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3-Amino-2-Bromopyridine

    • Product Name 3-Amino-2-Bromopyridine
    • Alias 3-Bromo-2-aminopyridine
    • Einecs 629-290-2
    • 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

    798992

    Cas Number 1837-58-7
    Molecular Formula C5H5BrN2
    Molecular Weight 173.01 g/mol
    Appearance Light yellow to brown solid
    Melting Point 55-59°C
    Boiling Point 270.5°C at 760 mmHg
    Density 1.728 g/cm³
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Synonyms 2-Bromo-3-pyridinamine
    Refractive Index 1.658
    Storage Temperature Store at 2-8°C

    As an accredited 3-Amino-2-Bromopyridine 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 25 grams of 3-Amino-2-Bromopyridine, securely sealed, labeled with product details, and hazard symbols.
    Shipping 3-Amino-2-Bromopyridine is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous chemical and must comply with local, national, and international shipping regulations. Appropriate hazard labeling and documentation are provided, and the chemical is transported in accordance with safety guidelines to prevent leakage or exposure.
    Storage Store 3-Amino-2-Bromopyridine in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep away from moisture and sources of ignition. Use proper chemical storage cabinets, preferably designated for organic compounds, and clearly label the container. Ensure appropriate personal protective equipment is available when handling.
    Application of 3-Amino-2-Bromopyridine

    Applications of 3-Amino-2-Bromopyridine in Industrial Manufacturing

    Our production of 3-Amino-2-Bromopyridine serves multiple advanced manufacturing sectors. Below, we outline major downstream applications based on verified industry use, with process-specific compliance, technical integration, and finished product relevance.

    1. Pharmaceutical Intermediate for Pyridine-Based Drug Synthesis

    Pharmaceutical manufacturers use 3-Amino-2-Bromopyridine as a key intermediate in synthetic routes for selective kinase inhibitors, antihypertensive agents, and other heterocyclic drugs. Its bromine and amino functionalities support regioselective functionalization, facilitating the construction of complex active pharmaceutical ingredients. Chemical engineers incorporate it during multi-step batch or flow synthesis prior to purification and crystallization phases.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF monographs (where applicable)
    • European Pharmacopoeia (Ph. Eur.) 11th edition guidelines
    • 21 CFR Part 211 Current Good Manufacturing Practice (cGMP)

    Typical usage ratio

    • 0.8–1.2 molar equivalents per target core structure, adjusted by process yield and impurity profile during scale-up

    Downstream process integration

    • Charged in initial coupling or cyclization reactions under controlled temperature (60–110℃)
    • Reacted with organometallic catalysts for further substitution
    • Precursor for protection/deprotection steps
    • Fed into purification (chromatography, recrystallization) after transformation

    Final product types

    • Kinase inhibitor drug substances (e.g., for oncology therapies)
    • Antihypertensive compounds (e.g., pyridine-based APIs)
    • Fluoroquinolone antibiotics precursors
    • Anti-inflammatory agents

    2. Agrochemical Synthesis: Herbicide and Fungicide Active Ingredient Building Block

    Agrochemical formulators use 3-Amino-2-Bromopyridine to access substituted pyridine rings present in new-generation herbicides and fungicides. Its reactivity allows custom ligation steps for tailor-made biological actives. Production chemists control purity and residual solvents to meet strict agro-grade regulations, integrating the material during the core scaffolding phase of technical substance manufacturing.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA 40 CFR Part 158 Pesticide Registration Requirements (USA)
    • REACH Regulation (EC No 1907/2006) for agro-intermediates
    • ISO 17025 quality system for analytical testing

    Typical usage ratio

    • 1.0–1.3 equivalents per substituted heterocycle, variable by crop target and downstream derivatization

    Downstream process integration

    • Integrated during nucleophilic substitution or amide/ester coupling
    • Applied in high-pressure reactors for further halogenation or alkylation
    • Cleaved or further functionalized en route to final technical concentrate
    • Undergoes in-process QC for isomeric purity

    Final product types

    • Selective post-emergence herbicides (pyridine derivatives)
    • Systemic fungicide actives
    • Seed treatment chemicals
    • Pre-emergence residual weed control actives

    3. OLED & Electronics: Functional Material Precursor

    Manufacturers of OLED emissive layers and specialty electronic materials utilize 3-Amino-2-Bromopyridine to construct functionalized pyridine units critical in charge transport layers and other organic semiconductors. Precision is essential in electronic applications, so all incoming lots undergo extended QA for metal and halide trace content. The compound is introduced during controlled C–N and C–C coupling reactions with downstream fine-tuning of layer properties.

    Industry compliance standards

    • RoHS Directive 2011/65/EU: Restriction of Hazardous Substances
    • REACH Substances of Very High Concern (SVHC) Tracking
    • ISO 9001:2015 for electronic chemical quality management
    • IEC 61249-2-21 for halogen-free requirements (as applicable)

    Typical usage ratio

    • 5–20% mol fraction in multi-component organic precursors, depending on desired functional density

    Downstream process integration

    • Direct dosing in Buchwald–Hartwig or Suzuki-Miyaura cross-couplings
    • Polymerization initiator or terminal block input
    • Feeds vacuum deposition or solution-based film casting steps
    • Employed prior to spin coating and layer annealing

    Final product types

    • OLED emitter molecules
    • Organic semiconductors for thin-film transistors
    • Pyridine-based hole and electron transport materials
    • Specialty display dye precursors

    4. Dye & Pigment Synthesis

    Colorant manufacturers incorporate 3-Amino-2-Bromopyridine to construct complex azo and anthraquinone dye intermediates. Its dual functional groups provide tools for extended conjugation, enhancing color strength and light fastness. Production teams monitor reaction end-points and downstream filtration to maintain batch consistency, as required by international textile and printing regulatory bodies.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances
    • DIN EN ISO 105-E01 for wash fastness of textiles
    • EU REACH Annex XVII for dye ingredient registration
    • GOTS (Global Organic Textile Standard) for pigment use

    Typical usage ratio

    • 0.2–0.6 weight equivalents in relation to primary chromophoric substrates; adjusted for desired color depth

    Downstream process integration

    • Introduced after initial diazotization or sulfonation of core dye structures
    • Participates in electrophilic aromatic substitution or condensation reactions
    • Feeds into neutralization and slurry dispersion units
    • Subjected to vacuum filtration before packaging the intermediate

    Final product types

    • Disperse dyes for polyester textiles
    • Reactive azo dyes for cotton finishing
    • High-performance inks for inkjet printing
    • Anthraquinone-based plastic colorants
    Free Quote

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

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    Certification & Compliance
    More Introduction

    Understanding 3-Amino-2-Bromopyridine in Our Production Line

    A Direct Look at 3-Amino-2-Bromopyridine from the Manufacturer's Perspective

    Walking through our synthesis bays, you quickly learn which intermediates get the job done, which cause headaches, and which support ambitious R&D. Few heterocycles have earned their keep quite like 3-Amino-2-Bromopyridine. After years handling this compound at scale, I can say it offers a rare mix of reactivity, selectivity, and reliability in both classic discovery labs and full-batch pharmaceutical operations.

    What Makes 3-Amino-2-Bromopyridine Worth Attention?

    We produce this material under tightly controlled conditions because it responds with subtlety and power in downstream chemistry. With its pyridine ring, amino group at the third position, and bromine at the second, you get a springboard for two-point derivatization—both amine and halo handle belong to the same molecule, giving direct routes to various libraries of bioactive compounds. Our chemists see this as a toolkit for chemoselectivity, allowing cross-coupling where needed, or introducing substitution patterns that would otherwise need roundabout routes.

    Model and Specifications from a Manufacturer’s Bench

    We don’t trade in generics here. Our batches follow a trusted model developed in response to both customer requests and our own internal benchmarks. Every kilogram we ship comes with crystalline purity above 98.5%, based on in-process HPLC monitoring and final batch GC-MS. We maintain a moisture content below 0.3%, confirmed by rigorous Karl Fischer titration. Materials that leave our plant come in free-flowing, light yellow powders—avoiding the sticky, high-impurity cakes we sometimes see in resupplied drums from less meticulous refineries.

    Our strict batch documentation covers melting point, color index, and residual solvents, knowing that micro-impurities slip into API development if you leave quality slipshod. We use high-purity DMF and control temperature gradients at multiple synthetic steps, avoiding over-bromination or loss of the amino group. Waste management processes reclaim reaction solvents and minimize hazardous byproducts, reflecting how our plant’s engineering connects directly to the product you see in your flask.

    Why End-Users Ask for This Molecule Over Others

    Requests for 3-Amino-2-Bromopyridine don’t happen at random. Seasoned medicinal chemists expect it to open new structure-activity relationships in kinase inhibitor research or anti-infective scaffolds. The molecule’s structure allows Suzuki or Buchwald-Hartwig couplings with impressive, repeatable yields, even under slightly impure or varied catalyst conditions. The bromo-pyridine backbone doesn’t just slip quietly into the background—it establishes the starting framework for more complex, functionalized pyridines.

    In our daily discussions with process scientists, I hear a single theme: time saved at the bench or in kilo-lab validation means an edge in the crowded patent landscape. Several of our customers confirm shorter campaign times and more predictable purification cycles with our batches, which ties directly to reduced troubleshooting and higher project throughput. That claim isn’t marketing—it shows up in actual yield data, time-stamped and audited during technical transfers.

    Long-Term Value From Process Tuning and Quality

    Production scale-up places a harsh spotlight on impurities. Once, an overseas client requested 3-Amino-2-Bromopyridine for scale-up, but their prior supplier left residues of dibrominated byproducts, complicating purification and increasing solvent waste. Here, we stick to validated routes, avoid over-reagent dosing, and continually monitor bromine equivalence. We also use automated titration to avoid leaving unreacted pyridines—a detail you learn matters when running larger recalibrations.

    In process chemistry, margins stack over a thousand subtle choices. For us, real-time spectra, tight solvent recycling, and batch-to-batch documentation wind up shaving days off campaign timelines. These savings aren’t easily seen in paperwork, but they show up when you aren’t debugging a stuck column at 2 a.m. If you're moving toward pharmaceutical registration or considering GMP manufacture, minimizing unknown peaks and regulatory hassles isn’t negotiable.

    The Practical Edge: Comparing to Closely Related Pyridine Derivatives

    Our team routinely debates the merits of 3-Amino-2-Bromopyridine versus similar molecules—like 2-Amino-3-Bromopyridine or unhalogenated 3-Aminopyridine. Start working with these, and differences in reactivity become unmissable. The bromine at the second position on the ring creates an eager leaving group for nucleophilic substitutions, yet remains stable enough for storage and shipping. Amino substitution at the third site simplifies certain routes to arylated or heteroarylated compounds—for example, selective borylation and cross-coupling reactions. In contrast, switching the positions, as in 2-Amino-3-Bromopyridine, typically shows lower yields and fussier purification due to steric clashes and rearrangement side reactions.

    Simple 3-Aminopyridine doesn’t support the same breadth of transformations; the lack of a leaving group limits downstream diversity. This means drug discovery teams often turn to our product as a multi-function jump-off point. On a kilo scale, predictable reactivity removes surprises in downstream coupling or derivatization. Having seen shipper’s manifests from major markets, including North America, Europe, and India, I can say with confidence that seasoned buyers recognize the difference firsthand between clean, well-characterized material and mixed-origin cargo.

    Safety in Handling and Storage Directly from the Shop Floor

    Safe handling always sits front-of-mind in our factory. Every batch comes off the reactor under closed systems, minimizing airborne dust and dermal exposure. We keep product sealed in high-density polyethylene barrels, with vapor guards and desiccant packs to keep product dry—3-Amino-2-Bromopyridine resists most slow hydrolysis, but trace water can alter shelf-life on a multi-month scale. Our warehouse temperatures stay below 25°C, sharply reducing batch degradation or caking.

    Lab mistakes usually point back to simple lapses—open bags near sinks, repackaged drums after customs inspections, or uncontrolled environment during quick bench work. We go over these real-world risk points when passing on safety information to our customers, not just box-ticking with a copied safety data sheet. We also support teams with small sample sizes for method development—or help them identify extraction or repurification options if stocks pick up contamination.

    From Small-Scale to Industrial Production: Insights from Real Batches

    Scaling up isn’t just a matter of running a bigger reactor or prolonging the same procedure overnight. Early on, we learned that exothermic reaction steps risked forming tar or hazardous byproducts, so we've implemented in-situ cooling and staged addition of reagents in every run. Sampling valves allow us to collect fractions at regular intervals, letting us catch reaction drift or impurity spikes before they ruin a full batch. Chasing kiligram-to-ton scales means investing in monitoring and feedback, not just batch output.

    Collaborations with pharma clients often lead to improved synthetic sequences—sometimes, a tweak in condensation temperature or choice of brominating agent, such as NBS versus Br2, helps suppress problematic byproducts. Our team keeps detailed logs so that once a gain is made, it’s banked for future productions, not lost on a notepad or in a departing chemist’s head.

    Market Trends and Requests We Hear Weekly

    Research activity around nitrogen-rich heterocycles hasn't slowed, and 3-Amino-2-Bromopyridine often sits near the top of requested intermediates for antiviral, antitumor, and agrochemical research. Development teams keep pushing boundaries in combinatorial synthesis, and they demand intermediates that don’t clog up pipelines with tough-to-remove impurities. Since we stock fresh inventory with rapid turnover, buyers avoid concerns with degraded, aged, or cross-contaminated supplies.

    We hear from formulation teams working on patent extensions, generic launches, and modification of legacy API profiles—all pointing back to the need for reliable core intermediates. Time lost troubleshooting unreliable supply chains piles up fast in both small and mid-size companies. We address those needs through steady schedules, transparent documentation, and full traceability, refusing to ship partial or back-mixed batches even when market demand surges.

    Supporting Discovery and Development Teams with Real Answers

    From our experience, chemists want to know what happens if a batch reacts unexpectedly, or if a new catalytic system fails to meet benchmark yields. Rather than shrugging and offering generic process notes, our technical support shares the specifics from our process logs and offers direct feedback for troubleshooting. For projects scaling from grams to hundreds of kilograms, we collaborate to minimize downtime and optimize purification. If users need to validate large-batch synthesis in a new region, we ensure all batch records and certification data are in line with regulator expectations.

    Feedback has shaped our routes in concrete ways. For example, a recent customer requiring rapid lead optimization saw off-target spots in their TLC and ambiguous mass spec traces. Drawing on our logs, we recognized a common impurity stemming from incomplete aminolysis at the penultimate step. By tweaking addition rates and monitoring for byproduct formation, they quickly resolved the bottleneck, saving time and lowering startup costs.

    Environmental Responsibility Linked to Real-World Processes

    All chemical production produces byproducts—it’s not possible to wish them away with slogans or paperwork. Our plant recycles halogenated waste in closed-loop reclamation, and bromine scrubbers keep vapor below safe regulatory thresholds. Solvent use—especially DMF and acetonitrile—receives careful tracking; we recover and purify solvents onsite, following principles of responsible circular usage. These practices don’t just reduce costs or meet compliance—they improve operator health and cut down on community risk.

    We’ve modified our plant design over the last decade, adding real-time emission monitors and upgrading our effluent treatment units. Reduced-odor processes and better fume hoods help our operators stay safe, and cleaner waste streams mean less post-treatment. Scale-up used to bring worries about environmental impact, but real changes in technology and management have shown we don’t have to trade quality for sustainability. I see the benefits in lower penalties, smoother permit renewals, and better local relationships.

    Technical Support Grounded in Daily Operations

    Hands-on guidance distinguishes a genuine manufacturing partner from a distant supplier. From initial method scouting through to validation, we offer direct process notes—from our own shop floor—outlining everything from preferred glassware coatings to actual reaction temperature maps used in several key campaigns. Equipment operators share tips on reducing static build-up, minimizing caking risk during drumming, and handling minor off-color product spots when shipping times exceed normal ranges.

    Questions from customers don’t end after a shipment leaves dock. Teams frequently consult with our chemists to optimize extraction for minor byproducts or tweak workup protocols for unfamiliar scale sizes. Our familiarity with the molecule shortens time troubleshooting, so researchers avoid dead-ends and focus on making progress. The value lies in practical knowledge built through real-day, real-volume production—not in passing on a warehouse-sourced spec sheet.

    Looking Ahead: The Role of 3-Amino-2-Bromopyridine in Future Chemistry

    From experience across countless molecules, I see 3-Amino-2-Bromopyridine’s demand holding strong as medicinal chemistry broadens into new indications, and material science projects seek modular, readily adaptable scaffolds. The twin reactivity and stability make it a staple for both innovation and scalable manufacture.

    Our investment in rigorous quality, environmental stewardship, and direct technical support keeps this compound accessible to discovery teams and large-scale production users alike. The stories and feedback from the bench drive us to keep refining, batch after batch—knowing that consistent production, honest answers, and safe handling build trust and keep the science moving.