Products

3-Nitrobenzoyl Chloride

    • Product Name: 3-Nitrobenzoyl Chloride
    • Alias: m-Nitrobenzoyl chloride
    • Einecs: 209-215-5
    • 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

    710973

    Productname 3-Nitrobenzoyl Chloride
    Casnumber 121-19-7
    Molecularformula C7H4ClNO3
    Molecularweight 185.57
    Appearance Pale yellow to yellow crystalline powder
    Meltingpoint 69-72°C
    Boilingpoint 305°C (decomposes)
    Density 1.49 g/cm3
    Solubility Reacts with water; soluble in organic solvents such as acetone and chloroform
    Purity Typically ≥98%
    Synonyms m-Nitrobenzoyl chloride; 3-Nitrobenzoic acid chloride
    Smiles C1=CC(=CC(=C1Cl)N(=O)=O)C(=O)Cl

    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 3-Nitrobenzoyl Chloride, 25g: Supplied in a sealed amber glass bottle with a secure screw cap and chemical hazard labeling.
    Shipping 3-Nitrobenzoyl Chloride should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It is classified as a hazardous material and must be handled according to regulatory guidelines, using proper labeling and documentation. Transport should be conducted by trained personnel following all safety protocols for corrosive and toxic chemicals.
    Storage 3-Nitrobenzoyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as water, strong bases, and oxidizing agents. Protect it from moisture and direct sunlight. Store in a corrosive-resistant container and ensure proper labeling. Use secondary containment to prevent accidental spills or leaks.
    Application of 3-Nitrobenzoyl Chloride

    Applications of 3-Nitrobenzoyl Chloride in Industrial Manufacturing

    As a direct producer of 3-Nitrobenzoyl Chloride, we serve various specialized industrial sectors. The following scenarios illustrate how manufacturers incorporate this raw material into critical downstream applications under established regulatory systems and technical requirements.

    1. Synthesis of Pharmaceutical Intermediates

    Pharmaceutical manufacturers use 3-Nitrobenzoyl Chloride as a key acylating agent when producing advanced intermediates for APIs, especially in the fields of antihypertensive and neuroactive therapies. The compound acylates amines or alcohols in multi-step reactions, forming nitrobenzoyl derivatives required for constructing complex drug molecules. Staff conduct these reactions under standardized cGMP conditions to ensure batch integrity and traceability. The product’s integration into process stages such as amidation or esterification directly impacts intermediate purity, thereby influencing the API quality.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF Monographs and General Chapters (for related intermediates and process controls)
    • FDA 21 CFR Parts 210/211 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs
    • EU EudraLex Vol 4 GMP Guidelines

    Typical usage ratio

    • 0.8 to 1.3 molar equivalents, based on the limiting substrate in intermediate synthesis. Adjustments depend on reaction yield optimization and minimization of residual chlorides.

    Downstream process integration

    • Utilized in initial acylation steps during multi-step organic synthesis
    • Incorporated as the acyl chloride for preparation of nitrobenzamide or nitrobenzoic ester intermediates
    • Handled within jacketed glass or stainless steel reactors under inert atmosphere
    • Managed with in-process purification and HPLC-based intermediate assessment

    Final product types

    • Precursors for antihypertensive agents (e.g., sartan family intermediates)
    • Intermediates for CNS-modulating pharmaceuticals
    • Benzamide and benzoate-related APIs
    • Process-development samples for FDA/EMA submission batches

    2. Development of Agrochemical Active Ingredients

    Agrochemical manufacturers introduce our material into synthetic pathways for potent herbicide and pesticide actives. 3-Nitrobenzoyl Chloride’s reactivity with amines and phenols supports production of intermediates in urea-, carbamate-, and oxazolone-type compounds. These actives confer selectivity or resistance properties for commercial crop protection products. Facilities carrying out large-scale agrochemical synthesis apply strict environmental and worker-safety monitoring due to the use and disposal of halogenated by-products.

    Industry compliance standards

    • FAO/WHO Recommended Specifications for Plant Protection Products
    • EPA 40 CFR Part 158 Data Requirements for Pesticides
    • REACH Annex XVII Restrictions (for hazardous substance handling and emissions)
    • ISO 9001:2015 Quality Management Systems (for production traceability and release)

    Typical usage ratio

    • Generally 1.05 to 1.20 molar equivalents in acylation steps, controlled for full conversion with post-reaction hydrolysis to minimize residual chloride content.

    Downstream process integration

    • Charged into reaction vessels during intermediate stage acylation of catalyst, urea, or amine functionalized compounds
    • Processed with active cooling and pH control to limit side reactions
    • Crystallization and solvent exchange employed for product isolation before onward formulation
    • Implementation of in-line monitoring to check for complete reaction and minimize environmental releases

    Final product types

    • Herbicide precursors for phenylurea and triazine derivatives
    • Pesticide intermediates for carbamate and benzoxazole actives
    • Active ingredients for crop protection formulations
    • Sample reference standards for agrochemical regulatory dossiers

    3. Liquid Crystal Monomer Precursors for Advanced Materials

    Materials science laboratories and display manufacturers utilize 3-Nitrobenzoyl Chloride when constructing high-dielectric or specialized monomers for use in liquid crystal displays (LCD) and related optoelectronic devices. The nitrobenzoyl group imparts rigid planar structure and electronic polarization, making it suitable for synthesizing aromatic ester or ether monomers. Downstream processing requires high-purity input and controlled esterification, supporting stringent end-use performance and clarity standards.

    Industry compliance standards

    • IEC 61747-1 LCD Standards for Display Devices
    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • REACH Annex XIV Authorization for Use in Polymer Synthesis
    • ISO 9001 for Quality Assurance in Advanced Material Manufacturing

    Typical usage ratio

    • 0.95 to 1.10 molar equivalents with respect to the target hydroxyl or amine compound. Fine-tuned to maximize monomer yield while avoiding by-product coloration or side reactions.

    Downstream process integration

    • Applied in step-growth polymerization for monomer functionalization
    • Involved in esterification reactions producing high-purity LCD monomers
    • Conducted in continuous-flow or batch processes with in-line UV monitoring for color and purity
    • Purification via column chromatography or crystallization to electronic-grade specifications

    Final product types

    • Aromatic ester monomers for LCD alignment layers
    • Liquid crystalline polymer intermediates
    • Photonic materials for optical filters and display matrices
    • High-purity additive for electronic-grade materials

    4. Synthesis of Specialty Dyes and Pigment Precursors

    Dye and pigment producers select 3-Nitrobenzoyl Chloride to introduce nitrobenzoyl functionalities during the preparation of azo and anthraquinone dye intermediates. The compound’s reactivity ensures the accurate placement of functional groups that impact color fastness, solubility, and shade in textile, leather, and industrial coatings. Strict impurity control is enforced throughout the process to achieve consistent chromatic properties and comply with export restrictions on banned aromatic amines.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – Textile Chemical Safety
    • EU REACH Regulation Annex XVII (Aromatic Amine Restrictions)
    • ISO 105-A02:1993 – Color Fastness Testing Requirements
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • 1.00 to 1.15 molar equivalents per azo or amine nucleus, adjusted to balance conversion and minimize excess nitrobenzoyl chloride in effluent streams as per environmental requirements.

    Downstream process integration

    • Participates in acylation of aromatic amines during azo dye synthesis
    • Used in the derivatization and modification phases of dye intermediate creation
    • Production employs stainless steel or glass-lined reactors with temperature and pH control
    • Includes process water monitoring and activated charcoal treatment to capture residual chlorinated species

    Final product types

    • Azo and anthraquinone dye intermediates
    • Specialty pigments for automotive and plastic coatings
    • Reactive dyes for wool and cotton processing
    • Textile printing ink components meeting export compliance

    5. Fine Chemical Synthesis for Industrial Catalysts

    Catalyst manufacturers require 3-Nitrobenzoyl Chloride as a selective acylating agent in the preparative chemistry of organometallic and coordination catalysts. Functionalizing ligands or supports with the nitrobenzoyl group enhances activity, stability, or selectivity in polymerization and petrochemical processes. Precision in stoichiometry and reaction condition control determines the reproducibility of catalyst performance in downstream manufacturing.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Specialty Catalysts
    • REACH registration for substances used in further catalyst production
    • Chemical Facility Anti-Terrorism Standards (CFATS) – for US based storage and handling
    • Responsible Care® Management System for process safety

    Typical usage ratio

    • 0.90 to 1.05 molar equivalents matched to the ligand target. Range controlled for thorough functionalization while reducing reagent excess that may affect catalyst properties.

    Downstream process integration

    • Ligand acylation or modification using controlled addition techniques
    • Employed during pre-catalyst or chelating agent formation steps
    • Integrated into flow synthesis systems for catalyst batch production
    • Post-synthesis purification by filtration or precipitation to ensure high-purity catalyst supports

    Final product types

    • Homogeneous and heterogeneous catalyst intermediates
    • Chelating ligands for polymer and fine chemical synthesis
    • Functionalized supports for petrochemical cracking units
    • Pre-catalyst solutions for laboratory and pilot plant use

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    Certification & Compliance
    More Introduction

    3-Nitrobenzoyl Chloride: Practical Know-How from the Manufacturer’s Side

    Clear Definition, Real Use

    3-Nitrobenzoyl chloride often appears in discussion among those who work with pharmaceutical intermediates, fine chemicals, and advanced materials. Our facility produces this compound under the model number NBC-03, focusing on purity and batch repeatability. As manufacturers, we notice requests for this material often come alongside inquiries about similar halide derivatives, usually with questions about how this product performs and what it means for their next process. Day-to-day, most inquiries focus on active ingredient synthesis, specialty polymers, or dye intermediates. The backbone of its use comes from the marked reactivity of the acyl chloride group joined to a nitro-substituted aromatic ring, which influences many downstream reactions.

    Watching the Chemical Profile

    Once a chemist uses 3-Nitrobenzoyl chloride in a reaction, the aromatic positioning of the nitro group hits home. The meta-nitro placement affects electron-withdrawing and influences both the speed and outcome of acylations, especially versus the ortho or para isomers. What this means in the flask, as we see in analytical runs, is a different product profile and more precise control over side reactions. Manufacturers using this for peptide coupling, for example, find it doesn’t cause the overactivation seen with some more electron-rich counterparts. In our own regular batch controls, we test for appearance, melting point, and purity by HPLC and GC, targeting a purity minimum of 99%, which supports process reliability down our clients’ lines.

    Uses That Matter to Active Synthesis

    Teams in pharmaceuticals ask for 3-nitrobenzoyl chloride because they trust it during the steps to create APIs. Others rely on it in polymer chemistry, where acyl chlorides help anchor desired features or functional groups. Many requests come from projects developing dyes, aramid fibers, liquid crystals, or even agricultural actives. These requests are often tied to tight timelines, and we see the downstream partners seek flexibility: they might test it as an intermediate for new small-molecule leads this month, or in a novel monomer route the next. Our production line adapts to requests for both kilo and ton quantities, with a synthesis route designed to minimize the byproduct formation that sometimes plagues smaller shops working with nitro aromatics.

    Differences from Other Benzoyl Chlorides

    Manufacturers who have switched between 3-, 2-, and 4-nitrobenzoyl chloride quickly appreciate the importance of substituent location. The 3-nitro variant can offer the best reactivity for some coupling chemistry, often without the steric hindrance of the ortho isomer, and less electronic density than the para. By managing production and handling at-scale, we minimize unwanted hydrolysis, a known risk with all acid chlorides. The specific nitro placement also impacts color stability and offers a longer shelf-life in suitable packaging. Over years of experience, we refined our drying and packing processes, using tight-seal lined drums to keep each kilogram in specification until the lids open on a customer’s floor.

    Lessons Learned in Real Manufacturing

    A good example from our lab floor involved a run where the input 3-nitrobenzoic acid started with trace moisture, causing unwanted hydrolysis during chlorination. Our team responded not by tweaking the end-stage, but by rigorously upgrading drying infrastructure upstream. Real-world chemical production always demands respect for seemingly small workflow details—this holds for 3-nitrobenzoyl chloride as much as any fine chemical. Years ago, feedback from one of our dye-manufacturing clients prompted adjustments in our quenching steps, cutting residual byproduct from 0.6% down to less than 0.2%. Every iterative change reflects ongoing partnerships with process engineers solving daily scale-up problems, rather than distant, hands-off suppliers.

    Why Purity and Crystal Habit Matter

    By hands-on standards, the story rarely ends at an assay number. We pay attention to the granular details like polymorphs and batch-to-batch consistency. Variations in crystal habit can affect downstream operations—clogging feed hoppers, producing dust, or slowing dissolution—all issues raised to us by real production chemists running hundreds of kilograms. Through repeated feedback cycles, we dialed product drying and micronizing steps, adjusting sieves and agitating flows. None of these elements appear on a datasheet, but they matter: smoother downstream handling turns a good intermediate into a trusted one. Our in-plant QA team runs parallel trials with customer-supplied handling protocols, updating drying and particle size controls when they see a blockage or a slow flow report come back.

    Handling, Safety, and the Everyday Reality

    Getting 3-nitrobenzoyl chloride from synthesis to shipping takes more than just drums and labels. Each lot requires careful moisture exclusion during inert gas packing. This workday reality is driven by the natural reactivity of acid chlorides with air and water—even minor slips cause off-odors and hydrolysis. We research and measure atmospheric controls, using nitrogen purges and selecting barrier materials that cut down on moisture ingress, based on recorded shelf-life studies and feedback from long-distance shipments. Lab and warehouse workers suit up in gloves and goggles not out of protocol, but out of real experience with splashes or spills that sting and corrode. Our teams developed procedures that catch leaks or pressure build-up before they cause losses, tying procedures to direct lessons learned over repeated campaigns, not theorized from a manual.

    Integration in Downstream Process Chemistry

    We hear from process chemists in peptide synthesis who select 3-nitrobenzoyl chloride specifically to reduce racemization during coupling. Others working in dye manufacture prefer the meta nitro because it tunes chromophore properties and supports stable end-use color. Customers also point out that this nitro derivative offers a cleaner reactivity in substituted aryl couplings than non-nitrated analogs—meaning the purification steps down their own lines are easier and waste is less. Manufacturers using more basic or para-substituted benzoyl chlorides often spend more time removing colored impurities or hydrolysis products. Each feature directly influences the cost-per-batch in actual plant operations.

    Packaging Improvements Born from Experience

    We moved from single-layer bags to double-sealed, lined drums for shipping after evaluating the moisture sensitivity of 3-nitrobenzoyl chloride alongside port weather logs. During a shipment to a coastal client, condensation rendered part of a cargo batch unusable. As a response we instituted a two-stage packaging audit, combined with passive humidity indicators. These quality upgrades came not from abstract requirements, but from listening to customer pain points. While many fine chemicals leave the factory as solids, the handling difference between a low-dusting, properly crystalline 3-nitrobenzoyl chloride and a clumped, powdery mess impacts not only process yields but operator satisfaction and safety.

    Managing Byproducts, Quality, and Waste

    Environmental and workplace safety pressures force responsible producers to rethink their chlorination strategies. Over the past decade, we moved from older thionyl chloride-based routes towards cleaner reagents, focusing on waste reduction. Our investment in scrubber upgrades reflects experience gained during routine plant audits where we recorded SOx vent measurements. Byproducts such as HCl are neutralized in-situ, cutting vented acid output by more than half over five years. For runs making 3-nitrobenzoyl chloride, we recover and reuse solvents wherever possible, integrating distillation columns sized to batch output and staffed by trained operators. Every new order presents an opportunity to further dial in both quality and process efficiency.

    Quality Commitment—Not Just a Slogan

    Having produced thousands of batches, we notice discrepancies that data sheets often miss: slight color shifts, textural changes, unusual odors—all subtle markers of upstream variation. We spot trends using digital batch records and on-site staff with years of training in both the theoretical and practical sides of chemistry. The best outcomes for users always stem from real-world vigilance: regular glassware maintenance, batch records linking raw material lots, and fast response to contamination. We also engage third-party analytical labs for confirmation assays—not as a requirement, but as a check against drift and a builder of trust with recurring clients. These steps allow us to promise—and regularly deliver—material that meets the expectations of demanding process chemists and production engineers.

    Supporting Global Supply Chains

    The global reach for 3-nitrobenzoyl chloride continues to grow, especially as new generics and specialty material projects launch worldwide. As a manufacturer, we have seen a sharp increase in demand from emerging pharmaceutical hubs and specialty polymer plants. Meeting these evolving needs demands not just capacity, but agility—reacting to regulatory changes, REACH guidelines, and customer customizations that go beyond standard material offerings. We work closely with logistics partners to monitor customs issues, transit times, and even container temperature variations, preventing delays or degradation. Teams in our supply chain and compliance offices keep close records on import documentation, realizing how a missed stamp or unreadable label can slow production at a customer’s plant on another continent.

    Comparing Costs and Investing in Improvements

    Constant competition from older, less expensive or poorly controlled product sources challenges every factory manager. Yet over the years, the true cost of off-spec or slow-reacting 3-nitrobenzoyl chloride always catches up—in re-runs, higher byproduct removal, or compliance headaches with disposal. That knowledge led us to invest in new control software, data logging hardware, and faster feedback loops between manufacturing, QC, and customer service. Chemical manufacturing—at its best—relies on a partnership between plant and customer: an ongoing cycle of feedback, troubleshooting, and adjustment.

    Adapting Batch Sizes for Project Needs

    Some customers need tons at a time, filling continuous reactors or long campaign runs. Others want reactive samples for new candidate drug projects, sometimes in just the hundreds of grams to shake down routes and flush out analytical methods. Our team learned not to treat these runs as one-size-fits-all: small-lot synthesis occurs in a part of our site with specialty glass reactors, segregated from the tonnage scale steel reactors that handle bulk orders. This division keeps cross-contamination to a minimum and allows the same material to launch a pilot program in a pharma startup or keep an established production line moving smoothly.

    Developing Custom Grades and Blends

    Certain downstream users want more than standard 3-nitrobenzoyl chloride. We’ve worked with partners who ask for very fine or coarse material, specified through particle size distribution studies we conduct in-house. Others require lower residual solvents, especially those in regulated markets, so we back up every shipment with a batch-specific certificate of analysis and offer supplementary checks by Karl Fischer titration or GC-MS. Still others ask for improved flow characteristics, addressed by small adjustments in crystal habit and drying. No matter the request, every tweak comes from direct dialogue with process engineers, not broad product literature.

    Upgrading Equipment for Cleaner Production

    Over years of experience, a clear truth emerged: handling nitrobenzoic derivatives safely and reliably at scale demands both equipment upgrades and operator retraining. After a 2017 incident where a legacy rubber gasket failed under load, introducing a contaminant, we moved our production lines to Teflon-lined systems. This investment cut product contamination rates by more than 80% across subsequent campaigns and allowed new automation software to track temperature spikes in near real time. These improvements were driven by necessity—more than a few challenging situations in our early days taught us that every dollar spent improving infrastructure pays back in stability and customer trust.

    Practical Advice to the Field

    Succeeding in process chemistry rarely means always sticking to the book. Supply leaders purchasing 3-nitrobenzoyl chloride look for certain critical assurances: closed packaging, reliable delivery, rapid technical support, and responsiveness to urgent production issues. As manufacturers, we adapt repeatedly—changing materials of construction, investing in scrubbers, and shifting production schedules around unforeseen equipment issues or raw material delays.

    Looking Forward: Continuous Improvement in Chemical Manufacturing

    Managing complexity and scale becomes a straightforward exercise in discipline and data. Product lines only thrive through open communication, rigor in every batch step, and attentiveness to client feedback—lessons learned and applied by our team over decades working with demanding chemistries. Owning mistakes, quickly correcting course, and investing in newer, cleaner, safer technology remains our baseline. Every new ton of 3-nitrobenzoyl chloride produced under our roof echoes these lessons, building trust batch after batch, year after year.

    Real-World Outcomes

    Our customers measure success by yield, purity, and simplicity in their own downstream processes. In practice, these goals happen when their 3-nitrobenzoyl chloride arrives with the right reactivity, the correct crystalline structure, and a level of documentation and technical backup that answers questions before they arise. Feedback loops run both ways: as manufacturers, we mature with every production run, every deviation identified, every improvement seeded by close partnership with our partners. Over time, this approach leads to longer relationships, smoother projects, and reliable supply to a marketplace that values both speed and substance.

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