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HS Code |
697118 |
| Cas Number | 585-55-5 |
| Molecular Formula | C7H4BrNO3 |
| Molecular Weight | 230.02 |
| Iupac Name | 3-nitrobenzoyl bromide |
| Synonyms | m-Nitrobenzoyl bromide |
| Appearance | Yellow to orange solid |
| Melting Point | 57-60°C |
| Boiling Point | 312°C |
| Density | 1.74 g/cm3 |
| Solubility | Decomposes in water; soluble in most organic solvents |
| Pubchem Cid | 11682 |
| Ec Number | 209-562-3 |
As an accredited 3-Nitrobenzoyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Nitrobenzoyl Bromide, 25g: Supplied in an amber glass bottle with a secure screw cap and tamper-evident seal, labeled with hazard information. |
| Shipping | 3-Nitrobenzoyl Bromide is shipped in tightly sealed containers, under cool and dry conditions, away from direct sunlight and incompatible substances. Proper hazardous material labeling is required due to its corrosive and toxic nature. Transportation complies with local and international regulations for hazardous chemicals to ensure safe and secure delivery. |
| Storage | 3-Nitrobenzoyl Bromide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong bases, oxidizing agents, and water. It should be protected from light and sources of ignition. Use secondary containment and clearly label containers. Store at room temperature or as specified by the manufacturer’s guidelines. |
Applications of 3-Nitrobenzoyl Bromide in Industrial Manufacturing3-Nitrobenzoyl Bromide serves as a critical intermediate in multiple specialized chemical manufacturing processes. Direct customers in the pharmaceutical, agrochemical, colorants, and polymer industries rely on its specific reactivity and functional group modification capabilities to drive downstream synthesis and formulate unique end-use products. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers utilize 3-Nitrobenzoyl Bromide as an acylating agent in the synthesis pathway of non-steroidal anti-inflammatory drugs (NSAIDs), antibacterial compounds, and other APIs. Precise coupling with amino or hydroxyl-containing intermediates enables the formation of benzamide and ester derivatives. Maintaining strict trace impurity control, process engineers dose the material into batch reactors under chilled, anhydrous conditions to achieve high-purity intermediates for regulated final APIs. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingAgrochemical formulators employ 3-Nitrobenzoyl Bromide in synthesizing herbicidal and fungicidal precursors based on substituted benzoyl moieties. The reagent reacts under controlled temperature and inert atmosphere conditions with heterocyclic or aromatic amines, creating stable intermediates for further transformation. Stringent monitoring of byproducts, such as inorganic bromides, ensures compliance with downstream purity standards and regulatory thresholds for crop protection chemicals. Industry compliance standards
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3. Specialty Dye and Pigment ManufacturingProducers of specialty dyes and pigments incorporate 3-Nitrobenzoyl Bromide during the construction of nitro-substituted aromatic scaffolds. The bromide acts as an acylating agent with primary aromatic amines or phenols to provide specific chromophore frameworks, supporting dispersion stability, lightfastness, and intense coloration. Tight control over side reactions and bromide byproduct removal underpins meeting quality requirements for advanced colorants destined for plastics and textiles. Industry compliance standards
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4. Liquid Crystal Polymer (LCP) Monomer PreparationChemical engineers in high-performance plastics utilize 3-Nitrobenzoyl Bromide for functionalizing aromatic diol and diamine monomers, essential in producing tailored liquid crystal polymers. The reagent facilitates targeted acylation, precisely building monomers that impart dimensional stability and heat resistance in polymers. Process chemists rigorously monitor residual bromide and nitro impurities to conform to polymer-grade monomer specifications used in electronics and automotive sectors. Industry compliance standards
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Every chemical we produce carries the fingerprint of hard-earned knowledge. 3-Nitrobenzoyl Bromide offers a great example. We have watched its role shift and expand as specialty chemical applications demand more nuanced reactivity and purity. Decades on the shop floor and in the lab have taught us that synthesis runs do not pardon short-cuts. Because this compound finds its way into pharmaceutical research, dye intermediates, and fine chemicals, reliable production means keeping every critical factor in check—from the grind of starting materials to moisture management. Our systems for producing 3-Nitrobenzoyl Bromide avoid the batch-to-batch inconsistencies that sometimes crop up in trading stock or repackaged lots. We stick fastidiously to high-purity standards because weaker grades turn up as headaches later in the synthesis chain. This is not just about compliance but usability for real chemists, so every batch faces strict QA with full documentation.
Product consistency starts with accessible, predictable materials. Our 3-Nitrobenzoyl Bromide, known in the shop as batch model NB-ZB193A, consistently tests above 99% by HPLC. The compound flows as off-white crystalline flakes, denser than the yellowish hues some resellers offer. That color difference rarely shows up in casual visual checks but comes clear during solid-state NMR or melting point analysis. Our teams chase out even slight process contaminants, including unreacted bromide or ortho-nitro byproducts. We track free acid numbers, examine water content by Karl Fischer, and batch-release nothing that fails strict IR fingerprinting. Moisture can cascade into hydrolysis downstream, so we dry and package under argon. Over the years, customer feedback has confirmed that our packaging—amber glass under vacuum seal—prevents the caking and clumping that sometimes turns up in loosely wrapped alternatives.
Applications drive every decision in synthesis. For 3-Nitrobenzoyl Bromide, researchers and process chemists usually want it for acylation and coupling reactions. It fits with nucleophilic substitution chemistry, offering a route to prepare amides, esters, and a range of fine intermediates for agrochemicals or pharmaceuticals. Over the years, requests have come in for downstream compatibility reports: which solvents carry the compound best, what temperatures keep unwanted reactions at bay, which labor-saving devices handle this product safely. Our internal data and client feedback show that using tightly dried dichloromethane and running reactions at temperatures below 40°C limits hydrolysis or side-reactions. In scale-up, yield stumbles often trace back not to the main reaction but to the mishandling of storage or small but critical variable in the starting material. Our own R&D teams have found that tight temperature controls inside glovebox synthesis, and pre-dried glassware, reduce batch losses.
Experience in production has forced us to respect how fragile 3-Nitrobenzoyl Bromide can be once exposed to humidity or unwashed processing lines. We have seen both minor impurities and trace moisture tip entire kilo-scale runs into expensive reworks. It doesn’t matter how well a reaction sequence looks on paper—sloppy handling at the initial acyl halide step invites emergency calls and wasted projects. We have driven hard on staff training and batch traceability. The presence of unseparated o-nitrobenzoyl bromide or unreacted starting acid usually shows itself during the first attempted acylations downstream. Laboratories confirm this before we do—nobody wins when that happens. We document every step of the drying, packing, and storage regime, with a sharp eye on even routine maintenance work. This vigilance maintains the confidence customers need, especially for regulated end uses.
One of the questions we get from project chemists circles back to the difference between 3-Nitrobenzoyl Bromide and its relatives like 4-Nitrobenzoyl Bromide or plain Benzoyl Bromide. After years on the line, we see these distinctions play out in steric demand, reaction pathway predictability, and environmental residue profiles. The 3-nitro group on the aromatic ring not only shifts electronic density but tunes the rate at which nucleophilic substitution occurs. That slight change sharpens selectivity when incorporating this compound into heterocycles or nitrogenous APIs. We’ve tracked dozens of pilot runs and see slightly higher yields for certain amino acid derivatives when the meta-nitro is used, compared to the para-substituted compound. Chemists who try to swap out other benzoyl bromides sometimes report sticky emulsions or incomplete conversions. We have developed a library of comparative data, showing not just reactivity changes but how these products behave in real-world glassware or reactors.
Sales talk often focuses on purity, but what arrives at the customer’s dock deserves equally close scrutiny. Industry experience taught us early to never take packaging or transit lightly. Bromide-based acylation agents show a strong tendency to degrade or clump if they see ambient air or stray solvents. We spent years working with both freight handlers and lab partners, trialing multiple packaging geometries. Only amber bottles—double-sealed and vacuum-wrapped—have passed the real test. Reports from customers confirm that product pulled straight from our packaging holds true to analysis, versus the partial decomposition often seen from sources that skimp on moisture barriers. We tested shipping profiles through three seasons, including high-temp transit, and keep backup plans for long-distance deliveries. This attention pays off with solid customer trust and fewer post-sale headaches for both sides.
Production brings its share of hazards. We owe a safe workplace not only to our staff but to downstream users as well. Years of small incidents drove us to double down on closed-system transfers, real-time air monitoring, and rigorous personal protection protocols. The pungent, lachrymatory nature of 3-Nitrobenzoyl Bromide means even minor leaks are swiftly detected and handled. In the plant, we draw from supplier material data but overlay that with lessons learned in the real world, such as valve and seal selection or quick-response containment drills. Our environmental protocols include thorough solvent capture and scrubbing, not just for compliance but for genuine ecosystem protection. We collect feedback on product hazard management from users and adapt procedures to suit not just our lab, but typical research or pilot plant setups found in customer operations.
Modern chemical businesses run on reliability. Past experiences with third-party intermediates showed us the need to keep tight, nearly end-to-end control over supply. Not every trading company holds the same documentation or oversight—batch mixing sometimes wipes out subtle, hard-earned process controls. We choose raw material suppliers by full-spectrum audit and require consistent COA documentation beyond ordinary thresholds. Regular dialogue with research partners gives early warning if contamination or batch inconsistency ever slips through, letting us solve problems before they turn into lost time or revenue. Our full traceability model indexes every step from raw material intake to final QC signoff and outbound shipment. By involving customers in our review cycle, we foster genuine working partnerships, not just transactional delivery. Trust builds best where transparency is part of daily operations—customers know who made each batch and why it arrived as ordered.
Years at the intersection of manufacturing and research have taught us never to stand still. Emerging application fields—whether in peptide conjugation, advanced pigment synthesis, or agrochemical innovation—bring new challenges for the acylation sector. Customers come with synthesis puzzles, often driven by novel regulatory restrictions or process retooling. Our role as a producer means direct adaptation, not just a menu of existing product codes. We have redesigned batch sequences, tweaked drying curves, and reworked reactor throughput to answer calls for faster delivery or alternate solvent compatibility. Customer-centric technical dialogue helps us anticipate demand waves, such as rising interest in green chemistry or changes in waste management. As protocols in pharmaceutical labs move away from high-chloride waste or single-use solvents, our production team supports test runs with new packaging, allergen-free options, and higher-barrier shipping materials. The learning goes both ways: challenges in scale-up show up first at the production line, not in back-office meetings.
One aspect the chemical world often underestimates is the role of technical support that comes from real production, not just a customer service script. Over years of tough reactions and troubleshooting, our teams have talked through every scenario: failed coupling reactions, clumped deliveries, yield drops after a wet winter shipment. In-house chemists and production workers pool daily practical know-how. That feedback cycle drives updates to both process and customer guidance—no generic advice, just facts born from doing. This depth of understanding means that phone advice is based on experience, not documentation alone. The best feedback loop happens when users in the field share their experience with unexpected byproducts or scale-up hitches; we log that knowledge and it changes how we produce and describe 3-Nitrobenzoyl Bromide tomorrow.
Real-world production never settles. The market and science throw up new challenges every season. Our process engineering team tracks not only current purity but identifies changing impurity profiles as upstream suppliers adjust plant operations or feedstock sources. Shift teams notice patterns in production downtime, bottlenecking, or solvent usage. This awareness led us to rework how raw nitric acid is handled, optimize bromination cycles, and reduce batch times without spiking by-products. We cross-check each improvement by trial-run batch records, pure bench chemistry, and direct customer collaboration. The resulting process doesn’t just yield a certificate for the file drawer; it delivers more usable material for end users.
Standards change over time. We watch regulatory advisories and export trends to avoid surprises. Some global markets now require even more rigid halide content limits or restrict certain solvents in production. Because we carry full-step batch records, we can pivot and meet those requirements. We have been part of industry-wide trace impurity studies for 3-Nitrobenzoyl Bromide and have provided anonymized samples for inter-laboratory comparison. Maintaining this transparency reduces risk for customers, who work in ever-tighter regulatory frameworks on their end. They rely on knowing actual lot data, not just a target spec. Direct dialogue also highlights overlooked end-user concerns—like the desire for downsized packaging to reduce material waste, or for reformulated dust-suppression to fit new air quality laws in certain jurisdictions. Staying responsive means our production always reflects not just internal best practice but active, two-way communication.
Long experience in chemical manufacturing shows innovation doesn't come from theory alone. We run pilot programs, sometimes funded by cooperative R&D, testing new uses for 3-Nitrobenzoyl Bromide inside fluorescent dye chemistry or enzyme inhibitors. Discovery always brings hiccups, from odd reactivity profiles to new side-reaction spectra. Our success relies on using cumulative plant experience along with collaboration from end users, who report back with clear eyes on what works in scale, not just at the bench. With increased demand for specialty benzoyl bromides in high-purity form, our teams evaluate emerging synthetic routes that minimize hazardous byproducts and simplify downstream purification. The learnings from each run update our protocols, and no improvement remains hypothetical—everything must survive the reality check of scaled production and actual customer workflows. This tight cycle between production and R&D generates the niche expertise that trading companies or distant brokers rarely provide.
In two decades of making specialty intermediates, our reputation has not survived on paperwork but on production that delivers—batch after batch, season after season. Every lot of 3-Nitrobenzoyl Bromide carries the weight of repeated feedback: yields that match the promise, packaging that protects, support that solves real-lab setbacks, and records that prove what’s inside. It’s not marketing that earns trust in this business, but a grounded, experience-driven commitment to better material. Customers know the difference after just one shipment—the proof is always in the reaction flask.