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HS Code |
308629 |
| Iupac Name | 2-(Trifluoromethyl)pyridine-3-carboxaldehyde |
| Cas Number | 870778-61-1 |
| Molecular Formula | C7H4F3NO |
| Molecular Weight | 175.11 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 75-80°C at 7 mmHg |
| Density | 1.373 g/cm³ |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Smiles | C1=CC(=C(N=C1)C(F)(F)F)C=O |
| Inchi | InChI=1S/C7H4F3NO/c8-7(9,10)6-5(4-12)2-1-3-11-6/h1-4H |
| Refractive Index | n20/D 1.489 |
As an accredited 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 2-(Trifluoromethyl)pyridine-3-carboxaldehyde, tightly sealed, with hazard and product labels. |
| Container Loading (20′ FCL) | 20′ FCL can be loaded with 10-12 metric tons of 2-(Trifluoromethyl)pyridine-3-carboxaldehyde, packed in sealed drums. |
| Shipping | 2-(Trifluoromethyl)pyridine-3-carboxaldehyde is typically shipped in sealed, chemical-resistant containers under ambient conditions. It should be protected from moisture and direct sunlight. The shipment complies with relevant hazardous material regulations, clearly labeled, and accompanied by appropriate safety documentation such as an SDS to ensure safe handling during transport and delivery. |
| Storage | Store 2-(Trifluoromethyl)pyridine-3-carboxaldehyde tightly sealed in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as oxidizers and strong acids. Protect from moisture and direct sunlight. Use appropriate chemical-resistant containers and ensure proper labeling. Store in accordance with local regulations and laboratory safety guidelines, preferably in a dedicated flammable chemicals cabinet. |
| Shelf Life | 2-(Trifluoromethyl)pyridine-3-carboxaldehyde is stable under recommended storage conditions; typical shelf life is 24 months in tightly sealed containers. |
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Purity 98%: 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Molecular Weight 173.09 g/mol: 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde with a molecular weight of 173.09 g/mol is used in custom organic synthesis, where accurate stoichiometry and reproducibility are achieved. Melting Point 42–44°C: 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde with a melting point of 42–44°C is used in solid-phase extraction protocols, where reliable phase transition supports efficient separation processes. Boiling Point 184–186°C: 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde with a boiling point of 184–186°C is used in vapor-phase peptide coupling, where thermal stability benefits process optimization. Stability Temperature up to 60°C: 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde stable up to 60°C is used in storage and handling applications, where prolonged shelf life and integrity are maintained. Particle Size <10 μm: 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde with particle size less than 10 μm is used in high-performance chromatography, where enhanced separation efficiency is achieved. Water Content ≤0.3%: 2-(Trifluoromethyl)pyridine-3-carBoxaldehyde with water content not exceeding 0.3% is used in moisture-sensitive synthetic reactions, where side reactions are minimized. |
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The search for precision and reliability in chemical synthesis rarely takes a straight path. Many reactions demand not just the right reagent, but one that performs consistently under varied reaction conditions. Our experience manufacturing 2-(Trifluoromethyl)pyridine-3-carboxaldehyde has shown us the broad potential of this molecule, especially for researchers developing pharmaceuticals, agrochemicals, and specialty materials. Years of feedback and direct laboratory use make clear that it's the subtle differences in molecular structure and handling that set it apart from similar compounds.
Every chemical manufacturer faces daily reminders that product consistency is essential for complex syntheses. We understand the requirements for 2-(Trifluoromethyl)pyridine-3-carboxaldehyde, not just because we produce it, but because our technical team regularly supports chemists pushing to unlock new reactions. The compound, recognized for its trifluoromethyl group at the 2-position and the reactive aldehyde at position 3 on the pyridine core, offers reactivity that chemists recognize as crucial for fine-tuning biological activity in targeted molecules.
The fluorine atoms in the trifluoromethyl group introduce significant electron-withdrawing capability. This property shapes both reactivity and stability, which matters for labs focused on nucleophilic additions, cross-coupling reactions, or forming unusual heterocycles. Many researchers have singled out this molecule for its handling compared to other pyridine carboxaldehydes – especially in routes involving condensation or cyclization. Early development projects in our own hands revealed that, compared to isomeric or non-fluorinated analogs, this aldehyde consistently provides both high yields and cleaner profiles in product mixtures. Less time spent on purification or troubleshooting means smoother research workflows.
In the past, inconsistent product batches have derailed timelines for both our clients and our own R&D partnerships. This lesson has driven us to pay close attention to every stage, from raw material sourcing, controlled reaction parameters, to tailored purification strategies. Our offering of 2-(Trifluoromethyl)pyridine-3-carboxaldehyde typically reaches a purity above 98%. This is not just a number on a certificate, but a reflection of repeated batch consistency checked by GC, NMR, and HPLC—methods chemists trust. As a chemical manufacturer who regularly faces audits and project reviews, we've learned that trace impurities, sometimes overlooked by bulk traders, can lead to unexplained reaction failures or downstream interference in bioassays.
Clients in pharmaceutical discovery and custom synthesis come back to us not because we offer formal specifications, but because they know we've stress-tested this compound through our own contract synthesis projects. Technical support doesn’t stop with a sale; when an unexpected chromatogram or yield drop appears, our technical staff helps track down the cause, drawing on in-house analytical archives that document subtle variations batch to batch.
Laboratory feedback has always been a guide post for our own improvement. Many users describe that 2-(Trifluoromethyl)pyridine-3-carboxaldehyde integrates into their synthetic workflows without the unpredictable reactivity swings seen in other aromatic aldehydes. One frequent challenge with competitive carboxaldehydes is instability during handling, sensitivity to air, or volatility losses at room temperature—these real-world problems cut into yields and waste valuable starting material.
We’ve tested shelf-stability across different storage temps and found that our product maintains high integrity, even after repeated opening. Years of experience with product packaging led us to switch to tightly sealed amber glass bottles, which significantly reduced degradation during shipping or storage. Less time spent re-ordering or double-checking storage means more time pushing forward in discovery settings.
Some competitors’ offerings, particularly from non-integrated distributors, have shown unacceptable levels of by-products such as residual pyridine, non-reacted starting materials, or oxidized derivatives. These contaminants often go undetected until a project slows down. Direct control over our own production lines allows us to inspect every lot, guaranteeing the absence of process-side impurities. This practical quality assurance, rather than just paper-based compliance, wins trust among experienced researchers.
2-(Trifluoromethyl)pyridine-3-carboxaldehyde doesn’t just sit in catalogues; it finds a role in the heart of research projects aiming at the next generation of pharmaceuticals and crop protection agents. The electron-withdrawing trifluoromethyl group transforms the electronic nature of the pyridine ring, boosting its ability to serve as a key intermediate in medicinal chemistry. Examples include synthesis of kinase inhibitors, anti-viral scaffolds, and novel heterocyclic frameworks.
Our R&D partners working on small molecule libraries have pointed out its ability to produce high-fidelity analogs during SAR studies. The aldehyde’s position facilitates selective modifications to the ring, supporting late-stage functionalization and rapid construction of new analogs. In agricultural chemistry, the molecule often acts as a backbone for active substances targeting pest resistance with lower environmental persistence. Multiple patent applications cite derivatives formed from this building block—demonstrating its real-world impact rather than a theoretical advantage.
Specialty material manufacturers also rely on this aldehyde for its behavior as an intermediate in the preparation of advanced dyes, ligands, and complex functional molecules. The ease of further transformation allows rapid development and adjustment of molecular properties, whether tuning solubility or binding strength for a new application.
Anyone working in chemical synthesis recognizes that choice of intermediate governs the ease of process optimization. Side-by-side examination shows that compared to 3-(trifluoromethyl)pyridine-2-carboxaldehyde or non-fluorinated analogs, our 2-(Trifluoromethyl)pyridine-3-carboxaldehyde offers enhanced stability and more predictable reactivity. Isomeric forms can introduce unwanted isomer separation problems in downstream processing. The lack of electron-withdrawing fluorine substituents in other aldehydes shifts reactivity so far that subsequent reactions – such as nucleophilic additions or cyclization steps – often require more stringent conditions, higher temperatures, and give lower selectivity.
We have seen feedback from medicinal chemists who, after switching from less-substituted pyridine aldehydes, achieved not only improved yields but also avoided formation of side products such as tars and polymeric material. These improvements become critical at project scale-up, where reworking or additional purification dramatically increases costs and lead times.
Handling differences also matter. Non-fluorinated pyridine carboxaldehydes have demonstrated greater moisture sensitivity, leading to self-condensation or hydrolysis during storage. Our trifluoromethylated version resists this fate, giving researchers confidence both at the bench and during longer term stockpiling for multiple project runs.
Making thousands of liters per year of 2-(Trifluoromethyl)pyridine-3-carboxaldehyde trains us to notice subtle production challenges that impact quality. Rather than relying on off-the-shelf purification, we invested in multi-stage distillation under inert atmosphere, combined with rigorous in-process analytics. Routine batch logs highlight any deviation, supporting continuous improvement and the highest reproducibility from lot to lot.
Our scale allows us to provide consistency not only for gram-scale R&D, but also for clients scaling up to pilot or production volumes. In customer audits, we regularly supply stability testing records over multiple years, showing no significant purity loss under standard ambient or refrigerated conditions. Real-world durability like this reassures both project managers and regulatory reviewers that the compound won’t complicate registration or scale-up.
End users have shared that they notice shorter reaction optimization cycles and fewer troubleshooting incidents when projects incorporate our batches as opposed to generic alternatives. Because we partner with labs at every stage—from early R&D through registration—this reliability translates into reduced overall project risk.
The increasing regulatory focus on trace contaminants and batch traceability means that manufacturers with direct process control bear greater responsibility. Our own experience with audit trails and compliance reviews prepared us to offer not only standard analytical certifications, but also in-depth impurity profiles, stability testing data, and reliable recall tracking.
We recognize that laboratories are under mounting pressure to minimize process hazards, especially as pyridine derivatives often draw attention for their volatility or combustion risk. Through careful lot-to-lot quality validation and adherence to best practices in packaging and labeling, we mitigate these concerns and offer users detailed transport and storage guidance based on real shipments under various climates.
Every team searching for new molecular solutions faces the pressure of tight deadlines and demanding targets. Based on our hands-on production experience and the hard-earned knowledge from thousands of reaction runs, 2-(Trifluoromethyl)pyridine-3-carboxaldehyde has proven value where reliability, purity, and reactivity matter most. A continuous focus on process improvement and direct feedback from global research partners has shaped the compound into a robust choice for both discovery and development settings.
Standard catalog suppliers or traders often lack insight into the challenges researchers face at the bench. In contrast, our involvement in joint development projects shows us where minor impurities or handling quirks can disrupt entire workstreams. Years of first-hand observation teach that a chemically pure, well-characterized intermediate makes the difference between wasted cycles and rapid project milestones.
Customer case studies underline that access to technical support—rooted in genuine production expertise—can accelerate problem-solving and allow researchers to tap the full potential of complex intermediates. This is not just about supporting sales, but about becoming a trusted technical resource as well.
Innovation does not stop at the laboratory scale. Feedback from R&D partners fuels production enhancements, whether adapting purification regimes or optimizing supply chain logistics for bulk shipments. We've worked closely with clients scaling syntheses from the gram bench top phase to multiple kilograms, adapting our processes to handle increased demands for throughput without compromising purity or traceability.
Production data collected over years highlight key factors such as temperature stability, packaging robustness, and sensitivity to light or oxidation. In-house stress testing ensures that no significant changes occur, even under prolonged shipping or storage. Because of this, institutions trust us with time-sensitive projects, from early-phase discovery to late-stage process validation and even regulatory submission.
Direct feedback loops with end users in pharmaceutical, agrochemical, and specialty materials sectors keep us informed about evolving requirements—driving both process refinement and new application exploration.
Ultimately, real progress in fine chemicals relies on building blocks that researchers trust to deliver precise and repeatable outcomes. As chemists and manufacturers, we see how every aspect—from sourcing and synthesis through rigorous analytics—impacts not only individual project success but also advances in science and application. 2-(Trifluoromethyl)pyridine-3-carboxaldehyde stands as a product shaped by real-world feedback and technical discipline, supporting the creativity and determination of teams at the forefront of chemical discovery.
By engaging directly with users and collecting data at every stage, we have learned that the best research outcomes stem from open communication and genuine technical insight, not just certificates or attractive catalog entries. The story of 2-(Trifluoromethyl)pyridine-3-carboxaldehyde illustrates how experienced manufacturing, continuous improvement, and long-term partnership come together to deliver value for scientists worldwide.