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HS Code |
634716 |
| Productname | 3-Chloro-4-Fluorophenol |
| Molecularformula | C6H4ClFO |
| Molecularweight | 146.55 g/mol |
| Casnumber | 700-36-7 |
| Appearance | White to light beige solid |
| Meltingpoint | 51-54 °C |
| Boilingpoint | 220 °C (approximate) |
| Density | 1.44 g/cm3 |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1O)Cl)F |
| Inchi | InChI=1S/C6H4ClFO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H |
As an accredited 3-Chloro-4-Fluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a tamper-evident cap, labeled "3-Chloro-4-Fluorophenol, CAS 700-37-8, for laboratory use only." |
| Shipping | 3-Chloro-4-Fluorophenol is shipped in sealed, chemical-resistant containers to prevent leaks and contamination. Packages are clearly labeled with appropriate hazard information. It is transported according to local and international regulations for hazardous materials, ensuring safe handling, storage, and delivery, and often requires temperature control and protection from moisture during transit. |
| Storage | 3-Chloro-4-Fluorophenol should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers and bases. Protect from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent accidental release or exposure. Use appropriate personal protective equipment when handling. |
Applications of 3-Chloro-4-Fluorophenol in Industrial Manufacturing3-Chloro-4-Fluorophenol serves as a specialized intermediate in several mature chemical segments. As the direct producer, we focus on downstream sectors where demand is driven by efficiency, compliance, and end-use safety. The application details below reflect real processes and industrial standards embedded in established manufacturing chains. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)Leading pharmaceutical companies use our material to synthesize API core structures for antimicrobial and anti-inflammatory drugs, where specificity in halogen-substituted phenol derivatives allows precise modulation of biological activity. In these controlled environments, raw material selection follows strict quality audits, and our batches undergo comprehensive trace analysis for residual solvents and impurities. Partners adjust input ratio based on stoichiometric requirements in key Suzuki or nucleophilic aromatic substitution steps, ensuring optimal yields and conformance to registration dossiers. Industry compliance standards
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2. Agrochemical Synthesis – Herbicide and Fungicide IntermediatesAgrochemical formulators utilize this material in stepwise building of complex aromatic scaffolds, especially where controlled electron density adjustment on benzene rings is required for target selectivity. In multistep syntheses, the compound typically links to cyano or ester functionalities through palladium-catalyzed cross-coupling, followed by downstream protection or halogenation steps. Traceability and batch uniformity are mandatory due to downstream registration with regulatory bodies. Industry compliance standards
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3. Specialty Dye and Pigment PrecursorsManufacturers in the dye and pigment sector incorporate this compound as a controlled halogen source for modifying chromophore structures, addressing color fastness and shade stability challenges required by automotive, plastic, and ink industries. The material often enters diazotization or azo coupling reactions as a mono-substituted phenol, influencing hue intensity and solvent resistance. Batch analytics focus on absence of trace metals and halogen purity due to downstream impact on color uniformity. Industry compliance standards
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4. Electronic Chemicals – Liquid Crystal Material IntermediatesProducers of specialty electronics chemicals apply this compound as a halogen donor in the construction of biphenyl or phenoxybenzoate cores essential for liquid crystal materials in advanced displays. The aromatic substitution pattern introduced by this raw material supports both thermal stability and dielectric anisotropy demanded by TFT-LCD manufacturing. Evaluation of each lot includes gas chromatography for trace organics, supporting consistency in optoelectronic device performance. Industry compliance standards
Typical usage ratio
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We have been making 3-Chloro-4-Fluorophenol for years, paying close attention to customers who need more than just another substituted phenol on their production line. This compound, known by its CAS number 1673-26-3, carries a molecular formula of C6H4ClFO. Many in the industry see it as just another halogenated phenol, but the interplay of both chlorine and fluorine atoms in the structure delivers very specific performance characteristics. The real value lies in this dual substitution pattern, something that ordinary monochloro or monofluoro analogs simply don’t match.
From our point of view, 3-Chloro-4-Fluorophenol stands out for those who are synthesizing complex molecules such as pharmaceuticals, agrochemicals, or specialty dyes. The presence of both electron-withdrawing groups directly influences the reactivity, enabling more precise transformations during downstream processing. We’ve seen customers favor this compound when striving for higher selectivity during substitution or coupling reactions, achieving greater yields and avoiding excessive by-product formation.
Every batch runs through a well-controlled process, monitored with the same scrutiny we would expect if we were using these materials ourselves. While many technical grade materials flood the market, we maintain narrow specifications for assay and related substances. Content purity often surpasses 99%, limiting unknown impurities and ensuring color and odor profiles stay consistent. This matters in both laboratory-scale use and commercial productions, where unpredictable impurities can interrupt entire runs or require additional chromatography.
Physical characterization is more than a checkbox. Melting point, sometimes overlooked by traders, gets our special attention, since a narrow range confirms product identifiability and supports shipment integrity. Typical batches of 3-Chloro-4-Fluorophenol appear as off-white to pale yellow crystals, a characteristic look that our experienced operators verify visually on top of instrumental analysis. Over time, we have improved our drying process to control residual moisture, something we found critical for certain coupling reactions that demand low water content.
Pharmaceutical teams usually prioritize precise site-selective reactivity, and that is where the 3-chloro and 4-fluoro arrangement provides clear benefits. The position of the halogens controls nucleophilic aromatic substitution, making this intermediate valuable for those building aryl ethers, esters, or more complex aryl scaffolds. In our ongoing supply partnerships, we often hear that its predictable reactivity profile trims down optimization time during lead compound synthesis, saving weeks of laboratory effort.
Crop protection and agrochemical research groups use this material for building active ingredients and for the preparation of advanced intermediates. The presence of both halogen atoms not only improves synthetic control but also tunes the physicochemical properties of the target molecule, such as changing solubility, lipophilicity, or metabolic stability. These small shifts can make the difference between a promising molecule and one discarded during field tests.
Some manufacturers underestimate the role of by-product minimization. Through process feedback, we’ve adapted our own synthetic route over the years, trimming out high-boiling tars and volatile by-products that tended to appear in off-patent commercialization runs. We found that maintaining a consistent batch color and crystal habit correlates directly with successful scale-up for customers, particularly those moving from pilot to full-scale manufacture.
Some buyers wonder if they could substitute with more typical building blocks, such as 4-chlorophenol or 4-fluorophenol. From our experience, single-halogenated phenols don’t always provide the selectivity or electronic effects required for modern organic synthesis. The synergistic influence of both a chlorine and a fluorine on the aromatic ring adjusts reactivity in ways single substitutions cannot replicate. It’s common to see increased ortho- and para-directing tendencies, facilitating selective reactions at specific positions.
In the context of medicinal chemistry, we have seen direct comparisons in customer programs. Simple 4-chlorophenol yields in coupling steps drop in the presence of competing nucleophiles, where the 3-chloro-4-fluoro variant holds up and reduces side-product formation. Analytical chemists often point out how the UV-visible absorbance and NMR signatures differ, which supports structure confirmation and separation steps. We often field questions about making custom analogs, but in reality, the dual-substituted core remains the most versatile for a wide range of derivatization chemistry.
An overlooked difference appears during handling and storage. Mono-halogenated phenols may exhibit instability or a slower response during purification. The dual-substituted 3-Chloro-4-Fluorophenol resists oxidation and discoloration over time, even when storage conditions are less than ideal. This has practical implications for research teams holding inventory between projects, keeping their stock usable without additional purification steps.
We learned early on that process optimization directly impacts cost, consistency, and environmental footprint. Sourcing high-quality starting materials like resorcinol or related aromatics makes a noticeable difference. We run halogenation under controlled conditions, always focusing on conversion, temperature balance, and waste minimization. Operator skill also plays its part—manual oversight at key reaction points complements automated systems and prevents batch failures.
Few realize how storage impacts safety and quality. Even stable phenols can pick up moisture or trace oxidants if exposed for long periods. Our storage protocol relies on tight-sealed, inert-lined drums or glass containers, kept cool and dry. Shipments are buffered by desiccants and vapor barriers. These measures help our product arrive at your lab or plant in good condition every time, keeping rework and loss rates low.
We regularly update our internal logistics based on customer feedback. In some regions, we've shifted from bulk shipment to multi-kilo pack sizes, reducing exposure and easing handling. This move cut down on product loss and saved time for process teams, especially those in regulated sectors. Every detail counts: label adhesive, drum lining, lot tracking, and documentation play their part in keeping downstream processes running smoothly.
3-Chloro-4-Fluorophenol gets respect in the plant, both for what it can do and for its hazards. Like most halogenated phenols, it calls for cautious handling. Through our years making and packaging it, we’ve seen how operator training, streamlined workspace design, and effective air management reduce incident risk. Most inhalation and skin contact issues stem from inattention during weighing or transfer, not large-scale leaks. Gloves, eye protection, and localized venting keep our operators and the environment safe.
We place waste management at the top of priorities. Neutralization and disposal of process residues involve regulated collection, pH control, and managed incineration. Any releases, even minor spills, receive immediate attention and thorough documentation. By minimizing waste during synthesis and packaging, we not only comply with regulations but also build customer confidence in the supply chain.
Environmental responsibility matters even before regulators point out problems. We refine our synthesis to cut high-persistence by-products and use in-plant recycling where possible. We take pride in supplying material that does not add unnecessary burden to waste streams at customer sites, particularly those operating under strict discharge permits. The reality is, small process improvements upstream translate into thousands of liters of saved solvent and lower emissions downstream.
Manufacturing specialty intermediates puts us in constant contact with customers across the globe. Requests for documentation, updated specifications, or alternative packaging modes come in regularly. Many of our process tweaks began as responses to customer challenges: minimizing dust during transfer, controlling solubility for fluid-bed reactors, or reducing dark impurities that complicated downstream purification. Our R&D team works not in isolation, but with direct feedback and data from both pilot and production scale users.
Batch history and traceability anchor our improvements. Each drum delivered carries forward a story of small changes—sometimes an extra filtration step, a tighter drying cycle, or improved wash protocols. We share those process histories openly with long-term partners, recognizing that transparency builds trust and keeps both sides aligned on quality expectations.
Open communication proved its value during volatile market swings, such as abrupt changes in feedstock prices or transportation bottlenecks through major ports. By prioritizing stable output and clear forecasting with our customers, we maintain not just orders, but long-term relationships. In our experience, staying proactive about schedule risk or quality issues earns repeat business far more reliably than the lowest bid.
Our relationship with research teams often extends beyond the point of sale. Technical dialogue goes as deep as the chemistry requires—from spectral analysis troubleshooting to suggestions for alternative reaction conditions. Academic and industrial researchers both benefit from shared process data and access to analytical profiles. We provide not just routine COAs, but full NMR, GC-MS, and, when needed, trace heavy metal screens. Our in-house chemists field technical questions directly, so responses carry the benefit of hands-on process knowledge rather than stock answers.
For development-stage pharmaceutical programs, we support reference sample requests and offer multi-gram to multi-kilo transition batches, enabling teams to validate scale-up without disruption. For new application areas—such as advanced materials or niche catalysts—we work with formulators to align purity and particle size specifications to actual end use, not simply the lowest common denominator.
In situations where researchers encounter unexpected challenges, whether a crystallization anomaly or instability during storage, our technical staff investigates actively. Adjustment of pH, exploration of solvent compatibility, or just a different drying profile have each emerged from ongoing customer dialogues. This two-way collaboration has produced some of our most robust process improvements and avoided costly reformulation projects for customers.
We watch the specialty chemical market change year to year, as applications for halogenated phenols expand. Regulatory shifts in agrochemicals and active pharmaceutical ingredient manufacturing raise the bar for quality, purity, and documentation. We’ve strengthened our in-process testing and finalized documentation to meet the evolving standards—whether state, national, or international. Consistency in supply, tight impurity controls, and willingness to partner on new program requirements underpin our approach.
Differentiation is not about being the lone supplier, but about consistency, process transparency, and genuine technical support. We track market entrants and competitive products, benchmarking our product against what’s available from others. What we see is a gap in experience and response time: many large producers distance themselves from direct customer contact, relying on paperwork instead of chemistry-driven support. We fill that gap with both reliable product and open-access expertise, making sure customers can move smoothly from bench to plant.
As downstream requirements grow more complicated, such as the move toward greener syntheses or regulatory-compliant packaging, we invest in developing new variants or delivery modes when it adds real value. Some of the latest requests include pre-weighed, sealed packaging for automated chemical feed systems and online access to batch certificates. We continue building systems that guarantee rapid, accurate, and clear delivery of both product and supporting documentation.
Long-term manufacturing has taught us to prefer practical solutions to theoretical ideals. Trials with alternative solvents, agitation methods, or different crystallization tanks have occasionally failed but more often revealed subtle ways to trim costs, improve purity, or cut cycle times. We keep logs on each process change, evaluate outcomes not just by the numbers, but by the challenges they solve for actual users. Problems like dust generation, low bulk density, or difficult dissolution inform next generation improvements.
We urge users to share observations from early trials or repeated batches, whether positive or negative. Field reports on filtration speed, batch color, or storage outcomes can uncover improvement opportunities that may not surface in controlled lab trials. Our door remains open for ongoing information exchange. Honest user feedback helps us refine both our offering and our service, setting us apart in a market where most rely on fixed specifications and one-way communication.
Our approach means learning from decades of both success and mistakes. By remaining open to change, attentive to detail, and actively partnering with each customer, we continue advancing the quality and reliability of 3-Chloro-4-Fluorophenol. The end result is not just a chemical, but a partnership grounded in shared technical standards, practical improvements, and mutual trust.