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4-Methyl-3-Nitrobenzoyl Chloride

    • Product Name 4-Methyl-3-Nitrobenzoyl Chloride
    • Alias 4-Methyl-3-nitrobenzoyl chloride
    • Einecs 217-720-5
    • 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

    247700

    Chemicalname 4-Methyl-3-Nitrobenzoyl Chloride
    Casnumber 121628-44-0
    Molecularformula C8H6ClNO3
    Molecularweight 199.59 g/mol
    Appearance Yellow crystalline powder
    Meltingpoint 73-77°C
    Boilingpoint 328.2°C at 760 mmHg
    Density 1.39 g/cm³
    Solubility Reacts with water, soluble in organic solvents like dichloromethane
    Purity Typically ≥98%
    Smiles CC1=CC(=CC(=C1)N(=O)=O)C(=O)Cl
    Inchikey MYCHZFJWWHYDJN-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, tightly sealed, labeled with hazard warnings, chemical name, CAS number, and manufacturer details.
    Shipping 4-Methyl-3-Nitrobenzoyl Chloride is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous material, following all relevant regulations. The chemical is transported with proper hazard labeling, accompanied by safety documentation, and stored in cool, dry conditions to prevent decomposition or accidental release.
    Storage 4-Methyl-3-Nitrobenzoyl Chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and direct sunlight. Keep it segregated from incompatible substances such as bases, strong oxidizers, and water. Store under an inert atmosphere if possible, and clearly label the container. Use proper personal protective equipment when handling.
    Application of 4-Methyl-3-Nitrobenzoyl Chloride

    Applications of 4-Methyl-3-Nitrobenzoyl Chloride in Industrial Manufacturing

    Our facility produces 4-Methyl-3-Nitrobenzoyl Chloride for integration into a range of specialized downstream processes. This compound serves as a key intermediate in the synthesis of advanced materials, pharmaceuticals, crop protection chemicals, and specialty dyes. Below, we detail established industry scenarios with supporting standards, formulation ratios, process roles, and representative end products as confirmed by long-term supply relationships with industrial manufacturers worldwide.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antibacterial Agents

    Pharmaceutical manufacturers use this material for acylation steps in the production of quinolone and fluoroquinolone antibiotics, where its molecular structure enables selective reactivity during ring closure transformations. Quality control measures govern impurity profiles and lot reproducibility as set by international pharmacopoeial requirements during API development and validation, ensuring consistent batch-to-batch performance in finished drug substances distributed to the regulated global market.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.), USP, JP standards for finished API
    • FDA cGMP (21 CFR part 211)
    • WHO/ICH impurity guideline Q3A/B

    Typical usage ratio

    • 0.9–1.1 equivalents per substrate molecule in coupling or acylation step; stoichiometry adjusted per synthetic pathway and impurity monitoring

    Downstream process integration

    • Dosed during intermediate amine acylation; introduced under controlled sub-ambient conditions to maintain reactivity and control side product formation in pilot and industrial reactors

    Final product types

    • Bulk quinolone and fluoroquinolone APIs (e.g., norfloxacin, ciprofloxacin)
    • Antibacterial pharmaceutical intermediates
    • Contract-manufactured generics distributed under EU/US DMF registration

    2. Agrochemical Intermediate in Herbicide Synthesis

    Technical-grade applications in crop protection manufacturing rely on the compound as a building block for constructing heterocyclic herbicide actives. Downstream synthesis involves coupling with protected amines or aromatic cores, where dosage and purity determine the environmental persistence and selectivity profile of the resulting active ingredient. Production facilities observe strict batch release criteria to meet both regional and multinational regulatory controls on raw input traceability and final active content in formulated products.

    Industry compliance standards

    • FAO/WHO Good Laboratory Practice (GLP) for pesticide manufacturing
    • REACH (EU) registration for intermediates
    • ISO 9001:2015 for agricultural input manufacturing
    • OECD Test Guidelines for pesticide actives

    Typical usage ratio

    • 1.0–1.2 moles per target scaffold; adjusted for conversion yield during stepwise multistage synthesis

    Downstream process integration

    • Bulk addition in acylation or condensation reactors; monitored introduction to ensure no unreacted chloride persists in downstream formulation

    Final product types

    • Triazole-based and chloronicotinyl herbicides
    • Granular and suspension concentrate herbicide formulations
    • Technical-grade herbicide actives for field application

    3. Specialty Dye Intermediate for Azo and Anthraquinone Pigments

    Manufacturers of high-performance organic colorants utilize this substance as a selective acylation agent to construct tailored dye intermediates, facilitating fine-tuning of chromophore properties required in applications like plastics, printing inks, and electronics. Process controls during large-scale dye manufacture target fastness, heavy metal content, and precise color reproducibility demanded by downstream OEMs for compliance and contract specifications.

    Industry compliance standards

    • EN 71-3 (Toy Safety: Migration of Certain Elements)
    • ETAD Code of Practice for dye stuff purity
    • REACH SVHC restrictions
    • RoHS 3 Directive for electronic applications

    Typical usage ratio

    • 0.8–1.1 equivalents per dye precursor, optimized for yield and minimal color by-product formation in pigment condensation reactions

    Downstream process integration

    • Feed to acylation step in pigment reactor lines, typically under solvent-phase conditions with automated pH and temperature monitoring

    Final product types

    • Azo pigments for high-performance plastics
    • Anthraquinone-based printing inks
    • Color masterbatches for filament spinning

    4. Advanced Liquid Crystal Monomer Synthesis for Electronic Displays

    High-purity grade is employed by liquid crystal monomer manufacturers, where the highly specific chloride group allows for controlled functionalization and elimination during the creation of rigid biphenyl or terphenyl building blocks. This route yields high-clarity, thermally stable liquid crystals needed for advanced display panels. All incoming lots are controlled for trace metal and residual acidity to fit OEM criteria and international electronics quality assurance standards.

    Industry compliance standards

    • IEC 61249-2-21 (low-halogen substances in electronic materials)
    • ISO 9001:2015 certified supply chains for LC components
    • RoHS (Restriction of Hazardous Substances Directive)
    • Internal QC protocols for polarizing film and TFT grade materials

    Typical usage ratio

    • 0.95–1.05 equivalents adjusted per monomer structure, verified by real-time HPLC analysis for ring structure integration efficiency

    Downstream process integration

    • Metered into closed-system reactors during core monomer functionalization steps under anhydrous and inert conditions

    Final product types

    • Biphenyl and terphenyl liquid crystal monomers
    • Specialty display-grade LC mixtures
    • LC modules for TFT-LCD panels and OLED applications
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    Certification & Compliance
    More Introduction

    4-Methyl-3-Nitrobenzoyl Chloride: Background, Use, and What Sets It Apart

    Direct From the Manufacturer’s Floor

    The reality of producing 4-Methyl-3-Nitrobenzoyl Chloride goes far beyond catalog entries and spec sheets. Every batch starts with careful sourcing, precise handling of raw materials, and a focus on reaction control that dictates final quality. This compound, made under controlled chlorination of 4-methyl-3-nitrobenzoic acid, comes out as a pale yellow to light brown crystalline powder. We’ve manufactured it for years, producing for both domestic and global customers who count on consistency in every drum.

    Years of plant experience show that maintaining tight temperature control during chlorination helps cut side-product formation. Small mistakes at this stage affect downstream purity, impacting any further transformations in customer plants. That is why those details, often lost in transaction documents, matter most in the real production environment.

    At our facility, we monitor moisture closely during storage and packaging. Benzoyl chlorides are notoriously reactive with water. High humidity during packaging encourages hydrolysis, not only degrading the product but also making it unsafe to handle due to HCl off-gassing and physical clumping. By engineering dry-air packaging rooms, we preserve the sharp characteristics our customers expect—no pasty residues or failed reactions. Every operator here knows shortcuts cost more than they save.

    Why This Compound Matters in Industry

    4-Methyl-3-Nitrobenzoyl Chloride is not a household name, but its impact runs deep in specialty chemicals, pharmaceuticals, and crop science. Its unique reactivity at both the acyl and aromatic rings sets up clear opportunities. We see most demand for it in custom synthesis, where chemists build complex molecules and want both the activating ability of a benzoyl chloride and the electron-pulling effect of the nitro group, all while retaining a methyl function. These features open up chemo-selectivity adjustments not easy to manage with simple benzoyl chlorides.

    Take pharmaceutical intermediates, for example. Many downstream compounds originate with acylation steps, where unreactive or unstable reagents fail under industrial conditions. The methyl group on the benzene ring shifts electron density, making the nitro-substituted benzoyl chloride more finely tuned in Friedel-Crafts acylations and amidations. End users in R&D labs and pilot plants get higher yields and cleaner separations thanks to narrow by-product profiles. At scale, this saves solvents, time, and costly purification resources.

    Pesticide active ingredient synthesis has also used this compound in fine-tuning substituent effects on biological activity. Early years of manufacturing, we partnered with agrochemical labs for small pilot quantities. Their feedback: acyl chlorides with nitro groups presented handling risks but brought real value in selectivity and overall efficiency at the assay level. Over time, we improved logistical controls, upgrading packaging protocols and shipment stability.

    Typical Model, Specifications, and Real-World Production Notes

    Our core product, 4-Methyl-3-Nitrobenzoyl Chloride, leaves the plant above 99% purity (GC). Each lot carries a moisture level below 0.2% by Karl Fischer titration. These numbers only tell part of the story. We do batch releases only after additional impurity screening for substituted benzoyl chlorides and over-chlorinated derivatives—contaminants not always listed in simplified COAs.

    More than a decade of hands-on production has taught us that true end-user value comes from ensuring not just nominal purity, but eliminating any invisible “wild cards” that threaten downstream reaction profiles. For example, a stray 3,5-dinitro isomer greatly impacts crystallization behavior and can jeopardize an entire run. Our attention to detail in monitoring reaction exothermicity and gas evolution helps consistently sidestep these pitfalls.

    Particle size distribution is another key aspect. Most resellers overlook it, but anyone who has scaled up acylation reactions knows how bulkiness and dissolution rate swing drastically with inconsistent granule size. Our fine-crystalline form is kept within a 45–150 micron median, easing handling and improving dissolving characteristics in both small lab glassware and hundred-liter reactors. We don’t acid-wash or use anti-caking agents that can introduce foreign ions—many other sources ignore these impurities at the expense of user safety or process reliability.

    Careful Handling in Packaging and Shipment

    Transport and storage challenges with benzoyl chlorides have shaped our in-plant protocols. We use air-tight UN-certified poly-liners inside HDPE drums. Each liner is triple-checked for integrity, as any micro-breach invites moisture to start slow hydrolysis. This diligence traces back to several bad industry incidents from years ago— failed couplings and line blockages occurred at customer sites stemming from under-monitored transit packaging. Over time, we moved away from basic bags and laminated jugs, which showed unexpected micro-leaks under long-haul stress.

    Our own logistics staff are trained to spot the early signs of destabilization—slight pressure in the drum, odors, or small crusting that hints at early degradation. An incident with a rival shipment once forced a full reactor cleanup at a pharma plant abroad, costing days in schedule slippage and hundreds of kilos in lost product. Since then, we've added stricter pre-shipment checks and require updated compliance certificates from all in-house staff, not just third-party auditors.

    Sourcing and Sustainability Considerations

    Supply chain pressures over the past decade have shifted how we source starting materials. Since many benzoyl chloride derivatives come from multi-stage processes with nitration and selective methylation, traceability ensures sustained product quality. We source 4-methyl-3-nitrobenzoic acid from vetted local partners who share our commitment to process transparency. This gives us confidence there are no contamination risks from heavy metals or banned solvents, issues that too often haunt poorly regulated suppliers. We routinely audit vendor processes and sample incoming batches before any transfer to production lines.

    While energy consumption in batch chlorination remains higher than other acyl chloride preparations, we've invested in closed-loop systems capturing and treating HCl byproduct. Over time, we moved away from venting and dilution wastes, instead recovering HCl for internal neutralization and offsite recycling—a practice now common among larger producers seeking to limit environmental liabilities. Handling even minor effluents from this synthesis, especially during startups and shut-downs, is no side note; slip here, and compliance bodies sweep in fast.

    Real-World Use Scenarios

    Chemistry departments and development labs often use 4-Methyl-3-Nitrobenzoyl Chloride as a reliable acylation agent. The compound also finds value in building complex molecules like benzamide derivatives or specialty dyes, where nuanced electronic effects allow for distinct chemical pathways not accessible through unsubstituted benzoyl analogs. We have seen requests for customized grades from major pharmaceutical manufacturers that want trace-level impurity certificates. They drive their R&D using our material for new active agents, coupling the acyl chloride with heterocyclic or amino substrates.

    Custom API producers rely on the methyl+nitration pattern that this compound offers, giving direct access to next-step nitroaniline or nitrobenzamide endpoints. They report improved yields and process robustness when using our tight-mesh powder form compared to coarse-grained alternatives. These operational outcomes don’t show up in data sheets, but after years of feedback, we’ve made process modifications based on this kind of real-world user experience.

    Agrochemical customers, who run high-throughput screens on molecule variants, use our product for direct acylations and for creating libraries of analogs in active ingredient research. The right substitution pattern speeds up structure-activity relationship studies, offering them compound diversity without introducing reactive sites that later cause shelf-life or formulation issues. Batch-to-batch consistency matters more in these settings than headline purity, something we learned early on after a major client’s automated system shut down from an input deviation just 0.2% off spec.

    Differences From Other Benzoyl Chloride Derivatives

    4-Methyl-3-Nitrobenzoyl Chloride stands apart from basic benzoyl chloride, 3-nitrobenzoyl chloride, and even the popular 4-methylbenzoyl chloride. Its electron-withdrawing nitro group lowers the ring’s electron density, which in turn reduces unwanted side reactions during acylation or amidation. Compared to 4-methylbenzoyl chloride—widely used for its selective reactivity—our nitro-methyl variant generates fewer by-products with stronger deactivation, making separation and purification steps much smoother.

    The presence of both methyl and nitro in fixed positions gives it a sweet spot between reactivity and selectivity. From a synthetic chemist’s perspective, the nitro exerts a strong meta-directing influence, while the methyl increases lipophilicity, changing solubility and making certain targets accessible that would stall with other substitutions. This is something only those with process visibility—seeing side streams and byproducts, not just the end product—fully understand.

    Basic benzoyl chloride, while cheaper, often triggers side-reactions that complicate production and slow scale-up. Introducing just the methyl group (as in 4-methylbenzoyl chloride) brings benefit in steric effects, but without the nitro, the electronic modulation lacks punch for designer intermediates. We have observed in repeated process validations that the nitro group, as present in 3-nitrobenzoyl chloride, increases compatibility with nucleophiles but sometimes at the cost of process safety and stability. Our compound balances these competing factors, based on actual run histories and numerous customer trials.

    Overdosing on alternative substituted benzoyl chlorides can result in contaminated runs, extra purification burdens, or waste disposal headaches. We routinely walk clients through side-by-side application testing, confirming that our carefully controlled product profile helps them avoid these expensive missteps. Even minor contaminant profiles in competitor products—with as little as 0.3% unidentified peaks in GC—can translate into hours of unplanned labor on remote sites.

    How Industry Feedback Drives Improvements

    Customers running full-scale production — not just milligram synthesis — have unique expectations. We supply pilot plants in pharma and fine chemical fields, where engineers run reaction sequences over weeks. Their feedback tells us more than lab-scale results ever could. A key learning: our packaging, attention to impurity content, and particle size uniformity often count for more than headline purity or cost per kilo. In one case, a client’s step-growth polymerization nearly failed due to a competitor’s higher bulk density grade. By working with production staff directly, we adjusted sieve protocols, yielding a form that dissolved and met feed targets precisely.

    International regulatory landscapes shape real improvement. While not every market enforces the same standards, we supply clients who must meet varying interpretations of purity and impurity reporting—particularly in Europe and Japan. Their compliance teams regularly push us for even deeper visibility on trace-level contaminants and process origins. Instead of treating this as a paperwork routine, we have invested in incremental improvements on onsite analytics and reporting. Reliability in traceability gives our clients an operational advantage over users of lower-grade, inadequately documented products.

    Shipping into regions with harsh climates or extended transport times led us to refine container choices and internal handling instructions. Field reports from the Middle East and Southeast Asia highlight temperature spikes, humidity shocks, and customs storage delays as key threats to chemical stability. Years ago, we faced several instances of visible caking and reduced performance in far-off batches. Each event has taught us to stay vigilant and proactive in process controls—from drum sealing to last-mile loading protocols — and to update our staff training accordingly.

    Supporting Customers Long After Shipment

    Chemical users today want more than box-ticking supply—they rely on regular feedback and troubleshooting from their sources. Our technical support teams connect production chemists directly with plant operators. Frequently, customers require help with downstream process issues, whether during initial reaction setup, during NMR impurity analysis, or while troubleshooting unexpected color changes in their product slurry. Because we are real producers, not intermediaries, our staff can pull up actual batch records and laboratory notes, not just spreadsheet summaries, offering actionable solutions.

    On more than one occasion, clients have reached out mid-campaign about unexpected MS peaks or off-odors from a new run. We review not only the analytics, but also specifics of packing dates, drum numbers, and moisture logs to circle in on the problem without delay. This level of partnership proves critical when a hundred-liter reactor hangs in the balance—chasing mysteries with quick-response data saves genuine production days and resource loss.

    Our in-house chemists conduct annual workshops with preferred users, sharing updated best practices and process improvements drawn from year-to-year plant learning. They cover practical methods: quick-dissolve preparations, stability improvements, handling precautions in humid transition periods, and options for managing any accidental hydrolysis or off-gassing events. This approach, rooted in real production and daily use knowledge, helps long-term customers boost both yield and safety outcomes.

    Building Product Value through Trusted Manufacturing

    In the end, 4-Methyl-3-Nitrobenzoyl Chloride’s true value only comes through deep attention to production realities and customer feedback. Knowing each step—from raw materials to shipping container—matters far more than check-box compliance. As a manufacturer, we live with the consequences of each decision, good or bad. We’ve learned that value comes not just from what’s on a label, but from ongoing commitment to process control, open client dialogue, and continuous problem-solving in real time.

    Through floods and shortages, pandemics and new regulatory twists, the markets keep changing. The only way to stay relevant is by pairing hands-on production knowledge with direct customer support. For 4-Methyl-3-Nitrobenzoyl Chloride, that means sweating the details others skip, and standing with users as both supplier and partner in every campaign. This conviction has shaped not only our product, but also how we see our role in the fine chemical value chain.