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3,5-Dichloro-4-Fluorobenzotrifluoride

    • Product Name 3,5-Dichloro-4-Fluorobenzotrifluoride
    • Alias 3,5-Dichloro-4-fluorobenzotrifluoride
    • Einecs 401-090-9
    • 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

    720007

    Productname 3,5-Dichloro-4-Fluorobenzotrifluoride
    Casnumber 74489-94-4
    Molecularformula C7H2Cl2F2
    Molarmass 213.99 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 175-177 °C
    Meltingpoint -15 °C (approximate)
    Density 1.54 g/cm³
    Solubilityinwater Insoluble
    Refractiveindex 1.505
    Purity Typically ≥98%
    Flashpoint 67 °C
    Vaporpressure 0.52 mmHg at 25 °C
    Smiles FC1=CC(Cl)=C(C(F)(F)F)C(Cl)=C1
    Storagetemperature Store at 2-8 °C

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 100 grams of 3,5-Dichloro-4-Fluorobenzotrifluoride, labeled with hazard warnings and chemical details.
    Shipping 3,5-Dichloro-4-Fluorobenzotrifluoride is shipped in tightly sealed containers, away from incompatible substances and moisture, under ambient temperature. Transport must comply with local and international regulations regarding hazardous chemicals. Appropriate hazard labeling is required. Ensure containers are upright and secure during shipping to prevent leaks or spills. Handle with protective equipment if opened.
    Storage **3,5-Dichloro-4-Fluorobenzotrifluoride** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances like strong oxidizers. Protect from heat, moisture, and direct sunlight. Store away from ignition sources and ensure proper labeling. Use secondary containment to prevent leaks and restrict access to trained personnel only. Follow all relevant safety guidelines.
    Application of 3,5-Dichloro-4-Fluorobenzotrifluoride

    Applications of 3,5-Dichloro-4-Fluorobenzotrifluoride in Industrial Manufacturing

    3,5-Dichloro-4-Fluorobenzotrifluoride serves as a key intermediate within several downstream sectors where chemical reliability and precision integration define product consistency. We manufacture this material to meet global standards and performance expectations for specialty production environments. The following scenarios illustrate targeted industrial uses where this compound enters the value chain, providing essential functionality and supporting rigorous compliance frameworks.

    1. Agricultural Crop Protection Intermediates

    This compound functions as a core building block in the synthesis of advanced agrochemical active ingredients, enabling the downstream production of herbicides and fungicides with specific halogenated profiles. Our material supports large-scale manufacturing processes designed to achieve traceability and product purity mandatory for regulated agricultural markets, and suppliers select it for its stability during multi-step synthesis under chlorination and fluorination conditions.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)
    • GB 2763 - China National Food Safety Standard for Maximum Residue Limits
    • ISO 9001:2015 Quality Management for chemical intermediates

    Typical usage ratio

    • Applied at 12–20% of the total batch mass in intermediate reaction steps; exact ratio varies based on target active compound molecular design and desired yield.

    Downstream process integration

    • Charged into closed system reactors following initial halogenation phase during multi-step aromatic substitution; reacts under controlled temperature (60–100°C) and pressure with proprietary base catalysts before further derivatization and condensation.

    Final product types

    • Halogenated herbicide actives (e.g., flurochloridone, trifluralin derivatives) for formulated crop protection agents.
    • Late-stage pesticide intermediates for formulation export.

    2. Pharmaceuticals – Advanced API Intermediate Synthesis

    Our material provides a critical halogenated aromatic core for the synthesis of select active pharmaceutical ingredients (APIs), primarily within the synthesis chain for small-molecule anti-infective and CNS pharmaceutical sectors. Downstream formulators rely on this compound for consistent impurity profiles and defined reactivity profiles in multi-step chlorinated aromatic reactions under GMP conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary) for designated APIs
    • European Pharmacopoeia General Chapter 2034 (Residual Solvents)
    • China GMP 2010 Edition

    Typical usage ratio

    • Added at 6–11% per reaction batch, adjustable based on API yield targets and downstream step efficiency.

    Downstream process integration

    • Introduced after initial aromatic ring construction within multi-step organic syntheses, followed by nucleophilic substitution or Condensation with secondary amines and ketones, adhering to validated process protocols for trace impurity control.

    Final product types

    • Active pharmaceutical ingredient intermediates for anti-infectives
    • CNS-active API scaffolds used in downstream tablet and injection formulations

    3. Specialty Fluorinated Polymer Synthesis

    This material enters the specialty polymers sector as an integral monomer or functional additive for high-performance fluorinated polymers and copolymers, targeting applications that demand both chemical resistance and low dielectric constants. Polymer manufacturers utilize it in tightly controlled feed ratios to achieve engineered polymer chain architectures.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (EU chemicals registration)
    • ISO 9001:2015 for polymer process control
    • UL 94: Flammability Standard for Plastic Materials
    • ASTM D543 (Chemical Resistance of Plastics)

    Typical usage ratio

    • Between 3–8% by weight in monomer feedstocks; dosing precision is critical to final polymer molecular design.

    Downstream process integration

    • Fed into pressure-rated polymerization vessels along with primary monomers under inert atmosphere (N2 or Ar); functionalization occurs by co-polymerization, typically between 100–180°C, with real-time FTIR or NMR monitoring for conversion rates.

    Final product types

    • Specialty fluorinated copolymers for electronics encapsulation
    • High-durability coatings used within chemical processing equipment

    4. Electronic Chemicals – Liquid Crystal and Semiconductor Process Chemicals

    Electronics and display manufacturers specify this compound for its defined halogen pattern, which supports the synthesis of specialty aromatic compounds used in liquid crystal mixtures and as an etchant precursor in semiconductor cleaning. The material’s purity and trace metal content align with demanding electronic chemicals supply requirements.

    Industry compliance standards

    • SEMI C93 (Standard for Electronic Grade Organic Chemicals)
    • IEC 62474 (Material Declaration for Electronic Industry)
    • RoHS (2011/65/EU Restriction of Hazardous Substances in Electronics)
    • ISO 14001 Environmental Management for chemical processes

    Typical usage ratio

    • Range of 2–7% in precursor solution formulations; ratio determined by required molecular alignment profiles in liquid crystal or purity in wet process chemicals.

    Downstream process integration

    • Introduced into aromatic synthesis campaigns producing specialized liquid crystal components, or into wet etching chemical manufacturing, using closed-system liquid feeding with inline conductivity and particle count controls.

    Final product types

    • High-purity liquid crystal compounds for TFT-LCD and OLED displays
    • Photoresist and etching process chemicals for semiconductor wafer fabrication

    5. Fine Chemicals – Aromatic Performance Additives

    The product acts as a precision aromatic building block within the fine chemicals industry, especially for the downstream synthesis of specialty performance additives such as UV stabilizers and selected dyes. Manufacturers in these markets require traceability and reproducibility in batch-to-batch performance for demanding industrial formulations and retail shelf stability.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 14001 for controlled environmental impact in fine chemical synthesis
    • EN 71-3 (Migration of Certain Elements in Toys, for colorant safety)
    • GHS (Globally Harmonized System) labeling for downstream distribution

    Typical usage ratio

    • Added at 4–10% of additive precursor mass; adjusted based on stability testing and end-use application requirements.

    Downstream process integration

    • Charged into multi-reactor aromatic substitution processes, typically after solvent control and before color-forming or stabilizer coupling reactions, with product tracked by HPLC and spectroscopic analysis in QC labs.

    Final product types

    • UV stabilizer additives for automotive or packaging plastics
    • Specialty dye precursors for high-performance industrial and textile use
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    Certification & Compliance
    More Introduction

    3,5-Dichloro-4-Fluorobenzotrifluoride: Our View on a Key Specialty Chemical

    A Daily Encounter in Our Manufacturing Process

    Walking through a modern specialty chemicals plant, you constantly notice vessels filled with complex aromatic compounds. Among those, 3,5-Dichloro-4-Fluorobenzotrifluoride often stands out because of its distinct role in synthetic chemistry. This compound, sometimes referred to in shorthand as its model number, CAS 173611-13-9, has become a necessary intermediate in our lineup. From our experience working with hundreds of different halogenated aromatics, few manage to offer the versatility packed into this molecule.

    Molecular Profile: What Sets It Apart

    In our facility, we manufacture 3,5-Dichloro-4-Fluorobenzotrifluoride as a transparent to pale yellow liquid, with a boiling range typically starting a little above 180°C. The molecular formula is C7H2Cl2F2CF3, combining two chlorine atoms, a fluorine atom on the ring, and a trifluoromethyl group. These seem like small details, but each atom has a purpose: Cl and F substitutions shift reactivity and physical properties in ways that aromatic chemists immediately value. The density and vapor pressure give us clues about handling and storage, but chemists usually pay more attention to the stability conferred by the electron-withdrawing groups. This ensures consistent shelf-life, which matters for projects running six months to a year.

    Not Just a Link in a Chain

    It’s tempting to think of specialty intermediates as generic stepping stones. Yet every step in a complex synthesis brings its own set of problems. Our technical team deals with these day in, day out, and experience with 3,5-Dichloro-4-Fluorobenzotrifluoride tells us the product solves several pain points in downstream processes. The unique combination of halogen and trifluoromethyl groups means it doesn’t just plug into a synthetic route anywhere; it plays best in select agrochemical and pharmaceutical pathways where a high degree of electronic tuning is essential.

    In the Real World: Application Insights

    Most production batches leaving our line support R&D teams or pilot plants synthesizing advanced intermediates for crop protection compounds and certain active pharmaceutical ingredients. Our colleagues in these sectors push for high selectivity, reaction efficiency, and reproducibility. Based on feedback from long-term partners, switching from unfluorinated or non-chlorinated benzotrifluorides to this molecule typically boosts both yield and environmental profile—like reduced byproducts and cleaner separations. We often see our product serve as a starting block for nucleophilic aromatic substitution or for constructing more elaborate fused structures. Such postsquenching transformations rely on the careful arrangement of substituents, which this molecule delivers out of the gate. For plants pushing toward lower-waste processes, this aspect moves the needle.

    Comparing with Similar Intermediates

    Many buyers begin by comparing 3,5-Dichloro-4-Fluorobenzotrifluoride to close cousins like the dichloro or monochloro analogs, or variants bearing just a trifluoromethyl or a single fluorine. Our production team faces the real differences in crystallization, volatility, and solubility head-on. The combination of three strong electron-withdrawing groups secures greater resistance to side reactions than dichloro- or monofluoro-only options. This permits higher reaction temperatures or longer dwell times if needed, widening the processing window. Operators running continuous systems learn to appreciate the molecule’s consistent liquid form over a broad temperature range because it minimizes blockage and fouling risks.

    In our hands, handling safety also takes a front seat. It doesn’t bring the acutely toxic or flammable hazard profile that often comes with heavily halogenated aromatics. That allows us to maintain a safer work environment and investigate optimization at larger scales without running into roadblocks with safety or containment. Over the last decade, we’ve seen regulatory attention shift toward greener chemical routes. The clear, reproducible structure and stability of this compound make it much easier for customers (and for us as a manufacturer) to maintain transparent records and pass compliance checks.

    How We Handle Quality Control

    Making sure the end product meets quality benchmarks means hands-on analysis, round after round. Every batch that leaves our plant gets rigorously checked using gas chromatography and proton NMR. We target a minimum purity of 99%. Customers sometimes request even tighter specs—like ultra-low water or acid content—because that can make or break performance in sensitive pharmaceuticals. Achieving this level of purity requires precise reaction control, careful quench and extraction, then multi-stage distillation under reduced pressure. Here’s where experience counts: we’ve optimized the distillation cut points and inert-atmosphere storage so the shelf life rarely dips below twelve months.

    Our technical support team keeps close tabs on feedback from downstream users. Sometimes, minute variations in impurity profiles pop up. We treat that data as fuel for continuous improvement. We’ve spent years dialing in our processes to minimize isomerization and unwanted side products, relying heavily on spectroscopic fingerprinting and batch retention for rapid troubleshooting. The result: pharma and agrochemical clients consistently log fewer downstream purification challenges—saving both time and solvent.

    Our Approach to Supply and Logistics

    Shipping sensitive chemical intermediates has taught us a few things about packaging and transport resilience. We use fluorinated HDPE drums or stainless steel IBC totes, depending on order size and customer preference. Each shipment leaves with tamper-evident seals and a full analytical report from our in-house QC lab. International buyers place a premium on robust documentation and certification for each lot, which we provide alongside standard transport papers.

    Long-term customers value predictable supply above everything else. Even slight interruptions in availability can set off a domino effect that jeopardizes key launches or registration deadlines. For this reason, our site management continually adjusts inventory buffers and adjusts batch scheduling, prioritizing this intermediate during pre-seeding and pre-drug-registration seasons. Our direct link to key raw material suppliers insulates us from many market disruptions that have cropped up over the last two years. We put in the hours to make sure buffer stocks remain in line with production forecasts. Our logistics crew continually revisits routes and partners to keep lead times tight, often adjusting on the fly if sea or rail delays threaten delivery schedules.

    Developing New Uses and Collaborations

    We treat every inquiry about novel applications for 3,5-Dichloro-4-Fluorobenzotrifluoride as a chance to learn. The most compelling recent collaborations have come from outside the traditional agrochemical and API spaces. Coatings formulators and specialty polymer producers have begun investigating this compound for introducing site-specific reactivity or improving weatherability of finished products. By sharing analytical data and reactivity profiles with collaborators, we see new routes opening up, such as fluorinated polymer backbones for electrolytes or high-performance dielectric materials. Our R&D team takes pride in partnering closely on pilot batches, shifting reaction conditions and purification strategies to suit emerging needs. This approach has led to patent filings and new commercial processes.

    For our own internal pipeline, we focus on cutting steps and solvents every year. Solvent-recovery and energy management are ongoing challenges, so we continually tweak our flowsheets and utilities. At every turn, safer reagents and milder conditions take precedence. We’ve benchmarked dozens of other halogenated aromatic intermediates for waste output, with 3,5-Dichloro-4-Fluorobenzotrifluoride repeatedly performing in the range of less than 20 kg non-recoverable waste per ton of output, when handled in our updated process trains.

    Common Pitfalls and How We Address Them

    Producing and supplying this compound reliably means tackling a few repeating headaches. Moisture ingress can impact purity and downstream reactivity, leading to side product formation or loss of yield. Our answer has been closed-loop nitrogen blanketing through each stage and routine spot checks by Karl Fischer titration. Another recurring lesson is related to the buildup of low-boiling impurities in distillation. Proactive column maintenance and in-process GC tracking detect excursions before they affect product shipment. Our staff training goes beyond the basics to include routine batch data review, ensuring deviations can be flagged and corrected early.

    We also know the pitfalls of upstream raw material variability. At least twice a year we carry out deep-dive audits with our suppliers, testing not just the raw materials but also their own supply chains for stability. It’s taken years to find the right partners and cultivate mutual transparency—a major win for everyone relying on end-to-end traceability. In regulatory inspections, we present batch records tracing back every raw material lot, fielding questions about reaction byproducts with detailed analytical results at hand.

    Market Dynamics and Trends

    Changing regulations, particularly those targeting persistent organic pollutants, have pushed the industry away from certain heavier halogenated aromatics. Our product offers a valuable alternative, bringing reduced environmental risk by comparison. Over several years, downstream players have accelerated adoption thanks to published toxicological and environmental fate data available in the public domain. Formulators in crop science have told us that this compound’s lower bioaccumulation score and efficient transformation during synthesis unlock green chemistry claims that help them compete.

    Customers who once imported from a patchwork of sources now emphasize local, reliable manufacture. They want a direct line to the producer, not a web of brokers. This shift played to our strengths as we’ve invested both in process intensification and transparency. Our team leads virtual and in-person audits, opening our plant to scrutiny by external QA, regulatory, and procurement teams. We maintain a regular schedule of internal risk reviews and welcome third-party safety consultants for fresh perspectives.

    A Manufacturer’s Perspective on Product Selection

    Project teams evaluating intermediates often weigh cost, supply chain confidence, and technical fit. We believe that long-term cost baselines are anchored in product reliability. For this chemical, fewer failures mean less downtime, reduced wasted solvent and raw materials, and faster project timelines. Over the last decade, we’ve seen clients who switched to 3,5-Dichloro-4-Fluorobenzotrifluoride from less stable analogs cut cycle times by up to a quarter. We know this isn’t a theoretical gain, but one we’ve witnessed through back-to-back annual reviews.

    What matters most to buyers, in the end, is how an intermediate affects the whole synthesis—not a one-line cost metric. Formulators on the ground appreciate the repeatability we offer: they get the same performance run after run. Life science researchers have noted the reproducibility of their data with our product, circumventing setbacks from off-quality lots. Process engineers highlight improved clean-in-place return times due to the chemical’s lower tendency toward residue buildup. Our technical support team remains on call to troubleshoot, share in-depth data, or adapt the product’s properties for new requirements.

    Benefits from a Sustainability Lens

    Sustainability runs deeper than paperwork; it affects almost every decision on the production floor. From day-to-day experience, waste minimization and energy savings take priority alongside regulatory compliance. Early efforts to recycle solvents and optimize thermal integration paid off quickly, reducing our overall footprint. Downstream users have doubled down on greener chemistry commitments, steering toward intermediates that offer more with less. In this spirit, our process engineering group tracks and publishes utility consumption data, benchmarking against sectoral standards.

    In the last batch life cycle analysis, we logged a 30% reduction in process water use compared to prior years, aligning with broader industry improvements. Our product design and stewarding teams keep a close eye on the newer, outcome-based regulations shaping the chemical landscape—especially those targeting fluorinated and chlorinated aromatic molecules. Participating in industry consortia, we contribute data sets on environmental fate and support collaborative studies into safer, more effective alternatives. But our in-house findings still point toward the trustworthiness of 3,5-Dichloro-4-Fluorobenzotrifluoride as an intermediate with compelling process, safety, and environmental metrics.

    The Way Forward

    Looking over all these years, our experience in producing and supporting 3,5-Dichloro-4-Fluorobenzotrifluoride has revealed where to focus our attention: batch consistency, supply chain resilience, and open communication with teams across the value chain. Each challenge—from moisture management to evolving EHS standards—gave us new tools and instincts for safeguarding product integrity.

    We work to stay ahead through applied R&D, routine process audits, and collaborative troubleshooting with partners. Our team keeps an eye on advances in catalysis and alternative synthetic methods that could one day reshape how we make and use halogenated aromatics. Most of all, our approach centers not only on chemistry, but on the practical needs of those who rely on these intermediates—from bench-scale researchers to full-plant engineers. Decades of manufacturing expertise count because they shape decisions not only about what works, but how best to deliver on those promises over thousands of tons and across years of changing industry demands.