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3-Chloro-4-Methylbenzonitrile

    • Product Name 3-Chloro-4-Methylbenzonitrile
    • Alias 3-Chloro-4-methylbenzenecarbonitrile
    • Einecs 256-437-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    483443

    Product Name 3-Chloro-4-Methylbenzonitrile
    Cas Number 7073-62-3
    Molecular Formula C8H6ClN
    Molecular Weight 151.59 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 51-54°C
    Boiling Point 266-268°C
    Density 1.18 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Flash Point 114°C
    Structural Formula ClC6H3(CH3)CN

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled "3-Chloro-4-Methylbenzonitrile, 100g," hazard symbols and handling instructions clearly displayed.
    Shipping 3-Chloro-4-Methylbenzonitrile is shipped in tightly sealed containers, protected from moisture and incompatible substances. It is classified as a hazardous material and handled according to local, national, and international regulations. Proper labeling and documentation ensure safe transit, and temperature controls may be applied to prevent decomposition during transport.
    Storage 3-Chloro-4-Methylbenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Proper labeling and secondary containment are recommended to prevent leaks. Personal protective equipment should be used during handling to minimize exposure risks.
    Application of 3-Chloro-4-Methylbenzonitrile

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

    As a direct manufacturer, we supply 3-Chloro-4-Methylbenzonitrile to critical chemical sectors requiring selective nitrile intermediates. Our material consistently meets batch-to-batch purity and processability demands for established downstream segments. Below we detail the substance’s use across key industrial scenarios, specifying compliance regimes, formulation practices, processing touchpoints, and typical finished product examples.

    1. Agrochemical Active Ingredient Synthesis

    Agrochemical formulators utilize 3-Chloro-4-Methylbenzonitrile as a central building block in the synthesis of pyridine and pyrazole-based herbicides and fungicides. In these applications, the nitrile group proves essential for subsequent chlorination and cyclization steps. We cooperate with downstream processors focusing on selectivity and throughput when integrating our raw material into large-scale agricultural active ingredient manufacture.

    Industry compliance standards

    • ISO 9001-certified quality management systems
    • REACH Registration (EC No. 1907/2006, Annex IX intermediates)
    • European Crop Protection Association (ECPA) Responsible Care commitments
    • FAO/WHO Maximum Residue Limits (MRLs) monitoring for final actives

    Typical usage ratio

    • Used at 15–35% of total molar input for nitrile intermediates per active ingredient batch, adjusted based on downstream yield targets and impurity control requirements

    Downstream process integration

    • Added at the initial condensation or coupling reaction stage, prior to heterocycle formation in multi-step synthesis; strict in-process QC on residuals and byproducts

    Final product types

    • Selective herbicide technical concentrates
    • Systemic fungicide actives for fruit and cereal protection
    • Bulk intermediates for further formulation into ready-to-use crop protection products

    2. Pharmaceutical Intermediate Production

    Pharmaceutical manufacturers source our 3-Chloro-4-Methylbenzonitrile for conversion into key intermediates required for non-steroidal anti-inflammatory drugs and certain central nervous system (CNS) therapeutics. The material’s consistent nitrile functionality supports safe and reproducible transformation in hydrogenation and amide coupling stages under GMP-monitored environments, with traceability from raw material to final API.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidelines
    • United States Pharmacopoeia (USP) / European Pharmacopoeia (Ph. Eur.) trace impurity reporting
    • FDA 21 CFR Part 211 requirements for drug substance intermediates
    • EDQM TSE/BSE risk evaluation for all aromatic intermediates

    Typical usage ratio

    • Employed at 10–25% w/w in advanced intermediate synthesis; adjusted to maintain reaction selectivity and impurity profile setpoints per downstream specification

    Downstream process integration

    • Fed directly into palladium-catalyzed hydrogenation steps or amidation batches in multi-step pharmaceutical syntheses, with batch segregation and documentation for full chain-of-custody

    Final product types

    • Pharma-grade intermediates for NSAIDs
    • Precursors for CNS drug molecules
    • Fine chemical intermediates for contract API manufacturing

    3. Liquid Crystal Intermediate Processing

    Performance electronics component makers incorporate 3-Chloro-4-Methylbenzonitrile within the synthesis routes of high-order nitrile derivatives required for specialty liquid crystal (LC) compounds. The product provides controlled aromatic backbone for downstream fluorination and subsequent alkylation, ensuring alignment, dielectric, and thermal properties match panel manufacturing standards.

    Industry compliance standards

    • ISO 9001 and ISO 14001 certified production systems
    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU)
    • IEC 61249-2-41 standards for electrical component content
    • REACH Annex XVII restriction review for electronic applications

    Typical usage ratio

    • Typically dosed at 8–18% by mass as a structural intermediate, aligned with targeted LC precursor yields and purity requirements for finished mixtures

    Downstream process integration

    • Introduced after initial nitration and halogenation in multi-stage aromatic derivatization; further processed through fluorination and esterification before blending into LC mixtures

    Final product types

    • High-stability liquid crystal blends for display panel manufacturing
    • Nematic LC host compounds
    • Advanced organic semiconducting materials for flat panel and mobile applications

    4. Dye Intermediate Manufacturing

    Dye and pigment makers employ 3-Chloro-4-Methylbenzonitrile as a precursor in the fusion of selectively halogenated benzonitrile compounds forming anthraquinone and azo dye chromophores. The controlled introduction of this substituent supports color fastness, solubility, and brightness requirements crucial for polymer fiber and specialty ink end uses.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Code of Practice
    • Oeko-Tex® Standard 100 appendix for colorant impurities
    • REACH SVHC (Substance of Very High Concern) screening
    • ISO 9001 quality systems for batch traceability

    Typical usage ratio

    • Formulated at 10–20% of chromophore precursor charge, subject to final shade strength and viscosity adjustment for downstream dye application method

    Downstream process integration

    • Charged at condensation or nucleophilic substitution stage preceding coupling and purification; undergoes sulfonation, reduction or diazotization as required for target dye family

    Final product types

    • High-durability disperse dyes for synthetic fibers
    • Azo and anthraquinone colorants for industrial inkjet inks
    • Specialty pigments for decorative coatings and plastics

    5. Specialty Chemical Intermediates for Polymer Additives

    Producers of high-performance polymer and plastic additives integrate 3-Chloro-4-Methylbenzonitrile within the synthesis of stabilizers, flame retardants, and plasticizers. Its defined reactivity facilitates controlled introduction of functionalized aromatic residues during additive manufacture, supporting target compatibility and thermal stability profiles for advanced polymer matrices.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • REACH compliance for polymer additive ingredients
    • ISO 17025 laboratory verification for migration and purity
    • SOCMA ChemStewards® Responsible Care participation

    Typical usage ratio

    • Charges range from 5% up to 22% of additive pre-polymer input, with refinements based on targeted polymer performance and regulatory migration limits

    Downstream process integration

    • Integrated at aromatic substitution step before functionalization, followed by blending, granulation, or extrusion into finished additive concentrates

    Final product types

    • Phosphorus-based flame retardant masterbatches
    • Stabilizer additives for automotive polymers
    • Plasticizer intermediates for high-performance PVC and engineering plastics
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    Certification & Compliance
    More Introduction

    3-Chloro-4-Methylbenzonitrile: Reliable Building Block for Chemical Synthesis

    Understanding 3-Chloro-4-Methylbenzonitrile

    Delivering quality and consistency across several industries starts with producing dependable specialty chemicals. Among our portfolio, 3-Chloro-4-Methylbenzonitrile stands out for its unique structure and reactivity. It carries the chemical formula C8H6ClN, with a molecular weight of 151.6 g/mol. This compound appears as a crystalline powder. Our process ensures controlled particle size distribution and low impurity content, supporting the demanding requirements of advanced synthesis.

    Shifting focus to how this nitrile behaves compared to other similar benzene derivatives, its value lies with the strategic placement of the chloro and methyl groups. This arrangement offers specific electronic effects for downstream chemical processes. Clients have found its performance stable under a variety of reaction conditions, and it handles purification steps with less complication than isomers or unsubstituted alternatives.

    Product Model and Specifications

    Our standard production line for 3-Chloro-4-Methylbenzonitrile achieves a minimum purity of 99.5%, measured by gas chromatography, with moisture content consistently under 0.1%. We apply manufacturing methods that limit residual solvents and restrict trace organics—removing complications in scale-up or further transformation. Particle size is monitored tightly during milling and sieving, because uneven particle size costs time during dissolution or filtration.

    We have responded to years of customer feedback by optimizing for stability under shipment and long-term storage. Packed in high-density polyethylene drums with tamper-evident seals, each batch is accompanied by a certificate of analysis, referencing all tested traits—so users can trust the material at every step of their process.

    Applying 3-Chloro-4-Methylbenzonitrile in Synthesis

    This molecule serves as a pivotal intermediate in pharmaceutical and agrochemical manufacturing. It enters a wide array of catalytic coupling reactions and offers a steady base for constructing more complex aromatic compounds. In our experience, downstream manufacturers choose this compound for nitrile-to-amide or amine conversion routes, because the methyl group improves solubility in organic solvents, while the chloro group invites regioselective substitution.

    Production lines for active pharmaceutical ingredients rely on this building block to control reaction selectivity and minimize side reactions. Several herbicides and fungicides, especially those built on benzamide or aniline cores, begin with 3-Chloro-4-Methylbenzonitrile. Its consistent purity reduces the risk of byproduct formation during hydrogenation or Grignard coupling.

    Our partners in material science have put this compound to work in electronics intermediates as well, pointing to its clean fragmentation under controlled pyrolysis, which allows smooth functionalization for specialty polymers that require both electron-withdrawing and -donating side chains.

    Key Differences from Related Benzonitriles

    Among halomethylbenzonitriles, the 3-chloro-4-methyl configuration brings subtle but important changes in reactivity. Comparing this to, for example, 2-chloro or 4-chloro analogs, our customers report that this molecule’s substitution pattern provides greater control in directed ortho-metalation. Chemists value this extra handle when they need to add further substituents selectively.

    Other isomers often present purification difficulties, as their polarity and melting points shift less predictably during organic extraction. Our users in process development teams have noted that impurities clear faster by crystallization, because the methyl group disrupts close molecular packing just enough to keep the product flowing. Chloro-4-methyl substitution also resists unwanted nitration and halogen exchange, so yield losses remain minimal during transformations involving strong bases or acids.

    In contrast to unsubstituted benzonitrile, the extra functional groups enable selective cross-coupling via Suzuki or Buchwald-Hartwig reactions. Yield increases and byproduct reduction in these markets have encouraged expansion of our production lines. For instance, while methylbenzonitrile alone tends not to provide sites for future elaboration, chloro-4-methyl derivatives position chemists to run multi-step programs without backtracking.

    Production Methods and Quality Control

    Producing this chemical begins with a carefully designed aromatic halogenation and methylation strategy. Our reactors feature closed-loop temperature and agitation controls, tailored to prevent side reactions commonly seen in open systems. Using high-purity chlorinating agents yields materials free from polychlorinated byproducts, which otherwise make downstream purification costly and time-consuming.

    Each batch is subject to spectroscopic and chromatographic analysis, revealing even minor contaminants such as ortho- or para-isomers. Over the years, continual improvement projects in our production lines have centered on minimizing these trace compounds. Raising reactor cleanliness standards, regularly calibrating process analyzers, and isolating storage of key intermediates all contribute to high reliability—season after season.

    We partner with accredited laboratories for independent verification of purity. Regular retention-sample analysis means long-term stability is assured, as each drum delivered matches reference spectra archived back at the plant. Any change in upstream suppliers receives deliberate vetting and site audits, ensuring incoming raw materials support our rigorous process expectations.

    Practical Handling, Storage, and Transport

    Experience teaches that moisture and airborne particulates threaten the quality of high-purity organics. Our facility integrates positive-pressure clean areas for decanting and sampling. Workers handling this product wear dust-control garments and use closed transfer methods to contain any risk of external contamination. We monitor warehouses for temperature swings and humidity, since repeated exposure—even to ambient air—promotes hydrolysis or clumping, which interfere with reliable dosing and weighing.

    With our established logistics partners, we schedule direct shipments to minimize hold times at ports or depots. Data loggers accompany every large-volume shipment, recording possible environmental excursions. Our bulk clients in Asia, Europe, and North America benefit from routine tracking reports, so delays or storage incidents can be investigated in real time. Supply chain transparency has made a real difference during complicated periods, such as severe weather or trade bottlenecks.

    Our containers resist both corrosive splashes and UV exposure, leaving no leachables or degradation products. For global customers, we group shipments for compatible hazard classes, cutting additional regulatory paperwork. Staff receive annual training on up-to-date transport laws—an important safeguard after jurisdictional changes over the last decade.

    Supporting Customers Beyond Supply

    Supplying a specialty intermediate involves more than just moving powder from one place to another. We view each shipment as a promise of reliability. Whether a client operates a single pilot reactor or manages a multi-tonne annual contract, our technical team remains involved, helping troubleshoot off-spec readings or unexpected process behavior.

    Some clients develop new processes that need samples with alternative particle sizes or unique solvent packages, so our plant engineers adjust drying and milling operations as needed. Others ask about process toxicology or risk analysis, and our regulatory affairs staff reviews literature and historical batch records to provide up-to-date answers. These partnerships often grow beyond routine supply, as customers turn to us for advice on scale-up tactics, secondary sourcing, or waste management options.

    We run customer feedback sessions twice a year, which have prompted several advances in lot traceability, packaging, and documentation. Our response to a widespread request for faster turnaround on analytical data led to new investments in chromatography automation, reducing turnaround windows from days to hours, and letting users qualify their inventory before a production run begins.

    Safety and Environmental Commitment

    Producing halogenated intermediates responsibly demands a long-term vision for both worker and environmental health. All employees in our plant undergo regular hazard communications training and participate annually in simulated leak and spill drills. Local authorities and neighbors receive updates about our containment infrastructure, including secondary containment, vapor scrubbing, and real-time air quality telemetry.

    Our waste stream management includes solvent recycling, incineration partnerships, and multi-stage aqueous treatment for process water. These measures reduce both local emissions and global environmental footprint. Our engineering teams designed custom scrubbers specifically for halo-organic offgassing, lowering annual emission rates below statutory limits. We invest back into research projects that look for alternatives to traditional chlorinating agents and strive for safer, renewable input materials.

    Packaging standards keep product secure during both export and return, and every empty drum managed through our post-use recycling initiative receives batch-specific cleanliness verification and tracking to end-user reprocessing vendors. This model meets or exceeds the norms in major production jurisdictions, including North American, European, and East Asian regulatory programs.

    Continuous Innovation and Industry Trends

    Chemical markets keep evolving, driven by regulation, consumer demand, and advances in process technology. In the last five years, end-users focused heavily on green chemistry metrics. Our research and pilot plants trialed alternative synthesis strategies, looking to cut hazardous waste and energy consumption for 3-Chloro-4-Methylbenzonitrile. We implemented batch-to-batch tracking with robust digital records, allowing both us and our customers to measure traceability, from starting materials to final use, across years.

    Customers now push for even tighter impurity profiles, not only for downstream safety but to minimize regulatory review cycles on final products. Our compliance department connects directly with downstream regulatory submissions teams, sharing real-time updates on any change to production or testing procedures. Collaboration at this scale beats the old model of static specifications—users demand transparency and documented reliability.

    We remain engaged with trade associations and technical committees monitoring global supply chain security and ethical sourcing. Regional shifts in raw material availability, along with unpredictable geopolitical factors, have made agile inventory planning essential. Investments in inventory management solutions and extra warehouse capacity have protected our delivery performance, so we can ship—on schedule—regardless of market turbulence.

    Looking Ahead—Partnership for Success

    We view each drum or pallet of 3-Chloro-4-Methylbenzonitrile as part of a continuous chain of progress in applied chemistry. Long-term partnerships with academic, industrial, and regulatory bodies have fed back into how we refine our processes and invest in laboratory infrastructure. In our plant, production is more than a technical task—it represents a commitment to accuracy, accountability, and sustainably shared knowledge.

    As market pressures change and user requirements become more demanding, our teams stay ready to adjust process parameters, validate new raw material sources, and deliver unbiased technical support for both new users and long-term partners. Our record stands on every lot we make, and the expertise in our business reflects years of practical experience producing high-value intermediates under real-world production pressures.

    For those seeking a benzene-based intermediate with a reliable track record in both large-volume chemical synthesis and demanding specialty applications, 3-Chloro-4-Methylbenzonitrile from our plant has earned its place through performance, transparency, and ongoing collaboration. We welcome ongoing exchanges with partners who face new formulation, scale-up, or regulatory questions—so that together, we keep pushing boundaries, keeping safety and quality at the center of every step.