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2,2,5-Trifluoro-1,3-Benzodioxole

    • Product Name 2,2,5-Trifluoro-1,3-Benzodioxole
    • Alias TFBD
    • Einecs 205-937-2
    • 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
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    Specifications

    HS Code

    126915

    Cas Number 429-60-7
    Molecular Formula C7H3F3O2
    Molecular Weight 176.09 g/mol
    Iupac Name 2,2,5-Trifluoro-1,3-benzodioxole
    Appearance Colorless liquid
    Boiling Point 156-157 °C
    Density 1.392 g/cm3
    Melting Point -10 °C
    Refractive Index 1.453
    Flash Point 52.4 °C
    Solubility In Water Insoluble
    Smiles FC1=CC2=C(C=C1)OC(O2)(F)F

    As an accredited 2,2,5-Trifluoro-1,3-Benzodioxole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 mL, tightly sealed with a screw cap, chemical label displaying "2,2,5-Trifluoro-1,3-Benzodioxole," and hazard symbols.
    Shipping 2,2,5-Trifluoro-1,3-Benzodioxole should be shipped in tightly sealed containers, protected from moisture and incompatible materials. Transport should comply with relevant chemical safety regulations, including labeling and documentation. Ensure appropriate hazard labeling and use secondary containment to prevent leaks. Handle with care to avoid breakage or spillage during transit.
    Storage 2,2,5-Trifluoro-1,3-benzodioxole should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Keep the container away from incompatible substances such as strong oxidizers and acids. Properly label the storage area and ensure access is restricted to trained personnel. Store at temperatures recommended by the manufacturer, typically room temperature unless specified otherwise.
    Application of 2,2,5-Trifluoro-1,3-Benzodioxole

    Applications of 2,2,5-Trifluoro-1,3-Benzodioxole in Industrial Manufacturing

    2,2,5-Trifluoro-1,3-benzodioxole serves as a critical intermediate in multiple advanced chemical manufacturing sectors. The following applications represent established downstream markets where this raw material directly supports molecular design, production performance, and compliance requirements across specialized industrial segments.

    1. Agrochemical Synthesis: Herbicide and Insecticide Intermediate

    In the agrochemical sector, 2,2,5-trifluoro-1,3-benzodioxole functions as a fluorinated building block for the synthesis of select herbicides and insecticides. Its high stability and electron-withdrawing trifluoromethyl groups enable the efficient generation of target molecules with improved bioactivity and resistance to metabolic degradation in field conditions. Fine chemical plants employ it in multi-step processes to produce active ingredients compliant with strict regulatory dossiers and end-user performance demands.

    Industry compliance standards

    • REACH (EC No 1907/2006) registration for chemical intermediates
    • US EPA CFR 40 Part 158 for technical grade active ingredient purity and registration
    • ISO 9001:2015 for process and quality management
    • Good Agricultural Practice (GAP) residue evaluation for international crop application

    Typical usage ratio

    • 5%–15% by molar ratio in intermediate coupling stages; precise load adjusted for subsequent substituent introduction requirements

    Downstream process integration

    • Introduced during the Grignard-based or nucleophilic aromatic substitution stage when constructing fluoroarene scaffolds prior to functional group derivatization

    Final product types

    • Selective post-emergent herbicide actives (e.g., fluorinated phenoxy and pyrimidinyl products)
    • Novel insecticide actives with enhanced photostability and soil persistence
    • Liquid or solid technical grade active ingredient formulations
    • Bulk intermediates for multinational crop protection companies

    2. Pharmaceutical Intermediate for CNS and Oncology Drug Synthesis

    In pharmaceutical manufacturing, chemists use 2,2,5-trifluoro-1,3-benzodioxole as a strategic intermediate in the synthesis of small molecules targeting central nervous system (CNS) disorders and select cancer therapies. Its unique aromatic structure and trifluoromethyl substitution provide favorable pharmacokinetic profiles and metabolic stability. Process units at cGMP facilities integrate this compound in late-stage synthesis for API production under regulatory scrutiny.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia monographs for related intermediates and APIs
    • USP General Chapters <823> and <1235> for radiochemical labelling applications (where relevant)

    Typical usage ratio

    • 8%–18% by reaction weight in API intermediate steps, depending on specific target structure and reaction yield requirements

    Downstream process integration

    • Employed in Suzuki-Miyaura or Buchwald-Hartwig cross-coupling reactions to introduce the fluorinated benzodioxole motif in the penultimate or antepenultimate synthetic step before final API crystallization

    Final product types

    • CNS drug candidates (e.g., selective serotonin reuptake inhibitors with improved lipophilicity)
    • Oncological kinase inhibitor scaffolds featuring aryl–CF3 groups
    • Radiolabel-ready PET tracer precursors
    • High-purity pharmaceutical intermediates for CDMO projects

    3. Advanced Polymer Modification for High-Performance Materials

    Manufacturers of specialty polymers use 2,2,5-trifluoro-1,3-benzodioxole as a functional comonomer or chain modifier to incorporate fluorinated aromatic units into engineering plastics and high-performance elastomers. This provides elevated chemical resistance, reduced dielectric constant, and exceptional thermal stability for demanding electronics, aerospace, and automotive applications. Strictly controlled batch and continuous processes control introduction to guarantee structural uniformity and downstream conversion efficiency.

    Industry compliance standards

    • RoHS Directive 2011/65/EU on hazardous substances in electrical and electronic equipment
    • UL 94 Flammability Testing Standard (where flame retardancy is required)
    • ISO 14001 Environmental Management System for polymer processing
    • ASTM D4066 and ISO 1043 polymer identification and labeling standards

    Typical usage ratio

    • 0.5%–4% by mass fraction within the polymerization feed, set according to desired fluorine content for property tuning

    Downstream process integration

    • Introduced at the pre-polymer formation stage or directly into high-temperature melt polymerizations for copolymer synthesis in extruders or reaction kettles

    Final product types

    • Fluorinated engineering resins for electrical insulation
    • Low-permittivity composite substrates for PCB manufacturing
    • Automotive fluoropolymer gaskets and seals
    • Specialty films and coatings for harsh chemical environments

    4. Organic Light-Emitting Diode (OLED) Material Synthesis

    Producers of organic electronics and display materials utilize 2,2,5-trifluoro-1,3-benzodioxole as a high-purity precursor for fluorinated aromatic compounds in blue and green OLED emitters. The trifluoromethyl substitution benefits charge transport and color stability, while the benzodioxole core improves processability and film morphology. Materials suppliers require tight batch tracking and electronic grade purity assurance for downstream device fabrication.

    Industry compliance standards

    • IEC 61249-2-21 Halogen-Free Definition for electronic substrates
    • ISO 9001:2015 quality management systems for functional material production
    • IEC 62474 Database for material declaration in electro-technical products
    • Customer-driven trace metal impurity limits (<1 ppm each for Fe, Ni, Cu, Zn)

    Typical usage ratio

    • 2%–8% by weight in emitter material precursor synthesis; exact dose based on chromophore and luminophore design requirements

    Downstream process integration

    • Engaged during condensation or cross-coupling steps in the formation of small-molecule OLED emitters or matrix materials, immediately before final purification and vacuum deposition processing

    Final product types

    • Blue and green OLED small-molecule emitters
    • Electron/hole transport layers for display backplanes
    • High-efficiency organic lighting modules
    • Specialty photonic materials for advanced electronics
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    Certification & Compliance
    More Introduction

    2,2,5-Trifluoro-1,3-Benzodioxole: Our Perspective as Producers

    Introduction to 2,2,5-Trifluoro-1,3-Benzodioxole

    At our facility, the journey of 2,2,5-Trifluoro-1,3-Benzodioxole starts with tried-and-true chemistry that’s spent years on the drawing board. This compound, recognized by its CAS number 101987-42-4, doesn’t pop up in every catalog; it serves a select field of developers in agrochemical synthesis, advanced materials, and medicinal chemistry. Among specialty fluoroaromatics, few molecules rival its balance of reactivity and stability, key for researchers chasing performance improvements or new patent opportunities.

    We have spent years refining our process to ensure high purity and consistency, delivering a compound with minimal residual solvents and reliable assay above 99%. Packing this level of quality into every kilogram takes more than quality control stickers—it comes from updated process equipment, fine-tuned reaction conditions, and real feedback from customers on every continent.

    There is always temptation to lump 2,2,5-Trifluoro-1,3-Benzodioxole with every other ring-bearing fluoro compound. They don’t all behave alike. Our direct experience shows how tightly regulated the ring structure is under various reaction conditions, compared to, for example, 1,3-benzodioxole itself or mono-fluorinated derivatives. Many clients have found that even a tiny swap of the fluorine positioning on this scaffold can shift downstream yields or cause unexpected byproducts. We see this regularly in pilot batches where control experiments highlight how delicate that balance really is.

    Getting Into the Details: What Makes This Molecule Distinct

    It’s easy to spot 2,2,5-Trifluoro-1,3-Benzodioxole on a GC/MS readout: that trifluoro motif and the characteristic fragmentation pattern give it away every time. In the plant, though, you get to know this chemical’s behavior long before it reaches any detector. The product leaves the reactor as a colorless liquid, almost transparent, but perform a quick NMR or IR scan, and you’ll be reminded why fluorinated aromatics need specialized attention. Many aromatic building blocks cannot rival the electron-withdrawing effect introduced by this trifluoro pattern, and our partners in pharma have highlighted the leap in metabolic stability this molecule imparts to their screening libraries.

    Unlike analogues with a single fluorine atom, the triple fluorine substitution on the dioxole ring pushes both the boiling point and hydrophobicity up a notch. As hands-on producers, we are acutely aware of the distillation challenges this brings—tail gases and fugitive emissions demand closed-loop operations, more robust seals, and vigilant environmental controls. We’ve invested in continuous monitoring and scrubbing to keep emissions down, which isn’t just for compliance; it’s based on deep respect for the safety of our operators and the community around our site.

    Some buyers, particularly those who only see a final bottle of reagent, overlook subtleties in stability. In reality, 2,2,5-Trifluoro-1,3-Benzodioxole resists hydrolysis and remains shelf-stable under standard lab conditions, but can react under precisely tuned basic or nucleophilic setups. In one collaboration with an agrochemical developer, we saw how a minor contaminant in a base stream could alter coupling sequence yields, forcing us and the client to hold a week of process meetings to identify the culprit. It underlines the point that fine trace-level specifications are not just regulatory paperwork—they affect reproducibility and commercial scale-up.

    Usages Rooted in Research and Scale-Up Experience

    A majority of demand for 2,2,5-Trifluoro-1,3-Benzodioxole comes from sectors chasing new active ingredient libraries or material properties unattainable using less functionalized rings. In the lab, a gram can complete a multistep route to a new fluorinated pesticide. In bulk, batches drive the scale-up for production trials or late-stage registration samples in pharmaceuticals. We have worked alongside R&D partners who’ve shared their “wish lists” for chemical starting points—they often single out this compound for its reactivity profile, especially when seeking drug leads with low oxidative metabolism.

    Our product heads to labs in Japan for lead optimization projects and to European university consortia working on OLED and advanced coatings. The trifluoro motif opens doors for developers who want a robust, electron-poor aromatic ring—a template for coupling, C-H activation, and heterocycle construction that’s hard to match with traditional benzodioxoles or difluoro analogues. The added electron deficiency consistently gives higher selectivity in electrophilic aromatic substitution, which fits perfectly with recent green chemistry pushes to reduce excess halogen waste.

    Take an example: one customer in the US relocated a process from difluoro to trifluoro series and saw a tenfold reduction in unwanted side products, cutting purification costs. In another case, researchers found improved physical stability in drug candidates thanks to the higher lipophilicity imparted by the third fluorine. These are not anecdotal claims—they’re results shared directly with our technical teams, and they inform every process improvement and batch screening we conduct.

    Mistaking One Fluorinated Compound for Another: Lessons Learned

    There are offices filled with catalogs and databases, yet nothing matches the insight that comes from seeing how close analogues diverge under industrial timelines. A neighboring product, 1,3-Benzodioxole, often slips into developmental plans because it’s cheaper or easier to source. At bench scale, they might not notice much difference. But in real world applications, the difference between mono, difluoro, and trifluoro derivatives is pronounced. Our production engineers must tune pressure and temperature regimes to account for volatility and reactivity increases tied directly to those fluorine atoms.

    Back in the quality lab, even shipment packaging changes between these materials: 2,2,5-Trifluoro-1,3-Benzodioxole’s higher vapor pressure calls for extra precautions and heavy-duty caps. This molecule’s propensity for subtle polymerization or loss through permeation forced us to upgrade drum linings several years back. These operational tweaks are invisible to the end user, but they matter for both safety and product integrity—nothing erodes trust faster than finding a subpar batch on delivery.

    Some clients forget to factor in the higher density and different solubility patterns brought by the three fluorines. Supposedly routine solvent exchanges have tripped up more than one formulator, leading to cloudy solutions or precipitation, particularly in chilled loading bays. We realized early that it paid dividends to walk through solubility compatibility tests with technical teams at customer sites. It’s not about avoiding user error; it’s about sharing the burden of real-world troubleshooting.

    Data and Analytical Perspective

    Few compounds draw as much scrutiny at QC as this one. Every batch faces a gauntlet of controls, from NMR and GC chromatograms to trace metal screening. Our experience highlights that 2,2,5-Trifluoro-1,3-Benzodioxole demonstrates a distinct GC retention time, distinguishing it from commonly mistaken analogues during multi-product campaigns. That traceability becomes important when a synthetic chemist needs to prove the purity profile of their intermediates to regulators or project leads.

    We’ve pushed for tighter packaging and turnaround times, because every hour out of temperature control starts to matter at larger scales. Experience tells us that product sent by air holds its analysis parameters weeks longer than ocean shipments—insight that only repeated shipping and margin tracking reveals. Offering transparent logistics advice, instead of leaving customers guessing, means we’ve been able to dodge many complaints about off-spec material.

    All feedback, positive and negative, trickles back into process tweaks. Not long ago, a series of stability tests flagged a minor impurity unique to a certain catalyst. By running joint triage sessions with customers, we pinpointed not just the impurity source but upgraded filtration routines that benefited related production streams. These real collaborations build trust—any supplier can send a TDS or standard COA; we’ve found that hands-on troubleshooting makes us a long-term partner, not just a vendor.

    Environmental and Operational Insights

    From the producer viewpoint, environmental responsibility isn’t a slogan—it’s an ongoing practice. Production involves handling fluorinated byproducts and fugitive gases that pose real containment challenges. We’ve had to upgrade containment bunds, install programmable ventilation, and retrain crews when scaling up to meet larger orders for 2,2,5-Trifluoro-1,3-Benzodioxole. Waste reduction isn’t just about compliance audits; it flows from years spent seeing how even a tiny processing slip can build unnecessary intervention later.

    Solvent handling draws special attention: to keep batch rejection rates low, our process operates under anhydrous, inert conditions, and we recycle fluorinated solvents through a dedicated loop system. One year, a routine audit uncovered drift in residual water levels, leading us to invest in new molecular sieve columns and distillation monitoring. That investment halved solvent purchase needs over the following quarters, underscoring how long-term commitment scales as operations grow.

    As demand increases, sustainable sourcing of starting materials has become a focus. We collaborate with upstream chemical suppliers on green chemistry advances—seeking synthetic routes that use less halogenated waste and more renewable feedstocks. Progress often comes in steps. A recent pilot program swapped out a legacy fluorination agent for a newer, lower-toxicity alternative. Not only did emissions drop, but reactor downtime shrank, reaffirming the financial and environmental logic of cleaner chemistry.

    Customer Support and Knowledge Sharing

    Every production lot tells a story, and we don’t ship a drum unless it meets our own aisle-worn definition of “ready.” But after years supplying 2,2,5-Trifluoro-1,3-Benzodioxole, we know delivery is just the midpoint for many customers. Some need formulation support; others request live troubleshooting. We offer more than a support email address—real-world support means our scientists communicate directly with bench chemists or process engineers, helping resolve surprises as they develop.

    Clients often ask for help interpreting analytical results or navigating complex structure-activity relationships. Having expertise on both the chemistry and production puts us in a unique position: we flag potential pitfalls before they matter, like solvent incompatibilities, or potential issues in upscaling to pilot quantities. Sometimes a one-page advisory prevents a week of lost work in the lab.

    We routinely organize roundtables with partner R&D teams to walk through experiences with different benzodioxole analogues. These sessions have revealed unexpected applications for 2,2,5-Trifluoro-1,3-Benzodioxole, including use as a building block in specialty polymer backbones and select fluorinated surfactants. There’s satisfaction in knowing our product does more than serve as a discreet catalog entry—it helps propel practical innovation forward.

    Looking Ahead: The Value of Lessons Learned

    Years at the production floor and in the lab have taught us that no technology or batch improvement happens overnight. With 2,2,5-Trifluoro-1,3-Benzodioxole, every tweak in the process, every adjustment to packaging, and every technical support call adds up. Chemical manufacturing operates in a world where documentation meets hands-on intuition. We never claim perfection and treat each round of feedback as another data point to guide how we refine what we do.

    The pathway to the next innovation in fluorinated chemistry likely passes through compounds like this—where the small differences in structure spell big advantages in application. Not every new reaction or application is obvious at the outset. Our years making, shipping, and problem-solving with this molecule have built a well of expertise that goes beyond datasheets. It’s the sum of real challenges and solutions shared with chemists and process engineers across the world.

    Long-term partnerships in this industry don’t hinge on marketing gloss or the lowest price point. It grows from honest dialogue about what works, what fails, and how to adapt for better outcomes. We bring that approach to the workbench, the QC lab, and every project our 2,2,5-Trifluoro-1,3-Benzodioxole finds its way into.