3-Pyridinecarboxylic acid, 6-fluoro-2-methyl-

    • Product Name: 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl-
    • Chemical Name (IUPAC): 6-fluoro-2-methylpyridine-3-carboxylic acid
    • CAS No.: 73039-57-1
    • Chemical Formula: C7H6FNO2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    551699

    Compound Name 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl-
    Molecular Formula C7H6FNO2
    Molecular Weight 155.13 g/mol
    Cas Number 55298-74-5
    Appearance white to off-white solid
    Melting Point 150-155°C
    Solubility Sparingly soluble in water, soluble in organic solvents
    Smiles Cc1nc(cc(c1)F)C(=O)O
    Inchi InChI=1S/C7H6FNO2/c1-4-6(8)2-3-5(9-4)7(10)11/h2-3H,1H3,(H,10,11)
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with a screw cap; labeled with chemical name, concentration, hazard warnings, and manufacturer information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl-: Typically loaded in 25kg fiber drums, total 8–10 MT per 20′ FCL.
    Shipping Shipping of **3-Pyridinecarboxylic acid, 6-fluoro-2-methyl-** requires compliance with chemical transport regulations. The substance should be sealed in suitable, properly labeled containers, protected from moisture and light. Accompany with a Safety Data Sheet (SDS). Handle as potentially hazardous; avoid direct contact. Transport via certified carriers, following all relevant local and international guidelines.
    Storage 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, and well-ventilated area. Avoid exposure to strong oxidizing agents and strong bases. Label containers clearly and keep away from incompatible substances. Follow all relevant safety protocols and refer to the MSDS for additional storage guidelines.
    Shelf Life Shelf life of 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- is typically 2–3 years when stored in a cool, dry place.
    Application of 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl-

    Purity 98%: 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal side reactions and optimal yield.

    Molecular weight 155.12 g/mol: 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- of molecular weight 155.12 g/mol is used in organic synthesis workflows, where precise molecular mass supports accurate stoichiometric calculations and product consistency.

    Melting point 127°C: 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- with a melting point of 127°C is used in solid-phase compound development, where thermal stability enhances process reliability.

    Particle size <50 μm: 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- with particle size <50 μm is used in catalyst preparation, where fine particles improve dispersion uniformity and catalytic efficiency.

    Stability temperature up to 110°C: 3-Pyridinecarboxylic acid, 6-fluoro-2-methyl- with stability temperature up to 110°C is used in high-temperature reaction media, where maintained compound integrity ensures consistent performance.

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    Certification & Compliance
    More Introduction

    3-Pyridinecarboxylic Acid, 6-Fluoro-2-Methyl—A Perspective from the Manufacturer’s Floor

    Understanding the Structure and Specialty of Our Compound

    3-Pyridinecarboxylic acid, 6-fluoro-2-methyl, often recognized through its unique substitution pattern on the pyridine ring, stands apart among heterocyclic carboxylic acids. The core structure, featuring a fluorine atom at the 6-position and a methyl group at the 2-position, brings distinct reactivity compared to unsubstituted nicotinic acids or mono-substituted versions. During synthesis on the shop floor, the placement of each substituent shapes not only physical properties like melting point and solubility but also the compound’s interaction with various reagents, intermediates, or catalysts. We have observed subtle differences in reaction yield and crystallization behavior that can only be appreciated through hands-on production.

    This molecule’s niche resides in how the electron-withdrawing fluorine and the electron-donating methyl tug the pi system in different directions. Such an arrangement changes acidity and reactivity—a fact chemists in our process lab have exploited for years. Downstream, our partners find the 6-fluoro-2-methyl combination especially valuable for creating pharmaceutical building blocks, agrochemical intermediates, or as a reference standard in research. Direct bench work has shown that this substitution pattern improves coupling efficiency and sometimes enables shorter synthesis routes compared to related compounds lacking the double substitution.

    The Production Journey—Lessons from the Reactor

    Volume production of this acid tests the limits of both equipment and operator skill. We have refined our oxidation and halogenation steps over the years to improve consistency and reduce impurity profiles. Each batch, whether tens of kilos or more, undergoes careful monitoring at crucial points. NMR and HPLC tell only half the story—the other half comes from hands sharpening their craft, reading subtle cues: the color of an intermediate, flow rates, the finicky onset of precipitation. Scaling up fine organics like this rarely follows a textbook path; solvent choices, temperature ramps, and isolation techniques all pivot on experience gained through difficult learning curves.

    This synthesis provides regular reminders that theory and practice do not always align. For example, the introduction of the fluorine atom requires meticulous control, as side products can proliferate when heat or reagent purity slips. Operations benefit from the discipline in reviewing every chromatogram before moving ahead. Any lapse costs time and raw materials. These lessons have led us to enhance our cleaning protocols, invest in custom glassware, and maintain a strong partnership between chemists and operators. Tight quality control closes the loop—mass balance tracking and impurity profiling enable us to ship product with confidence, batch after batch.

    Distinct Physicochemical Traits in Daily Work

    This compound’s dual substitution presents both challenge and opportunity. Purity standards tighter than 99% sometimes become necessary, especially for customers working in regulated spaces. Our staff find that the presence of the methyl at C-2 reduces water solubility compared to the parent compound, which has ripple effects on product handling, blending, and formulation. Dust control in powder handling, safe storage to avoid cross-contamination, and documentation for every step have emerged as critical tasks honed through day-to-day repetition.

    Fluorine’s presence gives an additional point of differentiation versus isomeric counterparts or unsubstituted pyridinecarboxylic acids. Beyond its influence on reactivity, fluorine also affects spectral fingerprints. Fingerprint signals in our in-house FTIR and mass spec readings allow teams to rapidly verify identity, even against libraries of similar chemicals. Technicians in our QC lab rely on these details to avoid costly errors during packaging or shipment.

    Applications—Firsthand Industry Observations

    Every request we receive carries its own story. Academics exploring new drug scaffolds request small quantities for high-throughput screening, while larger industry clients seek consistent quality for scale-up of advanced intermediates. We routinely see use in Suzuki-type cross-coupling, as the 6-fluoro substitution lowers activation barriers for certain catalysts. Colleagues in the R&D division highlight the way this molecule unlocks access to fluorinated pyridine rings—a motif increasingly common in medicinal chemistry for metabolic stability.

    Some clients working on crop protection agents explain that the methyl group provides better metabolic resistance in target weeds and insects. Others note the value in reference standards, where distinguishing between closely related compounds is essential for robust analytical methods. From direct conversations, the market has shifted in recent years with a greater push for fluorinated heterocycles. As demand grows, we find that delivering tight batch-to-batch consistency, flexible packaging, and technical documentation wins long-term business even more than price.

    Real-World Differences from Other Pyridinecarboxylic Acids

    Over time, our team has handled dozens of pyridine derivatives. Even among seemingly similar compounds, surprises abound. Handling regular 3-pyridinecarboxylic acid, we see much higher solubility in polar solvents while its methyl-fluoro cousin remains stubbornly less mobile—a factor that matters during clean-in-place routines or filter press operation. The 6-fluoro-2-methyl version brings sharper odor and different hygroscopicity, prompting us to use sealed drums with special liners for transport on humid days.

    Chemical behavior shifts as well. In Suzuki couplings, for instance, the 6-fluoro group gives the expected reactivity boost, but sometimes throws off downstream hydrogenation steps. We have learned from several campaigns that reaction pathways optimized for mono-substituted pyridine acids often falter with the double-substituted structure, requiring fresh pilot runs. The additional cost of reagents such as specialized bases or ligands asked for by the double-substituted structure, pays off through higher target yields and cleaner conversions.

    Safety and Handling—Lessons Learned by Doing

    On the manufacturing floor, safe handling practices develop through both training and cumulative experience. Our people know the subtleties of this compound: dust forms easily, so operators favor closed systems and local exhaust. During product transfer, anti-static measures go in place; gloves and goggles have saved more than one team member from accidental exposure to dust, which can be irritating if ignored. Cleanup down to parts per million is essential to avoid carryover in multi-purpose reactors. Every scrap of spilled powder must be gathered, logged, and disposed of in line with documented procedures—sloppy habits bring risks no team is willing to accept.

    The acid function means corrosion will eventually creep in on uncoated steel surfaces, so inspections happen with clockwork regularity. Our technical team–some with decades of hands-on experience–often recommend ceramic-lined reactors and transfer lines for critical runs. Proper labeling and tight inventory control earn their keep here, preventing costly mix-ups and intrusive compliance audits. Many of these insights arise not from safety datasheets or compliance checklists, but from shared stories and practical wisdom passed around during shift changes.

    Responding to Market Shifts and Sourcing Pressures

    Market turbulence has shaped the way we source raw materials used for 3-pyridinecarboxylic acid, 6-fluoro-2-methyl. Years ago, we saw prices double for certain reagents, and our supply chain team still keeps secondary sources and inventory buffers in play. Recent increases in the popularity of fluorinated intermediates have lengthened lead times from global suppliers—our approach involves forward planning and, at times, creative procurement. Partners sometimes ask for sustainable or “greener” options; while fluorination often leans on established chemistry, we explore catalytic approaches or higher atom economy transformations where possible without jeopardizing product reliability.

    Fluctuations in client demand put a premium on flexible batch sizing. Some years, major customers require steady truckloads for months; other times, projects end suddenly and excess inventory builds up. Waste minimization, product recovery from off-spec lots, and circular approaches—such as reclaiming solvents—feature just as prominently as fresh synthesis in our day-to-day work. These adaptations flow from the reality that chemical production rarely happens in a vacuum, and successful players learn to adjust without compromising core quality.

    Quality and Reputation—A Manufacturer’s View

    Repeat business with 3-pyridinecarboxylic acid, 6-fluoro-2-methyl comes not from faceless transactions, but from relationships built on reliability and candid conversations. Technical staff on both sides swap details about preferred packaging, stability testing, and logistics. We treat every spec deviation, no matter how small, as an opportunity to review procedures and learn. Our lot release sheets, raw chromatograms, and impurity profiles stand open to customer scrutiny because we value transparency, and feedback cycles build trust that outlasts fleeting market trends.

    Audits and site visits take place several times each year—regulatory inspectors, technical teams, even prospective buyers. Galleries of bench-top reactors and stacks of batch logs tell the story of a product’s journey, not just a number on a shelf. Continuous investment into analytical equipment, staff training, and equipment upgrades shows up in lower out-of-spec rates. Our team knows the reputational costs of a returned batch or missed delivery, and that motivation shapes every part of production, from raw material weighing to final packing.

    Future Trends—What We See from a Manufacturer's Angle

    Demand for fluorinated heterocycles will likely keep growing, especially as pharmaceutical research hones in on improved metabolic performance. Our partners in medicinal chemistry talk about the expanding role of rare substitution patterns and the challenge of finding reliable, cost-effective sources. We expect newer synthetic methods—perhaps biocatalytic, perhaps using more selective fluorination—to emerge in the coming years. Our R&D team, collaborating closely with academic and industrial labs, runs trials on alternative greener solvents, milder reaction conditions, and high-throughput reaction screening that promise both environmental and cost savings.

    Our approach to staying at the forefront depends on continued investment in talent development and the adoption of digital process controls. Automation and digital record-keeping help reduce deviation rates, ensure traceability, and speed up troubleshooting when Murphy’s Law intervenes. Openness to collaboration, with suppliers, customers, and even regulatory bodies, lets us move faster than if we held knowledge close to the chest.

    Working Side by Side with Customers—Lessons Beyond the Lab

    No substitute exists for the boots-on-the-ground value of client interaction. Over years of producing 3-pyridinecarboxylic acid, 6-fluoro-2-methyl, our engineers and sales team have grown adept at understanding not just written requirements, but the underlying motives: speed to market, reduced regulatory risk, technical support for troubleshooting, flexible MOQ. Custom packaging, clean documentation, rapid problem resolution—these take root in close dialogue, not just checklists or standards. More than one new application for this compound has grown out of customer discussions, site visits, or informal brainstorming sessions after a tough batch run.

    In-house experts hold regular conversations with process engineers at client sites, discussing details that might escape formal paperwork: handling idiosyncrasies, storage suggestions, disposal advice, or even forecasting supply chain constraints. Such engagement shortens problem-solving cycles and deepens mutual trust. Over time, the successes (and inevitable setbacks) from these interactions have cemented our product’s position not just in catalogs, but as a partner’s solution in laboratories, pilot plants, and full-scale production worldwide.

    Environmental and Regulatory Responsibility—Walking the Talk

    As regulations evolve, our manufacturing process keeps pace, not just for compliance but from genuine respect for safety and environmental stewardship. Waste streams from the production of 3-pyridinecarboxylic acid, 6-fluoro-2-methyl undergo careful segregation and treatment—solvent recovery, controlled incineration, and efforts to minimize halogenated residue in effluent. New guidelines from both local and international agencies raise the bar: limits on emissions and discharge, mandates for traceability, calls for data-driven hazard communication. Meeting these standards takes time, training, and resources—costs that pay dividends in reputational strength and community relations.

    Employees receive regular training not just on paperwork, but real-world accident scenarios: spill response, fire drills, ventilation checks. We invest in periodic third-party audits and welcome questions from neighbors or customers. Our laboratory’s history includes more than one near-miss—moments where lessons led to increased vigilance and improved engineering controls. Transparency has become part of our DNA, reflected in our willingness to discuss process changes, remediation projects, and continuous improvement initiatives with anyone who asks.

    From Factory to Final User—A Collaborative Endeavor

    3-Pyridinecarboxylic acid, 6-fluoro-2-methyl, as it moves from our reactors to users' workbenches, reflects thousands of small decisions, each informed by accumulated experience. While academic literature describes this molecule’s theoretical advantages, practical realization emerges only through the hands, eyes, and minds of people shaping matter day after day. Production scale, purity needs, packaging formats, and delivery timelines all find resolution through ongoing dialogue, incremental learning, and technical rigor. Partnerships flourish because expertise on both sides continues to evolve, informed by new science, new regulations, and a shared commitment to responsible innovation.

    Through decades of work with this product, we recognize that real value comes not just from catalog listings or technical purity, but from adaptability, openness, and a willingness to listen as markets and technology shift. As new uses arise, and as demand continues to evolve, our team stands ready to bring both depth of knowledge and willingness to innovate to every batch leaving our facility.