Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene

    • Product Name 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene
    • Alias DCNT
    • Einecs 401-050-9
    • 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

    775391

    Chemical Name 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene
    Cas Number 2252-50-8
    Molecular Formula C8H4Cl2F3NO2
    Molecular Weight 274.03 g/mol
    Appearance Yellow crystalline powder
    Melting Point 57-60°C
    Density 1.63 g/cm3
    Solubility Insoluble in water
    Purity Typically ≥98%
    Synonyms 3-Nitro-2,4-dichloro-5-(trifluoromethyl)toluene

    As an accredited 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g amber glass bottle with tight-seal cap, labeled with hazard symbols and product information, shipped in a secure protective carton.
    Shipping 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled as a hazardous chemical and handled according to relevant regulations. Transportation should comply with local and international guidelines for dangerous goods, ensuring appropriate safety and emergency procedures are in place.
    Storage 2,4-Dichloro-5-trifluoromethyl-3-nitrotoluene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep away from incompatible materials such as strong oxidizers and acids. Store at room temperature, and label clearly. Avoid exposure to moisture and ensure proper chemical waste protocols are followed.
    Application of 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene

    Applications of 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene in Industrial Manufacturing

    2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene serves as a key intermediate in the synthesis of specialty chemicals. Our manufacturing approach ensures strict quality control for various downstream sectors requiring this raw material for advanced transformation steps. The following sections describe principal industrial applications with detailed process and compliance references.

    1. Agrochemical Intermediate for Herbicide Synthesis

    Manufacturers in the agrochemical sector use this compound as a core intermediate in selective herbicide synthesis routes targeting broad-leaf weed control. During multi-step synthesis, the raw material acts as a halogenated aromatic building block, entering after initial nitration but before etherification or alkylation stages. Its reactivity profile enables formation of active ingredients such as fluorinated anilines utilized in post-emergent formulations. Process engineers adjust feed ratios to control conversion rates and achieve repeatable batch purity for downstream coupling reactions.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for agrochemical intermediates
    • China GB/T 22151.1-2008 for pesticide technical requirements
    • REACH (EC No 1907/2006) registration for import and production in the EU
    • US EPA Pesticide Registration requirements for included actives

    Typical usage ratio

    • 0.9–1.1 molar equivalents relative to the primary amination substrate
    • Adjusted according to specific reaction stoichiometry during batch or continuous processing
    • Small-scale validation at 100–120 g/L formulation loads for pilot samples
    • Final plant volumes for industrial runs depend on target throughput ranges

    Downstream process integration

    • Feeds into condensation or nucleophilic substitution steps in active ingredient manufacture
    • Reaction in stainless reactors with temperature control (80–110°C, often inerted with N₂)
    • In-process monitoring for residual nitrotoluene via HPLC
    • Products isolated by liquid-liquid extraction and crystallization before downstream formulation

    Final product types

    • Fluorinated herbicide actives (e.g., substituted anilines or benzotriazoles)
    • Granular and emulsifiable herbicidal formulations
    • Soluble concentrates for field use
    • Premixes for multi-active crop protection blends

    2. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical manufacturers utilize 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene as an advanced intermediate for non-steroidal anti-inflammatory drug (NSAID) and antifungal API synthesis. The material enters the flow after halogenation and nitration stages, facilitating aromatic modification during late-stage construction of pharmaceutical scaffolds. Chemists capitalize on the electron-deficient aromatic ring for regioselective substitutions, enabling downstream reduction and coupling with protected amines or heterocycles. Quality assurance teams monitor both starting material quality and final residuals to meet registration standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs for process and impurity control
    • FDA 21 CFR Part 211 for finished pharmaceuticals
    • EU GMP Vol 4 Part II for synthesis and isolation of pharmaceutical intermediates

    Typical usage ratio

    • 1.0 molar equivalent per synthetic step involving aromatic substitution or catalytic hydrogenation
    • Batch reactions typically run at 50–75 g/L substrate concentrations in pharma-grade solvents
    • Adjustment based on yield optimization during development work
    • Scale-up validated through process analytical technology (PAT) controls

    Downstream process integration

    • Introduction post-halogenation, prior to Pd-catalyzed coupling or nitro reduction steps
    • Integrated isolation and purification via column chromatography or crystallization
    • Strict analyte residue tracking to comply with Q3A/B impurity limits
    • Material transfers to GMP cleanrooms for final API assembly

    Final product types

    • NSAIDs with trifluoromethyl-substituted aromatic pharmacophores
    • Azole or triazole antifungals incorporating fluorinated rings
    • Intermediates for synthesis of personalized therapeutics
    • Pharmaceutical tablets and parenteral solutions

    3. Specialty Dye Manufacturing

    The pigment and dye industry deploys this raw material in the production of halogenated aromatic dyes and colorants, especially those requiring stability and defined chromaticity under UV exposure. The compound acts as a precursor for azo and anthraquinone derivatives used in plastics and fiber dyeing. Process engineers integrate it during azo coupling or electrophilic aromatic substitution, balancing purity versus reactivity to minimize color by-products. Strict stewardship is maintained throughout blending and post-treatment to comply with colorant safety protocols.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textiles
    • EN 71-3:2019 for migration of colorants in toys
    • Registration with REACH for dye ingredient supply in EU
    • ASTM D2256 for synthetic fiber colorant quality testing

    Typical usage ratio

    • 40–90 g per kg total dye batch in azo pigment blend formulations
    • Exact loading dictated by final color strength and tinting needs
    • Tuning of usage based on reactivity with diazonium partners
    • Evaluation in pilot production to avoid off-hue formation

    Downstream process integration

    • Acts as starting building block in in situ dye synthesis
    • Chemical coupling in aqueous or organic solvent conditions at 30–80°C
    • Post-processed via salting or spray-drying before milling
    • In-process UV-VIS monitoring for chromatic value and purity

    Final product types

    • Water-soluble textile dyes for polyester and nylon
    • Masterbatch pigment preparations for plastics
    • High-performance colorants for printing inks
    • Fluorinated azo pigments for industrial coatings

    4. Electronic Chemical Synthesis (Display Materials)

    This material supports advanced electronics manufacturing, functioning as a core intermediate for the construction of organic light-emitting diode (OLED) and liquid crystal display (LCD) components. Electronic chemical engineers value its halogenated, trifluoromethyl-substituted ring for imparting charge-transfer properties and UV stability to end-use molecules. Integration occurs prior to constructing small-molecule transport layers or color filter elements. Downstream yield, purity, and contamination trends are actively monitored to meet electronic chemical supply chain requirements.

    Industry compliance standards

    • IEC 62474 for reporting substances in electrotechnical products
    • RoHS Directive 2011/65/EU regulating hazardous substance content
    • IATF 16949 for supply to automotive electronic component manufacturing
    • SEMI S2 for chemical safety in semiconductor fabrication

    Typical usage ratio

    • 25–65 g per kg total OLED intermediate batch
    • Higher purity grades required at >99.5% for electronic chemical feedstocks
    • Ratio adjusted to device specification (e.g., blue or green emitters)
    • Batch blending precisely measured to control elemental contaminant profiles

    Downstream process integration

    • Input before Suzuki or Stille cross-coupling reactions for aryl building blocks
    • Reactor charging under inert gas, stringent moisture and dust controls
    • Extraction and recrystallization steps to ensure compositional consistency
    • Quality confirmed by ICP-MS and FTIR analysis pre-device integration

    Final product types

    • OLED emitter materials for advanced displays
    • LCD color filter precursors
    • High-purity small molecules for organic semiconductor devices
    • Functional intermediates for printable electronics

    5. Fluorinated Polymer Modifier Synthesis

    Producers of specialty plastics and coatings use the compound to introduce trifluoromethyl, chloro, and nitro functionalities during the creation of tailored polymer modifiers. These modifiers increase hydrophobicity, chemical resistance, and dielectric properties in base polymers. The integration occurs via nucleophilic aromatic substitution prior to chain extension or copolymerization. Careful control of final monomer conversion ensures that downstream modifiers meet global performance standards in demanding environments like wire insulation and chemical process tanks.

    Industry compliance standards

    • UL 94 Flammability Standard for plastic components
    • ASTM D543 for chemical resistance testing in plastics
    • ISO 14001 Environmental Management for specialty resin production
    • EU Regulation (EC) No 1935/2004 for polymer materials in food contact applications (where applicable)

    Typical usage ratio

    • 15–40 g per kg polymer feedstock during modifier synthesis
    • Adjustment follows physical/chemical target properties of end polymer
    • Screening at pilot scale for optimal balance of tensile strength and solvent resistance
    • Range depends on base resin/reactive group compatibility

    Downstream process integration

    • Prepolymer functionalization within small-batch glass reactors at 50–120°C
    • Addition before free radical or condensation polymerization steps
    • Removal of unreacted materials via solvent wash and precipitation
    • Structural validation by NMR and GPC prior to compounding or extrusion

    Final product types

    • Hydrophobic modifier additives for technical coatings
    • High-durability wire and cable insulation resins
    • Anticorrosive lining additives for chemical processing tanks
    • Functional fluorinated co-monomers for specialized plastics
    Free Quote

    Competitive 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene: Building Quality into Synthesis

    Understanding the Value of Precision Chemical Manufacturing

    Instead of approaching fine chemical production as just another process step, we place respect for molecules at the core of our work. Years spent in the plant, monitoring reactors in all conditions, reinforce that every batch of 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene tells a story. Even minor differences—temperature shifts, mixing rates, subtle pH swings—leave permanent marks on the outcome. Learning from experience, I have seen how careless sourcing or process shortcuts ripple through the supply chain, turning ambitious research projects into frustrating troubleshooting sessions. Our aim is different: we build in quality so scientists can focus on solving meaningful challenges, rather than backtracking over avoidable errors.

    Product Identity: Structure and Character

    2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene, often abbreviated for convenience yet treated with full technical diligence, stands out for its specific arrangement of functional groups. Within the aromatic ring, chlorines at the 2 and 4 positions work in tandem with a strong electron-withdrawing trifluoromethyl group at position 5, while a nitro group at position 3 rounds out the pattern. Every production run aims for chemical consistency, because research teams count on well-defined starting materials. Reliable molecular integrity means chemists aren’t fighting background noise, whether scaling up for pilot trials or assembling combinatorial arrays.

    Chemical formula: C8H4Cl2F3NO2. Its structure isn’t some off-the-shelf benchtop tool; it serves in advanced agrochemicals, sophisticated dyestuff intermediates, and pharmaceutical exploratory work where precise reactivity is everything. The unique substitution pattern delivers a specific reactivity profile, letting synthetic chemists manipulate electron density along the ring and achieve selective transformations most other toluenes simply cannot support.

    Specifications that Reflect Field Experience

    Years of hands-on manufacturing taught us what purity means for process reliability—not just for filling a column in a datasheet, but for keeping a synthesis on track at the end user’s bench. Purity for our 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene consistently reads above 99 percent by GC, with water content recorded down to the tens of parts per million by Karl Fischer titration. Color and physical appearance, though often treated as cosmetic by outsiders, matter to process engineers and analysts. Crystalline solid formation, without excessive oiling or discoloration, aids in downstream handling and accurate massing during scale-up. Trace impurities, particularly isomeric forms or over-chlorinated products, are tightly watched—our history with process mishaps and repeated corrective actions has taught every technician the consequences of letting tails persist.

    Quality Means Accountability, Not Just Compliance

    Quality control isn’t a box to check for us—it’s a set of direct actions, embedded from the earliest pilot batches to each regular run. Most chemical workers have war stories about poorly characterized intermediates derailing weeks of effort. Our in-process control checks go far beyond relying on supplier specs or accepting average numbers. By scrutinizing batch-to-batch variance using validated chromatographic methods, we catch trends that point to reactor fouling or subtle feedstock shifts before they snowball. Accountability comes down to giving researchers a real measure of confidence in their reactants—cutting down phone calls, sample retesting, or unnecessary troubleshooting that eats up grant money and resources.

    Practical Manufacturing: What Sets Our Approach Apart

    The plant floor poses more variables than any engineering text can capture. Reaction vessels see everything from sweltering mid-summer heat to deep-winter cold snaps. Every tank loading, washout, and charge of starting material gets logged and double-checked. We build and regularly validate cleaning protocols, knowing firsthand how residues from an earlier run can taint a new batch and require expensive do-overs. Process safety protocols keep our team secure—chlorinated-aromatic chemistry demands respect, due to potential off-gassing and heat release during certain steps.

    Solvent choice didn’t emerge from a theoretical ideal. We optimized after months of lab and pilot trials, balancing solvent performance with downstream removal and waste disposal challenges. Handling the trifluoromethyl group, for example, brought several rounds of trial-and-error before we reached high yields without excessive loss or decomposition. Sourcing raw halogenated aromatics relies on long-term relationships with established producers, because we’ve seen how supply interruptions or inconsistent grades tank reliability. These are lessons that come only from operators who live with their results—not traders who only handle paperwork.

    Distinction from Related Aromatic Intermediates

    Some may mistake 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene for its close chemical relatives, such as 2,4-Dichlorotoluene or 3-Nitrotoluene derivatives. Their reactivity diverges, due to strategic placement of the trifluoromethyl and nitro groups. Substitutions across the aromatic ring adjust the electron flow and reactivity in cross-coupling, nucleophilic substitution, and reduction steps. These chemical realities affect what’s possible in both discovery and scale-up. We pay attention to how our intermediate will behave as a substrate under a wide range of catalyst and pressure conditions—control over isomerism and side reactions saves significant time in process development.

    Comparing with generic dichlorotoluenes, our product’s trifluoromethyl group shifts physical properties—boiling point, solubility in selected solvents, and even chromatographic behavior during in-process analysis. The nitro functionality further tweaks its profile, facilitating key steps such as selective reductions to amines, which build into higher-value intermediates in fine chemical routes. Our familiarity with technical failures in substitution patterns lets us anticipate where selectivity breaks down, ensuring that clients avoid repetitive column chromatography or costly post-processing.

    Reliability at Scale: Avoiding the “Small Batch” Trap

    In a market crowded with repackagers and brokers, true scale manufacturing takes another level of commitment. Scaling aromatic intermediates highlights all the flaws hidden in laboratory syntheses. Our transition team tackles issues like seed crystal control, heat dissipation in multi-kilogram reactors, and waste stream management for halogen and nitro-containing compounds. Regulatory landscapes have tightened steadily—our plant stands up to periodic auditing and traceability checks, built over years of routine government and client inspections.

    Stability evaluation doesn’t stop at theoretical shelf-life predictions. We have lived through failed shipments and deformed packaging enough times to know the pains of product degradation during transit. Moisture ingress, vibration, and temperature swings in logistics pipelines all threaten sensitive organics, so we bundle shipments with robust, tested packaging that stands up to real-world handling. We select liners, seals, and drum materials with the same seriousness as the chemistry itself.

    Support for Chemical R&D and Industrial Synthesis

    Scientific programs depend on trusted sources of specialty intermediates. The research team shouldn’t lose time parsing ambiguities in purity reports or dealing with unpredictable residues that alter catalyst performance. Our product supports academic, government, and industry discovery teams by delivering what modern chemistry requires—transparency, not just technical compliance. We share real QC data, including full chromatographic traces, typical impurity profiles, and raw analytical curves, because nobody should operate from summary sheets alone. Our own technical team welcomes the challenge when a demanding process requires tighter control, alternate solvents, or custom particle sizing for a unique reaction need.

    Process chemists and formulators draw from foundation-grade intermediates. In our own plants, we’ve seen the costs—not just financial, but in time lost and morale—when a faulty intermediate or mischaracterized impurity forces a halt. We’ve responded to customer requests for precise particle cuts, custom blending, and even joint troubleshooting of scale-up failures. These interactions shape a product that adapts to the top requirements emerging from real-world use, not just theoretical “market demands”.

    Working Under Evolving Compliance Standards

    Manufacturing specialty halogenated organics under modern regulations means more than updating paperwork yearly. Each new customer inquiry and regulatory update prompts a full review of our environmental release controls, occupational health protections, and waste treatment strategies. Our team carries out air and wastewater testing not just to meet the law, but because the impact on neighbors and communities stays with us long after a batch ships. Years watching projects forced to switch suppliers for compliance reasons convinced us that transparent, locally valid records build trust that outlasts marketing brochures.

    Every operator knocking off a shift wants to know their plant sends out safe, non-contaminating products. So we partner with independent labs and keep our management system up-to-date, making sure chemical producers up and down the supply chain can verify that both listed and new substances are under control. Packaging carries all the pertinent hazard information, including GHS-aligned labeling, and we keep safety data sheets within easy reach for users and shipping partners.

    Applications: Beyond Niche Functions

    Research teams and process engineers look at molecules like 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene as gateways into broader chemical spaces. In our direct work with industry and academic partners, we have seen the product deployed as a central intermediate for the construction of complex heteroaromatics. Reactions that leverage the combined electron-withdrawing effects promote pathways that remain out of reach with simpler toluenes. Agrochemical innovators turn to this compound when designing new field-stable actives that must weather photolysis and microbial breakdown—properties inherited from judicious ring substitution.

    Dye manufacturers benefit from the reactivity tuning enabled by the nitro and trifluoromethyl groups, creating colorants with improved fastness and substrate penetration. Medicinal chemistry programs frequently require such multi-substituted toluenes as test-beds for structure–activity discovery, because the compound’s framework aligns with scaffolds in exploratory clinical candidates. Buying from a source with decades of focused specialty aromatic chemistry experience means avoiding delays, retests, or reorders due to incomplete intermediate performance.

    Responding to Industry Feedback: Lessons Built In

    Operators on the production line keep notebooks full of lessons hard-earned through missteps and successful runs alike. Some suppliers operate with a distance between office and plant; our site leadership walks the floor, takes feedback directly from the shift team, and tracks it through to process changes. Chemists working at the bench (and in the control room) flagged issues like solid breakage during shipping, or obscure odorous residues that resisted filtration. Fielding these calls led to overhauling our purification and packaging phases, and introducing finer in-line analytics before packing.

    No amount of sales speech compares with a regular report card from users in the field. Customers have pointed out batch-specific differences—sometimes in trace byproducts, sometimes in flowability or storage characteristics—and we have changed raw material sourcing or drying times in direct response. By making process changes public, we demonstrate not just legal compliance, but a visible commitment to continuous improvement as a manufacturer.

    Collaboration and Customization

    Specialty chemical users often operate at the technical limits of process and instrumentation. Some require custom particle sizes to enhance the dissolution rate in particular media; others look to improve recovery yields in high-throughput screening workflows. We answer these needs not through generic product variants, but through collaborative dialogue—tracing challenges to root causes, confirming on our own bench-scale reactors, and rolling out tailored process modifications at industrial scale. This approach isn’t a sales add-on, but part of adapting chemical manufacturing to the evolving landscapes of pharma, agro, and specialty industry work.

    Our technical service staff regularly find themselves working out impurity profiles alongside customer QC chemists. Shared analytical spectra, process logs, and deviation reports form part of each solution we build. Close collaboration rewards both sides—customers receive a material shaped to their process needs, and we build new process understanding into our plant-wide governance, making each subsequent production round that much more robust.

    Responsibility Beyond the Plant Gate

    Responsible care for 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene includes open communication about hazards, exposure controls, and responsible transport. Labels highlight real risks, so nobody in storage, transit, or handling receives an unwanted surprise. Waste minimization and solvent recovery anchor our daily operations, as we strive to keep resource use in line with global expectations for sustainable chemistry. We conduct internal safety drills, review near-miss reports rigorously, and tie corrective action to both operations and management review—because actual safety lies in follow-through, not just plans.

    Within our team, we pass on best practices for PPE, spill response, and first-aid procedures. We partner across the supply chain to encourage the same rigor, because gaps at one node can cascade, affecting worker health or creating environmental liabilities down the road. Through open dialogue and detailed documentation, we give downstream manufacturers the transparency they need for worker training and site audits.

    Trust Built Through Ground-Level Experience

    Real trust in a specialty intermediate, particularly one as nuanced as 2,4-Dichloro-5-Trifluoromethyl-3-Nitrotoluene, develops through hard-earned reliability. Each consignment leaving our plant carries both our technical reputation and our operational integrity. As manufacturers, we stake our standing not on certificates or batch numbers, but on the collective memory of every operator, shift supervisor, and QC chemist who keeps the process resilient. For the research scientist planning the next synthesis, the reliability of our product sets a foundation that extends from the first flask to pilot plant and commercial launch—freeing innovators to focus on breakthroughs, rather than patching preventable supply chain gaps.