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

2,4-Dinitro-1-(Trifluoromethoxy)Benzene

    • Product Name 2,4-Dinitro-1-(Trifluoromethoxy)Benzene
    • Alias 1-(Trifluoromethoxy)-2,4-dinitrobenzene
    • Einecs 221-836-2
    • 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

    485399

    Productname 2,4-Dinitro-1-(Trifluoromethoxy)Benzene
    Casnumber 1576-77-8
    Molecularformula C7H3F3N2O5
    Molecularweight 272.10
    Appearance Yellow crystalline powder
    Meltingpoint 65-69°C
    Solubility Insoluble in water; soluble in organic solvents
    Density 1.70 g/cm³ (approximate)
    Purity Typically ≥98%
    Storagetemperature Store at 2-8°C
    Smiles C1=CC(=C(C=C1OC(F)(F)F)[N+](=O)[O-])[N+](=O)[O-]
    Synonyms 1-(Trifluoromethoxy)-2,4-dinitrobenzene
    Hazardclassification Harmful if swallowed; irritant

    As an accredited 2,4-Dinitro-1-(Trifluoromethoxy)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25g amber glass bottle with a tamper-evident cap and hazard labels indicating toxicity and reactivity.
    Shipping 2,4-Dinitro-1-(Trifluoromethoxy)Benzene is shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified as a hazardous chemical and transported following regulations for toxic and environmentally hazardous substances. Appropriate labeling, documentation, and safety precautions are strictly observed to ensure safe handling and delivery.
    Storage **2,4-Dinitro-1-(Trifluoromethoxy)benzene** should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight, heat, and sources of ignition. Avoid storing with incompatible materials such as strong reducing agents or combustible substances. Clearly label the container and store in accordance with local regulations for hazardous chemicals, ensuring secondary containment to prevent spills.
    Application of 2,4-Dinitro-1-(Trifluoromethoxy)Benzene

    Applications of 2,4-Dinitro-1-(Trifluoromethoxy)Benzene in Industrial Manufacturing

    As a direct manufacturer specializing in fluorinated nitrobenzenes, we supply 2,4-Dinitro-1-(Trifluoromethoxy)Benzene to clients operating in advanced sectors where high-purity intermediates are essential to production quality and regulatory compliance. Our downstream partners rely on our rigorous quality management and precise formulation data to support sectors with demanding specifications and strict integration processes.

    1. Agrochemical Intermediate Synthesis

    Crop protection compound manufacturers utilize this compound primarily as a core building block in the synthesis of fluorinated herbicides and fungicides. Its trifluoromethoxy group enhances the physicochemical stability and bioactivity of target molecules. Manufacturing operations require stringent control over impurity profiles and batch processing conditions. We supply material with documentation for traceability and composition, supporting registrations in regulated markets.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • Sustainable Use Directive (2009/128/EC) for agricultural chemicals in the EU

    Typical usage ratio

    • Dosage forms for active ingredient synthesis: 0.3 to 1.5 mole equivalents per batch, adjusted based on target molecule and process route

    Downstream process integration

    • Added during early stage condensation or coupling steps in fine chemical operations
    • Integrated as a halogen or nitro group contributor in multistep molecular construction
    • Purified through distillation or recrystallization after reaction completion
    • Batches tracked under internal and customer traceability protocols

    Final product types

    • Fluorinated herbicide precursors
    • Systemic fungicide intermediates
    • Integrated pest management formulation components

    2. Pharmaceutical Research and Development

    Pharmaceutical companies incorporate this compound into structure-activity studies and lead compound optimization for novel APIs. The molecular scaffold enables unique interactions in early-stage drug discovery, especially in anti-infective and oncology programs. Our material meets research-grade specifications, with full analytical support for regulatory submissions and batch record management.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients (ICH Q7)
    • FDA 21 CFR part 211 for pharmaceutical manufacturing controls
    • IUPAC Nomenclature and chemical documentation accuracy
    • ISO/IEC 17025 Test & Calibration Laboratories Accreditation

    Typical usage ratio

    • Laboratory synthesis: 0.05 to 0.5 mmol per test batch, scalable to pilot plant use based on projected pharmacophore screening volume

    Downstream process integration

    • Introduced during lead molecule analog synthesis steps in medicinal chemistry labs
    • Serves as a functionalized aromatic core for molecular diversification
    • Processed in weighed aliquots with detailed batch documentation
    • Residues and intermediates managed under controlled substance procedures

    Final product types

    • Novel pharmaceutical lead compounds
    • Reference standards for analytical method development
    • Screening libraries for preclinical drug discovery

    3. Liquid Crystal and Display Material Manufacturing

    Producers of advanced liquid crystal materials select this compound as a precursor in synthesizing specialty fluorinated aromatic molecules. These intermediates contribute to electro-optical performance enhancements in thin-film display and switching applications. Our consistency in particle size and purity supports downstream reproducibility crucial for optoelectronic integration.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances
    • IEC 61249-2-21 for halogen content in electronic materials
    • JIS C 0950 for chemical substance management in electronic products

    Typical usage ratio

    • Typically 0.1 to 0.8 mol per synthetic batch, optimized according to the target liquid crystal phase and downstream formulation yield

    Downstream process integration

    • Enters as an acylation or substitution substrate in multi-step synthesis of anisotropic fluorinated aromatics
    • Intermediate purification by column chromatography or crystallization
    • Integrated into masterbatch for nematic or smectic phase mixtures
    • Quality control via high-resolution NMR and LC-MS

    Final product types

    • Custom liquid crystal monomers
    • Modified aromatic intermediates for display films
    • Functionalized fluorine-rich optical materials

    4. Specialty Polymer Additive Production

    Producers of high-performance engineering polymers and coatings employ this compound as a chain modifier or reactive additive, targeting improvements in chemical resistance and surface properties. The electron-withdrawing trifluoromethoxy and nitro functionalities impart unique compatibility with polyimides and aromatic polyethers for use in harsh environments.

    Industry compliance standards

    • UL 94 Flame Retardancy Standard for Plastics
    • ISO 10993 for biocompatibility where relevant
    • ASTM D256 for impact resistance of polymers
    • EN 60216 for electrical insulating materials thermal endurance

    Typical usage ratio

    • Incorporation rates from 0.5% to 2.5% by weight, adjusted according to polymer backbone reactivity and performance criteria

    Downstream process integration

    • Introduced as a co-monomer or functional additive during melt polymerization or solution blending
    • Processing temperatures maintained below decomposition onset (<250°C)
    • Residual monomer content verified prior to downstream film or molded part formation
    • Intermediate QC checks include FTIR and compositional titration

    Final product types

    • High-durability coatings and films
    • Specialty polyimide resins
    • Chemical-resistant polyetherketone blends
    Free Quote

    Competitive 2,4-Dinitro-1-(Trifluoromethoxy)Benzene 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-Dinitro-1-(Trifluoromethoxy)Benzene: Technical Insights from the Lab Floor

    Introduction: An Engineer's Perspective

    Walking through the distillation section, every batch release reminds us why certain intermediates make the cut for demanding synthesis routes. 2,4-Dinitro-1-(Trifluoromethoxy)Benzene turns heads among chemists who expect reliability. There’s no better way to describe it: this compound works through challenges in agrochemical and pharmaceutical builds that trip up lesser molecules.

    Real Form, Real Application

    We produce 2,4-Dinitro-1-(Trifluoromethoxy)Benzene in a tightly controlled crystalline form. Each granule reflects the strict moisture threshold and purity benchmarks demanded by complex synthesis work. Through years at the reactors, we know the batch-to-batch consistency relies on precise temperature surveillance and reaction timing. An off day in the plant can mean an impurity spike, so our staff double-checks every filtration and drying step. The yellow-orange crystals that reach your lab draw on this discipline; we take pride in providing material below 0.2% water, with HPLC showing purity above 99%.

    Production Rigor: Why It Matters

    No shortcut ever pays off when making 2,4-Dinitro-1-(Trifluoromethoxy)Benzene. Any process that doesn't keep the nitro groups under real control risks dinitrophenol byproducts or incomplete reaction—a waste of time and drums of solvent. We favor stepwise addition and multi-stage washing. This practical approach, hammered in from too many lessons learned in hot weather or during sticky distillations, holds contamination down and keeps downstream users out of trouble. By maintaining standardized conditions, our team delivers an on-spec product that moves seamlessly into halogenation, coupling steps, or other advanced modifications.

    Specifications Worth Noting

    We keep our specification sheet within arm’s reach, but most of what matters shows up in everyday handling. Our material melts between 75-78°C, flowing well under standard agitation setups. We measure melting point after every third run as an extra check that lot-to-lot differences won’t throw synthetic routes off. Each batch undergoes infrared verification so that customers can confirm identification without hassle. Moisture brings headaches, so our packing crew checks for clumping and records Karl Fischer measurements in the batch record, not just for regulatory box-ticking. This detail means the powder pours easily, loads well in flasks or continuous flow units, and doesn’t bring the risk of aggregation during storage.

    Why the Trifluoromethoxy?

    The trifluoromethoxy group confers unique properties that pure dinitrobenzenes cannot compete with. In practice, electrophilic substitution reacts more selectively, thanks to this group’s electron-withdrawing power. Chemists get tighter control over regioselectivity, limiting side reactions that drive up purification costs. We’ve seen innovation labs exploit these properties to open new synthetic routes—pushing beyond traditional nitroaromatics. The residue sits out of the aqueous phase on workup, further simplifying downstream steps. For agrochemical developers, the stability and low reactivity with water allow for expanded applications in field-ready actives.

    Performance in Downstream Chemistry

    At this point, our veteran process team knows which reactions sing and which ones sputter. We’ve supplied this molecule to teams focused on constructing intermediates for crop protection agents, APIs, and specialty dyes. The three fluorines sitting on oxygen drastically limit hydrolytic degradation, even in harsh process streams. Process chemists have told us this means less decomposition during challenging oxidation or coupling work. The nitro groups—activated yet not too eager—offer productive starting points for reduction, halogenation, and nucleophilic aromatic substitution. We see repeat orders not because of routine, but because process teams get predictable outcomes: high conversion, low levels of unidentified tars, and less time at the HPLC bench troubleshooting byproducts.

    Comparison to Alternative Nitrobenzenes

    Bench chemists often reach first for basic dinitrobenzenes—practical and cheap. Field feedback, though, shows that those base compounds struggle in scale-up, trailing off in reliability or introducing moisture sensitivity. Our 2,4-dinitro-1-(trifluoromethoxy)benzene holds together in ambient conditions, resisting chemical drift that ruins analogous dinitro series. The added benefit comes through the tailored electron withdrawal: reactions proceed under milder conditions, sparing solvent and keeping profiles cleaner.

    In a real-world campaign, we’ve watched as chemists using unsubstituted dinitrobenzenes waited for hours as reactions crawled to completion—losing yield and burning through extra clean-up. Our product, with the trifluoromethoxy driver, nudges the arrow toward higher conversions and lets reactors turn out more target intermediate per unit of feedstock. We use this in our own R&D, not just because of tradition but due to experience showing how fluoro-group stabilization matters in both bench-scale trials and production batches.

    Practical Storage and Handling

    After years stacking drums in both humid and controlled warehouse zones, we learned a few things no data sheet mentions. The compound needs no refrigeration yet resists degradation; not every nitroaromatic does. We recommend standard precautions—dry, sealed container—but don’t run into off-odors or color shifts after months under proper storage. Even during monsoon seasons or dry winter spells, our quality-control checks have flagged no drop in material integrity.

    For operators, granule size matters at scale. Too fine, and dusting becomes a nuisance during loading; too coarse, and incomplete dissolution slows things down. Through repeated feedback from process partners, we’ve tuned particle size so that the product charges into reactors without excessive build-up in feeders or hoppers. We don’t see caking, and material remains free-flowing, letting operators focus on chemistry, not mechanical issues.

    Why Synthetic Control Pays Off

    The synthesis of 2,4-dinitro-1-(trifluoromethoxy)benzene brings complexity but pays off in performance. We control nitro placement using controlled addition steps and close monitoring. Incorrect order, or skipping a stabilization session, creates off-spec products or eats into yields with unreacted intermediates. We’ve engineered our own solvent systems and adapted quenching procedures to fit both safety and quality needs. Our R&D continued refining details like agitator speed and addition rate, shaving minutes off cycle time but tightening control over the final product.

    We analyze every batch through NMR and HPLC. By listening to user feedback, such as tightening on impurities with overlapping retention times or slightly shifting drying protocols, we’ve cleaned up the product for both our pilot synthesis team and external research partners. Each lesson in batch failure drives improvements; corrections made on our floor show up in fewer call backs for downstream users.

    Environment, Health, and Safety Considerations

    Working around nitroaromatics, we prioritize operator safety and containment. Our process engineers put in triple containment for transfer lines, not as a regulatory checkbox but because leaks caused too many headaches early on. Scalable airflow management, emergency showers, and up-to-date PPE protocols keep our team secure without slowing batch flow. We monitor waste stream content and adapt neutralization agents—lessons from earlier runs stopped us shipping excessive acidic waste to third-party treaters.

    From an environmental lens, our choice of stabilized solvent blends and reduced waste keeps the impact light—customers downstream appreciate documentation showing how we've reduced emissions over several scaling campaigns. Benchmarking loss rates at the distillation stage, we fine-tune scrubber performance and minimize venting. It’s not just stewardship, it’s reducing hidden costs so the product price stays competitive.

    Supply Assurance

    Over the years, we saw how market shocks and interruptions hurt customers when sourcing through multiple middlemen. By handling synthesis, purification, and packaging in-house, we deliver directly, trimming timelines and giving clear answers when customers ask about availability. If a raw material runs tight, our inventory team anticipates needs because they run the forecast loop weekly. Shortages have hit the industry, but we buffer critical inputs—including nitric acid and trifluoromethoxyl intermediate—so customers don’t feel ripple effects.

    Our field technicians communicate with receiving chemists to solve issues the instant a question arises, bridging the gap between manufacturing and use. Over time, partnerships grew stronger because users know they’re working with the original producer, not a repacking or relabeling operation. Every label, drum, and certificate connects back to our QA records; we track everything batchwise, not just for regulatory sense but because process reliability shows up in our repeat customer base.

    Applications That Matter

    Putting 2,4-dinitro-1-(trifluoromethoxy)benzene to work spans industries. Agricultural research picked up our compound for development of crop protection actives needing robust aromatic frameworks. Medicinal chemists chase new target molecules, relying on the stability and reactivity of our product through multiple synthesis stages. Electronic materials research teams have found the trifluoromethoxy group offers a unique pathway to tuned dielectric properties—stories we documented through field collaboration projects.

    We don’t just ship product out the door. Our technical support teams talk synthesis details with users, reviewing conditions for nitration, alkylation, or coupling when results drift or something unexpected appears. Sometimes, a small shift in solvent or temperature solves scale-up issues due to the compound’s precise properties. This feedback loop built up our own in-plant training, as our chemists incorporate lessons directly into SOPs.

    Continuous Improvement by Listening

    Our team never takes consistent quality for granted. Monthly process reviews highlight areas for improvement—whether it’s double-checking incoming raw material purity or refining a solvent recycle protocol. A single complaint about speckling or color fade triggers a root-cause analysis. Those adjustments ripple forward, aligning current production with expectations from researchers and manufacturing partners.

    Industry advances move quickly, so we focus on adaptability. Recent cycles have included tighter particle size control and exploring bio-derived feedstocks for upstream intermediates. Slower crystallization protocols improved density and flow properties, based on storage data and user feedback during the rainy season one year. Our lab regularly pilots alternative hydrogenation schemes to further reduce nitro impurity traces, improving ease-of-handling without adding cost.

    A Community of Practice, Not Just a Transaction

    We maintain contact with customers after orders ship, inviting critical feedback for ongoing joint development. User insights on downstream problems shape future batches. For example, a medicinal chemistry partner noticed microcontaminants traced back to a resin change years ago—so we switched suppliers and documented the clean-up, communicating credit and changes directly. Such shared experience sharpens our internal practices and supports projects that need more than a datasheet or a certificate.

    Research institutes and industrial partners leverage trust built from dealing with a manufacturer invested in their results. Several innovation teams co-developed new processes, using our product as a linchpin. When specification targets changed based on route modifications in new projects, our support chemists collaborated to align batch release criteria within days. That kind of agility stems from keeping every stage under our roof, guided by real technical users.

    Conclusion: Knowledge, Not Just Chemistry

    Materials like 2,4-dinitro-1-(trifluoromethoxy)benzene serve as more than reagents on a shelf. Each kilogram shipped reflects years of chemical engineering, error correction, and exchange with working scientists. The value comes from knowing the quirks, strengths, and pitfalls of the compound, passing along practical advice and adapting to new challenges. In a chemical market that rewards short-term thinking, we bank our reputation on not just making a product, but continuously improving it to meet the real-world needs of partners who expect the best—because we've stood in their lab coats ourselves.