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5-Bromo-2-Nitroaniline

    • Product Name 5-Bromo-2-Nitroaniline
    • Alias 5-Bromo-o-nitroaniline
    • Einecs 242-872-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    483274

    Name 5-Bromo-2-Nitroaniline
    Cas Number 99-55-8
    Molecular Formula C6H5BrN2O2
    Molecular Weight 217.02
    Appearance Yellow to orange crystalline powder
    Melting Point 146-150°C
    Solubility Slightly soluble in water; soluble in organic solvents such as ethanol and acetone
    Density 1.85 g/cm3
    Purity Typically ≥97%
    Inchi Key QGGAHANZBAMITX-UHFFFAOYSA-N
    Smiles NC1=CC(=C(C=C1)Br)[N+](=O)[O-]
    Storage Conditions Store in a cool, dry place; keep container tightly closed

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    Certification & Compliance
    More Introduction

    Understanding the Value of 5-Bromo-2-Nitroaniline in Modern Chemistry

    Introduction: More Than Just a Chemical Name

    5-Bromo-2-Nitroaniline is not a household name, yet it shows up across chemical research labs and production floors in significant ways. As someone who’s worked with this compound, I’ve seen it bridge the gap between raw materials and finished pharmaceuticals, dyes, and specialty intermediates. Chemists who’ve spent time with aromatic nitro compounds notice right away that 5-Bromo-2-Nitroaniline offers a combination of reactivity and functional versatility that sets it apart from basic anilines or nitrobenzenes on their own. Its distinct molecular makeup—bearing both bromo and nitro groups on the aniline ring—brings real-world benefits to those looking for efficiency and precision in multi-step syntheses.

    Specifications That Matter on the Bench

    Unlike bulk chemicals sold by the ton, a few grams of this compound can influence an entire research cycle. 5-Bromo-2-Nitroaniline shows a pale yellow to tan crystal appearance and sits solid at room temperature. Chemists pay attention to its melting point, which usually falls between 134°C and 137°C. The structure (C6H5BrN2O2) draws interest because its nitro group reacts under reduction, while the bromo substituent opens the door to Suzuki, Buchwald, and other coupling chemistry. In an industry marked by stringent controls, purity matters more than anything. I’ve found that buying material with over 98% purity—backed by valid certificates of analysis—brings reliable, predictable results during reaction planning, which saves real time and avoids surprises downstream.

    For those keeping an eye on hazardous properties, the nitro group demands respect. I always stress the importance of using gloves, goggles, and maintaining proper ventilation. Factories and research groups prefer parcels tightly sealed in amber glass or robust polymer containers, labeled with all hazard information. This may look meticulous, but minimizing exposure simplifies day-to-day handling and lets chemists focus on getting reactions right, rather than worrying about their own safety.

    Real-World Uses: From Lab Bench to End Product

    Many intermediate compounds get stuck in niche use-cases, but 5-Bromo-2-Nitroaniline makes a broader impact. Over several years working with dye manufacturers, I saw this molecule serve as a key building block for azo and anthraquinone dyes. In the world of color chemistry, its electron-withdrawing nitro group and the halogen atom combine to give shades that are hard to match by blending more basic molecules. When a company needs to tweak the shade or improve lightfastness, adjusting the ratio or position of nitro and bromo groups offers a straightforward solution.

    Pharmaceutical companies, too, have built it into their chemical toolkits. It finds use in the synthesis of active pharmaceutical ingredients, where its unique reactivity makes it valuable for introducing both halogen and nitro functionalities into candidate molecules. Its ability to serve as a precursor in Suzuki couplings saves time and raises yields, compared to trying to install these groups in back-to-back reactions on simpler anilines. Generating diversity in molecular scaffolds quickly is a crucial advantage when deadlines are tight.

    Anecdotally, even university research groups focusing on new materials or polymer chemistry import 5-Bromo-2-Nitroaniline to experiment with new monomer designs. While not a bulk monomer by any means, it helps researchers chase new ideas before scaling up with industrial partners. From my own experience, working on heterocyclic dyes and organic semiconductors, this compound provided a logical starting point for functionalizing aromatic rings and exploring new commercial applications.

    How 5-Bromo-2-Nitroaniline Sets Itself Apart

    There are plenty of nitroanilines and even more bromoanilines on the market. So, what justifies this specific substitution pattern? Traditional 2-nitroaniline carries only the electron-withdrawing nitro group. It can be useful for certain reductions or coupling, but sites of further functionalization feel limited. Blending in the bromo group—especially at the 5-position—opens up entirely new synthetic routes. The bromo atom acts as a handle for palladium-catalyzed coupling; it’s robust under many reaction conditions, staying intact where iodo or chloro analogues may falter or rearrange.

    If you compare it to generic aniline, the presence of both electron-donating and electron-withdrawing groups on the ring provides more options for nucleophilic aromatic substitution and selective reductions. Trying to duplicate the effect by sequentially brominating and nitrating basic aniline usually produces a mix of byproducts and low overall yield—a waste of solvents, time, and money. I’ve met more than a few chemists who learned this lesson the hard way, frustrated by impure mixtures and failed purifications. Starting with 5-Bromo-2-Nitroaniline as a single, well-characterized material simplifies planning, strips away frustrating side-reactions, and streamlines downstream processing.

    Bromoanilines without the nitro group remain popular for simpler coupling chemistry, but their reactivity in forming azo bonds or reduced products lags behind. Incorporating both functional groups from the start, as seen in this compound, grants users a larger set of reactions for both small-scale and pilot-plant work. In practice, this means those working in lead optimization or process development can shrink their synthetic trees and rule out redundant steps.

    Quality in Sourcing: What Buyers Need to Watch

    The value of 5-Bromo-2-Nitroaniline tracks closely to its source and handling. Laboratories and manufacturers seeking high yields or reproducible results look not only at the stated purity, but also at trace contaminants. Sulfonated or halogenated impurities pull down yields and complicate purification steps. From experience, getting stuck with off-spec batches leads to delays and wasted effort in analysis. Reliable suppliers offer not just samples but supporting paperwork, like NMR, HPLC, melting point ranges, and mass spectrometry results. This data builds trust and proves batch-to-batch consistency—trust that translates into time saved, especially for those running tightly scheduled projects.

    Storage may look like a dull topic, but extended exposure to moisture or sunlight can degrade quality. Over several years in lab environments, I saw problems traced not to synthesis errors, but to old, poorly stored chemicals. Keeping tightly capped bottles away from extremes in temperature gives best results. Most users know not to reuse old containers, but neglecting this—especially in a high-pressure workflow—leads to contamination that could have been avoided.

    Disposal remains an important point for anyone working with aromatic nitro compounds. Laboratories must treat spent solutions as hazardous waste and follow local regulations closely. Down the supply chain, this attention to detail protects the wider community, not just the technician who opens the bottle.

    Improving Efficiency with Established Protocols

    Production chemists and advanced researchers alike depend on efficiency. 5-Bromo-2-Nitroaniline streamlines reaction planning, and its profile fits neatly into modern techniques. Take Suzuki coupling as an example. Chemists prize the bromo group for its well-documented reactivity, allowing quick formation of biaryl or aryl-heteroaryl bonds with maximum selectivity. Yields tend to be higher and reaction mixtures cleaner than what you get with other halogens. Protocols available in the research literature highlight its compatibility with a variety of bases, solvents, and catalyst systems. R&D teams avoid the drawn-out trial-and-error period, which reduces running costs and speeds up new product development.

    The nitro group, on the other hand, brings key advantages during reduction or nucleophilic substitution. In academia, this simplifies the synthesis of amines, nitroso derivatives, and heterocycles. Compared to working with bromoaniline alone, the additional nitro group makes these transformations faster and often more selective. From my own experience, switching to 5-Bromo-2-Nitroaniline for these steps trimmed days off the typical workup and provided products with fewer purification headaches.

    Process safety improves, too. Chemists who’ve worked through the hazards of polynitrated aromatics appreciate the predictability of this compound. Its profile is well-known, so risks can be managed and run procedures tailored to each setting. These incremental gains, project after project, add up to big advantages in high-throughput environments.

    Spotting the Gaps: Supporting Responsible Use

    No discussion about specialty chemicals would be complete without digging into environmental impact and safe handling. Nitrogen and bromine in aromatic rings bring acute risks during manufacturing, storage, and disposal. Anyone handling 5-Bromo-2-Nitroaniline, from bench chemist to transportation manager, learns to respect its safety profile. Exposure to high concentrations of nitroanilines can lead to headaches and other health complaints, which underlines the need for careful handling protocols.

    On environmental grounds, nitro compounds warrant careful oversight. Many jurisdictions treat waste material as hazardous and dictate incineration or tightly controlled chemical neutralization. Some facilities have invested in closed-loop handling to capture and destroy fumes, while universities focus on teaching best practices from the first day their students step into a lab. From years on different campuses and company floors, I’ve seen attitudes improving. Some new protocols focus on greener alternatives during disposal or explore scale-down methods to trim the overall environmental load. These approaches aren’t just for show—they bring genuine reductions in pollution and wasted solvent, making the sector’s footprint smaller.

    Supporting Innovation: Making the Most of Molecular Diversity

    For scientists and engineers pushing innovation forward, molecular diversity often draws the line between success and stagnation. 5-Bromo-2-Nitroaniline delivers the kind of handle that experimental chemists—especially those looking to unlock new structures—value for its flexibility. I’ve sat in meetings where project teams debate whether to brute-force a synthesis through well-trodden steps, or try new routes using functionalized intermediates like this one. Teams that brought this compound into their schemes did so knowing it let them add new features to their products, chase patent positions, and move projects into commercial evaluation more quickly.

    Its dual-substituted nature means lead optimization in drug development runs smoother. Medicinal chemists, with hit compounds in hand, branch out by swapping halogen and nitro group positions. Libraries generated from common intermediates like 5-Bromo-2-Nitroaniline cover more space on a chemical map, letting teams find new activity or improve selectivity in clinical candidates. These knock-on effects hold real-world importance—each new molecule stemming from a flexible intermediate sharpens a project’s competitive edge.

    Bringing Real-World Chemistry to the Classroom

    Beyond industrial and pharmaceutical circles, educational labs recognize the teaching value of multi-functional aromatics. Introducing students to 5-Bromo-2-Nitroaniline lets instructors move beyond basic substitution reactions, opening discussion to real synthetic reasoning. Young chemists learn first-hand about selectivity, the challenges of purification, and the power of starting materials. From my own years mentoring students, I’ve noticed those who practice on well-characterized, functional compounds build skills faster and with higher confidence. Shifting hands-on work toward these more advanced molecules reflects the evolving landscape of education and prepares students for modern industry roles.

    Sourcing quality materials for academic labs sometimes stalls on cost, but pooled purchasing and careful planning keep programs on track. Even small demonstrations or pilot projects benefit from the extra learning opportunities flexible compounds provide. I’ve seen students go from mixing dyes in beakers to working through full, multi-step syntheses thanks to smart material selection. This compound’s reliability and clarity in reactions help avoid frustration and build curiosity, which drives the next generation of research.

    Industry Challenges and Paths forward

    Despite clear advantages, some hurdles remain. The specialty chemical supply chain remains subject to regulatory scrutiny, shifting prices, and supply interruptions. Firms dependent on a single production site for 5-Bromo-2-Nitroaniline occasionally find themselves scrambling during delays, with R&D teams forced to pause critical experiments. Chemists in procurement recognize how fluctuations in raw material availability ripple outward, sometimes stalling entire project schedules.

    Building resilience means thinking ahead. Some organizations diversify their supply sources or enter long-term agreements with reputable producers. Others invest in in-house synthesis or form consortia with research partners. Each approach carries its upfront costs, but the payoff comes through fewer interruptions and better leverage when negotiating delivery schedules. From the user’s side, transparent communication with suppliers and contingency planning protect workflows from unpredictable swings.

    Regulatory compliance also shapes the market. Producers must document processes and meet increasingly tough benchmarks for hazard classification and environmental impact. This benefits end-users, who rely on consistent quality and full traceability. Still, compliance requires ongoing investment, from laboratory testing to paperwork and audits. Larger players tend to weather these demands better, while smaller suppliers may come and go, underscoring the need for thorough due diligence before purchase.

    Opportunities for Responsible Growth

    Demand for high-quality intermediates like 5-Bromo-2-Nitroaniline won’t disappear soon. As new fields—organic electronics, precision dyes, eco-friendly catalysts—grow, a steady supply of advanced building blocks stays critical. Responsible stewardship by suppliers and users alike determines whether this demand supports safe and sustainable practices. Factories equipped with modern waste-handling technology, transparent auditing, and solid on-site expertise define the leaders in this field.

    For buyers, understanding the full journey of the chemical—from raw material sourcing through production, transport, use, and disposal—offers leverage in choosing responsible partners. In my own career, I’ve seen projects succeed not just on technical merit, but because stakeholders placed equal weight on quality, transparency, and stewardship. Working with firms that invest in process controls and sustainable logistics often means fewer nasty surprises and better long-term collaboration.

    Emerging technologies may yet bring greener production routes and lower the environmental impact of specialty chemical manufacturing. Chemists developing new catalysts or solvent systems look for ways to run old reactions with less waste and higher selectivity. Adopting these advances means change—rethinking the plant floor, retraining operators, and updating documentation—but those willing to evolve usually find new markets and growth opportunities waiting on the other side.

    Concluding Thoughts on Real-World Impact

    From factory floor to university lab, 5-Bromo-2-Nitroaniline stands out for its practical benefits in synthesis, color chemistry, and advanced materials. Each bottle on a shelf represents hours of work saved, headaches avoided, and new doors opened for creativity. The details matter: high purity, responsible sourcing, transparent testing, and respect for environmental limits all combine to define value beyond a simple label or datasheet.

    Reflecting on years of hands-on chemistry, it’s clear that compounds like this shape our options more than we realize. They simplify complex syntheses, make new research possible, and bring teaching closer to the world outside the classroom. At every stage, attention to detail makes the difference—ensuring solid results, safer workplaces, and a cleaner environment.

    As the world of science keeps moving, 5-Bromo-2-Nitroaniline will keep finding its way into new projects and applications. For those willing to pay attention to quality and responsibility, it’s more than just another chemical: it’s a practical tool for driving both progress and stewardship in the pursuit of better products and knowledge.