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3-Nitro-4-(Trifluoromethoxy)Aniline

    • Product Name 3-Nitro-4-(Trifluoromethoxy)Aniline
    • Alias 3-Nitro-4-(Trifluoromethoxy)benzenamine
    • Einecs 629-044-9
    • 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

    888292

    Chemical Name 3-Nitro-4-(Trifluoromethoxy)Aniline
    Cas Number 720-94-5
    Molecular Formula C7H5F3N2O3
    Molecular Weight 222.12 g/mol
    Appearance Yellow solid
    Melting Point 65-69 °C
    Density 1.56 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C=C1N)[N+](=O)[O-])OC(F)(F)F
    Inchi InChI=1S/C7H5F3N2O3/c8-7(9,10)15-5-2-1-4(11)3-6(5)12(13)14/h1-3H,11H2
    Storage Conditions Store at room temperature, in a cool, dry place
    Synonyms 4-Amino-3-nitro-(trifluoromethoxy)benzene

    As an accredited 3-Nitro-4-(Trifluoromethoxy)Aniline 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, sealed with PTFE-lined cap, labeled with chemical name, hazard pictograms, CAS number, and safety information.
    Shipping 3-Nitro-4-(Trifluoromethoxy)aniline should be shipped in tightly sealed containers, protected from light and moisture. It must be handled as a hazardous material, following all relevant chemical regulations. Shipping should occur via authorized carriers specializing in chemicals, with appropriate labeling, documentation, and safety measures to prevent leaks or accidental exposure.
    Storage Store **3-Nitro-4-(Trifluoromethoxy)aniline** in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Properly label the storage container and use secondary containment if possible. Always follow institutional safety protocols and wear suitable protective equipment when handling this compound.
    Application of 3-Nitro-4-(Trifluoromethoxy)Aniline

    Applications of 3-Nitro-4-(Trifluoromethoxy)Aniline in Industrial Manufacturing

    As a specialized producer, we supply 3-Nitro-4-(Trifluoromethoxy)Aniline for advanced industries requiring precise performance and compliance with stringent process demands. Below are key sectors utilizing this material for end-use formulation and production.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use this compound in the multi-step synthesis of specific active pharmaceutical ingredient (API) intermediates—especially for fluorinated heterocycle drugs and advanced nitroaromatics. It takes part in ring-closing reactions or acts as a precursor for protected amine introduction. The chemical’s stability ensures consistent reactivity over repeated process batches and meets trace impurity limits set by the pharmaceutical sector.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA)
    • Pharmacopoeia monographs: USP, JP, and EP as applicable
    • ISO 9001:2015 Quality Management for Fine Chemicals

    Typical usage ratio

    • Batch processes commonly employ 3-10 mol% relative to the targeted pharmaceutical intermediate, adjusted for route specificity and yield optimization.

    Downstream process integration

    • This raw material enters as an early-stage coupling agent or aromatic feedstock during the construction of complex molecules in active intermediate lines.
    • Typically reacts via nucleophilic substitution or reduction before downstream isolation and purification.

    Final product types

    • Advanced pharmaceutical intermediates for oncology, antiviral, and CNS drug classes
    • Building blocks for fluorinated fine APIs
    • Pathway-specific protected amines
    • Precursors for active nitroaromatic compounds

    2. Crop Protection Active Ingredient Production

    Agrochemical producers rely on this compound in the synthesis of next-generation herbicide and fungicide active ingredients, integrating its electron-withdrawing trifluoromethoxy group to improve activity and durability in field conditions. It undergoes selective nitration and amination steps delivering more stable, targeted pesticide molecules with low off-target toxicity.

    Industry compliance standards

    • ISO 9001:2015 for Agrochemical Manufacturing
    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO manual on Pesticide Specifications
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU)

    Typical usage ratio

    • Used at 5-20% molar basis in multi-step syntheses depending on targeted crop protection molecule potency and synthesis route.

    Downstream process integration

    • Acts as an aromatic precursor in key nitration, etherification, and reduction stages for crop protection compound construction.
    • Feeds directly into pilot and production-scale reactors for active substance formation.

    Final product types

    • Selective triazole and pyridine-based fungicide actives
    • Novel fluorinated herbicide agents
    • Intermediate structures for insecticide formulation
    • Seed treatment active compounds

    3. Performance Coating Additive Synthesis

    Specialty coating manufacturers incorporate the material into the synthesis of advanced additive monomers and cross-linking agents for top-tier solvent-borne and powder coatings. Its chemical structure imparts improved chemical resistance and hydrophobicity, meeting rigorous demands for high-durability industrial surfaces and automotive OEM coatings.

    Industry compliance standards

    • ISO 9001:2015 Quality Systems
    • OECD TG 405/406 for chemical safety
    • Restriction of Hazardous Substances Directive (RoHS, EU) for finished coatings
    • ASTM D5402 for solvent resistance

    Typical usage ratio

    • Typically 1-7% by weight as a monomer component in specialty resin and additive synthesis; dosage depends on final property targets.

    Downstream process integration

    • Introduced during resin pre-polymerization or as a reactive diluent, allowing for integration of trifluoromethoxy and nitro functionality in final matrices.
    • Employed in pilot reactors and continuous reactors for industrial-scale production.

    Final product types

    • Industrial top coats for heavy equipment
    • Automotive refinish and OEM clear coats
    • Chemical-resistant floor coatings
    • Specialty powder coating formulations

    4. Electronics Liquid Crystal Intermediate

    Advanced electronics manufacturers use this aniline derivative to synthesize halogenated and fluorinated intermediates for liquid crystal materials. Its molecular features enable fine-tuning of dipole moment and viscosity in final liquid crystal mixtures, supporting improved electro-optical response in display applications such as LCD panels and organic light-emitting diodes (OLEDs).

    Industry compliance standards

    • IEC 62474 Declarable Substance Standard for Electronics
    • ISO 14001:2015 Environmental Management
    • RoHS 3 (Directive 2015/863/EU)
    • CQC Mark for chemical components in displays (China)

    Typical usage ratio

    • Usage commonly ranges 0.5-5 mol% relative to bulk liquid crystal precursor streams; precise levels set by dopant profile and target electro-optic property.

    Downstream process integration

    • Integrated during key coupling or reductive amination steps in the compound library expansion for new LC mixture prototypes.
    • Supplied in purified form directly to display material synthesis units.

    Final product types

    • Intermediate mesogens for liquid crystal display applications
    • OLED host and dopant compounds
    • Halogenated aryl intermediates for LC formulation
    • Specialty LC mixtures for high-speed panel production

    5. Specialty Dye and Pigment Intermediate Production

    Dye and pigment manufacturers utilize this compound to develop new chromophore architectures for high-performance dyes, especially in fluorescent, laser, and technical textile applications. The strong electron-withdrawing trifluoromethoxy group helps generate stable, colorfast pigments under various environmental conditions, while the nitro group supports deeper, intense shade generation in finished products.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile safety
    • ISO 13320 for particle size analysis of pigments
    • CFR Title 21, Part 74 (US) for color additives in specialty coatings and plastics
    • EN 71-3 Safety of Toys: Migration of certain elements (for pigments in toy coatings)

    Typical usage ratio

    • Used in 3-11% by mass as an intermediate in azo, anthraquinone, or heterocyclic dye synthesis, dosage adjusted by chromophore target and batch size.

    Downstream process integration

    • Participates in diazotization, coupling, or reduction stages to build novel chromophore components in dye manufacturing batch reactors.
    • Feeds purified streams to pigment synthesis and finishing lines for high-purity dye production.

    Final product types

    • Fluorescent and laser dyes for imaging and optical applications
    • Technical textile dyes with high UV stability
    • High-intensity specialty pigments for plastics and inks
    • Water-based pigments for industrial coatings
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    Certification & Compliance
    More Introduction

    3-Nitro-4-(Trifluoromethoxy)Aniline: A Producer’s Perspective

    Reliable Chemistry, Lasting Value

    Decades in the lab have led us to respect every raw material and process step that makes the difference between a sample and a tonne. 3-Nitro-4-(Trifluoromethoxy)Aniline does more than fill a chemical slot on a list; it answers a direct need from research and commercial teams focused on fine-tuning aromatic amines with electron-withdrawing and electron-donating groups in specific substitution patterns. Our facility has produced high-spec aromatic intermediates for over 25 years, supporting agrochemical formulators as well as pharmaceutical innovators with components whose reliability keeps the rest of their process on track.

    Consistency from Molecule to Barrel

    Our 3-Nitro-4-(Trifluoromethoxy)Aniline presents as a well-defined, solid product—bright yellow under proper lighting, with melting points checked against internal references daily. The model we deliver today reflects a pathway honed through scale-up challenges: from selective nitration, through custom work-up, to careful crystallization and drying. Typical purity surpasses 98 percent by HPLC, as confirmed batch-to-batch. This benchmark grew from feedback during both process chemistry trials and full-scale manufacturing, where impurities in aromatic amines often set off color, yield, or safety problems downstream.

    Other producers hit snags with consistency from lot to lot, particularly if their refining focuses only on bulk throughput or if filter cake washing does not remove trace acids. We run wider TLC monitoring and routinely chart trace-level byproducts by GC-MS. A well-run batch secures more than assay; it guards the reaction profile’s predictability later, whether in nucleophilic aromatic substitution, reduction, or diazotization.

    Practical Application: Beyond the Catalog

    Chemists do not buy intermediates out of habit. Every kilo of 3-Nitro-4-(Trifluoromethoxy)Aniline sits inside a real synthesis, mapped to a patented molecule, a bioactive fragment, or a candidate for a performance coating. Over the years, our material found its main markets in auxiliary building blocks for active agrochemical ingredients, in advanced specialty dyes, and in the medicinal chemistry of experimental small molecules.

    The placement of the trifluoromethoxy group at the 4-position extends the reach of this aniline into areas that require both lipophilicity and metabolic robustness. Fluorinated groups shift physical and biological properties far more than methyl or methoxy chains; we see product designers exploiting the reduced polarity and increased C–F bond strength for enhanced membrane penetration or hydrolytic resistance. Nitro substitution at the 3-position lends the aromatic core a distinct reactivity pattern. In our own reduction columns, we watch the transition to the corresponding diamine, or other downstream amine derivatives, proceed cleanly when starting material avoids residual metals or unreacted starting aryls from previous steps.

    Troubleshooting Upstream and Downstream

    Every step from benchtop synthesis to finished product gets real-world scrutiny. Labs pursuing only milligram-scale output may tolerate minor side reactions that are a major headache on multi-kilo production. For 3-Nitro-4-(Trifluoromethoxy)Aniline, control at the nitration junction is non-negotiable; the ortho and para directing effects require tight temperature and acid ratios. Under-dosed acid or small disturbances in cooling lead to incomplete conversion or mixed regioisomers. Strict attention to reagent handling, slow addition, and staged washing boosts not only the isolated yield but downstream purity by eliminating need for repeated reprocessing.

    On the flip side, granule size and dryness affect how the product feeds into following stages at our customers’ plants. Clumps, electrostatic charges, or moisture residues upset dosing tanks and reaction lances. We’ve built in slow ambient drying, monitored by moisture probes, to keep the delivered product free-flowing and right-sized for both automated and manual dispensing.

    How It Differs From Close Relatives

    In our experience, chemists often compare 3-Nitro-4-(Trifluoromethoxy)Aniline to standard nitroanilines or trifluoromethoxyanilines that lack the combined substituent layout. The presence of both the 3-nitro and 4-trifluoromethoxy groups creates altered electron distribution not shared by simpler analogs. Reduction paths differ substantively; the nitro group’s mild activation from the electron-withdrawing trifluoromethoxy alters reactivity, which impacts catalytic hydrogenation selectivity and the formation of side products.

    Many aromatic amines with only a nitro or a fluoro-containing substituent lack the versatility for introducing specific reactivity for subsequent cross-coupling or substitution. The unique electron profile our product offers can allow for milder conditions in Buchwald-Hartwig aminations or Sandmeyer-type transformations, and that detail matters for downstream yield and waste treatment.

    Another striking property emerges during analytical quality checks. Our team noted that the combined groups shift the UV absorbance spectrum; this can be useful not just for tracking purity, but also allows user labs to monitor process endpoints more sensitively. The product’s higher fluorine content compared to mono-fluorinated or methyl-substituted anilines shows up in NMR and mass spectrometry, which can make for traceable markers in multi-step syntheses or even for detecting cross-contamination in shared facilities.

    Why Purity Drives Progress

    Purity is the gatekeeper in chemical production. Any impurity can seed analytical drifts, color shifts, or off-spec odors. For us, reliable results come only by tracing back every deviation to a source—whether glassware fouling, a leaky seal, or a warehouse storing incompatible solvents. At the core, 3-Nitro-4-(Trifluoromethoxy)Aniline must meet not only internal spec sheets but also the response curves our customers design into their processes. We hear from process chemists that trace levels of ortho-substituted isomers will linger through the pipeline, affecting both reaction selectivity and regulatory compliance. We answer with real-time monitoring and corrective action instead of last-minute adjustments.

    Batch reports matter, but years in the business have shown us that customer audits matter more. Seeing how different plants measure quality, code data, and trace sources tells us how to strengthen internal discipline. We’ve implemented a double-layer sampling protocol at dispatch, both for legal accountability and for technical backtracking should any concern ever arise.

    Toward Sustainable Manufacturing

    Attention has shifted sharply in the chemical sector toward cleaner production. Aromatic nitrations often draw scrutiny for acid use, solvent emissions, and byproduct handling. Rather than chase after temporary “green” labels, we’ve grounded our environmental steps in regular process tweaks that reduce spent acids, cut washwater volumes, and reclaim organic solvents. Over time, these minimize both the emissions profile and supply chain interruptions. By steadily shifting towards closed-loop solvent recovery for the mother liquor and solid waste, not only do we lighten disposal volumes, our product leaves a gentler trace on both the factory floor and the transport corridor.

    We also link purification and waste heat capture. Heating crystallizer streams from existing reaction lines, instead of drawing new fuel, trims the factory energy load. These aren’t showpiece projects—they save money, keep us operating at profit even in lean years, and give purchasing teams honest reasons to trust in the continuity of our supply.

    Supporting the Next Generation of Synthesis

    Markets move in cycles, but one fact remains: research teams do not wait for supply chains to catch up. The demand curve for well-characterized, high-purity 3-Nitro-4-(Trifluoromethoxy)Aniline tracks with new agrochemical scaffolds, pharmaceutical leads, and advanced electronics. Each year we see orders not just grow in size but diversify as more end-uses surface. Coating technologies use our product for selective surface reactions, while medicinal chemists draw on its unique steric and electronic properties to improve metabolic half-lives or adjust target-binding selectivity.

    We’ve partnered with pilot-scale startups and global firms working under strict regulatory frameworks, from early-stage exploratory programs to scaled manufacture. Every collaboration teaches us tricks around handling, analytics, and sped-up troubleshooting—where a steady intermediate can shave months off a discovery-to-commercialization timeline.

    Lessons Learned from the Plant Floor

    No flowchart or sales leaflet captures the moment a high-stakes order bottlenecks. Our own history brims with missed targets, sudden supply drops, or contamination scares—each a learning curve. Consistent training, cross-checks, and on-call technical staff build the resilience a specialty product line needs to avoid repeat mistakes. Whenever a customer reported a false-negative in purity, or a blocked reactor transfer, we found the root causes stood right on the plant floor: insufficiently calibrated pumps, or missed step in the raw material acceptance.

    Direct feedback from users shapes our process upgrades, not bureaucratic review alone. If an R&D customer reports difficulty dissolving material, or complaints arise around caking after long transit, we adjust not just packing material but also the way we dry and sieve product before shipping. Handling quirks do not always signal a chemistry flaw—they often point to overlooked human routines or climate changes in warehouse scheduling. We respect these reports and rework both our SOPs and our storage cues.

    Tracing Progress by Standards

    Quality standards shape more than compliance forms—they support tangible, at-scale trust. Each container of 3-Nitro-4-(Trifluoromethoxy)Aniline walks through rigorous checkpoints: from raw material verification, in-process monitoring, to final packing under inert atmosphere. Auditors demand digital traceability, and years ago we automated batch record linkage so each order stays tied to its process history. Our regular practice includes stability testing at intervals up to 12 months under standard and accelerated settings. This data backs both our label claims and reassures downstream users that even after months in storage, their material reacts as expected.

    The science in manufacturing does not end with the batch. Regulatory attention grows around trace organofluorine and nitroaromatic emissions. We monitor not just product purity but workplace air, effluent, and surface residues. By proactively measuring these after each batch run, we intercept trouble before it blooms into rework or recall.

    Supporting Research and Regulatory Teams

    New users often ask about the safety margin and compliance history of our 3-Nitro-4-(Trifluoromethoxy)Aniline. Over years, we have learned the regulatory needs in North America, Europe, and some emerging markets. Documenting traceability, impurity profiles, and shipping records forms part of our routine. Our teams have worked through dozens of customer audits and third-party verifications, where tracking the smallest deviation in paperwork or sample data could mean a month’s delay or a lost contract.

    Documentation and transparency no longer form the last step—they start the process. If a technical team calls for a confirmatory COA or gap-filling safety documentation, our onsite analytical groups support them rapidly. Supply chain traceability rests not only with us; it matters upstream with suppliers of haloaromatic and fluorinated building blocks, and we only engage partners that meet stepped-up documentary standards.

    Why Product Differences Matter Downstream

    Small distinctions make big consequences as the synthetic burden increases. 3-Nitro-4-(Trifluoromethoxy)Aniline, distinct from its simpler cousins, brings downstream value that shows up in higher yield, better color, or faster purification. Its solubility, filtration behavior, and acid-base stability provide developers new levers to adjust complex, multi-step productions. Substitute another product and process teams suddenly compensate with extra solvents, longer isolation steps, or more frequent rework. Reliability, honed in-house, always finds validation in how little unplanned downtime or batch loss our customers report back to us.

    Sometimes the biggest difference between usable and outstanding intermediates starts with listening to the plant manager, the shift technician, or the shipping loader. Decades of listening gave us an edge in improving the handling and supply of difficult aromatic amines.

    Toward Continuous Improvement

    Challenges in manufacturing will always be present. Weather, raw material prices, energy shortages, or new regulatory standards—each can shape output and risk. Our answer has been steady investment not in flash-in-the-pan process tweaks, but in robust people, plant routines, and real-time process feedback. Regular recalibration, equipment upgrades, sustained analytics, and internal recertification close the loop from the lab to the loading dock. Sometimes, process optimization means pausing production to review what small inefficiencies creep in; at other times, it means calling in a team from off-shift just to fix an unexpected issue before a shipment deadline.

    Continuous improvement for us means honest, data-driven decisions. Process deviations are logged, analyzed, and used to adjust operations—be it in better washing steps, fouling precautions, or environmental controls. We keep our improvements grounded in both operator experience and emerging technical literature, not simply commercial targets.

    Looking Ahead

    Demand for sophisticated intermediates like 3-Nitro-4-(Trifluoromethoxy)Aniline will keep evolving. As medicinal, agrochemical, and advanced material chemists design new molecules, the expectations for quality, ease of handling, supply continuity, and regulatory clarity keep getting stricter. Producers who adapt, listen, and invest in plant and people will stay relevant, while those who lean on past specifications risk falling behind.

    With every batch, delivery, or technical support exchange, we add another stake in the trust our customers put in us. Our approach to producing, packaging, and dispatching 3-Nitro-4-(Trifluoromethoxy)Aniline rests on the lessons learned from every step of the process. Future enhancements in green chemistry, process automation, and customer communication will only make that product—and our partnership—stronger.