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3-Amino-2-Bromo-4-Picoline

    • Product Name 3-Amino-2-Bromo-4-Picoline
    • Alias 3-Amino-2-Bromo-4-Methylpyridine
    • Einecs 629-626-9
    • 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

    602309

    Chemical Name 3-Amino-2-Bromo-4-Picoline
    Cas Number 112023-87-7
    Molecular Formula C6H7BrN2
    Molecular Weight 187.04
    Appearance Light yellow to brown solid
    Melting Point 79-83°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents like DMSO and methanol
    Synonyms 2-Bromo-3-amino-4-methylpyridine
    Smiles Cc1cc(N)nc(Br)c1
    Inchi InChI=1S/C6H7BrN2/c1-4-2-5(8)9-3-6(4)7/h2-3H,8H2,1H3
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 3-Amino-2-Bromo-4-Picoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g amber glass bottle is tightly sealed, labeled "3-Amino-2-Bromo-4-Picoline," with hazard warnings and product details clearly printed.
    Shipping 3-Amino-2-Bromo-4-Picoline is shipped in tightly sealed, chemically resistant containers under cool, dry conditions. It is handled as a hazardous material, requiring proper labeling and documentation. Shipping complies with relevant transport regulations, and protective packaging prevents leaks or damage during transit. Only authorized carriers are used for its distribution.
    Storage 3-Amino-2-Bromo-4-Picoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure proper labeling and access only to trained personnel. Recommended storage temperature: 2-8°C (refrigerated conditions).
    Application of 3-Amino-2-Bromo-4-Picoline

    Applications of 3-Amino-2-Bromo-4-Picoline in Industrial Manufacturing

    3-Amino-2-Bromo-4-Picoline is a key intermediate used in several downstream speciality chemical production sectors due to its unique brominated and aminated pyridine structure. Below, our technical team outlines major industrial applications, regulatory frameworks, process roles, and end product types where this raw material serves as a strategic building block.

    1. Pharmaceutical Intermediate for Oncology Drugs

    This material is a central intermediate in synthesis routes for kinase inhibitors and heterocyclic APIs used in targeted cancer therapeutics. Process chemists incorporate it during heterocycle assembly or direct substitution stages. This molecule supports high-selectivity reactions for phenylpyridine-based pharmacophores within controlled environments, adhering to stringent GMP requirements. Process engineers monitor impurity profiles and recrystallization parameters for batch validation. API manufacturers compound it at strictly controlled dosage ratios, referencing established regulatory documents for impurity specifications before scale-up for clinical and commercial production.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • US FDA 21 CFR Part 211 for pharmaceutical manufacturing
    • China Pharmacopoeia standards for chemical drug APIs

    Typical usage ratio

    • 0.5 – 1.2 molar equivalents per target API, adjusted based on desired substitution pattern
    • Ratio determined by multi-step synthesis sequence and yield optimization

    Downstream process integration

    • Introduced during N-arylation and cyclization stages
    • Used in protected and deprotected forms for intermediate isolation
    • Employed in final impurity removal through preparative chromatography

    Final product types

    • Active pharmaceutical ingredients (APIs) for oral oncology drugs
    • Bulk intermediates for targeted therapeutic agents

    2. Agrochemical Synthesis for Fungicide and Herbicide Actives

    Agrochemical manufacturers integrate this raw material into multi-stage synthesis processes for producing substituted pyridine herbicides and pyridinyl-substituted triazole fungicides. The amino and bromo groups enable selective coupling with haloalkyl, phenoxy, or azole intermediates to yield crop protection compounds featuring improved bioactivity and environmental breakdown. Regulatory dossiers reference specific agronomic and analytical standards for all reaction stages, with cross-referencing to pesticide MRLs and impurity cutoffs. Batch records and analytical certificates confirm compliance ahead of contract formulation and bulk supply activities.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • US EPA 40 CFR Part 180 for pesticide residues
    • OECD Good Laboratory Practice (GLP) for chemicals
    • REACH registration for substances imported into the EU

    Typical usage ratio

    • 0.8 – 1.4 molar equivalents per target agrochemical
    • Adjusted for multi-step coupling and ring closure efficiency

    Downstream process integration

    • Fed into condensation or cross-coupling reactors at step two or three in synthesis
    • Removed by aqueous work-up before formulation with adjuvants
    • In-process QC for residual solvent and byproduct tracking

    Final product types

    • Active ingredients for systemic and contact fungicides
    • Pyridine-derived selective herbicides for post- and pre-emergent applications
    • Blends for formulated pesticide concentrates

    3. Electronic Chemical for OLED Material Synthesis

    Producers of organic light-emitting diode (OLED) materials deploy this amine-bromopyridine derivative in the construction of electron transport layers and light-emitting functional materials. Advanced materials teams use the compound in Suzuki–Miyaura or Buchwald coupling reactions to engineer electron-rich and electron-deficient heterocycles, achieving target energy gaps and charge mobility for display device manufacture. Cleanroom protocol, elemental analysis by ICP-MS, and sub-ppm metal residue controls are enforced in all production and purification operations. Route-of-synthesis and materials traceability records are maintained as per ISO and customer audit requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for advanced electronics chemicals
    • IEC 61249-2-21 for halogen content in display industry materials
    • JEITA guidelines for organic EL material purity
    • Chemical substance control regulations under China RoHS

    Typical usage ratio

    • 0.9 – 1.15 molar equivalents per OLED emitter or transport molecule
    • Ratio optimized for copper-catalyzed aryl-amine couplings

    Downstream process integration

    • Reacted in high-throughput flow reactors for batch and continuous production
    • Undergoes rigorous HPLC/GC-MS monitoring for trace contaminants
    • Supplied either pre-packed or in bulk for in-house downstream synthesis

    Final product types

    • Electron- and hole-transport materials for OLED panels
    • Custom small-molecule emitters for display technologies
    • Precursor compounds for OLED device integration

    4. Intermediate for Dye and Pigment Preparation

    Specialty dye and pigment manufacturers employ this compound for constructing brominated pyridine chromophores in advanced colorant production. Its high nucleophilicity and site-selective reactivity support synthesis of azo, anthraquinone, and other functional chromogenic systems, primarily for industrial printing and textile coloration. Quality assurance teams monitor metal and halogen impurities, leveraging analytical certifications and batch traceability as required by major textile and ink regulations. Consignment samples undergo compatibility trials in pilot plant before moving to scaled industrial dye house operations.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for chemical safety in textile colorants
    • EN 71-3 for heavy metal content in colorants for toys
    • ISO 13320 for particle size distribution in pigment suspensions
    • ZDHC MRSL compliance for effluent control in dye manufacturing

    Typical usage ratio

    • 0.6 – 1.3 equivalents per colorant molecule based on chromophore complexity
    • Ratio fine-tuned for azo or anthraquinone dye pathways

    Downstream process integration

    • Introduced into coupling or ring-closure reactions
    • Subjected to crystallization and washing for impurity removal
    • Validated via pilot-batch for shade reproducibility before full-scale production

    Final product types

    • High-performance pigments for plastics and coatings
    • Reactive and disperse dyes for textile applications
    • Colorant concentrates for inkjet and specialty printing
    Free Quote

    Competitive 3-Amino-2-Bromo-4-Picoline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 3-Amino-2-Bromo-4-Picoline from a Manufacturer’s Perspective

    What Sets Our 3-Amino-2-Bromo-4-Picoline Apart

    Our in-house production of 3-Amino-2-Bromo-4-Picoline demonstrates what chemical manufacturing brings to the table when the process aims straight for practical use and quality. As a manufacturer who spends every day transforming precursor chemicals into this methylated, aminated, and brominated pyridine, I see the priorities clearly. Product consistency, from batch to batch, makes or breaks reliability for downstream synthesis. That’s why our work starts with stringent in-process controls throughout synthesis, isolation, and purification.

    Making Each Step Count in Quality

    Supplying 3-Amino-2-Bromo-4-Picoline in volumes tailored both for the bench and large-scale runs calls for continuous investments. Our lab team tracks parameters meticulously across each run. The melting point, color, and NMR spectra are measured every time—we don’t move on unless every data point lands inside our internal specs. Loss on drying, residual solvents, and foreign ions add to our checklist, not as box-ticking, but because we’ve seen these variables affect partners’ yields or crystallization further down the chain.

    We choose our raw bromopyridine feeds based on impurity profiles that we’ve screened ourselves, rather than relying on upstream supplier claims. That approach shrinks the risk of introducing unexpected byproducts which can complicate HPLC or GC cleanups in our customers’ hands. Delivering what we promise is one thing; proactively reducing headaches for synthetic chemists speaks louder.

    Form, Presentation, and Handling in Real Labs

    3-Amino-2-Bromo-4-Picoline leaves our production in a pale to light-brown crystalline form, easily handled by hand, spatula, or scoop. Since the molecule responds to moisture, each container is triple-sealed and each drum or bag includes a quality certificate with analytical results from the exact batch inside.

    We understand the world of organic intermediates doesn’t pause for sluggish supply chains. Our shipments rarely stop at the local market; global destinations experience stable, tamper-proof packaging because partners everywhere deserve to open containers as fresh as those we check in our own QC lab.

    Why the Methyl Group Matters

    Chemists choose 3-Amino-2-Bromo-4-Picoline for that single methyl group at the 4-position. Adding only a methyl can shift electronic effects across the whole pyridine ring, making key coupling or cyclization steps possible that plain 3-amino-2-bromopyridine can’t deliver. Over the years, we’ve worked closely with researchers aiming for the sharpest selectivity in heterocycle synthesis. This small substitution often enables unique selectivity and can swing regioselectivity in N-alkylation, Suzuki couplings, or nucleophilic aromatic substitutions.

    Users tell us the extra methyl group provides more than a tweak. They experience cleaner reactions and discover access to substituted pharmaceutical intermediates, some destined for kinase inhibitor programs, or agrochemical screening. Instead of listing the molecule as a mere catalog entry, we monitor how synthetic programs and scale-up projects shift as new constraints and green chemistry push toward more atom-economical methods. In dozens of cases, 3-Amino-2-Bromo-4-Picoline helps chemists reduce waste or save time by minimizing protecting group steps—chemistry that fits changing expectations for sustainability.

    Our Model Numbering and Real-World Meaning

    In our internal tracking, each production batch receives its own identifier tied to a production log and a retained sample. This means if someone returns to us six months down the road with a new analytical request, we can quickly match their lot to our archived batch. We don’t treat this as mere bureaucracy—anyone who has traced a hard-to-find contaminant knows this narrows the search. Our confidence comes from full traceability, built into our systems from the first weigh-out to the final drum seal.

    Major Applications: What Customers Actually Make with It

    From direct conversation with medicinal chemists through our technical support line, most demand for 3-Amino-2-Bromo-4-Picoline centers on Suzuki-Miyaura cross-coupling or Buchwald-Hartwig aminations. The bromo group, tethered to that exact position, gives unrivaled reactivity in transition-metal catalyzed bond formations. Compared to unfunctionalized picolines, this product saves researchers weeks of multi-step synthesis. In agricultural R&D, teams use our picoline derivative as a building block toward herbicide and insecticide cores—where site-selective coupling means fewer byproducts and easier purification.

    Outside the pharma and agro domains, the versatility of 3-Amino-2-Bromo-4-Picoline makes it well-suited for fine chemical synthesis and pigment applications that require strict control over purity and substitution pattern. Sometimes a substitution at one ring position means the difference between effective downstream cross-coupling and an unworkable synthetic route.

    How Our Product Differs from Other Pyridine Intermediates

    Over the years, we have supplied both 3-amino-2-bromopyridine and methylated versions. The core difference lies not only in physical properties but in how the ring substitution alters solubility, melting point, and reactivity in catalysis. The methyl group at the 4-position increases lipophilicity, which becomes critical in certain drug or agrochemical design steps. Some customers attempted to introduce the methyl group after installing other substituents, only to find messy side products. By offering the methylated product directly, researchers save time and lower the risk of ring chlorination or overbromination.

    Compared to non-brominated analogs, our product enables direct entry to arylation or amination—in contrast, chlorinated derivatives display less reactivity under similar coupling conditions and often require higher temperatures or generate off-target products. Our own teams have tested these conditions on parallel projects for both internal and external customers, so this is an insight born of hands-on troubleshooting, not solely literature reference.

    Customers sometimes compare 3-Amino-2-Bromo-4-Picoline to isomeric pyridines. From a synthetic perspective, substitution pattern drives everything. Many reactions depend on the position of nitrogen in the ring, and both amino and bromo groups set the stage for further chemistry. Our experience tells us that a minor shift in position—say, swapping the bromo group to the 5-position—decreases reactivity or introduces side reactions which slow down project timelines for contract synthesis or pilot scale runs. With the 2-bromo and the 3-amino, and methyl at the 4-position, the pathway fits snugly with most Pd-catalyzed cross-coupling protocols.

    Technological Choices in Manufacturing

    Producing gram or kilogram quantities of 3-Amino-2-Bromo-4-Picoline means walking a narrow path for reaction conditions. Too dry a run can reduce yield; too much solvent makes isolation a hassle. Among our process chemists, experience counts for more than theoretical debate. The decision to quench at a particular pH, or to fractionate over silica versus liquid-liquid extraction, isn’t decided in a meeting room. Results from past process runs drive every tweak.

    We adapt our purification methods depending on target impurity profiles and volume, always going for reproducible recovery rates over theoretical max yields. Any manufacturer who has scaled a delicate pyridine derivative knows the pain points: incomplete amination or overbromination pop up if temperature or addition rates fluctuate. In our line of work, adjustments are recorded with each batch, then used to inform scale-up or tech transfer to partners. Staying close to the process and listening to operators on the floor keeps surprises to a minimum.

    Why Analytical Verification Counts Every Time

    Among the recurring issues in chemical development, off-spec batches due to unnoticed impurities account for more lost effort than almost any other problem. It’s one reason why we invest so heavily in in-house analytics, and why we retain reference standards not only for the main product but for expected byproducts and degradation products. LC-MS, GC, and NMR serve as our front line, and we employ standards run against both fresh and aged samples. Only labs with access to the actual production process can spot trends that point to emerging issues—this can’t be done with third-hand materials from resellers or brokers.

    Comparative test results from scale-up batches have exposed issues nobody spotted until gram quantities rolled off the line. For instance, a subtle yellow tint or minor change in the 1H NMR often reveals process water infiltration or slight batch-to-batch variability, which can derail an entire custom synthesis. Partner feedback draws attention to such anomalies, and we often adjust our drying or recrystallization routines to eliminate those variables.

    Packaging and Transport—Seeing the End-User’s Side

    Our shipments arrive triple-layered to block out moisture and air. Containers have inner foil seals beneath screw caps, and every bulk drum is filled under inert gas. We’ve heard about complaints from those who have received material from informal third-party handlers—clumped, colored, or off-odor. Those issues never remain abstract; when you field the call from a lab stuck waiting on a backordered or ruined input, the lesson sticks. Our commitment is direct: finished goods don’t leave the plant without a visual and assay check.

    Upon delivery, our partners unpack and sample direct from the original container, minimizing risk of contamination or exposure. We offer material tailored for both research and commercial users, each time committing to the same checks and reporting. Our technical and after-sales team follows up to make sure things don’t just look right but perform to expectation in reaction setups. This feedback loop shows up in how we revise SOPs annually.

    Environmental and Safety Responsibilities

    Any chemical manufacturer aware of today’s regulatory climate recognizes that compliance doesn’t just happen at the end of the line. Each step, from solvent use to effluent treatment, integrates controls to ensure environmental and occupational health standards meet local and global regulations. Our waste minimization and recycling efforts expanded in the last five years as both partners and regulators increased scrutiny.

    Handling halogenated and aminated pyridines requires focused safety protocols. Our operators wear full protective kit and handle all final isolation behind protective barriers. Unexpected exotherms or gas evolution, detected via real-time monitoring, prompt immediate intervention long before any incident. We share any near-misses at internal safety meetings and fold those lessons back into both new and established SOPs. Troubleshooting risky points has even reduced incidents in unrelated product lines.

    Continuous Improvement Based on Real Feedback

    We measure our success not just by how much 3-Amino-2-Bromo-4-Picoline we ship, but by how consistently it supports successful chemistry for our partners. Requests for custom specs or technical advice often turn up gaps in public literature or vendor data—problems that only hands-on manufacturers can solve. Our chemists bring up customer questions in their weekly meetings, adjusting formulation, drying, or packaging to address new pain points. Sometimes these requests prompt us to revisit an old control point that’s quietly drifted as equipment ages or suppliers change. We close that loop, make the correction, and watch for improvements in the next round.

    Scientists in academic, pharmaceutical, and industrial labs face relentless pressure to improve synthesis yields, reduce impurity fingerprints, and shorten project timelines. That’s a world we know firsthand, not as spectators but as participants. We push to adapt our manufacturing, analytics, and logistics to suit new assay standards and downstream targets as these pressures evolve. Regulatory hopes, green chemistry ambitions, and new analytical insights turn what used to be “good enough” into a constant challenge. Our frontline experience tells us that every tweak in our process—whether extra testing, a dryer storage box, or a new liner for a drum—carries ripple effects throughout the supply chain.

    Staying Connected with Users Beyond Delivery

    Feedback from real labs catches things no data sheet alone can capture. A customer calling about slightly longer dissolution times, or color variance under daylight, uncovers details missed by a spec sheet. Every reported anomaly feeds our improvement process, and every performance report influences our process changes or analytical checks. Transparent, two-way communication beats blind compliance every time.

    Years of collaboration and troubleshooting bring home the value of responsiveness. A manufacturer carrying responsibility for product quality cannot afford to hide behind generic protocols and automated replies. Our structure encourages direct lines between chemists, plant operators, quality analysts, and those in contact with customers. In this working environment, individual accountability and mutual respect sustain standards and drive progress, batch after batch.

    Looking Ahead: Challenges and Opportunities

    3-Amino-2-Bromo-4-Picoline will remain a crucial tool for designing new syntheses and scaling up production of next-generation compounds. Markets and applications continue to diversify—whether aimed at pharmaceuticals, crop protection, advanced materials, or new pigments. Each sector brings new operational constraints and requests for more sophisticated analytical packages, greener processes, and logistics tailored to shifting regulations.

    We embrace these challenges because direct experience as a manufacturer reveals both frustration and opportunity. Early feedback from those developing new routes or upgrading existing ones points out where we can eliminate complexity or improve purity profiles. There’s no shortcut to building that expertise, but by keeping lines of communication open, investing in equipment, training, and ethics, and holding ourselves accountable, we secure both our own future and smoother outcomes for every partner downstream.

    Supplying 3-Amino-2-Bromo-4-Picoline is more than selling a specialty chemical. It’s a commitment to practical progress, technical dialogue, and ongoing partnership with everyone testing, transforming, and creating the chemicals that will shape tomorrow’s industries.