Anhui Liwei Chemical Co., Limited
Products

4-Bromo-3-Nitrophenol


    • Product Name 4-Bromo-3-Nitrophenol
    • Alias 4-bromo-3-nitro-1-hydroxybenzene
    • Einecs 246-362-3
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    226892

    Productname 4-Bromo-3-Nitrophenol
    Molecularformula C6H4BrNO3
    Molecularweight 218.01 g/mol
    Casnumber 4195-98-4
    Appearance Yellow crystalline powder
    Meltingpoint 140-144°C
    Density 1.95 g/cm³
    Solubilityinwater Slightly soluble
    Purity Typically ≥98%
    Smiles C1=CC(=C(C=C1O)Br)[N+](=O)[O-]
    Inchi InChI=1S/C6H4BrNO3/c7-4-1-2-5(9)6(3-4)8(10)11/h1-3,9H
    Ecnumber 224-083-7

    As an accredited 4-Bromo-3-Nitrophenol 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 of 4-Bromo-3-Nitrophenol, sealed with a tamper-evident cap and labeled with safety warnings.
    Shipping 4-Bromo-3-Nitrophenol is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be labeled according to hazard regulations and transported as a hazardous chemical, complying with international and local laws. The package must be handled with care and accompanied by a safety data sheet (SDS) for safe handling instructions.
    Storage 4-Bromo-3-nitrophenol should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it separated from incompatible substances such as strong oxidizers and strong bases. Proper labeling is essential. Personal protective equipment should be used when handling to prevent inhalation, ingestion, and contact with skin or eyes.
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    Certification & Compliance
    More Introduction

    4-Bromo-3-Nitrophenol: Chemical Details and Application Insights

    Introduction to 4-Bromo-3-Nitrophenol

    Everyday work in chemical manufacturing demands more than a passing understanding of the building blocks we supply. 4-Bromo-3-Nitrophenol (CAS 17692-56-9) has grown into a specialty intermediate recognized in several sectors, especially pharmaceuticals, advanced material research, and agrochemical development. Over years at our facility, we have seen the shift in demand for high-purity derivatives such as this, primarily driven by tighter process controls and the move toward more sophisticated synthesis routes.

    With the chemical formula C6H4BrNO3 and a molecular weight of approximately 218.01 g/mol, this compound comes as a yellow crystalline solid, a typical attribute resulting from both nitro and bromo substitutions on the benzene ring. Our batches regularly yield crystals with a melting range between 114–118°C, as verified in routine quality assurance runs. These physical traits, though simple at the outset, define crucial handling and application protocols for both bench-scale chemists and large-scale processors.

    Manufacturing Approach and Quality Control

    Our team synthesizes 4-Bromo-3-Nitrophenol through controlled bromination and direct nitration of phenolic precursors. Long experience has shown that careful stoichiometry and purification steps create a product that meets the strict purity levels demanded by downstream users. Finished material usually carries a purity of 98% or higher, a requirement for advanced pharmaceutical synthetic schemes.

    Routine HPLC and GC analyses, as well as NMR verification, confirm both structure and purity details. Particle size distribution affects reactivity in batch reactors and must fall within a defined range to ensure consistent downstream processing. We invest in proper filtration and crystallization, knowing that uniformity not only reduces customer complaints but also improves our processing yields over time.

    Applications and Real-World Usage

    As manufacturers, we rarely look at a product as just another SKU. 4-Bromo-3-Nitrophenol emerges in our production line not as an end but as an important step toward other valuable molecules. In pharmaceutical labs, chemists use this compound as an intermediate during synthesis of biologically active targets. Nitro and bromo substituents serve as reactive sites, offering flexibility in a variety of coupling or substitution reactions.

    Agrochemical innovators use it for the development of novel herbicides and related molecules. The nitro group often increases the binding affinity for biological receptors, while the bromine atom can tune compound stability. 4-Bromo-3-Nitrophenol also stands out among analytical standards and dye intermediates, owing to its robust chromophore—a benefit for spectroscopic detection.

    Researchers working on heterocyclic scaffolds and ring transformations routinely ask for this particular substitution pattern. Our technical support team receives requests for advice on reactivity and compatibility with modern catalysts, whether for Suzuki couplings or nucleophilic aromatic substitutions. By working closely with R&D chemists, we continue to optimize our process to minimize impurities that may interfere with scale-up or cause headaches in purification steps during later syntheses.

    Comparison with Other Phenolic Derivatives

    The phenol derivatives family covers a wide landscape, yet substitution patterns dictate much of their behavior. In the lab, our experience shows that replacing the bromo or nitro groups with alternatives—such as chloro or methyl—alters both the reactivity and safety handling profile. For instance, 4-Bromo-3-Nitrophenol shows improved selectivity in certain cross-coupling reactions compared to its chloro-analogue, owing to the higher reactivity of the bromo group under palladium catalysis.

    On the other hand, if a user switches to 2-bromo-4-nitrophenol, the position of the substituents changes steric and electronic characteristics, sometimes influencing yields or by-product formation. Our feedback records from repeat customers underscore the importance of batch consistency, because even minor differences from other suppliers result in failures during scale-up.

    Unlike 4-nitrophenol or 3-nitrophenol, the 4-bromo-3-nitro substitution provides a two-point activation for further derivatization. Synthetic chemists often leverage this pattern as a gateway for more intricate molecules in the design of therapeutics or agricultural chemicals. The balance of electron-withdrawing and halogen effects gives the compound unique attributes that alternatives cannot always provide.

    Handling, Storage, and Regulatory Observations

    Commercial production of 4-Bromo-3-Nitrophenol demands careful attention throughout every stage of synthesis and packing. The solid releases dust easily, so all open-handling areas require proper local exhaust and dust management. Our packaging lines seal the final product under inert atmosphere in multi-layer containers, ensuring a long shelf life and steady performance in the customer’s facility.

    Customers rarely encounter degradation if they keep the material away from strong bases or excessive moisture. We maintain temperature logs during both storage and shipping, which gives our quality group the track traceability to flag any accidental exposure during transit. Our clients repeatedly cite batch traceability and the attention to detail in packaging documentation as key reasons for long-term partnerships.

    Regulatory compliance shifts frequently, especially as authorities tighten oversight of intermediates with potential toxicity. Our compliance officers maintain a dossier of all applicable registrations and studies on environmental safety, so end-users face no surprises during audits or customer due diligence. Each outgoing shipment receives certification tied to production batches, ensuring full documentation for quality and safety teams.

    Challenges in Consistency and Purity

    In actual day-to-day operations, delivering consistently high-purity material forms the backbone of repeat business with R&D and manufacturing clients. Typical issues stem from residual brominated or nitrated by-products, while unreacted phenol traces could upset catalysis in sensitive processes. Our chemists regularly sample each reactor batch and adjust flow and temperature to limit over-reaction.

    Batch failures usually trace back to fluctuations in reagent quality or slight changes in water content. Over the years, we’ve put greater emphasis on robust supplier audits and routine lot sampling for all incoming raw materials. Automated monitoring technology in our plant lowers the occurrence of out-of-spec products, but in rare cases where a deviation occurs, we initiate full-scale investigations.

    Another challenge comes from scale-up runs commissioned by larger customers. Small differences in mixing or crystallization conditions can magnify impurity profiles. Meanwhile, endpoint detection for the bromination and nitration steps often means the difference between a smooth end-of-batch report and costly rework. By sharing lessons across our technical teams, we continually fine-tune conditions, knowing the impact of even short shutdowns on downstream supply chains.

    Emerging Applications and Market Feedback

    Feedback loops between our production group and users drive changes in how we work and what we offer. Researchers in materials science started requesting different micron sizes for thin-film applications, so we developed secondary processing steps with finer particle mills. In dye and pigment synthesis, we noticed a rise in demand for small-lot orders with documented history of contamination checks, especially for use in high-spec textile or ink formulations.

    Pharmaceutical clients have pressed for ever-lower tolerances on heavy metal residues, pushing our labs to adopt new purification technologies, including column chromatography and ion-exchange polishing. The dialogue with practitioners has resulted in faster release forms for some applications, including tailored packaging adapted for automated dosing equipment.

    Anecdotal reports from research teams have illustrated where poorly characterized lots had ruined months of synthetic work, especially in routes that depend on clean leaving groups for cross-coupling. This highlights the importance of technical transparency—batch chromatograms, impurity listings, and analytical data packages now accompany every shipment. As a result, we observe fewer quality-related queries and less process downtime for our customers.

    Toward Improved Sustainability in Synthesis

    For most specialty chemicals, sustainability has moved from a marketing point to a production requirement. Solvent recovery and waste minimization represent practical changes we made after regular review of our environmental metrics. For a time, bromination relied heavily on non-recoverable halogenated solvents. Now, we reclaim most of the process stream, sending less hazardous material downstream.

    Our process designers work closely with environmental engineers to cut waste, such as by optimizing molar excess and minimizing bleed of starting phenol derivatives. Periodic investment in exhaust and effluent treatment guarantees compliance, avoids fines, and upholds our obligations to the surrounding community. Over several years, measurable reductions in chemical consumption have also translated into lower costs for our users.

    Collaborative projects with research institutions help us identify greener catalysts for phenol functionalization. While challenges persist—such as the sometimes-slower reaction kinetics of new “green” processes—we find that dedicated attention to these changes expands available market opportunities, particularly among companies actively tracking their own environmental footprints.

    Supporting R&D Partnerships and Custom Solutions

    Our technical team values dialogue with synthetic chemists working at both the discovery and pilot-plant stages. Unique needs often arise, such as requests for isotopically labeled materials, solutions with precise concentration, or lot-based purity guarantees. Direct conversations lead to tailored production runs, and we regularly produce controlled impurity profiles or material user-formulated to exact research needs.

    Thanks to in-house production, we respond quickly when pilot plant partners encounter bottlenecks or require real-time feedback on formulation changes. Our analytical lab supports customers with on-call consultation for reactivity, safety, and troubleshooting unexpected by-products. These two-way relationships underpin a development culture inside the plant, where feedback reaches both plant operators and process engineers without the noise of layers between supplier and client.

    For academic teams, especially those working on grants or time-limited contracts, short lead times and clear technical documentation save projects from delays. We prioritize shipping of small lots for bench-scale users, making adjustments in packaging size and temperature controls to align with their storage capacities.

    Health, Safety, and Staff Training

    Working with phenol derivatives brings specific risks—skin, eye, and respiratory irritation can occur with improper handling. Our process engineers work closely with plant operators, providing ongoing safety training and regular hazard reviews. Updated safety data, including guidance on fire and spill responses, is distributed to every team member, not just to laboratory staff.

    By documenting real incident case studies and sharing learnings at monthly meetings, we foster a safety-minded environment. Near-miss tracking and direct task feedback minimize workplace injuries and help us improve batch yields by maintaining cleaner, safer processing environments. This discipline extends to outbound shipments, where proper hazard labeling helps ensure that no surprises await at the customer’s dock.

    Worldwide Distribution and Practical Considerations

    As demand shifts from local to global buyers, our export operations adapt so the product arrives in optimal condition, regardless of destination. Seasonal temperature tracking during international transport protects sensitive material from heat or freezing, which otherwise could affect crystal purity. Multi-laminate packaging reduces risk of cross-contamination.

    Rising regulations on transportation of hazardous materials mean logistics partners must understand special handling requirements. Team members in shipping and compliance departments maintain ongoing certifications updated to reflect the latest requirements in all major countries with whom we work. These efforts let customers receive shipments without unexpected administrative holdups or demurrage.

    Continuous Improvement in the Manufacturing Chain

    Every new batch of 4-Bromo-3-Nitrophenol brings a chance to refine both product and process. From installation of sharper reaction temperature controls to the addition of automated impurity monitoring, investments in our production line have translated into lower failure rates and fewer customer issues. Engineers and chemists work side by side, bridging gaps between theory and practical manufacturing.

    Frontline employees actively participate in process reviews, often catching discrepancies overlooked during desk-based audits. By moving away from siloed roles and encouraging open discussion about near-misses and process hiccups, we drive iterative improvements. Laboratory upgrades grow directly from feedback delivered by end-users dealing with evolving project demands.

    Digital record management now adds another layer of reliability, allowing quick traceability for every step from precursor verification to finished-goods release. This system hits particularly close to home for buyers in pharmaceutical and regulated industries, who rely on this transparency to guarantee compliance and protect intellectual property.

    Conclusion: Value from Practical Experience

    Long-term manufacture of 4-Bromo-3-Nitrophenol shapes both our understanding of specialty chemical markets and our respect for the complex challenges facing users in research and industry. The journey from raw material to consistent, high-purity product involves more than technical know-how—it centers on attentive production, collaboration with end-users, and a dedication to responsible, safe supply.

    Through hands-on experience, robust communication, and ongoing process review, we continue to deliver a compound that fits the demanding needs of today’s innovators. Our workforce remains focused on both immediate quality and the evolving requirements for safety, sustainability, and reliability in chemical manufacturing.