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HS Code |
890154 |
| Chemical Name | o-Fluoroaniline |
| Synonyms | 2-Fluoroaniline, o-Aminofluorobenzene |
| Molecular Formula | C6H6FN |
| Molecular Weight | 111.12 g/mol |
| Cas Number | 348-54-9 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 182-184 °C |
| Melting Point | 7-9 °C |
| Density | 1.189 g/cm³ at 25 °C |
| Refractive Index | 1.567 |
| Solubility In Water | Slightly soluble |
| Flash Point | 70 °C (closed cup) |
As an accredited o-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with screw cap, labeled "o-Fluoroaniline," hazard symbols, chemical formula, and safety precautions printed clearly. |
| Shipping | o-Fluoroaniline should be shipped in tightly sealed containers, away from incompatible substances and in accordance with local, state, and international regulations. Handle with care, using secondary containment if available. Label containers clearly with hazard information. Ship at ambient temperature, avoiding exposure to heat, flame, or direct sunlight to ensure safe transport. |
| Storage | o-Fluoroaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition. Keep it away from incompatible substances such as strong oxidizers and acids. The storage area should be made of materials resistant to chemical corrosion and equipped with spill containment facilities. Protect from moisture and direct sunlight. |
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Purity 99%: o-Fluoroaniline with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced by-product formation. Melting point 33°C: o-Fluoroaniline with a melting point of 33°C is used in organic electronic material fabrication, where controlled phase transition enhances device uniformity. Low moisture content: o-Fluoroaniline with low moisture content is used in dye manufacture, where it prevents hydrolysis and increases color consistency. Molecular weight 111.12 g/mol: o-Fluoroaniline with molecular weight 111.12 g/mol is used in agrochemical formulation, where it provides precise active ingredient dosing. Stability temperature 80°C: o-Fluoroaniline with stability temperature 80°C is used in catalyst development, where it maintains reactivity without decomposition. Particle size ≤5 μm: o-Fluoroaniline with particle size ≤5 μm is used in polymer additive blending, where it improves dispersion and uniformity in the polymer matrix. GC purity ≥98%: o-Fluoroaniline with GC purity ≥98% is used in reference material preparation, where it assures analytical accuracy in calibration standards. Refractive index 1.571: o-Fluoroaniline with refractive index 1.571 is used in optical sensor production, where it optimizes signal transmission properties. Low residual metal content: o-Fluoroaniline with low residual metal content is used in semiconductor processing, where it minimizes electronic defects in finished components. Assay 98.5%: o-Fluoroaniline with assay 98.5% is used in fine chemical synthesis, where consistent concentration leads to reproducible reaction outcomes. |
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People working in chemistry, pharmaceuticals, or advanced materials often cross paths with o-Fluoroaniline. The name itself might not mean much if you don’t spend your days looking over reaction schemes or planning syntheses, but in the lab, o-Fluoroaniline proves its worth over and over. Its structure—a benzene ring with both a fluoro and an amino group at the ortho positions—makes it a unique building block for a range of industries. Anyone who has spent time with aromatic amines knows the difference a single atom of fluorine can make for the reactivity and the direction a project might take.
Chemists really appreciate the consistency and reliability o-Fluoroaniline offers. This compound sports a molecular formula of C6H6FN, with a molar mass just under 112 grams per mole. The substance typically comes as a colorless to pale yellow liquid with a characteristic, slightly sharp odor. Even minor shifts in the molecular makeup—like moving the fluorine from ortho to meta or para—change the product’s behavior, and those familiar with aromatic substitution know that these details matter when designing reactions. Its boiling point usually sits close to 180°C, and it dissolves with ease in a variety of organic solvents, which opens up a lot of options in synthesis planning.
It’s the combination of good reactivity and manageable handling that stands out. O-Fluoroaniline holds up well in storage and doesn’t break down as easily as multi-functionalized or unstable aromatic amines. This stability makes a huge difference to process chemists who need their intermediate to behave exactly as predicted. In the broader market for aromatic amines, the ortho-fluoro version helps users avoid some headaches from uncontrolled byproduct formation—something that can cause countless hours of repeat purification if the wrong variant gets used.
O-Fluoroaniline might look simple, but it fills a pretty special role in the world of manufacturing. The pharmaceutical sector relies on it for both target molecules and as a clever starting material for medicinal chemistry programs. The fluoro group acts as a molecular “switch,” shifting electron densities and changing how the compound interacts with enzymes or receptors. Plenty of well-known and emerging active pharmaceutical ingredients owe their function to small tweaks made possible by intermediates like this one.
People who’ve spent time in the field know how important it is to control every step of a multi-stage synthesis. O-Fluoroaniline lets chemists introduce the amino group under milder conditions than some other options, which makes life easier downstream—less byproduct, fewer purification steps, and a smoother process overall. In the world of dye manufacturing, the presence of the fluorine boosts lightfastness and color stability, qualities that can set a dye apart from competitors that fade or change under sunlight or repeated washing. The agricultural industry also trusts o-Fluoroaniline as a life-saving intermediate for making crop protection compounds. It offers reliable performance and consistency, month in and month out.
Fluoroanilines appear in several positional isomers—ortho, meta, and para. The ortho version stakes out some special ground thanks to its unique reactivity profile. The proximity between the amino and fluoro groups creates electronic and steric effects absent in the para or meta versions. I’ve seen research programs stall because the wrong isomer landed on the benchtop; reactivity isn’t interchangeable between them. Ortho-fluoroaniline tends to favor certain coupling and substitution reactions over its siblings, which makes a big difference if you want tighter control over the final structure of a drug or dye.
Cost and availability also come into play. While all three isomers show up in catalogs, demand for the ortho version often runs higher in advanced synthesis, especially for medicinal chemistry. Competitors in the fine chemical world try to offer pure product, but smaller impurities—in the parts-per-million range—can seriously throw off a pharmaceutical synthesis. Reliable suppliers invest a lot in purification and quality testing, and only the ortho variant opens specific doors in downstream chemistry.
In regulated sectors, purity isn’t just a point of pride—it’s a hard requirement. If you’re working on a drug candidate, even minor contaminants can trigger false signals in your biological assays or spark unexpected side effects in animal studies. I remember hearing about a medicinal chemist whose project tanked because a batch of intermediate contained a tricky-to-detect meta isomer. That single impurity, even at a few percent, ruined weeks of downstream work. Chemists look for o-Fluoroaniline from producers who show actual transparency in their analytical testing, whether it’s with gas chromatography, NMR, or HPLC. The ortho product often gets chosen specifically because producers can provide traceable purity records and batch consistency.
Handling requirements for o-Fluoroaniline resemble those for other small aromatic amines. Proper ventilation and gloves keep things straightforward. Some solvents and grades offer lower impurities—for certain high-value projects, even residual water counts as too much. Downstream, the right quality here signals fewer headaches later: fewer chromatographic purifications, cleaner spectra, and faster development overall. Process reliability matters. Experienced workers notice fast when a batch starts showing color shifts or phase separations not typical for pure product.
More and more, the industry insists on paying attention to chemical stewardship—not just in words but in real practices. O-Fluoroaniline brings with it the typical risks of aromatic amines. Direct exposure needs to be avoided, both for workers and for the environment. Plants that use this compound with proper fume extraction and leak management sidestep accidents and environmental releases. Focusing on tight containment and routine checks makes a real difference, as anyone responding to a spill can tell you.
It’s common now for producers to run cradle-to-gate assessments, including how raw materials are sourced and what waste streams get created. Fluoroaromatics don’t break down as readily as classic hydrocarbons, so waste management plans should always involve secure, permitted incineration or chemical treatment. Research into greener synthesis routes continues, and I know plenty of labs where process chemists swap notes on tricks to lower energy consumption and reduce off-gas volumes. Customers, especially those tied to global supply chains or based in Europe, now expect full disclosure about process safety and environmental impact, often auditing suppliers directly.
Small missteps in sourcing or reaction setup can set back an entire medicinal chemistry campaign. This isn’t just about regulatory red tape—it’s about not missing the next big thing. O-Fluoroaniline, used correctly, supports high-yield, selective transformations. In my own work, I remember how switching from a para- to an ortho-substituted starting material unlocked a route I’d once set aside as unworkable. The improved reactivity let us skip a protection–deprotection step and pushed the yield into workable territory. The same story repeats in dye synthesis: the ortho variant helps introduce halogenation or acylation without scrambling selectivity, which really helps if you’re working to meet customer specs without endless rework.
Process engineers also pay close attention. The boiling point and volatility of o-Fluoroaniline match well with existing plant setups. It distills without fuss, and—a detail often overlooked—its lack of deep color or residue means less plant downtime between runs. This reduces maintenance overhead. Large-scale operations value that reliability as it translates directly into output and cost savings.
No product escapes scrutiny or the push for improvement. Challenges with o-Fluoroaniline mostly pop up around scale, purity, and environmental fingerprints. Production uses aniline as a starting material and involves halogenation steps. Depending on how these are managed, yields and impurity profiles can swing. Market demand is growing, so supply chains need to adapt—especially to changing regulations covering aromatic amine handling and residual fluorine compounds.
As green chemistry gains ground, process improvements aim to minimize hazardous byproducts and cut down energetic costs. A handful of producers now boast continuous-flow setups to cut waste and tighten quality control. Buyers appreciate not just a high-purity material, but also a certificate showing reduced solvent use or lifecycle emissions. It’s clear that the direction of research, and customer demand, is pulling the market to cleaner and more responsible products, not just cheaper ones.
For anyone troubleshooting problems with o-Fluoroaniline, collaboration always helps. Reaching out to colleagues, comparing analytical spectra, and even sharing real-world stories about failed batches or process tweaks saves time and money. The best solutions don’t always come from big investments but from small operational changes: running tighter solvent controls, tracking storage temperatures more closely, or swapping out seals on old glassware that leech contaminants over time.
End-users who demand clear documentation and chain-of-custody records get better outcomes. Working with reputable suppliers who welcome audits and lab visits also pays off in fewer recalls and less downtime. Regulatory frameworks are evolving, especially surrounding aromatic amines in the EU and Asia, so producers who stay ahead of compliance save everyone downstream from expensive, last-minute revalidation work. The rise in data transparency—even something like sharing detailed batch chromatograms—means fewer surprises during product launches or scale-up campaigns. It comes down to a culture of trust and open communication rather than paperwork alone.
As the needs of the pharmaceutical, dye, and agrochemical industries keep shifting, o-Fluoroaniline remains a trusted, flexible tool. Its unique reactivity profile, tied directly to the placement of its functional groups, keeps it relevant as a key intermediate for specialized synthesis. While competition always exists, real-world experience shows how the ortho variant opens doors not easily reached through other routes.
Embracing a product like o-Fluoroaniline means thinking not just about cost or immediate need, but about longer-term outcomes for safety, product performance, and corporate reputation. Anyone serious about advanced synthesis, from the bench chemist to the operations manager, ends up weighing these factors as part of broader decision-making. As regulations and customer expectations tighten, the most reliable producers will be those who combine chemical insight, operational discipline, and a genuine commitment to responsible sourcing and environmental protection.
The seasoned voices in the chemical industry keep coming back to a handful of central themes. Small differences at the molecular level—here, the positioning of a fluorine atom—can make or break a project. A steady supply of pure, well-characterized o-Fluoroaniline saves weeks of effort down the line. Producers who take customer feedback seriously learn fast where problems hide, whether in impurity profiles, packaging weaknesses, or documentation gaps.
Day to day, it pays to keep communication lines open, internally and with suppliers. Encouraging team members to flag early performance concerns or even minor handling issues creates a workplace where problems get solved before they grow. My experience shows that a culture of transparency and active engagement, not just compliance with the rulebook, breeds real safety and better outcomes for everyone.
O-Fluoroaniline keeps proving itself as a valuable chemical intermediate for today’s demanding industries. Whether you’re pushing boundaries in drug design, inventing new pigments, or keeping crops safer, its unique structure offers a starting point for progress. Real-world knowledge, clear documentation, and a shared commitment to high standards drive success with this product.
Looking back at my own time in the field, I see how products like o-Fluoroaniline sit at the intersection of tradition and innovation. They make new discoveries possible while demanding respect for safety, quality, and environmental responsibility. That blend—of careful stewardship and spirited progress—remains as important as ever for those pushing chemistry forward.