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4-Amino-5-Bromo-2-Methylpyridine

    • Product Name 4-Amino-5-Bromo-2-Methylpyridine
    • Alias 4-Amino-5-bromo-2-picoline
    • Einecs 629-798-8
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    881737

    Chemical Name 4-Amino-5-Bromo-2-Methylpyridine
    Cas Number 942506-94-1
    Molecular Formula C6H7BrN2
    Molecular Weight 187.04 g/mol
    Appearance Light yellow to brown solid
    Melting Point 94-98°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Smiles CC1=NC=C(C=C1Br)N
    Inchi InChI=1S/C6H7BrN2/c1-4-2-5(8)3-6(7)9-4/h2-3H,8H2,1H3

    As an accredited 4-Amino-5-Bromo-2-Methylpyridine 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-Amino-5-Bromo-2-Methylpyridine

    Applications of 4-Amino-5-Bromo-2-Methylpyridine in Industrial Manufacturing

    4-Amino-5-Bromo-2-Methylpyridine serves as a key intermediate in the synthesis of advanced molecules across select chemical sectors. Our plant focuses production on strict standards for each downstream application. Below are core industrial segments utilizing this compound with specific process, compliance, and end use details.

    1. Pharmaceutical Active Ingredient Manufacturing

    Major pharmaceutical companies use this material as a heterocyclic intermediate in the custom synthesis of small-molecule APIs, especially within the anti-infective, CNS, and oncology drug classes. Production teams employ this pyridine derivative in multi-step reactions, including amination, halogen exchange, and cyclization, to generate proprietary scaffolds. The dosing ratio depends on the desired yield and purity, with in-line QA checks to meet ICH and pharmacopoeial specifications before final scale-up.

    Industry compliance standards

    • ICH Q7 GMP guidelines for API manufacturing
    • Current USP, Ph. Eur., JP specifications for raw materials
    • 21 CFR Part 211 (cGMP - US FDA)
    • EU Directive 2001/83/EC (as applicable per finished medicine)

    Typical usage ratio

    • 0.15–0.35 mol per mol of target API intermediate; adjusted per reaction stoichiometry and impurity profile

    Downstream process integration

    • Charged during Stage 2–3 of multi-step chemical synthesis, often after initial amide or coupling formation

    Final product types

    • Small molecule pharmaceutical actives (e.g., kinase inhibitors, CNS agents, anti-viral compounds)
    • Intermediate reference standards for drug development

    2. Agrochemical Synthesis

    Agricultural chemical formulators utilize this molecule as a building block for the manufacture of selective herbicides and certain fungicides. The compound introduces both bromo and amino functional groups, enabling further derivatization to target specific enzyme inhibition in weeds or fungi. Formulation scientists strictly control ratios to optimize crop selectivity, and residue studies align with regulatory approvals in target markets.

    Industry compliance standards

    • EPA 40 CFR Part 180 (US pesticide regulation)
    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO specifications for active ingredients
    • REACH registration and SDS requirements (EU)

    Typical usage ratio

    • 0.10–0.25 mol per mol of final agrochemical active, with ratio determined by desired herbicidal spectrum and environmental fate assessments

    Downstream process integration

    • Input for Step 1 or 2 of chemical synthesis—commonly coupled via Suzuki or nucleophilic aromatic substitution before active ingredient isolation

    Final product types

    • Pyridine-based selective herbicides
    • Systemic fungicide actives for seed treatment
    • Pre-emergent weed inhibitors

    3. Advanced Electronic Materials

    Electronics chemical manufacturers require this specialty pyridine for the development of organic compounds used in OLED emitters and organic semiconductor precursors. The material enables incorporation of bromine into molecular frameworks, providing tunable electron transport properties and high thermal stability in display and photonic components. Ratio setting responds to end-device electrical and optical testing results.

    Industry compliance standards

    • IPC-4101B for base materials in electronic laminates
    • RoHS Directive 2011/65/EU (hazardous substances restriction)
    • REACH compliance for electronic chemicals
    • ISO 9001:2015 (QMS for specialty electronics components)

    Typical usage ratio

    • 0.03–0.08 mol per mol of target emitter or precursor during material design evaluations

    Downstream process integration

    • Introduced in the condensation or functionalization step to form the conjugated pi-system in OLED or photoconductor molecules

    Final product types

    • OLED display emitters (blue/green hosts)
    • Organic photoconductors for imaging drums
    • Organic thin-film transistor materials

    4. Custom Dye and Pigment Manufacturing

    Specialty dye producers select this compound as a reactive intermediate allowing for creation of azo, anthraquinone, and pyridine-functionalized colorants. Its presence gives enhanced shade stability and fastness on synthetic fibers and plastic surfaces. Operators calibrate usage based on chromophore formation and lightfastness tests, aligning process with environmental compliance for dye effluents.

    Industry compliance standards

    • EN 71-3 Migration of certain elements for colored plastics (EU Toys)
    • OEKO-TEX Standard 100 textile safety
    • GHS labeling regulations (CLP Regulation EC No 1272/2008)
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • 5–18 wt% of total molecular backbone in target dye; varies by required color index number and shade depth

    Downstream process integration

    • Molecule enters during step-growth polymerization or in diazotization/coupling for azo dye formation

    Final product types

    • Textile fiber dyes (nylon, polyester blends)
    • High-performance plastics colorants
    • Inkjet and digital imaging pigments

    5. Veterinary Drug Intermediates

    Animal health product manufacturers use this pyridine as an intermediate for the assembly of antibiotics and antiparasitic agents. Process chemists rely on its amino and bromo groups for selectivity during nucleophilic substitutions and cyclization stages. Usage ratio is informed by route optimization labs adhering to international veterinary GMP requirements and residue guidelines.

    Industry compliance standards

    • VICH GLs (Veterinary ICH guidelines)
    • GMP for Veterinary Medicinal Products (EU Directive 91/412/EEC)
    • USP Veterinary compendium (when applicable)
    • Global MRLs (Maximum Residue Limits) via Codex

    Typical usage ratio

    • 0.12–0.28 mol per mol of veterinary API precursor, matched to yield and impurity standards per batch analysis

    Downstream process integration

    • Fed during mid- to late-stage of synthesis, allowing for late-stage functionalization in the API assembly process

    Final product types

    • Antiparasitic actives (oral and injectable forms)
    • Veterinary antibiotics for livestock and companion animals
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    Certification & Compliance
    More Introduction

    4-Amino-5-Bromo-2-Methylpyridine: Engineering Precision for Modern Chemistry

    Stepping Into Specialty Materials

    The landscape of fine chemicals keeps evolving, yet there are building blocks that quietly push entire industries forward. Take a closer look at 4-Amino-5-Bromo-2-Methylpyridine: a compound that hardly ever makes it into mainstream conversation but proves vital in the hands of chemists and materials scientists. Its molecular structure isn't just a collection of atoms—it's a ticket to new possibilities in the lab, driven by a combination of selectivity and manageable reactivity that's hard to find elsewhere.

    What Sets the Model Apart

    Chemistry is full of familiar names and formulas, but few substitute for the high standards set by this pyridine derivative. The combination of bromine and methyl substitution on the pyridine ring introduces both bulk and site-specific electronic effects, which change the way this molecule interacts in a series of syntheses, especially for those looking to build complex pharmaceuticals or advanced materials. The amino group, positioned at the 4 spot, adds a layer of reactivity without overwhelming the rest of the molecule. It's almost like having just the right amount of ambition—not too idle, not too explosive.

    From firsthand experience in research settings, I’ve watched how compounds like this create pathways that simply aren’t available when using simpler pyridines. Colleagues in medicinal chemistry have pointed to its value during the early stages of drug design. The substitution pattern allows for direct coupling and fine-tuning, particularly when you want to steer a molecular scaffold toward higher selectivity or when trying to dodge unwanted side-reactions. I remember the challenge of tweaking substituents in nitrogen-containing heterocycles to tune solubility and bioavailability; this compound gave us more control when libraries started to stagnate on more generic scaffolds.

    Real Applications Beyond the Bench

    At first glance, it might seem like a solution looking for a problem, but demand for 4-Amino-5-Bromo-2-Methylpyridine stands as proof of its usefulness. Medicinal chemistry teams working on kinase inhibitors, for instance, often look toward heterocycles with customizable positions for late-stage diversification. The presence of both electron-donating and electron-withdrawing groups opens doors to targeted modifications, essential for the kind of structure-activity investigation that's at the heart of drug development. It’s not just the pharmaceutical sector that benefits. Material scientists, especially those tinkering with new organic semiconductors or advanced dyes, use it to impart thermal stability and introduce unique sites for subsequent functionalization.

    During my time in a contract research organization, synthetic bottlenecks used to keep clients and researchers up at night. Library synthesis needed starting materials that were robust enough to survive demanding conditions but open enough for a range of transformations. Switching to pyridine scaffolds like this allowed us to break up gridlocked workflows, avoid excess protection-deprotection steps, and tilt reactions toward our desired products.

    Specifications That Matter

    Specifications don't exist to check boxes—they're about achieving consistency batch after batch. In the projects I’ve worked on, confidence in purity can make or break months of planning. The standard for 4-Amino-5-Bromo-2-Methylpyridine sits comfortably at >98%, supported by both HPLC and NMR analyses. Light yellow powders dominate the high-purity batches, and a sharp melting point signals the product stands free from ambiguous byproducts or major degradation. This consistency means fewer headaches when scaling up from milligram experiments to kilogram production.

    Moisture and light sensitivity are present, as with many amines, but no more so than a typical bench chemist would face working with related aromatic compounds. Proper storage (sealed container, away from direct sunlight and humidity) keeps the material fresh and ready for action, whether it’s destined for a round-bottom flask or an automated synthesizer.

    Differences That Define Performance

    Ask anyone who’s dug into the world of pyridine derivatives and the first challenge is often about picking the right starting point. The amino group at position 4 is far from trivial; compared to its placement at position 2 or 3, this arrangement reduces both steric hindrance and directs many reactions toward more predictable outcomes. When competitive bromination or methylation comes into play, most analogues either lose their reactivity or create messy mixtures.

    Take, for example, 2-Amino-5-Bromo-3-Methylpyridine. You end up with competing routes for cross-coupling and greater risk of polysubstitution that complicates purification. In contrast, 4-Amino-5-Bromo-2-Methylpyridine narrows reaction profiles and leaves more useful space for functional group diversity later. The higher selectivity shown in Suzuki and Buchwald-Hartwig couplings leads directly to cleaner reactions and higher yields—a reality borne out in thousands of organic synthesis reports.

    It can be tempting to reach for alternatives with similar ring systems or even swap the methyl for an ethyl, but those initial gut instincts rarely survive scale-up. In lab-scale experiments, I watched colleagues try to skirt bottlenecks with supposedly cheaper isomers, only to wind up wrestling with decreased solubility, sluggish reactivity, or side products that poisoned downstream steps. For researchers who need reliability, consistent supply, and confidence that tomorrow’s batch will match today’s, this 4-amino-5-bromo-2-methyl scaffold wins out almost every time.

    Supporting Accuracy and Trust in the Supply Chain

    Navigating specialty synthons demands attention to detail and a strong supply chain. Reliability isn’t just about compliance—it’s about safety and transparency. Suppliers work with batch analysis certificates, regulatory compliance reporting, and impurity profiling. Third-party testing and traceability have become part of the fabric of responsible sourcing. Quality systems that I’ve encountered focus on minimizing unknowns, providing documentation at every stage, from initial synthesis through packaging and distribution.

    In my own procurement roles, I’ve looked for clarity not only in analytical results but also in storage histories and supply chain records. Consistency starts well before a bottle lands on a laboratory shelf. Regular audits from pharmaceutical customers and exacting standards keep the industry honest, rewarding those who deliver on their promises.

    Toward Sustainable Choices and Responsible Use

    The chemical industry’s reputation often hinges on how it deals with the aftermath of innovation. For pyridine derivatives, waste minimization and greener manufacturing techniques are gaining ground, mostly in response to both regulatory pressure and genuine interest in sustainability. Many manufacturers have adopted cleaner synthetic routes, using fewer halogenated solvents and recycling reaction media where feasible. In one project, a partner supplier provided options with closed-loop manufacturing systems, which not only reduced byproduct streams but also cut costs over the long haul.

    I have seen colleagues apply stepwise purification and advanced crystallization methods, significantly reducing the use of hazardous materials downstream. Improving atom economy and cutting energy use per kilo produced builds not just a better product but a smaller ecological footprint.

    Challenges Lurking on the Horizon

    The march of regulation continues, especially across North America, Europe, and parts of Asia. Keeping up with shifting limits on impurity levels or restrictions on specific halogen uses presents a constant challenge for producers. As these rules get tougher, companies face decisions: invest in cleaner technologies and better process controls or risk losing access to global markets.

    From the buyer's side, demand for traceable origins and more transparent documentation remains relentless. Researchers want to know how the compound was made, whether there are any hidden contaminant risks, and what measures are in place to ensure safety in transit and storage. Some of this vigilance stems from spectacular failures in unrelated sectors, but it means more relationships built on trust, data, and detailed communication. The experience of vetting new suppliers often involves reading through technical files and third-party audits, leaning heavily toward those who can explain every step that the compound has taken from raw material to finished flask.

    Potential Solutions and the Path Forward

    Meeting tighter quality standards doesn’t need magical thinking; it’s about sticking to proven best practices. For supply partners, adopting practices such as in-line monitoring, robust batch tracking, and early adoption of greener manufacturing materials will keep demand high. I’ve watched small firms invest in process automation, using real-time data to catch deviations before they get out of control. That translates to better product and fewer recalls, which benefit every pocket of the laboratory ecosystem.

    For those in research and development, the answer lies not only in technical specs but also in relationships. Staying close to suppliers, requesting tailored batch analysis, and demanding transparency with every transaction lets chemists focus on discovery, not on routine troubleshooting. I’ve lost count of the times a trusted supplier saved our timelines by flagging a storage issue or providing tailored documentation before we even thought to ask. This kind of partnership forms the backbone of responsible science.

    Conclusion: Shaping Reliable Results in Dynamic Industries

    Modern chemistry—especially where the stakes are highest—faces constant pressure to innovate and deliver. Key building blocks like 4-Amino-5-Bromo-2-Methylpyridine take on more responsibility than most people realize. By offering a rare mix of selective reactivity, consistent purity, and practical storage, this molecule gives researchers the confidence to chase new ideas and meet ever-tightening standards. The journey doesn’t stop at the point of sale; the trail of documentation and stewardship grows longer and more complex, matched only by the drive toward cleaner manufacturing and more ethical sourcing.

    Whether setting up a medicinal chemistry campaign or diving into the world of advanced materials, having the right building block means fewer surprises and more successes. The difference comes from a mixture of careful design, hard-won experience in the field, and an industry-wide commitment to doing better—batch after batch, and year after year.