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2-Chloro-5-(Trifluoromethyl)Phenol

    • Product Name 2-Chloro-5-(Trifluoromethyl)Phenol
    • Alias 2-Chloro-5-(trifluoromethyl)phenol
    • Einecs 241-420-5
    • 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

    424429

    Productname 2-Chloro-5-(Trifluoromethyl)Phenol
    Chemicalformula C7H4ClF3O
    Molecularweight 196.56
    Casnumber 118-25-0
    Appearance White to off-white solid
    Meltingpoint 54-58°C
    Boilingpoint 207-209°C
    Density 1.495 g/cm3
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents such as ethanol and acetone
    Smiles CC1=CC(=C(O)C=C1)C(F)(F)F
    Refractiveindex 1.528
    Synonyms 2-Chloro-5-trifluoromethylphenol; PCMX-TF
    Storagetemperature Store at room temperature, keep container tightly closed
    Flashpoint 96°C

    As an accredited 2-Chloro-5-(Trifluoromethyl)Phenol 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 2-Chloro-5-(Trifluoromethyl)Phenol, tightly sealed with a screw cap and labeled appropriately.
    Shipping 2-Chloro-5-(Trifluoromethyl)Phenol is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous material, following all relevant transportation regulations. Appropriate labeling, safety documentation, and use of secondary containment are required to prevent leaks during transit. Store and ship at ambient temperature unless otherwise specified.
    Storage Store 2-Chloro-5-(trifluoromethyl)phenol in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and bases. Keep the container tightly closed and protected from moisture and direct sunlight. Use appropriate chemical-resistant containers and ensure proper labeling. Handle with gloves and eye protection to avoid direct contact or inhalation.
    Application of 2-Chloro-5-(Trifluoromethyl)Phenol

    Applications of 2-Chloro-5-(Trifluoromethyl)Phenol in Industrial Manufacturing

    2-Chloro-5-(Trifluoromethyl)Phenol plays an essential and highly specific role as an intermediate or functional additive within select chemical manufacturing sectors. Our production capabilities deliver this compound at the required purity for direct industrial use, supporting downstream partners in stringent regulatory environments. Below we outline established application scenarios from our production customers, specifying technical integration, compliance responsibilities, targeted formulation ranges, and key finished goods.

    1. Synthesis of Veterinary Pharmaceutical Intermediates

    Veterinary active substances, especially certain phenolic antiseptics and antimicrobials, frequently use this compound as a functional intermediate. Customers integrate it in the formation of halogenated phenol motifs required for broad-spectrum formulations, controlling byproduct profiles through closely monitored process conditions. The compound contributes to intermediate steps critical to pathogen resistance and finished dosage quality.

    Industry compliance standards

    • VICH GL3 Stability Testing
    • ISO 9001 for API manufacturing facilities
    • Chinese Veterinary Pharmacopoeia (CVP) for quality reference
    • FDA CFR Title 21 (specific to veterinary APIs)

    Typical usage ratio

    • Input: 0.8–2.1 molar equivalents in target aromatic substitution or coupling reactions (adjusted based on desired substitution pattern and impurity control strategy)

    Downstream process integration

    • Charged during condensation or halogen exchange stages
    • Subjected to subsequent esterification or amide coupling
    • Monitored for content/purity by HPLC or GC methods during intermediate transfer

    Final product types

    • Injectable veterinary formulations (antimicrobial agents)
    • Oral poultry and livestock medicine premixes
    • Topical livestock antiseptics

    2. Agrochemical Active Ingredient Development

    Leading crop protection manufacturers use our material in the synthesis of phenolic building blocks for selective herbicides and fungicides. It enters narrowly defined reaction windows to maximize yield of specific trifluoromethylated aromatics, which form the molecular backbone of high-value actives deployed in regulated agricultural markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 analytical method validation
    • REACH Regulation (EC) No 1907/2006 for imported/intermediate chemicals
    • China’s Pesticide Registration Requirements

    Typical usage ratio

    • Charging 1.0–1.5 mole ratio as precursor for aryl ether or amide coupling; batch-dependent optimization depending on catalyst system and solvent base

    Downstream process integration

    • Intentionally added following initial Friedel–Crafts acylation or nitration step
    • Purified under controlled crystallization post-coupling
    • Captured in route-specific QA for active ingredient precursors

    Final product types

    • Post-emergent herbicide bulk actives (granular, EC)
    • Systemic fungicide technical concentrates
    • Combined formulation additives for seed treatment products

    3. High-Performance Polymer Additives (Specialty Coatings)

    Specialty resin and surface coating producers adopt this phenolic compound when formulating advanced, halogenated thermoset or fluorinated copolymers. Its controlled release enables enhanced thermal stability and weathering resistance in demanding environments, supporting the production of high-end coatings for industrial and electronic applications.

    Industry compliance standards

    • ISO 12944 (Protective Paint Systems)
    • RoHS Directive 2011/65/EU (Control of hazardous substances for electronics)
    • ASTM D5529-01 (Thermal and environmental stability testing of polymers)
    • GB/T 22374-2018 (China chemical coatings industry standards)

    Typical usage ratio

    • Employed at 0.2–1.2% by resin mass for anti-corrosive additive requirements; ratio selected based on required thermal threshold and resin reactivity

    Downstream process integration

    • Dosed into pre-polymerization blending reactor
    • Subjected to high-shear mixing in presence of other monomers/catalysts
    • Evaluated by accelerated weathering and color stability QC

    Final product types

    • High-build marine protective coatings
    • PCBs and EEE component varnishes
    • Industrial machinery anticorrosion primers

    4. Fine Chemical Synthesis for Photographic Chemicals

    Manufacturers in the imaging and photographic chemicals sector utilize this molecule for synthesizing electron-rich phenolic couplers and image stabilizers. Its trifluoromethyl substitution offers unique reactivity that impacts color fade resistance and image-layer stability in complex multilayer films, where purity and lot reproducibility prove critical.

    Industry compliance standards

    • ISO 9001 (Quality Management in Fine Chemical Synthesis)
    • ISO 18902 (Imaging Materials – Processed Films and Prints)
    • ANSI IT9.2 (Photographic Processing Chemicals Specifications)
    • REACH Annex VI for specialty fine chemical substances

    Typical usage ratio

    • 0.5–1.7 mole equivalents as substrate in color coupler core formation; ratios adjusted per final dye structure and sensitivity demands

    Downstream process integration

    • Introduced during diazotization, alkylation, or coupling steps for color former synthesis
    • Subjected to solvent-driven fractionation
    • Analyzed by LCMS for trace impurity profile control

    Final product types

    • Color photographic couplers (multilayer film types)
    • Photographic stabilizer concentrates
    • Analog film developing process chemicals

    5. Specialty Biocidal Additives for Industrial Water Treatment

    In industrial water systems, especially cooling towers and pulp/paper process streams, this compound serves as a selective biocidal intermediate where chlorinated phenol structure is specified for efficacy against microbial biofilm. Partners in large-scale water treatment add it within synthesis pathways for advanced, non-leaching biocidal agents, where persistent activity and regulatory noncontroversy are essential.

    Industry compliance standards

    • EPA FIFRA (40 CFR Part 158, Pesticide Registration Requirements)
    • EN 1276 (Bactericidal efficacy in industrial water)
    • ISO 14001 (Environmental Management Systems for chemical plants)
    • China Water Treatment Chemicals Product Standard HG/T 3668

    Typical usage ratio

    • Utilized at input levels of 0.3–1.0% by active biocide precursor mass; ratio governed by water chemistry, biofilm burden, and treatment cycle demands

    Downstream process integration

    • Added to reaction vessel post-neutralization of base matrix
    • Stabilized with chelating agents and formulated for slow release
    • Quality-tested for release profile and stability under operational system simulation

    Final product types

    • Industrial cooling water biocide concentrates
    • Pulp and paper circuit anti-microbial agents
    • Circulating water anti-fouling formulas
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Chloro-5-(Trifluoromethyl)Phenol: A Closer Look from the Manufacturer’s Bench

    Experience Meets Innovation in Specialty Phenols

    For decades, our team has been producing aromatic compounds with a sharp focus on purity, safety, and performance. 2-Chloro-5-(Trifluoromethyl)Phenol (CTFP) stands out as one of the more technical phenolics we manufacture, distinguished by its molecular structure and the practical advantages that structure confers. Over years of process improvements, we have tuned both the yield and repeatability of this compound to satisfy both custom synthesis houses and larger scale formulators in agrochemical and pharmaceutical sectors.

    Getting to Know 2-Chloro-5-(Trifluoromethyl)Phenol

    CTFP, with CAS number 118-92-3, presents itself as a pale solid with a distinctly sharp, medicinal odor due to its phenolic backbone. On the production line, we prepare this molecule to rigorous specifications, typically targeting over 99 percent assay by HPLC. Impurities receive special scrutiny—halogenated and fluorinated byproducts can introduce real downstream complications, so lot-to-lot consistency is not negotiable.

    Its phenolic hydroxyl group gives this compound a notable chemical reactivity, yet the chloro and trifluoromethyl substituents on the ring lower its overall nucleophilicity compared to other phenols. These structural tweaks increase resistance to oxidative degradation and lend stability desirable in certain synthesis routes, particularly where formulation requires shelf longevity.

    How CTFP Shapes Manufacturing Practice

    Every year, we scale up batches of CTFP not simply to meet generic demand, but to solve concrete synthetic challenges. Just a few years back, a mid-tier crop protection manufacturer approached us about developing more robust pre-emergence herbicides. Their previous supplier’s batches varied in both melting point and water content, which played havoc with downstream hydroxyalkylation. Our process fixes water under 0.1% by KF and controls color (APHA scale) tightly, because even minor deviations can alter reactivity and solubility profiles.

    From our point of view, the value of CTFP is not just its chemical skeleton but what it enables down the line. Many custom chemists rely on its selective ortho/para-directing nature when assembling more complex rings, such as during the preparation of specialty benzoxazoles or substituted phenoxy acids. The electron-poor nature of the aromatic ring, compared to simpler chloro- and methylphenols, means halogen exchange or further trifluoromethylation proceeds at predictable rates. Troubleshooting these transformations is a lot easier with a supplier who has seen the pitfalls at scale.

    What Sets This Compound Apart?

    It’s common for new clients to ask how CTFP sets itself apart from the endless catalog of phenols on the market. The short version comes down to its dual electronic and steric effects. Most basic phenolic compounds—take para-chlorophenol or para-trifluoromethylphenol—offer one modifier group on the ring. CTFP, though, places both chloro and trifluoromethyl groups meta to the hydroxyl. This dual effect not only reduces nucleophilicity but also adds bulk that influences crystal packing and solvation in many solvents.

    These changes matter a lot when you’re formulating for bioactivity or stability. In agrochemical trials, formulations based on CTFP derivatives tend to show enhanced rain fastness and resistance to UV breakdown compared to those relying on unsubstituted phenol. In medicinal chemistry, we have seen requests for ultra-low impurity CTFP for coupling steps, since the presence of chlorine and fluorine often boosts both metabolic stability and target specificity.

    Safety and Handling Rooted in Practical Know-How

    Our experience has shown that CTFP poses some specific handling considerations. Its volatility is lower than unsubstituted phenol, but at elevated temperatures or during prolonged storage, vapor deposition can pose issues. Standard plant engineering controls—local exhaust, sealed reactors, active carbon traps—help us minimize airborne concentrations. The acute toxicity profile, intermediate between simple chlorophenols and highly fluorinated phenols, demands clear protocols. Over time, we have designed drum linings and packaging that sharply reduce leachable contaminants, as both chlorine and fluorine atoms can interact with certain polymers—something more common in long-haul shipments.

    Reactivity toward bases and organometallics is tempered, which is a blessing during more elaborate chemical synthesis. We rarely see runaway reactions in neutral or moderately basic environments, and our customers often praise the manageable exotherm profile. On the downside, the same electronic stabilization that boosts its value in synthesis also slows down direct substitution, so process chemists may need to adjust time or temperature to compensate.

    Manufacturing Ups and Downs: A Manufacturer’s Perspective

    Producing CTFP at scale never happens with a paint-by-numbers approach. The introduction of trifluoromethyl groups relies on specialty fluorination chemistry, which brings hazardous reagents and BY-products that push our environmental and safety teams to stay vigilant. We use dedicated vessels and validated scrubber systems, proven with real-world batch data and regular third-party inspection.

    The biggest lessons over the years haven’t come from lab-scale successes, but from resolving last-minute snags in isolation. Phenolic compounds can polymerize or discolor if the pH or temperature tracking system drifts, even for an hour. In one instance, a failed agitator allowed a local hot spot, leading to red-brown discoloration. The batch failed release. We ran a full root-cause analysis, established stricter monitoring, and rebuilt remote sensing redundancy. In practical terms, our customers received an update within one business day, and we worked with them to bridge the supply gap with advance notice.

    Real Costs and Value in the Specialty Aromatic Market

    The price of a kilo of CTFP doesn’t just reflect commodity utility; it represents years of process tuning, vigorous raw material controls, and compliance with both global and regional regulatory regimes. The trifluoromethyl group, for example, requires sourcing quality fluoroalkylating agents and verification of supply chain stability. The days of depending on unrelated suppliers faded after COVID-19 shutdowns exposed weak links. We have since developed an in-house bank of critical intermediates.

    Shipping CTFP to customers in North America, Europe, and East Asia has taught us that every region brings its own compliance quirks. We have seen customs spot-checks zero in on fluoroaromatics due to environmental rules. Early, open communication with our downstream partners—whether during the documentation of waste codes or during the neutralization of wash effluents—keeps paperwork aligned and shipments on time.

    Applications: Lessons from the Field

    Sitting in on technical calls with end-users, the most common refrain is a request for consistent assay and freedom from trace metals. Both agrochemical and API developers report that minor variations in starting phenolic content can ripple through late-stage product yield, stereochemistry, and impurity profile. Our process relies on real-time in-line monitoring, which helped one long-term partner improve their coupling step yield by trimming excess phenol to under 0.2 percent, shaving hours off purification.

    Researchers in crop science value CTFP’s resistance to microbial breakdown, a feature we validated with independent soil and water testing. Because the molecule has a relatively high logP, it shows strong partitioning into lipophilic phases, which minimizes leaching from treated substrates. This effect can translate to better field performance in both dry and wet climates. In pharma, its predictability during aromatic substitutions or oxidative couplings allows medicinal chemists to focus on novel therapeutics—without babysitting a tricky starting material.

    Voices from the Manufacturing Floor

    Much of our insight into CTFP’s properties bursts from shop-floor stories. Take the veteran in charge of distillation, who swaps inline filters quarterly after logging minor signs of fouling—he caught an early sign of excessive iron one spring, traced to wear in reactor baffles. Tweaking materials of construction improved the iron profile, and product complaints related to discoloration vanished. Our blending crew insists on staged temperature ramps for drying: it avoids superficial crust formation and ensures thorough, deep drying.

    Packing drums for long transport, experienced hands know to check for subtle shifts in pH and to reject even faintly off-color lots. Keeping the line between over-vigilance and “good enough” walks a fine edge, but builds a trust our customers rely on.

    Comparisons and Decision Points

    Many buyers initially compare CTFP with simpler phenolics, like 4-chlorophenol or 2-trifluoromethylphenol, primarily on price. In side-by-side trials, though, the functional advantages compound quickly. 4-chlorophenol, for instance, lacks the hydrophobicity stopping power of the trifluoromethyl group and usually falls short in both environmental stability and metabolic resistance. In direct substitutions, trifluoromethyl phenols run hotter and often react unpredictably due to incomplete electronic stabilization.

    For end users facing regulatory review, the combined presence of both substituents in CTFP frequently allows them to meet tighter residue and breakdown requirements than legacy products. In our own pilot plant, switching solvents and temperatures to match the solubility of CTFP required upfront adaptation, but ultimately reduced waste generation and reprocessing over time.

    Environmental and Regulatory Realities

    Handling products with fluorine always flags intensive scrutiny. Regulatory frameworks shift every season; our compliance officers constantly update waste codes, reporting methods, and transportation documentation for products like CTFP. We’ve invested in closed-loop waste neutralization, so fluoride ions don’t leave our site untreated, and we keep toxicological data up to date through both in-house and third-party laboratories.

    From the manufacturing standpoint, every environmental report isn’t just a compliance checkbox—it reflects the reputational risk where performance lapses have lasting impact. One slip in reporting, one batch leaking, can erase months of hard work. Our live lab dashboards and traceable batch titles help us maintain transparency not only with auditors but with our partners who depend on us for reliable, timely updates.

    Continuous Improvement: Future-Proofing Production

    Research doesn’t stand still. We’re running long-term studies on alternative synthetic routes to reduce hazardous byproducts, not just in finished lots but throughout the production cycle. Our R&D group measures everything from solvent recovery efficacy to total energy consumed per ton produced, pushing incremental gains that lower both cost and footprint. Failures are discussed openly in our weekly reviews; missed yield targets lead to root-cause sessions—never blame games.

    End users paying a premium expect more than purity. They expect traceability, a willingness to adapt specs for special runs, and responses informed by real shop-floor experience. When a large pharma customer references a concern with reactivity drift following a plant switchover, our technical liaison walks through the process audit with them, referencing batch histories and comparing key process parameters, rather than hiding behind generic specs.

    Bottom Line for Buyers: Real-World Reliability

    We don’t frame CTFP as a miracle molecule. It’s a reliable building block, built to specification with full transparency. Our goals circle around less waste generation, longer shelf life, and helping our clients hit tighter process windows. The value in a product like CTFP comes from relationships built on decades of hands-on troubleshooting, materials science, environmental stewardship, and the confidence that each drum, each sample, and each delivery will behave just as promised.

    Choosing the right phenolic intermediate shapes not just process efficiency but future regulatory security and product shelf life. Based on years at the tank, on the plant line, and at the formulation bench, we can say that 2-Chloro-5-(Trifluoromethyl)Phenol earns its place among high-performance intermediates, giving chemists and engineers more dependability—and more margin to innovate—batch after batch.