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3-Fluoro-2-Methylphenol

    • Product Name 3-Fluoro-2-Methylphenol
    • Alias 3-Fluoro-o-cresol
    • Einecs 618-452-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    853902

    Chemical Name 3-Fluoro-2-Methylphenol
    Molecular Formula C7H7FO
    Molecular Weight 126.13 g/mol
    Cas Number 461-72-3
    Appearance Colorless to pale yellow liquid
    Boiling Point 192-194 °C
    Density 1.17 g/cm³
    Flash Point 82 °C
    Purity Typically ≥98%
    Refractive Index 1.539
    Solubility Slightly soluble in water; soluble in organic solvents

    As an accredited 3-Fluoro-2-Methylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-Fluoro-2-Methylphenol, sealed with a screw cap and labeled with hazard warnings.
    Shipping 3-Fluoro-2-Methylphenol is shipped in tightly sealed containers, protected from light and moisture, and stored at controlled room temperature. Proper labeling and documentation accompany the shipment, complying with relevant chemical transport regulations. Personal protective equipment should be used when handling. Ensure the package is upright and secure to prevent leaks or spills during transit.
    Storage 3-Fluoro-2-Methylphenol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. It should be protected from light, moisture, and heat. Appropriate personal protective equipment (PPE) should be used when handling. Store under chemical safety protocols according to local regulations.
    Application of 3-Fluoro-2-Methylphenol

    Applications of 3-Fluoro-2-Methylphenol in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Fluoro-2-Methylphenol primarily for advanced synthesis sectors where its fluorinated structure and precise reactivity enable access to value-added compounds. Below are focused application scenarios reflecting real industrial deployments, with explicit reference to integration points, compliance requirements, and downstream product outcomes.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    This raw material enters pharmaceutical routes as a key fluorinated building block in heterocycle assembly, offering specific substitution patterns critical for structure-activity relationship (SAR) optimization. Medicinal chemistry groups employ it in multi-step syntheses for selective inhibitors, anti-infective scaffolds, and oncology candidates. Workflow typically involves nucleophilic aromatic substitution (SNAr) or Ullmann-type couplings, where the methyl and fluoro signatures direct reactivity and later derivatization steps.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Part II
    • USP/NF monographs for relevant intermediates
    • REACH Annex XVII, if supplied to EU-based pharma sites

    Typical usage ratio

    • Variable, typically 0.2–1.5 molar equivalents relative to target intermediate; precise ratio determined by stoichiometry and route efficiency.

    Downstream process integration

    • Charged at initial or intermediate coupling stages of API synthesis; involvement spans aromatic halide substitution or phenol-directed transformations prior to late-stage derivatization.

    Final product types

    • Oral solid APIs containing fluorinated aromatic motifs
    • Active molecules for oncology, anti-inflammatory, or CNS disorders
    • Key intermediates for patent-protected drug substances

    2. Agrochemical Synthesis for Herbicide and Fungicide Actives

    Chemical crop protection firms utilize this building block for synthesizing specialty actives where ortho-fluoro substituted phenols are responsible for enhanced metabolic stability and field longevity. The compound integrates into downstream processes employing phenolic etherification or acylation to achieve N-heterocycle frameworks, subsequently transformed into field-tested agrochemical agents.

    Industry compliance standards

    • FAO/WHO specifications for pesticide actives
    • ISO 9001:2015 for agrochemical manufacturing
    • REACH registration and CLP requirements (Europe)
    • US EPA active ingredient disclosure and tracking

    Typical usage ratio

    • 1.0–2.5% by weight in target reaction mass, adjusted to ensure conversion with minimal residuals and compliance with impurity thresholds.

    Downstream process integration

    • Reacted during initial condensation or cyclization steps forming the aromatic core; involved in batch and continuous-flow synthesis units for active ingredient production.

    Final product types

    • Selective herbicides with fluorinated phenol groups
    • Fungicidal agents with ortho-fluoro aromatic features
    • Stabilized agrochemical technical-grade concentrates

    3. Monomer and Modifier in Advanced Polymerizations

    In specialty polymer and resin manufacturing, formulators employ this raw material to introduce rigid, thermally stable, and fluorinated aromatic segments. It acts as a co-monomer or chain stopper in polyaryl ether, polyamide, and advanced fluoropolymer syntheses, delivering targeted dielectric, hydrophobic, and process-resistance coefficients required for electronics, membranes, and filtration applications.

    Industry compliance standards

    • UL 94 (Flammability safety for polymers used in electronics)
    • IEC 61249 for halogen content limits in laminates
    • ISO 9001:2015 for specialty chemical manufacturing
    • RoHS Directive (2011/65/EU) for electronics-related use

    Typical usage ratio

    • 0.5–5.0% by mass as a reactive modifier or co-monomer, tailored depending on final property requirements and backbone composition.

    Downstream process integration

    • Fed into polycondensation or polyaddition reactors; dosing controlled based on molecular weight targets, reactivity indices, and minimization of free monomers in the cured resin system.

    Final product types

    • Printed circuit board (PCB) laminates with low dielectric loss
    • Membranes for corrosive filtration systems
    • High-performance insulation films with enhanced weather resistance

    4. Fine Chemical Intermediate for Aryl Fluorination and Specialty Aromatic Derivatives

    Producers of dyes, UV absorbers, and aroma chemicals integrate this fluorinated raw material in signature aryl fluorination strategies. It allows for precise positioning of fluorine in the molecular structure, which is essential for achieving unique spectral absorption coefficients or olfactory notes in end products. Typical downstream steps involve controlled oxidation, nitration, or sulfonation, yielding final chemicals with defined fluorinated profiles.

    Industry compliance standards

    • ISO 17025 (testing and certification of specialty chemicals)
    • ETAD Responsible Care (for dyes and pigments)
    • IFRA Code of Practice (for flavor and fragrance intermediates, where relevant)
    • REACH registration according to annual tonnage supplied

    Typical usage ratio

    • 0.3–2.0 equivalents depending on downstream aryl substitution pattern; adjusted based on subsequent transformation and purity targets.

    Downstream process integration

    • Dosed into electrophilic aromatic substitution or oxidation units; sequence tailored to final product’s required substitution pattern and color/UV properties.

    Final product types

    • UV stabilizers for plastics and coatings
    • High-purity dyes with enhanced fading resistance
    • Fragrance and aroma intermediates featuring fluorinated aromatics
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    Certification & Compliance
    More Introduction

    3-Fluoro-2-Methylphenol: Practical Advantages in Modern Synthesis

    Understanding Our Chemical Craft

    Producing 3-Fluoro-2-Methylphenol has given us front-row insight into how subtle structural changes lead to dramatic differences in end-use applications. This compound, sometimes pegged under CAS number 2352-18-1, routinely helps drive innovation and refinement in specialty synthesis. We’ve witnessed the ways in which a methyl group at the ortho position and a single fluorine at the meta position create more than just a small adjustment to a phenolic backbone—they open new pathways for efficiency, reactivity, and adaptability.

    Specification Details and What They Mean

    Our batches of 3-Fluoro-2-Methylphenol register high purity, typically upwards of 98% by HPLC, with water content kept low, usually below 0.2%. As with all intermediates leaving our reactors, trace byproducts and unreacted starting materials calling for further purification rarely arise, but when they do, we catch them before packaging. Rigorous GC and NMR analysis supports our in-house quality controls; this attention to analytical clarity prevents downstream surprises for customers relying on sharp consistency.

    Liquids such as this phenol derivative carry a recognizable melting point if crystallized, often near 24–28°C, and a boiling range around 195–198°C at atmospheric pressure. The pale yellow appearance signals a clean product free from unnecessary tints or residues, with minimal odor outside what’s expected from phenolic compounds. We standardize every drum and small package by re-examining reactivity and confirming the absence of common organic impurities, which helps downstream users avoid costly reprocessing.

    Efficiency for Pharmaceuticals and Agrochemicals

    The pharmaceutical sector seeks compounds with ortho and meta functionalization, and we see the demand for 3-Fluoro-2-Methylphenol stay steady as a precursor in the development of next-generation APIs and their intermediates. Medicinal chemists, aiming to manipulate electron density or metabolic resistance, choose fluorinated rings for improved bioavailability and metabolic stability. Our clients often use this product as a step in building core fragments of selective kinase inhibitors or antiviral scaffolds; adding both methyl and fluorine influences both the pharmacokinetic and pharmacodynamic profiles.

    In crop protection, formulating molecules for optimal pest resistance rarely happens through one-step solutions. The electron-withdrawing fluorine group paired with a methyl provides performance advantages—stability against environmental degradation and tailored lipophilicity for targeted action. It bridges the demands for potency with environmental safety, allowing formulation teams to dial in specific application profiles without escalating costs or regulatory hurdles.

    Improved Performance: What Makes This Molecule Stand Out

    Fluorine doesn’t just add novelty to the ring. Our chemists have studied its impact on hydrogen bonding, acidity, and solubility. By installing a fluorine at the 3-position and a methyl at the 2-position, reactivity toward electrophilic aromatic substitutions shifts compared to simple phenol or cresol isomers. This opens doors in constructing ether, ester, or carbamate derivatives where positional selectivity must be tightly controlled. As a result, researchers working along the value chains for dyes, materials, and coatings select 3-Fluoro-2-Methylphenol for proprietary reactions that fail with less selective options.

    Regular methylphenol (commonly called cresol) or other mono-fluorophenols often fall short in these procedures. Either their reactivity is misaligned with catalyst or solvent systems, or downstream protection/deprotection schemes become too expensive. Our compound’s dual functionality—electron-withdrawing and donating—contributes to brevity in multi-step reactions, reducing wasted materials and manufacturing time.

    Reliable Supply: Mitigating Market Fluctuations

    Customers often voice concern about erratic availability and variable quality. Having built our infrastructure with redundancy, our team scales batch volumes in response to confirmed demand, always maintaining raw material reserves to avoid downtime. We learned early that running just-in-time with an intermediate as nuanced as 3-Fluoro-2-Methylphenol invites risk; we choose not to cut corners, instead prioritizing resilient supply chains.

    On more than one occasion, global events or regulatory shifts disrupted the routes others use to access similar intermediates. By refining our own synthesis pathway—eschewing hazardous reagents where possible, investing in closed-loop handling, and fine-tuning reaction conditions to squeeze every kilogram—we've kept both reliability and competitive cost structures intact. Shipping stability, storage compatibility, and ease of transfer into your existing workflows remain top-of-mind in every design tweak we make.

    Real-World Handling: From Our Facility to Your Lab

    The practical side extends to logistics. Drums and smaller containers we use for 3-Fluoro-2-Methylphenol avoid excessive handling hazards. Material remains free-flowing, resists premature polymerization, and maintains long-term shelf life under standard indoor conditions. We clearly label, double-check for container compatibility, and coordinate with freight partners experienced in both small-lot and tonnage transport. Our in-house storage—climate-controlled and isolated—prevents cross-contamination.

    Feedback from formulation and pilot plant teams around the globe guides every upgrade we implement. Whether it’s optimizing pourability for high-throughput synthesis or refining thresholds for detection of trace solvents, each adjustment feeds back to our next batch. That loop tightens every year, shaving down complaint rates and boosting end-user confidence. The collaboration doesn’t stop after shipment leaves our dock.

    Supporting Regulatory and Sustainability Demands

    Pushing forward on compliance, we document every step—not just in broad-strokes marketing, but granularly, molecule by molecule. Our environmental monitoring confirms that each run produces minimal vent emissions and manageable liquid wastes. Tight recycling protocols for solvents and cleaning reagents let us offer assurance that each liter supplied not only meets technical grades but leaves a lighter footprint than legacy chemical processes.

    Regional and global authorities place increasing scrutiny on trace impurity profiles, especially for building blocks touching human health or food production. We’ve invested in routine batch testing for regulated substances and can supply detailed impurity breakdowns on request. Our experience walking through site audits from major multinational customers, and collaborating on their registration dossiers, means faster onboarding and less lost time validating new suppliers.

    Customers have signaled growing interest in greener synthetic options. Drawing on our R&D, alternative routes now reduce hazardous waste and improve raw material efficiencies. As our purchasing partners move toward carbon accounting, our documentation simplifies their reporting, setting the stage for both ongoing partnership and mutual recognition of responsible production.

    What Matters: Customer Experience Sets Direction

    The true test comes not only from laboratory spec sheets but in real-world consistency and support. End users crafting grams or scaling up to metric tons depend on stable melting and boiling points, tight GC purity, and responsive technical backup. We don’t just hear about problems after the fact; regular dialogue means we learn what is working and where process pain points crop up. Over time, many users return with requests to expand use into new verticals—dyes, OLEDs, or specialty polymers—trusting our transparency and willingness to tweak parameters as their needs evolve.

    Some manufacturers stick rigidly to legacy batch sizes, but we built semi-continuous lines capable of meeting lab-scale startups and full commercial quantities without major interruptions. For new project launches and pilot-scale demonstration, our technical staff adjust solvent profiles, impurity targets, and even packaging volume to help clients get up to speed quickly. Once running, we offer seamless transition into long-term supply contracts, passing along logistical learning so fresh operators get up to speed with minimal handholding.

    Comparing 3-Fluoro-2-Methylphenol with Other Isomers and Analogues

    Newcomers sometimes group phenol derivatives without appreciating how a fluorine-methyl combination affects reactivity. Compared against 3-Methylphenol or 2-Fluorophenol, our product delivers unique advantages. The methyl group at position 2 activates the ring, increasing ortho-para reactivity for certain transformations. The 3-fluorine stabilizes metabolic liability, key in pharma and agro applications. Together, they strike a balance between electron donicity and withdrawal, assisting site-selective functionalization where simple mono-substituted rings lag behind.

    Differences continue into downstream processability: the body of evidence from our labs and user facilities highlights how other cresol or fluorophenol isomers may require harsher conditions, risk side-product formation, or fail to achieve clean conversion yields. By contrast, 3-Fluoro-2-Methylphenol enables milder, more efficient conditions, and reduces waste handling costs. As process industries face rising pressures from both regulators and their own management to minimize energy input and maximize extraction efficiency, this compound continues to outperform.

    Solubility profiles, refractive indices, and volatility under typical reaction conditions—each parameter has driven users to select our material over less tailored options. In practice, it holds its own in small-scale R&D as well as integrated multi-ton campaigns; we see little need to force customers into rigid volume tiers, preferring instead to track evolving projects and scale accordingly. For users working in tight control range chemistries, our compound’s reproducibility saves both time and rework on the bench.

    Building the Path Forward: Lessons from the Production Floor

    Our shift operators know the steps by heart—each charge, each purification, each drying protocol. Over the years, we’ve trained team members on the origins of process upsets and how prompt in-process checks prevent deviation. Regular root cause analyses of even the rarest off-spec batch keeps the discipline sharp. Only by maintaining direct control from raw material warehousing through finished goods release do we retain the flexibility to make small-batch customizations. It’s a hands-on operation, informed by historical runs and shaped daily through collaboration across production, QA, and shipping.

    Sourcing high-quality starting materials took years to perfect. Direct relationships replace opaque market chains, and we maintain deep reserves to guarantee ongoing runs. Efficient energy management practices—heat recovery, energy tracking, and smart scheduling—further anchor production against rising labor and utility costs. It’s a dynamic landscape, and every lesson feeds back into new investments and efficiency upgrades.

    Committed to Progress: Ongoing Refinements Meet Real Demands

    3-Fluoro-2-Methylphenol isn’t just a product; it’s the outcome of countless decisions that prioritize customer needs and technological progress. Real-world experience teaches us that manufacturing excellence comes not from theoretical optimizations, but hands-on troubleshooting, informed adaptation, and constant communication with users at all stages of the value chain. As regulations tighten and performance standards rise, we find new ways to stretch capacity, sharpen analytical precision, and minimize unwanted byproducts—all while balancing the imperatives of cost, sustainability, and safety.

    Every batch represents an investment of time, learning, and care. Our sales and technical teams support project launches, trouble-shoot unexpected results, and respond rapidly to questions about process adjustments or impurity profiles. This continual exchange of expertise lets us improve not only the product itself, but the entire customer experience. As we look forward, evidence from both laboratory trials and commercial-scale campaigns reinforces one clear message: the careful crafting of 3-Fluoro-2-Methylphenol drives advances across diverse fields, and we are committed to being a reliable partner as your science progresses.