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3-Nitro-5-(Trifluoromethyl)Phenol

    • Product Name 3-Nitro-5-(Trifluoromethyl)Phenol
    • Alias 5-Hydroxy-2-nitrobenzotrifluoride
    • Einecs 243-393-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    594815

    Chemicalname 3-Nitro-5-(Trifluoromethyl)Phenol
    Molecularformula C7H4F3NO3
    Molecularweight 207.11 g/mol
    Casnumber 99809-90-6
    Appearance Yellow to orange solid
    Meltingpoint 77-80°C
    Solubility Soluble in organic solvents like DMSO, slightly soluble in water
    Synonyms 5-(Trifluoromethyl)-3-nitrophenol
    Structure Benzene ring with nitro group at position 3, trifluoromethyl group at position 5, and hydroxyl group at position 1
    Pubchemid 15166747

    As an accredited 3-Nitro-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, 25 grams, screw cap, white hazard label detailing “3-Nitro-5-(Trifluoromethyl)Phenol,” chemical formula, and safety pictograms.
    Shipping 3-Nitro-5-(Trifluoromethyl)Phenol should be shipped in tightly sealed containers, protected from light and moisture. It must be labeled as a hazardous chemical and handled by trained personnel. Adequate cushioning and secondary containment are essential, and transport must comply with all relevant local, national, and international regulations for hazardous substances.
    Storage **3-Nitro-5-(Trifluoromethyl)phenol** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong bases and oxidizing agents. Protect from moisture, direct sunlight, and heat. Store at room temperature, and ensure chemical is clearly labeled and accessible only to trained personnel.
    Application of 3-Nitro-5-(Trifluoromethyl)Phenol

    Applications of 3-Nitro-5-(Trifluoromethyl)Phenol in Industrial Manufacturing

    3-Nitro-5-(Trifluoromethyl)Phenol is a highly specialized chemical intermediate valued for its performance as a building block in advanced material synthesis, crop protection active ingredients, and specialty dye manufacture. Our production process ensures traceability, consistent assay, and alignment with global industrial regulations across key downstream sectors.

    1. Agrochemical Synthesis: Key Intermediate in Herbicide Manufacturing

    Agrochemical formulators frequently incorporate 3-Nitro-5-(Trifluoromethyl)Phenol as a core building block in the synthesis of selective post-emergent herbicides. Downstream users rely on its chemistry during the condensation step to construct essential aromatic scaffolds. Its functional groups provide stability and enhance activity for selective weed control formulations, where trace impurities and batch consistency are closely monitored for registration purposes. Additive ratio depends primarily on target active molecule yield and the specific crop protection product design.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • REACH (EC) No 1907/2006 Registration for Substances
    • EPA 40 CFR Part 158 (USA) Requirements for Agrochemical actives

    Typical usage ratio

    • 5–18% of total synthesis batch weight, adjusted according to target yield and stoichiometry for the desired active ingredient.

    Downstream process integration

    • Reaction vessel charge during first condensation or nitration step for active ingredient core formation. Subsequent product isolation and purification before downstream formulation.

    Final product types

    • Selective herbicide technical concentrates
    • Active ingredient intermediates for pre-emergent weed control
    • Aromatic-based agrochemical actives

    2. Pharmaceutical Intermediate for Fluorinated Drug Synthesis

    The structured fluorine and nitro positioning on this molecule makes it attractive for pharmaceutical synthesis teams producing advanced APIs, especially in antineoplastic and anti-inflammatory drug research. Chemistries that require aromatic ring modification utilize this raw material during the late-stage intermediate coupling or amidation reactions, facilitating pathway flexibility for medicinal chemistry programs. Production lots require conformance to strict impurity profiles and trace metal limits to align with drug regulatory submissions.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) General Chapters for Excipients/Intermediates
    • European Pharmacopoeia (Ph. Eur.) Purity and Residual Solvent Limits
    • China Drug Master File (DMF) Requirements

    Typical usage ratio

    • 3–8% by molar ratio in the specific synthetic step; varies with target molecule framework and scale-up process.

    Downstream process integration

    • Intermediate addition point during aromatic substitution, nitro reduction, or amidation sequence, tracked via in-process analytical control prior to API isolation.

    Final product types

    • Fluorinated pharmaceutical intermediates
    • Specialty APIs for oncology or inflammation indications
    • Advanced medicinal chemistry screening compounds

    3. Fine Chemical Precursor in Specialty Dye and Pigment Manufacturing

    Dye and pigment producers exploit the electron-withdrawing properties of 3-Nitro-5-(Trifluoromethyl)Phenol in the formation of high-performance colorants, especially for applications requiring lightfast and solvent-stable output. The compound enters synthesis protocols as a nitration precursor, enabling targeted color modification while meeting tight batch reproducibility and purity requirements to support industrial and textiles-grade pigment clients.

    Industry compliance standards

    • OEKO-TEX Standard 100 for Textile Chemicals
    • EN 71-3 Safety of Toys (Migration of Certain Elements) for pigment use
    • ISO 14001 Environmental Management for effluent controls
    • European REACH SVHC Candidate List (Screening for restricted impurities)

    Typical usage ratio

    • 6–12% of precursor feed depending on dye structure and intensity targets; rate adjusted for batch color consistency and solvent compatibility.

    Downstream process integration

    • Introduced in aromatic ring coupling or alkylation stages of pigment/dye synthesis; subsequent oxidation and filtration yield the finished pigment.

    Final product types

    • Fluorinated azo dyes for synthetic fabrics
    • High-performance organic pigments for inks and coatings
    • Specialty solvent-based colorants for plastics

    4. Intermediate for Electronic Material Precursors

    Producers of liquid crystal and specialty electronic materials use this compound as an aromatic intermediate for synthesizing advanced functional materials. Its electron-withdrawing trifluoromethyl and nitro groups offer needed attributes for designers seeking enhanced dielectric properties, thermal stability, and defined reactivity. This molecule typically feeds into multi-step syntheses of monomers or specialty additives, and raw material QC addresses both trace metals and halogen content essential for high-purity electronic applications.

    Industry compliance standards

    • IEC 61249-2-21 (Halogen-Free Requirements for Electronic Components)
    • RoHS (Restriction of Hazardous Substances in Electronics) Directive
    • ISO 9001:2015 for electronic material manufacturing
    • JIS C 5016: Testing for electric insulation materials

    Typical usage ratio

    • 2–7% of polymer synthesis feed or monomer precursor reaction stream; usage determined by final dielectric or optical property specification.

    Downstream process integration

    • Reaction input for aromatic amination or coupling reactions, forming the backbone for specialty fluorinated monomers. In-process assay and purification ensure fit-for-purpose material grades.

    Final product types

    • Liquid crystal intermediate precursors
    • Specialty electronic polymers and resins
    • Functional additives for display and circuit boards
    Free Quote

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    Certification & Compliance
    More Introduction

    3-Nitro-5-(Trifluoromethyl)Phenol: Insights from the Manufacturing Floor

    Getting to Know 3-Nitro-5-(Trifluoromethyl)Phenol

    Making 3-Nitro-5-(Trifluoromethyl)Phenol has given our team a close-up view of its value, quirks, strengths, and how it changes downstream formulations. This compound, commonly recognized by its CAS number 118-33-0, finds its place in advanced syntheses across agrochemical, pharmaceutical, and specialty chemical sectors. We began process development years ago in response to rising demand for performance intermediates carrying both nitro and trifluoromethyl groups on the same aromatic core. The fine-tuning required for its manufacture taught us that this molecule packs more punch per ring than many simple phenolic derivatives.

    Our production pathway uses carefully controlled nitration and trifluoromethylation, balancing energetic reagents, precise temperature profiles, and selective workup sequences. The resulting product, a pale yellow crystalline powder, emerges in high purity with minimal residuals from upstream steps. We analyze every batch using gas chromatography, NMR, and mass spectrometry, ensuring no ambiguous isomer or impurity creeps in. Over countless cycles, even trace metal impurities have been rooted out and consistent melting points have become the norm. Such results did not arrive by chance or by copying any recipe from literature. Reality on plant scale points out every small pitfall the books don't discuss.

    Understanding Its Uses in Real-World Chemistry

    By direct experience with customer feedback, we see that 3-Nitro-5-(Trifluoromethyl)Phenol never fits neatly into a single category. The pharmaceutical chemists prize it as a building block for assembling heterocycles and as a key intermediate in antimicrobial synthesis. Agrochemical researchers value its electron-rich ring for designing new crop protectants with unique bioactivity profiles. Analytical labs turn to its distinctive structure to build calibration standards or derivatize sensitive analytes. Some producers of pigments, dyestuffs, and specialty plastics leverage the molecule's thermal stability and electronic properties in their proprietary blends. Seasoned buyers know that substituents at the 3- and 5-positions change product reactivity in unexpected ways compared with less functionalized phenols.

    A strong feature that defines its behavior is the interplay between the electron-withdrawing nitro and trifluoromethyl groups. This combination shifts the reactivity of the phenolic OH, complicates hydrogen bonding, and tunes solubility in a distinctive fashion. We see this effect daily in how clients formulate new compounds. Compared to simple nitrophenols, reaction rates in substitution and coupling steps shift noticeably. On the other hand, its fluorinated backbone imparts resistance against base hydrolysis, an advantage in harsh process conditions where traditional phenols decompose or discolor. Hands-on chemists learn these tricks after a few pilot batches, but insights save more time when shared directly.

    Hands-On Differentiation from Similar Phenolic Compounds

    We deal with requests for related structures—3-nitrophenol, 4-nitrophenol, 2-trifluoromethylphenol—on a weekly basis. Each has its champions. Arguments often arise over why 3-Nitro-5-(Trifluoromethyl)Phenol justifies the premium. Here, our experience lays out clear boundaries. Not all substituents produce equivalent reactivity, solubility, or handling properties.

    Against parent 3-nitrophenol, trifluoromethylation creates a pronounced shift in lipophilicity. Downstream, this means better partitioning in hydrophobic environments or less tendency to undergo sulfate conjugation in biological contexts. Compared to mono-fluorinated or mono-nitro analogs, this dual-substituted molecule resists oxidation more robustly, and the nitro group stabilizes the ring against nucleophilic attack during synthesis. No off-the-shelf substitute steps in for its role in site-selective alkylations or arylations because the two groups impose a strong electronic map across the ring.

    Our technical team often points out that, for every substitute, someone has already mapped the reaction failures—lower yields, color impurities, or unexpected byproducts. Relying on the dual substituent pattern prevents such setbacks. Others who experiment quickly report back to us that “analogues did not deliver the same results” or “byproduct profile changed completely”. The repetitions become lessons in the lab logbooks of R&D groups around the world.

    Current Model and Quality Principles

    Process knowledge shapes every lot of 3-Nitro-5-(Trifluoromethyl)Phenol that leaves our site. Our current output offers a purity consistently above 99%, driven by refined crystallization steps and tightly managed reagent addition rates. Over the years, customer returns have dropped because we scrutinize intermediate residues as thoroughly as the finished goods. Such transparency pays off long term, giving better shelf-stability, optimal color, and confidence in downstream transformations.

    Specifications reflect this production heritage. Appearance—clear, pale yellow powder with no dust or discoloration. Moisture content stays well below one percent when shipped in lined, sealed drums. Trace metals fall below parts per million. We maintain heavy metal screening with atomic absorption analysis, keeping even trace levels of Fe, Cu, or Zn at bay—critical for pharmaceutical synthesis or radical coupling steps. Particle size tuning gets rare attention but can be arranged with specialized milling prior to filling. Most customers report the product dissolves briskly in common organic solvents and shows minimal filter residue, eliminating nuisance filtration in pilot plant settings. Not every supplier keeps this level of focus, but continuous improvement means surprise-free runs for scale-up teams.

    Role in Sustainable and Efficient Chemistry

    On sustainability, making 3-Nitro-5-(Trifluoromethyl)Phenol raises clear challenges not all plants are prepared for. Handling energetic nitrating agents and fluorinated precursors requires first-hand safety experience and significant investment in environmental controls. We’ve seen how improper vent management or solvent reuse shortcuts give rise to regulatory headwinds. Years of process optimization have enabled us to recycle process water, minimize organic waste, and abate NOx emissions to levels well below local standards. Raw material sourcing receives as much attention as product yield, especially as fluorinated aromatics can originate from high-GWP industrial chemistry. Our switch to low-emission providers and green chemistry alternatives—like catalytic nitration—grew out of direct involvement in process hazards and compliance audits, not abstract promises.

    This practical experience means deliveries are timely and regulatory paperwork comes complete, avoiding audits, fines, or border delays that can derail time-critical projects. Labs seeking to build sustainable pipelines know to start with reliable, responsible input materials—3-Nitro-5-(Trifluoromethyl)Phenol included.

    Continuous Product Evolution Driven by Real Applications

    Patterns of usage continue to evolve. In the past five years, more customers demand tailored analytical documentation, traceability records, or manufacturing details for regulatory filings. This shift comes from new markets, especially as drug and pesticide developers register products in regions with stricter data requirements. We assemble full traceability files from our own batch records, ensuring all input materials, intermediates, and reaction controls hold up under scrutiny. Real-world cases where clients faced issues with audit trails taught us the value of detail in documentation. Auditors call for raw data, but only experience with those audits predicts where the trouble spots may lie.

    Batch-to-batch variability draws attention from customers controlling major synthesis campaigns. Unexpected color shifts or melting point drift, even if minute, spark investigations. Learning from every instance has led us to invest in redundant in-process monitoring, both online and offline. Adjusting filtration rates, solvent ratios, or agitation speed can make or break a run in practice, not just on paper. Feedback goes directly from customers to process engineers who see it implemented at bench and plant level. Changes aren’t handed down from an office removed from shop floor realities but are hashed out by the same people who have to make them work.

    No week passes without a new question or request for innovation. Operations run daily trials for alternative solvent systems or green chemistry options, sometimes at a customer’s request, other times by anticipating regulatory or market shifts. By accepting the pains of pilot-scale learning, we shortcut the delays trial-and-error impose on any new industrial process. We know from hard experience that small tweaks—cooling profile, reagent feed order, or workup handling—impact end-user success, not just our numbers. Every time feedback or research points out ways our product could solve a downstream challenge—be it solubility, processing, or regulatory compliance—we aim to bake that know-how into each lot produced.

    The Competitive Edge of Experience and Trust

    Buyers today want material that’s not only fit for purpose but that arrives backed by supply predictability, technical support, and responsiveness. For 3-Nitro-5-(Trifluoromethyl)Phenol, that difference hinges on supplier experience—and we see which projects finish on time and which stall because of poor source material. Early on, clients come to us with “mystery batch” samples from brokers, only to face solubility quirks or reactivity outliers. We welcome running side-by-side comparisons and backing our process history with references and direct data. Logical skepticism from R&D and procurement teams benefits from our transparency—we share test runs, impurity maps, and use-cases where our product outpaced alternatives.

    Years doing this work show that trust builds steadily. New clients may request small validation samples. They often run comparison studies and track how our material handles in their particular environment—what color forms on heating, how reproducible the yields, how smoothly the product integrates, and if there’s batch lapse or shipment trouble. Over time, returns drop, re-orders rise, and less effort gets spent on troubleshooting, freeing up teams for the bigger questions in research or production.

    Major projects highlight the risk of sourcing from companies with thin manufacturing experience or trading-only backgrounds. Delays, hidden contamination, or inconsistent supply chains cause missed deadlines or failed scale-up. Projects that begin with robust, direct-from-manufacturer products—like our 3-Nitro-5-(Trifluoromethyl)Phenol—advance faster and smoother, unlocking new process chemistry with fewer surpises.

    Addressing Challenges Honestly

    No honest commentary ignores challenges. Handling hazardous reagents—nitrating and trifluoromethyl sources—demands not only engineering controls, but decades of operational vigilance. Worker safety stands above all else. We maintain multi-stage containment, continuous air monitoring, and invest in employee training because accidents cost more than any delay or process upset. Scaling up to drum quantities means not just duplicating lab results, but conquering heat transfer, mixing, dust control, and isolation headaches. Failures happen—reactors clog, filters blind, unexpected pressure surges occur. By maintaining open books, tracking incidents, and always sharing lessons inside the team, experience accumulates and operations stabilize.

    Upstream raw material market shocks—fluorinated aromatics in particular—affect lead times and cost. We forecast future needs with suppliers and maintain buffer stocks, aware that market volatility can halt ongoing chemistry R&D at client plants. Only with foresight and dialogue with our partners do we keep fluids moving and avoid downtime. Regulations shift: as society examines fluorinated chemicals more closely, we continually revisit waste streams, emissions, and handling protocols. Meeting evolving international standards calls for agility and a willingness to invest, not shortcuts.

    Shipping and storage issues crop up for phenols—oxidation, moisture uptake, and packaging compatibility all come into play. We field requests for custom drum lining and offer technical guidance on warehouse humidity control. Each of these adaptations answers a real-world failure—someone’s sample degraded, tests failed, or shelf life came short. Only consistent self-auditing and feedback bring the knowledge needed to avoid repeat mistakes.

    Partnering for Progress in Chemical Synthesis

    The landscape keeps changing, and we anticipate further growth in demand for specialized, multifunctional intermediates such as 3-Nitro-5-(Trifluoromethyl)Phenol. As fewer sites maintain the capability to produce these compounds at scale—and with environmental and safety standards rightly rising—our direct hands-on focus provides an edge. We keep plant operators, chemists, and customer support in close contact, ensuring nimble responses to both routine and outlier requests.

    One trend we see, especially from multinationals, pushes for end-to-end traceability, sustainability audits, and transparent environmental practices for every kilogram delivered. This push boosts confidence for regulator-facing projects, new product filings, and high-volume purchasing. We engage, not only with paperwork assurances, but also with in-facility visits and open technical dialogue. The feedback loop between client and producer sharpens product quality, performance, and project momentum.

    As research frontiers expand, and discovery cycles shrink, direct support from manufacturers becomes more valued. We support formulation experiments, share technical data, and work through process adaptation hand-in-hand with teams who depend on predictable inputs. No two customers use 3-Nitro-5-(Trifluoromethyl)Phenol in quite the same way, yet every feedback and requirement, from reaction kinetics to storage concerns, reshapes our practices. By choosing partners who share their process knowledge and support, chemists in pharmaceuticals, agriculture, materials, and analytics empower breakthroughs beyond routine sourcing.

    Continuous learning and transparency, both within our plant and outward toward our clients, turn what could be a generic commodity into a critical building block for advanced chemistry. In every step, from raw material selection to equipment maintenance, documentation practices to technical support, our commitment shapes the performance, reliability, and long-term success of projects that rely on 3-Nitro-5-(Trifluoromethyl)Phenol.

    We see ourselves not as mere suppliers, but as partners in progress for those building the next generation of pharmaceuticals, agrochemicals, and specialty materials. With every lot produced, our expertise passes along—quietly enhancing the accuracy, safety, and outcomes for research and manufacturing teams who depend on quality from the ground up.