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HS Code |
616841 |
| Iupac Name | 5-cyano-2-fluorobenzaldehyde |
| Molecular Formula | C8H4FNO |
| Molecular Weight | 149.12 g/mol |
| Cas Number | 116432-95-8 |
| Appearance | Off-white to light yellow solid |
| Melting Point | 57-62°C |
| Boiling Point | No data available |
| Purity | Typically ≥98% |
| Density | No data available |
| Smiles | C1=CC(=C(C=C1C#N)C=O)F |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory tract |
| Synonyms | 5-Cyano-2-fluorobenzaldehyde; 2-Fluoro-5-formylbenzonitrile |
| Refractive Index | No data available |
As an accredited 5-Cyano-2-Fluorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle, tightly sealed, labeled “5-Cyano-2-Fluorobenzaldehyde,” with hazard warnings and batch information. |
| Shipping | 5-Cyano-2-Fluorobenzaldehyde is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. It is classified as a hazardous material; therefore, transportation is in accordance with international chemical shipping regulations, accompanied by a Safety Data Sheet (SDS) and appropriate hazard labeling to ensure safe handling and compliance. |
| Storage | 5-Cyano-2-Fluorobenzaldehyde should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizing agents. Keep in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Ensure appropriate labeling and avoid exposure to heat and direct sunlight. Use suitable personal protective equipment when handling the chemical. |
Applications of 5-Cyano-2-Fluorobenzaldehyde in Industrial Manufacturing5-Cyano-2-Fluorobenzaldehyde serves as a strategic intermediate for diverse downstream sectors, integrating into several precision chemical production routes. Below, we detail its industrial deployment across core application areas, highlighting compliance considerations, processing parameters, formulation guidelines, and real-world product end uses. 1. Pharmaceutical Intermediates SynthesisPharmaceutical manufacturers utilize this compound in the synthesis of advanced heterocyclic scaffolds, particularly in the production of active pharmaceutical ingredient (API) intermediates for oncology and anti-infective drugs. Its reactive aldehyde and cyano functionalities allow for step-specific incorporation within multi-stage synthesis schemes, frequently forming a building block for subsequent cyclization or substitution reactions in regulated manufacturing environments. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingThe compound finds significant use in the agrochemical sector, particularly for the synthesis of fluorinated pyrazole, triazole, and phenyl-nitrile herbicides and fungicides. Due to its combined electron-withdrawing fluorine and cyano groups, it provides chemical stability crucial for the manufacturing of crop protection agents under tightly regulated safety and environmental protocols. Industry compliance standards
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3. Organic Electronics and OLED Material SynthesisManufacturers in the organic electronics sector employ the material as a key intermediate for constructing π-conjugated systems and functionalized aryl aldehydes, which act as precursors for light-emitting layers and charge transport materials in OLED displays and related optoelectronic devices. Reactivity and substitution capabilities support complex molecule assembly with precise atomic placements. Industry compliance standards
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4. Specialty Dye & Pigment Intermediate ProductionThe compound is utilized by specialty dye and pigment producers to introduce specific fluorine and nitrile groups into aromatic structures, enhancing the color fastness, thermal stability, and solvent resistance of high-performance pigments applied in automotive coatings, plastics coloration, and textile dyes. Its chemical structure enables targeted modifications in multi-step pigment synthesis processes. Industry compliance standards
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5. Advanced Material Research for Fine Chemical DevelopmentChemical R&D and pilot-scale fine chemical plants leverage the compound as a precision-functionalization agent in SAR (structure-activity-relationship) screening and new molecule construction. Used for developing novel fluorinated building blocks, its reliable reactivity profile supports reproducibility in laboratory-to-pilot transitions, critical in custom molecule projects for specialty sectors. Industry compliance standards
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Years of chemical synthesis have taught us there’s seldom a shortcut to reliable performance. Our experience manufacturing 5-Cyano-2-Fluorobenzaldehyde has shown us how a single building block can influence the success or failure of a downstream process. This compound, with molecular formula C8H4FNO, stands out for its specific reactivity and its ability to serve as a versatile intermediate in pharmaceutical and agrochemical syntheses. Its precision design—a benzaldehyde ring substituted with both cyano and fluorine groups—plays a decisive role where selectivity and yield matter most.
The pairing of a cyano group at the 5-position and fluorine at the 2-position isn’t accidental. After countless batches and process optimizations, we’ve noticed how this structure affects reactivity. The electron-withdrawing character of both substituents modifies the aldehyde’s behavior in condensation and nucleophilic addition reactions. This fine-tuning can reduce the risk of side products, particularly for pharmaceutical intermediates where purity makes all the difference. Working with standard benzaldehyde derivatives, uncontrollable reactivity or unpredictable byproducts often complicate purification. With 5-Cyano-2-Fluorobenzaldehyde, the process engineer and the bench chemist both benefit from fewer surprises and more stable yields.
Every manufacturer can claim purity; our long-standing partnerships with downstream formulators keep us accountable. Our consistency develops from years of optimizing crystallization, filtration, and drying steps. Here, color and melting point tell their own stories: a pale to light yellow solid, sharp melting within a narrow range, and a distinct, pungent odor recognizable to anyone who’s worked with aromatic aldehydes. Our lot records confirm that water content and residual solvents remain well controlled, so customers receive a product they can blend or transform directly, without additional pre-treatment. This saves time, reduces waste, and minimizes complications with solvent compatibility.
Raw material fluctuations affect the entire industry, not just the producer. We’ve learned to secure stable supplies of key starting materials—fluorobenzene and suitable cyanation agents—to buffer against price shocks and ensure unbroken production. Each batch navigates a sequence of controlled temperature reactions, monitored by inline spectrometry and confirmed by off-line NMR and HPLC. Human oversight remains critical. Automated systems will flag an impurity, but only seasoned eyes can spot anomalies ahead of time. Years of scale-ups and troubleshooting put us in a position to ship material out the door that meets the same specification every time, regardless of scale.
This molecule continues to show up in essential syntheses for active pharmaceutical ingredients, especially those targeting CNS disorders and metabolic diseases. As a manufacturer, we see how subtle changes in intermediate quality echo downstream. When the aldehyde group engages in a Knoevenagel condensation, or when it’s reduced, the presence of the cyano and fluoro substituents affects regioselectivity and the types of side products that form. Agrochemical research circles have also turned to this compound in the search for novel active agents, using its unique substitution pattern to access otherwise inaccessible scaffolds.
Our direct customers often develop complex molecular libraries. They demand not only precise purity, but also reliable analytical data for regulatory filings and patent submissions. Their feedback has helped us refine our own documentation, making sure every shipment includes up-to-date certificates of analysis and retains enough reference material for retrospective studies. Regulatory scrutiny only intensifies, and as a supplier, the traceability of each drum or bottle now reaches far beyond our warehouse walls.
Confusing this material with its isomers or with mono-substituted benzaldehydes can disrupt a project for weeks. Traditional 2-fluorobenzaldehyde or 5-cyanobenzaldehyde each behave differently under catalytic or base-mediated conditions. The presence of both groups narrows the reaction scope but allows for advanced selectivity. In practical terms, we see shorter purification times, fewer repeat syntheses, and a lower likelihood of problematic byproducts.
For certain medicinal chemistry pathways, the dual electron-withdrawing groups reduce the rate of unwanted aldol and Cannizzaro side reactions. Researchers aiming for high-throughput synthesis notice the difference after running only a handful of test reactions. The final purity translates into cost savings—not just in terms of yield, but also in terms of analytical labor and paperwork.
Handling a compound with both cyano and aldehyde functionalities calls for careful containment and environmental controls. Over the years, we’ve invested in closed-system transfer technology, tailored ventilation, and solvent recovery, not only to protect operators but also to manage compliance with tightening environmental regulations. As the regulatory climate evolves, successful manufacturers stay one step ahead, refining protocols for waste reduction, emission limitation, and safe packaging.
We also recognize that customers increasingly expect transparency regarding sustainability and ethical supply chains. In response, we audit our own raw material suppliers with an eye to both compliance and human rights. Operating at this level allows us to offer more than paperwork—we can share best practices, process improvements, and even responder insights with our customers, helping their compliance teams both predict and prevent regulatory snags.
Markets for fine chemicals don’t stand still, and over the past decade we’ve adapted our process to changing customer requirements. With the onset of stricter limits on residual metallic impurities, we’ve transitioned away from catalyzed routes that might introduce difficult-to-remove traces. Simple claims are never enough; thorough monitoring of metals, halides, and other critical contaminants ensures that what passes our QC will also pass external audits. Regular review sessions with our most demanding customers help us align our product’s technical profile with their most recent regulatory updates and patent filings.
We’ve also taken lessons from troubleshooting production hiccups—learning under fire when a minor change in source material suddenly introduces an impurity detected by an overseas customer’s sensitive analytical equipment. These scenarios push us to further tighten controls and document every measurable parameter, reinforcing relationships built on shared problem-solving rather than hollow promises.
Serial feedback cycles have changed our priorities year by year. For research pharma groups conducting screens with small quantities, we pack in smaller lots with detailed analytical data, accommodating quick turnarounds. Pilot and full-scale manufacturers benefit from drum lots with batch-to-batch consistency, given that a sudden change in impurity profile or residual solvent composition can compromise entire campaigns. Our internal training programs, which rotate bench chemists through various stages of production, ensure broad expertise and a collective memory of past successes and pitfalls.
Repeat customers often reach out with process-specific requests—such as particle size distribution or solvent compatibility details. Instead of generic assurances, we draw on our own experience carrying out representative reactions or stability studies, showing that our data aligns with their experimental needs. This collaborative approach means we don’t just ship a product, but remain invested in its successful use, with technical documentation that addresses concerns such as photostability, volatility, and shelf-life.
No batch is perfect in theory; real-world realities force manufacturers to develop robust risk management strategies. Early on, an unexpected power outage during crystallization led to off-spec material, prompting us to update power redundancy and install additional process monitoring. On occasion, a subtle shift in water content altered product form, which required quick coordination with logistics partners and rerouting to qualified solvent recovery. These operational lessons translate into more reliable supply chains and quicker corrective action when things don’t go as planned.
As organizations expect greater documentation, our approach integrates electronic recordkeeping and real-time environmental monitoring, ensuring traceability from reactant delivery to finished product shipping. These systems not only reduce manual error, they also create auditable trails for quality assurance and customer peace of mind.
Advanced process analytics have turned real-time spectroscopic feedback into more than just buzzwords. In our facility, FTIR and Raman tools allow on-the-fly identification of key intermediates and prompt adjustments. Staff trained to interpret these signatures intervene before small deviations become large. Efficiency gains show up as shorter cycle times, less wasted material, and a reliable output that allows customer schedules to proceed without last-minute surprises.
Sourcing improvements don’t just reduce costs—they enable independence from single points of failure. Dual sourcing of chemicals and maintenance partnerships for key equipment have limited shutdowns and demonstrated that stability, not just price, matters to downstream projects. These concrete changes allow us to support projects anywhere in the development pipeline, guaranteeing material availability for both initial pilot runs and late-stage scale-ups.
Decades of dialogue with application chemists, regulatory affairs specialists, and supply chain managers have shaped not just our product, but also our perspective. Markets demand shorter lead times and greater product adaptability, without sacrificing the reliability necessary for regulated applications. Our response—automation balanced by experienced operators, documentation paired with accessible expertise—reflects an industry that prizes both consistency and rapid adaptation to new challenges.
This compound reminds us every day the payoff grows with the ability to combine craftsmanship and thorough scientific oversight. Isolated molecules are easy to describe in an academic setting; supplying dependable material, batch after batch, for real projects, requires every ounce of practical know-how and mutual respect between maker and user. A reputation for stability doesn’t come from marketing alone; it comes from a hundred decisions, revisited and improved each production cycle.
Standing at the manufacturing interface, we see shifts across the chemical landscape. Research aims move from one class of actives to another, but the fundamentals of reliability don’t change. Delivering 5-Cyano-2-Fluorobenzaldehyde in forms and quantities that meet specific, evolving needs ensures our role as a true partner, not just a material supplier. Day-to-day experience maintains our focus on quality, safety, and responsiveness, because real users deserve more than compliance—they deserve commitment and care that grows from long-term engagement with the molecules that matter most.