster trust and help partners avoid reinventing the wheel. Working together, we design continuous improvement cycles, building higher-performing intermediates that reduce waste, speed throughput, and ensure downstream compliance.

    We see real advances blooming from a manufacturer’s willingness to provide not just product, but accumulated know-how. Many times, teams bring their own raw material and analytical doubts to the table; we conduct comparative testing and offer solutions backed by decades of hands-on chemistry—methods as well as mistakes.

    Looking Forward: Building Confidence in Sourcing

    From first kilo to full container load, 4-Chloro-3-Nitrobenzonitrile reflects the sum of real process oversight, stubborn attention to customer needs, and responsiveness to global shifts. Every insight carved into our methods comes from working through supply crunches, quality investigations, and customer R&D hurdles. Over years, we’ve set up systems that reward precision, information sharing, and continuous improvement—not buzzwords, but tools that keep our partners’ processes running predictably and safely.

    Our commitment as a chemical manufacturer runs deeper than supplying a spec-compliant intermediate. We treat every batch as an opportunity to enforce standards, prevent regulatory surprises, and support the innovations that shape better medicines, safer crops, and deeper colors in daily life. This means showing up for audits, opening our books and archives, and investing in the facilities and people who make small-molecule chemistry work on a global scale. There isn’t a substitute for the rigor built into years of learning, and our customers know to look for it—not just in a certificate, but in every question answered and every solution offered.