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3-Nitrobenzoyl Chloride

    • Product Name 3-Nitrobenzoyl Chloride
    • Alias m-Nitrobenzoyl chloride
    • Einecs 207-737-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    887468

    Cas Number 121-90-4
    Molecular Formula C7H4ClNO3
    Molecular Weight 185.56 g/mol
    Appearance White to pale yellow crystalline powder
    Melting Point 67-69 °C
    Boiling Point 273 °C
    Density 1.51 g/cm³
    Solubility In Water Decomposes
    Purity Typically >98%
    Refractive Index 1.599
    Storage Conditions Store in a cool, dry place, protected from moisture and light
    Flash Point 138.8 °C
    Odor Pungent

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

    Packing & Storage
    Packing 250g amber glass bottle with screw cap, labeled "3-Nitrobenzoyl Chloride." Hazard and handling warnings clearly printed on packaging.
    Shipping 3-Nitrobenzoyl Chloride should be shipped in tightly sealed containers, protected from moisture, heat, and light. It must be labeled as a corrosive and hazardous material, following DOT regulations. Transport in compliance with all local, state, and international regulations, using UN-approved packaging and appropriate hazard labeling.
    Storage 3-Nitrobenzoyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sunlight, moisture, and incompatible substances such as strong bases and oxidizing agents. It should be kept under inert gas, if possible, to prevent hydrolysis. Proper chemical storage cabinets designed for corrosive or moisture-sensitive chemicals are recommended.
    Application of 3-Nitrobenzoyl Chloride

    Applications of 3-Nitrobenzoyl Chloride in Industrial Manufacturing

    As a manufacturer of 3-nitrobenzoyl chloride, we deliver high-purity intermediates for select industrial sectors that demand consistent quality, traceability, and regulatory compliance. Below are the principal application scenarios where this material enables key synthesis steps in high-value, regulated downstream industries.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize 3-nitrobenzoyl chloride as a core acylating agent in the synthesis of specialty APIs and advanced intermediates, particularly for nitroaromatic-based drug candidates targeting anti-infective and oncological indications. The material reacts at controlled stages of the multi-step pathway, ensuring product integrity and facilitating downstream purification that meets stringent regulatory protocols. Careful adjustment of molar ratios and reaction conditions allows for high yields with minimal impurity formation, contributing to batch reproducibility and regulatory filing readiness.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (cGMP Drugs)
    • EU Guidelines for APIs (EudraLex Vol. 4, Part II)
    • Chinese Pharmacopoeia for API Synthesis

    Typical usage ratio

    • 0.9–1.3 molar equivalents per reactant, adjusted according to the specific API intermediate yield across batch-scale and continuous processes, with further optimization based on critical impurity profiling

    Downstream process integration

    • Directly charged during the acylation step in nitroaromatic intermediate formation
    • In-line addition monitored by HPLC/GC for real-time process control
    • Followed by quenching/neutraliation prior to downstream purification (crystallization, extraction, or chromatography)

    Final product types

    • Nitrobenzamide-based API intermediates
    • Key starting materials for third-generation anti-infectives
    • Specialty intermediates for anti-cancer bulk actives
    • Chemical building blocks for finished solid-dose drugs

    2. Agrochemical Active Ingredient Synthesis

    Leading agrochemical formulators incorporate 3-nitrobenzoyl chloride in regulated syntheses of nitroaromatic-based herbicide and fungicide actives. Its high reactivity and defined purity support tightly controlled process windows that prevent by-product contamination and secure product registrations in major markets. Trace-level monitoring and restricted handling protocols are critical at this stage, ensuring full documentation and comparability across multiton batches in both tolling and captive manufacturing environments.

    Industry compliance standards

    • FAO/WHO Specification for Agrochemical Technical Material
    • ISO 9001:2015 Quality Management System for Agrochemical Production
    • REACH Regulation (EC No. 1907/2006) for Europe
    • China Pesticide Administration Regulations (ICAMA)

    Typical usage ratio

    • 1.0–1.2 equivalents depending on the specific herbicide or fungicide backbone; adjusted in pilot trials to minimize unreacted acid chloride and maximize target conversion, as verified by LC-MS and residue analysis

    Downstream process integration

    • Metered dosing to the key condensation or coupling stage during technical grade actives production
    • Batch and continuous flow compatibility, with inert atmosphere handling
    • Preceded and followed by pH-controlled washes to eliminate traces of unreacted material

    Final product types

    • Nitrobenzamide herbicide technicals
    • Nitro-substituted phenoxyacetic fungicide intermediates
    • Registered bulk active ingredients for formulated pesticides

    3. Liquid Crystal Monomer Production for Electronic Displays

    Specialty electronics chemical firms apply 3-nitrobenzoyl chloride in the precision synthesis of liquid crystal monomers, essential for tuned dielectrics in LCD and OLED manufacturing. Accurate dosing ensures molecular uniformity and phase transition control in downstream blending, which directly impacts the electro-optical performance of finished display panels. Compliance with low-halogen and electronic-grade purity benchmarks is mandatory, given stringent customer and regulatory QA protocols for the electronics supply chain.

    Industry compliance standards

    • IEC 61249-2-21 (Low Halogen Materials for Electronic Components)
    • RoHS Directive 2011/65/EU (Restricted Substances)
    • JPCA-ES-01 (Japan Electronics Packaging Standards for Liquid Crystal Materials)
    • ISO 9001:2015 with electronics-sector addenda and traceability modules

    Typical usage ratio

    • 0.95–1.10 equivalents, tailored per monomer structure and functional end-use requirements as verified by end-group titration and NMR analysis

    Downstream process integration

    • Introduced in the synthesis phase of the nitroaromatic segment of advanced LC monomer preparation
    • Monitored for exothermic control and batch uniformity
    • Downstream purification using high-resolution distillation or column chromatography to achieve electronic grade purity

    Final product types

    • Liquid crystal monomers for TFT-LCD display fluids
    • Specialty optical materials for OLED devices
    • Photo-alignment materials for advanced display panels

    4. Specialty Dye and Pigment Synthesis

    Manufacturers of specialty colorants rely on 3-nitrobenzoyl chloride for the production of nitroaromatic intermediates in select organic dyes and high-stability pigments used in industrial inks, security printing, and plastics coloration. Controlled dosing and sequential reaction planning enable vibrant, stable chromophores with minimal side reactions, supporting compliance in food-contact and toy safety applications where required. The process must adhere to heavy-metal-free protocols and account for potential TSE/BSE risk assessment where pigments enter sensitive supply chains.

    Industry compliance standards

    • EN 71-3 (Safety of Toys: Migration of Certain Elements)
    • US FDA 21 CFR 178.3297 (Colorants for Polymers)
    • ISO 12402-7 (Pigments in Plastics for Food-Contact)
    • OEKO-TEX Standard 100 (Textile Dye Safety)

    Typical usage ratio

    • 1.0–1.5 equivalents, selected based on chromophore construction and desired dye or pigment shade; closely managed by in-process UV-Vis monitoring and end-use compatibility checks

    Downstream process integration

    • Reactant in nitroaroyl coupling or Friedel–Crafts acylation stages of dye intermediate synthesis
    • Inline crystallization and washing steps for purity enhancement
    • Formulation into concentrated pastes or powders after final precipitation

    Final product types

    • High-performance pigments for plastics and coatings
    • Organic dyes for security or anti-counterfeit printing inks
    • Textile and polymer colorants meeting toy and food-contact specification
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    Certification & Compliance
    More Introduction

    Introducing 3-Nitrobenzoyl Chloride: Factory Insights and Usage Perspectives

    3-Nitrobenzoyl Chloride represents a chemical raw material that stands out for both its reactivity and its reliability in downstream organic synthesis. With years of hands-on experience in the manufacturing process and collaboration with chemists in pharmaceutical and dye sectors, we've developed a practical understanding of why this compound attracts steady, long-term demand. Every batch comes off our production line with careful monitoring; consistency and purity matter more for this specialty chemical than just about any other detail.

    Understanding 3-Nitrobenzoyl Chloride: Characteristics Built from the Ground Up

    This compound starts with a clear mission on the bench: deliver a highly reactive acyl chloride group attached to a nitro-substituted aromatic ring. We focus on delivering a purity level upwards of 99 percent, measured by HPLC and confirmed by NMR and GC where possible. Given the robust yellow crystalline powder it forms, we avoid contamination at all production points. Even trace moisture quickly triggers hydrolysis, and for this reason, packaging and storage happen under tight control—sealed drums, desiccant, and temperature-regulated warehouses. Alongside our experienced operators, every ounce draws on a workflow that addresses hazards and reactivity with deep respect for safety and accuracy.

    Intended Uses: How 3-Nitrobenzoyl Chloride Drives Modern Synthesis

    Laboratory benches and pilot plants count on this molecule for a reason: it unlocks specific organic transformations that many alternatives can’t match. The nitro group offers electron-withdrawing strength, altering the usual reactivity of the benzoyl chloride backbone, opening pathways that phenyl- or 4-nitro analogs close off. In our client feedback, the most frequent application remains the preparation of amides and esters. Synthetic routes for pharmaceuticals and advanced polymers depend on the predictable reactivity and clean conversions this intermediate delivers. Dyes and pigment manufacturers push for the most reliable nitrobenzoyl chloride because the finished colors tie directly to the starting material's quality—any impurity risks off-shades and weak performance.

    Compared to more common benzoyl chlorides, the presence of the nitro group at the 3-position—meta to the ring junction—changes the energetic profile of the reaction. It slows down unwanted side reactions, increases selectivity toward target products, and provides a handle for further transformations downstream. We’ve partnered with fine chemical producers to dial in this advantage during scale-up. Our technical support team compares laboratory test results with production-scale outcomes, which helps minimize batch-to-batch variation. Chemists working on peptide backbone protection mention greater control during acylation steps. Others use the compound in agrochemical intermediate production, all chasing the same outcome: higher yields, less byproduct, simpler purification.

    Specifications, Processing Realities, and Daily Factory Challenges

    We target a melting point for 3-Nitrobenzoyl Chloride in the 74 to 77 degrees Celsius range. Material arriving much outside this band signals off-spec synthesis or contamination, prompting us to halt shipment until we resolve the cause. Chloroform, dichloromethane, and acetonitrile provide the most commonly used solvents in our own pilot testing, ensuring rapid dissolution and transfer across the customer supply chain. The necessity for anhydrous conditions carries into loading and shipping: droplets of water in the cargo dock force a complete repack for quality assurance.

    Odor offers another indicator for experienced handlers—3-Nitrobenzoyl Chloride possesses a sharp, pungent smell that shifts with impurity levels. Workers receive direct training to spot the difference between normal and “off” batches by nose as well as machine. We use noncontact infrared thermometers during transfer, since exothermic hydrolysis releases both hydrochloric acid vapor and heat. Ventilation systems built into our filling area direct corrosive vapors through scrubbing towers, where real-time pH meters track acid removal effectiveness. Practical experience has taught us that scale introduces new challenges; minor leaks at lab scale become serious air quality risks on the tonne scale, so our safety engineer audits each batch movement weekly.

    Comparing to Other Benzoyl Chlorides: More than a Structural Change

    Chemists familiar with basic benzoyl chloride notice differences immediately when handling the 3-nitro variant. The extra nitro group at the meta position shifts both electron density and reactivity. Our technical partners report that acylation rates drop modestly, but reaction selectivity gets a clear boost. This difference matters for peptide chemistry, where protecting group removal or downstream coupling reactions often challenge clean separation and high assay. 3-Nitrobenzoyl offers stronger resistance to hydrolysis under neutral conditions versus unsubstituted counterparts, which makes storage and shipment less vulnerable to ambient humidity than more reactive variants like 4-nitrobenzoyl chloride.

    Our own head of process development notes that engineers spend less time addressing breakdown byproducts in wastewater lines, since the nitro group moderates the reactivity responsible. While both 2- and 4-nitrobenzoyl chlorides see niche use, the 3-position ensures a balance between functional group manipulation and process manageability. This quality means fewer corrosion hassles for steel lines and reactors—a benefit for both operators and maintenance teams. In pharmaceutical scale-up, this reliability in handling leads to real-world savings in plant downtime.

    Handling, Storage, and Regulatory Observations

    Direct handling of 3-Nitrobenzoyl Chloride requires fully enclosed transfer systems in our facilities. Operators run through multi-step training before receiving access to material tanks. Full PPE, splash goggles, double-layer gloves, and face shields become routine—not as a matter of compliance, but a response to the compound’s inherent irritant properties. Chloride dust accumulates easily around screw seals and transfer connections; we run checks each morning before plant startup, cleaning out residue with vacuum and solvent wipes. Our experience confirms that any deviation in storage—especially a broken seal or wet pallet—results in rapid quality loss. Drum labeling includes both chemical hazard codes and production batch traceability; if a problem arises, we isolate affected stock within minutes thanks to plant-wide digital tracking.

    From an environmental viewpoint, 3-Nitrobenzoyl Chloride’s risk profile compels respect. Any accidental release to drain causes localized acidification and nitroaromatic contamination. Our facility captures all wash-down and cleaning water for onsite treatment: caustic scrubbing followed by neutralization and detailed analysis before discharge. Regulatory inspections almost always spend extra time reviewing how we segregate storage and waste flows from benzoyl chloride lines. This scrutiny comes from the compound’s potential to form toxic byproducts; we take extra care to meet or surpass safety standards for emissions and effluents.

    From Raw Material to End Product: An Insider’s View of User Experience

    Feedback from customer labs provides the sharpest assessment of how 3-Nitrobenzoyl Chloride performs in real-world synthesis. Chemists on the floor often cite crystalline purity, but process engineers go further: they evaluate how the batch handles during weighing, transfer, and dosing. Too much clumping or dustiness signals an issue—so we control not just particle size by sieving, but also moisture content by oven-drying and sealed packaging. Several partners in small-molecule pharma remarked that our material produces better separation profiles during HPLC analysis, streamlining their QA. These advantages grow obvious as the scale of operation grows; headaches avoided during gram-scale trials become full-scale relief during kilo or tonne runs.

    Colleagues in pigment manufacturing describe the importance of batch brightness and consistent reactivity for high-value azo dyes. Minor differences in substituent position change not just color but also fastness and processability of the final product. We’ve supported these users by offering technical sheets summarizing which reactions most benefit from the selectivity boost brought by the 3-nitro configuration; synthetic pathways for advanced agrochemicals use this specificity to skip purification steps and avoid side reactions that otherwise waste both time and material.

    Continuous Improvement from Factory to User

    Experience in synthesis and bulk handling shapes our production adjustments year after year. After repeated feedback on dust generation and caking, we overhauled the crystallization stage, adding a cooling jacket to control particle growth and switching to sealed air-lift dryers to avoid agglomeration. Several years ago, a batch tracked to a chlorinated solvent carryover highlighted the need for more robust in-process monitoring, and we now run GC on every shifted lot to prevent recurrence.

    Like many specialty manufacturers, we balance raw material variability with output stability by adopting multi-step purification at scale. Our operators, chemists, and plant managers sit down quarterly to examine deviation reports, tracking anomalies back to their process roots. The goal always remains to supply 3-Nitrobenzoyl Chloride with as few surprises as possible—a matter of professional pride as much as regulation. Nitrogen sparge systems at the packing stage became standard after an incident of mild hydrolysis during a seasonal humidity spike led to a short batch recall. Since then, temperature and humidity data loggers archive shipping and storage conditions, allowing any downstream issue to be traced back transparently.

    Comparing Laboratory and Industrial Production: Factory Lessons

    On the laboratory bench, 3-Nitrobenzoyl Chloride often shows up in small vials, handled en passant with a pipette and tight-fitting septum. Industrial batches demand much more—specialized bulk transfer hoses, dual-stage vapor control, and multiple points of purity testing before and after crystallization. Having worked both at the bench and in the main plant, our staff sees the gap between synthesis on the gram scale and production on the tonne scale. Minor traces of iron or copper from reaction vessels end up amplified after crystallization; diligent cleaning and vessel passivation take care of this issue. The labor that goes into batch tracking pays off during a customer audit, as records provide a chain of custody viewers can trust.

    Laboratory staff focus on target molecule yield and side reaction suppression. Our production crew, in contrast, trouble-shoots mechanical losses, filter flow rates, and drum-bung torque settings. These details, invisible on a datasheet, shape product reliability for end users. A minor mistake—such as incomplete drying or overexposure to ambient air—translates into unexpected acid byproduct or degradation. Repeated practice and disciplined upgrades turn lessons into routine, helping us deliver the reliability advanced synthesis demands.

    Supply Chain Considerations and Global Trends

    Recent years have exposed the vulnerability of chemical supply chains. Pandemics, logistics delays, and feedstock shortages strain both small and large buyers of 3-Nitrobenzoyl Chloride. Direct feedback from our purchasing department highlights the impact of raw material interruptions, which ripple across the whole batch-planning calendar. For those depending on precision synthesis, delays in delivery often force rescheduling of multi-step sequences reliant on timely arrival of intermediates. As a manufacturer, we maintain buffer inventories and coordinate closely with upstream suppliers of nitration grade benzoic acid and phosgene alternatives to offset raw material volatility.

    Global shifts in regulatory frameworks, including environmental and safety standards, also steer product availability. We monitor updates from REACH in the EU and TSCA in the US, tailoring production accordingly. Cleaner production methods move up the priority list since regulators have flagged both nitroaromatic intermediates and acyl chlorides for tighter scrutiny. Our plant responded with upgrades to waste minimization and emission capture systems, treating them not as compliance burdens but as necessities for future-proofing both plant operation and customer confidence.

    Future Directions: Evolving with Needs, Shaped by Experience

    Continuous engagement with both academic users and industrial partners shapes our R&D. Advanced uses of 3-Nitrobenzoyl Chloride, such as in custom-designed ligands and catalyst scaffolds, often start with academic research and end with production-scale requests. Keeping a finger on the pulse of tool chemistry trends allows us to forecast demand surges and decline cycles—helping both us and our customers plan ahead.

    Experience has taught us to view each production batch as more than a statistic—it´s an output that stands between a chemist and their goal, a process engineer and plant efficiency, an operator and trouble-free handling. The value of 3-Nitrobenzoyl Chloride grows over time, not from marketing, but from accumulated reliability, hard-won improvements, and open dialogue with those who use it at every step. Every upgrade, process tweak, and feedback cycle improves both current quality and future confidence for those who depend on specialized reagents to spark the next innovation.