Anhui Liwei Chemical Co., Limited
Products

Phenol, 4,5-Difluoro-2-Methyl-


    • Product Name Phenol, 4,5-Difluoro-2-Methyl-
    • Alias 4,5-Difluoro-2-methylphenol
    • Einecs 407-290-0
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    120848

    Chemical Name Phenol, 4,5-Difluoro-2-Methyl-
    Molecular Formula C7H6F2O
    Molecular Weight 144.12 g/mol
    Cas Number 412-87-3
    Appearance Colorless to pale yellow liquid
    Melting Point 27-29°C (estimated)
    Density 1.3 g/cm³ (approximate)
    Solubility In Water Slightly soluble
    Flash Point 88°C (estimated)
    Refractive Index 1.520 (approximate)
    Smiles Cc1cc(F)c(F)cc1O
    Inchi InChI=1S/C7H6F2O/c1-4-2-5(8)6(9)3-7(4)10/h2-3,10H,1H3
    Pubchem Cid 177370
    Pka Approx. 9.7

    As an accredited Phenol, 4,5-Difluoro-2-Methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for **Phenol, 4,5-Difluoro-2-Methyl- (25 grams)** is a sealed amber glass bottle with a secure screw cap.
    Shipping Phenol, 4,5-Difluoro-2-Methyl- should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must comply with applicable hazardous material regulations, using appropriate labeling and documentation. Store and transport in a cool, ventilated environment, away from ignition sources. Specialized packaging may be required depending on quantity and destination.
    Storage Store **Phenol, 4,5-Difluoro-2-Methyl-** in a tightly closed container, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizing agents. Keep in a cool, dry, well-ventilated area, protected from moisture. Ensure containers are properly labeled, and limit exposure to air. Use secondary containment to prevent spills, and store away from food and drink. Handle using appropriate personal protective equipment.
    Free Quote

    Competitive Phenol, 4,5-Difluoro-2-Methyl- prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@liwei-chem.com

    Get Free Quote of Anhui Liwei Chemical Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Phenol, 4,5-Difluoro-2-Methyl—An Essential Intermediate from the Manufacturer’s Bench

    A Practical Introduction from the Chemists Behind the Drums

    Working hands-on with fine chemical synthesis every day, I have developed a particular respect for specialty substituted phenols like Phenol, 4,5-Difluoro-2-Methyl-. Fluorinated aromatic compounds do not roll off the assembly line by accident; they need precise attention from raw material handling to final filtration. This specific molecule has carved out a respected spot among building blocks for crop-protection agents, advanced pharmaceutical leads, and modern materials research. The subtle effects a pair of fluorine atoms and one methyl group can have, compared to other phenols or fluorinated benzenes, still fascinates me. Beyond paper theory, these variations deliver changes across reaction outcomes, end-product properties, and scale-up reliability.

    Manufacturing Approach: Refining Reactivity and Purity

    Producing 4,5-Difluoro-2-Methylphenol means more than following reaction recipes. It all starts with secure sources of key starting materials—usually methylated and fluorinated aromatics, whose supply chains we manage for both purity and consistency. Even minor impurities in precursors can create headaches downstream. Careful temperature controls, choice of halogenation sequences, and the timing of methyl addition steer the reaction toward the desired structure while limiting over-fluorination or ring rearrangements. Throughout this process, by-products demand close attention; even slight contamination with mono- or trisubstituted impurities will show up in the analytical profile.

    Our team screens each lot by NMR, GC-MS, and HPLC—not just for regulatory paperwork but to ensure the compound behaves as expected for our customers. These practical steps allow us to support scale-up confident that what left the reactor matches the intended connectivity and purity. Such vigilance is not optional in today’s regulated markets; we have seen numerous synthetic routes fail at the bench scale because a shortcut led to “good enough,” only to find trace by-products scramble customer R&D downstream.

    Physical Traits in Practice

    Among the family of difluorophenols, this 4,5-difluoro-2-methyl variant stands out for a specific melting range and a recognizable, sharp aromatic odor. Its solubility profile lands somewhere between the more hydrophobic trifluorophenols and simpler phenolic starting materials, landing as partially soluble in water yet well tolerated in ether, dichloromethane, and most polar aprotic solvents. This difference shapes both application and handling—we select reactors and transfer lines that resist both acidic and organic fouling, and our on-site air handling controls any vapor emissions.

    Experience shows that pure lots display a crisp white crystalline or pale solid appearance, which helps catch process deviations before analytical confirmation. If a batch appears off-color or sticky, that usually signals either trace oligomerization or accidental over-fluorination, both of which our QC technicians resolve before shipping. Customers in pharmaceuticals often need material below certain heavy-metal thresholds; we track this by using reactors and workup glassware designed to minimize metal leaching.

    Comparison to Similar Products

    Having synthesized dozens of phenolic derivatives, the addition of two fluorines at the 4 and 5 positions and a methyl at position 2 on the ring changes everything—from acidity to nucleophilicity. Simple phenol or monofluorophenols might dissolve more readily in water or react faster with acyl chlorides, but their metabolic stability and electron density do not align with what the difluoro-2-methyl group brings. Many groups try 3,5-difluorophenol for certain agrochemical scaffolds and find that the 4,5-difluoro-2-methyl analog produces markedly different yields or selectivity in downstream reactions. Sometimes a one-atom shift in position makes the difference between a useful intermediate and a dead end. Clients developing active pharmaceutical ingredients or high-performance coatings often demand this exact substitution pattern for its impact on hydrogen bonding and metabolic routes.

    Our custom synthesis chemists see, in real time, that substitution patterns do not exist simply to "check a box"—they serve as a practical determinant for reactivity and biological compatibility. This material blocks unwanted metabolic oxidation at specific points on the ring, letting formulators push their leads further in both early- and late-stage research. Certain projects have tested both 2,4- and 4,5-difluoro analogs and confirm that the latter’s steric profile opens up coupling opportunities that never succeed otherwise. We document and share these real-world application results with our partners, offering not just a product, but also manufacturing and synthetic insights that save time downstream.

    Applications in Our Clients’ Workflows

    Crop protection labs often rely on this molecule when developing new herbicide scaffolds or fungicidal leads. Its resistance to metabolic degradation, introduced by the gem-difluoro motif, ensures that actives last longer in the field and require lower application rates per hectare. We have supported several multinational agchem companies as they pivot their synthetic routes toward these difluorinated phenols to avoid rapid soil or sunlight breakdown. They see real differences compared to plain methylphenols or even monofluoro analogs—difluorination toughens the molecule for harsher environmental exposures.

    In pharmaceutical research, our partners often insert this compound into screening libraries aiming for CNS-active drugs, anti-infectives, or enzyme inhibitors. Our hands-on process design guarantees material with controlled moisture and halide content, as even small amounts of HCl or water can interfere with sensitive downstream reactions or biological tests. Several innovative APIs, still confidential under current NDAs, have adopted 4,5-difluoro-2-methylphenol to confer both lipophilicity and metabolic shunt resistance. Scientists keep coming back to the same chemistry—wherever improved blood-brain barrier penetration or metabolic stability is essential, this molecule ends up on the test list.

    Beyond life sciences, materials research teams use this compound as a precursor for high-performance polymers and liquid crystal displays. Polyaromatic resins incorporating this difluorinated phenol offer increased glass transition temperatures, improved dielectric properties, and robust UV stability without extensive post-synthesis modification. We have provided tons-scale lots for clients reworking their resin compositions, often troubleshooting together to develop workup procedures that retain the delicate substitution and avoid ring-defluorination under high heat.

    Hands-On Quality Control and Batch Consistency

    Where analytical certificates end, our on-site experience begins. In practice, tight pH adjustment during extraction, careful solvent drying, and immediate product isolation lead to smaller impurity tails and more consistent lots—something our clients appreciate when moving from bench to kilo scale. Time and again, I see the difference when chemists actually run trial reactions with small samples; batches handled inattentively yield less product, cause pressure spikes, or foul test reactors by mid-reaction.

    To ensure performance across diverse projects, every production cycle starts by revalidating analytical standards. Old standards can degrade or react, shifting spectra and confusing interpretation. We maintain up-to-date calibration batches and run parallel tests—ironically, some of the most meaningful quality feedback comes directly from our repeat customers who spot trace off-types or color changes in a batch before instruments confirm it. We view such dialogue as a lifeblood of continual improvement.

    Scale-Up Nuances Only a Manufacturer Notices

    Something R&D chemists rarely experience is the process drift possible when moving from flask to reactor. Solvent choice, agitation rates, and even the nature of fluorination reagents all demand revision with increased volume. We never scale from milligram to production runs in one step; there is always a sequence of intermediate builds, staged to watch for exotherm management and side-product formation. We have seen how a seemingly minor change in quench order can yield excess tar or color changes—lessons we have documented and share openly with clients considering custom synthesis or technology transfer.

    Continuous improvement in batch size also means examining filtration, drying, and packaging. Fluorinated phenols can volatilize or adsorb to filters if not treated sympathetically. We design drying cycles to retain product profile and avoid excessive heat, which may drive off one of the substituents or introduce yellowing from ring-opening by-products. Our product ships in sealed, inert gas-purged containers, with inert liners to resist both acidity and occasional residual reactivity.

    Worker and Environmental Safety, Informed by Practice

    Fluorinated aromatics, including our 4,5-difluoro-2-methylphenol, call for special stewardship at every production step. The volatility and odor of this class means our people wear full-face respiratory protection, especially in large-scale charge-ups. Our site ventilation and air scrubbing systems remove any off-gassing before it leaves the plant. Our liquid and solid waste collection protocols ensure no volatiles or residues enter drains or ground, using incineration approved for halogenated residues. We provide practical, updated safety training directly from workers’ own handling experience, not just hazard sheets. Regular feedback from those charged with routine cleaning and drum packing gives us new ideas for safer procedures.

    Environmental regulations demand compliance documentation for every kilogram produced or shipped. Our routine audits track process waste output, recycle streams, and endpoint chemical fate, in line with national and global reporting. We maintain open logs of exposure events and process deviations, approaching each as a learning tool. Over years of operation, we have built up reliable draining and quench setups that let us neutralize acidic process streams without introducing fire risk or excessive fumes.

    Sourcing and Customer Collaboration—A Manufacturer’s Philosophy

    As a producer, we view every order for 4,5-difluoro-2-methylphenol not as a transaction but as an engagement. Connecting with the scientists or engineers who will use this material guides our planning, from scheduling campaign runs to setting aside tight-spec batches for urgent R&D needs. We share not only product but experiences—practical tips for dissolving, weighing, or integrating the compound into larger syntheses. Clients often invite us into troubleshooting, especially during process validation or pilot plant commissioning.

    Regular communications, sometimes on short notice, let us align our next production campaign with emerging demands. During peak project surges, we can adjust vessel schedules to ensure just-in-time delivery, saving clients costly downtime or last-minute substitutions. In one instance, a global agchem partner flagged a new impurity detected at their site, and we mobilized our analytical team to recreate their findings, refine the purification, and supply a clean batch within that quarter.

    Continuous Innovation in Synthesis Methods

    Our R&D team constantly revisits the chemistry behind 4,5-difluoro-2-methylphenol. Even small advances—switching from batchwise to continuous flow addition, or trialing greener fluorination reagents—make significant impacts on safety and sustainability. Recent years brought in newer supported catalysts that allow for lower waste, reduced energy needs, and improved yield reliability. Each improvement goes into our procedural notes and gets cross-validated within the team before global roll-out.

    In direct partnership with universities and technology developers, we sponsor studies that identify next-generation routes for difluorinated aromatics, looking to phase out older, riskier reagents. Results allow us to offer both “standard” and “green” options for scale-up clients. Not all new chemistry wins on its first try, but this spirit of experimentation means better process resilience and, often, lower environmental burden.

    What Sets Our 4,5-Difluoro-2-Methylphenol Apart

    Feedback from formulation chemists, scale-up engineers, and regulatory teams across industries tells us this molecule stands apart in its performance reliability. While alternative phenols might lower raw material cost or slightly simplify transport, the uniquely substituted 4,5-difluoro-2-methyl ring has no direct substitute for most of its applications. Reliable purity, verified batch-to-batch consistency, and chemical expertise form the core values we bring. A trader or reseller can list the product, but only those with hands directly in the chemistry can guarantee optimized production and honest technical support.

    This approach underscores not just what the product is, but how it performs where it matters: on our client’s bench, in reactors and analytics, absorbed into project pipelines with minimal deviation from expected outcomes. And our commitment extends beyond simple supply—through dialogue, technical documentation, cross-validation of analytical data, and ongoing refinements, we build real partnerships grounded in applied chemistry.

    Partnering for the Long Run

    We encourage project leaders, process developers, and chemists aiming to push boundaries with high-substitution phenols to draw from real manufacturing experience. Challenges often arise in practice—odd clumping in a powder, vessel fouling, or compatibility issues with specialized solvents. Our background in hands-on production and continuous improvement equips us to solve such problems. Working together, from exploratory batches to commercial roll-out, enables all parties to anticipate hurdles and address them before they compromise scale or product integrity.

    With every lot, we verify not just chemical but practical readiness, supplying supporting technical data, shipping advice, and, critically, field-tested handling instruction. Over years in the specialty aromatic business, we have seen how upstream vigilance turns into downstream savings—through higher yields, fewer batch failures, and, ultimately, better-performing final products for the world’s labs, fields, and factories.