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2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid

    • Product Name 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid
    • Alias 2-Nitro-4-(trifluoromethyl)benzeneacetic acid
    • Einecs 636-502-0
    • 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
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    Specifications

    HS Code

    683314

    Product Name 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid
    Cas Number 120945-70-0
    Molecular Formula C9H6F3NO4
    Molecular Weight 249.15 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 120-124°C
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO and methanol
    Purity Typically ≥98%
    Smiles CC(C1=CC(C(F)(F)F)=CC=[N+]([O-])=C1)C(=O)O
    Inchi InChI=1S/C9H6F3NO4/c1-5(9(15)16)6-2-3-7(8(4-6)12(13)14)10 11 12/h2-5H,1H2,(H,15,16)
    Storage Temperature Store at 2-8°C
    Synonyms 2-Nitro-4-(trifluoromethyl)phenylacetic acid
    Safety Information Harmful if swallowed, irritating to eyes, respiratory system and skin

    As an accredited 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid, 10g," with hazard symbols and lot number, securely sealed.
    Shipping 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid should be shipped in tightly sealed containers and protected from light and moisture. Due to its chemical properties, it must comply with regulations for hazardous materials, including proper labeling and documentation. Shipping should be via certified carriers specializing in chemical transport, ensuring safety and regulatory compliance throughout transit.
    Storage 2-Nitro-4-(Trifluoromethyl)phenylacetic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect it from direct sunlight and moisture. Ensure proper chemical labeling and restrict access to trained personnel. Use appropriate secondary containment to prevent spills or leaks during storage.
    Application of 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid

    Applications of 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid in Industrial Manufacturing

    As a specialized manufacturer of 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid, we supply this intermediate to key sectors that demand stringent quality, consistent performance and traceable compliance. Below, we detail primary downstream industrial applications with clear breakdowns of regulatory standards, formulation parameters, production integration points, and the types of finished products derived from this material.

    1. Pharmaceutical Intermediate for Advanced API Synthesis

    Pharmaceutical companies utilize this compound as a crucial building block when constructing complex active pharmaceutical ingredients, particularly in heterocyclic and aromatic APIs where electron-withdrawing functional groups are required. Its introduction at the early stage of multi-step synthesis routes ensures the electronic environment and reactivity needed for subsequent condensation, halogenation, or coupling steps, especially in products targeting central nervous system or anticancer applications, as specified by established drug master files and process validation protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA)
    • European Pharmacopoeia Monographs for intermediates (when registered as per CEP dossiers)
    • Certificate of Suitability to the Monographs of the European Pharmacopoeia (CEP)

    Typical usage ratio

    • 0.8–3.5 molar equivalents relative to the target API backbone, depending on the synthetic route; process chemists adjust based on target molecule and impurity profile requirements

    Downstream process integration

    • Reacted in the initial or secondary alkylation/aroylation steps during API raw chain assembly; involved prior to protecting group removal or intermediate isolation under controlled inert atmosphere

    Final product types

    • Antipsychotic API intermediates
    • Kinase inhibitor intermediates
    • Fluorinated pharmaceutical precursors
    • Specialty drug substance fragments

    2. Agrochemical Intermediate for Herbicide Synthesis

    Crop protection manufacturers employ this raw material as a precursor in the synthesis of new-generation selective herbicides, where the nitro and trifluoromethyl substitutions enable improved plant uptake and soil persistence. The material’s entry into key coupling or rearrangement steps ensures optimal transfer of electronic characteristics to core herbicidal scaffolds, supporting efficacy at field scale as demonstrated in regulatory submission dossiers and pilot studies.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (Agrochemicals)
    • ISO 9001 Quality Management for technical grade materials
    • REACH Annex VII–X safety and environmental data
    • EPA 40 CFR Part 180 (US establishment of tolerances for pesticide chemical residues)

    Typical usage ratio

    • 5–12% w/w of key step intermediates, selected according to target molecule and scale-up requirements; technical managers adjust load based on process yield and downstream conversion rates

    Downstream process integration

    • Fed into condensation/fluid-bed reactors during phenoxycarboxylic or substituted pyridine herbicide active ingredient synthesis; typically loaded after base formation and before oxidative or reduction clean-up steps

    Final product types

    • Trifluoromethylated herbicide actives
    • Pre-emergence herbicidal concentrate bases
    • Selective broadleaf weed control actives
    • Granular agrochemical premixes for field application

    3. Functional Monomer for Fluorinated Polymeric Materials

    Specialty polymer producers utilize this compound as a functional monomer or endcapper in the manufacture of advanced fluorinated resins and specialty coatings, where the trifluoromethyl group provides improved solvent resistance and unique dielectric properties. Its incorporation at controlled loadings into custom aromatic building blocks allows precise tuning of physical characteristics in specialized wire enamels or insulator films designed for electronics and semiconductor industries.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • IEC 61249 Series (Base materials for printed circuits - halogen content determination)
    • ISO 10993 (Biocompatibility, for medical-grade polymers as needed)
    • ISO 9001:2015 Quality Management for production lots

    Typical usage ratio

    • 0.5–7% molar incorporation into polymer backbones or as a functional end-group, depending on required dielectric constant and hydrophobicity; material formulators set dosage after lab-scale curing and validation tests

    Downstream process integration

    • Introduced during pre-polymerization or chain extension in condensation or addition reactors; typically dosed as a solution in aprotic solvents to ensure uniform distribution in resin matrix before crosslinking or extrusion

    Final product types

    • Electronics-grade dielectric coatings
    • High-performance fluorinated resin wire enamels
    • Low-k insulator films for microelectronics
    • Specialty hydrophobic coatings

    4. Intermediate for Synthesis of Fluorinated Aromatic Fine Chemicals

    Producers of specialty fine chemicals incorporate this compound as an advanced intermediate to introduce both nitro and trifluoromethyl functionalities onto aromatic fragments, addressing the demand for tailored molecules in industries such as analytical reagents and performance additive sectors. Its reactivity supports Suzuki, Heck, or Ullmann couplings in downstream customization, facilitating precise modification per client specification files and small-batch contract orders.

    Industry compliance standards

    • ISO 17034 (General requirements for the competence of reference material producers, for analytical reagents)
    • ISO 14001 (Environmental management systems for specialty chemical plants)
    • REACH registration for supply within the EU
    • Custom client validation and batch testing as per project specifications

    Typical usage ratio

    • 1.5–9% w/w in reaction feed, selected based on the transformation pathway and product configuration; R&D teams adjust input to match stoichiometry in high selectivity couplings

    Downstream process integration

    • Charged during cross-coupling reactions or introduced as a core scaffold in controlled aromatic substitution; material added after catalyst pre-activation or under phase-transfer conditions for efficient conversion

    Final product types

    • Fluorinated reference standards for analytical laboratories
    • Custom aromatic additives for plastics and elastomers
    • High-purity intermediates for OLED and specialty dye synthesis
    • Contract-manufactured functional molecules for research institutes
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    Certification & Compliance
    More Introduction

    2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid: A Manufacturer’s Perspective

    Introduction

    Every time our reactors turn over a new batch of 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid, we reflect on how much our understanding of specialty chemicals has evolved since we first handled its synthesis. This compound stands out for its unique combination of a nitro group at the ortho position and a trifluoromethyl group at the para position on the phenylceaetic backbone. Years spent refining conditions and managing scale-up have shown how the subtleties in its structure, like the interplay between its electron-withdrawing groups, set the tone for its reactivity and stability.

    Commitment to Purity and Consistency

    As chemists who produce this compound at scale, we have come to appreciate that consistency is not just a marketing phrase but a discipline. Running the process from nitration through crystallization brings challenges, especially in mother liquor management and control of by-products. Maintaining narrow specification on purity — including traces of related acids and unreacted starting materials — calls for careful monitoring during both the reaction and purification steps. We maintain our product at a typical purity over 98%, often reaching upwards of 99%, since any deviation can have ripple effects in the downstream transformations planned by our buyers, who may use this intermediate for agrochemical, pharmaceutical, or advanced material applications. The spectroscopic signatures we use for routine QA, from NMR signal reliability to consistent HPLC peaks, speak to the time and investment we dedicate to training, instrumentation, and batch documentation.

    Understanding the Chemistry: More than a Catalog Entry

    The most striking aspect of 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid is its dual electron-withdrawing motif. In discussions with R&D customers, we‘ve learned that the precise arrangement of nitro and trifluoromethyl imparts not just reactivity but selectivity in downstream coupling, alkylation, or condensations. The CF3 group forces a change in the acidity of the alpha methylene, making C–H activation more feasible compared to simpler phenylacetic acids. At the same time, ortho-nitro creates a powerful resonance effect, which can guide synthetic chemists in targeted modification of the molecule, notably in heterocycle formation or in introduction of chirality at the benzylic position.

    Batch Manufacturing: What Sets Us Apart

    Batch synthesis differs from continuous processes not just in size but in the level of personal attention each batch receives. Our production does not rely on handed-down recipes; it comes from day-to-day adaptation to reactant quality, operator vigilance, and attention to waste stream management. During monsoon months, we tighten humidity controls and recalibrate our dryers. In every batch, our operators check not only the overall yield but side product patterns in TLC, ensuring no shift in impurity profile. By maintaining direct oversight, we control the narrative often lost in bulk commodity environments.

    Unlike traders or distributors, our relationship with the product goes beyond a shipping label. We monitor storage conditions to minimize acid degradation, temperature cycling, and light exposure. Over the years, we’ve identified that shipping this acid in dark, airtight containers and limiting excess headspace during packaging cuts down on peroxide and radical formation, which otherwise can change the appearance and behavior of the compound. These firsthand adjustments are hard-won lessons chemical traders may ignore, leading to end-user headaches we’re keen to avoid.

    Meeting Regulatory and Environmental Demands

    Global regulations have become increasingly complex, especially as EHS officers tighten their scrutiny of nitro and trifluoromethyl-containing compounds. We align our process documentation and waste disposal strategies not because of legal minimums but from a sense of duty to people and planet. Process steps are audited to minimize nitrophenol by-products and fluorinated waste. Instead of quick band-aid solutions, we invested in solvent recovery: our distillation plant now closes the loop on much of the acetic acid and aprotic solvents used upstream. Our compliance doesn’t just rest on a handful of certificates but on transparent logs shared during client audits, showing batch genealogy and waste handling trails.

    Applications: Not Just a Building Block

    In regular dialogues with formulation chemists and process developers, we understand that 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid isn’t a mere stepping stone. Each structural feature gives it an edge in synthesis. The nitro group more than doubles the electrophilicity of the aromatic ring compared to unsubstituted counterparts, while CF3 tweaks solubility and increases metabolic stability in drugs under development. Lab chemists often call us for advice on solvent compatibility and reaction temperature, seeking practical suggestions on minimizing hydrolysis or controlling decarboxylation during scale-up.

    Its bench-to-reactor versatility is evident in its adoption across pharma labs seeking to introduce fluorine and nitro substituents into active molecules. Similar utility is recognized in agrochemical research, where specific substitution patterns drive new modes of biological action. By tuning pH and temperature, product recovery stays robust, and side reactions are minimized, optimizing both cost and quality for the next step.

    Comparisons: Learning from Our Own Portfolio

    Making and selling phenylacetic acids of different substituents offers us daily lessons. A product with only a nitro group, for instance, handles very differently—yield, crystallization temperature, and even smell set them apart. We have observed that adding a CF3 group usually increases solubility in halogenated and polar aprotic solvents, but can create challenges in moisture sensitivity. Colleagues working with 2-nitrophenylacetic acid, lacking the trifluoromethyl group, notice sharper melting points and reduced volatility. When scaling up a batch of 4-(Trifluoromethyl)Phenylacetic Acid without the nitro group, downstream reactions often require longer times or harsher conditions, highlighting how the nitro's instability can actually be harnessed as an advantage when handled with skill.

    Through experience, we’ve come to recognize that the greatest difference arises in the ease of purification. The simultaneous presence of nitro and trifluoromethyl groups can complicate crystallization and make mother liquor recycling less predictable, especially compared to methyl or chloro analogs. Knowing this, our operators set aside more time for endpoint checks, and our QC team often batches pilot-scale purification trials before mainline scale-up. This intense attention to detail, and our willingness to retool methods, sometimes leaves clients surprised at the stability and clarity of our acid even after months in real-world storage.

    Packaging and Handling Realities

    Shipping 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid brings its own demands. Over the past decade, we’ve refined our approach to container choice, loading technique, and post-arrival storage advisories. We switched several years ago from single-bag plastic liners to laminated barriers, after evidence of gas permeability unexpectedly altered minor product parameters during long-haul transport. We follow up with clients not out of contractual obligation but simply because we share the responsibility for what happens to our chemicals. We have learned that taking time to explain simple precautions—like storing away from alkaline substances—reduces caking, lowers the frequency of clarification calls, and boosts reliability in repeated syntheses.

    Any producer will face questions about unusual odors, container swelling, or unexpected browing if storage guidelines aren’t met; we keep channels open for users to call our production leads directly, which draws out feedback we can use in future cycle improvements. Sketching out product histories and listening to specific user issues means we spot pattern changes faster, whether from new container sourcing or shifts in raw material supplies from our own upstream vendors.

    Supporting End Users Beyond the Lab

    Our work doesn’t finish at the factory gate. Whether a kilo or a multi-drum order, we look ahead to the customer’s downstream process, anticipating possible obstacles. Our technical team routinely walks through recommendations for optimal dissolution, hints on adjusting reaction stoichiometry, and even contingency suggestions for impurity knockdowns. This open exchange closes gaps between synthesized material and end application, something we see reflected in customer retention and repeat orders.

    Sometimes, a user will run routine analytics and spot a minor signal—say, a miniscule impurity coeluting in the LC-MS. Rather than waiting for a complaint, we proactively share data on background trace levels or typical shifts after long-term storage, setting realistic expectations for the analytics teams at the user end. This trust in full transparency anchors every transaction, allowing our partners in R&D and manufacturing to plan ahead and make rapid adjustments with full context.

    Reliability Borne From Experience

    In a chemical plant, change happens from the ground up. Some improvements arrive after failure or from customer complaints; others grow slowly from iterative process changes. We routinely gather operators, R&D chemists, and logistics coordinators to analyze weak points. Several key aspects have seen year-over-year upgrades: filtration systems, moisture control, trace metal monitoring, and solvent recycling. Unlike volume-driven players, our focus on process optimization often leads us to make small, unglamorous decisions that–over dozens of batches–pay off in reliability and trust.

    No amount of digital automation can fully substitute human instinct. Spectral analysis is checked by eye, not just algorithms. If an operator notices a minor shift in the color of the acid before drying, it triggers immediate double checks. This hands-on sensibility, collected from years on the line, means our product has a record of real-time adaptation, not just adherence to static procedures.

    The Role of Deep Knowledge in Specialty Manufacturing

    Lab-scale chemistry and plant-scale production share core concepts but diverge sharply in the day-to-day. Handling 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid in hundreds-of-kilo batches brings new issues: thermal buildup in exothermic steps, fouling in transfer lines, and shifts in crystallization behavior. Years of accumulated plant data, matched with open communication between lab and shift operators, move us steadily forward. Our technical crew is as likely to draw on advice from a veteran process chemist as from the literature, using all tools available to solve unexpected issues. Keeping our finger on the pulse of evolving green chemistry principles, we re-examine process segments to reduce direct and indirect hazards, from dust minimization to selective solvent choices based on lowest life cycle emissions. Experience has driven us to pilot new approaches–like microfiltration instead of gravity separation–not just to look good on audits, but to actually simplify and strengthen routine operations.

    Anticipating Future Needs

    The field isn’t static. Over time, research chemists move toward greater fluorination, hitching future molecules to growing trends in metabolic stability or new biological targets. We anticipate requests for tighter impurity profiles, tailored particle sizes, and faster delivery turnarounds. Platform upgrades pivot on client feedback–whether a need for an alternate solvent residue limit or an interest in a new application. Our R&D group keeps tabs on recent studies in medicinal chemistry, monitoring which molecular motifs migrate from the literature to pilot plant. That proximity to market trends, rooted in actual manufacturing know-how, means our feedback loops are short, and each improvement quickly translates to process robustness and client trust.

    Solving Real Problems as a Producer

    The role of a manufacturer is often overlooked by those who interact only with packaged product or catalog pages. Closer in, the picture is different. We handle the raw smell of nitroaromatic intermediates, the noisy filtration pumps, the unplanned stops during vacuum distillation, and the hard choices in waste treatment. Day-to-day operations remind us that real value emerges not just from technical know-how but from resilience, collaboration, and willingness to learn from error. By sticking with a product across its full lifespan—sourcing, manufacturing, QC, and shipping—we develop a clarity about both strengths and weaknesses.

    For clients developing new processes, we serve as a sounding board for troubleshooting challenges that only surface at scale. For those in regulated industries, we compare regulatory notes and share safety perspectives. In this way, every batch we create is more than a commodity; it becomes a proof of our adaptation, attention, and partnership. While market prices and supply chains can fluctuate, the reliability of a real manufacturing relationship decouples product quality from the kind of instability that affects intermediaries. The difference lies in our investment and our daily presence on the production floor.

    Conclusion: What It Means to Stand Behind a Specialty Chemical

    Our responsibility is clear: we make 2-Nitro-4-(Trifluoromethyl)Phenylacetic Acid not to a formula alone but to the reality of end user needs, anticipated challenges, and the small adjustments that add up to long-term trustworthiness. Unlike catalog firms or trading houses, we possess both the failures and successes in every shipment. The acid’s unique structure, refined through numerous production campaigns, continues to test and improve our understanding, not only of chemistry but of the wider production ecosystem. Each shipment we see leave our site carries with it a record of scrutiny, dialogue, and process discipline that no datasheet can fully capture.

    Every customer, from a research bench to a multinational formulation plant, interacts with our product at a critical stage in their own innovation journey. We recognize that, and we treat the work with the seriousness and care it deserves. In an evolving industry, that mindset doesn’t just result in a quality chemical. It builds a culture of openness, accountability, and mutual growth—qualities that define the best outcomes in specialty manufacturing.