2-Amino-4-Methyl-5-Bromopyridine

    • Product Name: 2-Amino-4-Methyl-5-Bromopyridine
    • Chemical Name (IUPAC): 2-amino-5-bromo-4-methylpyridine
    • CAS No.: 54231-35-5
    • Chemical Formula: C6H7BrN2
    • Form/Physical State: Crystalline powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    792054

    Productname 2-Amino-4-Methyl-5-Bromopyridine
    Casnumber 19798-29-9
    Molecularformula C6H7BrN2
    Molecularweight 187.04
    Appearance Light yellow to brown solid
    Meltingpoint 90-95°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storagetemperature Store at room temperature
    Smiles Cc1cc(Br)nc([nH]1)N
    Inchi InChI=1S/C6H7BrN2/c1-4-2-5(7)9-6(8)3-4/h2-3H,1H3,(H2,8,9)

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

    Packing & Storage
    Packing Opaque amber glass bottle, 25 grams, with tamper-evident cap, hazard labels, chemical name, purity, lot number, and safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Amino-4-Methyl-5-Bromopyridine ensures secure, moisture-free, and stable packaging for safe international transport.
    Shipping 2-Amino-4-Methyl-5-Bromopyridine is shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport is carried out according to regulations for hazardous chemicals, ensuring stability and safety during transit. Packaging is designed to prevent leaks or spills, and appropriate labeling is provided to indicate its chemical and hazard classifications.
    Storage 2-Amino-4-Methyl-5-Bromopyridine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Store in a chemical-resistant, labeled container at room temperature, and ensure proper handling to prevent moisture ingress and contamination. Use in accordance with safety guidelines.
    Shelf Life 2-Amino-4-Methyl-5-Bromopyridine has a typical shelf life of 2-3 years when stored properly in a cool, dry place.
    Application of 2-Amino-4-Methyl-5-Bromopyridine

    Purity 98%: 2-Amino-4-Methyl-5-Bromopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity profile.

    Melting Point 120°C: 2-Amino-4-Methyl-5-Bromopyridine at melting point 120°C is used in organic synthesis reactions, where thermal stability facilitates controlled reaction conditions.

    Molecular Weight 187.04 g/mol: 2-Amino-4-Methyl-5-Bromopyridine with molecular weight 187.04 g/mol is used in medicinal chemistry development, where precise molecular incorporation supports accurate compound design.

    Particle Size <50 µm: 2-Amino-4-Methyl-5-Bromopyridine with particle size less than 50 µm is used in solid formulation processes, where fine powder dispersion enhances mixing uniformity.

    Stability Temperature up to 80°C: 2-Amino-4-Methyl-5-Bromopyridine stable up to 80°C is used in high-temperature synthesis pathways, where decomposition risk is minimized for reliable product quality.

    Water Solubility 1 mg/mL: 2-Amino-4-Methyl-5-Bromopyridine with water solubility of 1 mg/mL is used in aqueous reaction systems, where moderate solubility supports homogeneous reactor conditions.

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    Certification & Compliance
    More Introduction

    Introducing 2-Amino-4-Methyl-5-Bromopyridine: Reliability in Chemical Synthesis

    A Closer Look at the Model and Specifications

    2-Amino-4-Methyl-5-Bromopyridine stands out among pyridine derivatives for its unique pattern of functional groups and its value in organic synthesis. As someone who’s spent years observing the quiet evolution of chemical reagents, I recognize the understated importance of these small but mighty molecules. The structure consists of a methyl group at position 4, an amino group at position 2, and a bromine at position 5 on the pyridine ring. This particular configuration gives it reactivity you don’t find in more basic analogs. With a molecular formula of C6H7BrN2, users can expect a powder that ranges from white to pale yellow, often with a faint characteristic odor—if it drifts up at all.

    Most batches consistently deliver a melting point in the range of 95–98 °C, which can tell you quite a bit about purity—any drift here can wave a red flag. Purity standards tend to hit at least 98%, typically verified by HPLC or GC, and for people working on scalable chemical processes, that reliability turns a routine check into genuine peace of mind. Storage in a cool, dry place away from light and strong oxidizers remains the best practice, mainly to guard against degradation. Packing is usually in double-sealed bags inside protective barrels, not just as a matter of tradition but because years of shipping experience have shown how unforgiving moisture and air can be for this kind of material.

    Usage Patterns: More Than a Building Block

    Pyridine derivatives make up a class of compounds that see use across pharmaceuticals, agricultural chemistry, dyes, and beyond. 2-Amino-4-Methyl-5-Bromopyridine enjoys a fair bit of attention from medicinal chemists looking for reliable “handles” on complex molecules. The combination of bromine and amino groups on the same ring lets researchers get creative with cross-coupling reactions or nucleophilic substitutions. In my experience, amine functionality on a pyridine backbone opens the door to plenty of late-stage functionalization in small molecule synthesis—a useful tool when timelines force tough shortcuts in the lab.

    What strikes me as essential about this compound is its role in generating intermediates for anti-viral and anti-tumor agents. Many life-saving therapies draw their complexity from careful placement of electrodonating and electronegative groups, a feature that 2-Amino-4-Methyl-5-Bromopyridine delivers straight from the bottle. Researchers have made inroads in kinase inhibitor development and even some central nervous system drugs by exploiting the selectivity available here. It’s not a stretch to say this molecule carries a kind of silent weight in drug discovery—rarely headlining, but always present.

    Agriculture also benefits. Agrochemical developers often reach for halogenated pyridines to confer resistance traits or target specific metabolic pathways in pests. While not as famous as classic herbicidal actives, these underlie improvements in selectivity, shelf-life, and application rates. Every season, production managers weigh the trade-offs between yield and environmental burden, and compounds like this tilt the balance by allowing lower application doses or new modes of action.

    What Sets It Apart?

    It’s one thing to claim a product is unique; it’s another to stand up to comparison. 2-Amino-4-Methyl-5-Bromopyridine brings together functional groups that drive both reactivity and selectivity. Many competitors rely on either amine- or bromo-substituted pyridines, but the presence of both transforms reactivity windows for Suzuki, Buchwald, or Ullmann reactions. For organic chemists churning through fragment-based design or library screening, this combination means fewer protecting group headaches and more direct paths from bench to compound collection.

    From practical experience, the operational differences matter. For example, take the solubility profile. While halogenated amines often push the limits of solubility in typical organic solvents, the methyl group here slightly nudges the balance in favor of better handling. Those hours wrestling with gooey, half-soluble reaction mixtures or chasing crystals that collapse before filtration—it gets old fast. With this compound, improved solubility simplifies purification, reduces loss on work-up, and generally keeps things moving. When scale-up comes into play, this sometimes means the difference between a clean process and a week lost to troubleshooting.

    Safety isn’t just a box to tick. Pyridine rings and halogen substituents can raise eyebrows due to potential toxicity or bioaccumulation, but strict adherence to occupational exposure limits and attention to ventilation minimize real-world hazards. Over the years, health and safety protocols have improved drastically across the industry. Most chemical handling setups now operate with closed-transfer systems, local exhaust ventilation, and strict personal protective equipment requirements. That kind of infrastructure changes risk perception—back in the day, you couldn’t always count on such safeguards. Today, a solid implementation makes handling compounds like this routine instead of risky.

    Challenges and Real-World Solutions

    Nobody in process chemistry expects an easy ride. Every compound has quirks, and 2-Amino-4-Methyl-5-Bromopyridine is no exception. Some common snags: batch-to-batch purity inconsistencies, occasional trace metal contamination from bromine sources, or off-odors that signal side reactions. Every research group develops its own troubleshooting playbook. Frequent verification using NMR and mass spec isn’t just busywork; it reflects the unpredictable nature of starting materials.

    One solution starts at the supplier level. Reliable partners publish comprehensive batch analysis and even retain reference samples so that users who detect issues downstream can trace the root cause. A few forward-thinking labs take up the challenge of in-house purification—recrystallization or even preparative HPLC—especially when regulatory filings require bulletproof traceability. In some countries, regulators now nudge manufacturers to declare known side-product or residual solvent levels upfront, which trims time and frustration both for quality assurance teams and for chemists pushing to file regulatory documents.

    Waste management once caused headaches across the specialty chemicals industry. Disposal of halogen-containing waste drew scrutiny from environmental agencies, especially in the last two decades. Many facilities shifted to on-site neutralization reactors or even integrated recovery, tracking halide levels before discharge. The move wasn’t just regulatory box-ticking—it cut costs and built goodwill in local communities. Anybody who’s sat through a heated city planning meeting knows why that matters.

    Sourcing raw materials isn’t without its drama. Geopolitical instability, natural disasters, or even shifts in commodity pricing can jolt supply chains overnight. Some manufacturers adapted by diversifying sources and setting up dual-path synthesis protocols, swapping out key reagents when disruption hits. That kind of resilience goes well beyond the chemistry itself—it’s a survival trait for modern producers.

    Trust and Track Record Matter

    Experience shapes how you judge a product’s real value. I’ve watched labs hedge their bets on unproven suppliers, drawn in by lower job-lot pricing, only to face delays when supplied material failed basic QA. Teams relying on clinical timelines or pilot-plant schedules simply can’t afford such hiccups. Building trust, for both supplier and user, means more than just accreditation letters or certificates. It means demonstrating a pattern of reliability across years and projects—being able to pick up the phone and get a straight answer from somebody who knows what they’re talking about.

    For chemists in discovery or development roles, reputation outpaces novelty every time. Testimonials from users in peer-reviewed literature, or real-world case studies from companies with skin in the game, trump flyers or promotional articles. Over time, a narrative forms around which suppliers deliver consistent product, respond quickly to incidents, and adjust their formulations to customer needs. Such relationships fuel both scientific innovation and business growth.

    A culture of transparency at the manufacturing level boosts confidence, especially during scale-ups or regulatory reviews. Open access to batch records, impurity profiles, and process controls lets downstream users forecast yield or trouble spots before the first round of testing. In my own career, more than one rushed project relied on clear communication with a supplier’s technical team to overcome bottlenecks. If you’ve ever had to explain an unexpected impurity at a regulatory meeting, you know just how valuable these conversations become.

    Comparing Alternatives

    It helps to keep perspective. Plenty of amine- or bromo-substituted pyridines see routine use. Some offer lower cost per gram, while others show slightly higher purity out of the box. What they lack, though, is the balance of reactivity that 2-Amino-4-Methyl-5-Bromopyridine offers. A one-for-one substitution rarely pans out without tweaking synthesis or purification steps. In projects where budget and timelines both run tight, simplifying the chemistry wins out over marginal savings.

    Green chemistry, though still aspirational for some, plays a bigger role with each passing year. Efforts center on reducing hazardous byproducts, improving atom efficiency, and optimizing solvent recycling. 2-Amino-4-Methyl-5-Bromopyridine slots into many synthetic routes with less need for toxic activators or stochiometric reagents compared to some of its peers. Some teams report fewer side reactions requiring hazardous cleanup as a result. As regulations keep tightening around waste management, that edge only grows sharper.

    Automation further changes the equation. Robotic synthesis platforms benefit from reagents with predictable solubility and minimal long-term storage degradation. This compound consistently meets those benchmarks, which allows for more predictable process control—a crucial factor in research and early-stage manufacturing alike.

    The Road Ahead: Innovation and Responsibility

    No single compound can claim all the glory for the advances in modern chemistry, but 2-Amino-4-Methyl-5-Bromopyridine draws attention precisely because it solves real problems. As drug pipelines face pressure from both public health goals and investor expectations, the spotlight falls on reagent quality and versatility. Regulatory watchdogs keep pushing the bar higher on traceability and impurity profiling. In response, most high-volume users now demand digital batch records and real-time analytics as standard, not as add-ons. This level of oversight wasn’t even on the horizon just a decade ago.

    Education plays a role nearly as important as innovation. Chemists—whether in academia, industry, or startup settings—share both failures and successes, contributing to a broader understanding of where reagents like this add value or introduce pitfalls. The modern research landscape encourages open communication, both to prevent costly duplication of effort and to flag issues like cross-reactivity or poor downstream compatibility before they have a chance to derail projects. Students and junior researchers benefit from this collective knowledge, building technical confidence that pays off in years to come.

    I’ve seen broader industry initiatives aimed at pairing reliability with ethical sourcing. For manufacturers, this requires verifying that bromination sources meet both environmental and human rights standards. Pressure from investors and activist groups now nudges corporate procurement offices to dig deeper. Supply chain mapping once seemed like an exotic exercise for multi-nationals, but now even niche suppliers face demands to show not just “what,” but “where” and “how.” This kind of due diligence stands to reshape how specialty chemicals enter the global market.

    Building for the Future: From Bench to Business

    The story of 2-Amino-4-Methyl-5-Bromopyridine mirrors that of many specialty reagents—quietly essential, rarely newsworthy. In a world of ever-changing project needs and shifting market demands, reliability and transparency become differentiators. Scientists, purchasing agents, and project managers all look for reagents that can absorb the bumps and detours of real-world development. Every time a compound enables a breakthrough or just saves a few days in the work queue, it demonstrates its worth behind the scenes.

    Business strategy evolves with the tools available. Increasingly, customers expect more than product—they expect partnership. Suppliers that regularly check in, provide training, or invite client feedback ultimately earn business for the long haul. With each successful shipment and satisfied user, a product line cements its reputation—not just in sales figures, but in the shared stories of progress and discovery.

    Innovation isn’t static. Modular synthesis tools, digital inventory management, and real-time analytics continue to shape how people buy and apply products like 2-Amino-4-Methyl-5-Bromopyridine. Agility in responding to these shifts determines who leads and who follows. For anyone who’s pulled long hours to troubleshoot a stalled route or chased down a missing package on a deadline, the value of reliability becomes crystal clear.

    As the next generation of scientists takes the helm, they inherit not just tools, but the culture of care, rigor, and responsibility that previous users have built. By choosing and stewarding materials thoughtfully, they further a tradition of discovery grounded in trust and progress. 2-Amino-4-Methyl-5-Bromopyridine, in its way, helps write that story.