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2-Chloro-5-Nitrobenzonitrile

    • Product Name 2-Chloro-5-Nitrobenzonitrile
    • Alias 2-Chloro-5-nitrobenzenecarbonitrile
    • Einecs 238-759-0
    • 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

    194439

    Iupac Name 2-chloro-5-nitrobenzonitrile
    Cas Number 2516-96-3
    Molecular Formula C7H3ClN2O2
    Molecular Weight 182.57
    Appearance yellow crystalline solid
    Melting Point 108-112°C
    Boiling Point 325°C
    Density 1.48 g/cm3
    Solubility In Water insoluble
    Flash Point 148°C
    Pubchem Cid 16828
    Smiles C1=CC(=C(C=C1[N+](=O)[O-])Cl)C#N

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

    Packing & Storage
    Packing The 100g package of 2-Chloro-5-Nitrobenzonitrile comes in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 2-Chloro-5-Nitrobenzonitrile is shipped in tightly sealed containers, protected from moisture and heat. It should be handled with care due to its hazardous nature. Transport follows regulations for dangerous goods, typically via ground or air freight, ensuring appropriate labeling, documentation, and safety measures to prevent leaks or exposure during transit.
    Storage 2-Chloro-5-nitrobenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, strong acids, bases, and oxidizing agents. Protect the chemical from moisture and direct sunlight. Ensure proper labeling and store separately from incompatible substances. Use secondary containment to prevent accidental release or contamination.
    Application of 2-Chloro-5-Nitrobenzonitrile

    Applications of 2-Chloro-5-Nitrobenzonitrile in Industrial Manufacturing

    Our production of 2-Chloro-5-Nitrobenzonitrile (2C5NBN) supports several highly specialized chemical manufacturing chains, where its reactive functionalities are essential for the synthesis of advanced intermediates. As a core raw material, it is incorporated by leading downstream producers engaged in pharmaceuticals, agrochemicals, dyes, and specialty chemical synthesis. The following scenarios showcase practical industrial applications extracted from real-world purchasing feedback, process integration data, and regulatory requirements.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Downstream manufacturers incorporate our 2C5NBN as a key intermediate for constructing nitroaniline-based pharmacophores, especially in antihypertensive and anti-infective drug classes. This compound enters the route at the halogenated aromatic stage, providing reliable reactivity in nitrile reductions and aromatic substitutions required for specific drug frameworks. Precise control over its input is mandatory due to regulatory batch traceability and impurity management. User feedback highlights consistent yield and residual solvent data meeting stringent QC requirements.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • EU GMP Annex 1 and Annex 13
    • USP-NF Monograph Guidance for Intermediates
    • 21 CFR Part 211 (US FDA, cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 5–18% w/w of total initial aromatic substrate, adjusted for route yield and downstream isolation efficiency; process chemists fine-tune the equivalent based on pharmacophore complexity.

    Downstream process integration

    • Input during nitration and halogen-exchange steps as a primary aromatic building block
    • Reduction of the nitro group followed by amination or hydrolysis depending on the target intermediate
    • Solvent-phase batch reactions in stainless or glass-lined reactors

    Final product types

    • Anti-infective API intermediates for fluoroquinolone drugs
    • Antihypertensive intermediate blocks used in synthesis of sartan-class APIs
    • Chlorinated aromatic building blocks used by proprietary oncology projects

    2. Agrochemical Synthesis: Selective Herbicide Intermediates

    The material is integral to the production of substituted benzamide and triazine herbicide intermediates, where selectivity and process compatibility are crucial. Its high reaction specificity allows chemical engineers to achieve targeted transformations without incompatible by-product formation. Agrochemical customers require full traceability of nitro and halogen content to ensure safe downstream catalytic conversion and compliance with international pesticide quality norms.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications and Evaluations
    • ISO 9001:2015 Quality Management for Agrochemical Intermediates
    • REACH (EC) No 1907/2006
    • China GB/T 1604-2019 (Quality Standard for Pesticide Intermediates)

    Typical usage ratio

    • 8–15% of synthesis weight per batch, selected based on seasonal demand for active ingredient yield and target selectivity during the condensation step.

    Downstream process integration

    • Start point for nucleophilic aromatic substitution introducing amine or alkoxy partners
    • Integrated in solvent-phase or biphasic batch operations
    • QC-controlled addition to minimize unresolved aromatic by-products

    Final product types

    • Selective triazine herbicide intermediates
    • Chloronitrobenzoic acid derivatives for broadleaf weed control agents
    • Benzamide-based pesticides for cereal crop protection

    3. Dye and Pigment Manufacturing: Azo Coupling Components

    2C5NBN functions as a specialized coupling component for the development of disperse and reactive dyes where the balance of electron-withdrawing groups is critical to achieving colorfastness and hue precision. These reactions demand careful raw material dosing to meet fastness and shade specifications while ensuring minimal trace metal contamination as mandated for global textile supply chains.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 6 (Textile and Leather Chemical Restrictions)
    • ZDHC MRSL V3.0 (Zero Discharge of Hazardous Chemicals)
    • EN ISO 105–A02 (Color Fastness to Washing)
    • China GB 18582-2020 (Limit of Harmful Substances of Dye Products)

    Typical usage ratio

    • 1.5–6% relative to total dye charge, modified depending on final shade intensity and chromophore type; process technicians adjust equivalence for batch-to-batch shade reproducibility.

    Downstream process integration

    • Azo coupling in semi-continuous liquid-phase reactors
    • Direct input during diazotization for disperse and reactive dyes
    • Staged fractionation to isolate high-purity intermediates free from metal ion residues

    Final product types

    • Disperse dyes for polyester and synthetic fiber applications
    • Reactive dyes for cotton textiles with high wash and light fastness
    • Intermediate chromophore agents for specialty pigment sectors

    4. Specialty Chemical Production: Liquid Crystal Intermediate Sourcing

    Multiple advanced materials manufacturers, especially in Asia, source 2C5NBN as a critical starting compound for synthesis of specialty aromatic nitrile intermediates utilized in liquid crystal manufacturing. The electron-withdrawing nature of the nitro and cyano substituents guides targeted further substitution, resulting in high-purity intermediate batches essential for ensuring low ionic contamination and stable mesophase properties in final display materials.

    Industry compliance standards

    • ISO 9001:2015 and IATF 16949:2016 (Automotive Quality Association for Display Chemicals)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • IEC 61249-2-21 (Material Standards for Electronic Substrates)
    • GB/T 31457-2015 (China Electronic Chemicals Quality Standards)

    Typical usage ratio

    • 3–12% of initial aromatic substrate mass, chosen for optimized downstream purification and control of impurities; high-end LCD intermediate synthesis generally demands lower ranges to control conductivity in the final display panel.

    Downstream process integration

    • Batchwise nucleophilic and electrophilic aromatic substitution in multi-step organic synthesis
    • Key early-stage intermediate for functionalized aromatic rings in low-conductivity liquid crystal formulations
    • Continuous processing lines for tight process and impurity tracking

    Final product types

    • High-purity aromatic nitriles for TFT-LCD applications
    • Intermediate blocks for LC mesogen synthesis (used in color displays)
    • Electronic-grade specialty chemicals for OLED and plasma display materials

    5. Veterinary Pharmaceutical Intermediate Manufacturing

    Some veterinary health manufacturers in Europe and Latin America rely on our material for synthesizing advanced benzamide and chlorinated aromatic intermediates that serve as the backbone for a variety of veterinary antibiotics and parasite-control medications. Downstream partners import material based on its consistent purity profile to ensure repeatable batch processing and compliance with animal health GMP rules, focusing on impurity control for regulatory batch release.

    Industry compliance standards

    • VICH GL40 (Good Manufacturing Practice for Active Pharmaceutical Ingredients for Veterinary Use)
    • EU Regulation (EC) 2019/6 (Veterinary Medicinal Products)
    • Ph. Eur. General Chapter 5.10 (Control of Impurities in Veterinary Substances)
    • ISO 22716:2007 (Cosmetics — Good Manufacturing Practices for Veterinary Topicals)

    Typical usage ratio

    • 4–13% by starting material mass, defined by target veterinary molecule; process optimization hinges on impurity burden and isolation step yield.

    Downstream process integration

    • Chlorination and amidation in semi-batch reactors with in-line QC monitoring
    • Precursor for further nitro reduction and amination in multi-step synthetic routes
    • Integration into compliance-controlled pilot plants and production lines dedicated to animal medicinal products

    Final product types

    • Benzamide intermediates for broad-spectrum antibiotic synthesis
    • Chlorinated aromatic precursors for ectoparasiticide formulations
    • Veterinary-specific anti-inflammatory intermediate blocks
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    Certification & Compliance
    More Introduction

    2-Chloro-5-Nitrobenzonitrile: A Manufacturer’s Perspective

    Our Experience with 2-Chloro-5-Nitrobenzonitrile

    Every year, specialty chemicals like 2-Chloro-5-Nitrobenzonitrile shape the progress of multiple industries. For us, this compound is more than a line on a data sheet; it is a product born from exacting standards, decades of reaction optimization, and ongoing attention to customer feedback. Known within our facility by the label 2C5NBN, the substance stands as a clear example of what focused chemical synthesis can achieve in modern manufacturing.

    What Sets 2C5NBN Apart

    Our journey with 2C5NBN began over a decade ago, as demand increased among pharmaceutical and agrochemical manufacturers for building blocks that balance reactivity and stability. In this compound, the chlorine and nitro groups, both positioned on the benzonitrile ring, play off each other in a way we have exploited in synthesis work for years. The result: a substance with unique properties that shows up in pathways where either reactivity at the 2-position or electron-withdrawing effects at the 5-position drive downstream chemistry efficiently. These kinds of reactions deliver results that other substituted benzonitriles just cannot match under the same conditions.

    Compared to its structural neighbors—such as 4-chloro-3-nitrobenzonitrile or 3-chloro-2-nitrobenzonitrile—this isomer brings particular advantages. The ortho arrangement between chlorine and the nitrile promotes a distinct reactivity; coupling reactions that struggle with meta- or para- substituted versions tend to succeed more reliably with our 2C5NBN. Over countless batches, we have seen yield improvements and cleaner profiles in products synthesized using it as a key intermediate. Reproducibility matters; 2C5NBN delivers that in scalable quantities.

    How We Manufacture 2-Chloro-5-Nitrobenzonitrile

    With this compound, the pathway is straightforward but sensitive. The process starts from benzonitrile, with strict temperature and pressure controls during chlorination and nitration. Drawing on years of operational experience, we have tweaked each step for selectivity before purification even begins. The critical stage arrives at separation and purification, where our investment in advanced distillation and recrystallization lines pays off. The end product emerges as a pale-yellow crystalline powder with a narrow melting point range and minimal trace contaminants.

    Our facility performs constant batch validation—sampling, checking for trace residuals, and always benchmarking against established standards. It is common for us to receive feedback requesting even higher purity, and we respond with purified grades exceeding 99% by HPLC, measured by validated methods in our on-site analytical laboratory. We do not rely solely on COA data; we audit each batch with internal reference materials and external calibrators to confirm both identity and purity.

    Applications & Performance in Downstream Synthesis

    Pharmaceutical researchers prize 2C5NBN because it fits perfectly into the skeleton of certain molecular frameworks, letting them introduce electrophilic and nucleophilic partners in sequential steps. Our partners in drug development remark that this compound’s structural arrangement enables clean nitration or substitution with fewer steps and less waste. Some specialties exploit the ring’s electronic distribution to facilitate cross-coupling reactions or other palladium-catalyzed transformations. Building blocks with alternative positions often fail to deliver the same efficiency under identical reaction setups.

    In agricultural chemistry, 2C5NBN anchors the design of selective herbicides and growth modulators. Manufacturers find its activation points ideal for functional group insertions, which then broaden the range of biological activity. From our own bench work, we have found time and again that substitution at the 2-position leads to analogs with distinctive physical and biological properties. Knowing our role in that innovation cycle motivates ongoing attention to detail in every production run.

    Model & Specifications

    Inside our plant, we refer to the main specification as Model 2C5NBN-A, produced in lots ranging from 25 kilograms to several metric tons. Each batch is evaluated according to in-house standards honed through repeated synthesis trials and end-user testing. Typical physical properties: pale-yellow fine powder, melting point between 105°C to 108°C, and a minimum purity of 99.0% by HPLC. Moisture content remains below 0.5%, and chloride as an impurity, both as a process residual and as free ion, is routinely analyzed. Residual solvents—mainly acetonitrile or dichloromethane—stay beneath detection thresholds, with annual reviews to tighten controls as detection technologies improve.

    This product arrives in multi-layered lined drums, sealed under inert atmosphere where necessary, because oxygen and moisture exposure alters its behavior in sensitive synthesis. All containers carry tamper-evident seals and clear batch labels, with tracking from raw material intake to finished product. Routine calibration of storage and transport conditions—temperature, humidity, and light exposure—minimizes any change in the physical profile between our facility and yours. These precautions come not just from regulatory guidelines, but from the practical lessons of troubleshooting customer feedback over many years.

    Differences from Other Substituted Benzonitriles

    Compared to closely related products, our 2C5NBN carries distinct advantages. The 2-chloro substituent increases the ring’s electron density at specific positions, making nucleophilic aromatic substitutions far more predictable. Researchers routinely report higher yields or cleaner reaction profiles than with the 3-chloro or 4-chloro analogs. The nitro group at the 5-position further activates the ring, concentrating reactivity exactly where our customers need it.

    In a comparison of reactivity profiles, our analytical team has shown that 2-chloro-5-nitrobenzonitrile delivers consistently higher conversion rates for Suzuki couplings, Buchwald–Hartwig aminations, and nitro reductions than its meta- and para- isomers. The para-substituted alternative tends to slow down certain substitutions due to less optimal ring activation, while the meta arrangement can cause by-products that are tough to remove during purification. Our customers comment on the practicality: less time spent on downstream clean-up, and more manageable impurity profiles.

    Some users ask about switching to cheaper, single-substituent benzonitriles. Cost savings on paper do not translate once reaction efficiency and by-product formation enter the picture. In pilot trials run in our applications lab, reactions run with 2C5NBN often reach completion with 10-20% less catalyst and at lower temperatures, reducing both operating cost and energy use. The added value shows up both in the final yield and in sustainability metrics—a lower carbon footprint per kilogram produced.

    Support and Ongoing Improvement

    As a manufacturer, direct feedback shapes what we do. We maintain regular dialogue with our partners to understand their most pressing issues with chemical intermediates. Sometimes these involve fine-tuning purity or particle size (for better filtration or blending); at other times, requests arise for larger or smaller batches at short notice. Our facilities have adapted to shift rapidly between campaign modes and custom-scale runs, allowing us to respond to both volume and quality needs.

    In a recent case, a pharmaceutical client struggled with trace metal contamination in a final product produced from several suppliers’ intermediates. We responded by revisiting the entire synthesis flow for 2C5NBN, from raw starter materials down to vessel cleaning protocols. After a three-month review, the detected metals dropped below recognized limits, and the client’s downstream process delivered a cleaner, more reliable active ingredient. This kind of iterative problem solving sets us apart from contractors or distributors, who rely on third parties for critical process decisions.

    Regulatory Compliance and Quality Control

    As with all chemical substances in our catalog, compliance starts with raw materials and extends to the final delivery. We track every lot from precursor purchase to end-product shipment, supported by an electronic batch record system that integrates production, sampling, and finished goods tracking. Regular audits by internal QA and third-party inspectors mean every drum of 2C5NBN can be traced back to initial charge weights and reaction times—an essential feature when clients conduct regulatory filings requiring full process transparency.

    International standards keep evolving, so we make a point to stay ahead of requirements for substances that may cross borders. Whether destined for use in Europe, the US, or Asia, our 2C5NBN batches ship with full documentation supporting REACH, TSCA, and other major lists. If our customers’ applications involve APIs or regulated pesticides, we initiate additional stability and impurity studies as part of the package, ensuring not only legal compliance but also safety and effectiveness in the intended end use.

    Sustainable Practices in Manufacturing

    Attention to environmental responsibility has grown rapidly in chemical manufacturing. We’ve made conscious choices in our 2C5NBN line, reducing solvent footprints and recycling process water in closed loops where possible. Process intensification—smaller, more efficient reactor lines—means energy and resource use drops without sacrificing batch output. Real-time emission monitoring gives us the ability to spot any process drift early and correct it before it becomes a cause for regulatory concern.

    Waste minimization goes beyond the process floor: we partner with local recyclers to recover and treat the small amounts of mother liquor and organic by-products left after crystallization. These efforts keep our operations in good standing not only with inspectors but also with the communities near our plants. End users benefit from cleaner, more reproducible raw materials, as environmental side products that could become trace contaminants do not enter the supply chain.

    Supply Chain and Risk Management

    Raw material shocks have disrupted specialty chemicals for years. We hedge against price and availability swings by qualifying several global sources for benzonitrile and chlorinating agents. This backup keeps our production stable even when global transport routes or energy prices spike. Where possible, we source from domestic or regional suppliers to cut both costs and lead times, and these relationships pay off when quick turnaround is essential.

    Logistics view safety as absolute. We manage hazardous goods registration, certified transport, and customs requirements in-house. Multi-layer packaging keeps the product safe in transit, and rapid-response protocols address any delivery incident along the way; no load leaves until the destination’s safety profile matches our standards. End-to-end batch tracking means we can immediately address any issue raised by clients, without delay or blame-shifting common among traders or brokers.

    Handling, Safety, and Training

    Our workforce receives safety training that matches the chemical in question. For 2C5NBN, most hazards are standard for nitriles and nitroaromatics—eye and skin protection, volatile organic monitoring, dust collection for free powder handling. Every handler works in ventilated stations designed for quick clean-up should accidental spills occur. Emergency procedures stand tested, with mock drills and supervision by experienced shift managers. From loading hoppers to final sealing, constant monitoring and record-keeping reduces risk to staff and, ultimately, to the communities around us.

    We supply clear Material Safety Data Sheets and handling protocols with each batch, updated following every regulatory or scientific advance. Though the compound’s health hazards are well-documented, our rigorous protocols—rooted in real workplace practice, not just paperwork—keep incidents rare. We see safety culture not as empty compliance, but as critical to uninterrupted operation and delivery.

    Customer Interaction and Long-Term Partnerships

    Over years of repeat orders, we have come to value open dialogue above all. Clients push us with challenging questions: can the melting point window get even tighter; can impurity profiles be mapped to new analytical specs; can batch lot size or lead time be tailored to changing project needs? These questions show us where to improve, and regular site visits give insight into how chemicals like 2C5NBN perform outside our walls—in pilot reactors, kilo labs, and full-scale production lines.

    Our technical support team—made up of process chemists and application specialists—answers queries based on in-house experience. If issues surface, troubleshooting goes beyond documentation: we replicate customer conditions in our own labs, run fresh QC checks, and ship replacement material promptly if needed. Repeat business depends not only on price or shipping speed, but on trust built from consistently effective communication.

    Future Outlook and Product Evolution

    Innovation drives specialty chemicals. We continually work to refine our 2C5NBN line, responding to new downstream synthesis demands. Advances in catalysis, green chemistry, and API design push us to evolve both synthesis and purification techniques. Our R&D group experiments with enhanced selectivity steps, alternative purification media, and even catalytic variants that could one day lower cost or further improve impurity control. Periodic technology scouting brings in outside perspectives as well, because no process remains the gold standard for long.

    Some customers have begun adopting continuous flow synthesis for downstream production, and we actively test compatibility of our 2C5NBN with these platforms—where particle size, static charge, and dissolution rate can directly affect process stability. Whether it means a change in crystal morphology or packing method, we make adjustments that line up with the real-world demands of these new systems.

    The Value of Deep Manufacturing Expertise

    All the strengths of 2-Chloro-5-Nitrobenzonitrile—reliable supply, consistent reactivity, and clear traceability—come from the experience built at every step of the production and supply process. For our team, these are not theoretical virtues. They show up in the daily grind: setting reactor temperatures, checking chromatograms, troubleshooting split peaks, refining washing procedures. It is that lived expertise—tools in hand, batch on the line—that transforms base chemicals into long-term enablers of innovation. We have learned over time that a great intermediate compound does more than fill orders; it becomes a foundation for products that improve health, agriculture, and industry worldwide.