|
HS Code |
856242 |
| Product Name | 2-Fluoro-5-formyl-3-methylpyridine |
| Molecular Formula | C7H6FNO |
| Molecular Weight | 139.13 g/mol |
| Cas Number | 864860-58-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | Approximately 220°C |
| Density | 1.18 g/cm³ (estimated) |
| Purity | Typically ≥ 97% |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Smiles | CC1=CN=C(C=C1F)C=O |
| Storage Conditions | Store at 2-8°C, tightly closed |
| Synonyms | 5-Formyl-3-methyl-2-fluoropyridine |
As an accredited 2-Fluoro-5-formyl-3-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed, labeled with hazard warnings, chemical name, purity, batch number, and handling instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2-Fluoro-5-formyl-3-methylpyridine securely packed in HDPE drums, 160 kg per drum, total 80 drums. |
| Shipping | 2-Fluoro-5-formyl-3-methylpyridine is shipped in tightly sealed, chemically resistant containers to prevent leakage and contamination. Packages are clearly labeled according to applicable regulatory standards. During transport, it is protected from moisture, heat, and direct sunlight, and handled by trained personnel following all safety protocols for hazardous chemicals. |
| Storage | 2-Fluoro-5-formyl-3-methylpyridine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and protected from moisture. Store separately from incompatible materials like strong oxidizing agents. Use appropriate chemical-resistant containers, and label them clearly for safe identification and handling. |
| Shelf Life | Shelf life of 2-Fluoro-5-formyl-3-methylpyridine: Stable for at least 2 years when stored under recommended dry, cool, and dark conditions. |
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Purity 98%: 2-Fluoro-5-formyl-3-methylpyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it results in high-yield and low-impurity final products. Melting Point 54°C: 2-Fluoro-5-formyl-3-methylpyridine with a melting point of 54°C is used in agrochemical development, where it provides controlled processability during compound formulation. Molecular Weight 139.12 g/mol: 2-Fluoro-5-formyl-3-methylpyridine of molecular weight 139.12 g/mol is used in medicinal chemistry research, where it ensures precise stoichiometric calculations for reaction optimization. Stability Temperature up to 120°C: 2-Fluoro-5-formyl-3-methylpyridine stable up to 120°C is used in high-temperature reaction protocols, where it ensures structural integrity during synthesis. Low Moisture Content (<0.5%): 2-Fluoro-5-formyl-3-methylpyridine with low moisture content is used in sensitive organic transformations, where it minimizes hydrolytic side reactions for cleaner product profiles. Particle Size <50 μm: 2-Fluoro-5-formyl-3-methylpyridine with particle size less than 50 μm is used in catalyst preparation, where it enables rapid dissolution and uniform dispersion in reaction mixtures. |
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Chemists know the race for useful, manageable intermediates never really stops. Every year, the demand for compounds that fill unique roles in research and manufacturing grows. Among these, 2-Fluoro-5-formyl-3-methylpyridine has become something of a quiet workhorse. This compound—precise in structure, with a fluorine atom on the second position, a formyl group at the fifth, and a methyl at the third—may not be on the tip of everyone’s tongue, but those who’ve worked at the bench know its value. I’ve watched research colleagues light up when it arrives because its profile promises both versatility and reliability in synthesis.
Let’s talk specifics. Chemists often reach for pyridine derivatives because these six-membered nitrogen-containing rings show the right balance of stability and reactivity. In this molecule, each substitution tweaks the electron distribution, shaping its behavior. The presence of fluorine on the ring matters—a lot. Fluorine is one of the most electronegative atoms, so its position affects hydrogen bonding, metabolic pathways, and sometimes even biological activity in final products. For folks hunting for improved pharmacokinetics or resistance to metabolic breakdown, these are attractive features.
The aldehyde group, sitting at the fifth position, makes this molecule remarkably reactive towards condensation and coupling reactions. Aldehydes, by their nature, act as go-to handles for forming carbon-carbon bonds. Some of my peers in medicinal chemistry see it as a way to quickly build out more complex scaffolds, while others in agrochemicals look for that functional group to dial in activity or environmental stability. The third-position methyl further modulates the physical and chemical properties. Unlike larger substituents that can throw off solubility or handling, the methyl group here keeps the compound manageable—a simple tweak with noticeable effects.
Labs can gain a lot by picking this compound when building out libraries of new molecules. In drug discovery, pyridine rings frequently pop up in candidates for anti-infective, anti-inflammatory, or even anti-cancer drugs. The pharmaceutical world prizes unique variants—it helps skirt patent thickets and gives researchers fresh ground to test new hypotheses. Over the years, I’ve seen teams use this molecule as a starting material for synthesizing more sophisticated heterocyclic frameworks. The aldehyde functionality makes it easy to attach new arms, run condensation reactions, or print the core onto resin beads for high-throughput screening.
Specialty chemical producers use this pyridine as a stepping stone toward advanced catalysts. The combination of electron-withdrawing and electron-donating groups attracts attention from those developing metal ligands with fine-tuned selectivity or activity. Plus, the fluorine acts as a probe in NMR experiments, which is a subtle but appreciated bonus when troubleshooting complex reactions.
Product consistency remains a top priority. Every bottle or drum should meet strict purity standards. Look around: high-purity material increases reproducibility and lowers the chance of mysterious results later in development. Analytical standards usually target purity above 98%, with trace metals and water contents checked carefully. When a researcher picks up 2-Fluoro-5-formyl-3-methylpyridine for a reaction, there’s confidence that batch variation won’t trip things up. Reliable melting and boiling points, solid IR and NMR spectra, and clean mass spectrometry data all foster trust, and these features get verified with every production run.
People rarely talk about handling, but it’s worth a mention. The product usually comes as a crystalline solid or liquid, depending on temperature. This form helps with weighing and transfer—two tasks that sound trivial, but matter a lot when precision counts. In smaller scale labs, airtight bottles and proper refrigeration can extend shelf life and prevent oxidation or hydrolysis.
The catalog listing tells half the story. Real value shows up in action. In my experience, researchers need intermediates that deliver results without fuss. 2-Fluoro-5-formyl-3-methylpyridine isn’t flashy, but it quietly enables reactions that expand chemical space efficiently. Consider the boom in AI-driven drug design; scientists now prioritize quick, diverse analog synthesis. Reliable intermediates keep the campaign moving because they remove bottlenecks and reduce troubleshooting time.
Not all pyridines behave the same, either. The placement and nature of ring substituents matters. Here's where practical knowledge beats generic catalog chatter. Specific substitution patterns—like having fluorine at the second and a formyl at the fifth—change the way reagents attack the ring and steer reaction outcomes. In some syntheses, closely related pyridines without a fluorine might decompose, polymerize, or stall while this derivative quietly pushes the process forward.
Some people think any pyridine will do, but as someone who's tried plenty of them, subtle differences in behavior make all the difference. Swapping the fluorine to another position or dropping the methyl group can give a completely different set of challenges. Without the methyl, a molecule might dissolve too quickly, or crystallize with stubborn polymorphs. Moving the formyl changes its reactivity, which might tank a whole route developed over months.
Many labs encounter hurdles when working with more common pyridine aldehydes. Compounds lacking a fluorine may show greater sensitivity to light and oxidation, making long-term storage a headache. Others without a methyl group drift across partition coefficients in unpredictable ways, throwing off attempts at purification. This particular derivative lessens those headaches, which can save weeks of troubleshooting. During a round of scale-up for a peptide synthesis project, my group couldn’t get the core fragment to react well with 2-formyl-3-methylpyridine—the reaction sat for days with little conversion. Swapping to the fluorinated analog made the entire process click. Sometimes, it really comes down to these little tweaks.
One of the more exciting aspects involves multi-step synthesis programs. Route scouts and process chemists often use 2-Fluoro-5-formyl-3-methylpyridine as an entry point to create functionalized bipyridines, ligand libraries, and substituted azines for advanced applications. In the world of OLED development, fluorinated pyridines can influence charge mobility or stabilize blue-emitting cores. I’ve listened to physical chemists debating the merits of different substituents late into research meetings. When the need arises for backbone shifts or electron balance, this compound gets high marks.
Agrochemical innovators prize the molecule’s handle for derivatization—think barnyard run-off and crop resilience. Researchers look for structures that degrade predictably in soil or resist breakdown until they’ve done their job. The aldehyde and fluorine groups modulate both environmental fate and bioactivity. Any practitioner who’s struggled to maintain shelf life knows why these matters cut deep—no one wants to recall a field batch just because it didn’t last on the shelf.
Trust in a chemical supply hinges on quality and transparency. Labs only build confidence by seeing batch analyses, having contaminants held in check, and getting copies of spectra included. I have come across researchers who track down a supplier’s quality records before placing a critical order. That transparency isn’t just a formality: each missing part can cost months in delays or force someone to redo decades-old routes. Transparency also helps meet regulatory needs. Authorities want to know which impurities sneak through and how they track through each synthetic stage. This level of detail, matched by clear documentation, makes a real difference for both newer startups and established players alike.
From an environmental perspective, fluorinated organics do draw scrutiny. Teams aim to ensure waste gets collected, treated, and managed so it doesn’t end up in irresponsible landfill or water flows. Recent reviews point to ongoing advances in fluorine chemistry—ways to capture, degrade, or recycle fluorine-containing intermediates without stalling research. Being responsible with this compound extends past the chem bench, reaching into purchasing, disposal, and environmental stewardship. If a lab tracks all incoming and outgoing materials, problems get spotted before they escalate.
In recent years, there’s been steady, even rising, demand for specialized pyridines like this one. Some reasons might surprise outsiders. It’s not just pharmaceuticals or advanced electronics, though those play a part. Institutions focused on academic research want access to new building blocks for mechanistic studies or to make labeled probes for trace analysis. Metabolic trackers benefit from the fluorine’s unique signature, which helps map out biological pathways in ways that other atoms cannot.
Material scientists exploring conductive polymers or coatings sometimes include this molecule to tweak properties in the final formulation. Experiences in polymer labs taught me the frustration of inconsistent batches—small amounts of impurities in intermediates can ripple through to product performance in surprising ways. Reproducible chemistry starts with a clean, well-characterized ingredient.
Every compound faces challenges, and 2-Fluoro-5-formyl-3-methylpyridine is no exception. One recurring issue involves the sourcing of key raw materials for its production. Supply chain interruptions can throw schedules off-track. Some facilities rely on suppliers located far from research hubs, increasing transit time and risk of delays. Building robust partnerships with domestic distributors and fostering transparent communication helps labs avoid dry spells.
Another challenge sits in scaling synthesis from gram to kilogram quantities. Laboratory routes often work well on the bench, but odd byproducts or heat management issues show up when escalating. Teams may need to rethink crystallization, solvent selections, or even switch up purification hardware. Years of work in contract synthesis have shown me clients rarely forgive surprises on delivery timelines, making anticipation and planning essential.
One solution comes from investing in adaptable production lines. Synthesis facilities with modular reaction setups, easy solvent swaps, and access to real-time analytical tools can meet changing order sizes without sacrificing quality. Strong lines of communication between researchers, procurement staff, and suppliers build trust and secure reliable access when demand spikes suddenly.
Every positive story I’ve seen about 2-Fluoro-5-formyl-3-methylpyridine, and practically any chemical, includes open lines of communication. From confirming spectral data to clarifying order specs, mistakes get caught early when people aren’t afraid to ask and triple-check. Online tools now make it easier to share structural information, batch numbers, and even photographs of containers—this accessibility builds confidence and keeps projects moving. Conversation about alternatives or substitutes happens quickly when expectations are transparent.
Teams don’t just lean on suppliers for stock; they rely on them for technical troubleshooting and recommendations. Seasoned chemists know what it feels like to get stuck. Sometimes swapping one derivative for another—a change that seems small—transforms a whole campaign. Personal relationships with trusted vendors open up access to new options and early notification about developments in inventory or regulation.
Young chemists or those new to 2-Fluoro-5-formyl-3-methylpyridine benefit the most from hands-on training and access to troubleshooting guides. Practical lessons—how to weigh, dissolve, and store this compound, and how to spot contamination—keep mistakes rare. I remember my early days at the bench, where clear labeling and shared stories about mix-ups kept everyone safe. Distributors who provide clear, readable instructions, practical use-cases, and real spectra make learning quick and lasting.
Resource platforms, video walk-throughs, and FAQs grow in value. In today’s research environment, new hires or rotating project staff can ramp up more quickly when guides are on hand. Taking pride in training reduces accidents, failed batches, and even folk-lore myths about which compound substitutes for another. Good documentation, well-maintained storage, and clear teamwork make these compounds assets instead of liabilities.
Discussions often drift towards cost, but it pays to distinguish between sticker price and overall project value. I’ve seen projects grind to a halt over a cheap, low-quality chemical, only to resume at full speed once a high-purity, reliable product arrives. Wasted time, lost batches, and long troubleshooting sessions cost far more than most chemicals themselves. Going with 2-Fluoro-5-formyl-3-methylpyridine from a trusted, transparent supplier helps avoid these pitfalls, delivers more consistent results, and supports large-scale studies or product launches.
Bulk purchasing and long-term agreements may yield savings for heavy users, but flexibility, responsiveness, and documented batch quality frequently overtake minor cost differences. Saving ten percent on an intermediate matters far less if it leads to an unexpected research standstill.
Excitement around molecular innovation keeps this compound in the spotlight. The chemistry community pushes new boundaries and, with it, asks more from each building block. The drive for greener, faster, and more selective transformations means more chemists are interested in derivatives like 2-Fluoro-5-formyl-3-methylpyridine. Emerging work on cross-coupling, stereoselective transformations, and late-stage functionalization all find a home here.
Ongoing collaboration between suppliers, universities, and industrial scientists will likely open up new derivatives and production methods, making molecules more accessible. Conversations grow especially interesting around sustainable sourcing—using bio-based feedstocks or low-emission production lines. These trends promise a future where everyone wins: improved product access, safer handling, and reduced environmental burden.
Chemists share stories of the molecule’s successes and hiccups alike. Sometimes, these tales teach more than any datasheet. In my own work, developing new ligands for metal catalysts meant tinkering with scores of pyridine derivatives over months. Reaching for 2-Fluoro-5-formyl-3-methylpyridine became a habit when speed and reliability mattered. The clarity of NMR spectra, the consistent reaction times, and the manageable physical handling always moved things forward. Talking with peers, I’ve heard similar satisfaction—small constants in a sea of changing variables. Each substitution pattern changes the unpredictable world of chemical synthesis just enough to keep discovery rolling without having to reinvent the wheel each step.
In summary, the story of 2-Fluoro-5-formyl-3-methylpyridine runs alongside the story of modern laboratory work. It’s a tale of incremental progress, meticulous attention, and the willingness to invest in small parts of bigger solutions. Scientists who rely on trusted intermediates know how these molecules grease the gears of innovation. Each round of compound testing, each early-stage screen, and every late-night troubleshooting session depends on having reliable materials like this one available. The chemistry world is full of bright minds and eager hands, looking for the right nudge to make a hard problem solvable. For many, this compound helps deliver that nudge—quietly, effectively, and repeatedly.