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2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid

    • Product Name 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid
    • Alias 2,6-Dichloro-4-(trifluoromethyl)benzylacetic acid
    • Einecs 410-090-2
    • 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

    155836

    Productname 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid
    Casnumber 21606-51-3
    Molecularformula C9H5Cl2F3O2
    Molecularweight 273.04
    Appearance White to off-white solid
    Purity Typically >98%
    Meltingpoint 104-106°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.61 g/cm³
    Smiles C1=CC(=C(C(=C1Cl)Cl)C(F)(F)F)CC(=O)O
    Inchi InChI=1S/C9H5Cl2F3O2/c10-6-1-5(9(12,13)14)2-7(11)8(6)3-4(15)16/h1-2H,3H2,(H,15,16)
    Synonyms 2,6-Dichloro-4-trifluoromethylphenylacetic acid
    Storagetemperature 2-8°C
    Hazardclass Irritant

    As an accredited 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, cylindrical HDPE bottle containing 100 grams of 2,6-Dichloro-4-(trifluoromethyl)phenylacetic acid, labeled with hazard warnings and handling instructions.
    Shipping **Shipping Description:** 2,6-Dichloro-4-(trifluoromethyl)phenylacetic acid is shipped in tightly sealed, chemically compatible containers to prevent leaks and contamination. Shipments comply with relevant chemical transport regulations, including appropriate labeling and documentation. The product is handled as a non-flammable, potentially hazardous chemical and may require temperature control and secondary containment during transit for safety.
    Storage 2,6-Dichloro-4-(Trifluoromethyl)phenylacetic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases, oxidizers, and reducing agents. Protect from moisture and direct sunlight. Store at room temperature or as specified on the product label. Ensure proper labeling and maintain access to Material Safety Data Sheets (MSDS).
    Application of 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid

    Applications of 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid in Industrial Manufacturing

    2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid serves as a specialized intermediate in several advanced chemical manufacturing sectors. Our production integrates strict quality controls to support industrial customers in regulated downstream segments. This section outlines specific industrial applications, compliance obligations, manufacturing ratios, process integration, and typical end products relevant to actual users.

    1. Agrochemical Synthesis—Herbicide Intermediate

    Leading crop protection companies select this acid as a key building block in making selective herbicides. Its dichloro and trifluoromethyl functionality allows precise molecular modifications essential for modern weed management products. Industrial customers benefit from traceable production lots and stable purity for downstream coupling and esterification steps.

    Industry compliance standards

    • ISO 9001:2015 certified production and documentation systems
    • REACH registration for use in agrichemical intermediates
    • OECD Good Laboratory Practice (GLP) for process validation
    • EU Directive 1107/2009 on plant protection product residues

    Typical usage ratio

    • 5–15% w/w in active ingredient synthesis batches, adjusted based on downstream molecular targets and process yields

    Downstream process integration

    • Acts as a coupling component in amidation or esterification during active ingredient assembly
    • Introduced at the conjugation stage before solvent extraction and purification

    Final product types

    • Post-emergent and pre-emergent herbicide actives
    • Selective graminicides for cereal crops
    • Custom-formulated agricultural chemical blends
    • Intermediate salts for proprietary glyphosate alternatives

    2. Pharmaceutical API Intermediate—Chlorinated Aryl Building Block

    Pharmaceutical manufacturers utilize this compound for synthesizing advanced APIs, especially where halogen-functionalized aryl groups improve potency or metabolic stability. Our material features low residual solvents and controlled impurity profiles to support stringent GMP workflows demanding rigorous traceability.

    Industry compliance standards

    • ICH Q7A GMP for API manufacture
    • USP and Ph. Eur. monographs for input intermediates
    • FDA 21 CFR Part 211 for handling and segregation
    • Certificate of Analysis for all delivered lots

    Typical usage ratio

    • 3–10% relative to other aromatic intermediates in the coupling step, tailored to API synthetic route and desired yield

    Downstream process integration

    • Used as an electrophilic aromatic acetic acid in Suzuki-Miyaura or Buchwald-Hartwig coupling reactions
    • Feeds directly into multi-step complexation with heterocyclic scaffolds

    Final product types

    • Arylcarboxylic acid-derived pharmaceuticals
    • Complex halogenated active ingredients for CNS and oncology pipelines
    • API intermediates for contract manufacturing organizations (CMOs)
    • Investigational New Drug (IND) substances

    3. Specialty Chemical Synthesis—Electronic Material Precursors

    Manufacturers involved in upstream electronics chemicals select this molecule for its high-electron-withdrawing profile, used for producing photoresist monomers and specialty fluorinated materials. Controlled particle size and low moisture content in our batches facilitate tight specification adherence for high-performance coatings and electronic applications.

    Industry compliance standards

    • RoHS compliance for electronics supply
    • ISO 14001 for environmental management in production
    • IPC-1752 for material declaration in electronics
    • Supplier qualification under OEM electronics QMS

    Typical usage ratio

    • 1–8% based on targeted substituted aromatic loading in downstream photolithographic or dielectric resin systems

    Downstream process integration

    • Feeds into nucleophilic substitution or cross-coupling to produce polymerizable monomers
    • Used during prepolymer formulation datasets for electronic coating grades

    Final product types

    • Photolithography photoresist monomers
    • High-dielectric polyarylates and fluorinated resins
    • Electronic circuit board coatings
    • Specialty optoelectronic materials

    4. Fine Chemical Intermediate—Custom Agro Synthesis and Traits

    Custom synthesis contract manufacturers leverage this acid in designing proprietary biological activity modifiers primarily for niche agro and seed trait sectors. Strict impurity and trace metal controls, batch homogeneity, and rapid scale-up capability support effective process optimization and formulation stability.

    Industry compliance standards

    • ISO 17025-accredited analytical verification
    • Compliance with China National Standard for agro intermediates (GB/T 20784)
    • Safe management under Globally Harmonized System (GHS) guidelines
    • US EPA regulations for new chemical inputs in crop innovation

    Typical usage ratio

    • 2–12% dosage as a structural modifier in high-throughput trait development, modifiable according to mutation target or biostimulant screening method

    Downstream process integration

    • Introduced as a functional linker or blocking group early in combinatorial agrochemical synthesis
    • Used prior to fractionation and biological screening

    Final product types

    • Patent-pending herbicide analogs
    • Novel growth regulator chemical scaffolds
    • Biostimulant precursor libraries
    • Seed trait-modifying conjugates for R&D
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    Certification & Compliance
    More Introduction

    Introducing 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid: A Manufacturer’s Perspective

    Building Chemistry from the Ground Up

    At our facility, daily operations revolve around translating laboratory discoveries into industrial realities. Among dozens of compounds running through our line, 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid stands out for its performance in specialty chemical synthesis. Our team handles every step, from sourcing raw chlorinated aromatics to the last shipment, keeping hands-on oversight at each phase. We understand what it takes to create molecules not just in theory, but in real, working batches hundreds of kilos at a time.

    Molecular Backbone and Batch Consistency

    In industrial settings, getting the fine details right changes everything. 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid—a mouthful for most—shows a unique profile in reactions involving organofluorine intermediates. The presence of two chlorine atoms at the 2 and 6 positions and a robust trifluoromethyl group at the 4 position creates a molecule less prone to unwanted side reactions. From our experience, this matters most during scale-up runs, where impurities seen at gram scale often multiply unpredictably.

    Our product comes as a pure, white crystalline powder, handled and packed under controlled conditions to limit moisture and cross-contamination. The melting point and purity, confirmed by HPLC and proton NMR at every batch, do not just match the technical spec sheet—they reflect what actually goes into reactors. Lab clients notice batch-to-batch uniformity in their yields, and our regular customers rarely have to pause for unexpected chromatographic separations.

    Specifications That Matter on the Floor

    End-users working in pharmaceuticals or crop-protection intermediates look for more than a chemical name. Our batches typically show purity above 99% by HPLC, and our lot validation includes spectral data, moisture content, and residual solvents. Experience has taught us that tiny variations at this point ripple through an entire production run downstream. Process engineers frequently share that they spend less time troubleshooting when the input quality is stable.

    Typical packaging formats include 25-kilogram fiber drums lined with double-sealed polyethylene bags. Sensitive shipments sometimes move in smaller packs for pilot synthesis groups. Every container is labeled with both production history and analytical results—most clients dig into these records during their internal QA but often say they value the transparency compared to blind-batched imports.

    Facing Challenges Behind the Scenes

    Manufacturing 2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid isn’t just a textbook sequence. The handling of halogenated intermediates calls for rigid containment to minimize exposure risks, and consistent treatment of waste streams burdens our facilities with extra scrutiny from authorities. This is not the sort of job that can be rushed or outsourced lightly. We’ve experienced that a reliable product starts on the shop floor, long before the bottles are filled and sealed. Working closely with our safety team and investing in solvent recovery systems has saved us from interruptions more than once.

    On-site chemists and operators run regular checks on storage stability. Over two decades, we have refined systems for inert-atmosphere transfers and real-time analysis, learning from batches that shifted color or lost purity due to unfortunate air ingress. Our line’s reputation didn’t come overnight or by cutting corners—each tweak stemmed from a direct lesson, sometimes expensive, always remembered.

    Where the Acid Finds a Home

    2,6-Dichloro-4-(Trifluoromethyl)Phenylacetic Acid works mostly as an intermediate, rarely as a finished goods ingredient. Its core applications cluster in sectors chasing new pesticide actives and pharmaceutical scaffolds. Developers working on new pyrazole or benzyl-substituted pharma agents often use this molecule to introduce both electron-withdrawing and halogen features, tuning biological activity precisely.

    Process teams facing scale-up hurdles reach out to us specifically for this acid after finding less substituted analogs generate too many unknown side products in late-stage couplings or brominations. One customer, after switching to our source, reduced purification steps by a third in their sulfonylamide route. These case studies shape our production priorities and, from time to time, feed back into how we purify each run.

    Comparing with Other Phenylacetic Acids

    Plenty of phenylacetic acids cross our plant, each with their own quirks. The difference with 2,6-dichloro-4-(trifluoromethyl)phenylacetic acid is that the combined halogen load stabilizes the aromatic ring during demanding syntheses. Less-substituted cousins, like 4-trifluoromethylphenylacetic acid or plain dichlorophenylacetic acids, tend to give lower selectivities under oxidative conditions. A single missing chlorine or a smaller alkyl group often leaves end-users with more unreacted starting material—they relay these headaches back after comparative trials.

    Our technical team interacts with R&D chemists at several multinationals, sharing actual reaction snapshots. Projects that once depended on more labile intermediates have switched to this acid, finding fewer byproducts and better throughput. Real-world differences show up not just in published yields but in cleanup time, tank turnaround, and waste treatment, all areas where marginal improvements matter in a manufacturing lineup.

    Supporting Modern Synthesis

    Modern chemistry demands substrates that push boundaries, particularly as new regulations limit legacy active ingredients in agroscience and pharma. The rise of fluorinated building blocks reflects demand for better metabolic stability and lower dosages. Our acid answers these calls with a structure that delivers both. We maintained in-house capacity as others shifted to low-volume traders, preferring to fine-tune each lot based on customer feedback. Some pilots in agrochemical development need only grams, whereas generic pharmaceutical lines pull our acid by the hundred-kilo lot over fiscal quarters.

    Research customers like to interrogate every bit of supporting data before a purchase. We’re used to it. Full analytic reports, impurity profiles, and even details down to the glassware cleaning logs travel with each batch. Not every supplier offers this level of detail. We do, because output only performs when input is predictable. Repeatability decides who stays in the inner circle of suppliers for critical reactions—and we work to keep ourselves there.

    Safety Continues to Shape Production and Industry Demand

    An acid carrying chlorines and fluorines requires more than just a steady hand. Production lines require shielded reactors, vent scrubbers, and staff training that absorbs half a working week or more. Operators learn to treat every valve and transfer line as a potential weak point, especially in monsoon season or during unplanned power stoppages. One year, stray condensation halted a week’s production. That downtime forced us to overhaul insulation procedures, and invest in a backup generator—changes that paid off in the years that followed.

    Across the industry, growing awareness of occupational exposure and environmental loading presses manufacturers to go further than regulatory minimums. We respond to this by integrating on-line monitoring, redundant containment, and less hazardous cleaning cycles. These investments rarely wow on a balance sheet short-term, but the freedom from production halts, regulator interventions, and staff turnover keeps output flowing.

    Environmental Responsibility: Lessons from the Front Lines

    Waste acid and solvent are unavoidable here, especially with multi-halogenated compounds. We manage these by solvent distillation and closed-loop recycling, efforts that stemmed from an incident a decade ago when a neighboring operator’s discharge fouled local water and brought oversight to our entire sector. Since then, our site’s discipline on waste tracking, storage, and cleanup never relaxed, not even under cost pressure.

    Visits from chemical auditors teach us new tricks every year—from mineral-based adsorbents to improved reaction quenching—and we’re quick to adopt these where practical. Older plants still struggle; our newer lines, with greater automation and leak detection, tick under stricter controls. Suppliers or would-be customers touring the facility see firsthand the extra hours spent handling the tail ends of chlorinated acid streams. These efforts might not show in the catalog, but they build trust, and that translates over time into stable business.

    Responding to Market Shifts

    Over the last decade, market requirements for 2,6-dichloro-4-(trifluoromethyl)phenylacetic acid swelled or shrank based on projects in the agri-chem and pharma spaces. Early years saw feast-or-famine cycles based mostly on patent cliffs and the race for new, more potent herbicidal backbones. Standing firm as a manufacturer gave us the chance to invest in capacity lines that absorb these swings, balancing custom lots with standard inventory.

    We receive requests for kilo-to-ton quantities, urgent timelines, altered impurity profiles, and often the hope for just a smaller MOQ on short notice. Our plant’s flexibility, shaped by years of direct feedback, helps us move outside the rigid “standard item” trap—something large contract plants, focused on volume rather than specialty, cannot often manage. Production managers from major client sites call periodically to discuss tweaks, whether that be smaller pack sizes, altered drying methods, or even experimental stabilizer additions. As a dedicated manufacturer, recognizing these needs and acting on them forms a daily rhythm.

    Validating What We Sell, Not Just Shifting Boxes

    Bottom-line, 2,6-dichloro-4-(trifluoromethyl)phenylacetic acid means more to us than a catalog number. Few companies accept every returned drum, or review every minor complaint, but our feedback loop closes as directly as possible. Each batch serves as both a technical achievement and a learning process—customers rarely see all the hours invested upstream during line trials, analytical troubleshooting, or operator retraining.

    The confidence our regulars display in reordering year over year reveals more about real-world product performance than any certificate or number on a spec sheet. We track usage patterns, listen closely to reported successes and bottlenecks, and use those as the foundation for every process improvement. This cycle creates a product that proves itself in tough, output-driven settings.

    Staying Ahead: Challenges and Opportunities

    Every year, regulatory expectations, client demands, and new synthetic methodologies shift the ground beneath chemical manufacturers. Adapting process routes, optimizing waste capture, and updating staff skills cost time and resources, but failing to keep pace brings long-term penalties nobody wants. We invest in outside technical training, risk analysis, and incremental upgrades based on both our own failures and those we see across the industry.

    Complexity in chemistry never dwindles; it only shifts. Advances in catalysis or reaction conditions need more flexible manufacturing setups. For us, partnering directly with process innovators—rather than waiting for a distributor’s summary—keeps us ready to tweak or overhaul lines as new needs emerge. Recent trends indicate a higher demand for customizations: altered melting points for formulations, unique impurity footprints for regulatory submissions, and even co-developed packaging protocols for highly sensitive syntheses.

    A Manufacturer’s Promise: Chemistry, Not Just Commodity

    We treat 2,6-dichloro-4-(trifluoromethyl)phenylacetic acid not as a generic box-ticker, but as the outcome of years experimenting, fixing, and refining. Our focus stays on product stewardship, open technical dialogue, and proactive adaptation of process needs. From new reaction partners to legacy transformation routes, this acid, once a niche specialty, holds substantial ground in today’s synthetic toolbox.

    Every decision along our process line takes into account safety, scalability, and changing customer requirements. Remaining in manufacturing for a compound as complex as this acid only makes sense if the feedback loop—between plant, product, and client—remains unbroken. By maintaining both physical control and technical dialogue, we ensure the acid keeps earning its place in demanding pipelines. That is how reliability, in practice, proves itself, batch after batch, year after year.