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5,7-Difluoroindole

    • Product Name 5,7-Difluoroindole
    • Alias 5,7-Difluoro-1H-indole
    • Einecs 853-811-1
    • 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

    482495

    Chemical Name 5,7-Difluoroindole
    Molecular Formula C8H5F2N
    Molecular Weight 153.13 g/mol
    Cas Number 172198-25-1
    Appearance White to off-white solid
    Melting Point 62-66°C
    Boiling Point Unknown
    Smiles C1=CC2=C(C=C1F)NC=C2F
    Inchi InChI=1S/C8H5F2N/c9-5-1-2-6-7(3-5)11-4-8(6)10/h1-4,11H
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light
    Synonyms 5,7-Difluoroindole; Indole, 5,7-difluoro-

    As an accredited 5,7-Difluoroindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle labeled "5,7-Difluoroindole," featuring hazard symbols, lot number, and chemical purity details.
    Shipping 5,7-Difluoroindole is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous material, complying with safety and transportation regulations. Proper labeling and documentation are ensured, and the package is cushioned to prevent breakage or leakage during transit. Store in a cool, dry place upon arrival.
    Storage 5,7-Difluoroindole should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep the chemical away from incompatible substances such as strong oxidizers and acids. Store at room temperature or as recommended on the manufacturer's safety data sheet. Ensure proper labeling and restrict access to authorized personnel only.
    Application of 5,7-Difluoroindole

    Applications of 5,7-Difluoroindole in Industrial Manufacturing

    5,7-Difluoroindole serves as a critical raw material in multiple advanced chemical production processes. As a manufacturer, we supply this compound for high-value applications in pharmaceutical synthesis, agrochemical intermediates, OLED materials, specialty dyes, and advanced material research platforms.

    1. Pharmaceutical Intermediate Synthesis

    5,7-Difluoroindole forms a key structural core for various active pharmaceutical ingredients, particularly those requiring precise fluorine substitution patterns on the indole ring. It enters the production chain as a building block in heterocyclic coupling, mainly in targeted oncology and CNS drug programs. Customers leverage its reactivity for Suzuki-Miyaura or Buchwald–Hartwig amination to yield fluorinated scaffolds in API pipelines. Handling must observe strict trace impurity controls, as final APIs must meet regulatory specifications for residual fluorinated aromatics.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs for specified APIs
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia CP2020 QC guidelines for indole derivatives

    Typical usage ratio

    • 10–25% by molar ratio in cyclization or halogen exchange reactions, adjusted based on substitution position requirements and downstream yield targets

    Downstream process integration

    • Introduced in the early-stage coupling or condensation process following protection group installation; reacts under mild base conditions before downstream acylation or sulfonylation

    Final product types

    • Targeted anti-cancer drug intermediates
    • CNS modulators with tetrahydroindole cores
    • Fluorinated tryptamine analogs for final API formulation
    • Pilot-scale intermediates for pharmaceutical validation batches

    2. Agrochemical Synthesis

    Within agrochemical manufacturing, 5,7-Difluoroindole functions as a synthetic precursor for high-performance fungicides and herbicides. The unique di-fluorination enhances pest resistance and field stability in downstream products. Industrial-scale processes typically use it in alkylation or glycosylation to introduce tailored functional groups, improving soil persistence and molecular binding in commercial formulations.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (Europe)
    • US EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemical Residues in Food)
    • Chinese GB 2763-2021 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • 5–18% by weight in active ingredient precursor reactions; dosage adjusted for chain extension lengths and substituent patterns of target compounds

    Downstream process integration

    • Added during the heterocycle construction stage after initial condensation with acylating agents; processed under controlled temperature for regioselectivity

    Final product types

    • Indole-based herbicide intermediates
    • Fluorinated fungal growth inhibitors
    • Seed coating additives
    • Chemical intermediates for soil remediation agents

    3. OLED Electronic Materials

    5,7-Difluoroindole finds advanced application as a monomer or intermediate in organic light-emitting diode (OLED) electronics. Research groups and material suppliers use its electron-withdrawing fluorine atoms to modulate band gaps and improve charge mobility in organic semiconductors. Integration occurs during ligand or host material synthesis for blue and green-emitting layer development, contributing to device lifespan and thermal stability.

    Industry compliance standards

    • RoHS 2015/863/EU Directive on the restriction of hazardous substances in electronic equipment
    • ISO 9001:2015 Quality Management Systems for electronic component manufacturing
    • IEC 62321 Determination of certain substances in electrotechnical products
    • ANSI/IPC-6012D Qualification and Performance Specification for Rigid Printed Boards

    Typical usage ratio

    • 1–6% by mass in emission layer formulations, tuned according to the device architecture and desired emission wavelength

    Downstream process integration

    • Dosed during aryl amine reaction or copolymerization, often in high-purity atmospheres; purification steps follow to ensure electrical characteristics meet OLED device standards

    Final product types

    • Blue and green light-emitting monomeric host materials
    • Hole transport layer intermediates
    • OLED device research samples
    • Prototyping blends for display panel development

    4. Specialty Dyes and Pigments

    Manufacturers in the advanced dye industry utilize 5,7-Difluoroindole for synthesizing specialty functional dyes, such as those used in security printing, photoresist formulations, and textile coloration. Its unique substitution pattern allows for synthesis of colorfast, solvent-resistant compounds, and enhances fluorescence or deep hue formation in bespoke dye molecules. Strict control of residual fluorine and byproducts ensures regulatory acceptance in sensitive end uses, especially when applied to garment or labeling sectors.

    Industry compliance standards

    • OEKO-TEX Standard 100 for harmful substances in textiles
    • REACH Annex XVII (Regulation for substances of very high concern)
    • ISO 105 series (Color fastness testing in the textile industry)
    • ASTM D4300 (Lightfastness of colorants in plastics and coatings)

    Typical usage ratio

    • 2–12% by weight in dye precursor reactions; selection tailored to target color depth and fluorescence properties of end dye formulation

    Downstream process integration

    • Introduced during condensation with aromatic aldehydes or coupling agents in high-shear reactors; follows by column purification and solid-state blending as required by downstream dispersal method

    Final product types

    • Security printing fluorescent dyes
    • Photoresist color additives for semiconductor lithography
    • Industrial textile indole dyes
    • Pigments for solvent-based coating systems

    5. Advanced Material Research & Discovery Platforms

    Academic institutions and specialty material developers employ 5,7-Difluoroindole as a reference compound for the development of new fluorinated heterocyclic systems. Its unique reactivity profile is suitable for creating novel ligands, catalysts, and material precursors for research into energy materials, advanced sensors, and molecular electronics. Reliable supply and consistent purity support reproducibility in iterative research workflow, including combinatorial synthesis and high-throughput screening.

    Industry compliance standards

    • ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories)
    • GMP (Good Manufacturing Practice) for laboratory chemical reagents
    • Safety handling per GHS (Globally Harmonized System of Classification and Labelling of Chemicals)
    • Institutional chemical procurement and hazard assessment protocols

    Typical usage ratio

    • Variable, typically 0.5–5% based on screening array design, with concentrations optimized per experimental pathway

    Downstream process integration

    • Applied in parallel synthesis arrays, automated liquid handling platforms, and ligand modification reactions under inert atmosphere; follows assessment by HPLC and LC-MS for compound verification

    Final product types

    • Experimental hybrid materials for energy storage
    • Sensor probe functionalization elements
    • Fluorinated indole libraries for hit identification
    • Ligand precursors for transition metal-catalyzed processes
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    Certification & Compliance
    More Introduction

    5,7-Difluoroindole: Expanding the Toolbox for Fine Chemical Synthesis

    An Insider’s Introduction to 5,7-Difluoroindole

    At our manufacturing site, we focus on building foundation blocks for the wider chemistry world. One important compound we produce is 5,7-Difluoroindole. Our model for this raw material carries a CAS number of 25017-26-5, and through a set of robust synthesis and purification pipelines, we achieve high-purity batches that serve researchers, pharmaceutical developers, and a wide range of material science teams. This molecule has carved out a meaningful place in complex synthesis schemes, often relied on for its unique reactivity and well-defined structure, which contributes essential functionalities during the creation of active pharmaceutical ingredients (APIs), specialty additives, agrochemical compounds, and light-emitting materials.

    Understanding the Structure: More Than Substitution

    The indole backbone sits at the core of many natural and synthetic compounds. By introducing fluorine atoms at the 5 and 7 positions, chemists achieve two goals at once. The electronic properties of indole undergo adjustment, carving out new possibilities for downstream functionalization, and the resulting stability often increases due to the inherent resilience conferred by the fluorine atoms. From our position behind the reactors and purification columns, we learned firsthand how small tweaks in the molecular structure translate into real differences in functionality later in the process. For example, 5,7-difluoroindole resists certain oxidation pathways compared to its non-fluorinated relatives, making it a reliable scaffold when handling more aggressive conditions.

    Meticulous In-House Synthesis

    The journey from commercially available starting materials to 5,7-difluoroindole calls for careful calibration at every step. We oversee the entire process—from halogenation and cyclization to distillation and crystallization—ensuring strict control over batch consistency and contaminant levels. Our analytical chemists rely on advanced techniques—NMR, GC-MS, and HPLC validation with reference standards—to check that each lot leaves the plant fully meeting target specifications. Over many years operating this production line, we've identified several key factors that preserve the molecule’s integrity: maintaining water exclusion, optimizing temperature ramp rates, and choosing compatible reactor linings to hold caustic intermediates. This dedication limits batch-to-batch variation, a factor seasoned formulators and research teams cite as a central reason for sticking with our supply.

    Typical Specifications

    Most outbound lots of our 5,7-difluoroindole show assay levels greater than 98%, with melting points sitting reliably between 49–53 °C, and low single-digit ppm water content (Karl Fischer method). The crystalline powder appears pure white to off-white, but slight variation in shade sometimes shows up—usually due to batch size and drying methods, and never signaling compromised quality. Trace metals are tightly controlled, well below threshold regulatory limits for advanced pharmaceutical and electronic applications, a crucial point clients in regulated sectors frequently scrutinize.

    The Value of 5,7-Difluoroindole for Synthesis

    In the world of medicinal chemistry, introducing fluorine atoms often shifts metabolic fate, influences binding affinity, and enhances molecular stability. Medicinal chemists come to us specifically for 5,7-difluoroindole when standard indoles lead to poor drug-like properties or drop out in biological screens. Beyond pharmaceuticals, the same molecular design bumps up the performance of organic semiconductors, luminescent dyes, and fine chemical intermediates. During brainstorming sessions with clients developing new chemical entities, we see recurring interest in difluoroindole frameworks, which often appear in early patent filings or structure-activity relationship (SAR) explorations. And downstream users continue to report that our tight control over batch consistency makes process optimization in the lab or at pilot-plant scale more straightforward.

    Comparing with Other Indole Derivatives

    Across the chemistry landscape, a wide range of indole derivatives compete for attention. Some groups opt for substituted indoles at the 2- or 3-position, introducing alkyl, aryl, or halogen groups to influence either physicochemical properties or reactivity. In contrast, modifications at the 5 and 7 positions frequently lead to less predictable electronic effects, offering unique reactivity profiles. Over years supplying both mono-fluorinated and difluorinated indoles, we charted important differences. 5,7-difluoroindole delivers sharper differentiation in certain binding assays, and chemists report it often resists ring-opening and side-chain elimination seen with other isomers. These practical insights didn’t emerge from theoretical speculation alone; regular feedback from end-users—combined with in-house reactivity tests—have shaped our understanding of where this product shines and where alternatives might offer a better fit.

    Real-World Applications: Beyond the Bench

    Our product heads out the door to support a range of industries. Pharmaceutical R&D teams incorporate 5,7-difluoroindole into screenings for kinase inhibitors, serotonin receptor agonists, and anti-infective agents. Sometimes these result in new lead compounds, other times they illustrate how subtle molecular changes help bypass metabolic bottlenecks or boost selectivity. In agrochemical development, teams employ it to fine-tune hormone modulators and crop protection agents, chasing higher bioactivity or longer field stability. Electronics factories turn to our difluoro product as a building block in organic LEDs and conductive polymers, where the electron-withdrawing fluorine atoms shape both device performance and long-term reliability. Having traced the journey of each kilogram shipped—to both startup labs and established blue chips—it’s clear that the impact is broad and continually evolving.

    Challenges Sourcing High-Purity Difluoroindoles

    Providing this molecule at scale isn’t just a question of chemical know-how. Early on in our production journey, uptime suffered due to tricky purification steps and the need for fresh, moisture-free supplies of reagents. Even today, the global pipeline for fine chemicals faces recurring raw material shortages, stricter quality requirements, and fluctuating energy costs. Investment in improved distillation set-ups and in-line monitoring allowed us to bump up both volume and reliability. Each improvement was driven by hands-on troubleshooting, not just reading the latest methods in journals. Environmental compliance also becomes more demanding every year, so we've worked through dozens of process tweaks to reduce halogenated wastes and recycle solvents as much as possible. These experiences shape our view that reliability and sustainable manufacturing shouldn’t just come from paperwork or slogans; it calls for ongoing tinkering and close collaboration between floor technicians and process engineers.

    Product Handling and Storage Insights from Practice

    Many customers toting our product into the lab ask about storage and handling quirks. Over years of tracking customer reports and testing retention samples, we found that this difluoroindole enjoys decent shelf stability if kept away from moisture, light, and air. Occasional clumping doesn’t reduce quality, though it’s best to prevent cycling the container between hot and cold spaces. Resealing containers quickly keeps out humidity and stops the gradual build-up of byproducts. We stack plenty of inert gas–filled vials for our in-house R&D benchmarking, and this practice seems to extend active shelf life even during multi-month studies. Direct hands-on experience trumps any list of recommended procedures, so we share updates based on both our own lab practice and customer-provided observations.

    Addressing Synthesis and Scale-Up Problems

    Chemists scaling up from grams to kilograms bump into issues that just don’t show at small scale. Solubility quirks, vessel fouling, and unexpected side reactions turn into production-stoppers if ignored. Our in-house team spent a lot of time comparing different reactor coatings and solvent systems to stop corrosion and minimize side product formation. We also discovered an odd but useful fact: slow addition of certain reagents reduces impurity formation far more than any post-reaction clean-ups can achieve. In many cases, environmental humidity and temperature swings carry more influence on yield than any theoretical yield or published process. Our advice for customers tackling pilot or manufacturing scale-ups often comes from hard-won lessons, not from textbook guidelines: keep track of minor process deviations and don’t assume a straight transfer from literature values.

    Authenticity in Supporting Innovation

    We see a steady stream of proposal requests: new fluorinated indole derivatives, tweaks to side chains, explorations of higher substitution levels. Looking over the years of sales logs and correspondence with synthetic chemists, one pattern stands out—those who succeed tend to request authentic, high-purity samples up front. Specifiers choosing our difluoroindole over non-fluorinated or mono-fluorinated alternatives often flag stability and clean analytical “footprints” as the deciding factor. Sometimes an extra hour in the purification step at our plant saves weeks of troubleshooting at a customer site. That direct feedback loop strengthens our belief that investing in upstream quality always pays downstream dividends—fewer false positives, consistent assay results, better reproducibility in multi-arm studies, and cleaner IP protection for the innovators building on these synthons.

    Tackling Regulatory and Analytical Demands

    Pharmaceutical and electronics industries push for tight impurity profiles, documentation, and complete traceability. Every batch of our 5,7-difluoroindole gets full analytical documentation, trace impurity screening, and comprehensive batch records. Our plant operations integrate sample archiving with every production run, giving teams a backup should future audits or regulatory filings require original material retention. Customers navigating ever-tighter global standards find value in engineering our processes to provide “out-of-the-box” compliance for regulated workflows. We learned through audits and collaborations that generic assurances of “high quality” don’t win trust—frontline chemists and regulators want the raw data, and we deliver it with every shipment.

    Feedback and Constant Improvement

    Day-to-day, our team checks incoming queries about odd reactivity, batch color, or analytical blips. Few molecules get away with totally predictable behavior in all settings; 5,7-difluoroindole is no exception. We lean on our network of research partners and in-house development staff to investigate trends and solve root causes. Whether it’s swapping out a filter type, updating a drying protocol, or flagging a newly detected trace impurity, the cycle of feedback and adjustment keeps our product line competitive and relevant. Teams trusting us with exploratory projects depend on this kind of agility—not just a rigid “meets spec” mentality, but an open ear to process quirks.

    Sustainable Manufacturing Commitments

    Over the last decade, industrial chemistry changed dramatically. Sustainability isn’t just a checkbox; it shapes process design and purchasing decisions. We moved beyond traditional solvent systems, invested in lower-waste halogen sources, and upgraded exhaust capture across production lines. Little steps—like reclaiming mother liquors or tuning agitation rates—keep waste and emissions down. We also prioritize low-emission logistics—batch shipments get consolidated to minimize carbon footprint where possible. European and North American customers in particular ask pointed questions about lifecycle impacts, so providing transparent answers relies on real operational transparency.

    Why Consistency Counts for the End User

    Those using our 5,7-difluoroindole rarely just want “a” molecule—they want something predictable over the whole R&D cycle. Wizard chemists can sometimes work around inconsistent batches with extra purification, but that eats up time, budget, and reproducibility. Most of our repeat customers cite the reduction in troubleshooting and down-time as primary benefits. Whether it’s synthesizing a key reference compound, validating QC methods, or running months-long batch processing, the real value emerges in the laboratory record books—clean, simple handoffs from shipment to workflow, rather than puzzle-solving with every bottle.

    R&D Partnership: Sharing Experience for Better Outcomes

    As a manufacturer, we’re more than a mere raw material supplier. We see ourselves as practical partners for users exploring new territory—sharing insights won through daily work in the plant. Teams in academia and industry alike benefit from our accumulated understanding, especially during technology transfers, upscaling, or troubleshooting session by session. Each success story—whether published as a new compound in a scientific journal, or passed along quietly in the form of a working material for a patent—serves as proof of the compounded value built from reliable supply and real-world expertise.

    The Human Touch in Chemical Production

    Nothing replaces the experience gained by actually running a process, tracking down intermittent impurities, or stopping a runaway reaction by eye and hand rather than algorithm. Our plant operators and technical staff bring deep experience to each production lot. The quiet pride taken in shipping out a complicated molecule like 5,7-difluoroindole comes from the knowledge that it’ll form a vital part of somebody’s new product, regulatory filing, or research milestone. Real chemistry is done by people—our job is to empower those making tomorrow’s innovations by providing materials that meet their ambition.