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2-Bromo-6-Nitroaniline

    • Product Name 2-Bromo-6-Nitroaniline
    • Alias 2-Amino-3-bromonitrobenzene
    • Einecs EINECS 226-749-8
    • 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

    690462

    Name 2-Bromo-6-Nitroaniline
    Cas Number 29521-87-7
    Molecular Formula C6H5BrN2O2
    Molecular Weight 217.02 g/mol
    Appearance Yellow to orange crystalline solid
    Melting Point 147-150 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Boiling Point Decomposes before boiling
    Density 1.85 g/cm³ (estimated)
    Smiles NC1=CC(Br)=C([N+](=O)[O-])C=C1
    Inchi InChI=1S/C6H5BrN2O2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H,8H2
    Purity Typically ≥ 97%
    Storage Temperature Store at 2-8°C
    Synonyms 2-Bromo-6-nitrobenzenamine

    As an accredited 2-Bromo-6-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 2-Bromo-6-Nitroaniline

    Applications of 2-Bromo-6-Nitroaniline in Industrial Manufacturing

    As the primary manufacturer of 2-Bromo-6-Nitroaniline, we provide this advanced intermediate material to global partners engaged in specialty chemical synthesis. The following sections outline established, field-proven industrial applications, each with detailed parameters for real-world downstream manufacturing use.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers utilize this compound as a key intermediate in the synthesis of several nitroaniline-derivative drug substances, especially antibacterial and antifungal agents. It participates in stepwise chemical transformations involving reduction, acylation, and cyclization during multi-stage synthesis of regulated APIs.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • EU GMP Annex 1 for sterile products (where applicable)
    • Pharmacopoeias: United States Pharmacopeia (USP), European Pharmacopoeia (Ph. Eur.)
    • FDA Drug Master File (DMF) registration requirements

    Typical usage ratio

    • 5–8% by molar ratio in initial condensation or coupling steps; actual proportion adjusted based on synthetic route, target molecular yield, and byproduct profile

    Downstream process integration

    • Charged as an input intermediate after the protection of amine group; undergoes controlled nitration or bromination in closed reactor systems before subsequent purification/extraction steps

    Final product types

    • Generic and proprietary active pharmaceutical ingredients (e.g., nitroaniline-based antibacterials, antifungals, and specific anti-tubercular drugs)

    2. Agricultural Chemicals Intermediate (Herbicide and Insecticide Synthesis)

    Producers of crop protection solutions employ this compound within the synthesis of specialized aromatic amine-based herbicides and insecticides. It acts as a chain-initiating intermediate for the formation of heterocyclic pesticide scaffolds, contributing to targeted agri-inputs for regulated markets.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • EPA 40 CFR Parts 150-180 (USA), REACH (EC) No 1907/2006 (EU)
    • ISO 9001:2015 for agrochemical raw materials
    • China GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 2–6% by weight in initial batch charge; value set by final active ingredient structure and required selectivity during coupling steps

    Downstream process integration

    • Introduced in the aromatic amination or nucleophilic substitution phase; participates in halogen exchange or nitro-group reduction as part of the multi-step synthesis of active pesticide molecules

    Final product types

    • Selective pre- and post-emergence herbicides (e.g., substituted anilides) and insecticides (e.g., bromonitroaniline derivatives), technical-grade pesticide APIs

    3. Dye and Pigment Intermediate for Performance Textiles

    Specialty dye manufacturers apply this compound as an aromatic amine source for synthesizing azo and disperse dyes used in high-performance textile coloration. Its electron-withdrawing substituents make it valuable for shade modification and fastness enhancement in finished fabric applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile contact safety)
    • REACH Annex XVII (EU restriction of amines in dyes)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 9001:2015 quality management for dye production

    Typical usage ratio

    • 4–12% by weight based on target chromophore intensity and final shade requirements; increased dosage used for deeper, saturated hues

    Downstream process integration

    • Charged in the amination or diazotization step of azo dye synthesis; often coupled with couplers under controlled pH and temperature before isolation and drying of finished dyes

    Final product types

    • Disperse red/yellow dyes, direct dyes for cellulosic fibers, polyester and synthetic fiber dyes, color-fast textile pigments

    4. Specialty Chemical Intermediate in Electronic Material Synthesis

    The electronics industry sources this material for the production of advanced aromatic nitro compounds used in liquid crystal material, high-performance resin, and specialty photoinitiator manufacturing. Its chemical structure supports the development of intermediates that impart UV and thermal stability to final components.

    Industry compliance standards

    • IPC-4101 (laminate and prepreg standards for electronics)
    • IEC 61249-2-21 (halogen-free electronic material safety)
    • RoHS Directive 2011/65/EU (hazardous substances in electrical equipment)
    • ISO 14001:2015 for environmental management in electronic chemical production

    Typical usage ratio

    • 1–3% by weight in coupling formulations or as part of prepolymer blends; exact ratio specified by target dielectric properties and processability

    Downstream process integration

    • Added during nucleophilic aromatic substitution or cross-coupling reactions for synthesis of nitroaromatic intermediates, incorporated under inert atmosphere for high-purity electronics precursor batches

    Final product types

    • Liquid crystal display (LCD) additives, high-stability resin intermediates, specialty photoinitiators, advanced polyimide and polyamide electronics coatings

    5. Fine Chemical Intermediate for Veterinary API Production

    Animal health formulation plants use this material as an essential intermediate for the synthesis of veterinary drug actives structured around nitrobenzene frameworks. It enables manufacturers to achieve target bioactivity profiles and regulatory purity in veterinary anti-infectives.

    Industry compliance standards

    • VICH GL3 GMP (Good Manufacturing Practice for Active Pharmaceutical Ingredients used in Veterinary Medicinal Products)
    • Ph. Eur. 9.0, Japanese Veterinary Pharmacopoeia (JVP)
    • National GMP regulations for veterinary drug API (e.g., China Ministry of Agriculture Decree 201)
    • ISO 9001:2015 for fine chemicals

    Typical usage ratio

    • 6–10% by mol in the initial step of nitrobenzene-based veterinary API syntheses; optimization based on conversion yield and final impurity profile

    Downstream process integration

    • Loaded during primary condensation or amide formation steps, followed by selective reduction and catalyst-mediated functionalization for active veterinary compound creation

    Final product types

    • Veterinary antibiotics, antihelminthic agents, and animal feed additive APIs derived from nitroaromatic chemistries
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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-6-Nitroaniline: Rethinking Utility in Modern Synthesis

    Understanding the Substance

    2-Bromo-6-Nitroaniline carves out a niche for itself in the family of aromatic amines. The compound, built around a benzene ring, holds a bromine atom at one position, a nitro group at another, and an amine group in the mix. Its structure isn’t just a marvel of chemistry; it shapes exactly how the molecule interacts with other reagents and molecules in the lab. Each functional group tugs at the molecule’s electronic structure, giving it unique reactivity and, as many have seen, reliability across a sweep of synthetic routes.

    Choosing the Product: More Than a Catalog Entry

    A bottle labeled 2-Bromo-6-Nitroaniline doesn’t get anyone’s attention by name alone, but the compound’s value shows through during workbench application. For chemists handling multi-step syntheses or chasing routes to more complex targets, this molecule brings both selectivity and flexibility. I remember a synthesis project where minor changes to a ring system completely shifted downstream reactivity. As someone who’s tried cutting corners with regiosimilar compounds, that lesson came at a price: reactions that stalled, inconsistent yields, and purification headaches. The specific locations of the bromo and nitro groups matter as much as the presence of each. Subtle shifts in placement turn a game-changer into a letdown.

    Key Specifications That Shape Laboratory Work

    For practical work, good reproducibility comes from reliable sourcing. Every bottle should guarantee not only a set purity, but minimal impurities—halogenated species, regioisomers, or leftover starting materials can sidetrack delicate steps in a synthesis. Given the sensitivity of modern analytical techniques, impurities at even half a percent can complicate NMR or LC-MS readings and introduce ambiguity that derails an entire research cycle.

    Batch-to-batch consistency pays off, especially in larger research labs or manufacturing. Within my own work, even a small fluctuation in crystal habit or residual moisture shifts solubility or reaction kinetics. Long gone are the days of accepting “close enough” reagent quality; projects rise and fall on reproducibility. Experienced chemists know that poorly characterized, off-brand samples of similar compounds can introduce headaches in scaling up, or in meeting the requirements set by downstream pharmaceutical partners.

    Comparisons to Related Products: Why Placement Matters

    At first glance, some might lump 2-Bromo-6-Nitroaniline with any bromoaniline or nitroaniline. Chemically, they can look like siblings, but practical differences become obvious in the lab. Take 4-Nitroaniline. The position of the nitro group changes not only the electron density on the ring, but also how coupling reactions occur. Even seasoned chemists can fall into the trap of thinking that any ortho, meta, or para substitution pattern will “do just fine” in a pinch. In reality, that shortcut leads to lost days retesting protocols or second-guessing analytical results.

    Second, consider the way different isomers handle further substitution or cross-coupling reactions. The ortho relationship between nitro and bromo in 2-Bromo-6-Nitroaniline governs selectivity and sets up well-defined intermediates. Synthetic strategies that need precision benefit from this arrangement. In fields like medicinal chemistry, where the outcome of a downstream transformation can define a patentable entity, small structural details translate into significant gains or losses.

    Applications: From Concept to Implementation

    2-Bromo-6-Nitroaniline fills gaps in synthetic planning. In pharmaceutical research, it serves as a launchpad for building more elaborate molecules. Because bromine acts as a good leaving group in many cross-coupling reactions—think Suzuki, Sonogashira, or Buchwald-Hartwig couplings—it brings participation and selectivity that’s hard to replicate with other halogen positions. The nitro group, on the other hand, doesn’t just modify ring electronics; it opens up further modifications, allowing reduction to an amine or other functional transformations that can swing a project in new directions.

    This dual handle makes 2-Bromo-6-Nitroaniline a workhorse for researchers aiming for odd, otherwise-hard-to-build scaffolds. I recall one collaboration on heterocycle synthesis where we cycled through several nitroanilines, but only this compound delivered the clean reactivity required at a crucial step. Projects like these prove out the value of careful reagent selection—especially under budget constraints or urgent project timelines.

    Why Consistency and Quality Remain the Real Differentiators

    Across dozens of multi-gram preparations, what separates reliable products from their lower-grade competitors boils down to attention in raw material sourcing, control of synthetic conditions, and final purification. Inconsistency breeds problems for everyone downstream. Research groups count on vendors or suppliers to maintain careful controls—trace metals, residual solvents, or unintended byproducts can kill a promising route before it starts.

    With so many research budgets stretched thin, skimping on quality can seem tempting. From my own mistakes, I’ve learned that the up-front savings don’t really add up in the end. Low-grade samples bring uncertainty, re-tests, repeated troubleshooting, and the kind of frustration that chews up weeks of work. The best 2-Bromo-6-Nitroaniline options on the market feature clear batch analytics and certificates with every purchase, giving real-time confidence to those at the bench.

    The Value of Certifications and End-to-End Transparency

    Standardized certifications give buyers concrete assurance. Lab managers and researchers want transparency about origin, testing, and storage practices. Documentation pointing to compliance with recognized pharmacopeia standards or validated analytical methods makes tracking consistency simple and fast. I’ve worked both places where chemical stocks were a black box and where everything, down to humidity in the store room, carried a traceable record. The latter approach wins out every time, slashing downtime and preventing surprises when trouble hits.

    Trust is built on experience. An anecdote: I once ordered a batch made with little documentation; halfway through development, we realized the product wasn’t matching expected reactivity—HPLC showed minor, persistent impurities. Time lost chasing ghosts taught our group the real value of buying from transparent sources. Now, we scrutinize every new vendor, demanding data up front, no exceptions.

    Supporting Research with Adaptable Solutions

    Modern projects aren’t static. Research groups dive between catalysis, scale-up, formulation, and biological screening. No one wants to recalculate from square one because raw materials shift unexpectedly. Those who buy and use 2-Bromo-6-Nitroaniline rely on stable specifications and reliable logistics, but also, increasingly, on provider expertise. Feedback loops between R&D labs and suppliers—real discussion about run-to-run challenges, packaging needs, or even storage conditions—make projects move smoother, with fewer unpleasant surprises.

    Some of the more well-rounded companies now offer deeper support: application notes, reactivity testing, or case histories that spell out best practices. Junior researchers get up to speed faster. Senior chemists can push boundaries, leaning on technical teams for advice on purification or workup. Ownership of challenges on both sides encourages better science and more reliable returns on investment.

    The Environmental and Regulatory Landscape

    Few research chemicals escape the gaze of environmental or regulatory bodies. 2-Bromo-6-Nitroaniline isn’t an exception. The implications go beyond safe handling. The bromine and nitro groups demand care at every step—usage, storage, transport, and especially disposal. Labs making regular use of this compound factor in safety training, dual containment, and disposal methods that don’t threaten wider ecosystems. From my time in both academia and industry, I’ve watched labs tighten those controls, keeping up with new rules as governments adjust chemical control lists and waste treatment standards. Responsible sourcing increasingly drives which suppliers are chosen—those demonstrating cradle-to-grave stewardship stand out in bid proposals and funding reviews.

    Solving Supplier and User Challenges Together

    Ongoing improvement happens when suppliers and users work side by side. One solution for the evolving regulatory scene involves offering recycled packaging, batch-tracing software, or educational tools on correct handling and disposal. Labs stay compliant, reduce their footprint, and suppliers build lasting relationships. Digital tracking also pays off; investing in standard barcoding and cloud-based inventory tracking means reduced misallocation, fewer expired reagents, and streamlined ordering.

    After years of both simple and messy chemical management systems, I’ve seen how much smoother lab life runs with digital controls. It’s more than a convenience—these tools cut long-term risks, flagging outdated products before they reach critical reactions. For institutions facing higher scrutiny, clean digital paper trails ease audits, whether internal or regulatory.

    Addressing Industry Needs: Customization Matters

    Demand for 2-Bromo-6-Nitroaniline doesn’t move in a straight line. Some clients want it for pharma, others for dye intermediates or advanced materials. Each group brings slightly different requests—particle size, purity, packaging size, or shipping requirements. Successful suppliers take in feedback, making small but meaningful changes: tamper-evident packaging for added integrity, custom bottle volumes to match order scale, temperature-controlled shipping to avoid degradation on the road.

    Open channels between buyer and seller let these adaptations happen quickly. My own group once pressed for a low-iron variant after noticing trace contamination hurting catalyst performance. A supplier with flexible manufacturing—rather than fixed, “take it or leave it” models—delivered a customized product batch in record time. Outcomes like that turn a one-off purchase into a decades-long business relationship.

    Global Reach and Local Responsibility

    Chemistry doesn’t sit inside neat national borders. 2-Bromo-6-Nitroaniline travels from plant to researcher’s bench, crossing continents in the process. Sourcing on a global scale intersects with real-world issues—border regulations, documentation, and ethical production. As distribution chains stretch, the best partners are those upfront about supply chain transparency and labor practices.

    There’s a competitive edge for those who approach these challenges proactively. Those who anticipate interruptions—trade disputes, shipping delays, or raw material shortages—can pivot quickly. By building up local warehousing or working closely with logistics partners, reliable companies keep supplies steady, cushioning labs from sudden shortages. This has mattered greatly in recent years, where even routine shipments can hit unexpected snags. Closely knit networks up and down the supply chain have transformed “crisis” into only a minor inconvenience.

    Building a Safer, More Responsive Market

    Good products alone don’t build a robust chemical sector; engaged, informed users and responsive suppliers do. Training resources, whether shared digitally or sent with shipments, let labs use 2-Bromo-6-Nitroaniline safely and to its full potential. Regular updates from suppliers—bulletins on handling practices, changes in purity testing, or regulatory shifts—make a more resilient ecosystem for everyone. Where manufacturers treat their customers as genuine partners, responsive feedback loops generate product improvements faster and with less friction.

    Direct experience has shown me that commitment to education pays rich dividends. In labs with regular training and shared “lessons learned,” incident rates fall. Small investments in clear communication save researchers, managers, and suppliers the cost and stress of missteps, wrecked experiments, or worse, safety incidents.

    Navigating New Technologies and Digital Transformations

    Digitalization in the chemical industry now influences both sourcing and application of reagents like 2-Bromo-6-Nitroaniline. Data-driven ordering, real-time batch analytics, and automated restocking give research teams a sense of control. Even the way products are tracked and certified now benefits from secure online platforms. Documentation that once took days to retrieve finds a home in searchable databases, making due diligence nearly painless. In my earlier days, shuffling through stacks of paper for a missing chromatogram or batch certificate slowed projects and muddied regulatory compliance. The change to digital, collaborative data sharing marked a leap in productivity.

    Looking ahead, as automation seeps further into chemistry labs, so too does the need for reagents whose quality and behavior have been scrutinized and documented thoroughly. Automated systems don’t tolerate variation—any inconsistency heads straight for system alarms or failed runs. Reliable, well-characterized 2-Bromo-6-Nitroaniline means moving confidently from manual procedures to higher-throughput, robot-driven synthesis. Early adopters are already seeing gains: shorter development cycles, better scale-up reliability, and stronger case histories for intellectual property filings.

    Conclusion: The Path Forward for Chemistry Innovation

    The value that 2-Bromo-6-Nitroaniline brings to research and industrial chemistry rests on much more than basic specifications or a single-use case. It stems from layers of trust, collaboration, and a commitment to quality that move far beyond what’s printed on a label or certificate. Over decades, chemists build up a mental library of what works and what frustrates, learning that small structural or quality differences ripple out into massive downstream consequences. The product’s role grows out of hands-on experience, the evolution of safe practices, and constant dialogue between those at the bench and those shaping the supply chain.

    For any lab bench, pilot plant, or analytical suite looking to stretch boundaries or lock in reliable performance, the lessons learned around sourcing, using, and improving 2-Bromo-6-Nitroaniline form a roadmap. Each challenge—whether from regulatory compliance, technological disruption, or simple day-to-day workflow—finds its answer in a blend of science, transparency, and responsive support. The next chapter in chemistry calls not for generic commodities, but for trusted building blocks whose credibility has been earned with every synthesis and every successful project.