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2-Amino-6-Fluoropyridine

    • Product Name 2-Amino-6-Fluoropyridine
    • Alias 2-FLUORO-6-PYRIDINAMINE
    • Einecs 237-507-6
    • 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

    772259

    Cas Number 399-55-3
    Molecular Formula C5H5FN2
    Molecular Weight 112.10 g/mol
    Iupac Name 6-fluoropyridin-2-amine
    Appearance Off-white to light brown solid
    Melting Point 66-71°C
    Boiling Point 228.7°C at 760 mmHg
    Density 1.27 g/cm³
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles c1cc(F)ccc1N
    Inchi InChI=1S/C5H5FN2/c6-4-2-1-3-8-5(4)7/h1-3H,7H2

    As an accredited 2-Amino-6-Fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Amino-6-Fluoropyridine is supplied in a 25g amber glass bottle with a secure screw cap, labeled with safety information.
    Shipping 2-Amino-6-Fluoropyridine is shipped in tightly sealed containers to prevent moisture and contamination. Packages are labeled according to safety regulations and shipped by certified carriers, often under controlled temperatures. Handling instructions, hazard information, and safety data sheets (SDS) accompany each shipment to ensure compliance with chemical transport standards.
    Storage 2-Amino-6-Fluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Avoid excessive heat and ignition sources. Proper labeling and secure storage are essential to prevent accidental exposure or contamination. Use with appropriate personal protective equipment as recommended.
    Application of 2-Amino-6-Fluoropyridine

    Applications of 2-Amino-6-Fluoropyridine in Industrial Manufacturing

    2-Amino-6-Fluoropyridine serves as an essential building block in pharmaceutical synthesis, agrochemical formulation, and advanced material development. By leveraging advanced production control and strict quality protocols, we deliver this intermediate to enable high-precision industrial processes across multiple specialized sectors.

    1. Pharmaceutical Intermediate for Antiviral Drug Synthesis

    Major pharmaceutical companies utilize 2-Amino-6-Fluoropyridine in multistep syntheses of active pharmaceutical ingredients (APIs), especially for certain antiviral agents. The compound’s specific substitution pattern introduces desired electronic properties for later-stage heterocycle construction. Enabling manufacturers to produce small-molecule therapies, this intermediate enters reaction sequences through nucleophilic aromatic substitution and ring-closure processes. QC teams demand analytical traceability at every stage to satisfy DMF and global regulatory filings.

    Industry compliance standards

    • ICH Q7 GMP Guide (API manufacturing)
    • USP, Ph. Eur., JP relevant monograph references
    • Certificate of Suitability (CEP) for EU drug registration
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 0.5–4 molar equivalents relative to key starting material; laboratories select precise ratio based on API route and yield optimization

    Downstream process integration

    • Stages include nucleophilic substitution, amide coupling, heteroaromatic ring formation, and recrystallization
    • Material added in stepwise synthesis or one-pot telescoped reactions
    • In-process controls include HPLC purity profiling and residual solvent testing
    • Integrated with pharma-scale batch reactors and continuous processing lines

    Final product types

    • Pharmaceutical intermediates for licensed antivirals
    • Pyridine-derived kinase inhibitors
    • Precursor scaffolds for proprietary small-molecule drugs
    • Regulatory-submitted API process samples for scale-up validation

    2. Crop Protection Agent Precursor

    Agrochemical formulators use 2-Amino-6-Fluoropyridine to produce active ingredients in systemic fungicides and insecticides. The nitrogen-fluorine moiety improves metabolic stability and biological activity in final compounds. It undergoes N-acylation or further halogenation in synthesis schemes. Technical teams monitor reactivity profiles to enhance yield and pesticide selectivity, while maintaining compliance with residue and toxicity regulations.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • China GB 2763 (Maximum Pesticide Residue Limits)
    • REACH Regulation (EU) No 1907/2006
    • EPA 40 CFR Part 180 (US pesticide tolerances)

    Typical usage ratio

    • 2–10% by weight in synthesis step; adjusted based on target molecule backbone and desired fluorination profile

    Downstream process integration

    • Initial charge or mid-synthesis feedstock for active pesticide moieties
    • Reaction with acyl chlorides or boronic acids
    • Integration with continuous multi-phase reactors
    • Scalable post-synthesis purification by solvent extraction and crystallization

    Final product types

    • Fluorinated pyridine-based pesticides
    • Systemic fungicides for cereal grains
    • Novel insecticidal active molecules supporting global crop protection brands
    • Registration-ready technical-grade crop protection agents

    3. Manufacturing of Specialty Dyes and Pigments

    Producers of electronic-grade dyes and pigments select 2-Amino-6-Fluoropyridine for synthesizing high-stability pigments and display colorants. The fluorinated aromatic structure is introduced during azo coupling or condensation reactions, where heat stability and solvent resistance are required. Manufacturers run matched-lot syntheses and color consistency testing under ISO standards, targeting application in OLED and LCD display components as well as specialty plastics.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for pigment production)
    • EN 71-3 (Toy Safety—migration of certain elements, for colorant applications)
    • RoHS Directive (EU 2011/65, restricted hazardous substances in electronics)
    • DIN 55943 (Colorants—General requirements and test methods)

    Typical usage ratio

    • 3–9 mole % in pigment or dye precursor mixtures, selected for color intensity and shelf-life stability based on application

    Downstream process integration

    • Introduced in primary azo coupling or oxidative condensation reactions
    • Processed through solvent milling and spray-drying units
    • Subjected to high-purity filtration and drying to minimize impurities
    • End-line batch color testing to IEC display standards

    Final product types

    • Electronics-grade OLED colorant precursors
    • High-durability display pigments
    • Automotive polymer coloration masterbatches
    • Specialized inks for industrial marking systems

    4. Intermediate for Active Materials in Organic Electronics

    Advanced materials manufacturers use 2-Amino-6-Fluoropyridine as an intermediate in developing organic semiconductors for use in thin-film transistors, sensors, and light-emitting diodes. This raw material participates in cross-coupling and cyclization steps to build electron-transport frameworks. QC includes full spectral confirmation and heavy-metal monitoring per electronics industry protocols, ensuring reliable batch scalability for commercial device fabrication.

    Industry compliance standards

    • IPC-1752A (Material declaration for electronics)
    • IEC 62474 (Material declaration standard for the electrical and electronics industry)
    • UL 94 V-0 (Flammability standard for plastics used in electronics)
    • RoHS 3 (Directive 2015/863/EU, Restricted Substances)

    Typical usage ratio

    • 1–6 mole % in monomer synthesis batches, ratio chosen for polymer chain structure targeting specific device parameters

    Downstream process integration

    • Loaded in initial cross-coupling and ring-closing reactions
    • Purification via column chromatography for electronic-grade intermediates
    • Integrated into ink formulations for printable electronics
    • Final batch QC involves full IR/NMR confirmation and residue analysis

    Final product types

    • Thin-film transistor precursors
    • Organic light-emitting diode (OLED) active materials
    • Conductive polymer platform intermediates
    • Photodetector and sensor material prepolymers
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    Certification & Compliance
    More Introduction

    2-Amino-6-Fluoropyridine: Consistency and Reliability from the Source

    Direct from the Manufacturer: Our Approach to 2-Amino-6-Fluoropyridine

    Standing on the factory floor, the path from raw materials to refined product runs clear. Our journey with 2-Amino-6-Fluoropyridine connects research, scale-up, and full-rate production with the same hands that handle the solvents and gauge the reactions. Many chemists know the headaches that come from inconsistent intermediates—a batch that throws off a reaction profile or carries impurities into the final stage. We make a point to maintain batch-to-batch stability, carefully adjusting process parameters on the production line to deliver the same high standard every time.

    2-Amino-6-Fluoropyridine serves as a key intermediate in synthesizing many pharmaceuticals and agrochemical products. What makes it valuable comes down to the substitution pattern of the molecule: with an amino group at the 2-position and a fluorine at the 6-position on the pyridine ring, it opens unique options for building complex targets. In the world of medicinal chemistry, this structure creates a gateway for further functionalization—either as a nucleophile, or as a scaffold for Suzuki or Buchwald-Hartwig couplings. Teams looking for a reliable building block in heterocyclic synthesis know its reactivity can unlock novel kinase inhibitors or herbicidal agents that other pyridines can’t quite achieve.

    Our Scale and Specifications

    Daily work in a chemical plant brings a real respect for precise control. We synthesize 2-Amino-6-Fluoropyridine under strictly regulated conditions, using equipment built to handle both hazardous reagents and exact temperature profiles. Our technical crew monitors each stage, starting from the initial loading of the reactor vessels to the purification and crystallization steps. Moisture controls and exclusion of contaminants keep the final product free from hydrolysis or polymerization, which can cause headaches down the pipeline.

    The product leaves our plant in off-white crystalline powdered form, ran through a rigorous QC process before packing. Typical NMR and HPLC readings show a purity of at least 99%, with single-digit ppm levels of metals and aromatic impurities. Particle size holds tight limits for maximum solubility and blending, based on feedback from long-standing customers in contract pharma manufacturing. Each lot comes stamped with full traceability; our logs stretch back years, recording every lot of raw material and every parameter change.

    Usage in the Lab and at Industrial Scale

    Chemists often run into the problem of scale translation: a gram-scale experiment shows promise, but the pilot plant struggles to reproduce the yield or selectivity. Our direct knowledge of the full manufacturing sequence means we can flag common trouble spots early, like inadequate solvent recovery or off-ratio reactant charges. Our 2-Amino-6-Fluoropyridine moves smoothly from kilo to ton quantities for project needs—whether the use is in library development at an R&D center or in a production campaign for a registered API.

    Clients working with fluorinated heterocycles know the sensitivity of these materials. Minor levels of non-fluorinated analogs can poison late-stage reactions, especially for complex coupling chemistry. Purity and lot consistency draw demand from companies who don’t want to compromise at the intermediate stage, where a subtle impurity might escape early screening but show up later as a process deviation or regulatory concern.

    The staff at our quality lab coordinate shipments directly with clients’ technical groups, sharing analytical profiles and sample data. This lets formulation teams check compatibility and process robustness upstream—not after hundreds of kilos land on the dock. We keep records of common solvent systems and compatibility with various bases, since smaller manufacturers often call to discuss what works in scale-up and what to avoid. For experienced process chemists, these little pointers can mean the difference between weeks of troubleshooting and a smooth first batch.

    2-Amino-6-Fluoropyridine Versus Similar Pyridines

    The market for aminopyridines contains many options. Some producers push for 2-Aminopyridine or 2-Amino-5-Fluoropyridine as drop-in alternatives, but our conversations with development chemists tell a different story. The position of fluorine on the ring isn’t a trivial modification: it can change both the electronic characteristics of the ring and the available sites for further substitution. In a medicinal context, this difference can decide the metabolic stability or selectivity of a molecule and later influence the patent landscape. "Close enough" rarely works at the highest levels of synthesis.

    We hear about supply chain uncertainties from downstream users, especially those burned by variable quality when buying through traders. Many off-the-shelf grades of similar pyridines fail to meet the standards set by regulatory filings or large-scale plant runs, bringing in nitrosamine contamination or trace metals. Our response draws on decades of hands-on experience: maintain dedicated production lines, avoid cross-contamination from other fluorinated products, and run independent batch records for every lot.

    Switching between pyridine intermediates might look attractive on paper, but our customers remind us of the hidden long-term regulatory and synthesis headaches. Some competing products cut corners by blending batches or relaxing trace control to hit a price point; these shortcuts appear in inconsistent melting points, higher moisture content, or hard-to-remove colored byproducts. As a manufacturer, we see the defects others brush aside—because those "little things" can cause expensive rework or regulatory trouble for our partners.

    Experience Leads Accuracy: Why We Focus on the Details

    Looking back at our first batches years ago, the difference between "good enough" and "production-grade" stands out most in the details. Mastering the purification was no easy feat—with amination and fluorination reactions, trace halides and byproducts challenge even the best equipment. Tuning the quench and extraction steps prevents residual acids from degrading material in storage. Finishing one batch isn’t the same as being able to turn out consistent material year-round, through winter humidity and summer heat—for that, experience trumps calculation.

    We share technical learning openly with clients, because working together often solves persistent roadblocks. Sometimes, the challenge comes down to something simple: a patch of moisture in the drying room, or the need for fresh silica gel. Other times, a small pH shift in the mother liquor at the washing stage can knock the color and stability off-kilter. Building those controls into our standard operating procedures took years of gradual refinement—mistakes, shared solutions, and continual investment in equipment upgrades.

    The modern chemical supply chain puts pressure on quality and documentation. Our response is to run open batch records and provide detailed certificates of analysis on request, including chromatograms and impurity profiles. Many large clients want additional impurity specs or toxicity data for registration. Others need full transparency for compliance with international transport and storage guidelines. We keep these details organized and accessible, so any technician or auditor looking at our material sees the full trail.

    Solving Customer Problems—From Bench to Plant

    Nothing matches the value of hearing directly from end-users about problems that slowed their development campaigns. Early on, a customer reached out after finding persistent instability in a solid dose formula. Our lot met all published specifications, but a trace impurity left behind in the deprotection step caused sensitivity. We revisited our process, identified a harsher wash solvent, and retested at both lab and bulk scale. The change removed the impurity and tightened the melting point range. The next campaign ran without a hitch, saving weeks of lost time. It’s a small story, but it’s how manufacturers learn and adapt.

    Sometimes, the problems aren’t in the chemistry itself, but in logistics and supply risk. We keep a reserve stock of key inputs to hedge against raw material shortages, because our clients run time-critical campaigns. That means we can guarantee supply on tight lead times, rather than scrambling for imports. Production scheduling adapts to customer timelines, and our bulk handling processes cut down on potential damage during long-haul shipping.

    Technical engagement remains the backbone of reliability. Downstream partners frequently call our technical lead, sharing specifics about the reaction conditions they plan to use. That real-time feedback loop means we troubleshoot possible side reactions or dissolution issues early. We maintain a reference library of solvent systems, drying agents, and in-process analytic data, always ready to share with trusted customers.

    Analytical Support and Regulatory Confidence

    2-Amino-6-Fluoropyridine often enters regulatory-facing pipelines, either as a GMP intermediate or as part of a validated process for critical APIs. Registration packages often demand detailed impurity profiling, not just major components but all detectable side-products. Our in-house analytics cover LC-MS spectra, controlled drying, and even stability testing under various humidity and temperature regimes.

    Regulators expect clear records of purity, lot traceability, and manufacturing steps. Our documentation goes beyond routine quality checks—we map input lots, processing times, and in-process test results. Clients receive copies with shipments and direct access to our compliance group if any questions arise. Keeping the flow of information honest and complete builds trust, especially when the end product moves through several hands before reaching its final use.

    International shipments tend to bring extra scrutiny. We comply with global transport codes for hazardous goods, matching packaging and labeling practices to each region’s requirements. Recent changes around shipping certain fluorinated intermediates into Europe and North America led us to update MSDS protocols and re-train staff. Coordinating with freight partners prevents holdups at customs, and our technical team remains available 24/7 during transit windows.

    Continuous Improvement: What the Market Demands

    As demand for fluorinated building blocks grows, the pressure on manufacturing systems only increases. We hear from clients that upstream reliability is as important as price and purity. Late deliveries or inconsistent quality throw off whole production calendars, wasting capital and staff hours. Our investment in automated process controls and continual operator training keeps our line running smoothly—even during surges or supply chain disruptions.

    Every process revision starts with operator feedback. They know the real texture of the product, the sound of a pump going soft, or the shift in odor that follows a trace impurity. Adjustments to agitation speed, solvent swap times, or drying profiles come from real practice, not just lab theory. Each year, we invest in new dry rooms, improved filtration, and updated analytic tools to deliver material that matches the expectations set in the R&D lab.

    Looking ahead, we see opportunity in both higher margin bulk production and specialized small batches for targeted projects. Increasing interest in green chemistry drives experiments with alternative solvents and recovery strategies. We coordinate these trials with clients interested in new process approaches but cautious of regulatory surprise. These partnerships set the foundation for safer, cleaner future production.

    Chemistry Doesn’t Work Without Trust

    Selling 2-Amino-6-Fluoropyridine means more than moving inventory—it’s a continued commitment to end-users’ process goals and production safeguards. We know a failed batch costs more than money; it drains morale and sets back months of work. From the operator checking the reactor jacket to the QC scientist scanning the final IR spectrum, everyone on our team cares about delivering material that meets the highest standard.

    Our relationship with clients exists beyond the invoice. It’s the urgent call to confirm a reserve order, the request for extra spectral data, the shared sigh of relief at a successful campaign run. The people who use our material build life-saving medications, develop novel agrochemicals, and drive the next wave of chemical technology. Supplying them with reliable 2-Amino-6-Fluoropyridine is our contribution to those advances.

    We stay ready to adapt our operation and documentation to whatever the next challenge requires, and we remain open to technical cooperation of all kinds. Chemical manufacturing remains a craft built on trust, rigor, and pride in every drum and sample that leaves our facility. Our 2-Amino-6-Fluoropyridine stands for that commitment at every step.