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HS Code |
486227 |
| Product Name | 2-Fluorobenzaldehyde |
| Cas Number | 446-52-6 |
| Molecular Formula | C7H5FO |
| Molecular Weight | 124.11 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 185-187 °C |
| Melting Point | -10 °C |
| Density | 1.188 g/cm3 at 25 °C |
| Refractive Index | 1.548 |
| Flash Point | 67 °C |
| Solubility In Water | Slightly soluble |
| Smiles | O=CC1=CC=CC=C1F |
As an accredited 2-Fluorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Fluorobenzaldehyde, 100 mL, supplied in an amber glass bottle with a sealed cap, labeled with hazard symbols and product details. |
| Shipping | 2-Fluorobenzaldehyde is shipped in tightly sealed containers, protected from light and moisture, and clearly labeled as a hazardous chemical. It must be transported according to local, national, and international regulations for flammable and toxic substances, ensuring proper documentation and handling to prevent leaks, spills, or exposure during transit. |
| Storage | 2-Fluorobenzaldehyde 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 oxidizers and bases. Protect from direct sunlight and moisture. Store in a flammable chemicals cabinet, and ensure proper labeling. Follow all relevant safety protocols and local regulations for storage of hazardous chemicals. |
Applications of 2-Fluorobenzaldehyde in Industrial Manufacturing2-Fluorobenzaldehyde has advanced utility as a key intermediate in specialty chemical manufacture. Our production site supports customers by supplying high-purity material precisely aligned to varied downstream process specifications. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)Pharmaceutical synthesis utilizes this compound in the development of fluorinated aromatic cores for targeted APIs. The molecular structure meets strict requirements for controlled substitution in building blocks used in central nervous system drugs and anti-infective agents. We support global pharmaceutical partners with traceable quality and seamless integration in multistep API syntheses. Industry compliance standards
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2. Agrochemical Synthesis for Herbicides and FungicidesThe molecule provides a functionalized aromatic base in the workup of selective herbicide and fungicide actives. Production teams in the crop protection sector use it in the development of compounds offering enhanced environmental persistence and target selectivity. Our material supports precise halogen insertion steps in both pilot and full-scale agrochemical lines. Industry compliance standards
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3. Aromatic Fragrance Ingredient SynthesisPerfume and specialty fragrance producers employ 2-fluorobenzaldehyde for introducing controlled fluorine motifs into high-value aromatic aldehydes and related chemicals. Integration into fragrance blending enhances volatility, imparts distinct olfactory notes, and improves formulation stability for premium end-market applications. Our technical team delivers detailed batch analytics to support olfactory performance studies and regulatory traceability. Industry compliance standards
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4. Specialty Polymer and Resin ModifiersAdvanced materials engineers adopt this compound as a functional monomer for introducing fluorinated moieties in selected polymer matrices and coatings. Integration at the pre-polymer stage improves hydrophobicity, chemical resistance, and alters dielectric properties critical in electronics or technical coatings. Our plant capabilities support controlled supply from kilograms to multiple tons aligned with customer batch scheduling. Industry compliance standards
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5. Fine Chemical Manufacture for Dye and Pigment SynthesisColorant sector operators rely on this aromatic aldehyde to introduce fluorinated substituents during the synthesis of complex chemical dyes and pigments. The fluorine atom aids in tuning chromophore stability, solvent resistance, and photostability of specialty colorants for plastics, fibers, and inks. Our QC framework ensures trace impurity control meeting stringent downstream requirements. Industry compliance standards
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Competitive 2-Fluorobenzaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
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As a long-standing chemical manufacturer, we’ve seen the shift in requirements from bulk commodity outputs to unique building blocks that deliver consistency and performance. 2-Fluorobenzaldehyde falls into this class of fine chemicals, finding its way into applications where a standard benzaldehyde just doesn’t cut it. Our journey with this compound started years ago as we were searching for more selective options for our pharmaceutical and agrochemical partners, and its distinctive molecular structure immediately stood out.
With the fluorine atom anchored at the ortho-position, 2-Fluorobenzaldehyde offers a balance between reactivity and stability. In our daily operations, we run continuous batch synthesis using carefully controlled conditions, making use of toluene sulfonic acid catalysis or metal-catalyzed halogenation where necessary. Our 2-Fluorobenzaldehyde regularly enters the reactor as a clear liquid, usually above 98% purity, often up to 99.5% by GC when requested. Moisture and acidic impurities are monitored tightly, as customers have little tolerance for ingredient deviations, especially in key steps of pharmaceutical manufacturing.
In laboratories and kilolabs alike, the fluorine substituent unlocks new reactivity that ordinary benzaldehydes can’t achieve. Colleagues in intermediates synthesis remark on the robust electron-withdrawing effect at the ortho position, which pulls electron density and modifies attack at the aldehyde group. Chemical industry analysts increasingly cite this compound when discussing specialty aromatic intermediates, particularly where downstream derivatives depend on precise molecular control.
We’ve seen this in our work with both complex fragrance and pharmaceutical projects. 2-Fluorobenzaldehyde acts as a launching point for building blocks like fluoro-cinnamic acids, substituted styrenes, and even specialty heterocycles. It’s also made its mark on certain crop protection molecules, where downstream selectivity hinges on the proper placement of that single fluorine atom. Compared to the para-fluoro or meta-fluoro variants, the ortho isomer consistently leads to more distinct chemistry — from regioselective ring opening to unique nucleophilic substitutions later in the process.
Each drum or bottle we prepare comes with traceable batch data. We test for appearance, purity (by GC), water content (Karl Fischer), and acidity before anything leaves the plant floor. Customers often ask for low levels of residual toluene or dichloromethane, so we double-rinse glassware and purge containers with nitrogen. Odor serves as a quick check on bench-scale batches — a sharp, biting scent distinct from plain benzaldehyde — and helps our team verify product identity during sampling.
We maintain a standard packaged product at 25 kg per drum for bulk processes and also service the kilo-scale labs with as little as 250 grams at a time, ensuring no cross-contamination from other reactive aromatic aldehydes. It doesn’t matter whether we’re filling small jerricans or loading bulk containers; each process is tracked, personnel wear full PPE, and the safety team reviews all shipping modes for temperature and compatibility with seals and gaskets.
Many companies still rely on basic benzaldehyde for foundational chemistry, but those working at the edge of pharmaceutical and agrochemical innovation need structural differences that unlock selectivity. Adding a fluorine atom — especially in the ortho position — changes everything. Electron withdrawal reduces the rate of nucleophilic additions to the aldehyde, which can mean higher selectivity or a decreased rate of side-product formation in complex syntheses.
Some chemists point out that while para- or meta-fluorobenzaldehyde almost meet their project needs, downstream steps involving metal-catalyzed couplings or selective reductions just don’t work as efficiently as with the ortho isomer. That’s become obvious in customer feedback; a major intermediate plant referenced significantly increased yields and lower impurity levels when switching from the para derivative to our 2-fluorobenzaldehyde.
Physical handling makes a difference, too. Our compound runs as a mobile, colorless to pale yellow liquid at ambient temperature, with a boiling point near 181-183°C, making it less volatile and easier to store than lighter aromatic aldehydes. Lower vapor pressure translates into safer handling and reduced losses during storage. Our plant team appreciates that a solid or crystallizing aldehyde slows down filling and wrapping. With 2-fluorobenzaldehyde, line blockages are rare, and transfers proceed according to schedule.
Demand cuts across different sectors, but pharma stands out as the leading application domain in our experience. We’ve spent years connecting with chemists at R&D startups and long-established drug developers who rely on this fluorinated aldehyde to build active pharmaceutical ingredients (APIs) where standard precursors would never meet synthetic targets. In one recent project, a customer ran a reductive amination, using our 2-fluorobenzaldehyde as a critical intermediate en route to a fluorinated benzimidazole. Throughout the multistep synthesis, the position and presence of the fluorine atom determined not just chemical yield but also the ease of purification and stability of key intermediates.
Agrochemical companies face their own synthetic hurdles. Chlorination, coupling, and alkylation reactions behave differently with the ortho-fluoro derivative, especially when attempting selective substitution on the aromatic ring. Customers tell us that this improves their downstream yields and saves several hours per batch at the plant. In fragrance and specialty chemicals, certain musk and floral components arise from reactions involving 2-fluorobenzaldehyde, where end customers desire a unique profile inaccessible from parent benzaldehyde or other halogenated varieties.
We also respond to inquiries from material science labs looking for fluoroaromatic components that alter polymer characteristics or bring in desirable electronic properties. The interaction of the fluorine atom at the two-position creates subtle but crucial differences in the resulting materials.
Synthesizing and delivering a niche aromatic intermediate presents its own challenges. Unlike commodity solvents or acids, 2-fluorobenzaldehyde requires tight control at every production stage. Fluorination chemistry is notoriously demanding: exotherm management, reactor surface passivation, and careful gas handling become central issues. Even the minor by-products — such as 4-fluorobenzaldehyde or small quantities of over-oxidation products — must be tracked, separated, and minimized using process improvements and in-line analytics.
Once produced, product stability forms the next focus area. We design packaging with multilayer barriers to handle aromatic compounds, and invest in compatibility tests for drum liners and gaskets exposed to possible attacks by the aldehyde group or released HF. Each lot leaves with analytical verification, and warehouse staff rotate stock to minimize storage times, as fresh product almost always provides better downstream outcomes for our partners.
On the logistics side, shipping regulations around fluorinated organics often evolve. Our compliance team monitors regulatory updates for restrictions or new transport carve-outs, working directly with carriers to avoid temperature excursions or holding periods at customs. In over a decade of global exports, we’ve avoided serious delays by prepping every document — including Certificates of Analysis and all required labels — days before scheduled shipping dates.
Finding effective ways to minimize waste has become a priority. Our team implements closed-loop solvent recovery in the allelic step, neutralizes aqueous effluent, and properly ventilates storage spaces to protect both staff and product. Temperature and humidity controls in the packing area prevent product degradation. Hydrogen fluoride, one possible hazard in some older fluorination methods, is continuously scrubbed and neutralized in a monitored system before any vented gas leaves the building.
Our worker safety record matters just as much as our product quality. PPE requirements on our production line include gloves, splash goggles, and workwear rated for aldehyde and halogen exposure, going beyond the minimum local standard. Annual training refreshers keep our staff up to speed with the latest in chemical handling best practices, and emergency protocols undergo real-world drills to ensure no disruption to supply.
Most of our customers come with their own requirements and questions — can we provide tighter impurity specs, reduce certain trace metals, or supply in specialty packaging? Instead of generic responses, our technical teams work directly with site chemists to make modifications that work without losing batch consistency. There have been cases where downstream applications struggled with trace acid or water. By adapting our drying steps and switching to high-efficiency thin-film evaporation, we succeeded in delivering lower moisture content, letting customers skip an extra pre-synthesis purification round.
A bright spot has been the feedback loop we’ve developed. Users update us on how small tweaks in the synthesis affect their processes, and we introduce these learnings into the next runs. For example, one team working on fluorinated phenethylamines highlighted small aromatic impurity carryover. By changing a single process variable and running an extra short-path distillation step, we improved both appearance and odor, leading to higher approvals in subsequent QC checks.
A question new users often raise centers around the differences between 2-fluorobenzaldehyde and similar compounds like 3- or 4-fluorobenzaldehyde, or even other ortho-substituted aromatic aldehydes. Our first-hand experience repeatedly confirms that reactivity in side-chain formation, ring functionalization, and further halogenation occurs at a noticeably different rate. The ortho-fluoro effect not only drives electronic differences but can physically alter crystalline packing and solubility, impacting step yields and purification effectiveness in labs and on plant scales.
Our clients focused on final product consistency see that even a shift from ortho to meta takes them out of specification. Synthesis of certain active molecules relies on preserving substitution patterns, and the purity demands of regulated markets make substitutions a matter of regulatory compliance, not just chemistry. When a specialty dye manufacturer provided us feedback after a failed run using the meta-fluorinated aldehyde, we worked together to map out the root cause. In the end, only the ortho-fluoro product produced the desired hue and fastness in the final pigment batch.
Ongoing R&D within our team targets cleaner, safer routes to 2-fluorobenzaldehyde. High selectivity in halogenation, greener processes, and alternative fluorinating agents feature heavily in our trials. The push for safer, solventless methods has already led to pilot-scale tests with continuous flow reactors, limiting exposure to hazardous reagents and improving yield per reactor volume. As emerging pharmaceutical and specialty applications demand higher and higher purity, we continue refining our analytical approach, using ultra-high-performance chromatographs, NMR, and spectroscopic confirmations for each batch.
We remain attentive to sustainability concerns across the industry. Whenever downstream clients request lifecycle data, waste minimization figures, or emissions tracking, we provide transparent reporting. These collaborations drive mutual improvements — our efficiency gains help their own ESG reporting, and joint audit visits foster deeper understanding of shared supply chain challenges.
Having spent years watching 2-fluorobenzaldehyde move from our reactors to specialty labs and large-scale sites worldwide, we see this compound as more than just another molecule. It represents the synergy between advanced chemistry and hands-on production expertise. Every kilogram reflects the work of dedicated teams who understand that performance, safety, and compliance are not just buzzwords but core aspects of what truly sets a manufacturer apart.
For those building the next generation of drugs, crop solutions, or specialty materials, 2-fluorobenzaldehyde brings unique reactivity powered by its distinctive molecular geometry. Our commitment remains to ensure that each batch not only meets spec but matches the real-world demands of innovation-driven industries. Through continual investment in best-in-class production practices, logistical reliability, and direct customer engagement, we deliver more than just a product: we offer partnership grounded in decades of practical manufacturing experience.