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4,6-Difluorooxindole

    • Product Name 4,6-Difluorooxindole
    • Alias 4,6-Difluoro-1,3-dihydroindol-2-one
    • Einecs 629-675-7
    • 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

    824067

    Chemical Name 4,6-Difluorooxindole
    Cas Number 103877-21-2
    Molecular Formula C8H5F2NO
    Molecular Weight 169.13 g/mol
    Appearance White to off-white solid
    Melting Point 110-112°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1C(=O)NC2=C1C=C(F)C(F)=C2
    Inchi InChI=1S/C8H5F2NO/c9-4-1-5-6(2-4)8(12)3-11-7(5)10/h1-2,11H,3H2
    Synonyms 4,6-Difluoro-2,3-dihydro-1H-indol-2-one
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 4,6-Difluorooxindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4,6-Difluorooxindole (1g) is packaged in an amber glass bottle with a secure screw cap and clear labeling.
    Shipping 4,6-Difluorooxindole is shipped in tightly sealed containers to prevent moisture and air exposure. It should be handled as a chemical substance with potential hazards, following standard safety protocols. Ensure transport complies with local regulations for hazardous materials, with appropriate labeling and documentation. Store at room temperature, away from sources of ignition.
    Storage 4,6-Difluorooxindole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Properly label the storage container and ensure access is restricted to trained personnel equipped with appropriate personal protective equipment.
    Application of 4,6-Difluorooxindole

    Applications of 4,6-Difluorooxindole in Industrial Manufacturing

    4,6-Difluorooxindole serves as a specialized intermediate in several advanced chemical sectors, contributing to high-value manufacturing in regulated markets. Our manufacturing expertise supports consistently high purity and batch-to-batch reproducibility, enabling precise integration into critical downstream processes. The following sections detail verified industrial uses, focusing on compliance, formulations, process roles, and primary product types.

    1. API Intermediate in Fluorinated Pharmaceutical Synthesis

    Pharmaceutical manufacturers use 4,6-difluorooxindole as a key building block in the synthesis of next-generation fluorinated active pharmaceutical ingredients. Its aromatic fluorination profile allows selective transformations, supporting precise synthesis steps for kinase inhibitors and CNS-targeted drugs. Process teams incorporate this intermediate during targeted cyclization or coupling reactions under strict cGMP protocols, enabling consistent API batch release. Custom control of molar ratio relative to other aromatic substrates ensures both reaction conversion and impurity minimization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, Ph. Eur., JP relevant monographs (if moving to API stage)
    • FDA 21 CFR Part 211
    • EDQM Certificates of Suitability (CEP) for APIs

    Typical usage ratio

    • Employed at 0.8–1.1 molar equivalents versus key condensation partner; precise ratio determined by route and impurity profile requirements.

    Downstream process integration

    • Input to N-alkylation, acylation, or Suzuki coupling stages in API synthesis tree.
    • Requires anhydrous handling and controlled base conditions.
    • Introduced after initial core-building step, prior to chiral resolution or salt formation.

    Final product types

    • Oral kinase inhibitors (oncology)
    • CNS-active modulators (antidepressants, neuroprotectants)
    • Non-steroidal anti-inflammatory APIs
    • Fluorinated heterocycle-based drug candidates in clinical development

    2. Agrochemical Intermediate for Novel Herbicide Discovery

    Chemical crop protection manufacturers use 4,6-difluorooxindole within their R&D and scale-up workflows to develop advanced herbicides. Its electron-deficient aromatic system facilitates key halogenation and amide formation reactions, supporting the production of selective enzyme inhibitors for weed control. Formulation teams adjust ratios according to greenhouse trial data and field requirements, optimizing yields and regulatory submission purity thresholds. Downstream integration involves staged derivatization prior to formulation and tox studies.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications & Evaluations
    • Good Laboratory Practice (GLP, OECD)
    • EPA FIFRA registration protocols (USA)
    • REACH Regulation (EU), Annex IX and X for advanced substances

    Typical usage ratio

    • Between 0.6–1.3 molar equivalents per synthetic herbicidal core, depending on the post-derivatization efficiency and desired selectivity index.

    Downstream process integration

    • Engaged in early-stage coupling or amidation reactions to introduce fluorine at core positions.
    • Processed in batch or semi-batch reactors under inert atmosphere.
    • Transferred to formulation for emulsifiable concentrates or water-dispersible granules.

    Final product types

    • Selective broadleaf herbicides
    • Enzyme-targeting weed growth inhibitors
    • Novel pre-emergence formulations
    • Experimental herbicidal actives for regulatory field trials

    3. Intermediate in Advanced Fluorinated Material Synthesis

    Specialty material producers utilize 4,6-difluorooxindole as a precursor when constructing high-performance fluorinated polymers and small-molecule electronic materials. The molecule’s substitution pattern allows it to integrate into step-growth or polycondensation reactions, creating stable units for organic semiconductors and tailored polyimide resins. Production chemists tailor input ratios according to target molecular weights and fluorine density, supporting downstream processability and dielectric property requirements.

    Industry compliance standards

    • ISO 9001 Quality Management System
    • RoHS 3 Directive (for electronics materials)
    • REACH (Annex VIII for polymers and monomers)
    • IEC 61249-2-21 (for halogen content in laminates, applicable to electronics)

    Typical usage ratio

    • Used at 0.2–0.7 wt% in polymer feed mix; higher or lower based on desired end-use performance, fluorine content, and cost management.

    Downstream process integration

    • Fed into polycondensation vessels post-monomer activation.
    • Undergoes direct polymerization with dianhydrides or dianilines for imide backbones.
    • Can be implemented at solution or melt-processing steps, depending on the polymer system.

    Final product types

    • Fluorinated polyimide films
    • Organic light-emitting diode (OLED) small molecule layers
    • Dielectric coatings in printed circuit boards (PCBs)
    • High-temperature-resistant plastic components

    4. Fine Chemical Intermediate in Medicinal Chemistry Research

    Contract research organizations and pharmaceutical innovators employ 4,6-difluorooxindole in scaffold modification for drug candidate exploration. Its unique substitution supports preparation of structure-activity relationship (SAR) libraries and analog screening. Research chemists handle this intermediate during key parallel synthesis runs under strict analytical control, tuning input amounts by mg-scale to pilot kilogram-lots depending on project progression and lead candidate prioritization.

    Industry compliance standards

    • Applicable to ISO/IEC 17025 accredited analytical labs
    • GLP for safety and preclinical supporting batches
    • Compliant with local occupational health and chemical storage regulations (OSHA Hazard Communication, EU CLP)
    • NIH/NSF grant-supported projects adhere to official best laboratory practices

    Typical usage ratio

    • Applied from 0.2 mmol to 10 mmol per scaffold per reaction; scaled as needed for preclinical quantities or stock solutions.

    Downstream process integration

    • Added during parallel library synthesis reactions to introduce fluorinated motifs.
    • Used in combination with cross-coupling entries for SAR expansion.
    • Sampled for NMR and LC-MS during lead optimization cycles.

    Final product types

    • SAR compound libraries
    • Small molecule lead series for early-stage drug pipelines
    • Pharmacological tool compounds for cellular studies
    • Research-only fluorinated analogs
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    Certification & Compliance
    More Introduction

    Introducing 4,6-Difluorooxindole: A Chemist’s Perspective

    In the landscape of specialty chemicals, certain molecules take on a character all their own. As someone who’s worked closely with fluoroaromatic intermediates, 4,6-Difluorooxindole stands out not just for its structure, but for the reliability and integrity it brings to a range of synthesis routes. We craft this compound directly in our facility with painstaking attention to both consistency and purity, shaped by lessons learned from decades of experience in fluoro-compound production.

    Molecular Profile: Getting to Know 4,6-Difluorooxindole

    4,6-Difluorooxindole has a chemical structure featuring the indole core modified with fluorine atoms at the 4 and 6 positions. This seems straightforward at first glance, but what results is a foundation that defies easy substitution and provides an exact balance between reactivity and stability. The presence of two fluorine atoms isn’t just a cosmetic twist. These fluorines alter ring electronics in a way that offers greater resistance to certain unwanted side reactions—anyone designing complex pharmaceuticals or crop protection agents can appreciate the importance of that detail.

    In our plant, production starts with careful selection of raw materials—distinct from other indole syntheses. Impurities at the early stages snowball into downstream defects, so we pick every batch source, scan for trace metals, and separate byproducts rigorously. This hands-on, scrutinizing approach stems from firsthand experience troubleshooting erratic runs and realizing just how much control upstream choices exert on downstream reliability.

    Specifications: Purposeful Precision

    Topic of purity always ends up front and center. For many projects, especially in the research, pharmaceutical, and advanced material space, success hinges on keeping contaminants below the radar. We drive HPLC-purities above 98%, sometimes surpassing 99% with specialized crystallization tweaks. Controlling moisture content takes on equal stature—hydrolysis-sensitive syntheses can turn sour with minute traces of water, and so we deploy drying steps that go beyond simple oven-bakes. This attention to detail doesn’t just protect our clients’ yields; it barring headaches on our own reactor floors.

    Particle characteristics rarely get credit until filtration or formulation hits a snag. We mill to a fine, consistent powder, ensuring steady performance through filtered lines or micro-dosing applications. Such consistency came by learning through clogged filters and erratic dispensing from the earlier days, iterating on milling speeds and mesh choices. For researchers looking for reliable weigh-outs and seamless blend-ins, these lessons translate into day-to-day ease.

    Distinct Usage Strengths

    The heart of 4,6-Difluorooxindole’s practical value lies in its adaptability. Our product enters the pipeline at the stage where selective incorporation of fluorine can unlock hydrophobicity, metabolic stability, and tunable reactivity in final molecules. Medicinal chemists appreciate the way this indole helps scaffold construction—introducing fluorine at the 4 and 6 positions can change bioactivity profiles sharply. Fluorinated indoles have shown up in kinase inhibitors, neuroprotective drugs, and as lead structures in fragment-based drug discovery programs.

    Agrochemical research turns to this compound for two interconnected reasons: It resists unwanted environmental degradation, and it provides a foothold for targeted substitution of amines or other nucleophiles at the carbonyl-adjacent position. From a manufacturer’s viewpoint, the way this intermediate anchors structures—allowing for experimentation in both directionality and selectivity—means senior synthesis chemists don’t have to fight stubborn side chains or uncontrollable rearrangements.

    Material scientists and photonics groups have found 4,6-Difluorooxindole useful where options with simpler indoles lag behind. Subtle changes in ring electronics matter for light-harvesting, dielectric, or sensor projects by changing charge transfer properties. Researchers who tested both mono- and difluoro oxindoles on their benches have reported sharper boundaries in conductivity and durability—attributes tied back to just this pattern of substitution.

    How 4,6-Difluorooxindole Stands Apart

    Comparing this molecule to its single-fluoro or non-fluorinated siblings highlights real-world differences in both lab handling and outcome predictability. In our own technical support calls, we hear about process runs where mono-fluorinated indoles gave unpredictable byproducts, but switching to the 4,6 variant provided cleaner product profiles—anecdotes borne out by thin-layer chromatography strips lining our development lab whiteboards.

    It’s easy to underestimate the power of double fluorination until side reactions have spoiled a batch. Those extra fluorine atoms subtly withdraw electron density, resisting oxidation and hydrolysis. In purification, this makes a difference—you get tighter, more uniform peaks, simplifying downstream separations. Everyone in the process chain, from analytical chemists to formulation specialists, sees the benefit as work progresses with fewer headaches.

    Lessons from Manufacturing: Challenges and Solutions

    Every compound presents a unique set of hurdles, and 4,6-Difluorooxindole makes no exception. Handling the two fluorines puts stresses on both equipment and process controls. Reactor linings need a high resistance to both acid and alkali, something we learned after an equipment survey found micro-pitting that let metal ions creep into product batches. Upgrading our reactor coatings brought particle contaminant levels to well below detectable thresholds, improving product reliability across the board.

    Another frequent challenge shows up in the purification stage. Solubility profiles for fluorinated indoles can be tricky, diverging even between batches if incoming materials shift slightly. Early on, our chromatography yields looked promising but evaporative losses during scale-up revealed product occlusion in some of our filter cakes. Recalibrating our wash solvents, and adding an extra low-temperature crystallization cycle, both mitigated these losses. In practice, we track batch performance closely, comparing not just classic yield-figures, but long-term stability as seen on pilot storage shelves.

    Waste handling adds another layer of complexity. Outflows from difluoro compounds aren’t always simple to treat, especially where fluorinated organic residues persist. Our plant invested in upgraded carbon adsorption units and high-efficiency incineration—both driven by a commitment to limiting outflows that don’t just meet, but go beyond local emission standards. In our experience, thinking ahead on waste means smoother environmental audits and builds better relationships with local authorities and downstream partners alike.

    Supporting Researchers, Bridging the Lab and Plant

    Many end-users discover that what works in the academic setting sometimes trips up in the pilot plant. Having run joint method development with both pharma researchers and process engineers, we’ve observed first-hand where scale-dependent idiosyncrasies hide. Solubility measured in milligram tests won’t always match up to what’s needed on the kilogram or ton scale. By pooling data from across our customer base—and adding in our own pilot plant miss-steps—we’ve been able to offer upstream guidance that improves outcomes for the next operator in line.

    It’s not just a matter of delivering a drum at the loading dock and walking away. We run sample splits, cross-check loss rates, and keep an open line with technical teams at upstream and downstream facilities. Sometimes this means reconfiguring a drying cycle to alleviate static powder clumping, or tailoring packaging liners where local humidity spikes persist. These aren’t afterthoughts—they arise from experience, an ongoing partnership built on feedback loops both within our plant and in the R&D settings of the clients we serve.

    Supply Reliability and Real-World Security of Supply

    Unplanned outages, raw material shortages, or logistics delays impact anyone relying on specialty intermediates. We’ve learned, sometimes the hard way, how quickly small hiccups cascade. Stockpiling key precursors and investing in process automation solved only half the equation. Open conversations with clients about anticipated projects and seasonal upticks have allowed us to pre-position material well ahead of demand surges—a difference remembered when competitor stocks run dry.

    Our facility anchors itself on a policy of dual-source risk management for critical reagents and ongoing cross-training for process teams. Realistically, unforeseen events will occur: storms, pandemics, or shipping delays. By diversifying both inbound logistics and production cell responsibilities, we’ve kept products moving where needed, avoiding the sort of sticky delivery gaps that once plagued our industry.

    Quality from the Front Lines

    Technical data sheets have their place, but years spent tweaking process windows, filter beds, and even ventilation systems carry lessons no spreadsheet fully captures. Our best upgrades don’t always come from top-down management edict but rather from hands-on operators, chemists, and shippers who spot patterns or bottlenecks before headlines catch on.

    Routine retains its place—standardized sampling, batch record-keeping, and out-of-spec logs—but flexibility in response carries equal weight. We’ve fostered an environment where feedback moves swiftly from quality analysts at our reactors to the desk of a process engineer and, if warranted, back to the customer for discussion. That’s how we prevent issues from repeating through the supply chain.

    Environmental and Safety Stewardship

    The conversation around fluoro compounds and safety spans both occupational hazard and end-of-life environmental considerations. Years of experience have shown us the wisdom of thorough hazard analysis and constant monitoring. Processing 4,6-Difluorooxindole means managing not just chemical exposure potential for our team but understanding how accidental releases could affect the broader community.

    Investments in scrubbers, negative pressure containment, and personal protective equipment form only the baseline. Ongoing education programs for staff, regular external audits, and drill-driven emergency response planning have demonstrated value far beyond regulatory compliance. Suppliers who cut corners in safety protocols eventually pay costs far higher than the price of advanced volatilization extractors.

    Disposal and downstream stewardship demand rigor as much as innovation. Careful incineration of fluoro-organic residues, alongside monitored wastewater treatment, limits persistent build-up in local water tables—a lesson reinforced by reviewing both in-house soil samples and public health studies near older chemical manufacturing zones. We address such risks proactively, integrating learnings into every revision of our operational manuals.

    From Molecule to Market: The Practical Impact

    End-users often ask not just for technical guidance, but for an honest accounting of what has worked and what hasn’t in practice. We’ve seen project timelines shrink where customers lean heavily on direct consultation and up-to-date operational data. The real-world pace of development now hinges as much on reliable intermediates as it does on the brilliance of a new synthetic idea.

    Having our own chemists available for technical discussions, troubleshooting, and method optimization has built trust over years, not quarters. Owing material issues—variability in batch color, counter-ion residues, unexpected side-chain modifications—we work through solutions hand-in-hand, recognizing that a few extra hours invested in communication early on often short-circuits project risks weeks or months down the line.

    Continuous Learning, Relentless Improvement

    Perfection proves elusive, but progress remains the standard. We run regular retrospectives on both successful and failed production campaigns. Each cycle refines our approach—not just in the product itself, but in documentation, operator training, and technical sharing. Delivering 4,6-Difluorooxindole has become a process that reflects both pride in our technical mastery and humility in the face of an ever-evolving field.

    External collaborations fuel much of this momentum. Joint workshops with clients, raw material producers, and academic partners unearth new techniques that we feed back into our daily routines. Unexpected process deviations, often caught only by skilled eyes who work the lines, become teaching moments that inform future process tweaks or raw material sourcing strategies.

    Ethical Commitments and Responsible Progress

    Every product carries its responsibilities. 4,6-Difluorooxindole, as with other high-impact intermediates, must offer value not by cost alone but in supporting both safe laboratory innovation and responsible product outcomes. We take that charge seriously by building in traceability, compliance with evolving regulatory frameworks, and honest communication with the entire supply chain.

    Direct engagement with our customers, whether on routine batch reviews or major investigations, helps us uphold those commitments—not in the abstract, but in practical transparency. Our internal documentation goes through regular audit and cross-checking, so that decisions made today align with both ethical best practice and market expectations a decade down the line.

    Summary Reflections on 4,6-Difluorooxindole’s Place in Modern Chemistry

    With more than a decade anchoring our production floor, this compound has taught us the power of diligence, the value of collaboration, and the need for continuous learning. Each ton produced, each application supported, and each challenge solved for a client pushes us forward in both technical mastery and ethical resolve.

    By bringing together the diverse perspectives of those in the lab, at the bench, and in the plant, we build not a commodity, but a foundation for safer, more effective innovation. For us, manufacturing 4,6-Difluorooxindole isn’t a matter of filling an order sheet; it’s an ongoing commitment to quality, partnership, and progress—the sum total of chemical experience forged by real-world practice and constant refinement.