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4-Nitrobenzoyl Chloride

    • Product Name 4-Nitrobenzoyl Chloride
    • Alias PNBC
    • Einecs 209-036-6
    • 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

    242862

    Cas Number 122-04-3
    Molecular Formula C7H4ClNO3
    Molar Mass 185.56 g/mol
    Appearance Light yellow to pale brown crystalline solid
    Melting Point 78-80 °C
    Boiling Point 140-142 °C at 15 mmHg
    Density 1.54 g/cm³
    Solubility In Water Decomposes
    Flash Point 117.7 °C
    Refractive Index 1.598 (calculated)
    Purity Typically ≥98%
    Storage Temperature Store below 30 °C, keep tightly closed

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

    Packing & Storage
    Packing 500g amber glass bottle, tightly sealed, labeled with hazard warnings, product name "4-Nitrobenzoyl Chloride", CAS number, and supplier details.
    Shipping 4-Nitrobenzoyl Chloride must be shipped in tightly sealed containers, kept away from moisture and incompatible materials. Transport must comply with local regulations for hazardous chemicals, typically classified as a corrosive substance (UN 3261). Appropriate hazard labeling and documentation are required to ensure safe handling during shipping and delivery.
    Storage 4-Nitrobenzoyl chloride should be stored in a cool, dry, well-ventilated area, away from sunlight, moisture, and incompatible substances like strong bases, acids, and oxidizers. It should be kept in a tightly sealed container made of materials resistant to corrosion, such as glass. Always label containers clearly and store them in secondary containment to prevent accidental spills or leaks.
    Application of 4-Nitrobenzoyl Chloride

    Applications of 4-Nitrobenzoyl Chloride in Industrial Manufacturing

    4-Nitrobenzoyl chloride serves as a specialized acylation agent in multiple industrial supply chains. Our manufacturing expertise guarantees consistent quality for demanding production environments, supporting diverse chemical syntheses for downstream sectors. The following application scenarios describe real industrial uses, detailed with compliance and technical integration points for process engineers, formulators, and procurement professionals.

    1. Synthesis of Pharmaceutical Intermediates

    Pharmaceutical manufacturers incorporate 4-nitrobenzoyl chloride for stepwise acylation in the preparation of active pharmaceutical intermediate (API) building blocks, such as substituted benzamides and sulfonamides. In controlled GMP reactors, the compound reacts with amines or alcohols to deliver high-purity intermediates for final API assembly targeting anti-infective and CNS drugs. Multistage purification ensures batch traceability and content uniformity required for regulatory audits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monograph reference for intermediates
    • US FDA 21 CFR Parts 211 (finished pharmaceuticals) and 210 (manufacturing standards)
    • China GMP (Revision 2020) for chemical APIs and intermediates

    Typical usage ratio

    • 1.05–1.25 molar equivalents relative to nucleophilic substrate, adjusted to reaction kinetics and target intermediate structure

    Downstream process integration

    • Charged during batch synthesis after complete solubilization of base components in aprotic solvents (e.g., dichloromethane or acetonitrile)
    • Careful temperature ramping and staged addition to control exotherm
    • Immediate aqueous workup or phase separation post-acylation to remove residual acid chlorides

    Final product types

    • Nitrobenzamide derivatives for further functionalization
    • Sulfonamide pharmaceutical intermediates
    • Active pharmaceutical ingredients for anti-tubercular and anxiolytic drugs

    2. Synthesis of Agrochemical Actives

    4-Nitrobenzoyl chloride enables acylation steps for the creation of specialty benzoyl-containing agrochemicals, including selective herbicide and fungicide actives. Agrochemical process engineers use it for the benzoylation of precursor amines, directly impacting activity or selectivity in field application agents. Tight control of process impurities assists manufacturers in achieving required pesticide residue and environmental release specifications.

    Industry compliance standards

    • FAO/WHO pesticide specification requirements
    • ISO 14256-1:2020 (Crop protection product manufacturing)
    • REACH (EU) and TSCA (US) chemical registration, safety data documentation
    • China GB 2763-2021 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Equimolar amount (1:1) to amine or alcohol substrate, but can range from 0.95–1.1 depending on agrochemical formulation and impurity risk

    Downstream process integration

    • Added after mixing precursor and inert solvent, before neutralization or crystallization
    • Purification by distillation or liquid-liquid extraction to meet active content standards

    Final product types

    • Benzoylurea insecticide actives
    • Substituted nitrile fungicides
    • Pre-mix agrochemical actives for granule or concentrate production

    3. High-Performance Dye Intermediate Manufacturing

    Dye manufacturers utilize 4-nitrobenzoyl chloride for the acylation of aromatic amines, creating tailored intermediates for solvent and disperse dyes. Optimized reaction conditions contribute to improved chromophore performance in textile and plastic coloration. The process demands rigorous analytic controls to verify color yield and ensure impurity levels remain within specified limits for downstream end-use certification.

    Industry compliance standards

    • ETAD ecological and toxicological standards for dyes
    • OEKO-TEX Standard 100 restricted substances list
    • ISO 9001:2015 chemical sector quality control
    • China GB/T 17592:2006 (Dyes—Determination of banned azo compounds)

    Typical usage ratio

    • 1.1–1.3 molar ratios to aromatic amine base, modulated for desired chromophore purity and yield

    Downstream process integration

    • Used post-coupling reaction in dye intermediate flow line, typically in the final acylation phase
    • Followed by isolation and fine filtration before pigment conversion or standardization

    Final product types

    • Sequestered azo and anthraquinone dye intermediates
    • High-temperature disperse dyes for synthetic fibers
    • Color bases for automotive and packaging plastics

    4. Liquid Crystal Material Synthesis

    Advanced electronics producers select 4-nitrobenzoyl chloride to acetylate phenolic compounds toward production of biphenyl and terphenyl liquid crystal monomers. The precise introduction of nitrobenzoate moieties adjusts phase transition profiles, facilitating fine tuning of display properties for consumer electronics or instrument panels.

    Industry compliance standards

    • IEC 61340-5-1 electronic component handling
    • RoHS Directive (2011/65/EU) for hazardous substance content
    • ISO 9001:2015 for high-purity chemical production
    • China GB/T 30512-2014 (Restriction of hazardous substances in electrical equipment)

    Typical usage ratio

    • 1.0–1.05 molar to the functional base, minimized to reduce side-product formation in high-value monomer synthesis

    Downstream process integration

    • Acylation step after base monomer preparation in high-purity organic solvent systems (e.g., chlorobenzene)
    • Subsequent vacuum stripping and crystallization for phase purity

    Final product types

    • Biphenyl-based liquid crystal monomers
    • Terphenyl intermediates for advanced display technologies
    • Materials for high-definition flat-panel displays

    5. Polymer Additive Manufacturing

    Manufacturers in the plastics and coatings sector use 4-nitrobenzoyl chloride for the functional modification of specialty polymer additives. The chemical allows incorporation of nitrobenzoyl groups on polymer backbone or as end-group, enhancing reactivity or stability in UV-cure or thermoset systems. Accurate dosing and reaction control reduce risk of instability or crosslinking defects in the final composite.

    Industry compliance standards

    • REACH registration (EU) for polymer additives
    • ASTM D5630 standard for polymer additive content
    • ISO/TS 16179 Determination of certain substances in plastics
    • US FDA 21 CFR 177.1520 for plastics in food contact (where required)

    Typical usage ratio

    • Typically 0.5–2.0 wt% of reactive polymer feed, fine-tuned per desired end-group functionality and performance criteria

    Downstream process integration

    • Dosed in the modifier preparation stage, often prior to extrusion or bead polymerization
    • Residues monitored by GC/HPLC before masterbatch compounding

    Final product types

    • UV-cure resin additives for graphic coatings
    • Crosslinking agents in acrylic emulsions
    • Functional masterbatches for engineering thermoplastics

    6. Advanced Analytical Reagents Production

    Producers of analytical reagents rely on 4-nitrobenzoyl chloride for derivatization protocols in HPLC and mass spectrometry applications. The reagent reacts with primary and secondary amines to provide chromophore-labeled analytes, improving detection limits and reproducibility in laboratory and process QC. High purity, batch-to-batch uniformity, and certification of absence of specific classes of impurities remain critical for analytical usage.

    Industry compliance standards

    • ISO 17034:2016 (Reference material producers)
    • ISO/IEC 17025:2017 for calibration laboratories
    • USP Analytical Reagent Grade specifications
    • JIS K 8001 (General rules for chemical reagents in Japan)

    Typical usage ratio

    • Generally used at 1:1 molar ratio to target analyte for derivatization, with adjustment for instrument sensitivity and matrix background

    Downstream process integration

    • Added at derivatization step post-sample extraction, before chromatographic analysis
    • Excess reagent quenched and removed by aqueous wash or organic phase separation

    Final product types

    • Chromophore-derivatized standards for HPLC and LC-MS
    • Reference reagents for quality control testing
    • Nitrobenzoyl-labeled peptides for protein analysis
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    Certification & Compliance
    More Introduction

    Why 4-Nitrobenzoyl Chloride Remains a Steadfast Choice for Chemical Synthesis

    Introduction to 4-Nitrobenzoyl Chloride

    In day-to-day production at our facility, the value of consistency and reliability in raw materials stands out. 4-Nitrobenzoyl Chloride, with its chemical formula C7H4ClNO3, plays a critical role across many synthesis routes. Its pale yellow crystalline appearance is instantly recognizable to any chemist who works on benzoyl derivatives. As a manufacturer with direct oversight of the entire process—from sourcing precursor nitrobenzoic acid to careful conversion with thionyl chloride—we hold a deep appreciation for the product’s purity, reactivity, and predictable behavior in the lab and plant.

    Product Details and Specifications

    Each batch of 4-Nitrobenzoyl Chloride goes through strict quality assessments. Most production lines require a minimum purity of 99%, measured by gas chromatography or HPLC. Trace moisture or residual starting acid can cause secondary reactions, especially in amide-forming or esterification steps. For this reason, our team focuses on drying, filtration, and packaging steps that keep contaminants well below operational thresholds. Granule size matters less than reactivity, though for some customers, we supply both fine powder and crystalline solid based on intended dissolving or dosing methods.

    Melting point typically falls between 76 and 80°C. Its acidity and electrophilicity mean it should not be stored where moisture enters. Reactivity with water releases hydrogen chloride gas—a sharp reminder to keep workplace handling protocols front-of-mind. Our packaging lines always use airtight, corrosion-resistant containers that allow easy transfer without exposure.

    Comparisons to Other Benzoyl Chloride Derivatives

    Some projects require benzoyl chloride or 2-nitrobenzoyl chloride instead. The 4-nitro variant offers a subtle but valuable difference: the para-nitro group pulls electron density away, increasing the acyl chloride’s reactivity. This feature heightens yields in acylation of less reactive amines or alcohols, making it a mainstay for pharmaceuticals where efficiency matters. Chemists seeking milder conditions—less exothermic runs, more controlled substitutions—may prefer unsubstituted benzoyl chloride. But for forming esters, amides, or heterocycles with more stubborn nucleophiles, para-nitro often finishes the job where milder versions stall.

    In advanced materials and pigments, 4-nitrobenzoyl chloride brings about vibrancy and stability that other isomers do not match. Its inclusion tends to shift finished material properties, especially where electronic effects and color intensity are important. These subtle differences run through research journals and patent literature, often being the deciding factor when scale-up teams pick their preferred reagent.

    Production Process and Operational Considerations

    Our process starts with high-purity 4-nitrobenzoic acid, which we subject to chlorination using phosgene alternatives like thionyl chloride. The reaction demands precise temperature control: high enough for complete conversion, low enough to minimize decomposition. We run real-time monitoring for acid chloride formation, using infrared spectroscopy for functional group detection. Once the batch hits completion, we push any volatile residue out with dry nitrogen. Final purification comes through cooling crystallization, not solvent evaporation, to avoid introducing even slight yellow-brown impurities.

    From operator experience, incomplete neutralization at the quench or inadequate drying before milling introduces corrosive fumes or sticky batches that jam feeders. Repeated training and refined process steps reduce these issues. Spot checks for hydrolysis sensitivity keep packaging and storage lines clean. Finished product is weighed and sealed under inert atmosphere wherever feasible, especially for export consignments crossing variable climates.

    Applications and Value in Diversified Sectors

    Pharmaceutical companies view 4-nitrobenzoyl chloride as a workhorse intermediate. They use it to build up protected amino acids, peptide linkers, or tailor acyl groups onto modified sugars. Its utility extends to the dye industry, where forming nitro-substituted aromatics unlocks both structure and color stability. In research settings, it acts as a reference compound in mechanistic studies of nucleophilic substitution or Friedel-Crafts-type routes.

    No two customers approach this molecule from the same direction. Some prioritize rapid, exothermic acylation to maximize throughput on automated equipment. Others need a particularly crisp melting profile to sync with analytical methods. Our team’s conversations with digital ink producers, agrochemical developers, and academic labs all point to the same core requirement: keep impurities low and batch-to-batch reactivity steady. Failure in this regard doesn’t just impact laboratory work—it runs the risk of regulatory delays or lost time in scaled production runs.

    Many inquiries also cover regulatory checks necessary for pharmaceutical and cosmetic use. While 4-nitrobenzoyl chloride itself is an intermediate—rarely present in finished consumer products—we field regular questions from quality assurance departments about residual solvents, elemental impurities, and presence of byproducts like dioxins. These controls do not simply tick boxes for specifications. They aim to establish trust and traceability, especially for products moving across borders or into global supply chains.

    Addressing Challenges in Handling and Transportation

    Among industrial chlorides, 4-nitrobenzoyl ranks fairly manageable with proper facilities but carries its typical hazards: corrosiveness, a tendency to hydrolyze, and toxic byproducts. Training our staff matters more than process automation. A new operator introduced to its sharp odor during storage soon internalizes the importance of tightly sealed drums far faster than any manual or datasheet can explain. Our plant uses closed transfer systems wherever possible and designs emergency vent lines to scrub accidental HCl release with soda lime traps.

    Shipping 4-nitrobenzoyl chloride becomes its own exercise in risk management. Our barrels and vessels all meet UN-approved rating, not just for leakage but also for thermal insulation. Rail and truck shipments move under sealed, labeled containers, and we coordinate with forwarding agencies familiar with hazardous goods paperwork. Over the last twenty years, experience shows us that successful risk management pivots on clear chain of custody. Lost time recovering a compromised shipment often exceeds the value of the material itself, so we invest in redundant tracking, security seals, and local storage options to bridge shipping uncertainties.

    Global sourcing of raw acid influences site-by-site production costs but rarely impacts the purity of our outgoing product. Our facility’s equipment maintenance and housekeeping set the baseline for repeatable, safe quality. If any batch falls outside spec, our team destroys it rather than risk downstream disruption—a stance shaped by both internal incident reviews and hard-won trust with client teams.

    Environmental and Regulatory Considerations

    Modern manufacturing places relentless focus on effluent, emissions, and waste disposal. Legacy production routes for acyl chlorides once relied heavily on phosgene, but shifts in regulations and public health data have forced a near-universal move to thionyl chloride in closed reactors. We recover SO2 byproducts wherever feasible, diverting these gases for separate neutralization instead of venting them directly to atmosphere. Wastewater streams run through acid quenching, pH balancing, and activated carbon polishing steps before release. Periodic audits by environmental authorities push us to document every gram of loss and recovery.

    No production process remains entirely clean or waste-free. Over the years, we’ve seen innovation from colleagues across the sector: recovery of hydrochloric acid for use in parallel reactions, solvent recycle with demisting towers, and minimization of single-use plastics in packaging lines. Most changes spring not from external mandates but from incremental savings borne out by plant operators. These investments quietly shift the long-term footprint of a chemical plant and reflect well on the diligence of those who work here.

    Understanding Product Reliability and Customer Feedback

    Technical teams evaluating new sources often run comparison trials: a fresh 4-nitrobenzoyl chloride batch beside material from their old supplier. The difference, when it shows, is usually in reactivity time, yield loss from hydrolysis, or trace impurities. We routinely encourage feedback from lab supervisors, especially during method validation or pilot-scale up. A single missed performance target—say, a skipped dry-down step that lets in moisture—can trigger hours of troubleshooting downstream, so our batch records include both chemical analysis and operational notes from the floor.

    Feedback from customers regularly shapes protocol updates. Once, a batch displayed an off-target melting point by one degree. The investigation tracked back to slightly higher agitation speed during chlorination, which changed surface area and heat dissipation. The insight, recognized quickly by a technical customer, led us to standardize our agitation speeds across all product lines. Real improvements happen at the boundary between laboratory quality control and production line experience.

    Repeated conversation with clients working in fine chemical production reveals preferences for drum size, specific labeling details, and even stacking configuration for warehouses. We adjust to these metrics naturally over time. There’s a practical reality to fulfilling an order: not just meeting chemical purity targets, but making the logistics as simple and dependable as possible. Our teams invest as much attention in a sturdy, easy-pour container as they do in the chromatogram peak shape.

    Differences From Competing Products

    Many customers come to us after struggling with intermittent issues using other isomers or supplier batches—erratic foaming on dissolution, fouling of reaction vessels from colored residues, minor fluctuations in molar mass yields that crop up only in replicated runs. Through careful process control and traceability of all packing and transfer units, we reduce these variables to a minimum. Small differences in purification method, storage atmosphere, or even resin seals make outsized impacts on finished product usability.

    In technical applications, small compositional drift leads to bigger downstream performance swings. Products aimed at dye manufacture or advanced polymer research require precise, known material behavior. Our pure 4-nitrobenzoyl chloride batches, supported with full documentation of origin, handling, and in-process checks, stand up to repeated scrutiny from regulatory and R&D staff. A familiar pattern emerges over years of partnership: customers initially compare several sources on laboratory scale, lean into higher-quality batches for reliability at pilot and full plant scale, and standardize on suppliers that demonstrate hands-on knowledge of both chemistry and practical application.

    As projects advance in sophistication—from pharmaceuticals to specialty coatings—subtle parameter shifts separate robust suppliers from less engaged distributors. We focus on owning each step from precursor acid through finished drum, so every outgoing batch reflects both operator diligence and customer feedback. Where purity and reactivity matter most, experience-driven adjustments in drying, filtration, and storage process pay far greater dividends than chasing scale alone.

    Perspectives on Future Innovation

    Increasing customer attention to trace impurities, particularly for regulated industries, steers us toward incorporating more advanced real-time analytical tools on the production line. While classic wet-chemistry checks once sufficed for batch release, rapid scanning infrared and chromatography methods now catch deviations before a single drum gets sealed. Feedback loops from finished-product testing in downstream synthesis feed directly into protocol changes at the plant—closer partnerships with R&D chemists lead to faster refinement of process parameters.

    Emerging research continues to push the boundaries of where 4-nitrobenzoyl chloride fits. In pharmaceutical lead optimization, new linker strategies exploit the strong electron-withdrawing effect of the nitro group for site-selective acylation, backed by published studies showing superior yields compared to classical benzoyl chlorides. Materials scientists reach for the para-nitro version to tune fluorescence or color fastness in high-performance pigments. Our own collaborations with development teams at customer facilities often uncover unexplored applications or process efficiencies that only show up under production conditions, not in small-scale research articles.

    Sharing these application insights with production staff closes the loop between advanced chemical research and practical, reliable manufacturing. Operators who understand the impact of small process variables—solvent purity, drying time, refrigeration temperature—feel greater ownership over the finished product. Over time, this culture of accountability proves as valuable as any certification or quality assurance score.

    Technical Support and Partnerships

    Our customers rarely buy on price alone. In our discussions with process engineers and plant managers, the support network behind each drum carries as much value as the molecules inside. Direct lines to technical staff, flexible packaging runs, and documentation suited for international regulatory bodies make the difference during rapid project scale-ups or sudden audits. We consider these relationships core to our operation—the practical outcome is fewer plant disruptions, faster troubleshooting, and an open channel for continuous improvement.

    Clients sometimes request long-term storage or phased deliveries to match production windows, especially in regions where transportation exposure risk climbs during humid months. We maintain facility space and cold-room shipping options where justified by demand. For customers facing unique waste handling or post-use product reclamation requirements, our technical staff share handling experience and process modifications that have proven successful in-house. Real partnerships come from practical knowledge, not just product brochures.

    Closing Thoughts From the Shop Floor

    Years of experience handling 4-nitrobenzoyl chloride reinforce its deserved reputation as a foundational intermediate. Its uses stretch far across industries—from complex pharmaceutical synthesis to precision pigment creation—and each application uncovers new requirements for quality, reliability, and teamwork between supplier and end user. By focusing on meticulous production, real customer feedback, and incremental innovation, we build trust batch by batch. Those who spend time at the reactor or drum line know: small differences in process and attention make big impacts on industry success. We take pride in seeing our product stand up to the most demanding applications, delivering the reliability that keeps research, production, and innovation moving forward.