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4-Dimethylamino-3-Nitrobenzotrifluoride

    • Product Name 4-Dimethylamino-3-Nitrobenzotrifluoride
    • Alias 4-DMABTF
    • Einecs 223-479-2
    • 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

    962150

    Chemical Name 4-Dimethylamino-3-Nitrobenzotrifluoride
    Cas Number 3934-20-1
    Molecular Formula C9H9F3N2O2
    Molecular Weight 234.18 g/mol
    Appearance Yellow crystalline solid
    Melting Point 49-52°C
    Solubility Slightly soluble in water
    Density 1.42 g/cm3 (approximate)
    Synonyms N,N-Dimethyl-4-(trifluoromethyl)-2-nitroaniline
    Pubchem Cid 2847875

    As an accredited 4-Dimethylamino-3-Nitrobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 4-Dimethylamino-3-Nitrobenzotrifluoride is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping **Shipping Description:** 4-Dimethylamino-3-nitrobenzotrifluoride should be shipped in tightly sealed containers, protected from light, heat, and moisture. Store in a cool, well-ventilated area. Handle as a hazardous chemical, following applicable regulations for transport of toxic or irritant substances. Appropriate hazard labeling and documentation must accompany all shipments in compliance with local and international guidelines.
    Storage 4-Dimethylamino-3-Nitrobenzotrifluoride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and direct sunlight. Keep away from incompatible substances such as strong oxidizing agents and acids. Store at room temperature and ensure the storage area is clearly labeled and compliant with chemical safety regulations.
    Application of 4-Dimethylamino-3-Nitrobenzotrifluoride

    Applications of 4-Dimethylamino-3-Nitrobenzotrifluoride in Industrial Manufacturing

    4-Dimethylamino-3-Nitrobenzotrifluoride serves as a critical intermediate in a range of specialty chemical industries. With precise molecular structure and consistent lot quality, it enables downstream manufacturers to maintain stringent control over synthesis, formulation, and end-use product performance. Below are the main industrial applications with detailed process and compliance information.

    1. Pharmaceutical Intermediate for Fluorinated Active Pharmaceutical Ingredient (API) Synthesis

    Our material acts as a functionalized building block in the synthesis of complex fluorinated APIs, especially where electron-withdrawing groups are required to enhance bioavailability and metabolic resistance. The electron-rich dimethylamino and nitro functionalities make it suitable for nucleophilic aromatic substitution and condensation reactions, forming critical linkages in the production of advanced pharmaceutical compounds.

    Industry compliance standards

    • EU GMP Part II in chemical API synthesis
    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF monographs for relevant downstream APIs
    • REACH (EC 1907/2006) for supply within the EU

    Typical usage ratio

    • 10-20% w/w as a functional intermediate in multi-step API syntheses
    • Ratio varies by target API molecular complexity and reactivity demands

    Downstream process integration

    • Charged in the second or third step after initial halogenation or nitration
    • Condensed via Buchwald–Hartwig amination or nucleophilic aromatic substitution
    • Purified with chromatographic or crystallization approaches before subsequent synthesis steps

    Final product types

    • Active pharmaceutical ingredients for oncology and CNS disorders
    • Fluorinated drug precursor compounds
    • Intermediates for generic and specialty drugs

    2. Agrochemical Synthesis of Trifluoromethylated Herbicides and Fungicides

    This compound functions as a key starting material in the agrochemical sector, especially in the production of selective herbicides and fungicides containing trifluoromethyl groups. Its structural motifs enable synthesis of actives with increased field persistence and targeted biological activity against weeds or fungal pathogens in high-value crops.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines for pesticide raw material quality
    • ISO 9001:2015 for process documentation
    • European Regulation (EC) No 1107/2009 for agrochemical actives
    • EPA 40 CFR Part 158 (USA) for pesticide active technical materials

    Typical usage ratio

    • 5-15% in active intermediate processing, depending on the specific synthetic pathway
    • Adjusted based on the targeted substitution degree in final molecule

    Downstream process integration

    • Introduced during early-stage condensation or nucleophilic aromatic coupling steps
    • Transformed via reduction, halogen-exchange, or diazotization to produce active cores
    • Followed by formulation and granulation for end-use

    Final product types

    • Trifluoromethyl-substituted phenyl herbicides for soybean and corn fields
    • Fungicide actives for cereal crops
    • Intermediates for crop protection R&D

    3. Dye and Pigment Intermediate for High-Performance Textile Colorants

    As a halogenated, nitroaromatic compound, this raw material is utilized in the production of specialty dyes and pigments with high color fastness, chemical resistance, and thermal stability. It participates in diazo-coupling and reduction reactions to generate brilliant, persistent colors for technical textile applications and industrial polymers.

    Industry compliance standards

    • Oeko-Tex Standard 100 for restricted aromatic amines in textiles
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) list
    • EN 71-3 (European Toy Safety: migration of certain elements)
    • GOTS (Global Organic Textile Standard) for permitted auxiliaries

    Typical usage ratio

    • 8-12% as a diazo component in dye batch or pigment precursor synthesis
    • Varying with chromophore design and shade intensity requirements

    Downstream process integration

    • Reduced to corresponding amine for azo dye synthesis
    • Coupled under controlled pH and temperature for pigment formation
    • Integrated post-filtration into masterbatch or textile sizing formulation

    Final product types

    • Acid dyes for nylon and silk fabrics
    • Pigments for automotive fibers and industrial coatings
    • Masterbatch colorants for engineering plastics

    4. Electronic Chemical Intermediate for Liquid Crystal and OLED Materials

    This specialty nitrobenzotrifluoride derivative finds targeted use in the electronics industry as a key intermediate in the manufacture of liquid crystal monomers and OLED dopants. Its electron-rich and highly fluorinated structure enables downstream formation of rigid, thermally stable compounds needed for advanced display applications and organic semiconductors.

    Industry compliance standards

    • IECQ Hazardous Substance Process Management for electronics raw materials
    • RoHS Directive 2011/65/EU for restricted substances in electrical/electronic equipment
    • IPC-4101 for base materials qualification
    • ISO 14001:2015 for environmental management in electronics manufacturing

    Typical usage ratio

    • 2-7% in electronic chemical synthesis lines for monomer preparation
    • Adjusted based on target functional group density and downstream compound design

    Downstream process integration

    • Reacted in early monomer functionalization stages for LC and OLED precursor synthesis
    • Undergoes selective reduction and coupling for chain elongation
    • Subsequently purified by distillation or chromatography before polymerization or device fabrication

    Final product types

    • Liquid crystal intermediates for flat-panel displays
    • OLED emitter and transport layer materials
    • Functional monomers for advanced semiconductor coatings

    5. Intermediate for Fluorinated Polymer Synthesis

    As a functionalized aromatic with high fluorine content, our raw material supports the synthesis of specialty polymers, such as high-performance engineering plastics and fluorinated resins. These polymers require precise introduction of trifluoromethyl groups to impart chemical resistance, low surface energy, and stability under harsh service conditions in coatings, membranes, and specialty components.

    Industry compliance standards

    • ASTM D5630 for fluorine content in plastics
    • UL 94 for flammability certification in polymer components
    • REACH Annex XVII on restricted substances in polymer additives
    • ISO 10993-5 for biocompatibility when used in medical polymer equipment

    Typical usage ratio

    • 3-10% in polymer batch as a reactive chain modifier or monomer
    • Tuned for targeted mechanical, thermal, and chemical resistance properties

    Downstream process integration

    • Introduced during initial monomer preparation for step-growth or radical polymerization
    • May be functionalized further before copolymerization
    • Embedded in resin or masterbatch for film, coating, and molded part production

    Final product types

    • Fluorinated polyimide resins for aerospace
    • High-performance coatings for electronics and chemical processing
    • Fluoropolymer membranes for water treatment and fuel cells
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    Certification & Compliance
    More Introduction

    Product Overview: 4-Dimethylamino-3-Nitrobenzotrifluoride

    Experienced Chemical Manufacturing Meets Daily Industry Needs

    Working from the production floor of our chemical plant, we've handled plenty of specialty intermediates over the years, and 4-Dimethylamino-3-Nitrobenzotrifluoride stands out for good reason. Every week, batches move through reactors and columns as our operators work with this substance. We know this compound by the shorthand "DMANTF", recognized across dyes, agrochemical, and pharmaceutical sectors. From our own tanks and from the vantage of our QC lab, it's clear why manufacturers rely so much on specific properties it brings to the synthesis process.

    To understand the substance, we look at its structure: a benzene ring with both a dimethylamino group and a nitro group, and a trifluoromethyl group attached to the ring. These substitutions change both its reactivity and its solubility compared with more basic nitroanilines. Workers in our plant report that its crystalline form makes it less dusty than more common nitro aromatics—years of feedback from packing teams support this observation. In real terms, that means less powder escaping into the air during weighing and transfer, a definite advantage for maintaining a tidy working environment and cleaner maintenance cycles.

    Consistent Quality: How We Deliver Reliable DMANTF

    Nobody wants surprises in their raw materials, and that's especially true for our customers. We track every lot with tight GC monitoring and frequent HPLC checks so we catch impurities before they leave our gates. Experienced technicians keep moisture under control with careful drying, knowing this material typically absorbs less water than aminotriphenylmethane derivatives, making shelf life easier to manage. Granular batches pass through our bulk fillers and inspectors lift out any oversized clumps or undertreated fractions before sealing. These are not optional steps. Composite sampling across drums from a given lot lets us spot and address inconsistencies before they affect downstream use.

    We noticed years ago that customers in dye manufacturing pointed out the impact of residual starting amines and trace acidic impurities. Adjusting our purification section and pushing for more controlled nitration and filtration, we've steadily reduced such residues. When we walk the floor and see the real product being packed, it's satisfying to know the comments from R&D scientists halfway across the world have led to such real improvements at the plant.

    Features That Set DMANTF Apart in Industrial Use

    On a practical level, the differences from other nitrobenzotrifluorides matter during actual processing. The dimethylamino group increases electron density, which can speed up some coupling and condensation reactions. Chemists looking to install more complex groups downstream count on the reactivity difference over unsubstituted or mono-substituted analogues. In pharmaceutical intermediates, subtle reactivity changes often translate to shorter reaction times and higher yields, a fact we've documented in internal yield logs from projects run with and without DMANTF.

    We've seen this compound provide more robust coloration in certain disperse dye families. The final color strength shifts, sometimes favorably, due to the electron-donating nature of the dimethylamino group. We hear from customers that they like the consistency lot-to-lot, since batch color never wavers more than a few points against control. Our own colorimetric and chromatographic analyses back those field observations.

    Besides this, the trifluoromethyl group enhances both thermal stability and resistance to oxidative breakdown, which matters during multi-step synthesis or high-temperature operations. In polymer and liquid crystal chemistry, suppliers often ask for raw materials that keep integrity through harsher processing. DMANTF permits longer dwell times before decomposition compared to simpler nitrobenzenes—a property substantiated by our in-house DSC and TGA curves. Down the line, this can reduce waste and extend equipment run-times.

    Real-World Feedback: Listening to Users and Improving Production

    We pay attention to end users. Over the years, pharmaceutical contract manufacturers have told us how DMANTF simplifies the formation of key intermediates for active pharmaceutical ingredients (APIs). Its electron-rich nature enables certain nucleophilic substitutions that would stall using less activated systems. Batch records and lab book notes, passed along by technical teams, let us trace where material performance directly impacts output. That’s how our production group learned precisely what form and purity ranges best serve those drug development customers.

    Dye companies, handling hundred-kilo quantities, report smoother filtration and cleaner product isolation using our DMANTF. This isn't just a laboratory curiosity—we’ve handled return calls and follow-ups ourselves about unclogged filter presses and less backwashing. Our plant floor teams feel the impact in throughput and efficiency, too.

    We’ve also worked closely with agrochemical formulators running pilot-scale reactions. Staff on the customer side want not just purity but batch-to-batch reproducibility, since synthesis routes become costly otherwise. Trust built over years leads to real dialogue; we welcome samples sent to their pilot plants, and have incorporated direct feedback—sometimes down to tweaks in particle size distribution or careful targeting of low ppm-level metal traces. These iterative improvements come from real boots-on-the-ground experience, not just file-drawer specification lists.

    Green Chemistry and Worker Safety: Sustainability in the Plant

    The chemistry of DMANTF brings challenges. Traditional nitration routes use acids and generate strong off-gas. We’ve overhauled ventilation and fume scrubbing, backed by third-party audits, to keep emissions down and energy use manageable. As plant operators, not just managers, we see daily how upgrades—better emission abatement, modified solvent recovery, and drum-pack filters—matter for those who spend their careers beside the reactors.

    Worker safety shapes our choices. Closed transfers and dust control ensure operators want to handle the material shift after shift. On a hot day, it’s the difference between an easy drum changeover and an unpleasant, dusty cleanup job. We’re not outsiders drawing up process flowcharts—we sweep the floors ourselves, troubleshoot pump hitches, and roll pallets right into shipping. Newer handling equipment and less dusty product have reduced cleanup and cut down on PPE use, letting us focus labor on real tasks rather than corrective action.

    It’s not just about inside the gate. Downstream waste streams from our customers benefit from the chemical’s stability and controllable reactivity, leading to easier post-synthesis workup. These factors make a difference once you’ve handled hundreds of runs in real, sometimes imperfect, batch operations.

    Comparison with Other Nitrobenzotrifluoride Derivatives

    Chemists and engineers constantly weigh which aromatic intermediate fits their purpose best. What sets DMANTF apart boils down to its combined electron-donating and electron-withdrawing groups—a rare pairing. The dimethylamino substituent increases reactivity in condensation and coupling steps, while the nitro and trifluoromethyl groups confer enhanced stability against oxidation. We’ve processed mono-substituted nitrobenzotrifluorides and consistently find they require longer reaction times or harsher conditions for installation of complex side chains.

    In recipes calling for para-oriented synthon work, customers sometimes default to more standard nitrobenzenes, only to encounter bottlenecks in subsequent amination or reduction steps. Our own reaction screens make things clear: DMANTF needs less forcing conditions, reducing both energy input and time under heat. This matters—or even makes a project viable—in routes designed for sensitive payloads where thermal or oxidative stress must be tightly managed.

    Take colorant synthesis for textiles. Common nitrobenzenes can yield dull or unstable hues in the final product, sometimes fading during use or storage. Material from our plant supplies higher color fastness and brighter initial chroma due to the molecular influence that the dimethylamino and nitro groups bring, acting synergistically. Several major customers verify this through their own application-specific testing, and return to DMANTF as a reliable backbone even on bulk colorant projects.

    Specifications Tuned to User Experience

    From daily weigh-ups and tank feeds, we’ve learned that strict purity control alone doesn’t guarantee process success. Our technical team worked alongside plant operators to define optimal moisture content and allowable trace metals. We routinely dry final product below the percent range and routinely screen for ppm-level sodium, iron, and copper following actual customer process data—these aren’t just numbers, but figures drawn from field-trial feedback. Lot labels on our drums reflect these real-world learnings, not just book values.

    Crystal form and particle size get as much attention as purity. Engineers in dye or pharmaceutical synthesis often request tailored range, but through trials, we settled on a granular distribution that balances flow and ease of dissolution without caking or causing dust clouds. We back up these choices through hands-on test runs with our own process equipment rather than relying just on spec sheet recommendations. Each time we get a new application request, we work directly with end users to fine-tune our micronization or compacting step, integrating their nominated equipment constraints.

    Transport, Storage, and Customer Support Drawn from Long Practice

    Shipping specialty chemicals isn’t just a matter of shoving product into a drum and dispatching it. Experienced logistics staff handle packing to reduce shift in transit, avoid moisture uptake, and deal with temperature swings during ocean crossing or inland transit. We field our own trained warehouse crew to manage incoming and outgoing lots, maintaining proper rotation so stock doesn’t get stale—a common frustration in slow-moving specialty products.

    Many partners need storage procedures that hold up in real world conditions, not just climate-controlled warehouses. For DMANTF, we found that keeping the product in double-lined fiber drums, stored at moderate ambient temperature, mostly prevents moisture uptake and caking. Our technical support team—often the same chemists and operators who made the batch—stand behind our products. We respond to questions drawn from live process runs, and collaborate on troubleshooting when issues crop up.

    Historically, we’ve handled requests for ship-partial orders and even emergency air dispatch for critically timed projects. We take these as a sign of trust from plant-to-plant, and handle them with the same care as anything that gets our label.

    Continued Innovation: Evolving with User and Industry Demands

    Markets and user needs change rapidly, and we keep pace by investing in process upgrades and fielding feedback directly from chemists, formulators, and engineers. When regulations shift or a novel synthesis route calls for new purity, we pilot-test improvements on our own equipment. For instance, tighter limits on residual solvents drove us to add further purification columns, while periodic spikes in international orders led to a larger packing line for shorter lead times.

    We also work with technology partners to decrease the environmental impact of our output by using solvent recovery units and energy-efficient reactors. This benefits both our own community—operators, neighbors, local government—and customers who face increasing scrutiny on the lifecycle impact of their own products. We see ourselves as part of a broader process, not just a point source, and tailor upstream and downstream practices accordingly.

    Sometimes, a new application brings unforeseen challenges: maybe a customer requires DMANTF for a photoinitiator, noticing issues with isomer formation in highly sensitive downstream chemistry. Rather than passing off stock material and shifting responsibility, our plant managers and lab teams calibrate output—making adjustments in temperature profile, filtration media, or downstream drying—so the resulting product truly meets the later-stage needs. Only hands-on practice, daily plant walks, and long relationships can position a manufacturer to solve these specific challenges.

    Conclusion: Trust Gained Through Hands-On Production

    We see ourselves not just as suppliers, but as active participants in the processes our customers depend upon. The story of 4-Dimethylamino-3-Nitrobenzotrifluoride is written in the daily work of production, shipment, and support. Our plant floor is a place where innovation comes from experience and real-worn feedback, not theoretical ideals. We know the specific challenges of producing, handling, and delivering specialty chemical intermediates because we take each step ourselves—reactor by reactor, drum by drum.

    Over two decades, we’ve watched as new applications broadened, regulations evolved, and performance demands grew stricter. By staying in touch with both the molecule and those who put it to use, we’re able to deliver DMANTF that stands up to real-world scrutiny. Whether it’s making fewer headaches for plant operators, greener emissions, or more productive synthesis, we keep learning and building with every batch.