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6-Amino-5-Bromonicotinic Acid

    • Product Name 6-Amino-5-Bromonicotinic Acid
    • Alias 6-Amino-5-bromo-pyridine-3-carboxylic acid
    • Einecs 629-417-7
    • 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

    783643

    Productname 6-Amino-5-Bromonicotinic Acid
    Casnumber 630419-32-8
    Molecularformula C6H5BrN2O2
    Molecularweight 217.02 g/mol
    Appearance Off-white to light brown solid
    Meltingpoint ≥ 235°C (decomposition)
    Purity Typically ≥ 98%
    Solubility Slightly soluble in water; soluble in DMSO and methanol
    Smiles C1=CC(=NC(=C1Br)N)C(=O)O
    Inchi InChI=1S/C6H5BrN2O2/c7-4-1-3(6(10)11)2-9-5(4)8/h1-2H,(H2,8,9)(H,10,11)
    Synonyms 5-Bromo-6-aminonicotinic acid

    As an accredited 6-Amino-5-Bromonicotinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 6-Amino-5-Bromonicotinic Acid

    Applications of 6-Amino-5-Bromonicotinic Acid in Industrial Manufacturing

    6-Amino-5-Bromonicotinic Acid plays a critical role in multiple downstream sectors as a building block for specialty chemical synthesis. As a direct manufacturer, we support industrial partners by providing consistent quality adapted for regulated, high-value manufacturing workflows. Below we detail key applications with process-specific guidance.

    1. Pharmaceutical Intermediates for Anti-viral and Anti-cancer APIs

    Pharmaceutical production facilities use 6-Amino-5-Bromonicotinic Acid as a cornerstone intermediate in synthesizing pyridine-based drug molecules. This material contributes as a heterocyclic precursor in the pathway for oncology and anti-viral active pharmaceutical ingredients (APIs), specifically in systems that require precision halogenation and amination. This intermediate allows for direct attachment in selective Suzuki, Buchwald-Hartwig or SNAr couplings, supporting lead compound synthesis, scale-up for clinical batches, and process validation in regulated plants.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • EU GMP Part II for Chemical Intermediates
    • USP/EP monograph compliance for downstream APIs
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 5–50% relative to total mass of defined synthesis stage, with adjustment based on desired final yield, impurity profile, and API route-specific stoichiometry

    Downstream process integration

    • Charged at initial heterocycle assembly via palladium-catalyzed cross-coupling, then progresses through successive amide bond formation or selective reduction steps in API synthesis lines

    Final product types

    • Nicotinamide-based anti-cancer APIs (e.g., clinical trial materials for kinase inhibitors)
    • Antiviral precursor molecules with halogenated pyridine scaffolds
    • Process intermediates in custom synthesis for innovator pharmaceuticals
    • Chemical reference standards for regulatory submission

    2. Advanced Agrochemical Synthesis

    Agrochemical formulators use this compound for constructing brominated nicotinic acid derivatives, essential in the synthesis of modern herbicides, fungicides, and systemic crop protectants. The raw material facilitates the building of ring-structured moieties for high-specificity active ingredients, so process engineers precisely control purity and bromine positioning during downstream manufacturing. This compound’s properties help deliver targeted biological activity and robust field application profiles.

    Industry compliance standards

    • FAO/WHO Guidelines for Technical Materials and Formulations
    • ISO 9001:2015 Quality Management Systems for crop protection chemicals
    • European Community Regulation (EC) No 1107/2009 for Plant Protection Products
    • OECD Test Guidelines for Pesticide Residues

    Typical usage ratio

    • 10–30% of overall synthesis batch, varied according to desired final bromine incorporation and chlorination steps

    Downstream process integration

    • Feeds into multi-step synthesis lines after bromination of the pyridine ring, followed by chlorination, esterification, or amination based on target molecule specificity

    Final product types

    • Brominated herbicide intermediates (e.g., for selective broadleaf weed control)
    • Systemic fungicide precursors with enhanced field stability
    • Active agrochemical ingredients for custom formulations
    • Standard analogs for residue testing laboratories

    3. Development of Electronic and Optoelectronic Materials

    R&D and industrial teams in electronic chemical manufacturing integrate this raw material into synthesizing pyridine-containing ligands and small-molecule organic semiconductors. The substance supports device engineers working on organic light-emitting diode (OLED) layers, sensor films, and photovoltaic cell studies. Controlled halogenation patterns contribute to electronic bandgap tuning, making this input critical for achieving targeted electron transport and emission properties in molecular crystals and nanostructures.

    Industry compliance standards

    • IEC 61249-2 for halogen-free electronic materials
    • RoHS Directive (2011/65/EU) restricts hazardous substances
    • ISO 14001 Environmental Management Systems in electronics
    • Customer-specific electronic grade impurity controls (≤50 ppm Cl, ≤100 ppm Fe)

    Typical usage ratio

    • 2–8% by mass in precursor solvent reactions for small molecule synthesis; adjusted for polymer backbone functionalization requirements

    Downstream process integration

    • Dosed during ligand synthesis, followed by Suzuki or Sonogashira coupling to prepare light-emitting or charge-transporting materials; subsequent processing includes purification, crystallization, and thin film deposition steps

    Final product types

    • OLED emitter and host materials for display manufacturing
    • Organic photovoltaic compounds for flexible solar panels
    • Nanolayer sensor fabrication precursors
    • Electronic grade intermediate approvals for new device launches

    4. Synthesis of Specialty Dyes for Analytical and Diagnostic Applications

    Chemical suppliers providing inputs for analytical and medical diagnostic sectors adopt this intermediate to build pyridine-derived dyes and labeling agents. High-purity lots support consistent chromophore formation and conjugation in in-vitro diagnostics, molecular imaging, and reagent cartridge production. Strict control over bromine placement ensures desired spectral characteristics and compatibility with downstream bioconjugation systems, yielding reliable, calibrated results in lab testing and point-of-care diagnostics.

    Industry compliance standards

    • ISO 13485 Certification for medical device raw materials
    • REACH (EC 1907/2006) compliance for laboratory agents
    • GHS SDS requirements for labeling chemicals
    • CLP Regulation (EC No. 1272/2008) for hazard communication

    Typical usage ratio

    • 15–40% as primary scaffold for dye synthesis, with input mass scaled per fluorochrome molar ratio and conjugation efficiency

    Downstream process integration

    • Loaded into aromatic substitution reactions, followed by sulfonation or amidation steps for custom dye design; integrated with surface-activated particles or labeling linkers before final purification

    Final product types

    • Diagnostic reagent dyes for immunoassays and ELISA plates
    • Fluorescent labeling agents for molecular biology
    • Chromogenic sensors for clinical analyzers
    • Calibration and reference solutions for laboratory kits
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    Certification & Compliance
    More Introduction

    Introducing 6-Amino-5-Bromonicotinic Acid: Reliability Through Every Batch

    A Close Look at a Fundamental Chemical Building Block

    The chemical industry has corners bustling with innovation, yet certain molecules keep showing up at the foundation of ambitious research and process design. 6-Amino-5-Bromonicotinic Acid, easily found in the catalog under the model 6-ABNA, fits this slot in labs and production floors. This compound, with its distinct molecular structure — holding the smile notation of BrC1=CC(N)=NC=C1C(=O)O — brings a straightforward approach to synthesis challenges. It isn’t just the name or formula that brings folks back to this compound. What makes a difference is the predictability, consistency, and flexibility it offers.

    Every seasoned chemist remembers the time they wanted to push their experiments past the commonly used, often-characterless intermediates. While some chemicals force you to fudge your routes or put up with weak yields, 6-Amino-5-Bromonicotinic Acid holds a uniqueness that’s hard to find anywhere else. Not many molecules hand you the possibility of both amino and bromine chemistry on a strong pyridine backbone without demanding a redesign of your synthesis. Every batch I have handled or heard about has met the purity standards expected in pharmaceutical-grade source materials — often above 98% by HPLC — which means you rarely see unexpected spots in TLC or odd peaks crowding up the NMR spectrum. The acid group on the pyridine ring opens the door to coupling reactions that run cleaner, especially if you hate purifying side products.

    Value Stemming from Experience, Not Just Composition

    Many compound suppliers send out their wares with long lists of technical details, but the real test starts when you weigh the powder, watch it dissolve, and put it through its paces. Chemists working in drug discovery, agricultural chemistry, or even advanced materials see this firsthand. I remember colleagues in peptide synthesis praising how the amino position on this acid couples smoothly, maintaining integrity even as reaction temperatures climb. Some competitors ship in large crystal forms that gum up filters or make it a hassle to portion out small lots. The sturdy, finely powdered 6-Amino-5-Bromonicotinic Acid from reputable sources pours well and dissolves promptly in standard solvents, avoiding wasted time and frustration.

    Let’s get practical. Trying out alternatives can lead to oddball impurities, stubborn residues, or (worse) wasted months if you rely on chemicals prone to instability. Nitration or bromination after you’ve installed sensitive groups brings headaches; starting with a compound that includes both the amino and bromo groups from the beginning often delivers more reliable outcomes. I’ve seen projects grind to a halt while researchers scramble to tweak process steps just to handle an over-brominated or under-crystallized intermediate sourced elsewhere. Choosing 6-ABNA cuts out several steps, supports cleaner purifications, and allows chemists to focus on more interesting problems—not wasted glassware and chromatography columns.

    Application in Research and Production

    What sets this molecule apart is its adaptability. Pharmaceutical chemists know that attaching small fragments to a pyridine ring can help unlock tough-to-access analogs of important drugs — either by Suzuki couplings, amidation, or direct cyclization. Hard data often shows improved synthetic yields compared to older precursors that lack the ortho-amino and para-bromo configuration. Where other intermediates force you to sidestep and add protection-deprotection cycles, 6-Amino-5-Bromonicotinic Acid lets you jump ahead. The bromine serves as a clean handle for further transformations, while the amino group offers a path to rapid diversification through acylation or sulfonylation. In the right hands, this compound becomes the starting gun for dozens of cleaner, shorter syntheses.

    Some lab veterans find that the acid functionality travels well through even harsh solvent systems. Few alternatives can keep their structure intact — especially after repeated evaporation cycles or vigorous extractions. The robustness of solid 6-ABNA comes into play during scale-up. When you need to make gram or multi-kilogram lots, purity and handling ease matter much more than a fancy label or overproduced safety sheet. I’ve watched startup process teams shave weeks off development timelines because the material behaved predictably all the way from flask to drum.

    Handling the Material Day After Day

    Daily lab work is all about shaving off inefficiencies and nailing reproducible results. Some products in this space frustrate users by shipping in lumpy forms, or with a strange static cling that makes a mess in weighing boats. The best 6-Amino-5-Bromonicotinic Acid comes as a fine, neutral powder, easy to handle and resistant to caking, thanks to solid manufacturing controls. Solubility is strong enough in common solvents like dimethylformamide or DMSO to let you prepare stock solutions at whatever scale your workflow calls for. The compound may be stored at room temperature, needing no special refrigeration or elaborate humidity control, which makes life simpler for facilities with limited climate control.

    In the trenches of pharmaceutical development, small differences in input quality magnify downstream. From a batch chemistry standpoint, rolling out 6-ABNA with batch-to-batch consistency saves teams hours that would otherwise be spent troubleshooting or re-validating old results. Training new staff becomes simpler too — they run one set of controls and can trust their reactions will follow the expected path.

    Differences From Standard and Competing Compounds

    Some might wonder if the difference between this and other pyridine derivatives really matters. In hands-on work, the evidence builds up quickly. Most alternate compounds lack the combined amino and bromine functionality in this specific arrangement. You might find the amino group elsewhere or swap the bromine to another position, but that changes electron density, often forcing changes to catalyst loadings or calling for longer reaction times. Cheap substitutes save you a few dollars per kilo, but throw up yield losses, stubborn by-products, or batch variability that chew up profits at the commercial scale.

    Other similar molecules often limit synthetic creativity. For example, compare to 6-bromonicotinic acid or 5-aminonicotinic acid taken alone. Each delivers partial reactivity, but you’ll hit walls during attempts to diversify your molecule at multiple points. With 6-Amino-5-Bromonicotinic Acid present in your toolkit, cross-coupling on the bromine remains selective and energetic without the steric drag found in more heavily substituted rings. Most users report less need for additional purification steps, with cleaner NMR and LC-MS fingerprints to show for it. I’ve witnessed pilot plants shave days off their cycle times once they made the switch.

    Not every manufacturer gets this product right. I have seen poorly controlled processes that turn out coarse, off-white chunks with questionable melting points and visible contamination. Those who invest in well-controlled crystallization, frequent in-process checks, and robust drying protocols ensure that 6-ABNA ships in a form that works reliably across all common applications. Experience tells me it’s worth avoiding no-name knockoffs that skip these steps.

    What Chemists and Developers Can Expect

    6-Amino-5-Bromonicotinic Acid has become an obvious pick for both discovery projects and routine manufacturing. Once you bring it into your workflow, you notice less time spent chasing down artifacts in reaction monitoring, fewer costly test runs, and far more predictable batch outcomes. The molecule has supported everything from early-stage medicinal chemistry to intermediate production of API cores for anti-viral and central nervous system therapies. Even those working in specialty agrochemicals have found it a nimble option for building out new scaffolds, especially in the face of changing regulatory conditions and shifting supply chains.

    For scientists pushing at the boundaries of what can be built on a pyridine backbone, the combination of precision, reactivity, and user-friendly handling matters just as much as any certificate of analysis. The availability of this compound means faster progress in hit-to-lead optimization, clear decision points on reaction routes, and fewer missed deadlines in pilot plant campaigns. I’ve watched new chemists learn to appreciate reliability the hard way — after trialing lesser intermediates and seeing programs slow down or budgets balloon. Teams who bet on this molecule find progress, not headaches.

    Supply Chain, Longevity, and Responsible Use

    Modern laboratory managers worry about more than just cost per kilogram. With shifting regulations and tightening environmental standards, sustainable and transparent sourcing has become procedures worth scrutinizing. Experienced suppliers back up their product promises with clear information about batch origin, handling from raw material to finished good, and documentation that keeps risk managers content. 6-Amino-5-Bromonicotinic Acid, produced under current good manufacturing practices, checks these boxes when sourced from responsible providers. Every batch may be tracked, traced, and logged to guarantee no corners have been cut.

    Those running scale-ups appreciate sealed, UV-resistant packaging with tamper-proof indicators. I’ve never liked dealing with materials that degrade in light or spew dust upon opening. Good batches protect both the user and the compound itself, extending shelf life and preserving compliance records. This factor grows in importance for organizations serving regulated markets. Tight lot control and clear chain-of-custody procedures mean this product can enter serious pharmaceutical workflows or validated agricultural production lines without constant second-guessing.

    Improving Research Timelines and Delivering Value

    Lab managers and researchers live with the downstream effects of early-stage choices. A stubborn reaction, unreliable batch, or glassware clogged with char can set projects back weeks. With 6-Amino-5-Bromonicotinic Acid, the time and money saved upstream often shows up months later as new patents filed or product launches advanced on schedule. Studying process improvement cycles at several companies, I noticed that groups able to lock in stable, high-purity inputs were far more likely to hit quality milestones. Software can’t fix what raw chemistry breaks.

    The flexibility of this compound has helped teams explore both well-trodden and cutting-edge methodologies — from classic Buchwald-Hartwig aminations to site-specific halogen-metal exchanges under controlled cooling. If process chemistry matters, products that let you run hotter, push reactions longer, or avoid excess catalyst loads invariably translate to more robust, cost-effective campaigns. This is exactly where 6-ABNA earns its keep.

    Safety and Dealing With Changing Standards

    While nobody wants to spend all day reading safety data, real-world experience shows that choice of intermediate strongly influences both health risks and scale-up headaches. Pyridine derivatives carry characteristic odors and, in some cases, respiratory concerns at high dust levels or under careless handling. Thankfully, 6-Amino-5-Bromonicotinic Acid resists volatilization and dusting under normal conditions, making procedural precautions easy to implement. I always recommend nitrile gloves, splash goggles, and sealed containers — but it’s notable that most facilities log few, if any, reportable incidents with this product when handling guides are followed.

    As regulatory rules around pharmaceutical intermediates evolve, especially in larger jurisdictions, substances that ship with clear paperwork and established toxicology data simplify ongoing operations. Even when active ingredients shift, process engineers can stick with chemistry they understand and trust. Long-term users notice that compliance documentation, including batch traceability and residual solvent data, comes bundled with shipments from reputable sources. This level of transparency now forms an expectation — not a luxury.

    What Keeps 6-Amino-5-Bromonicotinic Acid in Demand?

    No chemical product solves every problem, but reliable workhorses deserve their reputation. 6-Amino-5-Bromonicotinic Acid has kept its place on lab benches and in pilot suites not because it looks fresh on a specification sheet, but due to the sheer hours of research it has made possible. In my experience, synthetic programs move more smoothly when the basics take care of themselves. Teams that don’t trip on unpredictable intermediates make more real discoveries — and get more credit for novel results that matter in the field or at the bedside.

    Its differentiation from lookalikes keeps delivering dividends: robust functional groups paired on an active ring, manageable stability profile, and a track record that satisfies both technical staff and risk managers. For anyone aiming to accelerate innovation, cut down on repeated troubleshooting, or lay the groundwork for new lead compounds, this product promises more returns than a shelf lined with “cheaper” but uncertain alternatives.

    Continuous Improvement and the Edge of Innovation

    If there’s an area where 6-Amino-5-Bromonicotinic Acid keeps surprising me, it’s in the way scientists repurpose it for ever-newer synthetic schemes. Innovative minds have used it to reach challenging heterocyclic compounds, step up selectivity in C-H activation, and open pathways to scaffolds impossible with less powerful starter materials. Each time a research group publishes a streamlined process or shares data on higher overall yields, this molecule tends to show up in the method. It rarely gets the glory, but every experienced chemist or project manager knows the gears keep turning because the starting line never let them down.

    There are still hurdles: new green chemistry demands better solvents, tighter waste streams, and greater efficiency. Here, 6-ABNA’s resilience and functional diversity let users test out methods requiring less energy, cutting down on solvent volume or catalyst loading. I heard a process leader in a pharma company credit the molecule with slashing their use of high-boiling solvents and speeding post-reaction work-ups — not exactly headline news, but crucial for efficiency and environmental impact.

    Looking to the Future

    The way forward in chemical manufacturing and lab discovery circles isn’t about revolutionary new intermediates every year. It’s about incremental improvements, technical trust, and building on a backbone that won’t shift under your feet. 6-Amino-5-Bromonicotinic Acid fits that vision. Its cost-effectiveness, batch quality, and well-documented supply chain mean fewer bad days, and more hours pushing at the frontier.

    While the market will keep introducing new reagents and smart molecules, some bets endure — simply because they’ve proven themselves in the toughest workflows, from exploratory benchtop synthesis to regulated bulk production. It’s a backbone item that asks little, delivers on promise, and stays adaptable without drama. For teams who care as much about reliable days as big breakthroughs, this compound looks set to keep earning its place for years to come.