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HS Code |
616928 |
| Cas Number | 643-13-0 |
| Molecular Formula | C6H5FO |
| Molecular Weight | 112.10 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | 12-14 °C |
| Boiling Point | 180-182 °C |
| Density | 1.221 g/cm³ at 20 °C |
| Refractive Index | 1.538 |
| Flash Point | 72 °C |
| Solubility In Water | Moderately soluble |
As an accredited 2-Fluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Fluorophenol, tightly sealed with a screw cap and labeled with hazard warnings. |
| Shipping | 2-Fluorophenol is shipped in tightly sealed containers constructed from compatible materials, typically glass or high-density polyethylene, to prevent leaks or contamination. It is classified as a hazardous substance and handled following regulations for flammable, toxic chemicals. Proper labeling, documentation, and temperature control are ensured during transportation to protect handlers and the environment. |
| Storage | 2-Fluorophenol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizing agents and bases. The storage area should be clearly labeled, with appropriate spill containment measures in place, and access should be limited to trained personnel wearing suitable protective equipment. |
Applications of 2-Fluorophenol in Industrial Manufacturing2-Fluorophenol serves as a key intermediate in multiple advanced industrial sectors, supporting efficient production of high-value chemicals, pharmaceutical ingredients, and specialty polymers. Our manufacturing expertise ensures consistent supply for complex downstream operations. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)Pharmaceutical manufacturers use 2-Fluorophenol as a primary building block to synthesize specific fluorinated aromatic compounds in APIs, particularly within anti-inflammatory and central nervous system drugs. Control over purity and impurity profiles remains critical during multi-step organic synthesis. Detailed formulation protocols mandate close monitoring of phenolic and fluorinated trace residues before final coupling or rearrangement stages, ensuring compliance with pharmacopoeia monographs. Our technical support teams regularly collaborate with formulation chemists to streamline batch scale-up while maintaining regulatory standards. Industry compliance standards
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2. Agrochemical Synthesis and Crop Protection CompoundsMajor agricultural chemical producers utilize 2-Fluorophenol as a core intermediate to develop fluorinated phenoxy herbicides and selective pesticides. It reacts in the early stages of active ingredient formation, offering controlled substitution patterns that tailor biological activity. Consistency in ortho-fluorine placement directly affects downstream selectivity and crop-safety testing in regulated field trials. We guarantee traceability from raw phenolic inventory through to packaged batch deliveries in line with agrichemical stewardship protocols. Industry compliance standards
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3. Synthesis of Liquid Crystal Materials for Electronic DisplaysProducers of advanced display materials employ 2-Fluorophenol in the creation of liquid crystal (LC) monomers and oligomers. Its precise fluorine substitution improves dielectric anisotropy and temperature stability in nematic LC phases. Industrial blending protocols demand chemically stable phenols with low ion content to meet strict defect level criteria in thin-film electro-optical device fabrication. Our chemical consistently meets these high specifications through plant-based purification and detailed quality control at each step prior to shipment. Industry compliance standards
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4. Manufacturing of Specialty Polymers and ResinsIndustrial polymerization plants integrate 2-Fluorophenol as a co-monomer in high-performance engineering plastics and specialty epoxy resins. Its substitution enhances flame resistance and chemical durability for advanced automotive and aerospace applications. Reactor charge sheets specify tightly controlled molar ratios and pre-blend protocols, while post-polymerization analysis ensures full conversion and excludes free phenolic residues. In-house application engineers support customer pilot plants with real-time technical guidance during scale-up runs and resin formulation tweaks. Industry compliance standards
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2-Fluorophenol steps into our catalog as a vital aromatic intermediate, finding frequent use in the synthesis of specialty chemicals, pharmaceuticals, and agrochemicals. Over the years of refining and scaling up this compound, the value comes not only from its reactivity and purity, but also from the technical hurdles we have learned to manage. This commentary draws from our production floor experience to shed light on what makes this product distinct, its core practical uses, and why thoughtful sourcing creates measurable differences in both process outcomes and finished goods.
With a molecular formula of C6H5FO and a CAS number of 367-12-4, 2-Fluorophenol appears as a clear to slightly yellowish liquid with a faint aromatic odor. In our own operations, we control for water content, acidity, and traces of by-products at each batch, because these aspects directly influence downstream outcomes, especially in pharmaceutical synthesis and pesticide formulation. The presence of fluorine ortho to the hydroxyl group creates significant electronic effects: reactivity shifts, solubility is altered compared with its non-fluorinated analogue phenol, and selectivities in substitution reactions can differ. The melting point and boiling range also change with fluorination, which matters for both scale-up and safe handling at the plant. These practical details are not afterthoughts—they shape heating protocols, storage systems, and purification strategies.
Many years of production have taught us that minor contaminants in aromatic intermediates do more harm than most users expect. Even trace halogen impurities from alternate routes—often below 100 ppm—cause unwanted side reactions in downstream synthetic applications. We rely on high-performance distillation and constant GC-MS tracking to control levels of chlorinated congeners, polymerization products, or residual acids, so our 2-Fluorophenol consistently offers purity well above 99%. Technical and pharmaceutical clients have pointed out that with strong incoming quality, their purification steps can often be trimmed, reducing overall solvent use and waste generation. These efficiencies don’t come from chemical formulae, but from a close partnership between analytical chemists and operations teams at the factory.
As a manufacturer, we keep a pulse on the research and commercial trends that dictate demand for specific building blocks. 2-Fluorophenol’s main value flows from its ability to introduce both a hydroxyl and a fluorine atom into more complex structures. Fluorine itself offers a unique set of advantages: it shifts metabolic stability, binding affinity, and physical behavior in pharmaceuticals. Medicinal chemists frequently request it for the synthesis of fluoroaryl ethers, carbamates, and sulfonates. In our experience, successful projects usually demand attention to the ortho relationship of F and OH—the substitution pattern ensures that resultant molecules exhibit increased acidity and different hydrogen bonding properties. Unlike para or meta isomers, this ortho compound tends to participate actively in selective couplings, nucleophilic substitutions, and esterification or acylation reactions with improved yields.
Comparing 2-Fluorophenol with analogous compounds—such as phenol itself, 4-fluorophenol, or 2-chlorophenol—clarifies why chemists keep asking for the ortho-fluorinated version. The electron-withdrawing effect of fluorine is strongest at the ortho position: this drops the pKa of the hydroxyl group, making the phenolic proton more acidic. In a practical sense, this means 2-Fluorophenol deprotonates easier under milder conditions, which opens up alternative synthetic strategies in the laboratory or production plant. It can also affect the rate and selectivity of electrophilic aromatic substitutions; we’ve seen customers favor this compound because it resists some forms of nitration or sulfonation that would otherwise cause undesired by-products when starting directly from phenol.
Another real-world distinction centers on toxicity and handling. Compared to 2-chlorophenol and 4-fluorophenol, the ortho-fluoro compound proves more manageable in terms of volatility and less prone to rapid air oxidation under controlled atmospheric conditions. This reduces losses during transfer and limits exposure, creating safer working conditions for plant technicians.
Scaling up organofluorine products from kilo-lab to production batches carries risks: reactor corrosion, batch-to-batch volatility, and the build-up of trace impurities all challenge plant engineers. Our process integrates fluorination at an intermediate stage—a strategy that controls side reactions and reduces corrosive hydrogen fluoride emissions. All storage vessels and equipment are fabricated with fluoropolymer linings to cut down on metal leaching and product degradation.
Customers from pharmaceutical and crop-protection sectors have occasionally asked for custom specifications, such as defined water content, reduced heavy metal content, or compatibility data with specialty solvents. We incorporate direct feedback into our process by modifying pre-drying steps, optimizing in-line purification modules, or adding nitrogen protections. Each design change is validated with real-world batch records, rather than relying solely on analytical data sheets. These are not simply technical improvements—they translate to fewer rejected lots, less downtime at customer facilities, and more predictable supply chains.
Unlike bulk phenol, 2-Fluorophenol’s relatively higher boiling point (187–189°C) and lower vapor pressure reduce evaporative losses in open systems and during prolonged reaction cycles. Users mixing small quantities into resin formulations or fine chemicals benefit from these properties: the addition phase runs cleaner, needing fewer vapor recovery provisions. In coupling reactions—such as those forming diaryl ethers or biaryl linkages—the ortho-fluoro group improves selectivity, based on our years of feedback from pilot-plant scale partners. In our downstream labs, we notice that hydroxy protection and deprotection steps, which sometimes stifle phenol derivatives, progress with higher conversion rates when using this compound.
In contrast, attempts to replicate the same transformations with 4-fluorophenol typically deliver lower yields and need more process debugging. Often, phenol itself generates too many side products, requiring labor-intensive purifications and rework. It’s the little adjustments in reactivity caused by the ortho fluoride that help avoid costly inefficiencies. For any process engineer chasing throughputs above 90% yield, these distinctions are not theoretical—they show up in the plant’s product loss reports.
Handling 2-Fluorophenol in a manufacturing environment calls for strict protocols. Our experience over hundreds of batches shows that airtight drums sealed under nitrogen make the product far more stable over time. Exposure to moisture or acidic vapors triggers minor polymerization and yellowing, complicating downstream use. Regular audits at packaging lines, and cross-checks between warehouse and QC personnel, catch these deviations early.
We also note its relatively modest toxicity for a halophenol, though strict personal protective equipment is non-negotiable. Unlike some other halogenated phenols, the skin absorption risk remains lower, but inhalation protection is always required in our workflow. Any leaking containers or spills get immediate attention, and all cleanup runs with pre-approved alkali neutralization.
Raw material volatility—particularly fluoro sources—affects production scheduling everywhere in the industry. We invest in stable contracts and local partnerships to bring in precursors with short lead times, cushioning a bit against market whiplash. At key points in the year, we run predictive inventory modeling, based on both macroeconomic signals and the immediate feedback from regular customers. In our experience, transparency about potential forecast shifts matters far more than chasing the lowest spot price. Most partners have come to appreciate upfront discussions around availability and quality, which in turn let product development teams adjust their project roadmaps in a realistic manner.
We have invested in modular distillation systems for surge capacity. Fast cleaning and setup cycles let us switch between larger and smaller production runs with minimal cross-contamination. This isn’t an academic ideal—it’s a change forced by the sharp swings in demand, particularly from the custom synthesis segment, and by customers requiring documented change control. For them, every transition must be tracked, and deviations logged, so that regulatory audits move forward without delays.
Our factory teams recognize that the organofluorine chemistry field often comes under scrutiny for its environmental impact—not just because of end-use toxicity, but through a whole-lifecycle view. We document emissions and manage liquid and solid waste through a closed-loop system. Working with local agencies, we collect and destroy waste streams containing persistent organofluorines, an effort that adds operational overhead but keeps us compliant with the tightening restrictions on hazardous discharge.
Green chemistry revisions are a constant topic. Five years ago, we replaced a key solvent system with a recyclable, lower-toxicity formulation, and the transition paid off in fewer permit headaches and smoother batch approvals. Incremental upgrades—from new filtration cartridges to better anti-static packaging—reduce risk both for our teams and for clients who need to pass environmental reviews.
Some of our best process improvements have come from fielding tough questions posed by chemists tackling new molecular targets. Projects across pharmaceutical, crop protection, and specialty materials regularly reach out for support in optimizing syntheses involving 2-Fluorophenol. One medicinal chemistry group needed ultra-low water content (<200 ppm) to prevent hydrolysis in a sensitive coupling step. Standard drying equipment and logistics were not enough. We redesigned part of our packaging line to allow inert gas blanketing and desiccation right up until seal, and added a rapid-response analytical station at the loading bay. This level of customization cost us in the short term but locked in longer-term partnerships because it made their own scale-up faster and less risky.
In another example, an agrochemical developer sent feedback about resin incompatibility when using a former supplier’s lot, pinpointing minor isomeric impurities as the culprit. We brought their technical team for an onsite review, ran side-by-side pilot trials using our material, and shared spectra. Clear communication around each process step allowed both teams to identify and fix issues in a single quarter, rather than through large-scale trial and error.
New derivative projects continue to push the demand for high-purity 2-Fluorophenol. Whether chemists are building advanced monomers for electronics, scaffolds for drug discovery, or specialty hardeners for advanced coatings, we keep a close technical exchange going. Recent academic collaboration explored fluorinated ligands for catalysis, which relied on consistent access to highly pure starting materials. The direct feedback from external partners has helped us shape quality specifications that anticipate the complications faced by R&D chemists, not just those defined by international standards.
Startups venturing into green pesticide formulations often experiment with alternative solvents or new coupling methods. Sharing batch-level performance histories and solvent compatibility notes, we help customize bulk supply packages that accommodate fast iteration, ensuring that researchers avoid stumbling blocks that raw batch variability can cause. By treating every inquiry as a technical conversation, not just a sales channel, we offer the accumulated experience of countless process cycles and problem-solving events along our own manufacturing journey.
Every product has boundaries. 2-Fluorophenol, despite its strengths, must be handled with respect for its reactivity—both in labs and in large-scale plants. Direct sunlight and open-air transfer cause oxidative color shifts that create downstream troubleshooting headaches. We encourage customers to discuss their own storage, handling, and blending setups during tech reviews, so the integration plans account for these quirks. Our quality team routinely shares tips gained from in-plant experiences: optimal transfer line materials, fast decontamination protocols, and fail-safe steps for inerting tanks.
For those needing nonstandard volumes, we offer intermediate bulk packaging, not just drums, reducing handling labor and minimizing exposure risk. The cost difference is often offset by better yield and lower pollutant generation through fewer transfers. We regularly share our batch histories during audits. This willingness to open our records builds credibility and deepens both technical and ethical trust.
Demands on product properties and regulatory compliance don’t stand still. The lessons we have drawn from scaling up our 2-Fluorophenol process—incremental hardware upgrades, smarter solvent selection, streamlined in-process controls—position us to react quickly as the boundaries of pharmaceutical and specialty chemicals shift. Skill sharing with advanced users and regulatory professionals ensures we avoid costly missteps. Regular, open feedback channels remain a key part of our manufacturing culture, feeding back new expectations into each future batch.
By emphasizing direct technical support and a factory-driven perspective, we offer more than just a product—our experience stands behind every shipment. Chemists, formulators, and process engineers who draw on both our quality guarantees and our bench-side insight gain a technical partner, not just a supplier.