|
HS Code |
702422 |
| Common Name | 3-Fluoropicolinic acid |
| Iupac Name | 3-fluoropyridine-2-carboxylic acid |
| Cas Number | 66975-47-5 |
| Molecular Formula | C6H4FNO2 |
| Molecular Weight | 141.10 |
| Smiles | C1=CC(=C(N=C1)C(=O)O)F |
| Inchi | InChI=1S/C6H4FNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3H,(H,9,10) |
| Appearance | White to off-white solid |
| Melting Point | 195-198 °C (lit.) |
| Solubility | Soluble in water and common organic solvents |
As an accredited 2-Pyridinecarboxylicacid,3-fluoro-(9CI) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a sealed 25g amber glass bottle, clearly labeled with name, CAS number, hazard codes, and safety instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Pyridinecarboxylicacid,3-fluoro-(9CI): 12 metric tons packed in 25 kg fiber drums. |
| Shipping | 2-Pyridinecarboxylic acid, 3-fluoro- (9CI) is shipped in sealed, chemically-resistant containers, protected from moisture and direct sunlight. Standard practice includes inner polyethylene bottles within cushioning materials, packed in sturdy outer cartons or drums. All shipments comply with relevant chemical transport regulations, featuring appropriate labeling for hazardous materials and supporting documentation for safe delivery. |
| Storage | **2-Pyridinecarboxylic acid, 3-fluoro- (9CI)** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Store away from incompatible substances such as strong oxidizers and bases. Ensure proper chemical labeling and secondary containment. Access should be limited to trained personnel following standard laboratory safety protocols. |
| Shelf Life | 2-Pyridinecarboxylicacid,3-fluoro-(9CI) typically has a shelf life of 2-3 years when stored in a cool, dry place. |
|
Purity 98%: 2-Pyridinecarboxylicacid,3-fluoro-(9CI) with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures improved reaction yield and minimal impurities in the final product. Melting Point 176°C: 2-Pyridinecarboxylicacid,3-fluoro-(9CI) with a melting point of 176°C is used in agrochemical formulation processing, where the defined melting range facilitates predictable process control. Molecular Weight 155.11 g/mol: 2-Pyridinecarboxylicacid,3-fluoro-(9CI) with a molecular weight of 155.11 g/mol is used in heterocyclic compound production, where precise mass enables accurate stoichiometric calculations. Stability Temperature 25°C: 2-Pyridinecarboxylicacid,3-fluoro-(9CI) with a stability temperature of 25°C is used in analytical laboratory applications, where ambient stability ensures reliable repeatability of analytical results. Particle Size ≤10 μm: 2-Pyridinecarboxylicacid,3-fluoro-(9CI) with particle size ≤10 μm is used in solid-state formulation research, where fine particle distribution enhances homogeneity and dissolution rates. |
Competitive 2-Pyridinecarboxylicacid,3-fluoro-(9CI) prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Producing specialty pyridine derivatives has long been a core part of our operations. Among these, 2-Pyridinecarboxylicacid,3-fluoro-(9CI) receives much attention from research chemists and pharmaceutical developers. Our engineers and production team work directly with this compound daily, refining our process with every batch. In the plant, we experience firsthand why small changes in molecular structure open up new downstream applications, and that’s what makes the 3-fluoro analog of pyridinecarboxylic acid a standout. As the manufacturer, we watch its demand grow as organizations pursue novel heterocyclic building blocks for medicinal chemistry and materials research.
We recognize that chemists require dependable input chemicals—no batch-to-batch guessing, no mystery impurities that spoil data or throw a wrench into expensive syntheses. Each production run gets tracked for melting point, purity (typically >98% by HPLC in our labs), and moisture content, as moisture especially can foul coupling reactions. Over the years, our process adjustments have dealt with the particular volatility of this fluorinated pyridinecarboxylic acid, so you don’t uncover surprises with residual solvents or co-products. What sets manufacturing apart from handling ready-made chemicals is troubleshooting live reactions and scaling filtration and drying steps to preserve integrity; it’s this hands-on experience that translates into cleaner product for researchers.
Ask anyone who spends time with pyridine derivatives in the plant: introducing a single fluorine atom at the 3-position on the ring changes both reactivity and handling compared to non-fluorinated or para-fluorinated cousins. This difference goes beyond chemical novelty. Hydrogen bonding, solubility profile, and behavior in coupling and metal-mediated transformations all shift, and the 3-fluoro isomer often brings out properties not present in the unsubstituted carboxylic acid or other isomeric fluorinated pyridines. These attributes make it valuable for projects targeting new active pharmaceutical ingredients, agrochemicals, and ligands in organometallic synthesis, as we’ve seen in direct collaboration with industry partners.
Most pyridinecarboxylic acid derivatives in commerce lean toward the unsubstituted or halogenation at the 4-position, simply because older technologies favored those regioisomers. Directing fluorination to the 3-position presents extra technical hurdles—side reactions and purification difficulties primarily. Our plant team, through repeated batchwork, discovered practical methods to keep side-product formation minimal. So we offer a 3-fluoropyridinecarboxylic acid that stands apart in terms of purity and batch consistency, rather than riskier samples from indirect synthesis or incomplete separation.
Compared to 4-fluoro analogs, the 3-fluoro product displays a different set of electronic influences. During pilot-scale projects with outside partners, we noticed improved selectivity in C–N and C–O coupling reactions. This made it a preferred starting material for certain libraries of kinase inhibitors, as noted by collaborating researchers. Ask around synthetic chemistry forums or at conferences and the value of positional selectivity for functionalization comes up routinely; having access to reliable material opens up more design space in medicinal chemistry.
In our observation, 2-Pyridinecarboxylicacid,3-fluoro-(9CI) often enters the process pipeline as a coupling agent for amide bond formation, especially in early-stage drug discovery. Contract labs and pharmaceutical companies leverage its fluorinated core to explore candidate molecules with altered metabolic stability or target selectivity. Over several years, our customers have reported its effective role as an intermediate for building more complex frameworks, especially those requiring a heteroaromatic backbone with a tailored electron density.
Colleagues in the field of coordination chemistry use this acid as a ligand precursor, benefiting from the fluoro group’s ability to tune electron-donating and withdrawing properties. Several patents cite the use of this building block in ligand design for asymmetric catalysis, as those who have worked hands-on with the compound can confirm. The ability to switch between the 3-fluoro and other substituted pyridines—with confidence that starting materials won’t introduce variable background effects—is crucial for these applications.
Consistent production of fluorinated heterocycles demands attention well beyond bench synthesis. During scale-up, different reactor conditions influence yield and impurity profile significantly. One recurring challenge involves fluorine-containing volatile byproducts, which can escape detection unless you have rigorous analysis in place. Our analytical group employs both NMR and HPLC routinely, screening for potential low-level contaminants. Purification sometimes introduces tough trade-offs—raise the yield but jeopardize purity, or lose a bit of material to deliver a cleaner product.
We keep close control on drying conditions. Some customers need moisture below 0.2% for sensitive coupling chemistry. Our facilities use vacuum ovens with in-line monitoring to manage residual water or solvent levels, drawing on direct feedback from chemists who encountered failed reactions due to residual moisture from other suppliers. It's hands-on troubleshooting like this, informed by returning customers, that guides our continuous improvements.
Shipping presents another concern. The product’s sensitivity to moisture and certain packaging materials means simple off-the-shelf containers don’t work. We developed lined HDPE bottles and double sealed packaging after hearing from customers about clumping or partial hydrolysis during transit. Regular factory audits and spot-checking have been fundamental here, further reducing surprises on arrival.
In modern synthesis, unambiguous data matters. Our team runs both proton and fluorine NMR on every lot, complemented by HPLC for purity, and FTIR for functional group analysis. Occasionally a customer requests custom data reports or extra impurity identification. We keep these records, not simply for internal compliance, but to arm users with actionable insights—documents that have helped avoid mid-project setbacks more than a few times. By manufacturing directly, we gain feedback cycles that just aren’t possible through distribution alone.
Trace metal contamination occasionally crops up with some batches, so we include routine ICP-MS scans when batches are targeted at organometallic usage. These checks come from experience—chemists have seen even sub-ppm levels derail catalyst studies, and we take pride in supporting trusted work by eliminating such variables at the source.
Several years back, small and mid-sized pharma began investigating more fluorinated heterocycles in their lead optimization efforts. The recent spike in these projects pulled 2-pyridinecarboxylic acid derivatives into focus for a wider range of researchers and process development teams. Our technical staff interacts regularly with R&D groups in Europe, North America, and East Asia, tracking new uses for the 3-fluoro isomer, especially in bioactive molecule synthesis. Providing technical background, not just an MSDS, often guides our development process—we incorporate industry trends and special requests directly into the batchwork.
Environmental and regulatory scrutiny on halogenated aromatics continues to climb worldwide. Our internal environmental compliance team works proactively to align waste handling and emissions with both local and international standards. This sometimes means adopting new purification technologies or investing in better scrubber systems long before regulatory deadlines. Our motivation stems from daily experience on the line: nothing stalls progress like a production standstill over environmental paperwork. By staying ahead, we maintain a steady output for our partners relying on timely deliveries.
Over regular correspondence, we noticed that many researchers struggle to trace supply chain issues with specialty heterocycles—unpredictable shipment times, variable purity, and unclear handling guidance. As producers, we commit to direct feedback loops between chemists and manufacturing staff, skipping layers of resellers. Customers who needed special particle size or tailored drying grew our technical support team into what it is now—capable of switching between routine high-throughput requests and small-batch, high-purity jobs as needed.
This year, our team completed a set of joint pilots with two European API developers to address persistent issues with batch variation. Back-and-forth communication refined our crystallization technique. Eventually, we supplied a run with purity and performance that met both their scale-up and regulatory requirements. Running these collaborations provides perspective impossible to gain from market summaries or catalogs.
Correct storage begins well before bottles leave our factory. We navigate between high and low humidity conditions across facilities, accounting for static buildup and bottle lining material. Our firsthand experience shows too many costly delays can track back to ignored storage advice or inadequate packaging. Using both customer feedback and in-house aging studies, we recommend sealed, low-moisture environments and quick use after opening. Any material returns or customer complaints trigger batch analysis and process review. These moments push us to revisit basic protocols and reinvest in more robust process controls.
Handling 2-Pyridinecarboxylicacid,3-fluoro-(9CI) in manufacturing scales brings new challenges compared to lab scales. Exact pH range for dissolution, solvent choices for recrystallization, and solid transfer methods all play a critical role in delivering quality material to end users. Every tweak in the process—mixing rate, temperature, or solvent vapor pressure—manifests in the product’s physical appearance, filterability, and stability. Years of in-plant sampling and batch logs drove us to standardize these process details and share pointers with partners on safe, effective usage.
Maintaining consistency from early production lots through large-scale regular supply is a challenge we take seriously. Regular investments in analytical equipment and process automation reflect the reality that, left unchecked, drift in operating procedures invites recurring problems. We maintain historical records of every run and analytical report, comparing across years and shifting conditions. Direct customer conversations sometimes reveal application-specific needs not anticipated at the development stage; rapid adaptation sets our production process apart from those limited by less flexible facilities.
In a global context, supply chain disruptions and tariffs have pushed many users to work with primary manufacturers instead of relying on less accountable middlemen. Our export and logistics staff anticipate regulatory, packaging, and labeling demands for each region, having spent time problem-solving on the ground for international shipments. Building this groundwork—based on years of actual delivery experience—helps secure uninterrupted supply for R&D pipelines or routine manufacturing runs.
Our background handling this compound day in and day out grants us a clear window into both strengths and pain points. We track performance not just by sales figures but by technical support calls, process feedback, and the ultimate impact on our customers’ research projects. Improvements to process yield, waste minimization, and delivery speed all spring from this loop of direct experience and honest self-assessment.
The field of pyridine derivatives continues to evolve, with emerging demands for purer materials, faster delivery, and wider regulatory approval. As the team at the manufacturing site, we see firsthand the impact of these pressures. Our aim remains reliable, adaptable supply—tightly controlled from starting material all the way through final shipment. By working at the source and staying in tune with chemists’ real-world needs, we help extend what can be achieved with 2-Pyridinecarboxylicacid,3-fluoro-(9CI) in tomorrow’s R&D breakthroughs.