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HS Code |
578813 |
| Iupac Name | 5-hydroxy-3-(trifluoromethyl)pyridine-2-carbaldehyde |
| Cas Number | 885276-14-2 |
| Molecular Formula | C7H4F3NO2 |
| Molecular Weight | 191.11 |
| Appearance | Solid |
| Solubility | Soluble in common organic solvents |
| Purity | Typically >98% |
| Smiles | C1=C(C=NC(=C1O)C(F)(F)F)C=O |
| Inchi | InChI=1S/C7H4F3NO2/c8-7(9,10)4-2-6(12)11-3-5(4)1-13/h1-3,12H |
| Synonyms | 5-Hydroxy-3-(trifluoromethyl)-2-pyridinecarboxaldehyde |
| Storage Conditions | Store at 2-8°C, protected from light |
As an accredited 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, screw cap, hazard labels displayed; product label lists “2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)-,” CAS number, and purity. |
| Container Loading (20′ FCL) | 20′ FCL container loading of 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- ensures safe, bulk, and secure international chemical transport. |
| Shipping | 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- is shipped in tightly sealed containers, protected from light and moisture. Compliant with relevant chemical transport regulations, it is packaged using appropriate hazard labeling. Temperature control may be applied as required, and safety data sheets are provided to ensure safe handling during shipping and upon receipt. |
| Storage | 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture, direct sunlight, and excessive heat. Store under inert atmosphere if possible, and always follow all relevant safety guidelines and local regulations for chemical storage. |
| Shelf Life | Shelf life of 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- is typically 2 years if stored cool, dry, and sealed. |
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Purity 98%: 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reproducibility of active pharmaceutical ingredients. Melting Point 120°C: 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- with a melting point of 120°C is used in solid-state catalysis research, where it offers thermal stability during elevated temperature reactions. Molecular Weight 191.11 g/mol: 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- with molecular weight of 191.11 g/mol is used in drug discovery screening, where it enables accurate dosage calculations and compound tracking. Particle Size <10 µm: 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- with particle size less than 10 µm is used in formulation of fine chemical reagents, where it improves dissolution rates and homogeneity in solution. Stability Temperature up to 80°C: 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- with stability temperature up to 80°C is used in high-throughput screening assays, where it maintains structural integrity during automated processes. |
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In the world of advanced chemical synthesis, certain building blocks end up pulling more weight than their understated label suggests. Our team has been making 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- for years, and the journey from handling rare starting materials to meeting the rigorous needs of global researchers often calls for clarity, patience, and consistency. Handling this compound means working with a structure where each atom matters—a trifluoromethyl group at the 3-position, an aldehyde at the 2-position, and a hydroxy group at the 5-position on the pyridine ring. The formula isn’t simply a string of descriptors; every group alters reactivity and performance, and the customer’s results can shift with a subtle impurity or an unclear lot.
Many compounds share functional groups that, on paper, promise similar reactivity. That illusion usually breaks under the scrutiny of actual experiments. The trifluoromethyl group on this molecule doesn’t just add another number to the formula; it shifts electronic effects across the ring. As chemists running the manufacturing lines, we’ve watched how substitution at the 3-position, coupled with a hydroxy group at the 5-position, creates a balance between nucleophilic and electrophilic behavior. We’ve noticed customers who previously used simpler analogs—such as 2-pyridinecarboxaldehyde or 5-hydroxy-2-pyridinecarboxaldehyde—discover new reactivity windows when switching to this version, especially where selectivity and yield need a push.
What frequently gets lost in documentation is how sensitive the material can be. The aldehyde group, by itself, attracts all kinds of intruders during storage and shipping. Introducing the trifluoromethyl group, with its strong electron-withdrawing effect, can temper some of that reactivity, but it doesn’t eliminate the need for careful packing. We seal every batch under nitrogen and track moisture content analytically—a practice honed after seeing more than one project stall at a customer lab because a trace of water sneaked in. Some batches get requests for extra quality documentation, and we see our role as more than simply delivering a drum or a vial; our production logs trace every precursor, each temperature cycle, and every purification step for transparency.
Our process for manufacturing 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- starts with selecting source chemicals with proven provenance. We rely on a sequence of reactions where managing temperature gradients, pH swings, and precise dosing of reagents drives the success rate. We perform thin-layer chromatography and HPLC (high-performance liquid chromatography) for every production lot, and results need to consistently show the desired isomer—nobody in our field enjoys surprises at scale-up. Over the years, feedback loops with customers have persuaded us to maintain a purity above 98 percent, since lower purities often create headaches during downstream coupling or oxidation reactions.
We supply material in multiple packaging formats. Volumes can range from gram-scale vials for R&D up to bulk drum supplies that support pilot and pre-commercial manufacturing. At every scale, our internal team runs a battery of verification tests, looking for residual solvents, minor byproducts, and shifts in melting or boiling behavior. A discrepancy, even minute, tells us something changed—sometimes the solvent batch quality, sometimes the temperature ramp wasn’t ideal. We don’t dump imperfect batches onto the market; the reject drum in our facility isn’t just theoretical.
Some buyers ask for 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- as a precursor in pharmaceuticals, especially for molecules that demand specific electron density in aromatic systems. Over the years, we’ve also supplied chemists exploring agrochemicals, electronic materials, and even niche organic pigments where the trifluoromethyl group influences color fastness. A frequent advantage comes from the hydroxy group at the 5-position, which allows selective functionalization. The site often acts as a convenient anchor for transformations that risk wandering in other analogs.
Unlike commodity pyridine derivatives, this variant calls for extra care in synthesis. We’ve fielded questions from customers trying to perform cross-coupling reactions, where the compound’s high purity and well-defined substitution patterns increase yields and cut purification time. Colleagues at scale-up have noted that using a material with less than 98 percent purity means running more chromatographic cycles, raising both cost and waste. A well-made batch saves hours and reduces the number of troubleshooting emails.
There’s no shortage of pyridinecarboxaldehyde derivatives on the market. What often separates one from another isn’t what’s written on the label but what the lab data show over long projects. Our 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- batches go through qualification with customers who track material with inventories tagged to each experiment, and subtle variations can throw off entire series of data. Other suppliers sometimes offer broader tolerance on purity or skip secondary impurity controls, but we’ve learned that—even when standards at the outset sound similar—long-term reliability drives repeat business.
Customers sometimes compare our product to simple 2-pyridinecarboxaldehyde or other hydroxy-pyridinecarboxaldehyde variants. Those molecules can function as intermediates, but without the trifluoromethyl group there’s a missed opportunity for increased metabolic stability or broader reactivity. Adding the hydroxy group in the right position encourages selective derivatization that cannot be matched by non-hydroxylated analogs. The precise arrangement determines which downstream reactions move efficiently; years of customer reports make the case better than any brochure.
Some years ago, our team tackled a run where residual acid from a prior step persisted through the process, only surfacing as inconsistent performance in client tests. Time in the plant taught us that standard neutralization steps can fail if not standardized around batch-to-batch variability. Learning from those lessons, we now track acid content at multiple stages and use internal reference standards calibrated against international benchmarks. Consultation with end-users led to further refinements, prompting us to develop semi-continuous flow methods for certain steps. Those processes give finer control, higher yields, and a familiar batch-to-batch fingerprint.
Every synthetic journey has friction points. One bottleneck involved handling raw materials whose sourcing sometimes triggered unexpected impurities or delayed delivery. Our records show that direct negotiation with precursor suppliers—insisting on full analytical disclosure and annual audits—brought down variability and improved timelines. We also increased storage capacity to cushion against logistics failures, especially after seeing how chemical supply issues can ripple outwards and affect research programs around the world.
The global reach of advanced synthesis demands agility. We register materials in accordance with importing region requirements, run analytical profiles as requested, and remain open to third-party validation. Responding to unique project demands sometimes means customizing documentation or sending reference samples for parallel testing—not every need fits a neat box.
Producing complex compounds like this one requires not only mastery over chemical methods, but also a responsibility for protecting employees and ecosystems. Our plant emphasizes closed-system operations, advanced air handling, and liquid-phase containment. The trifluoromethyl group, while beneficial for molecular performance, means downstream waste needs careful management. Regulatory agencies increasingly focus on trace fluorinated compounds in effluent, so each batch incorporates extra monitoring for organic fluorine. After implementing in-line waste monitoring several production cycles ago, we reduced effluent to below detection in most runs.
Worker safety stands as a daily practice, not just compliance paperwork. During material transfer, we use barrier protection and precision dosing pumps, which reduce accidental exposure, particularly with volatile intermediates. Emergency checks and frequent drills keep the team sharp. Plant workers rotate through training updates, learning not just what works, but also what fails. Small investments in new analytical detection, like Fourier-transform infrared spectroscopy, let us catch trace contaminants early, reducing hazard risks before shipments leave the loading bay.
We find the most fruitful relationships grow from open discussion of experimental details—good and bad. By supporting chemists as they develop new routes or troubleshoot unexpected reactivity, we gather feedback that shapes the next iteration of our product. A project with an academic group revealed how minor levels of residual palladium could compromise yields in sensitive pharmaceutical syntheses. Data shared back with us prompted an upgrade of our purification train, installing new scavenging columns. Those investments sometimes outpace market expectation, but long-run reliability rewards everyone involved.
Last year, an industrial partner reported that a change in raw material supplier elsewhere in their value chain had thrown off a project, as a previously undetected contaminant began to accumulate during a condensation step. Joint troubleshooting uncovered the issue, and we adjusted our own sourcing to provide a more robust input. The extra work trickled down into reproducible output and smoother process scale-up. These case studies reinforce why our focus remains as much on relationships and information flow as it does on the chemical reactions themselves.
Emerging fields constantly recalibrate the value of specialized intermediates. Recent work in fluorinated pharmaceuticals and specialty polymers puts extra emphasis on the value of 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)- in discovery chemistry. Access to high-purity, characterized material, consistently produced, has sped up project cycles and reduced the costly churn of retesting inferior lots. In some projects, the hydroxy group at the 5-position serves as a launchpad for further functionalization, while the trifluoromethyl group moderates bioactive properties.
From the factory floor, we see an uptick in requests for analytical transparency—customers want batch chromatograms, residual solvent profiles, and even supporting NMR spectra before committing to a purchase. We support those expectations, recognizing the long-term reward: teams make better decisions, and projects move forward without unnecessary retracing of failed steps. This trend, combined with more agile supply chain management across continents, is reshaping how we plan production cycles, stock critical inputs, and even train new chemists on our crew.
What sets a manufacturer apart over time isn’t marketing flourishes or glossy short-term wins; enduring trust is built batch by batch, shipment by shipment. Our facility has shipped metric tons of complicated molecules—some for everyday scale, others on a schedule so tight that missing a delivery window could cost weeks of research work. The most enduring feedback comes not just from big clients but also from those running small pilot labs, who notice when a product “just works” the way they expect.
We’ve tuned production, packaging, and analytical methodology specifically to the day-to-day challenges our customers face. For 2-Pyridinecarboxaldehyde, 5-hydroxy-3-(trifluoromethyl)-, that means respecting not just the letter of the label but the tougher, practical realities of advanced organic synthesis. Each step along that journey has taught us more about the tradeoffs, possibilities, and real stakes of modern chemistry—a perspective we carry into every batch that leaves our floor.