Products

4-Nitrobromobenzene

    • Product Name: 4-Nitrobromobenzene
    • Alias: 1-Bromo-4-nitrobenzene
    • Einecs: 210-804-9
    • 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

    651452

    Cas Number 586-73-6
    Molecular Formula C6H4BrNO2
    Molar Mass 202.01 g/mol
    Appearance Yellow crystalline solid
    Melting Point 125-128 °C
    Boiling Point 299 °C
    Density 1.76 g/cm³
    Solubility In Water Insoluble
    Refractive Index 1.641
    Flash Point 179 °C
    Pubchem Cid 11909
    Smiles C1=CC(=CC=C1Br)[N+](=O)[O-]

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

    Packing & Storage
    Packing The 4-Nitrobromobenzene is packaged in a 100-gram amber glass bottle, labeled with hazard symbols and chemical details.
    Shipping 4-Nitrobromobenzene is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It must be handled as a hazardous material, kept away from heat and incompatible substances, and shipped according to regulations for toxic and environmentally hazardous chemicals. Appropriate labeling and documentation are required for safe transport.
    Storage 4-Nitrobromobenzene should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizing or reducing agents. The storage area should be clearly labeled, and access should be limited to trained personnel. Protect from moisture and direct sunlight to maintain chemical stability.
    Application of 4-Nitrobromobenzene

    Applications of 4-Nitrobromobenzene in Industrial Manufacturing

    As a specialized producer of 4-nitrobromobenzene, we focus on supporting industrial clients in downstream segments that depend on reliable raw material inputs for strict synthesis processes. Below, we outline the key industrial applications where our product delivers defined functional value. Each segment addresses specific industry standards, precise formulation technology, integration steps, and the end-user goods manufactured by our customers.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize 4-nitrobromobenzene as a key halogenated aromatic intermediate in the multi-step synthesis of active pharmaceutical ingredients, particularly nitroaniline derivatives and various heterocyclic compounds. This material enters as a controlled electrophile during nucleophilic substitution or palladium-catalyzed cross-coupling stages, where reaction parameters must comply with Good Manufacturing Practice due to downstream use in regulated medicines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Guidelines for Active Substance Production (EudraLex Volume 4)
    • USP General Chapters for Residual Solvents and Impurities
    • U.S. Drug Enforcement Administration (DEA) List I Chemicals reporting where applicable

    Typical usage ratio

    • 0.6%–2.5% w/w of total batch mass, adjusted according to targeted yield and reaction stoichiometry in intermediate step formations

    Downstream process integration

    • Charged as a starting substrate or coupling partner during initial or mid-stream synthesis stages; typically introduced after solvent preparation, under nitrogen protection, and preceding catalyst addition in Buchwald–Hartwig or Suzuki couplings

    Final product types

    • Fluoroquinolone antibiotic intermediates
    • Oral antihypertensive precursor intermediates
    • Substituted aniline API blocks subjected to downstream hydrogenation and derivatization

    2. Agrochemical Synthesis

    Producers of crop protection ingredients employ 4-nitrobromobenzene in the synthesis of selective herbicide and fungicide intermediates, capitalizing on the electron-withdrawing nitro and bromo groups for regioselective transformation. The compound is utilized during the creation of key aromatic building blocks, particularly in processes requiring high functional group tolerance and consistency to comply with agrochemical production protocols.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Agrochemical Production
    • FAO/WHO Specifications for Pesticide Active Ingredients
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC 1907/2006)
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)

    Typical usage ratio

    • 1.5%–3% by weight of synthesis blend, based on batch scale, molecular yield, and substitution reaction scope

    Downstream process integration

    • Fed into aromatic aromatic nucleophilic substitution, C–N/C–C coupling, or reduction reactions for quinoline, benzimidazole or triazole structure assembly, preceding formulation and packaging

    Final product types

    • Intermediate scaffolds for triazole crop fungicides
    • Key intermediates in selective post-emergence herbicide synthesis
    • Precursors for plant growth regulator compounds

    3. Dye and Pigment Manufacturing

    The dye and colorant industry leverages 4-nitrobromobenzene in the regulated synthesis of dispersion, azo, and anthraquinone dyes. Its introduction provides a functional aromatic base for further derivatization steps, such as reduction to amines or subsequent diazotization, ensuring color strength and uniformity demanded by textile-specification standards.

    Industry compliance standards

    • OEKO-TEX Standard 100 for Textile Chemicals
    • REACH Annex XVII listing for restricted aromatic amines
    • ZDHC MRSL (Manufacturing Restricted Substances List)
    • ISO 9001 Chemical Management for Dye Synthesis

    Typical usage ratio

    • 0.7%–1.8% of total reactant mass per batch; proportion varies based on targeted chromophore intensity and substitution patterns for the chosen dye class

    Downstream process integration

    • Added during the aromatic coupling stage or as a halogen/nitro aromatic precursor, followed by reduction, diazotization, or coupling with phenols or polyaromatics, prior to color strength standardization

    Final product types

    • Bright yellow monoazo textile dyes
    • Disperse dyes for polyester fiber coloration
    • Anthraquinone pigments used in high-performance plastics

    4. Organic Electronic Materials

    Manufacturers in the field of specialty electronics exploit 4-nitrobromobenzene as a monomer or intermediate in the construction of advanced π-conjugated systems for organic semiconductors, OLED materials, and photovoltaic dye-sensitizers. The compound’s defined substitution pattern allows precise incorporation into polymer backbones through palladium-catalyzed coupling, with specifications to ensure electrical and optical purity.

    Industry compliance standards

    • IEC 62899-201: Test Methods for Printed Electronics
    • RoHS (Restriction of Hazardous Substances Directive) for Electronics
    • ISO 14001 Environmental Management in Electronic Chemical Production
    • ASTM F1357 Standard for Organic Semiconductor Materials

    Typical usage ratio

    • 0.2%–1.2% of monomer component in the polymerization reaction; dosage tuned for molecular weight control, polymer chain length, and functional device properties

    Downstream process integration

    • Charged into Suzuki, Stille, or Sonogashira coupling reactions during functional polymer precursor synthesis, preceding device fabrication and layer assembly

    Final product types

    • Precursor blocks for blue light-emitting OLED devices
    • Donor-acceptor type organic photovoltaic active layers
    • Semiconducting polymer chains for flexible circuitry

    5. Specialty Chemical Catalysts

    Catalyst manufacturers deploy 4-nitrobromobenzene as a precursor or ligand substrate in the synthesis of transition metal complexes, given its leaving group properties and functional aromatic structure. These intermediates enable the preparation of highly functionalized metal-based catalysts for fine chemical and pharmaceutical production, where traceability and batch quality must meet industry verification protocols.

    Industry compliance standards

    • ISO 17034 Reference Material Producers Quality System
    • ISO 9001:2015 for Fine Chemicals
    • GHS Classification and Labelling for Intermediate Handling
    • Responsible Care Management System (RCMS) for Chemical Producers

    Typical usage ratio

    • 0.5%–2.0% of batch reactant mass, with exact range dependent on complexation route and target metal center coordination

    Downstream process integration

    • Reacted in aromatic substitution or direct metalation stages for the fabrication of organometallic catalysts; typically fed before ligand exchange and purification

    Final product types

    • Palladium and nickel-based catalytic complexes for cross-coupling chemistry
    • Ligand-stabilized precious metal catalysts for pharmaceutical fine synthesis
    • Pre-activated catalytic powders for hydrogenation and C–C bond formation

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    Certification & Compliance
    More Introduction

    4-Nitrobromobenzene: Insights from the Manufacturer’s Floor

    Direct from the Facilities: What Sets Our 4-Nitrobromobenzene Apart

    As a chemical manufacturer, focus lands squarely on the daily realities of converting raw materials into highly reliable chemicals. In the production of 4-nitrobromobenzene, the smallest detail matters—from the selection of feedstocks to the checks and balances guiding every batch through the plant. The familiar yellow crystals of 4-nitrobromobenzene do more than fill request sheets; they anchor synthetic processes across pharma, agrochemical, and pigment manufacturing. Years of experience—and the daily scrutiny of purity, structure, and stability—form the backbone of our operation with this molecule.

    4-Nitrobromobenzene is known among chemists for its potential as a versatile intermediate. Its molecular formula, C6H4BrNO2, tells only part of the story. There’s a significance in each batch, tied to how bromine occupies the para-position to the nitro group on the benzene ring. This configuration opens direct access into challenging Suzuki and Buchwald–Hartwig couplings. One highlight from our experience: subtle shifts in purification temperature or washing protocol can cause minor color streaking or influence melting point, pointing to trace contaminants that can alter downstream yields for sensitive pharmaceuticals. There’s no substitute for hands-on process management when the goal is a consistently reliable raw material.

    Consistency Under Pressure: Manufacturing Quality at Scale

    Batch monitoring starts with the first drop of bromination, guided by both automation and on-the-ground intuition built over years. Analytical equipment does much of the heavy lifting, but the occasional off-target GC trace proves that checking beyond the readout is worth the effort. In one of the tougher seasons, we traced a quality deviation to a slight mismatch in the nitrobenzene’s supplier source, reinforcing the lesson that upstream quality checks hold as much weight as any internal protocol.

    Our tighter controls yield a 4-nitrobromobenzene typically showing a melting point of 125–128°C, fitting well with what the textbooks list, but it’s not numbers on a page that bring requests from process chemists. Instead, there’s trust built batch by batch—processed with exacting solvent removal, followed by careful storage away from excessive heat and light. In mainline production, stability against light and efficient separation of residual metals after bromination help reduce contamination risks. These controls mean smoother processing downstream, a point echoed by clients scaling their own syntheses.

    From Small Lab Synthesis to Kilo Scale: Adapting to Real-World Demands

    Scaling up always presents a reality check. During kilo-lot production, small changes in stirring speed or cooling rate can magnify discrepancies seen only on large scale. Early in our ramp-up phase, we caught a subtle rise in color impurities traced to a lagging cooling coil. These details seem trivial, but unchecked, they have a habit of reappearing when clients move from gram to multi-kilo synthesis. One can’t rely on procedural memory alone; records guide us, but hands-on troubleshooting catches issues missed by endless SOPs.

    We field questions nearly every week on alternatives and substitutes. Some buyers ask about switching from 4-nitrobromobenzene to isomers such as 2- or 3-nitrobromobenzene. The difference comes down to compatibility with cross-coupling reactions. The para-substituted compound consistently provides superior reaction control, generally affording purer end-products in biaryl synthesis. From years of dialogue with medicinal chemists, it’s clear: switching isomers isn’t just a matter of swapping one molecule for another—subtle electronic and steric effects change the pathway of each synthetic route.

    We’ve often been asked if 4-chloronitrobenzene or 4-iodonitrobenzene could serve as replacements. Chlorinated analogs sometimes reduce cost, but reactions are slower, often giving incomplete conversion, with leftover starting material complicating the work-up. On the flip side, iodo-variants accelerate reactions, but price and supply chain volatility create headaches for inventory managers. Bromine chemistry, sitting between the two, finds a unique sweet spot—allowing predictable reactivity, reliable cost, and stable supply.

    Applications in Pharmaceutical and Agrochemical Synthesis

    Much of the 4-nitrobromobenzene flowing from our lines finds its place in the earliest steps of active pharmaceutical ingredient (API) production. Medicinal chemists value it for building heterocyclic scaffolds where the nitro group serves as a masked amine or a functional handle for further elaboration. For us, it’s not just a matter of hitting purity specs on a COA sheet. If a batch carries residual water or trace halide byproducts, downstream processes using palladium-catalyzed couplings may show inconsistent yields or runaway exotherms. Years of feedback have refined our drying and filtration steps to preempt these issues.

    A handful of agrochemical manufacturers utilize 4-nitrobromobenzene in creating protective agents for crops. Here the requirements may differ in terms of impurity profile, but the overarching need for chemical stability and batch-to-batch reproducibility never fades. By listening to each sector’s process engineers and lab managers, we’ve dialed in specifications that buffer against the adventurous reactions often encountered in agrochemical research and scale-up.

    Navigating Supply Chain Surges & Regulatory Shifts

    Working in the manufacturing space means riding the waves of supply chain disruptions and regulatory reshuffles. A sharp spike in bromine costs a few years back created a scramble across the sector; despite pressures, we kept a steady focus on quality over short-term savings. Our experience shows that cutting corners eventually multiplies costs when key clients run into trouble downstream. Long-term contracts with feedstock suppliers, combined with periodic process audits, have helped us navigate such shocks without compromising either quality or supply.

    Regulatory demands shift every season. Whether it’s new scrutiny on hazardous waste minimization, or evolving best practices for solvent choice, the main challenge is staying ahead without overwhelming the plant floor with paperwork. We’ve found that working closely with environmental engineers early in process design, instead of as an afterthought, significantly reduces rework and keeps the compliance record clean. This ground-level approach supports safer operations while satisfying both local and international customer expectations on traceability and environmental footprint.

    Real Experience: Scaling Up and Handling Byproducts

    Process waste management looms large in any full-scale operation. The classic bromination of nitrobenzene generates hydrobromic acid as a byproduct, and handling it safely is every bit as critical as synthesizing the main product. Years ago, rapid improvement in containment and neutralization protocols reduced workplace exposure and improved plant hygiene, cutting unplanned shutdowns. This focus not only keeps operations running but bolsters long-term productivity—informed by decades of seeing how uncontrolled byproducts eat away at both facility infrastructure and worker safety.

    Improved reactor materials have also made a difference. Early operations dealt with corrosion when using less robust metallic surfaces. Upgrading to lined glass or specialized coatings provided not only longer reactor life but also minimized batch variability. Reducing the risk of cross-contamination—particularly between halogenated intermediates—translates directly into a dependable product for demanding applications. Regular staff training, not just for frontline operators but throughout the support teams, keeps everyone alert to subtle process deviations.

    Collaborating with Chemists: What Matters Most

    Over time, it becomes clear what matters to synthetic chemists buying 4-nitrobromobenzene from a manufacturer, as opposed to a distant trader or distributor. Direct lines of communication let us anticipate concerns—batch-to-batch reproducibility, impurity profiles, and even specifics like particle size for easier handling in automated dosing systems. Listening to recurring headaches from labs, we adjusted our drying and sieving protocols. A smoother-flowing product helped larger customers move from manual weighing to automated feeds, reducing bottlenecks in their own lines.

    Requests for special grades—extra-low metal content or finely tuned particle distributions—often stem from feedback out of R&D groups. Each time our team gets involved in troubleshooting, both sides learn. An example involved tedious filtration issues during a downstream reduction. After working alongside the chemist handling the work-up, we introduced a new filtration pad in our final step and shut down the repeated problem. These collaborations shape tweaks that ripple back through the production floor.

    Why Direct Manufacturing Experience Matters

    Every bottle that leaves our gates embodies hundreds of adjustments made and lessons learned—not just from technical manuals, but from genuine issues encountered at scale. When someone calls about off-spec melting points or unpredictable reactivity, a manufacturer’s response does more than pull from a specification sheet. Each answer comes informed by hands-on troubleshooting, not templated responses. Our records, date-stamped with every deviation, guide the tweaks that lead to the high-performing batches relied upon by our regulars.

    We’ve found that while many downstream users originally looked for the most competitive price, they returned for steady quality and open support lines. Whether the end use involves building a novel pharmaceutical or optimizing a pigment, they count on our operational transparency. A known impurity, flagged and disclosed, impacts planning less than an unexpected ghost in the analytics. That’s why full disclosure and readiness to discuss technical details remain key principles.

    Key Product Attributes: More Than Purity

    A batch of 4-nitrobromobenzene doesn’t draw all its value from purity alone. What consistently draws repeat orders are the factors behind the listed specs: moisture levels low enough to prevent clumping even through humid spells, free-flowing yellow crystals that resist caking under pressure, certificates detailing heavy metal content, and open access to batch-specific analytical data on request.

    Our 4-nitrobromobenzene supports critical reaction types in high-throughput drug discovery, scale-up, and pilot production. As process chemists move deeper into complex targets, batch traceability and consistent analytical support become more important than ever. Knowing the starting material’s full analytical profile—down to traces of dibrominated side-products—eliminates roadblocks during downstream troubleshooting. Our feedback loops with clients ensure quick turnaround when new purity requirements arise.

    Comparing Alternatives: What Chemistry Teaches Us

    No candidate chemical works in isolation. Our most experienced staff field regular questions about swapping in less expensive or more available compounds. With hands in both benchtop analytics and scaled reactors, the differences between 4-nitrobromobenzene, its ortho- and meta-isomers, and analogs like 4-chloronitrobenzene become more than theoretical. The para-substituted compound fits synthetic transformations that require robust yields without the steric struggles posed by other positions. Nothing beats case feedback from clients who ran into troublesome side-reactions with substituted isomers, only to return to our default after exhaustive troubleshooting.

    Product substitution, especially among halogenated nitroaromatics, often trades initial savings for reduced reliability. We’ve seen entire campaign schedules go off track due to unexpected reactivity or new purification demands. From our vantage point, the best approach is to weigh total process impact, not just the headline price of a kilo. Seasoned buyers soon realize that the few percentage points saved at purchase often vanish amid wasted solvent, lost time, or redesigns when reactions underperform. For manufacturers with upstream and downstream oversight, long-term relationships save everyone more headaches than quick market flips.

    Supporting Technical Teams: Transparency and Tailored Support

    Working directly with technical managers and process chemists, we prioritize open access to production and analytical records. Analysis reports, including NMR and GC spectra and impurity breakdowns, go beyond the minimum regulatory checklists. Our own technical teams run challenge batches to stress-test incoming raw materials and outgoing lots. This approach catches potential outliers—crystals forming slower or residual organics at the ppm level—before they leave our warehouses. Experience tells us the small effort up front makes downstream wins easier to capture.

    Knowledge travels both ways. Feedback from customers working on process optimization or scale-up trials often leads us to refine filtration, storage, or packaging—sometimes months before an industry trend becomes widely known. Open feedback keeps our technical and QC teams sharp; it also provides the edge clients need to carry projects across the finish line.

    Looking Ahead: Responding to Industry Challenges

    Supply chain strains, regulatory refreshes, and the drive for more sustainable practices challenge chemical manufacturers to respond quickly. While there’s no crystal ball for predicting the next shift in environmental regulation, factory audits, and deep engagement with raw material suppliers put us ahead of sudden turbulence. Monitoring process emissions and reducing solvent waste have become priorities—in part because long-term partners expect both performance and accountability.

    Recently, digital traceability and automated quality logging tools have joined our daily routines. These investments mean nothing unless the insights drawn at the plant pass directly to the hands of end users. For us, the aim is to build more open relationships, drawing on both process records and problem-solving experience to serve medicinal, agrochemical, and pigment chemists pushing the boundaries in their fields.

    Final Word: Manufacturer’s Commitment

    The expertise baked into every container of 4-nitrobromobenzene reflects decades of direct work in synthesis, production, and quality assurance. Our team’s willingness to tackle new problems, disclose what’s in each lot, and work side-by-side with troubleshooting chemists sets a standard that generic distributors struggle to achieve. The end result is more than a chemical; it’s a reliable foundation for ongoing discovery and scaled production across many industries.

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