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2-Bromo-4-Methylpyridine

    • Product Name 2-Bromo-4-Methylpyridine
    • Alias 2-Bromo-4-picoline
    • Einecs 613-415-2
    • 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
    VTB
    Specifications

    HS Code

    600280

    Chemical Name 2-Bromo-4-methylpyridine
    Cas Number 22282-99-1
    Molecular Formula C6H6BrN
    Molecular Weight 172.03 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point 220-222 °C
    Melting Point -13 °C
    Density 1.5 g/mL at 25 °C
    Purity Typically ≥98%
    Flash Point 101 °C
    Refractive Index 1.574
    Solubility Slightly soluble in water

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2-Bromo-4-Methylpyridine, sealed with a red screw cap and labeled for laboratory use.
    Shipping **Shipping Description for 2-Bromo-4-Methylpyridine:** 2-Bromo-4-Methylpyridine is shipped in tightly sealed containers, protected from moisture and light. It should be packed according to regulations for hazardous chemicals, typically requiring labeling as a corrosive and/or toxic substance. Shipment must comply with local, national, and international transport regulations, including proper documentation and handling by trained personnel.
    Storage **2-Bromo-4-Methylpyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Avoid exposure to heat and direct sunlight. Store under inert atmosphere (e.g., nitrogen) if possible, and ensure containers are clearly labeled. Follow all relevant safety and regulatory guidelines.
    Application of 2-Bromo-4-Methylpyridine

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

    2-Bromo-4-Methylpyridine is a key pyridine derivative utilized by advanced manufacturing sectors for the synthesis of complex molecules. As a direct manufacturer, we supply high-purity material engineered for stringent downstream production lines. Below, we outline the principal industrial application sectors, highlighting unique compliance routes, formulation ratios, technical integration, and representative end-use products.

    1. Pharmaceutical Intermediate for Antiviral Drug Synthesis

    Leading pharmaceutical producers incorporate this material as a building block in synthesizing heterocyclic compounds, especially for antiviral actives such as integrase inhibitors and non-nucleoside analogs. Our product allows precise halogen exchange and nucleophilic substitution under controlled conditions. Producers require traceable batch consistency and robust impurity control for regulatory filings. Usage parameters depend on target molecule design and impurity pathway management.

    Industry compliance standards

    • International Council for Harmonisation (ICH Q7, Q3A)
    • Good Manufacturing Practice (EU GMP Part II, US 21 CFR 211)
    • United States Pharmacopeia (USP-NF, relevant monographs)
    • Drug Master File (DMF) registration with FDA and NMPA filing standards

    Typical usage ratio

    • 5–15% molar basis in key condensation steps, adjusted for target conversion rates and downstream yield optimization

    Downstream process integration

    • Initial heterocycle construction phase for active pharmaceutical ingredient (API) synthesis; subsequent coupling and deprotection involve real-time purity monitoring

    Final product types

    • Antiviral and oncology drug substances (e.g., pyridine-based integrase inhibitors, kinase modulators)
    • Regulatory-submitted API intermediates

    2. Crop Protection Chemical Synthesis (Agrochemical Intermediates)

    Major agrochemical companies utilize this compound for the production of substituted pyridine herbicide and insecticide actives. The controlled reactivity of the bromo and methyl groups allows targeted derivatization, enabling access to active molecules with tailored biological selectivity. Producers require consistent physicochemical properties to ensure batch-to-batch uniformity during scale-up and technical registration.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Synthesis
    • FAO/WHO Specifications for Technical Grade Active Ingredients (Relevant for pyridine herbicides/insecticides)
    • OECD Good Laboratory Practice (GLP) for Agrochemical Intermediates

    Typical usage ratio

    • 8–20% weight basis in batch synthesis, depending on specific crop protection molecule and final activity design

    Downstream process integration

    • Intermediate input for etherification, halogenation, or Suzuki coupling in multi-step synthesis of technical-grade agrochemical actives

    Final product types

    • Pyridine-based herbicides (e.g., picolinic acid derivatives)
    • Insecticide intermediates and technical active ingredients

    3. Material Science – Specialty Polymer Synthesis

    Innovators in advanced polymers employ this material as a functional monomer precursor for the design of novel conductive and flame-retardant polymers. The compound introduces specific electronic modifications into aromatic polymer chains. Exacting purity profiles are required to avoid catalyst poisoning and to achieve the desired material performance metrics in electronic and construction applications.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006) for monomer sourcing
    • RoHS Directive 2011/65/EU for electronic polymer components
    • ASTM D5630 (polymer composition testing)

    Typical usage ratio

    • 2–8% molar introduction into backbone polymerization, varied according to polymer type and end-use functionality required (electrical resistance, flame retardance)

    Downstream process integration

    • Feeding into Suzuki or Stille cross-coupling process for functionalized aryl polymer chain initiation, with in-process analytical verification (GPC, NMR)

    Final product types

    • Specialty electronic polymers (e.g., OLED substrate intermediates)
    • Flame-retardant construction plastics
    • High-impact engineering resins

    4. Fine Chemical Synthesis for Dye and Pigment Manufacturing

    Producers of advanced colorants employ this raw material in multi-step syntheses to introduce tailored pyridine ring modifications, yielding high-stability dyes and pigments for electronic and textile markets. Strict controls on purity and side reactions promote consistent chromophore attributes and application performance, supporting batch-based or continuous processing environments.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Colorant Synthesis
    • EN 71-3:2019 (Toy Safety for colorant ingredients)
    • Oeko-Tex® Standard 100 (restricted substances for textile dyes)
    • REACH Annex XVII (restriction of hazardous substances in pigments and dyes)

    Typical usage ratio

    • 3–10% molar contribution to aromatic ring transformation in pigment precursor synthesis, modulated by hue and photostability targets

    Downstream process integration

    • Stepwise substitution and cyclization for advanced azo and heterocyclic dye synthesis, followed by purification and finishing to technical grade

    Final product types

    • Electronic display colorants
    • Industrial textile dyes and specialty pigments
    • High-performance printing inks
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    Certification & Compliance
    More Introduction

    Meet 2-Bromo-4-Methylpyridine: Precision for Modern Chemistry

    Our Experience with 2-Bromo-4-Methylpyridine

    We have been making 2-Bromo-4-Methylpyridine (CAS No. 3430-13-5) in-house for many years and have seen first-hand its growing importance in fine chemical and pharmaceutical synthesis. The compound builds on the well-known pyridine scaffold, but that carefully placed bromine at the 2-position and a methyl group at the 4-position set this molecule apart. Each time our customers draw upon this compound, it is for a reason rooted in practicality: reliable reactivity and clear downstream value in complex molecule development.

    Why Small Modifications Matter: The Story in Each Molecule

    Chemists often talk about “structure-activity relationships,” but only practice reveals how critical even a single atom’s placement can be. In the world of substituted pyridines, attaching a bromine and a methyl group to the ring changes the game. The methyl at the 4-position blocks unwanted reactions, and the bromine at the 2-position opens new doors in cross-coupling chemistry. We see it each time clients request custom analogs: those seemingly minor tweaks shape the chemical’s personality—its physical profile, its reactivity, and its sophistication as a building block.

    Looking Beneath the Surface: Physical Purity and Consistency

    Each batch that leaves our plant is checked for color, clarity, and exact composition. With 2-Bromo-4-Methylpyridine, even slight contamination can steer a pharmaceutical intermediate or agrochemical in the wrong direction. We have invested in high-precision distillation and controlled reaction conditions to keep trace halides, heavy metals, and other common residuals below detectable limits in all production runs. The bright, transparent liquid our partners receive stands as proof of our attention to detail, not just because regulatory agencies demand it, but because our team has seen what happens when shortcuts get taken. Reduced catalyst lifetime, unpredictable byproducts, or failed downstream steps all cost more than the time it takes to get the first steps right.

    2-Bromo-4-Methylpyridine’s Chemistry in Action

    What sets 2-Bromo-4-Methylpyridine apart is the reactivity at the bromine site. Direct reactions, especially Suzuki and Buchwald-Hartwig cross-couplings, work with high selectivity and good yield under the right conditions. Chemists find it especially useful in stepwise syntheses where they need to install different functionalities at tightly controlled points on the aromatic ring. In pharmaceutical research, this means building complex drug candidates with minimal side products and purifications. For agrochemicals, that reactivity can streamline the addition of active moieties while sidestepping competing transformations.

    Over the years, we have tested its performance both in gram-scale trials and kilo-scale production. The chemical’s behavior remains steady as the scale increases—no nasty surprises in purification, and no issues with side reactions that pop up only when larger reactors come into play. Those are points a casual trader will often gloss over, but production chemists notice the difference immediately.

    Model, Form, and Reliable Delivery

    We manufacture 2-Bromo-4-Methylpyridine both as a laboratory-grade reagent and in larger volumes for process chemistry. The chemical’s typical appearance is a pale to colorless liquid, and our regular shipments meet or exceed 98 percent purity by GC. We do not divert waste streams between batches; we produce purpose-built lots, all with the same attention to trace impurities and byproduct exclusion.

    In terms of logistics, the liquid physical state brings both an advantage and a requirement. It pours smoothly, and there are no issues with caking or moisture retention as seen with powders. At the same time, we use lined containers and nitrogen blankets to minimize the risk of oxidation or trace acid formation in transit. Turnaround times depend on batch size and destination, but our record shows delivery that fits site schedules without unnecessary waiting—because we build inventory based on forecasted demand, not just-in-case speculation.

    Comparing the Alternatives: Why Choose This Compound?

    Often, chemists face a choice among various bromo, methyl, or halopyridines. Each offers a different balance of cost, reactivity, and selectivity. For those chasing particular substitution patterns, 2-Bromo-4-Methylpyridine avoids the pitfalls of ortho-related side reactions common in mono-substituted analogs. Its methyl group at the 4-position adds steric hindrance, so the ring’s electronics and reactivity differ from those of 2-bromopyridine or 3-bromo-4-methylpyridine. With direct experience running scale-ups, we have found that more standard bromo-pyridines often struggle with selectivity or byproduct formation once other functional groups join the mix, whereas this compound holds its profile across a variety of reaction partners.

    Customers sometimes ask about cost drivers for this molecule compared to its isomers. The process for making 2-Bromo-4-Methylpyridine is more complex than single-site brominations, and it requires careful control of reaction temperatures and brominating agents to hit the exact regioselectivity. Our catalysis team has refined this multistep route so that overall yields are robust and consistent. Investment in better purification columns pays for itself in client satisfaction and repeat business—because every microgram of contamination can torpedo a million-dollar synthesis downstream.

    Real-World Applications: From Bench Development to Full-Scale Production

    Pharmaceutical scientists select this molecule to investigate new heterocyclic scaffolds for targeted therapies. Medchem teams favor it when exploring new kinase inhibitors, where subtle modifications to aromatic cores can improve drug-like properties. Its dual substituents also allow for tuning of water solubility and metabolic stability—features that have benefited more late-stage compounds than any catalog entry ever reveals.

    Our own manufacturing group has supported contract partners developing crop-protection agents that require the precise functionalization this molecule provides. In process-development work, the compound has proven well-suited to automated handling and is compatible with both traditional and emerging cross-coupling catalysts, including palladium complexes and modern nickel systems. That flexibility assures our customers of straightforward integration into their existing process flows, whether they handle twenty grams or two hundred kilograms per campaign.

    Sustainability and Process Improvements

    Production often creates waste streams, so each year we assess our methods for opportunities to cut waste, recycle solvents, and recover valuable byproducts from bromination steps. Our plant engineers have fine-tuned the process to cut the volume of hazardous waste per ton produced. Every improvement—whether it is a new scrubber, smarter solvent recovery, or improved heat management—directly benefits both our partners and the neighborhoods surrounding our sites.

    We have also moved toward sourcing starting materials from audited suppliers with proven track records on safety and sustainability. These choices do not always mean lower immediate costs, but over time, fewer surprises and more reliable production keep both our teams and our customers ahead. This approach leads to steady production without the disruptions that hit less robust supply chains during regulatory changes or raw material shortages.

    We share detailed production and handling information with our contract customers. We do not simply sell a drum, but support the whole lifecycle of the chemical. If a sudden process hiccup appears during scale-up at a partner site, our technical support group steps in: they have seen the molecule both from the perspective of synthesis and real-world use, so they can identify root causes based on years of hands-on problem solving. Few things matter more than this level of continuity in a field where lost time translates directly to lost revenue.

    Safety and Responsible Use

    As a manufacturer, we handle the hazards of bromine chemistry on a daily basis. Strict monitoring, engineering controls, and staff training shield workers and the community. For users, this means every lot arrives with comprehensive documentation on safe storage, handling, and recommended protective equipment. While crossing regulatory lines adds paperwork, it also strengthens safeguards throughout the chemical lifecycle.

    We routinely interface with regulatory bodies worldwide to track any changes in occupational exposure limits or emerging data on environmental impact. Feedback loops between regulators, manufacturers, and customers help raise the overall standards for all involved in this sector. We support research into safer chemistry and greener alternatives, while continuing to deliver the robust performance that research and industry need today.

    Tracing Authenticity and Avoiding Counterfeits

    The global market for fine intermediates continues to attract non-manufacturers and repackers. Anyone who has suffered from a contaminated shipment, delayed delivery, or mismatched documentation knows the cost of trusting an unknown source. We maintain full traceability of every production lot, from raw materials through finished goods, all the way to the packing line. Labs that purchase from us do so with confidence, knowing that each bottle matches the analytical data supplied, because the same team who produced it stands behind the certificate.

    Experience shows that cutting costs upfront rarely pays in specialty chemicals—especially intermediates like 2-Bromo-4-Methylpyridine, where even trace residue or unvetted handling can spell disaster for a downstream campaign. We offer both standard and custom lot sizes to meet changing research or production needs, with every container filled and sealed by the same hands that made the product.

    Improving Outcomes Through Technical Support

    Our chemists have used this compound in method development, optimization, and troubleshooting. We regularly advise partner labs on reaction choice, temperature settings, reagent stoichiometry, and expected side products. Practical suggestions, drawn from actually running these reactions with our material, keep projects on track. In one collaboration, a major biopharma firm encountered sluggish coupling reactions using commodity-grade 2-Bromo-4-Methylpyridine from a non-manufacturer; switching to our product eliminated reproducibility issues that had stymied the team for weeks.

    We have also helped formulation teams improve yields and reduce the number of purification steps, thanks to reliable material consistency. The difference becomes obvious in scale-up: there is no need to compensate for variations in purity or moisture, so equipment run-times and solvent usage both drop. These aren’t just numbers on a spreadsheet; they reflect real improvements to laboratory safety, environmental footprint, and project return on investment.

    Challenges in the Industry and Our Response

    The fine-chemical field races at the dictates of discovery and regulation. New methods disrupt old practices, and customers demand ever-greater transparency. We continue to refine our process in response to feedback and to remain competitive as regulations on brominated intermediates evolve. If a new best practice emerges from literature or commercial use, our team evaluates its impact and integrates it incrementally for maximum benefit.

    Supply chain disruptions—such as raw material shortages, rule changes, or transport delays—pose ongoing risks. By running our own plant, versus relying on external producers, we can pivot more quickly. Our staff closely monitors every lot, so if a problem appears, it gets resolved at the root, not after bottlenecks cripple manufacturing.

    Trust Earned with Experience

    Across hundreds of campaigns, we have learned that delivering consistent, high-purity 2-Bromo-4-Methylpyridine goes far beyond hitting a specification on a sheet. It requires vigilance, constant skill development, and a willingness to invest in long-term partnerships with both suppliers and customers. Our team takes pride in knowing that every shipment supports not only a reaction or a project, but the progress of human health, sustainability, and technology.

    We welcome collaboration and dialogue with every partner. The people making the chemistry—the people shipping it, testing it, and using it—determine the future of our field. We keep our standards high because we have seen what happens when others don’t.