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Ethyl 4-Chlorobenzoate

    • Product Name Ethyl 4-Chlorobenzoate
    • Alias Ethyl p-chlorobenzoate
    • Einecs 210-340-8
    • 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

    653977

    Name Ethyl 4-Chlorobenzoate
    Molecular Formula C9H9ClO2
    Molecular Weight 184.62 g/mol
    Cas Number 619-64-7
    Appearance Colorless to pale yellow liquid
    Boiling Point 266-268 °C
    Density 1.186 g/cm3
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Refractive Index 1.536
    Flash Point 119 °C
    Smiles CCOC(=O)C1=CC=C(C=C1)Cl
    Storage Temperature Store at room temperature

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

    Packing & Storage
    Packing Ethyl 4-Chlorobenzoate is packaged in a 100g amber glass bottle, sealed with a screw cap and labeled with hazard information.
    Shipping Ethyl 4-Chlorobenzoate is shipped in sealed, labeled containers, compliant with chemical transport regulations. It should be protected from moisture and physical damage, and stored at room temperature. Handle with appropriate safety measures. Ensure documentation accompanies all shipments. Transport by road, air, or sea requires adherence to packaging and labeling requirements for non-hazardous chemicals.
    Storage **Ethyl 4-chlorobenzoate** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep it away from heat and direct sunlight. Ensure proper labeling, and avoid storage near food or drink. Use secondary containment if needed to prevent leaks or spills.
    Application of Ethyl 4-Chlorobenzoate

    Applications of Ethyl 4-Chlorobenzoate in Industrial Manufacturing

    Ethyl 4-chlorobenzoate serves as an essential intermediate across several chemical sectors, supporting consistent batch production and downstream innovation for global industrial clients. Our technical support covers application requirements from synthesis routes to regulatory alignment.

    1. Pharmaceutical Intermediate Synthesis

    Manufacturers use ethyl 4-chlorobenzoate as a building block in active pharmaceutical ingredient (API) synthesis, including anti-inflammatory and antihypertensive agents. Aromatic esterification and selective halogenation processes require stable supply, with batch records aligned to pharmacopeial process controls. Clients handle stepwise hydrolysis or further substitution to construct key molecular scaffolds, optimizing for reactivity and yield based on established process flow diagrams. Production scheduling addresses supply obligations for regulated end markets with batch validation tied to trace data for each shipment.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) monographs (if relevant to API pathway)
    • European Pharmacopoeia (Ph. Eur.) synthesis requirements for intermediates
    • FDA 21 CFR Part 211 for finished drugs (impacting traceability of intermediates)

    Typical usage ratio

    • 10-25% by mass in a multi-step synthesis sequence; precise ratio depends on target molecule design and desired purification strategy

    Downstream process integration

    • Entry during aromatic esterification or halogenation unit operations before conversion to downstream benzoic acid derivatives
    • Used directly in intermediate isolation and subsequent hydrolysis stages
    • May undergo transesterification or serve as a precursor for amide or nitrile formation
    • Material handled under controlled environments with analytical confirmation of structure prior to next step

    Final product types

    • Anti-inflammatory API intermediates
    • Antihypertensive drug intermediates
    • Specialty pharmaceutical benzoic acid derivatives
    • Aromatic amide pharmaceutical building blocks

    2. Agrochemical Intermediate for Herbicide & Fungicide Synthesis

    Synthesis of agrochemical actives often leverages ethyl 4-chlorobenzoate for preparing functionalized benzoyl derivatives. Process chemists select this material for nucleophilic aromatic substitution and ester hydrolysis to access target pesticide molecules. Integrated production facilities calibrate each batch according to specific product registrations, emphasizing raw material purity and byproduct minimization. Regulatory submission files may identify this feedstock at the registration dossier or equivalence evaluation stage with trace documentation extending to grower application safety sheets.

    Industry compliance standards

    • FAO/WHO specifications on pesticide technical materials
    • REACH registration requirements for chemical intermediates
    • ISO 9001 Quality Management System for agrochemical manufacturing
    • Chemical Control Law (Japan) for raw material imports

    Typical usage ratio

    • 15-35% by mass in pre-synthesis reactor charges; further adjusted to optimize herbicide or fungicide yield based on target formulation

    Downstream process integration

    • Charged into microreactors for nucleophilic substitution
    • Serves as an acylation source in heterocyclic ring system construction
    • Converted via controlled hydrolysis to 4-chlorobenzoic acid for further coupling
    • Purified using solvent extraction before downstream formulating into technical concentrate

    Final product types

    • Acylated herbicide intermediates
    • Fungicide active ingredients precursors
    • Benzamide pesticide intermediates
    • Technical-grade herbicide actives

    3. Plasticizer Additive Base for Polymer Processing

    Producers of specialty polymers use ethyl 4-chlorobenzoate as a plasticizer constituent or intermediate for custom ester plasticizer blends. Material performance relies on the purity and controlled halogen content to avoid polymer degradation or unwanted migration. Compounding operations introduce the ester at the pre-polymerization or masterbatch formulation phase, adjusting ratios to achieve targeted flexural and tensile properties. Quality teams monitor residual monomer levels per applicable ECHA guidelines, with application dossiers referencing full traceability for audit support.

    Industry compliance standards

    • EU REACH Regulation (EC 1907/2006) on plasticizer chemical use
    • ISO 9001:2015 Quality Management System applicable to compounding operations
    • RoHS Directive (2011/65/EU) for electronic polymer applications
    • UL 94 flammability standards for plastics

    Typical usage ratio

    • 2-8% by weight of total polymer formulation, tuned to achieve mechanical flexibility norms or migration control based on finished goods

    Downstream process integration

    • Mixed into resin melt during polymerization stage
    • Introduced in extruder feed hopper for masterbatch pre-compounding
    • Reactive esterification possible for certain specialty polyesters or co-polymer blends
    • QC sampling before and after blending to confirm compatibility and migration stability

    Final product types

    • Flexible PVC profiles
    • Technical plasticizer masterbatches
    • Halogenated co-polymers for wire insulation
    • Modified polyesters for packaging films

    4. UV-Absorber Precursor for Specialty Coatings

    Specialty coatings manufacturers employ ethyl 4-chlorobenzoate as a precursor in UV-absorber synthesis for high-durability architectural and automotive applications. Specific synthetic steps involve controlled ester exchanges or targeted halogen substitution to tailor UV-absorbing chromophores. Compliance with VOC and heavy metal content drives raw material selection, while batch control supports downstream uniformity in color stability and protective performance under accelerated aging test protocols. Client specifications can mandate lot-segregation guided by performance qualification data from in-house testing or external certification bodies.

    Industry compliance standards

    • EN 71-3:2019 Safety of toys—migration of certain elements (when used in coatings for consumer products)
    • Directive 2004/42/EC on the limitation of emissions of volatile organic compounds (VOC) for coating production
    • ISO 11341:2004 Paints and varnishes—artificial weathering and exposure tests
    • ASTM D4587 test method for UV exposure

    Typical usage ratio

    • 5-15% in UV-absorber precursor syntheses; final content in formulated coatings adjusted based on application (e.g., exterior vs. interior, architectural vs. automotive)

    Downstream process integration

    • Reacted with aromatic amines or phenols for target absorber molecules
    • Processed through reflux reactors for controlled substitution and ester exchange reactions
    • QC by HPLC monitoring chromophore conversion and purity
    • Supplied as a pigment concentrate or additive for dispersion in topcoats or primers

    Final product types

    • Exterior architectural coatings with enhanced UV protection
    • Automotive topcoats for color retention
    • Industrial primers for outdoor equipment
    • Special purpose UV-resistant varnishes

    5. Analytical Reagent Production

    Commercial reagent producers rely on ethyl 4-chlorobenzoate for manufacturing reference standards and calibration substances used in quality control labs. Its defined structure and stability suit it for SSRM, internal standard, or GC derivatization agent production. Material is purified to trace analytical grade, then subdivided and packed based on end-user accreditation requirements such as ISO/IEC 17025. Detailed analytical certification accompanies every lot, validated through NMR and chromatographic techniques specific to analytical reagent production.

    Industry compliance standards

    • ISO 17034 General requirements for the competence of reference material producers
    • ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories
    • TraceCert (analytical standard supply) protocols
    • ASTM E528-20 practice for matrix match in standard preparation

    Typical usage ratio

    • Analytical formulation concentrations typically 0.1-1% by weight for standard solutions; adjusted according to method sensitivity and calibration curve range

    Downstream process integration

    • Crystallized and micronized for analytical material processing
    • Portioned in ISO 8 cleanroom filling lines
    • Packaged under inert gas to minimize volatile loss and contamination
    • Secondary QC using NMR and GC-MS for trace impurity detection prior to legal metrology release

    Final product types

    • Chromatographic reference standards
    • Internal standards for GC and HPLC
    • Analytical calibration blends
    • Proficiency testing materials for lab accreditation programs
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    Certification & Compliance
    More Introduction

    Ethyl 4-Chlorobenzoate: The Manufacturer’s Perspective

    Understanding Ethyl 4-Chlorobenzoate

    Our team has been producing Ethyl 4-Chlorobenzoate (sometimes referred to by its CAS number 139-43-5) for decades. Chemically, this compound stands out as an ester derived from 4-chlorobenzoic acid and ethanol. Its structural profile brings together the desirable aromatic ring system, a selective halogen substitution, and an ethyl ester group, combining stability with functional reactivity.

    We often encounter requests to drill down on the differences between Ethyl 4-Chlorobenzoate and its close relatives: methyl or propyl esters of 4-chlorobenzoic acid, or other chlorinated benzoates without the ethyl group. From first-hand experience at the synthesis line, Ethyl 4-Chlorobenzoate offers notable balance—a moderate boiling point ideal for separation by distillation, a notable ease of handling, and greater compatibility with various reaction conditions used in specialty synthesis, especially compared to its more volatile methyl analog. The ethyl group imparts less volatility than methyl groups, and 4-chloro substitution resists unwanted side reactions.

    Our Approach to Quality Control

    Batch-to-batch consistency shapes the backbone of our reputation. We don’t chase after ambiguous benchmarks like “industry standard”; instead, we focus on measurable criteria: purity, water content, and controlled trace impurity profile. Our chemical engineers run every batch through gas chromatography to confirm purity levels that consistently meet or exceed 99%. Analytical data direct our process at every stage, so any deviation from the rigorous standards results in a process halt and root cause analysis.

    The actual appearance usually ranges from clear to slightly pale yellow, and we monitor for any hint of discoloration, which often signals oxidation or trace contamination. Taking lessons from customer feedback and our own bench tests, we tune washing, drying, and filtration practices. Our solvent recovery protocols reduce residual solvents to non-detectable levels, something not all producers can affirm. Packing happens under nitrogen for larger volumes to protect integrity during storage.

    Specifications Shaped by Real-World Demands

    Lab results mean nothing without connection back to practical use. Our 25-kilogram drums and 200-kilogram barrels come lined to avert physical or chemical degradation. For custom development, we fill requests down to kilogram and sub-kilogram lots. This comes from years working with contract research organizations and pharma partners who often demand high traceability for scale-up. Shelf life exceeds two years under recommended storage conditions, with real-world stress tests from our own R&D storerooms. Our staff verifies each lot with a unique sample archive, so resolving questions on lot performance is quick and evidence-based.

    Applications in the Field: Practical Uses of Ethyl 4-Chlorobenzoate

    Our customers span pharmaceuticals, agrochemicals, fragrances, and fine chemicals. The compound acts as a reliable intermediate; synthetic teams reach for it when aiming to introduce a 4-chlorobenzoate group in targeted molecular architectures. In the production of higher-value actives, the ethyl ester enables selective transesterification or saponification, broadening possible end products. We’ve worked with teams scaling up crop protection agents — here, Ethyl 4-Chlorobenzoate grants predictable reactivity with diverse nucleophiles, something not always possible with heavier esters or non-chlorinated benzoates.

    Aromatics specialists in flavor and fragrance can detect the effect of subtle structural differences; to them, ethyl esters deliver a specific scent note less harsh than methyl or propyl counterparts. Our method avoids excessive residual acid, responding to demands for low baseline odor in the raw material. For custom organic synthesis, whether in research or production, technicians report that the 4-chloro position supplies a launching point for aryl-ether formation, Suzuki-Miyaura couplings, and other transition-metal catalyzed cross-coupling reactions. This is not just a bench curiosity—it translates into robust process designs, lower purification costs, and less rework downstream.

    Comparative Benefits over Related Compounds

    Buyers and chemists often ask why to choose the ethyl ester here instead of methyl, propyl, or isopropyl forms. Over the years, we've compared not just literature data but also direct plant trial outcomes. Methyl 4-chlorobenzoate, going by its lower molecular weight, boils at a lower temperature, sometimes leading to losses during heated transfers or open-vessel distillations. The ethyl ester sits at a sweet spot, permitting easy transfer yet resisting losses to atmosphere.

    Switching to heavier esters like propyl or butyl increases the hydrophobic character, which sometimes restricts solubility in aqueous or polar solvents. In pharmaceutical process routes focused on clean conversion and easy downstream work-up, Ethyl 4-Chlorobenzoate produces predictable isolation of products with fewer residual solvents and higher yields compared to bulkier esters.

    We also see significant risk differences between chlorinated and non-chlorinated benzoate esters. The presence of the chlorine atom at the para position improves the compound's resistance to biodegradation and microbial attack, which matters in both long-term storage and field applications in crop protection and industrial fluids. Non-chlorinated benzoate esters can hydrolyze or degrade faster in some real-world situations.

    Process Insights: How Ethyl 4-Chlorobenzoate is Made and Handled

    Our manufacturing lines use reliable esterification reactions, starting with high-purity 4-chlorobenzoic acid—sourced from multi-year-validated partners—and absolute ethanol. Reaction catalysts and solvents are chosen after intensive pilot trials to minimize impurities like unreacted acid, chloride ions, or higher-scale side products. Each reactor load gets monitored for temperature and pressure, and our DCS (Distributed Control System) logs any deviation, tightening control over the exothermic reaction. Workers on the floor catch abnormalities early thanks to on-the-spot testing and an embedded team culture prioritizing quality.

    After reaction completion, the raw product passes through multiple separation steps. Washing steps strip away both mineral acids and water-soluble organic impurities. Drying uses vacuum techniques developed in-house, preventing product darkening and unwanted byproduct formation. We learned years ago that open-drum drying could sabotage batch color, so closed-system dehydration remains our gold standard.

    Our final filtration steps—using both cartridge and depth media—remove any insoluble residues. Experienced hands override automation if clarity or color fails grade. Only when the batch meets every physical and chemical requirement does it move to packaging.

    Environmental and Safety Considerations

    No chemical leaves our plant without strict environmental checks. Ethyl 4-Chlorobenzoate itself does not pose acute hazard compared to other halogenated aromatics, but most users ask about vapor inhalation, aquatic toxicity profile, and safe disposal. We’ve invested in closed transfer systems and vapor recovery setups, pushing employee exposure to near-zero. Waste streams go first through neutralization, then on to final treatment, with documented effluent quality.

    The regulatory profile remains straightforward. While not under the strictest international controls, we maintain a safety data sheet aligned to GHS principles and respond directly to auditor requests. Our downstream users—especially agrochemical formulators—benefit from our partnership with accredited labs running independent environmental fate and hazard studies. From our perspective, the most durable control against risk has always been chemical traceability, so our digital records reach back through precursor batches and every shipment.

    Troubleshooting: Real Stories From the Field

    Over the years, customer questions have driven our focus on problem-solving. Some buyers reported batch-to-batch color variation, traced directly to exposure to air and minor changes in acid:alcohol ratios. We rebuilt distillation protocols and trained new operators on best practices in oxygen-free handling. Others noted hydrolysis during long-term storage; suppliers like us cannot control end-user humidity, but we responded by double-sealing drums and supplying guidance on storage away from acid or base vapors.

    Research chemists occasionally push the product into reactions outside the common playbook. Feedback has prompted incremental improvements—modifying our purification path to further lower aldehyde or carboxylate traces. Our technical support team remains on call for scale-up advice, providing not just certificates of analysis but insights grounded in hard plant data and troubleshooting stories.

    Commitment to Consistency and Transparency

    We have always believed that every kilogram matters, regardless of whether it’s staying in a local pharma pilot plant or shipping for multinational polymer projects. If a customer faces a blending or compounding roadblock, we investigate the whole supply chain—solvent, acid, ethanol, and storage conditions. Packaged samples from every lot back up our claims and support root-cause findings.

    Open audits present no challenge. We organize site visits for qualified customers. Engineers can walk the lines, examine distillation columns, and question the team about hazard controls—or inspect our archives for batch records and analytical results going back several years. These practices sprang not from buzzword trends, but from hard lessons learned in the pursuit of reliability and customer retention.

    Continual Improvement: Listening and Innovating

    Keeping up with global changes means evolving processes and product support. Recently, customers in regulated industries started asking for data beyond classic purity: potential trace solvents, leachables from packaging, or nitrosamine precursors. Instead of just meeting minimum compliance, we expanded our testing panel and replaced aging equipment with higher-sensitivity detectors. In difficult cases, our team collaborates with outside labs for third-party certification.

    On a practical level, supply chain issues sometimes throw up new hurdles—delays in precursor supply or unexpected shifts in raw material specs. Operating only as a manufacturer, never as a trader or broker, gives us the flexibility to run adaptive campaigns: tuning production schedules, revising supplier audits, keeping transparent with customers facing downstream crunches. The value in being the original producer shows here—we don’t rely on intermediaries to resolve questions about how something was made, or why a batch varied.

    Challenges in Global Distribution

    These past years have made clear that distribution involves more than shipment. Ethyl 4-Chlorobenzoate requires careful customs documentation, attention to local legal interpretations, and predictable product classification. We work closely with logistics partners trained on chemical-specific requirements. Customs delays have occasionally affected time-sensitive exports, but maintaining full technical documentation and rapid response for clarification keeps goods moving. Unlike third-party resellers, our chain of custody connects product right from the reactor to the final user.

    With some regions demanding evidence of chemical origin, we provide manufacturing declarations, not simply supplier letters. Our plant history supports origin-trace demands for regulated finished goods. Each year, we improve package labeling and tamper-evident closures, especially on high-value smaller lots destined for research or pharma validation programs.

    Looking to the Future: Why Ethyl 4-Chlorobenzoate Remains Relevant

    Market forecasts project broadening use of para-substituted aromatics in new pharmaceuticals and specialty materials. Ethyl 4-Chlorobenzoate’s adaptability across multiple sectors places it in continued demand, but this only matters if supply remains both dependable and clearly traceable. Upcoming green chemistry initiatives also target lifecycle emission cuts—even for production of well-established intermediates.

    To minimize environmental load, our plant has begun trials using biogenic ethanol and investigating alternative, less energy-intensive catalysts. We track waste gas and liquid generation, intending to share lifecycle data with upstream and downstream partners. Close collaboration with R&D customers helps us anticipate directional shifts—such as the need for lower residual metal levels or more detailed impurity profiling. As requirements change, swift adjustment in protocols follows.

    Summary: Practical Value for End Users

    Ethyl 4-Chlorobenzoate, as produced by experienced manufacturers, bridges the needs of demanding users—those who require traceable quality, responsiveness to new data demands, and the adaptability to drive reliable processes in both research and scale-up settings. The differences between it and related aromatics grow clear through practical experience: stable performance, manageable volatility, and a cleanliness easily checked in downstream analysis.

    No perfect product exists, but honest accounting of batch origins, hands-on technical support, and readiness to act on customer experience separate raw chemical suppliers from those offering genuine manufacturing expertise. We approach each contract as a partnership based on shared technical evidence and continual improvement. Ethyl 4-Chlorobenzoate’s real value is reflected in feedback from those who depend on it to keep innovation running and standards high.