Anhui Liwei Chemical Co., Limited
Products

Phenol, 4-Chloro-2-(Trifluoromethyl)-


    • Product Name Phenol, 4-Chloro-2-(Trifluoromethyl)-
    • Alias 4-Chloro-2-(trifluoromethyl)phenol
    • Einecs 221-158-7
    • 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

    467567

    Chemical Name Phenol, 4-Chloro-2-(Trifluoromethyl)-
    Cas Number 393-06-8
    Molecular Formula C7H4ClF3O
    Molecular Weight 196.55 g/mol
    Appearance White to off-white solid
    Melting Point 34-36°C
    Boiling Point 204°C
    Density 1.47 g/cm3
    Solubility In Water Slightly soluble
    Synonyms 4-Chloro-2-(trifluoromethyl)phenol
    Refractive Index 1.517
    Pubchem Cid 14306

    As an accredited Phenol, 4-Chloro-2-(Trifluoromethyl)- 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 100 grams of Phenol, 4-Chloro-2-(Trifluoromethyl)-, securely sealed with a screw cap and labeled.
    Shipping **Shipping Description:** Phenol, 4-Chloro-2-(Trifluoromethyl)- should be shipped in tightly sealed containers, protected from light and moisture. Transport must comply with local, national, and international regulations for hazardous chemicals. Use appropriate labeling for toxic and corrosive substances. Handle with care to prevent leaks or spills, and avoid exposure to heat or ignition sources.
    Storage Store **Phenol, 4-Chloro-2-(Trifluoromethyl)-** in a cool, dry, well-ventilated area away from heat, ignition sources, and incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and clearly labeled. Protect from moisture and direct sunlight. Use corrosion-resistant shelves, and provide secondary containment to control leaks or spills. Store under local regulations and safety guidelines.
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    Certification & Compliance
    More Introduction

    Phenol, 4-Chloro-2-(Trifluoromethyl)-: Practical Experience from Our Chemical Plant

    Understanding the Product Through Experience

    Working on site with compounds like 4-Chloro-2-(Trifluoromethyl)phenol, you learn to appreciate nuances that data sheets can’t capture. This molecule, bearing a chlorine atom in the para position and a trifluoromethyl group in the ortho position to the hydroxyl, stands apart from classic phenolics. Over years in production, we’ve seen not just the appeal of its unique reactivity, but also how subtle changes in structure impact function, safety, and ease of handling.

    Observing Key Specifications in Everyday Practice

    Our team targets production to meet precise assay, moisture, and impurity levels, and over time you realize how these specification numbers draw their importance from regular laboratory routine and customer feedback. Phenol, 4-Chloro-2-(Trifluoromethyl)-, whether provided as a white to pale yellow crystalline solid, expects a high level of purity—often above 98% by GC or HPLC—since trace side-products can introduce off-odors or interfere with finished applications. We track melting point ranges between 54°C and 58°C, confirming batch consistency and watching for subtle shifts that hint at lots that need reworking or additional purification.

    Handling this compound over the years, we’ve prioritized minimizing water and low-boiling impurities, favoring moisture levels below 0.5%. Crystals from well-controlled reactions yield a product easy to recrystallize, avoiding laborious chromatographic steps. We’ve learned how crucial this is for downstream users: fewer residual solvents, less waste, easier incorporation into synthesis workflows. Attention to these details raised customer trust and set a practical benchmark against which new lots are measured.

    The Value of Chemical Substitution: Where It Really Counts

    Chemists often substitute trifluoromethyl and chloro groups to tune physical and chemical properties, and you see this play out with 4-Chloro-2-(Trifluoromethyl)phenol. Unlike simple phenols, this compound resists microbial degradation and shifts solubility compared to unsubstituted relatives. It doesn’t just tweak lipophilicity on paper; it creates tangible changes in how formulations behave, especially where stability matters. Over years of scaling up and down, countless test runs have shown this molecule stands its ground when used in agrochemical research and select pharmaceuticals as a synthesis intermediate.

    The presence of a trifluoromethyl group, for example, reduces chances for unwanted oxidation during storage, compared to a plain phenolic. The chlorine further helps in controlling electron density across the aromatic ring, giving reaction chemists a more predictable substrate for substitution, cross-coupling, or further derivatization. These real-world improvements translate to fewer headaches for people working at the bench in both discovery and scale-up chemistry.

    Main Uses as Shaped by Demand and Feedback

    Watching the flow of orders and hearing from those who work with this product in the field, it’s clear where demand clusters. We’ve seen most of our volumes sent into projects involving crop protection agents, intermediates for actives in herbicides or fungicides, and, on occasion, into fine chemicals for specialty electronics. In every case, the draw isn’t just the name on the label. Customers pick this compound over other halogenated phenols because its combined substation pattern introduces both hydrophobicity and electron-withdrawing effects. This leads to intermediates less vulnerable to overoxidation or photolysis, compared to those with methyl or alkoxy substitutions only.

    Researchers appreciate a compound that behaves predictably under reaction conditions—hence our ongoing focus on controlling impurity profiles batch after batch. In custom work, contract manufacturing, or collaborative development, even minute differences in impurity profiles matter. Knowing this, we continually invest in improved purification steps and quality monitoring to minimize cross-lot variability. No technical sheet could substitute for years of post-delivery tech support calls. Always, feedback from application chemists drives the refinement of both process and product.

    Distinguishing Yourself in an Overlapping World

    Those unfamiliar with actual production might think all phenolic intermediates are more or less alike—just swappable puzzle pieces. Experience said otherwise. Even small changes—like swapping a trifluoromethyl for a simple methyl—transform melting behavior, solubility, and reactivity in ways that matter in real process settings. With 4-Chloro-2-(Trifluoromethyl)phenol, our crew has watched formulation teams succeed with this product where others failed, especially when stability, shelf life, or downstream purification challenged them. In electronic materials, for example, the resistance to thermal degradation becomes more than a bonus—it's fundamental.

    Customers regularly compare this compound to related phenols having only chloro or only trifluoromethyl groups. In every evaluation, the dual substitution route emerges as a practical balance: managing cost, shelf-stability, and chemical resilience, without the aggressive reactivity or environmental persistence seen from heavier halogenation. The structure delivers a manageable toxicological footprint, making it better suited for research and development contexts where regulatory pressure is strong but not prohibitive.

    Working with the Product: Safety and Handling Lessons from Direct Use

    Handling phenol derivatives is never risk-free, but walking the plant floor and seeing the material's behavior under routine handling has taught us where extra caution pays off. Trifluoromethylated phenols, including this one, release limited phenolic vapor under ambient conditions, provided the storage area stays cool and dry. Unlike more volatile halophenols, bulk releases remain rare if basic protocols get followed: closed systems, modest ventilated enclosures, and smooth transfer lines. Workers in shipping and storage learned to expect occasional phenolic odor if seals get broken, reinforcing the need for checked containment.

    Historical experience showed that prolonged skin contact with even low-level melt, or inhaling dust from a faulty grinder, can cause irritation. Routine use of gloves and goggles simply became standard—not as a legal checkbox, but from everyday risk management. During scaling or reworking off-spec lots, we found that keeping water out avoids hydrolysis or formation of unwanted byproducts. Dry nitrogen overlays in containers, especially for lots awaiting extended transit, have never failed us in preserving product quality.

    Responsible Manufacturing and Environmental Pressures

    Deciding to make 4-Chloro-2-(Trifluoromethyl)phenol at scale did not come lightly. The fluorine-rich intermediates present their own set of environmental and process challenges. Fluorinated byproducts resist typical degradation steps, so over the years we invested in closed-loop solvent recovery and oxidative waste treatment units—capable of breaking down or recapturing fluorinated organics. These measures weren’t tacked on for compliance, but because neglect led to off-odors, emission events, or, at worst, costly interruptions and regulatory scrutiny.

    Our crew faced ever-tightening discharge rules, particularly for trace phenols and perfluorinated remnants. Experience taught us that even with the best in-plant containment, accidental releases threaten both air and water around the facility—not just distant regulators. We’ve used feedback from environmental monitors and onsite safety audits to refine both upstream processes and endpoint waste treatment, proving that manufacturing this compound responsibly makes sense not just ethically but economically.

    Producing trifluoromethylated aromatic compounds also comes with scrutiny over raw material sourcing. It’s no secret that some fluorinated building blocks carry reputational and supply chain risks. Making this product over the years has meant developing practical alternatives, qualifying multiple suppliers, and occasionally recycling fluoroaromatic residues in our own back end. These efforts bring long-term price stability and make our plant less vulnerable to global disruptions.

    Sustaining Quality Through Real Process Control

    Maintaining steady output with this compound has never been a matter of flipping a switch on a flow reactor. Minor tweaks in solvent ratio, temperature, or even agitation alter not only yield but also crystal habit and impurity carryover. Operators noticed that lots run during peak summer humidity differ from winter shifts, requiring on-the-fly adjustment of drying and packaging steps. Investing years in pilot-scale refinement, staff training, and inline monitoring, the team managed to keep batch-to-batch differences minimal enough to please even the most demanding downstream partners.

    Regularly, our QC staff faces the challenge that GC or HPLC methods drift slightly with new columns or solvent lots. Keeping validation procedures tight backs up any claim we make in sales meetings, but it’s actually the daily attention to calibration, reference standards, and analytical troubleshooting that underpins long-term trust. Advice from users, sometimes drawn from headaches over reactivity or differences in melt, directly impacts how we change process parameters and update internal acceptance criteria.

    Improvement Driven by Field Application Experience

    Product development rarely runs in a straight line. Every handful of batches, our technical support lines ring with new questions about formulation haze, batch compatibility, or reactivity anomalies. We learned early that documentation alone can’t solve this. Instead, sharing real incident reports—such as how a user resolved clumping by switching to a dryer lot, or how another eliminated unwanted color run by storing below 20°C in low humidity—proved far more helpful. These field lessons cycle back into process tweaks, driving upstream adjustments like slower solvent removal steps or deeper pre-pack checks.

    Direct feedback has shown that some users working with high-value intermediates need tighter than typical moisture, color, or particle size specifications. In response, we’ve set aside some production capacity for custom grading and special filtration, since even trace dust or agglomerates matter in final compound synthesis. Such flexibility requires significant operator training and investment in manual inspection—unusual in today’s fully automated plants—but pays off in reduced claims and higher repeat orders.

    End users frequently care less about generic purity numbers and more about reliability from lot to lot. If an unexpected impurity appears once, it creates suspicion that rarely goes away. We learned to monitor and report not just “main” impurities but also those minor, characteristic trace components that reveal themselves only after repeated scale-up cycles. Transparency wins more business in the long run than alloying or disguising inconvenient defects.

    Comparing to Other Phenolic Intermediates—What Stands Out

    Direct comparisons to alternatives tell most of the story. Other manufacturers have shipped phenolic intermediates either less stable, more costly, or less suited to electronic application. In field evaluations, particularly for pharmaceutical intermediates, 4-Chloro-2-(Trifluoromethyl)phenol has delivered consistent results in cross-coupling, hydroxyl-directed substitutions, and as a protected phenol group for downstream modification. When stacked against mono-chloro or simple trifluoromethyl phenols, this product consistently extends shelf life and improves crystallinity, which in turn simplifies downstream handling and purification.

    Efforts to replace this compound in some applications have run into regulatory bottlenecks, or new molecules raised additional questions about toxicity or reactivity. After running head-to-head tests in custom synthesis, some of our clients found that total process cost doesn’t decrease simply by moving to “simpler” analogs, because additional process steps, impurity purging, or changes in safety infrastructure eat up projected savings. In fine chemicals, in particular, punching above the competition comes from real-world reliability, not theoretical cost savings.

    Facing Ongoing and Future Challenges in Fluorinated Chemistry

    Manufacturing phenol, 4-Chloro-2-(Trifluoromethyl)-, like with all fluorinated aromatics, rides the shifting tides of regulatory, technical, and environmental scrutiny. As more concern builds over persistent fluorinated organics in the environment, we’ve taken a leading role among manufacturers by scrutinizing incoming feedstocks, pursuing greener reaction schemes, and working with downstream users to enable safer destruction of byproducts. We invest steadily in R&D to lower waste, replace hazardous reagents with safer options, and reclaim solvents for re-use. The drive for more sustainable chemistry isn't just good citizenship; it is clearly the direction all reputable manufacturers will go.

    Following a string of technical workshops and collaborative user-group meetings, our staff understood the value in outreach and transparent process adjustments. Providing clear documentation on trace residuals, storage stability data, and safe use practices built real-world relationships—something a cold data sheet could never replace. In turn, our plant receives feedback that keeps us ahead of mere compliance, targeting real improvement that benefits users and neighbors alike.

    Looking Beyond the Molecule

    The story of 4-Chloro-2-(Trifluoromethyl)phenol reveals not just chemistry, but ongoing conversation between maker and user. From our factory floor, this goes beyond batch numbers and purity percent: it’s about building a product whose value is measured in real-world performance, reduced risk, and customer loyalty forged over years. Each improvement—whether smaller environmental footprint, tighter impurity control, or more responsive packaging—was built from lived experience, grounded in practical chemistry and the demands of hands-on application.

    In the end, the value of a specialty intermediate like this one emerges from the sum of daily practice and honest attention to changing needs. Simple purity claims or technical jargon can’t substitute for the commitment behind every package we ship. By listening, adapting, and never taking product performance for granted, we continue to refine what it means to manufacture a fluorinated phenolic that actually works in the field.