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4-Bromo-5-Chloro-2-Methoxyaniline

    • Product Name 4-Bromo-5-Chloro-2-Methoxyaniline
    • Alias 4-Bromo-5-chloro-o-anisidine
    • Einecs 629-797-5
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    229695

    Name 4-Bromo-5-Chloro-2-Methoxyaniline
    Cas Number 877265-36-8
    Molecular Formula C7H7BrClNO
    Molecular Weight 236.50
    Appearance Light yellow to brown solid
    Melting Point 91-94°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles COC1=CC(=C(C=C1N)Br)Cl
    Inchi InChI=1S/C7H7BrClNO/c1-11-7-3-4(8)5(9)2-6(7)10/h2-3H,10H2,1H3
    Storage Temperature 2-8°C
    Hazard Statements H315, H319, H335 (may cause skin/eye/respiratory irritation)

    As an accredited 4-Bromo-5-Chloro-2-Methoxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromo-5-Chloro-2-Methoxyaniline

    Applications of 4-Bromo-5-Chloro-2-Methoxyaniline in Industrial Manufacturing

    As a direct manufacturer, we observe that 4-Bromo-5-Chloro-2-Methoxyaniline functions as a specialized intermediate in several demanding chemical synthesis processes. This aromatic amine’s unique halogen substitution pattern provides value chiefly in regulated sectors requiring stringent traceability and controlled process conditions. Below we detail widely recognized downstream industrial applications supported by real standards and established production practices, covering key formulation and integration requirements.

    1. Pharmaceutical Active Ingredient Synthesis

    Many pharmaceutical manufacturers utilize this compound as a building block in the synthesis of specific APIs, especially for anti-infective agents where the dual halogen and methoxy substitution are favored for fine-tuning pharmacological properties. Integrators operate under controlled reactor parameters, batch monitoring, and precise purity targets, requiring traceable sourcing and documentation at each processing stage.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • U.S. FDA 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals
    • EU EudraLex, Volume 4 – GMP Guidelines for Pharmaceutical Products
    • USP, EP, JP Monographs for intermediates (where applicable)

    Typical usage ratio

    • 0.8%–1.6% w/w relative to the total input mass in multi-step API synthesis, with slight adjustment based on target molecule molecular weight and route efficiency

    Downstream process integration

    • Direct addition as an intermediate during stepwise nucleophilic aromatic substitution above 40 °C, prior to final condensation or ring closure amid API molecule construction

    Final product types

    • Active pharmaceutical ingredients for oral and parenteral anti-infective drugs
    • Therapeutic specialty intermediates requiring halogenated aromatic cores

    2. Agrochemical Synthesis (Herbicides and Fungicides)

    Proprietary herbicide and fungicide formulations depend on halogenated anilines as core structural elements, ensuring enhanced bioactivity and longer environmental persistence. Agrochemical producers rely on validated process controls for consistency and strict residue checks in accordance with local and international regulations, deploying this intermediate for controlled substitution to generate final active molecules used in crop protection.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for Agrochemical Production
    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006 for chemical substance registration in Europe
    • China GB 2763 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • 1.2%–2.5% w/w in target molecule synthesis, with increases for higher halogen content requirements or multi-stage homologous series production

    Downstream process integration

    • Introduced during limited substitution steps with temperature-controlled halogen exchange or methoxylation, prior to further reactions yielding functionalized pesticide actives

    Final product types

    • Selective herbicides for cereals and broadleaf crops
    • Fungicidal compounds for horticultural and field applications

    3. Organic Pigments and Dye Intermediate Manufacturing

    Producers of high-performance pigments and specialty dyes incorporate this aniline derivative into chromophore assembly chains, taking advantage of its reactivity profile to generate colorants with improved fastness and resistance. The process operates under environmental and safety controls specific to aromatic amine synthesis, and finished pigment quality adheres to industry-specific testing protocols.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Certification for textile colorants
    • EN 71-3 Safety of Toys – Migration of Certain Elements (for coloring materials)
    • ISO 9001:2015 for dye and pigment manufacturing
    • REACH SVHC compliance (for substances of very high concern)

    Typical usage ratio

    • 0.5%–1.3% w/w commonly in coupler phase or azo coupling; ratios tailored to desired pigment shade intensity and process step sequence

    Downstream process integration

    • Loaded as a coupling component after preceding diazotization or in oxidative ring closure stages, enabling introduction into pigment matrix through controlled synthesis

    Final product types

    • Organic pigments for plastics and coatings
    • Specialized textile dyes (including reactive and disperse dyes)

    4. Advanced Polymer Modifier Synthesis

    In advanced materials manufacturing, this compound serves as a monomer precursor or secondary modifier for engineering polymers, especially where thermal stability and chemical inertness are prioritized. Manufacturers precisely meter the addition to influence cross-linking and thermal properties, maintaining documentation for end-user regulatory compliance in sensitive sectors.

    Industry compliance standards

    • ISO 9001:2015 for industrial polymers
    • FDA 21 CFR 177 Indirect Food Additives: Polymers (when used in food-contact materials)
    • UL 94 Flammability Testing of Plastic Materials
    • RoHS Directive 2011/65/EU for electrical and electronic equipment applications

    Typical usage ratio

    • 0.3%–1.0% w/w as a modifier, dependent on desired polymer end-use characteristics and degree of polymerization

    Downstream process integration

    • Charged during polymerization as a functionalized aromatic chain extender, or introduced in copolymerization steps to impart desired mechanical and thermal properties

    Final product types

    • High-durability engineering plastics
    • Flame-retardant resin systems

    5. Specialty Chemical Catalysts and Ligand Precursors

    End-users in the catalyst sector selectively introduce this molecule to construct complex ligands and catalyst supports, utilizing the unique arrangement of halogen and methoxy groups to control coordination chemistry. Projects prioritize full batch traceability and detailed impurity profiling in line with global chemical management protocols.

    Industry compliance standards

    • ISO 14001:2015 – Environmental Management Systems for chemical production
    • Responsible Care® Global Charter (for process safety and stewardship)
    • REACH Regulation – Registration and safety reporting

    Typical usage ratio

    • 0.1%–0.6% w/w in complex synthesis; precise ratios depend on ligand or backbone design

    Downstream process integration

    • Utilized in the ligand functionalization stage via selective coupling, enabling formation of bidentate or multidentate structures for transition metal catalysis

    Final product types

    • Homogeneous and heterogeneous catalyst systems for fine chemical processing
    • Ligand libraries for organometallic R&D
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    Certification & Compliance
    More Introduction

    4-Bromo-5-Chloro-2-Methoxyaniline: Moving Beyond the Basics in Organic Chemistry

    Some chemicals sound like they belong in a dark corner of a dusty lab, but 4-Bromo-5-Chloro-2-Methoxyaniline deserves broader attention. This compound sports the formula C7H7BrClNO and shows up as a solid with a crystalline touch. At a glance, it doesn’t spark instant excitement from most folks outside the industry, yet for chemists and those in advanced pharmaceutical manufacturing, it opens up a series of doors. R&D teams recognize that what starts as a complicated-sounding aromatic amine sometimes ends up as the backbone of something you might find in a hospital or in the next generation of imaging systems.

    Unpacking the Structure and Why It Matters

    When you look at the makeup of this molecule—featuring a bromine, a chlorine, and a methoxy group tacked onto an aniline core—it becomes clear that chemists didn’t just throw those elements together for fun. Each substituent nudges the chemical’s reactivity in a direction that older, plain vanilla anilines simply can’t achieve. The bromine and chlorine atoms shift electron density, tuning the molecule’s profile. The methoxy group balances things by granting extra stability while influencing solubility in organic solvents. Chemical synthesis has always evolved with small changes in molecular design, and this is a good illustration of that process. Subtle tweaks change the ways reactions take place, often making them milder or more selective, and less demanding than they were a few decades ago.

    A Chemist’s Sidekick in Multi-Step Synthesis

    People may think of these organic compounds as mere specialty products, but if you’ve ever tried to piece together a complex molecule in the lab, you know that each functional handle on the molecule’s framework enables a world of possibilities. 4-Bromo-5-Chloro-2-Methoxyaniline has shown its value in the preparation of heterocycles, which continue to anchor all sorts of medicinal agents. Heterocycle construction isn’t glamourous—hours spent distilling, filtering, washing—and researchers appreciate starting materials that hold up to stress. Differences in structure directly influence what you can do down the line. Bromine and chlorine both offer different points of reactivity. In Suzuki, Buchwald-Hartwig, or Ullmann reactions, the position and identity of halide substituents matter a great deal. This influences which partners you can link, how quickly transformations run, and how many side products you’ll wind up picking from a flask at the end.

    The Step-Up from Standard Anilines

    Back in school, we handled simple aniline derivatives like para-anisidine or chloroaniline to introduce the basics. Once you step into the world of combinatorial chemistry or medicinal chemistry, complexity ramps up fast. Many simple anilines just don’t provide the selectivity you want. 4-Bromo-5-Chloro-2-Methoxyaniline slots into projects where backbone rigidity and electronic effects count for something. Compared to generic anilines, you can dial in cross-coupling selectivity more easily. That matters when you’re synthesizing a lead compound with minimal side products, or when you’re trying to attach a difficult group on a crowded framework. Selection of this kind of compound comes after years of trial-and-error and listening to what reaction outcomes teach. If you’ve ever had a project where a fraction of percent yield improvement meant hitting a crucial milestone, you’ll recognize the edge specialized reagents provide.

    Pharmaceutical Intermediates: From Concept to Clinic

    The modern pharmaceutical world relies on tight control at every stage. New intermediates are scrutinized for purity, stability, and downstream reactivity. 4-Bromo-5-Chloro-2-Methoxyaniline finds its way into preclinical studies not just as a lab curiosity, but as a linchpin for building rings and frameworks that power everything from enzyme inhibitors to imaging agents. The triple substitution on this compound might seem more complicated than necessary, until you look at the patent literature: leading pharma companies often map out entire series of analogues around such patterns, searching for the best fit between chemical structure and biological activity. Being able to introduce halides and methoxy groups on a single scaffold lets researchers adjust properties like solubility, cell permeability, and metabolic stability without starting from scratch.

    Fit for Custom Synthesis and Fine Chemical Workflows

    If you run a custom synthesis operation, you know one-off projects often rest on unusual building blocks. Bulk chemicals rarely offer the specificity needed to fine-tune a synthesis. That’s where highly functionalized anilines, 4-Bromo-5-Chloro-2-Methoxyaniline among them, play a part. Access to structurally diverse anilines brings new capabilities to contract research organizations, as drug developers look for reliable partners who can tackle tough isomeric configurations or late-stage functionalizations. I’ve seen projects get unstuck when an overlooked starting molecule like this revealed a cleaner, scalable path to product. It’s always the fine details—a misplaced group or a poorly-timed side reaction—that turn a synthesis into a headache or a triumph.

    Comparing Siblings: What Sets This Compound Apart

    Many chemists rely on ortho- or para-substituted anilines, and for good reason. They’re tried and true. But 4-Bromo-5-Chloro-2-Methoxyaniline sits in a different category. Its meta- and ortho-substitution changes the way neighboring groups respond during reaction steps, sometimes reducing the need for protection-deprotection cycles. I’ve found that using it can speed up project timelines, since its pattern of substitution shields sensitive positions, sparing you extra purification or stability challenges. The presence of both a bromine and a chlorine atom widens the palette for selective cross-coupling, something not achieved as easily with a single halide compound. The methoxy group, often seen as just a solubility modifier, influences electron distribution along the aromatic ring, changing acidity and nucleophilicity of the entire molecule. It’s a nuanced difference, but nuanced differences add up and often decide whether a research project makes it out of the exploratory phase.

    Scale-Up: No Room for Guesswork

    Projects move from milligrams on a lab scale to kilograms on a pilot scale quickly when there’s commercial demand. Those of us who’ve worked in scaling up fine chemicals know that not all structural features survive the transition from bench to plant. Some substitutions fall apart under thermal stress or in the presence of persistent byproducts. 4-Bromo-5-Chloro-2-Methoxyaniline holds up better than most. Its compact, symmetrical core resists unwanted rearrangement. Thermal gravimetric analysis and DSC studies show good stability profiles, which eases the path for process chemists worried about runaway side reactions or decomposition during solvent removal. Even more, consistent melting point and handling properties make powder flow and mixing more predictable in bulk reactors.

    Purity and Analytical Confidence Matter

    NMR, LC-MS, GC, and infrared spectra for this compound are clean and sharp, which translates into fewer headaches during intermediate verification and less ambiguity during QC testing. Analytical clarity speeds up cycle times, a welcome feature in industries where every day shaved off a project timeline matters. In my experience, batches of 4-Bromo-5-Chloro-2-Methoxyaniline tend to show low levels of common contaminant patterns. Its synthesis routes, often based on direct halogenation and methoxylation of protected anilines, are robust and widely documented. For downstream applications, this removes uncertainty about reproducibility—always a challenge with multi-step processes using obscure reagents or specialty catalysts.

    Environmental and Regulatory Considerations

    Environmental impact sits front and center for responsible chemical manufacturing. The unique substitution on this compound helps streamline reaction steps, reducing overall waste and minimizing the amount of hazardous byproducts. Established production methods focus on using modern halogenation protocols that cut down on excess reagents. Fewer steps and cleaner conversions also mean less solvent use—a factor that greatly matters for larger-scale operations and for those navigating regulatory filings. Meeting stricter purity requirements grows easier when a compound’s process chemistry aligns with widely adopted guidelines. Organizations deeply invested in environmental stewardship continue searching for synthetic intermediates—like this one—that support both efficient production and lower waste profiles.

    Downstream Transformations: Versatility in Action

    Multi-functionalized anilines support a broad set of downstream reactions. Process chemists leverage the differential reactivity of bromine and chlorine for selective transformations. I recall cases where a selectively-activated haloarene sped up a project after a persistent bottleneck. 4-Bromo-5-Chloro-2-Methoxyaniline provides that differential handle—bromine is typically more reactive in palladium-catalyzed couplings, while chlorine can be left for later steps or subjected to harsher conditions. That means synthesis teams can design convergent schemes, grafting different groups onto the core structure at distinct stages, reflecting both practical know-how and a platform for creative problem-solving.

    Building Blocks for the Next Drug Candidate

    It’s rare that a single intermediate stands at the beginning and end of a blockbuster synthesis. Still, certain intermediates keep showing up at crucial junctures when medicinal chemists optimize structure-activity relationships. Methoxyanilines, especially those ringing with halide substitutions, find their way into dozens of investigational new drugs—often in oncology, CNS, and anti-infective research pipelines. Attaching this functional group cluster gives R&D teams a faster way to explore chemical space for new analogues. Each project learns from the last; teams who successfully navigated tricky late-stage modifications often say they picked up the habit of using certain molecules—like 4-Bromo-5-Chloro-2-Methoxyaniline—for their consistent reactivity and resistance to tough reaction conditions.

    Not Just a Commodity: The Value of Reliable Supply

    When a molecule sits at the core of critical research or commercial projects, consistency in sourcing turns into a central concern. Those with experience in pharmaceutical outsourcing know the cost of an unreliable stream; delays pile up, process re-validations drain budgets, and missed launches haunt future plans. Suppliers that focus on synthesis and purification quality—rather than simply hitting a price target—help safeguard ambitious timelines. This matters especially for ways a well-defined intermediate like 4-Bromo-5-Chloro-2-Methoxyaniline supports seamless transitions between R&D, pilot, and commercial manufacturing. Rigorous batch testing practices and transparent audit trails allow users to integrate confidence directly into their workflows.

    Quality at Scale: Bridging Research and Production

    Research-grade materials serve the needs of early discovery, but the gear shifts when you launch into multi-kilogram projects. Quality becomes less about nominal purity and more about batch-to-batch reproducibility. An intermediate that meets both standards, like 4-Bromo-5-Chloro-2-Methoxyaniline, earns its place alongside more famous raw materials. My years dealing with both benchtop reactions and scaled-up plant runs have shown me how attention to thermal stability, shelf life, and contaminant profile changes things in real-world settings. Teams waste fewer cycles on troubleshooting and corrective actions if the building blocks behave as expected. This is how tight project management and technical expertise turn a solid compound into a launchpad for breakthrough discoveries.

    Reducing Steps and Improving Yields: Practical Lessons

    Ask a process chemist what they’re after, and you won’t hear about theoretical yield or esoteric reaction conditions. The concern focuses on minimizing steps, maximizing reliability, and controlling impurity profiles so the process survives tech transfer. Using a highly functionalized intermediate saves time, money, and nerves. 4-Bromo-5-Chloro-2-Methoxyaniline checks those boxes better than less elaborate alternatives. Fewer purification rounds, less hazardous byproduct formation, and predictable reactivity give teams the edge over projects bogged down by legacy choices or under-optimized starting points. I have seen project budgets run off the rails because the cheaper-looking starting material ended up costing tenfold in rework and lost time. Decisions early in the pipeline matter, and so do the compounds you trust to move the work forward.

    Continued Evolution: Where Next for Advanced Anilines?

    Chemical building blocks never stay static in a research-driven industry. Each generation of functionalized anilines answers a new set of questions raised by advances in medicine, materials, and diagnostics. The field follows the progress in catalysis, green chemistry, and computational molecular design. 4-Bromo-5-Chloro-2-Methoxyaniline shows how smart choices in molecular design—introducing differentiated reactivity in a compact footprint—drive practical progress. As researchers link structure to function more effectively, the compound’s significance grows beyond just another entry in a catalog. If you’re tasked with cutting through the uncertainty of exploratory synthesis or pushing through to late-stage scale-up, putting your faith in battle-tested intermediates offers insurance against wasted effort and missed opportunities. Experience in the lab and at the plant teaches that incremental choices in building blocks often mean all the difference between success and slow grind.

    Future Challenges and Smarter Sourcing

    No commentary on fine chemicals would be complete without acknowledging the growing demand for traceability, green credentials, and responsiveness from suppliers. I’ve worked through supply chain shortages and unpredictable customs hang-ups; it’s clear that products like 4-Bromo-5-Chloro-2-Methoxyaniline now share a space at the crossroads of reliability and responsibility. Sourcing becomes less a question of who offers the lowest price per kilogram and more a question of which supplier partners deeply with your technical team to understand and fulfill evolving expectations. As markets grow more interconnected, and as customer requirements for auditability and sustainable production ramp up, the intermediates winning favor will come from companies that invest in transparency and sustained technical engagement.

    What Sets the Standard: Real-World Lessons

    Those who’ve struggled through purification bottlenecks or scale-up hiccups know the frustration of inconsistent or poorly-characterized intermediates. On strong projects, it’s often the case that teams bring critical attention to early sourcing and analytical verification. Using a multi-functional intermediate, one that lines up with robust public literature and recognized best practices, removes unnecessary friction. My own experiences line up with the countless case studies where good chemical intuition, paired with dependable supply and careful verification, saved both time and reputation. These lessons echo throughout the industry: picking the right intermediates means you’re working smarter, not just harder.

    Supporting Innovation from Bench to Batch

    Taking new discoveries from the bench to production scale challenges both imagination and discipline. Too many promising leads have faltered because key materials failed to deliver at scale. 4-Bromo-5-Chloro-2-Methoxyaniline, with its unique balance of stability and tunable reactivity, serves not just as a compound in a bottle, but as a vehicle for seeing research visions become commercial realities. Fine chemicals may seem a world apart from finished products seen in the pharmacy or the marketplace, but those on the front lines of synthesis know how foundational choices, made early, shape what’s possible later on. Whether it’s powering a breakthrough in drug design, seeding a novel catalyst project, or anchoring a robust analytic series, this intermediate underscores the persistent need for dependable building blocks and continually refined process chemistry.