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HS Code |
567636 |
| Iupac Name | 1-bromo-2-nitrobenzene |
| Molecular Formula | C6H4BrNO2 |
| Molecular Weight | 202.01 g/mol |
| Cas Number | 577-19-5 |
| Appearance | Pale yellow solid |
| Melting Point | 45-47°C |
| Boiling Point | 272°C |
| Density | 1.74 g/cm³ |
| Solubility In Water | Insoluble |
| Smiles | C1=CC=CC(=C1Br)[N+](=O)[O-] |
| Flash Point | 131°C |
| Pubchem Cid | 11814 |
As an accredited 2-Nitrobromobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 100 grams of 2-Nitrobromobenzene, tightly sealed with a plastic cap, labeled with hazard symbols and chemical details. |
| Shipping | 2-Nitrobromobenzene is shipped as a hazardous chemical, typically packaged in tightly sealed containers to prevent leaks and contamination. It should be transported in accordance with local and international regulations for hazardous materials, including appropriate labeling, documentation, and use of compatible packaging to ensure safety during transit. Avoid exposure to heat and moisture. |
| Storage | 2-Nitrobromobenzene should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizing or reducing agents. Keep the container tightly closed when not in use. Store in a tightly sealed, appropriately labeled chemical-resistant container. Protect from direct sunlight and moisture to maintain stability and prevent hazardous decomposition. |
Applications of 2-Nitrobromobenzene in Industrial Manufacturing2-Nitrobromobenzene serves as a critical intermediate in modern chemical manufacturing, particularly valued for its reactivity in selective halogenation and nitroaromatic synthesis. Our factory supplies this raw material directly to industrial customers engaged in fine chemicals, crop protection, pharmaceutical building blocks, polymer additives, and dye intermediates manufacturing. Below are key application scenarios, detailing industry compliance, usage ratios, integration points, and the types of end products derived. 1. Agrochemical Active Ingredient SynthesisMajor agrochemical manufacturers use 2-Nitrobromobenzene in the production of herbicides and insecticides, especially as a halogenated intermediate in coupling and cyclization reactions. This raw material is frequently introduced in the synthesis of nitro-substituted phenyl ureas and carbamates, where precision in substrate purity and controlled reaction conditions is critical for synthesis yield and downstream plant protection efficacy. Formulators request narrow impurity specifications, given the strict compliance requirements in the crop protection sector. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate for API ManufacturingIn API synthesis, 2-Nitrobromobenzene acts as an essential intermediate for the assembly of substituted anilines and other aromatic systems, forming the basis for several anti-infective, analgesic, and central nervous system drug molecules. Pharmaceutical clients specify tight analytical controls and traceability throughout their procurement and production processes, often requiring material validated to pharmaceutical-grade GMP and full impurity profiling. The reactivity in nucleophilic substitution and Suzuki cross-coupling reactions determines the demand for high purity and consistent batch reproducibility. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Dye Intermediate in Colorant ManufacturingColorant and pigment manufacturers utilize 2-Nitrobromobenzene as a mono-substituted aromatic ring for the production of azo and nitro dyes. This application exploits its dual functional groups for selective diazotization and coupling, resulting in stable, vibrant color properties critical for textile, plastics, and ink industries. Downstream customers demand tight control of residual halogen content and sulfur impurities to guarantee dye solubility and batch-to-batch consistency. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Synthesis for Electronic MaterialsThe specialty fine chemicals sector integrates 2-Nitrobromobenzene as a precursor in the manufacture of high-purity aromatic compounds that serve in liquid crystal, photoresist, and specialty polymer production. These high-end applications focus on the material's ability to enable tailored substitution and direct further functionalization via Suzuki or Buchwald–Hartwig coupling. Customers from electronics and display industries require absolute trace metal and organic contaminant control, as sensitive products demand consistent reaction kinetics and minimal defect rates in end-use electronic components. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Polymer Additive and Crosslinker PrecursorPolymer and resin manufacturers use 2-Nitrobromobenzene in the design of functional additives and reactive crosslinkers, particularly where high-performance, crosslinkable benzene rings are required for heat and chemical resistance. The dual reactivity of the nitro and bromine positions ensures selective incorporation into polymer backbones, offering improved mechanical and ageing properties. End-user sectors such as coatings, adhesives, and advanced engineering plastics specify exact feed ratios and impurity levels for durable, safe, and compliant mass production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Every batch of 2-Nitrobromobenzene we produce traces its roots to decades of hands-on chemical synthesis. Generations of practical experience in handling halogenated and nitrated aromatics built our current approach. Here, the process starts with scrupulous selection of raw benzene derivatives. We take bromination and nitration a step at a time, controlling temperature and reactant addition rates in jacketed reactors equipped with real-time monitoring. Our teams closely supervise acid concentrations throughout, not only for consistency in product but also for reliable downstream reactivity in end use.
In the plant, we tackle not just theoretical yields but also real-world scale-up issues—layer separation, waste minimization, heat management. There’s no substitute for a person in the facility verifying the purity by GC and HPLC, confirming melting point, and watching for byproduct signals. With brominated nitroarenes, these details separate laboratory purity from kilogram-scale viability.
Our most requested line centers on 2-Nitrobromobenzene, molecular formula C6H4BrNO2, commonly known by its CAS number 577-19-5. Typical production lots fall in the range from 25 kg to multi-ton orders. We optimize each run for a GC purity consistently above 99%, lot after lot. Moisture content remains well below 0.2%, as confirmed by Karl Fischer titration—not just because it looks good on a certificate, but because residual water interferes with many synthetic reactions in downstream fine chemicals work.
Our crystalline product stores easily in drums or industrial bulk bags. Color appears as very pale yellow to light tan—variations that reflect differences in the starting benzene feedstock or bromine quality, without affecting end reactivity. We maintain particle size distribution with a goal of reducing dust yet allowing direct weighing into large-scale reaction vessels, helping operators minimize product loss and inhalation risk.
There’s a world of difference between a bottle marked “2-Nitrobromobenzene” and a drum that delivers clean, crystal material, run after run. Unseen impurities impede process development in pharmaceuticals, specialties, and crop science. Off-the-shelf commodity product, sometimes wafting from intermediaries with less attention to upstream controls, can frustrate scale-up. Synthetic routes frequently involve coupling reactions—Suzuki, Ullmann, or other cross-couplings—where trace isomers or heavy-metal contaminants throw off stoichiometry or lead to lower yields.
We avoid those headaches at the source. By keeping sodium and heavy metal contamination below 20 ppm, we maintain the reliability that experienced chemists expect. We work directly with customers at the process development stage, sharing batch certificates, impurity profiles, and—when their route demands—conducting bench-level tests with their other ingredients to ensure compatibility. The goal remains the same: less troubleshooting, more productive lab hours, and fewer surprises on the plant floor.
Much of the 2-Nitrobromobenzene making its way from our reactors finds a place as a versatile intermediate in medicinal and agrochemical synthesis. Manufacturing teams rely on its ortho substitution for targeted aromatic coupling steps. Demand often surges when a new API candidate moves from pilot plant to production, or when a crop protection product enters commercial scale.
Over time, we’ve supported companies making pharmaceutical building blocks—like substituted anilines and aryl amines—through careful amination and reduction strategies. Chemists value the ortho position for creating biphenyls, phenoxides, and fused heterocycles using well-known metal-catalyzed chemistry. Bromine’s reactivity, coupled with the electron-withdrawing nitro group, creates a compound that stands up to multiple transformation steps without excessive side product formation.
We’ve also observed a steady stream of requests from pigment and dyestuff makers. Here, the aromatic backbone and ortho substitution pattern let formulators fine-tune chromophore structures. The brominated nitro ring combines with other groups to produce colorants with tailored absorption, fastness, and solubility profiles.
In the world of brominated nitrobenzenes, position and purity are everything. There are close relatives on the market, including the para-isomer and the 3- or meta- substituted version. Our customers working with ortho-specific processes, especially those involving consecutive substitutions or cyclization, find the 2-position unlocks reactivity no substitute achieves.
Para-nitrobromobenzene, for instance, often fails to deliver the same conversion rates in certain cross-couplings. The electronic and steric effects differ just enough to demand careful selection. Some applications call for 1,3- or 1,4-disubstitution, but our experience in the pilot plant taught us that ortho compounds like ours consistently offer more reliable nucleophilic aromatic substitution performance. Our 2-Nitrobromobenzene grants control when building multi-ring systems, especially with transition-metal catalysis.
Comparing with chlorinated nitrobenzenes, brominated analogs like ours react more rapidly and selectively under most palladium-catalyzed conditions. This lets formulation scientists and synthetic chemists capitalize on higher yields and fewer byproducts. With the rising costs and regulatory pressure facing certain halogenated substrates, we’ve observed our product gaining favor in green chemistry development. It delivers reactivity without requiring excessive reagent loading or specialized apparatus.
Years of close work with this compound’s packing and logistics led us to develop information and protocols that address actual handling risks, not just theoretical ones. 2-Nitrobromobenzene emits only faint odor, but its dust can irritate skin and respiratory tract. We always advise wearing standard PPE and using effective dust collection at charging points.
Our product flows easily in climate-controlled settings, and we designed packaging that withstands regular transport jostling. Bulk formulations never clump into unusable mass, thanks to our drying and sieving steps. We take no shortcuts on labeling and hazard comms—the right information, clearly marked, in language operators use. Warehouse teams who handle large volumes need this material to act as expected, without surprises.
Storage in cool, dry areas prevents hydrolysis and maintains free-flowing crystals. In regions with temperature swings, our seals keep external moisture and oxygen at bay through well-tested liners. Over the years, we’ve helped dozens of clients implement upgrades to storage and transfer procedures, achieving safety alongside efficiency.
Having guided production lines through scale-up failures and batch inconsistencies, we know how ripples start upstream. Minor shifts in reaction temperature or acid strength during nitration cascade into altered impurity sets. If a chemist in a plant receives material from a batch that saw an uncontrolled exotherm, their next reaction may slow, fizz, or yield intractable byproducts. Dryers running slightly too hot risk impacting both color and melting point.
We monitor and record every lot, and through years of feedback from pharmaceutical and agrochemical process teams, updated our reactors, automation, and QC checkpoints. Overlooked batch variation costs time and raw materials at each stage downstream, so we maintain strict controls and run in-house pilot tests before moving to customer-scale deliveries.
As more manufacturers worldwide shift to GMP and ISO-driven production, they seek sources who demonstrate traceability and awareness of batch-to-batch reliability—not just statistical averages but quantifiable, reproducible results. Consumers of 2-Nitrobromobenzene, especially in regulated industries, have no tolerance for last-minute surprises. We back every batch with archived analytical data and retain samples to resolve any issue quickly.
Our team learned early the value of working directly with process chemists. Sometimes a reduction fails in a pharma lab, or a metal-catalyzed coupling falters. Root cause often comes down to a sub-spec impurity or an unforeseen physical property. We developed our protocols not to satisfy checkboxes on a document, but to ensure the researchers, plant operators, and production managers can actually run the chemistry they need smoothly at scale.
For those with specific particle size or custom purity targets, we run tailored crystallization or micronization steps. This approach evolved after years of troubleshooting in partnership with some of the best process development teams across North America, Europe, and East Asia. It doesn’t just solve a single problem; it builds trust for future campaigns, whether scaling to metric tons or producing pilot batches for a specialized intermediate.
Sometimes, adjustments go beyond the material itself. We work with customers to test packaging that suits their transfer systems, supply certificates of analysis matched with their regulatory compliance needs, and consult on optimal storage strategies. These are the practical details that decide whether a material will integrate into a complex, multi-step sequence or get stockpiled and sidelined.
Many of our long-term partners ask about trends with synthetic aromatics and regulatory landscapes. We notice increasing attention on sustainable chemistry, especially pressure to minimize halogen waste and reduce byproduct streams. Fortunately, 2-Nitrobromobenzene fits new, milder catalytic activation protocols, letting users hit output targets with cleaner profiles.
The pharmaceutical sector shows strong demand growth as new patent applications for complex APIs emerge—each requiring robust, reliable intermediates. Speed to market has become paramount, and that puts focus on suppliers able to deliver not just one-off shipments, but stable supply through the entire R&D and launch phase. Shortages or unplanned substitutions grind expensive projects to a halt, so consistency and lot traceability now hold equal weight to chemical purity.
In agrochemicals, product stewardship grows in importance. Reliable 2-Nitrobromobenzene lets developers focus on efficacy and environmental fit, instead of revalidating every shipping source. In pigments and dyes, small spectral shifts driven by undetected impurities mean lost batches or regulatory pushback. Many of our buyers now integrate supplier qualification as tightly into their own quality systems as any manufacturing step.
Years working on the factory floor, not just in R&D labs, taught us that real progress in chemical manufacturing comes from problem-solving and collaboration. Every time a batch passes QA not just in our lab, but in a client’s pilot vessel, it validates all the small process choices behind the scenes—steps such as investing in filtration upgrades, deciding between drum liners or bulk bags, tweaking crystallization cycles.
Our facility staff lead continuous improvement meetings, reviewing feedback from customer returns or unusual lab analysis, and comparing with outcomes in long-running partnerships. The direct producer’s perspective resets not only how we measure growth, but also how we communicate about our products. Transparent discussions about lot-specific analytical results, impurity fingerprints, and even shipment anomalies ensure stronger industry relationships.
Direct feedback cycles between manufacturing and users shape future batches—reducing process variability and driving specification improvements. This hands-on approach, open to adaptation, shapes our reputation with customers and brings mutual success.
At the end of every production campaign, our work stands not just in product delivered but in chemistry performed. We see the results not just in data sheets but in how smoothly our 2-Nitrobromobenzene works in the hands of customers, in their campaigns for new molecules, in time saved for plant teams, and in actual kilogram yields. Our experience shows that care at every process step—from raw materials to final packaging—delivers the most consistent, reliable product for competitive, global industries.
By keeping our focus steady on hands-on, real-world synthesis, we bring value that goes beyond the standard product listing. Building direct relationships with users, responding to process challenges, and learning from every run—these actions ensure the success not just of a batch or contract, but entire production pipelines. For anyone needing high-performing, consistent 2-Nitrobromobenzene, this is the difference a manufacturer delivers.