|
HS Code |
378314 |
| Chemical Name | 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- |
| Molecular Formula | C7H6FNO |
| Molecular Weight | 139.13 g/mol |
| Cas Number | 81565-18-4 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 220-223°C |
| Density | 1.18 g/cm³ |
| Smiles | CC1=CN=CC(F)=C1C=O |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light |
| Solubility | Slightly soluble in water; soluble in organic solvents |
As an accredited 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a screw cap and labeled for 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl-, chemical grade. |
| Container Loading (20′ FCL) | 20′ FCL: Chemical packed in 200L drums, 80 drums per container, net weight approx. 16 MT, suitable for safe shipping. |
| Shipping | 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- is typically shipped in tightly sealed containers, protected from moisture and light. It is transported in accordance with relevant chemical safety regulations, often as a hazardous material. Proper labeling, documentation, and use of absorbent packaging are required to prevent leaks or spills during transit. |
| Storage | 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and direct sunlight. Keep away from incompatible materials such as strong oxidizing agents. Storage should be at room temperature, and the container should be clearly labeled. Ensure safe handling to avoid spills and inhalation. |
| Shelf Life | 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- typically has a shelf life of 2 years if stored tightly sealed at 2–8°C, protected from light. |
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Purity 98%: 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yield and minimal byproduct formation. Melting Point 56°C: 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- with a melting point of 56°C is used in solid-phase organic synthesis, where the defined melting point enables precise temperature control during reactions. Molecular Weight 153.14 g/mol: 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- with molecular weight 153.14 g/mol is used in drug design programs, where accurate stoichiometry improves compound screening outcomes. Stability Temperature up to 120°C: 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- with stability temperature up to 120°C is used in high-temperature reaction processes, where thermal stability enhances product reliability. Solubility in DMSO 40 mg/mL: 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- with solubility in DMSO 40 mg/mL is used in medicinal chemistry research, where high solubility facilitates compound library preparation. Particle Size <10 µm: 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- with particle size less than 10 µm is used in fine chemical formulations, where uniform particle distribution enhances blending and reactivity. |
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In our journey with fine pyridine intermediates, we have always found that subtle structural modifications often open up new possibilities for both performance and results. Years of hands-on work in our suite of reactors have shown us just how a single atom can shift a whole synthesis pathway. The story of 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- is a good example. It may look modest on paper — a fluoro and a methyl group dressing up the pyridine ring — but the impact of these changes surfaces every time downstream chemists test it in their research or scale up a crucial process. The work here is not about hypothetical trends; it’s grounded in what actually happens on our production floor and what researchers report back across real-world applications.
In practice, adding a fluorine atom into a pyridine ring increases both chemical resilience and tunability. The methyl group at the 5-position can enhance certain biochemical interactions. Together, these groups protect the molecule from oxidative degradation during challenging condensation or cyclization. This aldehyde functions with a sort of “shield,” letting scientists chase more aggressive targets without the starting material falling apart early. Based on our direct observations, its behavior stands apart from more classic aromatic aldehydes or plain pyridinecarboxaldehyde. The fluoro substituent can also impact reaction rates in ways we have mapped through both feedback and our own analytical controls during batch validation.
We have learned the hard way that specification sheets never tell the full story. We run this product to a minimum 98% purity (HPLC) and confirm structural features through a set of spectral signatures before it leaves our floor. Boiling point and moisture sensitivity also shape its handling — we have seen bulk drums and small packs behave differently when exposed even briefly to humid warehouse air. This compound is a pale liquid with a recognizable odor, and that subtle scent will flag cross-contamination if quality protocols slip. Such surface-level details matter more often than not: minor residues in prep glassware actually alter subsequent yields if not fully purged, an issue plain pyridinecarboxaldehyde rarely poses.
Most producers chase speed and cost-cutting. We stick out for a reason: we trace every lot from raw feedstock all the way through isolation and packaging. We source high-grade halogenating agents and selectively fluorinate with careful temperature hold and feed control — too much heat and unwanted pyridine isomers creep in; too little and the conversion stalls. Our teams have grappled with these issues more than once, sorting through exotherm spikes in early days. Now, precise temperature programming and staged addition mean our output keeps tight lot-to-lot consistency, a comfort for scale-up chemists facing regulatory audits or internal QC deadlines.
Most requests for this compound come from pharmaceutical R&D specialists, agrochemical innovators, and those in niche specialty materials. In medicinal chemistry, the focus often falls on pairing the aldehyde directly to core scaffolds via reductive amination or further oxidation. That fluoro substituent allows researchers to dial in metabolic stability for lead candidates — an insight we’ve seen validated by customers running preclinical screens. Agrochemical labs have asked for this molecule as a building block in projects where moisture-resistant, biologically active heterocycles become a necessity for robust field performance. The interplay of electronic effects from those methyl and fluoro groups pushes activity into new territory, which is something not every pyridinecarboxaldehyde derivative can promise.
Colleagues sometimes ask about whether to stick with the tried-and-true 3-pyridinecarboxaldehyde or shift to this fluoro-methyl variant. From where we sit, the differences are not academic. Standard pyridinecarboxaldehyde lacks the resilient, electron-withdrawing influence of fluorine. This means it breaks down faster under certain acid- or base-catalyzed reaction conditions. The methyl group’s subtle steric effect can also tip selectivity in downstream cyclizations, which provides an edge in building more complex heterocyclic libraries. Straight 2-fluoro-pyridinecarboxaldehyde gets closer, yet without the boost from methyl at the 5-position, it cannot achieve the same level of metabolic and chemical stability — a point that matters in pilot-scale synthesis and early animal studies.
We have lived through scenarios where one batch dimmed the performance of a long-running drug lead program and we, together with the customer, traced it right back to the subtle difference in impurity levels. No amount of marketing can fix that sort of fallout. For us, E-E-A-T (Experience, Expertise, Authority, and Trust) means every lot undergoes three-point testing — in-house, external, and at the customer’s site — before we sign off. From the moment the precursor feeds enter our reactors to the moment the final packed vessel is sealed, lab technicians and QC teams double-check for micro-level contamination, which stems directly from the manufacturing equipment, not just the chemical process itself.
A few years back, demand spikes forced many in our industry to prioritize speed over solid documentation. We faced those pressures and made the decision to avoid speculative batch stacking. Instead, we built a made-to-plan production model where capacity flexes but records and quality checkpoints remain robust. This means our timelines run slightly longer but out-of-spec complications have dropped to virtually zero. Customers on tight regulatory timelines know exactly where every drum started — including time-stamped in-process records, chromatograms, and residual solvent levels — and this has kept their own compliance teams insulated from last-minute audit surprises.
In our early days, careless decanting and loose closures led to headaches: slight aldehyde losses through evaporation, and sometimes enough air exposure to build up peroxides. Since then, we moved to nitrogen-purged packing and specified every drum to hold not only the right quantity, but also a prescribed headspace integrity. Technicians trained on real-world mishaps take the extra time to check stoppers and seals before shipping — an effort rooted not in caution, but in actual batch failures. Storage away from open sunlight and dampness is critical. Warehouse surveys at our facilities and customer sites turned up that even indirect fluorescent lighting can yellow the product and start subtle degradation.
One recurring insight from working with university labs and scale-up partners is the need for flexibility. Some groups need bulk material for a multi-month drug candidate project; others require highly tailored sub-kilo amounts with screening certificates attached. As manufacturers, we are often asked if we can tweak impurity profiles for advanced analytics, or adjust drying steps to suit specific solvent tolerances. Our long-term partnerships arise from saying yes when it counts — not just with product specs, but also with packaging size, storage protocols, and transparent documentation. This willingness is not a marketing ploy; it’s necessity. We know how lost time and resources impact an ambitious research timeline.
We have seen more than a few pilot-scale setups grind to a halt when a starting material creates unexpected side-products. Each time, the solution involved critical examination not just of ingredient certificates, but also of our own process lines and cleaning protocols. “Are there traces of old product at the flange or in the condenser lines?” “Did the crystallizer trap get fully flushed prior to the new batch?” These are frontline questions our technical reps resolve alongside our customers. In this way, our technical documents, batch histories, and storage logs move from paper into practice, preventing cross-lot contamination or unwanted polymeric side-pathways.
Every fresh batch unlocks gradients of learning. Routine NMR gives way to advanced LC-MS/MS screening whenever impurity drift— even in trace levels — risks impacting a client’s target pathway. Spectroscopy and routine purity analysis become partnerships, not chores. Over the years, customer feedback has led us to perfect not only our chemical recipe but also our documentation and test methodologies, refining the process more than any consultant could advise. Existing analytical tools can catch most process impurities, but operator expertise — the kind built up only through repeated production — is what delivers integrity from start to finish.
Years in chemical synthesis engrain a sense of accountability extending well beyond lab doors. We adhere to a rigorous waste treatment protocol, minimizing fluoro-organic residues and using closed-system recovery for solvents. Regular internal audits confirm compliance not for box-checking reasons, but because a decades-old accident elsewhere in the industry made clear the risks. At every production shift, operators monitor for leaks and cross-contamination. Continuous safety drills and maintenance schedules maintain safe conditions — not just for regulatory display, but to guarantee that employees, customers, and the community remain protected. These hard-won lessons shape how we run: routine, predictability, and respect for the hazards built into our everyday dealings with fluorinated aromatics.
Modern supply chains demand that every stage be open to scrutiny. Each year, regulatory and partner audits become more intense. We respond by keeping every pathway traceable: raw material provenance, equipment maintenance, batch-by-batch protocol, and incident logging. Customers who once treated pyridine intermediates as simple commodities now ask for full chain-of-custody. Thanks to hard experience, it’s standard practice here. Not every manufacturer welcomes that, but as scrutiny escalates, skipping steps risks more than a lost batch: it means losing trust, a reputation, or even regulatory standing.
As drug discovery and agrochemical demands shift, researchers now require pyridine intermediates with finer control over electron density, metabolic fate, or solubility. We watch these trends not in analyst briefings, but by talking with the customers whose work depends on nuanced molecular design. Sometimes, a methyl group is the tip of the spear for a project; at other times, the fluorine’s unique electron profile is the entire reason for switching from a comparable intermediate. Fine-tuning our product line rarely hinges on producing more of the same. Instead, we orient each new production plan around the customers’ raw application data, adapting our pathway and QC steps on the fly.
Every lot of 3-pyridinecarboxaldehyde, 2-fluoro-5-methyl- reflects years of field lessons. Supply security challenges, advances in green chemistry, and the escalating demand for scalable, high-spec intermediates all shape our ongoing development. Upcoming tech—like flow-reactor platforms or automated impurity mapping—continues to influence our approach. As regulatory frameworks demand greater data transparency, we’re investing in even more rigorous documentation, from synthetic origin to post-sale technical support. Collaborative customers push us to expand not only capacity but also adaptability, knowing that the landscape of applied chemistry never stands still for long.
We are not just sending out drums of aldehyde; we’re forging tangible links with customers who need responsible sourcing, responsive support, and technical depth that stands up to real-world scrutiny. The value of 3-Pyridinecarboxaldehyde, 2-fluoro-5-methyl- is not locked in its structural novelty or even purity metrics; it’s built on the trust we earn through every batch, every technical resolution, and every collaborative advance in downstream science. Our experience as actual manufacturers has taught us to value precision, traceability, and partnership—not in theory, but as shared success stretching from reactor to research breakthrough.