|
HS Code |
102703 |
| Name | 4-pyridinecarboxylic acid, 2,6-difluoro- |
| Cas Number | 153034-51-2 |
| Molecular Formula | C6H3F2NO2 |
| Molecular Weight | 159.09 |
| Appearance | White to off-white powder |
| Melting Point | 172-176°C |
| Solubility | Slightly soluble in water |
| Smiles | C1=CC(=NC(=C1F)C(=O)O)F |
| Inchi | InChI=1S/C6H3F2NO2/c7-4-1-2-9-5(8)3(4)6(10)11/h1-2H,(H,10,11) |
| Pubchem Cid | 13610737 |
As an accredited 4-pyridinecarboxylic acid, 2,6-difluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with white screw cap, labeled "4-pyridinecarboxylic acid, 2,6-difluoro-, 25g," chemical hazard symbols included. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-pyridinecarboxylic acid, 2,6-difluoro-: Packed in sealed drums/cartons, maximizing capacity, compliant with chemical safety regulations. |
| Shipping | 4-Pyridinecarboxylic acid, 2,6-difluoro- is shipped in tightly sealed containers to prevent moisture and contamination. It is transported following standard chemical handling protocols, typically at ambient temperature. Proper labeling and documentation are provided, and shipping complies with applicable regulations for safe handling and transit of laboratory chemicals. |
| Storage | 4-Pyridinecarboxylic acid, 2,6-difluoro-, should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Avoid moisture and keep away from food or drink. Ensure proper labeling and limit access to trained personnel. Use chemical-resistant containers and store in designated chemical storage cabinets. |
| Shelf Life | Shelf life of 4-pyridinecarboxylic acid, 2,6-difluoro-: Stable for at least 2 years when stored in a cool, dry, tightly-sealed container. |
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Purity 99%: 4-pyridinecarboxylic acid, 2,6-difluoro- with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and purity in final compounds. Melting Point 220°C: 4-pyridinecarboxylic acid, 2,6-difluoro- with a melting point of 220°C is used in high-temperature organic reactions, where it provides excellent thermal stability during processes. Molecular Weight 173.09 g/mol: 4-pyridinecarboxylic acid, 2,6-difluoro- of molecular weight 173.09 g/mol is used in structure-activity relationship (SAR) studies, where it enables precise molecular modeling and optimization. Particle Size <50 µm: 4-pyridinecarboxylic acid, 2,6-difluoro- with a particle size below 50 µm is used in fine chemical formulation, where it ensures uniform blending and enhanced reaction efficiency. Stability Temperature 150°C: 4-pyridinecarboxylic acid, 2,6-difluoro- with stability up to 150°C is used in catalyst preparation, where it maintains chemical integrity under elevated processing temperatures. Water Content <0.5%: 4-pyridinecarboxylic acid, 2,6-difluoro- with water content below 0.5% is used in moisture-sensitive reaction systems, where it prevents hydrolysis and degradation of sensitive reagents. Assay ≥98% (HPLC): 4-pyridinecarboxylic acid, 2,6-difluoro- with assay ≥98% by HPLC is used in active pharmaceutical ingredient (API) development, where it assures consistent dosage and therapeutic efficacy. Solubility in DMSO 50 mg/mL: 4-pyridinecarboxylic acid, 2,6-difluoro- soluble at 50 mg/mL in DMSO is used in bioassay screening, where it supports high-concentration stock preparation for in vitro testing. Shelf Life 24 Months: 4-pyridinecarboxylic acid, 2,6-difluoro- with a shelf life of 24 months is used in long-term research programs, where it ensures reliable performance over extended storage periods. Purity by GC ≥98%: 4-pyridinecarboxylic acid, 2,6-difluoro- with GC-assayed purity of ≥98% is used in analytical method validation, where it provides a reproducible standard for precise quantification. |
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Working day in and day out with pyridine derivatives brings a unique insight into the delicate balance between performance and reliability. 4-pyridinecarboxylic acid, 2,6-difluoro-—often known in the lab by its CAS number 3939-09-1—stands as an example of how careful fluorination can enhance a molecule’s value. As a chemical manufacturer, every batch is an opportunity to deepen our knowledge and refine technique. We watch how the twin fluorine atoms at the 2 and 6 positions don’t just decorate the ring. They reshape electron distribution, impact solubility, and alter how the acid group interacts with its surroundings. Years of refinement have gone into making this compound useful beyond academic curiosity.
Fluorination changes everything. The basic scaffold—a pyridine ring—starts out familiar, but introducing two fluorine atoms makes a substantial shift in reactivity and binding selectivity. This puts 2,6-difluoro substitution far from a cosmetic change. It modifies hydrogen bonding and reduces basicity of the nitrogen atom, which in practice affects applications in ligand design and as an intermediate for pharmaceuticals. In our experience, this chemical stays less prone to unwanted side reactions during multi-step syntheses, especially where alternatives like unsubstituted 4-pyridinecarboxylic acid would show more reactivity than desired.
The acid’s unique balance of fluorine placement and carboxylic acid functionality brings advantages when precision is needed. In structure-activity relationship studies, it serves as both a building block and an experimental probe, making it stand out among both the unfluorinated and mono-fluorinated variants. This is not just a simple matter of swapping out substituents. Every modification on the pyridine ring means new crystal habits, solubility profiles, and separation challenges for the team on the production line. Tweaking conditions—solvent ratios, crystallization temperature, and pH—demands a trained hand and familiarity with the way these small changes play out at scale.
Most inquiries for 2,6-difluoro-4-pyridinecarboxylic acid come from labs engaged in pharmaceutical research, where tight control over the behavior of intermediates counts for more than raw reactivity. Drug discovery teams approach us with demanding purity requirements, seeking out this molecule for its ability to influence metabolic stability, lipophilicity, and receptor selectivity in their candidate compounds. Our production crew frequently communicates with formulators about the molecule’s role in targeting kinases or as a ligand in metal binding studies. We have seen this compound considered for applications in crop protection research, where subtle differences in substitution can spell the difference between a promising lead and a failed trial.
Beyond pharma, some of our longest-standing clients use this chemical for the synthesis of advanced materials and polymers. The twin fluorines enhance thermal stability in specialty applications—crucial for those pushing boundaries in battery chemistry, liquid crystals, or high-performance coatings. Requests often focus more on consistency across lots rather than record-breaking purity; our batch records serve as a testament to that demand. It is not uncommon to receive feedback from customers using 2,6-difluoro-4-pyridinecarboxylic acid in asymmetric synthesis or as a handle for further elaboration on the ring. This cross-industry need keeps us focused on process reproducibility at every scale.
We respect how sensitive this compound can be to slight changes in production. Fluorinated intermediates require strict control over temperature profiles and agitation rates to ensure uniformity. Even slight residual moisture in a reaction can throw off yields or purity, so our equipment choices always err on the side of redundancies in drying protocols. Routine HPLC and NMR checks throughout process refinement reinforce this attention to detail—no batch moves to the next stage without full spectra reviewed by our in-house analysts.
The experience gained from working with 4-pyridinecarboxylic acid, 2,6-difluoro- also means recognizing the barriers faced by our clients. Anyone who has tried to scale up a reaction with highly fluorinated intermediates knows the headaches: increased viscosity, need for specialized filtration media, and solvent choices that minimize decomposition or side product formation. Our process engineers run pilot batches under simulated end-user scenarios, striving to minimize headaches for downstream blending or formulation teams. Supply chain disruptions—sometimes as simple as a late delivery of anhydrous solvents—can impact lead times. Thus, we keep inventory lean but smart, always calibrated by feedback from our partners.
Anyone who has handled a range of pyridinecarboxylic acids knows not all behave the same. Our team’s workbench is lined with benchmark data comparing the 2,6-difluoro analog against its cousins. For users accustomed to the single fluorinated or non-fluorinated versions, transitioning to the difluoro variant means a steeper melting point and altered solubility patterns in both protic and aprotic media. The molecule’s increased hydrophobicity emerges as a consistent theme in our tests, influencing not only its isolation but also the way it integrates into further transformations. During scale-up, filters can clog and solubility in common solvents like methanol or acetonitrile drops compared to simpler analogs. Adjusting for this brings lessons learned directly back into our process optimization.
We see the mono-fluoro compounds behave differently regarding stability under mildly basic conditions—a feature some of our clients actively exploit during synthesis route design. The difluoro variant helps in cases where a more electron-deficient aromatic system is desired, effectively shifting the balance toward selectivity and away from unwanted side reactions. Among all pyridinecarboxylic acids we produce, only this one brings that finely-tuned balance between ring activation and resistivity to nucleophilic attack. Our team often works with partners developing new ligands, observing differences in metal complex formation between the difluoro, monofluoro, and non-fluorinated cases. Documenting these behaviors is as much a habit as it is a necessity for our batch records and quality design.
We’ve always believed that open dialog with researchers is integral: it keeps our knowledge sharp and our batches reliable. Regular feedback loops—researchers flagging subtle crystallization problems, process chemists sharing successful scale-ups—make their way back to our production notes. Over years, these conversations drive in-house improvements. A single customer’s need for a custom particle size or reduced chloride content can trigger broader changes in our crystallization setup. This two-way engagement does more than keep clients happy; it raises the whole industry standard for what to expect from specialty chemical manufacturing.
We encourage direct communication about pain points. In recent years, requests have ranged from specific enantiopurity in downstream transformations to maximized stability for prolonged storage. Our work on 2,6-difluoro-4-pyridinecarboxylic acid has included experiments in stabilizing agents and custom packaging solutions that protect against environmental moisture—challenges that don’t come up with less fluorinated relatives. Shipping routes, lead time forecasts, and special handling requirements have evolved continually as usage expands into new geographies and industries. We adapt alongside, knowing the job doesn’t end at the loading dock.
Fluorinated building blocks carry greater scrutiny from environmental and safety perspectives. We understand the difference that containment protocols and proper waste neutralization make. Our operations feature containment strategies for vapor and liquid effluents, grounded in years of troubleshooting. We invest in analytic methods that allow us to monitor trace fluorine content in our effluent streams. Feedback from regulatory agencies is not just a compliance checklist—it actively drives process improvements, from minimizing reagent excess to streamlining our purification steps.
We also run regular safety seminars for our production teams. Experience tells us that handling and transferring highly fluorinated compounds means attention to detail—from vented weighing stations to specialized gloves and eye protection. As fluorinated intermediates move through our storerooms, each drum gets tracked, logged, and double-checked before it leaves the facility. Accidents rarely happen in operations with a culture focused on shared responsibility; a point of pride among our crew, many of whom have decades of combined experience.
Consistency drives customer loyalty for specialized intermediates like 4-pyridinecarboxylic acid, 2,6-difluoro-. Each new batch enters a stringent regime of HPLC, NMR, and titration analyses mapped out in quality logs and signed by designated chemists. We do not dilute our standards to suit volume demands. Our lot release threshold came from repeat customer needs for low ppm levels of impurities, so trace-by-trace transparency matters. Export markets require special attention to documented provenance, and all certificates head out the door alongside real data, not just boilerplate assurances.
Every so often, customer audits bring insights impossible to plan for—an unexpected interaction with a filter aid, a subtle drift in melting point, or advice about solvent-saving. These interactions pull us forward. The story of 2,6-difluoro-4-pyridinecarboxylic acid production unfolds as the accumulation of these lived moments rather than preset templates. We have learned that success means not just hitting a spec sheet, but building resilient processes that adapt, correct, and improve as actual research needs evolve. If an upstream material supplier changes a drying technique, or if analytical thresholds shift in response to new regulatory science, our process evolves.
Experience living at the intersection of production and end user demand puts real responsibility on our shoulders. The world’s rapid push for innovation in pharmaceuticals and advanced electronics runs in tandem with the evolution of specialty intermediates. Each run of 4-pyridinecarboxylic acid, 2,6-difluoro- is a live experiment in precision and adaptability. Open curiosity—willingness to experiment, to tweak parameters, and document every outcome—powers our progress far more than the rote ticking of QA boxes.
We participate in professional chemical associations for the knowledge exchange opportunities. Industry gatherings bring together producers, researchers, and equipment manufacturers. They reveal new findings on improved purification strategies, safer packaging protocols, or innovative uses of difluorinated heterocycles in research. Every new insight gets considered by our in-house chemists for its relevance to 4-pyridinecarboxylic acid, 2,6-difluoro- and sister products.
Our perspective is shaped by years of direct involvement, from raw material selection to dispatching finished product. We know the difference between theoretical purity and actual process-friendly performance. Clients return year after year because we solve not only the expected, but also the unforeseen challenges that surface in high-stakes research and manufacturing.
Constant improvement runs through our work. We regularly revisit our manufacturing parameters, reformulate purification protocols, and roll out improvements learned from audit findings and shifting regulatory landscapes. Our staff gets ongoing training on new analytic techniques; feedback loops bring knowledge from bench chemists directly to the process control room. Analytical trends that suggest even minor instability trigger in-house investigations, no matter how minor. This discipline helps us meet requests for tighter specifications and enables rapid response to bespoke research demands.
Fluorinated intermediates like 4-pyridinecarboxylic acid, 2,6-difluoro- play a pivotal part in research and commercial innovation. They drive progress in areas from pharmaceuticals and crop protection to advanced materials. Decades of focused manufacturing expertise make us uniquely attuned to the intricacies of this compound. Our continuous collaboration with research and industrial partners ensures that the chemical performs as needed now, while flexible processes let us address the requirements of tomorrow.
Every production run tells a story woven from thousands of careful calculations, process tweaks, and quality controls. Feedback from every corner of the chemical ecosystem—researchers, procurement, regulators—gets distilled into our batch sheets and process controls. This compound’s value comes not just from the structure written on a bottle, but from the experience-driven reliability experienced by every scientist or engineer who puts it to work. We take pride in every kilo of 4-pyridinecarboxylic acid, 2,6-difluoro- that leaves our facility, knowing it is backed by the experience and commitment of a team dedicated to continuous improvement and chemical excellence.