Products

2-Nitrobenzoyl Chloride

    • Product Name: 2-Nitrobenzoyl Chloride
    • Alias: 2-Nitrobenzoyl chloride
    • Einecs: 209-034-6
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    501189

    Product Name 2-Nitrobenzoyl Chloride
    Cas Number 89-01-0
    Molecular Formula C7H4ClNO3
    Molar Mass 185.56 g/mol
    Appearance Light yellow to yellow crystalline solid
    Melting Point 38-42 °C
    Boiling Point 147-150 °C at 20 mmHg
    Density 1.515 g/cm³
    Solubility Reacts with water, soluble in organic solvents such as ether and chloroform
    Iupac Name 2-nitrobenzoyl chloride
    Synonyms o-Nitrobenzoyl chloride, 2-nitrobenzenecarbonyl chloride
    Flash Point 110.7 °C
    Refractive Index 1.619

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

    Packing & Storage
    Packing 250g of 2-Nitrobenzoyl Chloride is packaged in a sealed amber glass bottle, labeled with hazard warnings and handling instructions.
    Shipping **2-Nitrobenzoyl Chloride** should be shipped in tightly sealed containers under cool, dry conditions, away from heat, moisture, and incompatible substances such as bases and strong oxidizers. Ensure appropriate hazard labeling and documentation. It is classified as a hazardous material, requiring compliance with transportation regulations for toxic and corrosive chemicals.
    Storage 2-Nitrobenzoyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, direct sunlight, and sources of ignition. It must be kept away from incompatible substances such as water, alcohols, strong bases, and oxidizers. Properly label the container and use secondary containment to prevent spills or accidental contact.
    Application of 2-Nitrobenzoyl Chloride

    Applications of 2-Nitrobenzoyl Chloride in Industrial Manufacturing

    2-Nitrobenzoyl chloride serves as an efficient acylating agent across multiple industrial sectors, supporting advanced synthesis routes in bulk chemical manufacturing. Our material delivers narrow batch-to-batch purity and is engineered for stringent downstream requirements. Explore below the leading application scenarios where this compound provides specific functionality and integration value.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Leading pharmaceutical companies employ 2-nitrobenzoyl chloride in the synthesis of benzamide-based APIs and related structures, exploiting its nitro-substituted benzoylation profile for ortho-nitro functional group introduction. Reaction control and purity directly affect API yield and regulatory compliance. This feedstock appears most often in the benzoylation step during the assembly of anticonvulsants and select non-steroidal anti-inflammatory drugs (NSAIDs).

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4
    • U.S. FDA cGMP (21 CFR Parts 210, 211)
    • Chinese Pharmacopoeia general chapter for intermediates

    Typical usage ratio

    • 0.7–1.2 molar equivalents per target amine or alcohol substrate, finely tuned to maximize conversion and avoid overacylation

    Downstream process integration

    • Charged to the reaction vessel after primary substrate activation, under low temperature with controlled base addition to suppress impurities; followed by aqueous or organic work-up before product isolation and trace impurity removal by crystallization

    Final product types

    • Ortho-nitrobenzamide derivatives (e.g., in anti-inflammatory APIs)
    • Intermediates for anti-infectives and anticonvulsants
    • Amide-linked prodrugs requiring ortho-nitrobenzoyl protective groups

    2. Fine Chemical Synthesis of Dyes and Pigments Precursors

    Major colorant producers use 2-nitrobenzoyl chloride as a key building block for synthesizing anthraquinone, azo, and other nitrobenzamide-based dye intermediates. This material’s electrophilic acylation behavior enables the formation of high-purity nitro-substituted aromatic frameworks, which influence final dye chromaticity and stability during textile or ink fabrication processes.

    Industry compliance standards

    • OEKO-TEX Standard 100 (restricted substances)
    • REACH Regulation (EC) No. 1907/2006 for chemical registration
    • ISO 9001:2015 Quality Management for fine chemicals
    • ZDHC MRSL V3.1 (for textile dye components)

    Typical usage ratio

    • 0.8–1.5 molar equivalents relative to coupling reactants, adjusted to achieve target substitution patterns and color strength

    Downstream process integration

    • Introduced after preliminary diazotization or aromatic amine functionalization, followed by acylation, reflux, neutralization, and selective crystallization; impurities removed by solvent extraction or preparative chromatography

    Final product types

    • Nitrobenzamide dye intermediates
    • Anthraquinone-based pigments
    • Azo compound precursors for textile and ink dyes

    3. Crop Protection Chemical Synthesis

    Specialty agrochemical manufacturers depend on 2-nitrobenzoyl chloride in the production of specific herbicide and pesticide intermediates. The nitro-functionalized benzoyl moiety introduced using this raw material is crucial in molecular scaffolds that exhibit selectivity and systemic transport within crops. Process conditions emphasize safety and contaminant control due to downstream application requirements.

    Industry compliance standards

    • FAO/WHO Guidelines for the Quality Control of Pesticides
    • ISO 9001:2015 for agrochemical manufacturing
    • REACH Annex IV (for active ingredient registration)
    • China GB 21641-2022 for agricultural chemical safety requirements

    Typical usage ratio

    • 1.0–1.3 molar equivalents based on the nucleophilic substrate, with optimization to minimize unreacted acyl chloride/quench requirements

    Downstream process integration

    • Added after initial halide or amine functionalization within batch or continuous flow reactors, typically followed by neutralization with carbonate bases and solvent-driven purification steps

    Final product types

    • Nitrobenzamide-based herbicide intermediates
    • Nitroaromatic scaffolds for insecticides
    • Pre-formulated active ingredient blends for pesticide concentrates

    4. Photoinitiator Synthesis for UV-Curable Resin Formulation

    Manufacturers of specialty polymers and coatings employ 2-nitrobenzoyl chloride to synthesize photoinitiator molecules with high quantum efficiency for UV-curable resins. This component delivers controlled acylation required for multi-step routes to benzoin-derived initiators, which activate rapidly under UV exposure and catalyze crosslinking in inks, adhesives, and electronics encapsulation systems.

    Industry compliance standards

    • ISO 9001:2015 for photoinitiator manufacturing
    • RoHS 2011/65/EU (Restriction of Hazardous Substances for electronics)
    • REACH restriction list for photoinitiator components
    • European Printing Ink Association (EUPIA) guidelines

    Typical usage ratio

    • 0.9–1.1 molar equivalents per secondary alcohol or benzoin substrate, modulated according to target reactivity and minimization of over-chlorination

    Downstream process integration

    • Combined during the post-oxidation step for benzoin photoinitiator synthesis, followed by base-catalyzed workup and chromatographic purification, and supplied as a high-purity intermediate for UV resin blending

    Final product types

    • Photoinitiators for UV-cure inks and coatings
    • Photoactive additives for 3D printing resins
    • UV-reactive adhesives for microelectronics assembly

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    Certification & Compliance
    More Introduction

    2-Nitrobenzoyl Chloride: Practical Insights from Production to Application

    Living Daily with 2-Nitrobenzoyl Chloride: The Material Behind Specialty Synthesis

    Every chemist who walks the production floor knows each raw material as more than a line item. For years, our team has worked hands-on with 2-Nitrobenzoyl Chloride, seeing its behavior in bulk, running continuous and batch syntheses, troubleshooting reactors, and responding to the reality that this isn’t just another fine chemical—it’s a go-to building block for advanced intermediates and research needs. The daily reality of manufacturing, quality, and shipping reveals strengths and quirks that go unnoticed in high-level summaries.

    The molecule’s structure—a benzoyl chloride core with a handy nitro group on the ortho position—provides a reliable acylating function, letting it react cleanly with nucleophiles in well-worn synthetic routes. It acts fast, its electrophilic carbonyl only sharpened by the electron-withdrawing nitro ring substitution. That simple arrangement is why labs and plants order it by the drum: it works where it counts, in sulfa drug intermediates, dyes, agricultural custom synthons, and a handful of advanced polymer and lubricant additives.

    Understanding Its Specifications—Not Just Purity, but Reproducibility

    Experience with 2-Nitrobenzoyl Chloride starts before the vats, right at incoming quality control. Chemists recognize consistency across batches keys production reliability. Good material carries a pale yellow appearance, sharp benzoyl chloride smell, and strong moisture sensitivity—any off-colors or lingering HCl fumes can indicate early hydrolysis, often from storage or transport mishaps. We monitor melting point, GC purity, HPLC for trace organics, and water content, not to show off figures, but to ensure our regular customers can rerun their protocols without redesigning every time.

    While tight specifications might sound like marketing copy, down in the receiving warehouse real people open these kegs and depend on clump-free, uniform materials—fine enough to weigh precisely, granulated to avoid static, but not so dusty that it clogs charging ports in automated feeders. Any variance—a damp sample, a jammed auger—costs an afternoon and tempers, so even small parameter changes matter. The end users aren’t just chemists in a quiet lab. They’re running shifts in kilo labs and pilot plants, counting on predictable melting (usually 42–45°C), high GC-verified purity, less than 0.5% related substances as a practical threshold.

    Where Production Challenges Shape Daily Practice

    Making 2-Nitrobenzoyl Chloride at scale, the plant doesn’t dress up reaction basics. The core route starts from 2-nitrobenzoic acid, its chloride formation powered by traditional thionyl chloride or, for certain requirements, phosphorus pentachloride. This isn’t chemistry for show—it’s chemistry for yield and for downstream purity. Operations teams scrutinize gas scrubbing, acid scavenging, and solvent recovery, since every fraction of loss is a cost some customer will pay, or a defect someone will regret.

    The biggest lesson from long production experience: don’t mess around with moisture. The acyl chloride reacts with almost any water in the environment, so dehumidified storage, airtight drums, and nitrogen blanketing always beat last-minute interventions. Seasoned workers catch faint traces of hydrolysis in the odor or texture—evidence that even warehouse mishaps (opening barrels for 'just a quick look') can spoil an entire shipment. Each production campaign, we calibrate storage temperatures and monitor drum seals, not just to hit specs but to protect future reactions down the supply line.

    Putting 2-Nitrobenzoyl Chloride to Work: Common and Custom Applications

    Those of us managing supply for pharma know 2-Nitrobenzoyl Chloride by its performance in peptide acylation and API intermediate synthesis. Its persistent popularity stems from predictable reactivity and minimal by-product profiles. The ortho-nitro group adds a rigid electron demand, making nucleophilic attack on the carbonyl smoother and often speeding up the reaction over less activated benzoyl chlorides. Producing kilo-lots for medicinal chemistry means any slip in purity or particulate content drags down isolation yields and downstream conversions.

    Outside pharma, pigments and dyes sector chemists value the product for similar reasons—its functional group placement drives unique color and fastness properties in azo and anthraquinone structures. They care about reproducibility batch-to-batch, because small differences in the nitrobenzoyl component show up as color drift across pigment production runs. Custom agricultural manufacturers, dealing with smaller production volumes, prefer the ortho-nitro isomer because it enables them to spin out selective herbicide and plant growth regulators. Whether serving a kilo-lab or a hundred-ton pigment campaign, 2-Nitrobenzoyl Chloride delivers on expectations for reactivity and outcome.

    How It Stands Apart—Chemically and Practically

    Direct competitors, like plain benzoyl chloride or its meta- and para-nitro analogs, certainly serve in other syntheses, but anyone who’s run acylations with all of them sees the difference in yield, reaction time, and by-product formation. The ortho-nitro substitution changes not only the speed of the nucleophilic acyl substitution but also the selectivity of the resulting product—critical in multistep synthesis sequences where cleanup or separation after every reaction slows down a campaign or eats into margins.

    Physical handling varies, too. While regular benzoyl chloride smells sharper, it sits more neutral in color, whereas 2-Nitrobenzoyl Chloride’s pale yellow hue helps operators spot degrading material or cross-contamination at a glance. Chemically, the extra nitro group further restricts volatility during heating, making headspace control during large batch work more forgiving (though it still demands proper extraction and venting in high throughput lines). These process-specific differences aren’t just academic—they add up across thousands of kilos handled through a year.

    What We’ve Learned About Sustainability, Safety, and Compliance

    Continuous years of production reveal that regulatory compliance and safe handling aren’t side notes. The ortho-nitro group makes hydrolysis products more persistent in waste streams, so chemists adopting greener practices build extra steps into neutralization and effluent management. Everyone in the plant learns new protocols quickly. While in the lab bench phase, a researcher can get away with fume hoods and careful dripwise addition, bulk handling means pressure venting, double containment, and practice runs for every new piece of equipment.

    In response, our material ships with explicit handling instructions, not out of bureaucratic box-ticking, but from repeated real-world experience. Operators faced with leaking drums in the summer or stuck valves in an isolation train know the importance of dry air, non-metal seals, and avoiding contact with bases. Inconsistent handling spells profit loss—contaminated waste drums, failed batches, or, once, a production halt that lasted three shifts while we checked every possible water ingress point after a heavy rainstorm.

    After many years, our setup uses sealed transfer lines, dedicated nitrogen blankets, and temperature-controlled storage, all based on those practical lessons. New investments in vapor scrubbing and waste capture systems let us meet environmental guidelines and ensure nobody faces exposure hazards during decanting or repacking. We input these process strengths into updated safety sheets and recommend customer-side adaptations—quality production can’t survive surprise hydrolysis at the end user’s plant, so communicating these quirks protects output all the way to the finished compound.

    Adapting Supply Chains and Packaging to Harder Realities

    Logistics for 2-Nitrobenzoyl Chloride show up as a daily discipline. After losses traced back to poorly sealed shipping containers and fluctuating warehouse temperatures, we intensified audits and reviewed drum lining materials. Tight coordination with our logistics teams became standard, ensuring deliveries avoid long port layovers or unplanned warehouse moves. Moisture pickup along the way can undo months of careful batchwork, so every inbound and outbound shipment features real-time temperature and humidity loggers and strict packaging audits—not just for show, but because the evidence for damage is always clear in the first sample withdrawal.

    The choice of packaging—generally fluoropolymer-lined steel drums or HDPE kegs—comes directly from field complaints. Metal closures show signs of corrosion after a few months, so we pivoted to plastic fits and corrosion-resistant septa. For material going to humid climates, we double-bag and label clear usage windows to discourage unnecessary opening. Having a material rejected on arrival means not only financial loss but also strained customer relationships, so our focus from drum cleaning to batch dating remains uncompromising.

    Feedback from truck drivers, customs inspectors, and receivers led to further improvements. No one likes surprises—every packed drum now features extra tear tape, heavy-duty seals, and secondary covers. On-site teams at the receiving end have come to expect a little more from our drums: speedy sampling, easy drum turn, and unpacking that fits their actual floor space, not just theoretical guidelines.

    Real-World Troubleshooting: What Can Go Wrong, and How We Respond

    Our veterans remember the odd batch found sticky from partial hydrolysis—tragedy for downstream separations. So we built in routine batch stability checks, split samples, and long-term accelerated storage reviews. Material hitting the analysis bench late tells us straight away about upstream failings. Recurrent problems get tracked to their sources, whether in filter changes, raw material swaps, or misread tank sensors. The response isn’t just more paperwork. It's hands-on: cleaning the lines, training new hires, walking the drums down the line, and—most important—maintaining honest feedback with end users.

    Regular check-ins with large buyers result in faster issue detection, whether it’s slight off-odors (often seen with behind-schedule shipments) or reports of changed particle size (traced back one year to a minor shift in crystallization temperature). These findings go straight to batch records and get used in annual process improvements. In a market with new competitors every year, long-term relationships come from making real corrections, not just promising tighter specs on paper.

    The Market View—Why 2-Nitrobenzoyl Chloride Holds Its Place

    Researchers might temporarily substitute less expensive acyl chlorides or skip the nitro group hoping to cut costs, but years of customer data show most come back. It’s the exceptional performance in demanding syntheses—selectivity, clean conversion, and ease of workup. Researchers in competitive, IP-driven industries flock to specialty intermediates where trace by-products can kill product launch timelines or drive up rejection rates.

    Pharmaceutical innovators, pilot plant scale-up teams, and custom agrochemical shops—these aren’t distant users. Over the years, several have called or visited to troubleshoot their own syntheses using our batches. They want the physical material in hand to match on-paper data. When switching products, subtle changes—particle size, halide odor, chloride content—impact the first step, which often sets the tone for an entire multi-kilo process. The feedback loop between their bench and our factory lines ensures quality doesn’t lag as demand spikes or regulations shift.

    Thinking Forward: Opportunities and Improvements

    Plenty of routine and innovation share space on the production line. There’s growing pressure on all fine chemical makers to move away from harsh chlorination reagents, pushing research toward greener alternatives, less hazardous by-products, and renewable solvent systems. Every trial run at our plant brings opportunities for process tweaks, pilot campaigns with new dehydrohalogenation techniques, or small tweaks to improve throughput or reduce waste.

    We invest in process intensification—continuous flow routes, upgraded distillation systems, and closed-loop waste handling—responding directly to what end users report and what production teams encounter shift after shift. Several batch failures in one year led us to redesign our crystallization chamber’s airflow and automate temperature controls. Tweaks on paper deliver hours saved over quarters, but most important, reduce the unplanned overtime that wears down skilled staff and squeezes margins thin.

    Another forward trend comes from digital tracking and integrated quality systems. Each produced or shipped drum carries QR-coded records back to its batch, allowing customers to trace every physical inspection, test result, and handling incident before the material ever reaches their operation. When a European pigment company flagged a minor trace impurity in an HPLC scan, we traced it back to a supplier’s altered filtration method within two days and corrected it before the next campaign shipped.

    Lessons from the Field: What Customers Teach Us

    The reality of producing and distributing 2-Nitrobenzoyl Chloride is found as much in customer conversations as in reactor vessels. Regular meetings with R&D directors, plant engineers, and inventory managers keep product improvements grounded. They call out small shifts in lot color, trace residue concerns, or late-breaking stability questions, and rely on our direct answer—not a rep’s guess or third-party relay. These loops build ways to anticipate new needs, like smaller packaging options or adjusted crystallinity for novel dispensing equipment.

    Some requests seem minor—an extra desiccant packet, better drum stacking for limited warehouse heights—yet map straight onto production tweaks we adopt permanently. Collaborations with long-term partners streamline development cycles: shared test reports, direct pilot runs, and exchange visits where their chemists stand beside ours for real-time problem-solving.

    Continuous Growth: Building on What Works

    Reliable supply of 2-Nitrobenzoyl Chloride supports diverse chemical industries, far beyond the reach of a single lab or plant. Our experience, honed on the line and sharpened by every unusual request or shipping mishap, pushes us to combine old-school reliability with ongoing modernization. Each day shows new realities: climate-driven shipping routes, evolving compliance requirements, customer batch tracking requests, and shifting global markets.

    All this means 2-Nitrobenzoyl Chloride is more than a specialty compound. For our team, it represents decades of attention to real-world obstacles, from managing tightly sealed, moisture-free drums to tracking batch-level feedback across supply chains. That work supports every researcher, production chemist, and procurement officer who counts on one less thing going wrong in their campaign. In an industry where mistakes are expensive and time is finite, proven, consistent material makes all the difference.

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