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HS Code |
287001 |
| Product Name | 4-Fluoroindole-2-Carboxylic Acid |
| Cas Number | 496-23-1 |
| Molecular Formula | C9H6FNO2 |
| Molecular Weight | 179.15 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 242-246°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CC2=C(C=C1F)NC(=C2)C(=O)O |
| Inchikey | NAYGQXMFULWRKT-UHFFFAOYSA-N |
| Storage Temperature | 2-8°C |
| Synonyms | 4-Fluoro-1H-indole-2-carboxylic acid |
As an accredited 4-Fluoroindole-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g package of 4-Fluoroindole-2-Carboxylic Acid comes in a sealed amber glass bottle with a printed chemical label. |
| Shipping | 4-Fluoroindole-2-Carboxylic Acid is shipped in securely sealed containers, protected from moisture and light. It is classified as a laboratory chemical and handled according to standard safety regulations. Packages are clearly labeled and shipped via specialized couriers, ensuring compliance with all relevant chemical transport and hazardous material guidelines. |
| Storage | 4-Fluoroindole-2-carboxylic acid should be stored in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area—ideally at room temperature or as specified by the manufacturer. Store away from incompatible substances such as strong oxidizers, bases, and acids. Ensure proper chemical labeling and follow institutional safety protocols. |
Applications of 4-Fluoroindole-2-Carboxylic Acid in Industrial ManufacturingAs the original producer of 4-Fluoroindole-2-Carboxylic Acid, we focus on supporting key industrial sectors that rely on this specialty intermediate for targeted synthesis. Below, we detail its established roles in advanced pharmaceutical building blocks, crop protection research, chemical reference materials, and specialty dye intermediates, presenting application notes verified by actual end-use in global manufacturing chains. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical manufacturers incorporate 4-Fluoroindole-2-Carboxylic Acid during the construction of complex heterocyclic scaffolds for next-generation small molecule APIs, especially in the segment of kinase inhibitors and neuroactive compounds. Process chemists utilize its specific fluorinated structure to enhance bioavailability and metabolic stability when assembling key intermediates in multi-step synthetic routes. Industry compliance standards
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2. Agrochemical Research & DevelopmentAgrochemical innovators apply this fluorinated indole carboxylic acid during lead optimization efforts when screening new classes of herbicides and fungicides. Its role as a specialized intermediate lies in modification of active sites for improved plant uptake and metabolic stability, with use concentrated in research batches and pilot-scale synthesis for regulatory evaluation submissions. Industry compliance standards
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3. Analytical Reference Standard ProductionProducers of pharmaceutical and agrochemical analytical standards utilize this compound in preparing purity-characterized reference calibrants. Its molecular specificity supports high-precision calibration and system suitability testing in both QA laboratories and regulatory affairs units, where consistency and traceability are essential for certification of finished calibrants. Industry compliance standards
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4. Specialty Dye and Pigment Intermediate ManufacturingSpecialty dye manufacturers deploy this compound as an advanced building block to introduce fluorinated indole motifs in high-performance pigments. It enables tuning of photostability and color fastness, especially in dye classes for technical textiles and security inks, through late-stage substitution reactions in custom pigment synthesis. Industry compliance standards
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In the world of specialty chemicals, each molecular tweak carries big consequences for research and industry. Decades at the bench and in production lines have taught our team that there’s no shortcut to consistency, especially with fine chemicals like 4-Fluoroindole-2-Carboxylic Acid. Careful attention to purity, batch-to-batch reproducibility, and logistical reliability means more than just selling a material – it builds real trust with formulators and scientists who have zero tolerance for uncertainty.
4-Fluoroindole-2-Carboxylic Acid has become a go-to intermediate for many of our clients aiming to push the boundaries in pharmaceuticals, agrochemicals, and advanced materials. Our most widely produced grade falls under the model 4FICA-995. Laboratories demand a minimum of 99.5% purity, which our team verifies through HPLC, NMR, and GC-MS analyses calibrated on regularly sourced standards. Each batch must meet strict controls on residual solvents and moisture, with most production lots showing less than 0.3% by weight loss on drying. We ship this compound as a crystalline powder, free-flowing and easily handled in standard container formats. Shelf stability remains solid for several years, thanks to the tight wrapping and nitrogen-purged drums straight from our reactor. Real-world users have reported no issues with caking or degradation during storage under recommended conditions.
Chemists are familiar with indole as the backbone for countless molecular blueprints. Adding a fluorine atom at the 4-position, along with a carboxylic acid group at the 2-position, brings a distinct change in reactivity. With enough field data, we’ve seen how this compound often performs better as a key intermediate than other halogenated or plain indole derivatives. For instance, its electron-withdrawing fluorine influences selectivity on coupling reactions, helping researchers construct target molecules with fewer byproducts. In medicinal chemistry, the presence of fluorine not only modifies the metabolic stability of final candidates, but it also tunes binding affinities in structure-activity studies. These are not just theoretical benefits – we’ve worked alongside research teams who came to us after less substituted analogs fell short in real-life screens.
Compared with 4-chloro or 5-fluoroindole-2-carboxylic analogs, our customers have shown a preference for the balance of reactivity and stability found in the 4-fluoro variant. The lower tendency for side reactions, especially during amide or ester formation, translates to more successful synthesis and streamlined purification. Not every substitution delivers this reliable processability. Our technical team regularly sits down with clients, looking into analytics and troubleshooting reaction bottlenecks, and this hands-on approach keeps the knowledge base growing with each new challenge.
In pharmaceutical R&D, the compound shows up in several synthetic routes for kinase inhibitors, CNS actives, and enzyme modulators. From what we’ve observed on the production side, demand typically spikes during the early candidate optimization and process research phases. The 4-fluoroindole-2-carboxylic motif appears in a handful of granted patents, and more promising leads pass through our order books every year. Feedback from process chemists points to its predictable crystallization behavior and straightforward work-up as key factors for adoption.
For agrochemical innovation, clients reach out to us looking for ways to shift biological activity windows on indole-based scaffolds. Current biopesticides and plant growth agents benefit from the fine-tuned properties fluorine brings. One developer recently shared data showing a noticeable shift in selectivity profile by swapping out a hydrogen for a fluorine at the 4-position, underlining the impact even minor substitutions cause in field results. As a manufacturer, we frequently adjust sizing and batch schedules to account for agricultural researchers’ tight seasonal cycles, so responsiveness counts for a lot in these relationships.
In electronics and advanced materials, specialty indoles add value as functional monomers for polymers and optoelectronic films. Companies pursuing next-generation OLEDs, sensors, and organic transistors leverage the unique electronic effects of the 4-fluoro substitution to shape band gaps and device lifespans. These development partners rely on transparent impurity profiles, ensuring no hidden signal shifts during device scaling. Our lab collaborates closely, running custom pilot-scale syntheses or providing stability studies to meet the fast-moving pace in these industries.
Having worked through the scale-up process for a full spectrum of substituted indole carboxylic acids, we have seen where 4-fluoro-based compounds clearly diverge from their peers. One major lesson: not all halogen substitutions behave equally under harsh conditions. 4-Chloro and 4-bromo analogs, while structurally similar, tend to present greater challenges in downstream purifications. Our plant operators and QC analysts report that the 4-fluoro substitution strikes a sweet spot – it resists unwanted oxidation and hydrolysis without introducing intractable byproducts.
From the customer’s angle, we get calls when off-standard materials caused failed steps on automated synthesizers or unclear spots on purity traces. Unlike bulk intermediates, this molecule rewards attention to detail throughout the process. We have observed very few cases of batch-to-batch variability, mainly because solvent systems and temperature profiles get tuned specifically for this compound. Where some labs have faced solubility headaches with similar acids, the 4-fluoro variant dissolves cleanly in DMSO, DMF, and acetonitrile, making it friendlier for parallel synthesis and scale-up.
Comparing all these experiences to simpler indole-2-carboxylic acids, the introduction of the 4-fluoro group has repeatedly improved both handling and end-use possibilities. No single building block works across every project, but this particular structure has enabled new approaches in lead diversification and made it possible to reach candidates or functions that eluded traditional approaches. Our commitment lies in not just manufacturing this molecule, but building on the lessons learned from its real-world deployment.
We have not always enjoyed smooth sailing bringing fluorinated indole derivatives into regular production. Early on, raw material sourcing drew more challenges than expected, with parent indole stocks swinging in purity from vendor to vendor. Our solution involved negotiating fixed contracts with upstream suppliers and performing in-house distillation rather than relying solely on external audits. Yield volatility taught us plenty about reactor fouling and the quirks of direct fluorination – lessons that only hands-on troubleshooting can offer.
Scaling from gram to multi-kilo production demanded new equipment and rigorous training for plant staff. Our teams have learned to pay closer attention to trace metal catalysts and pH drift throughout each reaction stage. Only with close monitoring and repeated sampling did we hit the reliability thresholds our clients expect. Looking back at these efforts shows there is no such thing as a “routine” batch – each run carries a fresh opportunity for improvement or discovery.
We maintain a responsive feedback loop with scientists using our materials. This includes customizing drum and packaging formats, updating our Certificate of Analysis formats, and prioritizing user-inspired tweaks for the next campaign. By keeping a low barrier for customer communication, we often hear of new synthesis routes or biological screens years before they hit journals. Reliable information sharing cuts both ways, strengthening not only our product portfolio but also our own scientific community.
Quality assurance for 4-Fluoroindole-2-Carboxylic Acid centers on three main priorities: consistent chemical purity, minimal trace contaminants, and stable long-term storage. To uphold these, our processes employ closed-system crystallization, immediate vacuum packaging, and staged stress tests under varied humidity and light conditions. False economies at this step would cost our brand dearly. Retaining customer trust has always trumped short-term savings.
Following increasing attention to environmental footprints, we have fine-tuned the handling protocols for all indole derivatives. Production lines recapture as much solvent as possible, using in-line distillation and recycling methods. We regularly review waste treatment plans to keep discharge far below regulatory thresholds. Health and safety training for indoor staff covers all aspects of material handling, with environmental monitoring for any trace emissions of fluorinated byproducts.
From what long-term partners tell us, confidence grows because they see us treat health, safety, and the environment as integral to our identity – not as hurdles to check off. We continually update safety data sheets as new insights or regulatory advisories emerge. Having a full audit trail from raw starting materials to finished goods lowers risk, both for the users and our own team. Some would say these are just cost drivers; our experience says reputation is worth more than margin skimming.
We work closely with research institutes scaling up new routes, offering not just off-the-shelf solutions but advice grounded in the chemical realities of the shop floor. This means being ready to troubleshoot unexpected solubility swings, crystal morphology shifts, or purification bottlenecks on demand. Our clients rely on the fact that every sample, kilo, or package they receive traces directly back to controlled, repeatable processes, with transparent records and support built in. That requires experience from both the production and R&D sides, something our staff continues to draw on daily.
As new global standards and applications for indole derivatives evolve, so does our pipeline. We help steer early-stage projects by sharing synthetic pointers on how best to leverage specific features of 4-Fluoroindole-2-Carboxylic Acid for selectivity, resilience, or downstream modifiability. Partnerships like these have already yielded IP for several collaborators, reflecting a mutual drive to extend the boundaries of what this compound enables.
In one recent collaboration, an academic group trialed our material in a route for a lead CNS candidate, only to encounter unexpected humidity sensitivity at a key N-acylation step. By rerunning the process under our standard inert-atmosphere protocols, they rescued material with improved yield and clarity. Such case studies emphasize the practical know-how that grounds our offering in real science, rather than guesswork or marketing claims.
Ongoing regulatory changes have also inspired new levels of diligence in registration, shipping practices, and international documentation. Our dedicated compliance team stays current so that even the most challenging logistics or documentation hurdles do not block customer timelines. We have seen how just one missing certificate or mis-labeled batch can delay critical research by weeks; our approach always aims to make these headaches a thing of the past.
Demand for higher-specification, fluorinated intermediates keeps growing as drug, crop science, and technology sectors pursue ever more nuanced molecular targets. Our hands-on understanding of 4-Fluoroindole-2-Carboxylic Acid – from raw material procurement through to delivered package – gives us a unique edge in supporting new discovery. The lessons gained through years of iterations, setbacks, and customer problem-solving flow directly into every new batch out the door.
For us as a manufacturer, success depends on more than one-off sales; it lies in enabling those who build tomorrow’s medicines, materials, and tools with a clear path to repeatable, scalable chemistry. We invest in new process equipment, in staff training, and in cultivating partnerships that look past quarterly results to long-haul achievements. As expectations for quality, traceability, and reliability rise industrywide, our commitment stands: keep science mutual, practical, and open to the real work of chemical progress.