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Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride

    • Product Name Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride
    • Alias Methyl 5-amino-2-bromo-4-methylbenzoate HCl
    • 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

    664623

    Product Name Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride
    Molecular Formula C9H9BrClNO2
    Molecular Weight 278.53 g/mol
    Appearance Off-white to light yellow solid
    Solubility Soluble in water and DMSO
    Purity Typically ≥98%
    Storage Temperature 2-8°C (Refrigerated)
    Synonyms Methyl 5-Amino-2-Bromo-4-Methylbenzoate HCl
    Chemical Class Aromatic halide derivative
    Iupac Name Methyl 5-Amino-2-Bromo-4-Methylbenzoate hydrochloride

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

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    Application of Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride

    Applications of Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride in Industrial Manufacturing

    As a specialized manufacturer of Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride, we supply this intermediate to several sectors requiring tailored synthesis steps and strict quality assurance at industrial scale. The following application scenarios highlight how downstream producers integrate this compound to support regulated performance requirements, precise process efficiencies, and compliance-controlled end products.

    1. Advanced Pharmaceutical Intermediate Synthesis

    Pharmaceutical firms incorporate this compound into the synthetic route for the preparation of various small-molecule APIs, especially within the development of next-generation anti-inflammatory agents and certain kinase inhibitor drug candidates. Due to the brominated aromatic ring and amino substituent, formulation chemists exploit its reactivity for regioselective coupling and stepwise derivatization, maintaining process traceability and impurity thresholds to meet strict drug substance standards throughout clinical and commercial manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU GMP Annex 13 for Investigational Medicinal Products
    • Chinese Pharmacopoeia (ChP) API impurity guidelines (for China-based API manufacture)

    Typical usage ratio

    • 0.8–1.5 molar equivalents as a step intermediate, with final ratio adjusted based on stoichiometry demanded by target molecule synthesis. Process engineers calculate batch size by yield optimization and impurity control in the main coupling or condensation stage.

    Downstream process integration

    • Enters as a starting aromatic intermediate for palladium-catalyzed cross-coupling (Suzuki, Buchwald-Hartwig, etc.) or amide formation steps following solvent-based purification and specification release. Subsequent conversion to final API via hydrogenation, hydrolysis, or further acylation as dictated by product route.

    Final product types

    • Oral solid and injectable APIs, reference standards, pilot-scale preclinical compound batches
    • State-registered generic APIs and drug substance supply for CDMO partners

    2. Specialty Dye and Pigment Intermediate

    Manufacturers synthesize high-performance specialty dyes using this benzoic acid derivative as a key coupling precursor. The compound’s unique bromo and amino positions enable intensive chromophore development, resulting in dyes for demanding textile, plastics, and inkjet applications where lightfastness and chemical resistance profiles are critical. Downstream processes require close control of color development reactions and hydrolytic stability of intermediary products.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for eco-friendly textile dyes
    • EN 71-3:2019 for pigment compliance in toys and printable goods
    • REACH Annex XVII restrictions on aromatic amines and halogenated dye precursors
    • ISO 9001:2015 quality management systems for dye manufacturing

    Typical usage ratio

    • 0.5–2.0% by weight of total dye batch, depending on required color depth and covalent incorporation in azo, anthraquinone, or heterocyclic dye scaffolds. Adjustments reflect desired UV resistance and downstream dye purity specifications.

    Downstream process integration

    • Feeds into diazotization or nucleophilic aromatic substitution followed by condensation with coupling agents under regulated temperature and pH. Final dye intermediates undergo filtration, salting out, and spray drying prior to blending into masterbatch formulations.

    Final product types

    • Disperse dyes for polyester and synthetic textiles
    • Solvent-resistant pigments for plastics and coatings
    • Waterborne and solvent inkjet inks

    3. Agrochemical Active Ingredient Synthesis

    In agrochemical active manufacturing, formulators rely on the brominated amino acid derivative for the construction of unique heterocyclic scaffolds offering crop protection activity. This intermediate serves as a structural bridge in molecules designed for broadleaf weed control or as a building block in pyrazole and pyridine ring systems. Its use must meet hazardous substance restrictions and environmental safety limits typical for agrochemical feedstocks.

    Industry compliance standards

    • FAO/WHO Code of Conduct on Pesticide Management
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • US EPA FIFRA regulatory program (Federal Insecticide, Fungicide, and Rodenticide Act)
    • ISO 14001 environmental management for agrochemical synthesis

    Typical usage ratio

    • 0.4–0.7 molar equivalents per batch, calculated in relation to downstream heterocycle formation. Precise amount is varied in pilot-plant and commercial trials depending on overall yield and impurity formation profiles in targeted actives.

    Downstream process integration

    • Incorporated during initial cyclization or halogen exchange step for new active molecule scaffolds. Material is charged directly into reactor vessels, often as a dissolved solution in polar organic solvents, for controlled condensation and ring closure reactions.

    Final product types

    • Pre-formulation pesticide actives
    • Technical grade intermediates for selective herbicides
    • Field trial samples for regulatory submission

    4. Fine Chemical Research and Analytical Reference

    Certified standards and analytical reagent producers apply this compound for preparing traceable reference materials tailored for industrial QC labs and regulatory validation. Its defined aromatic structure, halogen and amino functionality provide critical matrix standards for HPLC, GC-MS, or NMR reference testing across pharmaceutical, environmental, and R&D sectors. Traceability, chemical identity, and stability are paramount, demanding robust documentation of lot data and reference storage conditions.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • ISO/IEC 17025 laboratory accreditation for analytical testing
    • USP <823> and Ph. Eur 2.7.1 for pharmaceutical impurity standards
    • OECD Mutual Acceptance of Data (MAD) guidelines for global chemical testing

    Typical usage ratio

    • 0.02–0.15% w/w when preparing analytical standards solutions or spiking samples; varies based on calibration protocol or sensitivity of detection method. Replicates and dilutions standardized by lab SOPs.

    Downstream process integration

    • Undergoes purity verification, homogenization, and gravimetric dilution before bottling into QC-certified reference vials. End users integrate these standards into method validation procedures and instrument calibration protocols.

    Final product types

    • Certified reference materials (CRMs) for chromatography
    • Analytical calibration standards for spectroscopic analysis
    • Trace impurity markers in pharmaceutical process QC
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    More Introduction

    Introducing Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride: Real-World Value and Practical Insights

    Behind the Name—A Compound with Purpose

    Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride doesn’t exactly roll off the tongue, but people working in chemical research or pharmaceutical development know it's more than just a technical label. This compound, often referenced by chemists for its molecular uniqueness, fills a spot that generic benzoic acid derivatives can’t fill. The model number attached to it, usually set by the producer, ties directly to its batch consistency and traceability, both practical details that make a real difference in everyday laboratory and industrial settings.

    Structure That Matters—Why This Compound Stands Out

    Let’s get to the heart of what this chemical is: a benzoic acid backbone, tweaked with a bromine at the 2-position, an amino group at 5, a methyl at 4, and set as its hydrochloride salt. For chemists, these tweaks aren’t just technical—they shape how the molecule will behave in reactivity, solubility, and stability. Bromine and methyl give it distinctive properties for building more complex molecules, especially in synthesis trees for drug candidates or organic electronics. This is not just a lab curiosity; these groups create opportunities for targeted reactivity, which is critical during steps where chemists might need precise control over how a reaction proceeds.

    Quality and Purity—A Key Factor Researchers Rely On

    Any researcher who has spent late nights troubleshooting experiments knows that impurities can derail progress. With Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride, purity specifications matter—often upwards of 98% or more. What sounds like a tiny margin is the difference between a clear reaction and a frustrating dead-end. This compound is typically delivered with reliable spectral data—NMR and HPLC reports are common tools for confirming its identity. For anyone running complex organics, cutting corners with quality means risking everything from reproducibility to safety.

    Uses—Connecting the Laboratory with Real-World Products

    Chemists reach for Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride for its flexibility in forming key intermediates. Pharmaceutical research teams value its amino group, which serves as a handle for constructing ureas, amides, or coupling with peptides. The bromine makes it an ideal starting point for Suzuki or Heck reactions, especially for late-stage functionalization where tweaking a molecule for activity can make or break a project. While the end-user may never hear about this specific building block, drugs, dyes, agrochemicals, or diagnostic agents that promote health or sustainable agriculture can trace critical steps back to this exact compound.

    What you find with this hydrochloride salt—rather than a free base or neutral form—is increased aqueous solubility. For those assembling complex molecules, this salt form often dissolves in water-based or mixed solvents without headache, which shortens time spent on initial solubility puzzles. My own work as a bench chemist showed me how delays compound when you spend hours coaxing a stubborn compound into solution. I remember spending weeks optimizing a route, only to realize that swapping an amine for its hydrochloride sped up purification and improved yields.

    Comparing with Other Benzoic Acid Derivatives

    Not every benzoic acid derivative will deliver the same result, especially when optimizing for selectivity or reactivity. Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride stands apart from simpler analogs—for example, a plain 5-aminobenzoic acid or a methylbenzoic acid. The specific pattern of bromine and methyl substitutions changes the reactivity profile, especially under catalytic cross-coupling reactions or directed ortho-metalation.

    In my own collaborations with medicinal chemistry teams, we found that a subtle structural difference between an ortho-bromo and an ortho-chloro derivative led to a tenfold change in the downstream yield of a target intermediate. That’s not marketing talk—it’s a typical story for chemists who have to justify every step to quality controls and budget holders alike. Bromine often outperforms chlorine in leaving group ability, opening up access to more robust coupling partners, which in turn gives more room for creativity in structural design. The methyl group, meanwhile, can block unwanted substitutions and force the reaction to happen where you want it.

    Getting a hydrochloride salt, versus a free amine, can be a game changer. Free amines often attract moisture and can turn sticky or degrade. The hydrochloride is not just easier to handle but can store longer without risk of amine oxidation, a concern that chemists dealing with scale-up especially dread. Practically, this means someone pulling a bottle after six months finds the same reliable compound, not a degraded mess.

    Solving Practical Problems: Stability and Handling

    People who work with sensitive molecules know how frustrating instability can be. Air and moisture sensitivity aren’t strangers in the world of substituted benzoic acids. As a hydrochloride salt, Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride handles exposure much better than many free amines or carboxylic acids. This helps labs reduce waste and repeated purchases. From experience, there’s nothing like opening a fresh container, only to find your material’s turned brown or clumpy from air exposure—especially weeks after you put it away in what you thought was good storage.

    Stability isn’t just about convenience; it’s also central for regulatory purposes. In the pharmaceutical industry, every intermediate must clear regulatory hurdles on impurity profiles, stability, and traceability. Having a well-behaved salt form makes documentation smoother and reproducibility more straightforward. It’s difficult enough shepherding a compound through the mazes of ICH guidelines without being tripped up by material that isn’t reliable over time.

    Academic and Industrial Experience: Making Synthesis Work

    During my own PhD years, working out multistep syntheses for active drug candidates, access to specialty intermediates like this one reduced the risk of stalls during crucial steps. In projects with industrial partners, cost and supply chain stability determined whether a route advanced from the whiteboard to the kilo lab. This hydrochloride salt, already more stable than a free amine, removed barriers—I didn’t have to plan for extra purification or worry about side reactions caused by environmental exposure. Once, I wasted days troubleshooting a methylbenzoic acid route because our substituent positions didn’t match what was needed for selectivity. Availability of precisely substituted intermediates changed the project’s timeline by weeks.

    Suppliers often provide detailed spectral analyses, which removes ambiguity and accelerates development timelines. Instead of waiting for uncertain results, teams get reproducible access to a key tool for drug discovery, dye development, or other fields where tailored aromatic compounds provide the foundation for innovation. Researchers choosing between this compound and alternatives should weigh not only the upfront cost, but also the hidden value—smoother reactions, less downtime troubleshooting, and a shot at better yields.

    Challenges and Potential Solutions

    One persistent challenge is keeping supply steady. Specialty chemicals like Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride depend on stable feedstocks and reliable logistics. Disruptions can arrive quickly, especially if a precursor chemical becomes scarce or a producer changes preparation routes. In the past few years, I’ve seen projects halted not for lack of innovation, but because a shipment delayed critical steps. That sort of bottleneck can dry up grant funding or break a development cycle.

    Building redundancy into supply chains would help. This involves sourcing from multiple vetted suppliers, maintaining clear communication on product specifications, and setting up frameworks for alternate sourcing. Plenty of labs already keep a log of trusted suppliers, but even so, verifying identity and quality remains an ongoing effort. Collaborative purchasing agreements and early warning supply indicators could buffer critical projects from the impact of the next big shortage.

    Shipping and storage present another issue. Hydrochloride salts are generally easier to handle than their base counterparts, but packaging can still be a vulnerable point. Strong humidity control and airtight packaging prevent degradation. Research organizations sharing tips on storage and handling reduces waste and surprise losses. I’ve swapped stories and advice with colleagues at conferences, learning practical tricks for storing sensitive materials—sometimes a simple desiccant packet in the container keeps the compound stable months longer. Industry best practices should be more widely shared, especially with new researchers.

    Safety and Environmental Considerations

    Anyone working with compounds containing bromine and aromatic amines must respect their hazards. Proper lab ventilation, gloves, and eye protection aren’t negotiable—old habits and shortcuts can burn even experienced chemists. The waste streams from reactions involving brominated intermediates should never be poured away casually. Most labs developed strict protocols, but newer operations sometimes cut corners under pressure, risking harm or regulatory backlash. Training must remain a priority, not just at the onboarding stage, but ongoing as chemical handling standards evolve.

    Long-term, methods to reduce hazardous byproducts could make a difference. For example, transition toward greener cross-coupling protocols, using water-based solvents or catalytic systems that minimize toxic reagents, shows real promise. Several recent papers detailed improved Suzuki and Buchwald-Hartwig couplings with benign conditions, reducing the environmental impact of making advanced intermediates. Adopting these practices means recalibrating standard operating procedures, but the downstream benefits spread beyond the lab—safer workplaces, cleaner waste, and less regulatory paperwork.

    Innovation and the Role of Reliable Intermediates

    Science progresses on the shoulders of robust intermediates. Without dependable, well-characterized starting materials, even the most creative synthetic routes stumble. In my involvement with start-ups and academic teams, access to compounds like Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride made the difference between screening five candidate molecules or fifty. Productivity and discovery scale up when supply bottlenecks fade into the background.

    Transforming a benchtop breakthrough into a scalable process takes more than just brilliant chemistry. It takes raw materials that you trust, supported by clear documentation and regular supply. This hydrochloride salt has shown staying power because it fills a genuine need—reactivity, physical stability, and ease of handling. As more advanced therapeutics, specialty dyes, or agrochemicals require fine-tuned aromatic intermediates, the role of uniquely substituted benzoic acids will only grow.

    Several published case studies tackled the direct use of this compound or very close analogs in late-stage functionalization. My peers in pharmaceutical process research echoed these findings: picking the right building block at the outset saves time, money, and headaches downstream. They reported that downstream regulatory filings, especially for clinical-stage drug candidates, were bolstered by solid purity data and well-understood impurity profiles linked to the hydrochloride salt.

    Cost versus Value—Making Smart Choices in Chemical Procurement

    Budget pressure never goes away in research, whether in academia, biotech, or industrial R&D. Buying high-quality intermediates sometimes gets squeezed below equipment or labor on the priority list. From experience, skimping on a key intermediate rarely pays off. Cheaper, low-grade batches can introduce impurities that echo through every subsequent step, requiring more purification, more solvents, more time spent on troubleshooting.

    Cost-benefit analyses should include not just sticker price, but hidden savings from improved reaction efficiency and reduced downtime. In group discussions, colleagues often cite cases where a slightly pricier, high-purity intermediate led to higher overall yield and less end-product testing. In some cases, premium lots of this hydrochloride intermediate led to scalable methods that survived tech-transfer from R&D to pilot plant, saving tens of thousands across a project.

    The Future—Directions for Benzoic Acid Intermediate Usage

    Looking forward, the demand for flexible aromatic intermediates will grow. With AI-driven medicinal chemistry and high-throughput screening, speed and reproducibility mean more than ever. Compounds with clear attributes—solid-state stability, proven batch-to-batch reproducibility, and regulatory-compliant documentation—set the stage for this acceleration. Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride meets these needs, both in its physical properties and its established track record.

    The push toward greener chemistry and sustainable production will shape the landscape. Sourcing brominated intermediates responsibly, minimizing hazardous waste, and transitioning to cleaner synthetic protocols serve both regulatory and environmental needs. Some of my recent projects turned to catalytic biotransformations as an alternative step—sometimes bypassing harsh halogenation conditions entirely. While not every process can be “green” from the start, every move forward counts.

    Mentorship and training should keep pace. As students and early-career scientists enter the world of chemical synthesis, clear guidance on the practical choices—when and why to pick a certain salt form, how to handle sensitive intermediates, where to look for best storage solutions—adds up to a more capable, confident workforce. Labs fostering this kind of practical wisdom see fewer wasted reagents and smoother project timelines.

    Conclusion—The Real-World Impact of a Specialized Benzoic Acid Derivative

    Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride might seem like a mouthful, but it’s a quiet enabler of chemistry that shapes the medicines, diagnostics, and materials society relies on. My work and conversations with others in the field confirm that reliable intermediates lay the groundwork for innovation, efficiency, and safety. Thoughtful procurement, responsible handling, and a commitment to ongoing best practices ensure that this compound continues to drive progress in both lab and industry. The difference often comes down to choosing tools with a proven record—tools that make groundbreaking science possible, one reaction at a time.