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HS Code |
722019 |
| Name | 3-pyridinecarboxaldehyde, 6-fluoro- |
| Synonyms | 6-Fluoronicotinaldehyde |
| Cas Number | 16532-79-1 |
| Molecular Formula | C6H4FNO |
| Molecular Weight | 125.10 |
| Appearance | Colorless to yellow liquid |
| Boiling Point | 223-225°C |
| Density | 1.25 g/cm3 |
| Melting Point | - |
| Purity | Typically ≥97% |
| Solubility | Soluble in organic solvents such as DMSO, ethanol |
| Smiles | C1=CC(=NC=C1F)C=O |
| Inchi | InChI=1S/C6H4FNO/c7-6-2-1-5(4-9)3-8-6/h1-4H |
As an accredited 3-pyridinecarboxaldehyde, 6-fluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, 25 grams, labeled "3-pyridinecarboxaldehyde, 6-fluoro-", hazard symbols, manufacturer, and lot number. |
| Container Loading (20′ FCL) | Container loading for 3-pyridinecarboxaldehyde, 6-fluoro- (20′ FCL): Secure drums or IBCs, ensure ventilation, comply with hazardous material regulations. |
| Shipping | 3-Pyridinecarboxaldehyde, 6-fluoro- is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The package includes hazard labeling per regulatory requirements and is handled as a hazardous material, with transport complying with DOT/IATA/IMDG guidelines. Temperature and light exposure are controlled to maintain product stability during transit. |
| Storage | Store 3-pyridinecarboxaldehyde, 6-fluoro- in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed when not in use. Handle under inert gas if possible to minimize moisture exposure. Use appropriate personal protective equipment and follow all standard laboratory safety procedures. |
| Shelf Life | 3-Pyridinecarboxaldehyde, 6-fluoro- typically has a shelf life of 2–3 years when stored tightly sealed, protected from light, and moisture. |
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Purity 98%: 3-pyridinecarboxaldehyde, 6-fluoro- with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in final drug compounds. Melting point 38°C: 3-pyridinecarboxaldehyde, 6-fluoro- at a melting point of 38°C is used in organic reaction processes, where it allows easy handling and efficient processing at moderate temperatures. Molecular weight 139.10 g/mol: 3-pyridinecarboxaldehyde, 6-fluoro- with a molecular weight of 139.10 g/mol is used in chemical research, where precise stoichiometric calculations enable accurate formulation of experimental compounds. Stability up to 50°C: 3-pyridinecarboxaldehyde, 6-fluoro- stable up to 50°C is used in prolonged reaction setups, where it maintains structural integrity and consistent reactivity without decomposition. Low moisture content: 3-pyridinecarboxaldehyde, 6-fluoro- with low moisture content is used in moisture-sensitive synthesis steps, where it reduces hydrolysis risk and maximizes product quality. Assay ≥99%: 3-pyridinecarboxaldehyde, 6-fluoro- with an assay of ≥99% is used in specialty chemistry applications, where high analyte concentration facilitates reproducible and reliable experimental results. Solubility in ethanol: 3-pyridinecarboxaldehyde, 6-fluoro- soluble in ethanol is used in solvent-based reactions, where it enables uniform mixing and efficient molecular dispersion. |
Competitive 3-pyridinecarboxaldehyde, 6-fluoro- prices that fit your budget—flexible terms and customized quotes for every order.
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In our facility, every batch of 3-pyridinecarboxaldehyde, 6-fluoro- comes from years of refining the process at scale. We focus on being consistent, straightforward, and clear in our approach to this specialty building block, which consistently finds demand in pharmaceutical synthesis and specialty chemical manufacturing. Its chemical formula, C6H4FNO, and structure—highlighted by a fluorine at the 6-position—gives it a unique reactivity that distinguishes it from standard pyridinecarboxaldehydes. As direct producers, we do more than fill orders; we understand what matters in reliable supply and performance.
Most customers ask what difference the 6-fluoro group makes. From our line experience, introducing fluorine at the 6-position changes both the electron distribution on the ring and the aldehyde’s handling behavior. Compared to regular 3-pyridinecarboxaldehydes, we see better stability and altered reactivity, which is useful in certain condensation and addition reactions. The fluorinated variant doesn’t just mimic the base compound—it adds new possibilities for medicinal chemistry, giving access to analogs with improved bioavailability and metabolic profiles.
Every lot is built from high-quality starting materials and finished under tightly controlled conditions. Over years in production, we’ve seen how trace moisture, solvent residues, or uncontrolled temperature shifts can reduce yield and introduce impurities difficult to remove by simple distillation. So, we invest in closed-system synthesis, including nitrogen purge and monitored reaction kinetics. Purity runs at no less than 98% GC, supported by HPLC and NMR analysis, because even a small impurity can throw off downstream steps in medicinal chemistry applications. Regular testing and archived spectra for every lot make it possible to trace back and verify quality concerns.
The crude product comes as a pale-yellow to light-brown liquid with a sharp odor typical of pyridine derivatives. Because small variations in appearance often signal underlying issues, our QC team reviews every batch by eye and by instrument. Water content stays below 0.2% by Karl Fischer titration. We keep free acid and related pyridines under strict control, typically below 0.5% total impurities. Packing involves fluoropolymer-sealed glass because alternative materials sometimes react with aldehydes, especially when the fluorine can leach into other plastics. Every drum and bottle is flushed, inerted, and labeled with full batch history so customers see the real source.
It’s never enough to just list storage temperatures or talk about “recommended” protective equipment. In real-world conditions, we know that 3-pyridinecarboxaldehyde, 6-fluoro- can attack some standard gloves or polymer gaskets over time, especially above room temperature or in humid environments. We chair quarterly reviews with production and shipping staff to catch design flaws in containers or loading practices. This has led to a switch to dual-seal closures and regular compatibility checks on all hoses and transfer equipment, steps that directly reduce the risk of leaks or contamination.
Chemists working on CNS drug discovery and anti-infective programs come back to this molecule for good reason. The electron-deficient ring is a favored starting point for synthesizing fused heterocycles and specialized intermediates, such as pyrazolopyridines or fluorinated azines. We have followed projects where a switch from non-fluorinated versions to the 6-fluoro analog led to improved binding in kinase assays and better metabolic stability in preclinical tests. The same reactivity that makes it appealing for large-scale pharma also supports smaller, research-driven customers who need new analogs for patent filings.
Beyond pharma labs, the 6-fluoro group changes physical properties enough to interest agrochemical teams—particularly where new modes of crop protection or lower toxicity profiles are tested. Customers from industrial R&D settings have explained that this is not a commodity aldehyde: the fine-tuning from the fluorine builds in subtle, but crucial, changes in liquidity, boiling point, or even crystallization behavior in multi-step routes.
We keep a process notebook with practical notes—what works, what gives trouble, what to avoid. Our team has tested a range of condensation partners for 3-pyridinecarboxaldehyde, 6-fluoro-, from primary amines in reductive amination, to boronic acids for Suzuki couplings after conversion to other intermediates. The key, in our experience, often comes down to careful temperature control and avoiding overexposure to air. The 6-fluoro position can sensitize the ring to side reactions with strong nucleophiles or Lewis acids, so cold traps and oxygen scrubbers should be in place when scaling up.
Customers have reported success with phase-transfer catalysts or carefully buffered reaction conditions, especially in scale-up for clinical trial materials. Solvent selection often affects both yield and isolation: while DCM and acetonitrile show acceptable yields, we see improved purity from ethereal solvents at scale, provided evaporation is tightly controlled.
Compared to its non-fluorinated cousins, this molecule holds up better in extended storage, resists hydrolysis, and shows altered chromatographic behavior. These differences don’t always look large on a data sheet—but in practice, they mean fewer surprise losses in reactivity and easier separations at work-up. Over ten years, we’ve fielded questions about substitutions at other positions: we keep close records and notice that only the 6-fluoro analog lines up with requests for enhanced selectivity and resistance to unwanted side reactions.
Direct communication with customers—especially those on tight project timelines—shapes how we run the line. Major pharmaceutical companies typically want greater batch traceability and absolute certainty in record keeping. That means our team reviews every deviation, samples incoming raw material more than some would consider necessary, and sends out monthly trend reports. In times of global raw material shortfalls, our long heritage sourcing fluorinated starting materials and controlling internal timelines has kept supply disruptions rare.
Emerging issues in regulatory requirements around residual solvents, trace metals, or batch reproducibility are daily themes in operations meetings now. We do not wait for downstream customers to flag problems: we pull from our own stability and stress test bank on every new batch, cycling samples at different temperature and humidity, tracking potential color shifts, polymerization, or oxidation profiles.
Handling specialty fluorinated aldehydes used to mean high energy input, poor atom economy, and hazardous effluent. Equipment upgrades—using closed loops, in-line solvent recycling, and real-time process monitoring—have dropped waste output per kilogram by more than 35% in our last three-year operational cycle. Switching to greener reagents in the oxidation and fluorination steps remains a multi-year project, constantly weighed against the unpredictable nature of some greener chemical alternatives. We collect, treat, and incinerate all fluorinated wastes at licensed facilities and pull regular audits from downstream handlers to keep public trust and meet rising compliance standards.
We also run return and re-use schemes for all bulk packaging, cutting single-use plastics out of mainline orders. By publishing our environmental impact metrics in supplier review meetings, we stake our reputation not just on words, but measurable reductions in waste.
Few products challenge us with as many regulatory and logistic hurdles as 3-pyridinecarboxaldehyde, 6-fluoro-. Not everyone outside direct production knows that specialized transport permits are needed for certain volumes, and many standard carriers lack the capacity to recognize the risks with poorly packed aldehyde derivatives. We keep a fleet of insulated temperature-controlled boxes on standby and run new training for logistic partners every quarter.
Unpredictable jumps in demand, especially around pre-launch phases for new drugs, have taught us the cost of not holding enough on-premises stock. We keep safety reserves to protect repeat customers from delays, accepting that the carrying costs are balanced by continuity of supply and customer loyalty.
The hunger for more fluorinated small molecules in therapeutic R&D means that products like 3-pyridinecarboxaldehyde, 6-fluoro- rarely stay on the shelf. More chemists have moved from commodity aldehydes to ours for work that needs new biological space or unique regulatory footprints—positions inaccessible to their competitors.
Looking ahead, pressures for sharper analytical profiles, faster lot release, and greener synthetic channels will only grow. Our process engineers are already experimenting with microwaved-assisted fluorination routes and supercritical fluid handling—reviewing every novel method on pilots, capturing both cost and risk profiles before rollout. These investments are not about hype: they let us compete both on quality and on environmental impact metrics.
We regularly sit down not just with researchers, but with plant managers, safety directors, and supply chain leads to review how well our product fits real-world workflows. Each cycle brings revised checklists, updated risk assessments, and fresh user insights. Chemists want easy-to-pour, low-foaming liquids; packers need non-slip drums and labeled seals that survive rough transit. Our response blends these needs into each batch and into every packing run.
We also collaborate with customers developing next-generation routes. They share early screening data or unpublished impurities with us, letting our process chemists adjust operating windows to counter new side reactions or isolate hard-to-separate byproducts. We see ourselves not just as a supplier, but as an extension of our customers’ chemistry toolkit.
Pharma R&D timelines are shrinking, and the appetite for rapid iteration on new molecule libraries grows every year. Simple, reliable access to specialty building blocks like 3-pyridinecarboxaldehyde, 6-fluoro- makes this possible. From gram-scale samples for first-step research to multi-kilo lots for process development, we scale output without compromising batch-to-batch consistency. We keep open lines between technical support and plant operations: if a customer flags a gelation issue at crystallization or reports trace new impurities, our engineers can review and respond within a working day.
We do not rely on sales scripts, but rather on in-house technical specialists who understand both bench chemistry and scale-up realities. Conversations with customers frequently drive key process upgrades: several improvements in throughput, stability testing, and packing stem directly from feedback sent by teams running overnight synthesis or handling late-shift deliveries.
Over the years, the best partnerships develop not just around pricing, but shared problem solving. Regular reviews with long-term customers help us identify chronic bottlenecks, whether those involve reaction workups, shipment delays, or container compatibility mishaps. Trust grows through transparency: we don’t hide deviations, but raise and resolve them openly, offering replacement or root cause reports when warranted.
Over fifty percent of our annual volume now ships to repeat buyers—many of whom have shared project milestones, regulatory submissions, or even final API approvals achieved using our material. We credit this not to marketing, but to the reliability baked into each stage of our process, from synthesis all the way to last-mile delivery.
No amount of abstract product description substitutes for the lessons learned at the production line. What matters day to day is reliability, clarity, and accountability—both for safety and for product performance. From picking raw material sources to controlling plant throughput and shipping on time, each small choice shapes the value customers see in molecules like 3-pyridinecarboxaldehyde, 6-fluoro-. Direct engagement with users, not just through datasheets but through real conversations and shared troubleshooting, forms the backbone of our success. The commitment goes beyond supplying chemicals—it is about enabling progress in research, supporting industry partners, and continually improving how we make and deliver every batch.