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HS Code |
795321 |
| Chemicalname | O-Fluorobenzaldehyde |
| Synonyms | 2-Fluorobenzaldehyde |
| Molecularformula | C7H5FO |
| Molecularweight | 124.11 g/mol |
| Casnumber | 446-52-6 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 182-184 °C |
| Meltingpoint | -3 °C |
| Density | 1.186 g/cm3 |
| Refractiveindex | 1.561 |
| Smiles | C1=CC=C(C(=C1)F)C=O |
As an accredited O-Fluorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 mL of O-Fluorobenzaldehyde, sealed with a screw cap, labeled with hazard and handling information. |
| Shipping | O-Fluorobenzaldehyde is shipped in tightly sealed containers, protected from light and moisture, and labeled per hazardous chemical regulations. It is transported in compliance with local and international guidelines, typically under ambient temperature, with necessary documentation for safe handling, indicating its status as a flammable and potentially harmful substance. |
| Storage | O-Fluorobenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from light and moisture. Store at room temperature and ensure proper labeling. Always follow local regulations and safety data sheet (SDS) recommendations for additional storage guidelines. |
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Purity 99%: O-Fluorobenzaldehyde with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reduced side-product formation. Melting point 26°C: O-Fluorobenzaldehyde with a melting point of 26°C is used in fine chemical production, where it enables easy handling during low-temperature processing. Molecular weight 124.11 g/mol: O-Fluorobenzaldehyde with a molecular weight of 124.11 g/mol is used in agrochemical research, where it provides consistent reactant quantification in formulation development. Stability temperature up to 60°C: O-Fluorobenzaldehyde stable up to 60°C is used in industrial batch reactions, where it maintains structural integrity under moderate thermal conditions. Low water content <0.5%: O-Fluorobenzaldehyde with water content below 0.5% is used in moisture-sensitive organic synthesis, where it prevents hydrolytic side reactions. Refractive index 1.555: O-Fluorobenzaldehyde exhibiting refractive index 1.555 is utilized in analytical detection protocols, where it allows precise compound identification in chromatographic analysis. Flash point 91°C: O-Fluorobenzaldehyde with a flash point of 91°C is used in laboratory-scale process development, where it offers enhanced safety during solvent handling and transfer. |
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Walking through the corridors of chemical development, I often see compounds that solve problems in ways only seasoned chemists notice. O-Fluorobenzaldehyde stands out among these. Produced as a pale liquid with a faintly bitter aroma, it carries the weight of the molecular formula C7H5FO. It’s not just different because it sports a fluorine atom at the ortho position on the benzaldehyde ring; that slight change sets off a chain reaction of new properties that turn heads in research and manufacturing. Working in chemical labs, I've watched O-Fluorobenzaldehyde slide into reaction flasks and reshape possibilities for pharmaceuticals, agrochemicals, and advanced material development.
Rolling up my sleeves in organic synthesis, the structure draws my attention: combining the well-known reactivity of the aldehyde group with the unique behavior fluorine offers. Chemists often use the ortho-isomer specifically for its predictable response in certain substitutions and condensations. For those not knee-deep in synthetic pathways, here’s why it matters: that placement of fluorine can nudge electron distribution on the ring, shifting how the compound reacts with nucleophiles and electrophiles. This isn't arcane theory—it changes the real-world results of multi-step synthesis work. Using O-Fluorobenzaldehyde, new scaffolds for medicines and crop-protection products show up where more common benzaldehydes would stall, or worse, give low yields. This metric is not theoretical; ask anyone troubleshooting dead-end routes in medicinal chemistry.
Some compounds look similar on a spec sheet but feel worlds apart at the bench. Pure O-Fluorobenzaldehyde typically arrives with high assay, often above 98%, and a boiling point hovering around 186-188°C. These specs draw skepticism unless you’ve seen the difference in work-up steps—product stability and trace impurity levels change outcomes in final applications. Water content may be low, but what matters even more on long runs is minimal byproduct formation. In my batches, a faint color change pointed toward degradation; careful storage under inert atmosphere and sealed vials made all the difference in shelf life and reliability. Any chemist counting on reproducibility ends up grateful for manufacturers that invest in extra purification or offer the isomer with tight specification tolerances.
Standard benzaldehyde works fine for classic reactions, but O-Fluorobenzaldehyde brings advantages you won’t see elsewhere. The ortho-fluoro group influences both activation and selectivity in substitutive aromatics. Nowhere is this more vivid than in heterocyclic construction and in the making of pharmaceutical intermediates. Many of today’s approved drugs rely on subtle modifications of standard frameworks; adding a fluorine at this position offers improved metabolic stability and altered biological activity. I remember a project where the ortho-fluoro motif helped dial in the right polarity for binding to a particular enzyme, outperforming the unsubstituted derivative by a wide margin.
Anyone who’s worked a day in custom synthesis knows that all fluorobenzaldehyde isomers are not born equal. Para-fluoro and meta-fluoro isomers show up often, but the ortho variant brings nuanced reactivity. The electronic effects of the ortho placement create both steric and inductive influence close to the aldehyde. In certain condensations and ring-closures, that twist tamps down on side reactions or directs incoming reagents more reliably. Working with O-Fluorobenzaldehyde in our own lab, I saw formation of unwanted tars plummet—a relief when purifying final compounds by chromatography. Some colleagues resist using ortho isomers, worried by slightly higher costs or handling concerns, but the time saved in downstream processes justifies the investment. Rationalizing this comes easy after a few failed runs with other isomers or derivatives.
Synthetic chemists and pharmaceutical scientists chase down value at every step. One product that has pulled its weight in medicinal chemistry is O-Fluorobenzaldehyde. During one series of indole syntheses, using the ortho-fluoro isomer allowed newer analogs to take shape, each extending potency or specificity. In flavor and fragrance research, small tweaks in the aromatic ring can mean the difference between harshness and smooth undertones. People underestimate how impactful these signals are in consumer products. Academic literature supports this: O-Fluorobenzaldehyde has appeared in patent filings and published studies for anti-inflammatory agents, fungicides, and dyes. Its adoption is built on practical impact, not just theoretical appeal.
Many buyers look at aromatic aldehydes and expect similar handling, but this one commands respect. In my own experience, improper storage unleashed slow decomposition that quietly undermined months of work. These details never make it into celebratory press releases but turn out to be what makes or breaks a research campaign. I’ve stored the compound in clear glass by mistake, ending up with yellowed product and mystery peaks in my NMR. It’s one thing to look at a certificate of analysis, another to see how a sample ages in your own hands. If your process can tolerate small impurities, you might dismiss these issues, but in regulated synthesis or preparation of building blocks, every trace counts. High-quality suppliers, in my experience, always encourage cold, dark storage and airtight seals, and they back this up with documentation on real-world stability testing.
Fluorinated aromatics underpin some of the most effective drug candidates on the market. Adding a fluorine atom can slow metabolic breakdown in the liver, let new treatments linger and do their job more effectively. During one therapeutic campaign, we built analogs based on O-Fluorobenzaldehyde as a starting point. Changing just one substituent increased not only potency but also oral bioavailability. Textbook chemistry helps you predict changes like these, but there’s something satisfying about chasing down a hit compound based on a well-picked starting material. In agricultural science, I’ve seen similar successes, with certain herbicides strengthened by this motif’s persistence in the field, reducing the rate of application and supporting sustainable practices.
Clients in the pharmaceutical and specialty chemical industries want consistent performance—not just a product that works on paper. O-Fluorobenzaldehyde checks these boxes when you source it carefully and follow best practices around use. Process chemists look for intermediates that shorten sequence length or provide clean transition to final products. There’s measurable improvement in pilot runs using O-Fluorobenzaldehyde instead of more basic aldehydes: less rework, higher isolated yields, smoother compliance during audits. This mirrors my own work, where better starting materials turned into direct revenue gains and shorter timelines. It’s not a silver bullet for every pathway but earns its reputation where robust, scalable chemistry matters.
Making decisions in research often comes down to striking a balance between price and performance. Some labs save on material costs by buying general benzaldehydes, skipping the added premium of the ortho-fluorinated isomer. Yet, across my projects, investment in O-Fluorobenzaldehyde paid off through fewer failed reactions, easier purifications, and clearer analytical readouts. Cost per gram drops sharply in bulk, making this product more approachable for larger projects. Teams that plan with efficiency in mind find value not in the sticker price but in the reduced labor and time required to deliver final products. These are hidden savings that rarely show up in basic quotes but loom large during multi-step syntheses.
No aromatic aldehyde is truly benign, and O-Fluorobenzaldehyde is no exception. Its vapor irritates the nose and eyes; gloves and proper ventilation stand as more than suggestions in a busy lab. Early on, I underestimated its potency and paid the price with headaches and watery eyes. Smart chemists prioritize quality PPE for themselves and the people they train. Good labeling, storage under inert gas, and knowledgeable waste disposal are as important as following reaction protocols. Data supports a cautious approach: exposure limits are not well defined for this compound, but lessons from related chemicals guide safe handling and disposal practices. Reminding new team members about these risks cements good habits for future work with novel aromatic intermediates.
Pressure to “go green” in synthesis grows every year. I’ve watched interest in greener aldehyde sources rise; some suppliers offer O-Fluorobenzaldehyde from recycled or renewable feedstocks. In day-to-day lab practices, minimizing solvent use and avoiding excessive purification steps lessens the environmental impact. Choosing O-Fluorobenzaldehyde sometimes makes it possible to run cleaner reactions with lower loadings of reagents or fewer side products. That translates into fewer resources spent on post-reaction cleanup and waste management. Regulatory agencies increasingly encourage these choices, and showing upstream improvements stays important in both compliance and internal sustainability goals.
Scaling from gram-scale research to pilot-plant production brings a host of new challenges. O-Fluorobenzaldehyde, with its moderate boiling point and volatility, behaves differently in reactors than on a bench-top. I have seen small changes in pressure or temperature introduce color changes or off-odors in large batches. Physical handling also shifts: drums must be carefully vented, and automated dispensing equipment managed to avoid leaks and exposure events. Companies specializing in scale-up services know how critical it is to control variables with this compound. Trust in a supplier and close monitoring of batch attributes make or break the scale-up process.
With chemical safety always evolving, regulatory stance on aromatic aldehydes and especially fluorinated derivatives can shift with little notice. O-Fluorobenzaldehyde fits into the broad risk categories for aromatic intermediates, but regional differences pop up between Europe, North America, and Asia. I’ve learned to keep documentation handy and review new compliance bulletins before moving product across borders. Forward-thinking organizations track classifications under REACH, TSCA, and other frameworks, while researchers dig into safety datasheets for current advice. This overhead might seem like a distraction, but it saves time and money during external audits or as new restrictions come into play.
Not every day in the lab revolves around rare or novel reagents, but having O-Fluorobenzaldehyde in stock has become routine for many in organic chemistry. Solvolysis, cyclization, and common condensations run more predictably when you can tune reactivity with confidence. Junior chemists start to recognize that picking the right isomer isn’t an academic exercise; it’s about getting to the result without headaches, missed timelines, or costly mistakes. In group meetings, teams pass around success stories that start with a new aldehyde flavor and end with a compound that lands funding or hits a milestone. These small victories stack up in commercial R&D and academic environments alike.
Anyone in the trade knows O-Fluorobenzaldehyde doesn’t just ride on its isomeric position. The fluorine atom in the ortho position locks in unique electronic and spatial traits. This attribute shapes not just reaction speed or selectivity but also downstream behavior like crystallization or extractability. During a purification train, a single drop in byproduct formation brought months of relief in repeated runs. The para and meta isomers have their advocates, but for cases where close-range electron withdrawal matters, the ortho reigns supreme. Product developers across pharma and agrochemical companies keep returning to this compound for its repeatability and performance.
Everyone in research aims to make an impact, whether on a molecule or a product line. O-Fluorobenzaldehyde forms part of the backbone where these innovations spring. In licensing, the freedom to operate with a fluorinated aldehyde of known provenance opens strategic doors. My own licensing projects looked better on both paper and during technical due diligence when intermediates matched published, peer-reviewed precedents. This builds trust with partners, auditors, and potential buyers.
Growth in new chemical entities depends on accessing and using such specialized building blocks. I expect to see more processes designed with O-Fluorobenzaldehyde at the core, especially as automation comes to fine and specialty chemicals. Robotic platforms rely on consistent, high-purity feedstocks, something this compound can routinely deliver when bought from quality sources. The demand for ever more specific, more predictable, and safer synthetic intermediates won’t slow down. Based on my track record and the increasing challenges facing both R&D and full-scale production, O-Fluorobenzaldehyde stands ready to answer the call.
For researchers and production teams, using O-Fluorobenzaldehyde is less about tradition and more about realizing practical benefits. Time after time, it’s turned tough syntheses into solvable projects and allowed routes that close the gap between idea and finished product. Cutting through the crowd of isomers and analogs, this one brings unique offerings not just in a test tube but in the value chain of modern science and manufacturing. Drawing on work at the bench and in scale-up, the verdict is clear: O-Fluorobenzaldehyde brings reliability, reactivity, and flexibility to every project it touches.