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6-Fluoro-2-Methylindanone

    • Product Name 6-Fluoro-2-Methylindanone
    • Einecs 629-022-1
    • 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
    VTB
    Specifications

    HS Code

    275516

    Chemical Name 6-Fluoro-2-Methylindanone
    Molecular Formula C10H9FO
    Molecular Weight 164.18 g/mol
    Cas Number 131140-98-2
    Appearance White to off-white solid
    Melting Point 54-57°C
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, away from moisture and light
    Solubility Slightly soluble in organic solvents (e.g., DMSO, methanol)
    Synonyms 6-Fluoro-2-methyl-1-indanone
    Smiles CC1CC(=O)C2=C1C=CC(F)=C2
    Inchi InChI=1S/C10H9FO/c1-6-5-9(12)7-3-2-4-8(11)10(6)7/h2-4,6H,5H2,1H3

    As an accredited 6-Fluoro-2-Methylindanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25-gram package contains 6-Fluoro-2-Methylindanone in a sealed amber glass bottle with a clear, tamper-evident safety cap.
    Shipping 6-Fluoro-2-Methylindanone is shipped in tightly sealed containers to prevent moisture ingress and contamination. The chemical is packaged according to standard hazardous material regulations, typically in amber glass bottles, cushioned within sturdy outer packaging. Careful labeling and documentation ensure safe handling during transit, with temperature and light exposure controls as needed.
    Storage 6-Fluoro-2-Methylindanone should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong oxidizers. Ensure proper labeling and secure storage to prevent accidental spillage or contamination. Use appropriate chemical storage containers.
    Application of 6-Fluoro-2-Methylindanone

    Applications of 6-Fluoro-2-Methylindanone in Industrial Manufacturing

    6-Fluoro-2-Methylindanone serves as a crucial building block in several high-value industrial chemical syntheses. Its unique chemical structure enables targeted transformations across pharmaceuticals, agrochemicals, fine chemical intermediates, and specialty polymer industries. Below are detailed application scenarios based on proven industrial practices.

    1. Pharmaceutical Intermediate for CNS Drug Synthesis

    The compound plays a significant role in the production of advanced intermediates for central nervous system (CNS) active pharmaceutical ingredients, facilitating the synthesis of selective dopamine receptor modulators. Our facility supplies this raw material to manufacturers who require strict batch traceability and documentation due to regulatory scrutiny. Downstream processes incorporate it at the heterocyclic scaffold construction stage, where fluorine substitution patterns significantly influence pharmacological properties. Integration into multi-step syntheses demands high purity and reliable supply, with precise control over isomeric composition to meet API requirements.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU EudraLex Volume 4, Part II
    • USP and Ph. Eur. monograph references for advanced intermediates
    • FDA DMF (Drug Master File) requirements for intermediates

    Typical usage ratio

    • 5–15% of total substrate input in CNS API precursor synthesis
    • Adjusted based on molar equivalence to targeted heterocyclic core formation

    Downstream process integration

    • Introduced during core condensation and cyclization steps
    • Utilized prior to Suzuki-Miyaura or Buchwald–Hartwig cross-coupling operations
    • Subjected to phase transfer catalysis or base-promoted alkylation depending on synthesis route

    Final product types

    • Advanced pharmaceutical intermediates for CNS agents
    • Dopamine receptor modulator drug substances
    • Anti-Parkinson’s API core structures

    2. Agrochemical Active Ingredient Synthesis

    Our material is widely used for synthesizing select fluoroindanone-based agrochemical actives that provide high soil stability and improved bioactivity in crop protection products. In this segment, customers require batch consistency for large-scale installations and close specification control to minimize by-products affecting environmental residue profiles. Downstream syntheses leverage the electron-withdrawing fluorine atom to enhance the target compound’s metabolic resistance, resulting in longer-lasting plant protection.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 and ISO 14001 process certification
    • REACH registration (EC No. 1907/2006) for imported raw materials
    • OECD principles of Good Laboratory Practice (GLP) for active substance dossiers

    Typical usage ratio

    • 8–18% by weight in the precursor formulation for indanone-type pesticide synthesis
    • Altered proportionally based on conversion rates in Friedel–Crafts or Mannich reactions

    Downstream process integration

    • Added at the first aromatic acylation or halogenation step
    • Serves as the core during formation of pyrazole or pyridine substitution patterns
    • Employed in solvent-based or continuous flow production lines

    Final product types

    • Herbicide and fungicide technical concentrates
    • Active ingredient APIs for selective weed control
    • Seed coating agents for commercial agriculture

    3. Fine Chemical Intermediate for Fragrance Ingredient Development

    6-Fluoro-2-Methylindanone is an essential intermediate in specialty fragrance compound manufacture, especially for high-value musk and floral notes which require controlled fluorination to achieve stability and volatility profiles. Downstream processors focus on minimization of impurities to safeguard olfactory performance. The compound is introduced into condensation, reduction, or cyclization protocols to form macrocyclic ketones and lactones, which are then further refined into proprietary fragrance bases.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • ISO 9235:2013 for aromatic raw materials
    • REACH compliance for industrial fragrance intermediates
    • HACCP-based factory-level quality controls

    Typical usage ratio

    • 2–7% of initial batch charge, depending on the backbone structure of the fragrance target
    • Adjusted for yield optimization in dimerization or cyclization stages

    Downstream process integration

    • Employed at the ring-expansion or subsequent esterification stage
    • Feeds into hydrogenation steps for musk compound synthesis
    • Subjected to fractional distillation and solvent extraction post-reaction

    Final product types

    • Fluorinated musk bases
    • Specialty floral fragrance intermediates
    • Fixative ingredients for high-end perfumes

    4. Monomer Precursor in Specialty Polymer Synthesis

    This raw material facilitates the production of advanced poly(indanone) and poly(aryl ether ketone) grades that require unique substitution patterns for high thermal resistance and chemical durability. Industrial polymerization protocols demand extremely low impurity levels and trace metal content, which we verify batch-wise. The compound is deployed as a core monomer or co-monomer feed in direct condensation or step-growth reactions, imparting fluorine functionality that enhances final polymer performance for technical components in demanding end-use sectors.

    Industry compliance standards

    • ISO 9001 Quality Management System for polymer raw materials
    • IEC 61249-2-21 for halogen-free high-performance laminates
    • UL 94 flammability rating prerequisites (where applicable)
    • RoHS (Restriction of Hazardous Substances) for electronics and electrical applications

    Typical usage ratio

    • 3–9% molar ratio in copolymer feed for specialty indanone-polyarylene ether synthesis
    • Adjusted in step-growth polymerizations to achieve desired Tg and mechanical profile

    Downstream process integration

    • Charged into melt-phase or solution-phase polymerization reactors
    • Combined with aryl dihalides and bisphenols under catalytic conditions
    • Integrated into in situ functionalization stages for custom polymer property development

    Final product types

    • High-temperature resistant polyindane copolymers
    • Engineering plastics for electronics housings
    • Specialty films and laminates for electrical insulation
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    Certification & Compliance
    More Introduction

    6-Fluoro-2-Methylindanone: Practical Insights from the Manufacturer’s Bench

    The Role and Nature of 6-Fluoro-2-Methylindanone

    Working hands-on with 6-Fluoro-2-Methylindanone every week, we see firsthand how this compound offers chemists a reliable core structure for building advanced molecules, especially specialty agroscience and pharmaceutical intermediates. Its unique indanone backbone incorporates a fluorine atom on the aromatic ring, bringing a change to reactivity and downstream applications. With the methyl group at the 2-position, it often acts as a stepping stone for more elaborate substitutions and ring modifications. Demand often originates from research teams in need of fine-tuned, tailored scaffolds for high-throughput screening or scale-up projects.

    Batch after batch, our quality control teams record the off-white crystalline appearance, typical melting range, and chemical stability as key attributes. Decades of incremental improvements have refined our process, yielding consistent material with impurity profiles well below common synthetic standards. Gas chromatography and NMR analyses guide every lot out the door. We know impurities, even in trace amounts, can skew entire projects or confuse analytical methods, especially as end users push the envelope in new organofluorine chemistry.

    From Raw Intermediate to High-Value End Use

    Several fields favor indanone-based fragments, but fluorinated versions stand apart. Medicinal chemists, for example, value the fluorine atom’s ability to change metabolic stability or receptor affinity—modifying a compound’s activity profile without a huge steric load. Crop protection R&D leans on these indanones for pre-clinical lead optimization, looking for better uptake or drought resistance through bioisosteric substitution. The 2-methyl group functions as a stable handle for further functionizations, such as Friedel-Crafts alkylations or Suzuki couplings.

    Our production process starts from readily available aromatic precursors; each step must maximize regioselectivity to place fluorine in precisely the right spot. Chlorinated indanones and non-fluorinated derivatives are common on the market, but these generally do not share the same reactivity profile. Non-fluorinated analogues lack the unique electronic effects brought by the fluorine, which often leads to different pharmacokinetics or downstream compatibility for coupling reactions. Many contract research organizations ask for multiple indanone isomers to directly compare their properties. We’ve seen plenty of reports where a single atom’s shift results in orders of magnitude difference in bioactive performance.

    Key Differences from Other Indanones

    A fluorinated indanone sets itself apart the moment it enters a reaction flask. Colleagues mention how un-fluorinated 2-methylindanone often shows less favorable selectivity when building multi-functional molecules. The electron-withdrawing effect of the fluorine directs further substitutions, changing both reactivity and yield. Downstream reactions sometimes progress more cleanly—less over-reaction and fewer byproducts—thanks to this single change. Over the years, we’ve optimized crystallization methods specifically for this isomer, as its solubility profile changes with the fluorine ring position.

    Bulk suppliers usually focus on more basic indanone derivatives due to their simplicity, but scale-up experience with this molecule is crucial. Our team’s hands-on knowledge with solvent selection and waste management increases yield and quality—details not learned from textbooks. Customers point out that alternative sources sometimes offer material with higher impurities or shifted melting points, directly impacting their process efficiency further down the line. Producing a high-purity, fluorine-containing indanone requires diligent distillation and purification, much more demanding than for simple unfunctionalized indanones.

    Sustainability and Manufacturing Considerations

    Direct experience with our reactors reveals how challenging fluorination reactions can be, especially on scale. Halogenation often means hazards, and keeping process temperatures and pressures within a safe range isn’t negotiable. Equipment corrosion can become a hidden issue. We’ve sourced specialized reactor linings and invested in continuous-flow technology to reduce byproduct formation and energy waste. Each batch produces data that guides us to safer, greener synthesis. Waste reduction over the last five years has resulted in lower handling costs and a measurable cut in emissions, something our downstream partners increasingly ask about.

    Third-party suppliers or traders usually do not manage their own waste streams, leading to regulatory blind spots or missed savings. Managing the whole process in-house gives us more control, both over the process and the final product. It pays to monitor emissions, track yields, and revisit raw material sourcing—improper handling often shows up in final product inconsistencies. In the last annual audit, our production data showed kilowatt-hour use per kilo of product dropped since integrating solvent recycling on-site.

    Downstream Applications and Chemical Flexibility

    Discovery teams see value in using 6-Fluoro-2-Methylindanone as a module for synthesizing pyrrolo- and benzo-fused frameworks. Medicinal chemistry campaigns rely on reliable indanone derivatives when screening for new kinase inhibitors or small-molecule probes. Academics have also started exploring the role of fluorinated indanones in photoresponsive materials—our technical team keeps up with those trends, collaborating with R&D partners to tune impurities below one percent for photochemistry benchmarks. Blending human expertise with automated analytics helps us respond quickly to new industry directions.

    The core skeleton of 6-Fluoro-2-Methylindanone enables rapid build-out of chemical diversity. It tolerates a variety of functionalization reactions—nitration, sulfonation, Grignards, and metal-catalyzed couplings—without decomposing or introducing significant side-products. This flexibility often turns into cost savings and efficiency as downstream users do not lose batches to impurity buildup or unexpected degradation. Teams using this compound for process optimization regularly share how purity impacts both reaction throughput and analytical reliability.

    Consistency in Processing and Delivery

    Consistent batch-to-batch quality is a regular topic in calls with our long-term customers. Their feedback, combined with our in-house process controls, means tweaks take place in real time, not through slow bureaucracy or off-site communication. Most users ask for documentation detailing lot numbers, testing protocols, and impurity profiles. We actually keep historic records stretching back years—our analytical team can trace small shifts in melting point or color and tie these shifts back to changes in incoming raw materials.

    Nearly every kilogram leaving our facility has a lifecycle story. From real-time in-line monitoring of key steps to final physical inspection, every layer of manufacturing ties back to experienced technicians on the ground. Our chemists cross-train in production and quality control, ensuring tight feedback loops between process optimization and daily execution. Crucially, we make it a priority to stay ahead of evolving international standards. This means our quality benchmarks gradually move upward, keeping pace with new testing methods and regulatory requirements.

    Supporting Research, Enhancing Outcomes

    Universities and industry labs come to us when their in-house syntheses are under strain—often because scale-up uncovers new challenges. They routinely share feedback about reaction reproducibility on larger volumes, where small differences in precursor quality have major downstream effects. Some chemists discover workup difficulties with cheaper or batch-inconsistent sources; switching to our material often clears analytical headaches, letting their teams focus resources on compound optimization instead of troubleshooting supply issues. Reliable starting materials give R&D teams more room to push into new applications, reducing stalled projects and duplicated work.

    We have observed shifts in demand cycles: project launches spike, followed by quieter periods as results are validated. This experience lets us manage production schedules without waste, avoiding excess inventory while maintaining enough capacity to meet urgent calls. Long-standing partnerships emerge from this cycle. Trust develops as users experience consistent deliveries—even under tight timetables or uncommon purity requirements.

    Challenges and Forward-Looking Solutions

    Though the manufacturing process is well-established today, we recall earlier hurdles with waste treatment and environmental compliance. Upgrading to closed-system reactors changed the picture—investment in better offgas scrubbers has cut emissions and boosted worker safety. Now, collaborative projects with materials suppliers target further reductions in process solvent use, looking to minimize environmental impact without compromising quality. Regulators expect traceability and rigorous reporting; hands-on experience smoothing audit procedures now pays off as standards become more demanding.

    Our technical team also explores emerging greener fluorination approaches. Swapping traditional halogenation agents for milder, safer chemicals is a key research area, inspired by feedback from industry partners facing stricter regulatory obligations. Not every promising lab method works on scale, so pilot trials, analytical monitoring, and production-led troubleshooting continue to drive progress. Even small incremental gains in yield or byproduct reduction can set new industry benchmarks.

    Supply chain security is another reality in chemical manufacturing. Periodic disruptions in key raw materials taught us to keep multiple vetted sources and maintain buffer stock. As global logistics change, especially for specialty fine chemicals, keeping a close relationship with upstream suppliers guards against batch delays or unexpected quality shifts. Tight feedback and robust recordkeeping support rapid adjustment, reducing the risk that external shocks ripple down to customers.

    Developments in Downstream Chemistry

    End-use applications of 6-Fluoro-2-Methylindanone keep expanding. Recent collaboration with a specialty pharma team involved late-stage functionalization of indanone cores for central nervous system targets. Here, the fluorine atom played a decisive role in boosting blood-brain barrier penetration for scaffolds that previously showed poor absorption. The methyl group provided the platform for regioselective modifications, accelerating analog synthesis in SAR campaigns. Downstream formulation chemists saw less batch-to-batch degradation, highlighting how small molecular changes made upstream affect everything later on.

    In the agroscience space, newer pesticide candidates rely on our indanone derivative for its metabolic stability and diminished photodegradation under field conditions. We have evidence from field partners that formulations built from this compound show improved residual profiles compared to non-fluorinated options. These properties translate into improved outcomes for end users, not just incremental chemistry improvements.

    Regulatory, Safety, and Operator Experience

    A hands-on production environment fosters deep familiarity with each step. Safety protocols evolve as new data emerges—not just to protect raw product, but every employee handling or packaging the material. Extensive operator training shifts with changing regulations, covering everything from proper PPE use to chemical storage best practices. We take pride in transparent site tours, showing research partners our real-world safety measures and continuous improvement cycle. Reviewing near-miss events and acting on operator feedback goes hand-in-hand with maintaining high-quality output.

    Lab trials and early scale-ups get easy support from our technical teams, whose experience bridges both the manufacturing and application sides. End users regularly request historical Certificate of Analysis reports to satisfy evolving quality and regulatory audits. Anticipating this, quality engineers tightly document every production shift, so we answer questions proactively rather than reactively. Customers mention regulatory process headaches reduced when supply partners understand both chemical and documentation landscapes—an edge that consistent, hands-on manufacturing experience delivers.

    Conclusion: A Product Backed by Real-World Expertise

    Every batch of 6-Fluoro-2-Methylindanone reflects technical know-how built over years of direct manufacturing. Conversations with chemists across drug development, materials science, and crop innovation shape continuous improvement. Persistent investment in cleaner synthetic routes, real-time analytics, and environmental safeguards ensures product reliability and safety. Upstream, ongoing dialogue with raw material suppliers mitigates supply chain shocks, while robust process controls support consistent, trusted performance.

    Instead of generic commodity chemicals, our daily attention remains fixed on real outcomes for users. Success stories from customers—faster development cycles, fewer failed syntheses, and more robust downstream chemistries—fuel ongoing investment in new methods and equipment. Knowledge moves both ways: insights from the bench flow back into process refinement, and challenges from the production floor spark innovative technical solutions. In an industry where every atom and impurity matters, a manufacturer’s experience makes the difference between just another chemical and a foundation for new advances in science and industry.