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5-Fluoro-2-Methylindan-1-One

    • Product Name 5-Fluoro-2-Methylindan-1-One
    • Alias 5F-MIND
    • Einecs 695-595-8
    • 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

    746584

    Chemical Name 5-Fluoro-2-Methylindan-1-One
    Cas Number 1807428-32-0
    Molecular Formula C10H9FO
    Molar Mass 164.18 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Synonyms 5-Fluoro-2-methyl-1-indanone
    Structure Type Aromatic ketone
    Solubility Soluble in organic solvents
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Smiles Notation CC1CC(=O)C2=C1C=CC(F)=C2
    Inchi Key VHRPDGQGBPQJKK-UHFFFAOYSA-N

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

    Packing & Storage
    Packing White, labeled HDPE bottle containing 25 grams of 5-Fluoro-2-Methylindan-1-One; tamper-evident seal, hazard symbols, and lot information included.
    Shipping 5-Fluoro-2-Methylindan-1-One is typically shipped in tightly sealed, chemical-resistant containers to prevent leakage or contamination. It should be handled with care, following all relevant hazardous material transport regulations. Shipment is usually via ground or air freight, labelled with appropriate hazard warnings, and accompanied by documentation such as an MSDS and shipping manifest.
    Storage Store **5-Fluoro-2-Methylindan-1-One** in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Ensure it is isolated from incompatible substances such as strong oxidizers and acids. Always follow laboratory safety protocols and use personal protective equipment when handling.
    Application of 5-Fluoro-2-Methylindan-1-One

    Applications of 5-Fluoro-2-Methylindan-1-One in Industrial Manufacturing

    5-Fluoro-2-Methylindan-1-One serves as a crucial intermediate for specialty organic synthesis in several tightly regulated industrial manufacturing sectors. With stringent compliance requirements and specific process integration points, industries utilize this ketone in targeted ways to manufacture high-value end products. Below we outline validated downstream scenarios, focusing on the technical implementation details and compliance framework relevant to each use case.

    1. Pharmaceutical Key Intermediate for CNS Active Compounds

    Pharmaceutical manufacturers select this raw material as a specialized intermediate for constructing advanced central nervous system (CNS) active scaffolds. The compound’s indanone structure offers regiospecific fluorine substitution, enabling downstream synthesis of select psychoactive pharmacophores through precise ring functionalization and alkylation steps in API development pipelines. Process chemists dose in carefully calculated ratios, with strict analytical surveillance to comply with global drug master file (DMF) protocols.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, Ph. Eur., JP—relevant monographs for impurity profiling of indanone derivatives
    • FDA Drug Master File (Type II) submission suitability
    • ECHA REACH registration of precursor substances

    Typical usage ratio

    • 3–8% by molar input in multi-step synthesis, adjusted based on desired yield and downstream purity targets; usually controlled within ±1% range in GMP plants

    Downstream process integration

    • Charged in the early condensation or cyclization steps as starting scaffold, directly subjected to organometallic transformations (e.g., Grignard, Suzuki coupling) to elaborate CNS-active molecules

    Final product types

    • Nootropic therapeutics APIs
    • Anti-parkinsonian drug intermediates
    • Novel antidepressant research compounds

    2. Agrochemical Fine Chemical Synthesis Intermediate

    Agrochemical formulators use this building block in the multi-step production of fluorinated heterocyclic actives, vital for selective herbicide and pesticide synthesis. The unique substitution pattern enhances both lipophilicity and metabolic resistance in target molecules, supporting the creation of next-generation products intended for regulated global markets. Production runs require documentation for trace impurity removal and full batch traceability.

    Industry compliance standards

    • OECD Minimum Requirements for Industrial Chemicals
    • FAO/WHO Specifications for Pesticide Technical Materials
    • EU Regulation 1107/2009 for Plant Protection Products
    • ISO 17025-accredited analytical release testing

    Typical usage ratio

    • 5–12% w/w in active ingredient precursor synthesis, variation tied to the specific halogen exchange or ring-closure efficiency required for targeted pesticide class

    Downstream process integration

    • Fed into fluorination or alkylation sequences preceding final heterocycle assembly, often as a core skeleton for production of triazole or indanone-based actives

    Final product types

    • Precursor for selective herbicides
    • Base intermediate for systemic insecticides
    • Fluorinated plant growth regulator building blocks

    3. Advanced Materials Synthesis for Organic Electronic Components

    Producers of organic electronic materials introduce this indanone derivative during the manufacture of fluorinated organic semiconductors. The electron-withdrawing fluorine facilitates controlled energy band engineering and enhances stability under UV and oxidative environments, important for advanced OLED and organic PV applications. Manufacturing strictly limits batch variance using in-process HPLC and NMR verification.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) and amendments
    • IPC-4101D: Qualification and performance of base materials for printed boards
    • ISO 9001:2015-certified electronic component manufacturing
    • REACH compliance for candidate list substances

    Typical usage ratio

    • 1–3% w/w in functional monomer or oligomer feedstock, proportional to desired charge carrier mobility and thermal stability requirements

    Downstream process integration

    • Mixed in early-stage oligomer synthesis, often undergoing subsequent Suzuki, Stille, or Heck polymerization to generate conductive or emissive layers

    Final product types

    • Organic light-emitting diodes (OLED) emissive layer intermediates
    • Organic photovoltaic cell absorber components
    • Thin-film transistor channel materials

    4. Specialty Fragrance & Aroma Synthesis Ingredient

    Fine chemical firms in the aroma industry utilize this compound as a precursor for rare indanone fragrances, valued for their persistent woody and musk notes. Its methyl and fluorine modifications allow distinctive odor profiles through oxidation and reduction cascades in proprietary synthesis routes, meeting international safety requirements for use in fragrances or aroma formulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • REACH Annex XVII for restricted fragrance substances
    • ISO 9235:2013 (“Aromatic natural raw materials — Vocabulary”)
    • Food Chemicals Codex, if targeted for flavor additive use

    Typical usage ratio

    • 0.5–2% w/w in reaction batch, dosage selected for yield optimization in target aroma precursor, with residual solvent limits closely monitored

    Downstream process integration

    • Inserted during lactonization or selective reduction to create alcohols or esters, used as intermediates for blending in complex fragrance compositions

    Final product types

    • Rare musk or woody base notes for perfume
    • Fine fragrance ingredient synthons
    • Aroma compounds for luxury personal care

    5. Custom Research Chemical Synthesis for Academic and Industrial R&D

    Contract research organizations and innovation labs use this specialty ketone as a starting material for molecular scaffold construction and mechanism-of-action exploration. The compound’s unique structure supports the formation of libraries of fluorinated indanone analogues, critical for SAR (structure–activity relationship) investigations across drug, material, and photonic research fields.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for non-clinical safety studies
    • ISO/IEC 17025 for analytical and research laboratories
    • OECD Test Guidelines for the Testing of Chemicals
    • Institutional review and chemical hazard communication protocols (GHS/CLP)

    Typical usage ratio

    • Variable: usually 1–10 mmol scale in library synthesis protocols, depending on the number of derivatives targeted and yield optimization requirements

    Downstream process integration

    • Employed in scaffold diversification libraries through late-stage fluorination, condensation, or asymmetric synthesis for research-scale preparation of analogues

    Final product types

    • Screening compounds for drug discovery
    • Probe molecules for mechanism studies
    • Specialty analytical standards for custom assays
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    Certification & Compliance
    More Introduction

    Understanding 5-Fluoro-2-Methylindan-1-One: A Deeper Look at a Unique Building Block

    Real-World Experience with 5-Fluoro-2-Methylindan-1-One

    In the chemical industry, innovation doesn’t slow down. Every new intermediate brings its own story. 5-Fluoro-2-Methylindan-1-One speaks for itself in the lab with its specific features. In the hands of process developers and synthetic chemists, it has become a reliable backbone for further modified indanone derivatives. Through years of production experience, we have witnessed researchers favoring this compound for its balance of reactivity and stability.

    At our plant, the process starts with a careful selection of fluoro and methyl sources. Our chemists scrutinize every batch because 5-Fluoro-2-Methylindan-1-One shows variability not just in yield but in minute traces of byproducts if even one variable drifts. The production must run controlled from the first step—adding the methyl group to the indanone scaffold to carefully introducing fluorine at the ortho position. Temperature racks up during methyl introduction, and timing matters for the fluorination. Small tweaks influence purity more than expected, so the recipe stays tight to scientific benchmarks.

    We developed solvent systems that avoid halogen scrambling, a common headache with similar indanones, and regularly invest in improved crystallization techniques to keep batches reproducible. The quality separates itself from run-of-the-mill indanones with erratic melting points and irregular grain. Our analysts patrol for any sign of residual reagents and can spot even tenths of a percent impurity by NMR and HPLC. The benchmark for 5-Fluoro-2-Methylindan-1-One is not just “high purity” anymore; today we target and regularly reach levels matching the standards expected in project-critical pharmaceutical synthesis.

    Why Structure Matters: The Role of 5-Fluoro-2-Methylindan-1-One in Synthesis

    Our customers come from pharmaceutical labs and specialty chemical makers searching for structurally advanced intermediates. 5-Fluoro-2-Methylindan-1-One steps forward with two major groups on the indanone skeleton—one methyl, one fluorine—both carefully positioned. This 2-methyl, 5-fluoro pattern cannot be easily substituted by just any indanone. In medicinal chemistry screens, the strategic placement enables distinct physiochemical shifts. The methyl group on the ring delivers electron-donating influence, and the fluorine brings its notorious electron-withdrawing signature, impacting metabolism rates and receptor binding for downstream targets.

    Our tech team encountered several project groups aiming to push older indanones toward better receptor selectivity. With 5-Fluoro-2-Methylindan-1-One, the results tended to shift binding profiles, allowing for tailored metabolic stabilities in new lead compounds. Fluorine makes all the difference—even a single atom alters solubility and oxidation resistance on clinical candidates in pre-formulation. The methyl group further boosts the molecule’s rigid character, preventing unwanted rotational isomerism and allowing tight SAR (structure–activity relationship) mapping. This balance is difficult to mimic with either 2-methyl indanone or 5-fluoro indanone alone.

    Comparisons: Not Just Another Indanone

    Anyone familiar with indanone derivatives knows that substituents can turn a simple compound into a powerhouse or a headache. Take 2-methylindan-1-one: it handles well in basic condensation reactions, but misses out on the beneficial shift in polarity seen with a fluorine atom at the 5-position. On the flip side, 5-fluoroindan-1-one can improve electron dynamics, but lacks the methyl-triggered stability that supports harsher transformations. Our daily practice shows that combining methyl and fluoro on the indanone core reduces side product formation, especially during late-stage alkylation or arylation.

    Several production teams that rely on 2-methylindan-1-one for scale-up processes report limitations during halogenation steps—often overreacting or degrading under strong nucleophilic conditions. Adding a pre-installed fluorine at the 5-position, as in 5-Fluoro-2-Methylindan-1-One, cuts these risks. In our facility, replacing legacy intermediates with this product halved cycle times for high-throughput parallel synthesis. Final products appeared cleaner without hours of extra chromatography.

    Working with 5-Fluoro-2-Methylindan-1-One in the Plant

    From a manufacturing perspective, we learned early that 5-Fluoro-2-Methylindan-1-One comes with specific requirements. The raw material selection, solvent control, and process timing affect every lot, and not every supplier delivers on consistency. We go through rigorous incoming inspections, NMR and IR fingerprinting, and repeated micro-crystallization tests before committing feedstocks into a cycle.

    Handling 5-Fluoro-2-Methylindan-1-One on the shop floor demands respect for its dustiness and risk when elevated temperatures enter the picture. The team works with closed systems and high-efficiency extraction, following both safety and efficiency protocols. It’s a step above the procedures reserved for undistinguished indanones. Product recovery relies on solvent stripping followed by vacuum drying, which locks in the product’s desired polymorph and stable yellow color.

    On the scale-up line, the chemists rely on analytical QC in real time. Any off-odor or discoloration could indicate phenolic breakdown or side-chain scission. In our continuous improvement program, we regularly tweak process points—monitoring not only purity but also product morphology, which impacts downstream filtering and blending. This goes well beyond typical GMP standards: every gram is scrutinized for trace impurities, which can cause headaches in late-phase medicinal chemistry programs.

    Performance in Analytical Testing

    Purity comes first to most of our buyers. Our 5-Fluoro-2-Methylindan-1-One routinely reaches HPLC levels above 99%. NMR integrations check out cleanly for every batch. Unlike some competing products, we run full spectrum analysis, including low-level GC-MS screening for trace halide isomers and solvent residues. Over time, our team found patterns in impurity profiles unique to the fluoro-methyl combination—certain halogenated byproducts and unreacted intermediates show up at levels below a part per thousand if the fluorination energy isn’t controlled precisely.

    Thanks to tighter control, we avoid the pitfalls reported with commodity indanone varieties, like drifting melting points and inconsistent powder handling. The product’s solid-state packing stays consistent, which simplifies storage and transport. We never get calls about bridging, caking, or unexplained color darkening—a common theme from users of generic indanones. Stability on the shelf lasts more than 24 months in controlled containers, and the crystals resist photodegradation under standard lab conditions.

    Adapting Production for Industry Needs

    Industry moves fast, and the last five years put pressure on everyone to deliver smarter, faster, and with fewer impurities. Some pharmaceutical clients send specific requests—whether it’s micronization for fine blending or DMF compatibility checks. Our QA/technical staff work alongside them, sharing batch-level chromatograms and sometimes running cooperative pilot batches in their equipment before final shipment. From this direct feedback loop, we adopted several improvements, such as streamlined washing protocols to shave solvent retention by a half percent and filtering at custom mesh grades. Clients who scale up to multi-kilo runs find better performance in downstream extractions and purification, saving their own time and solvents.

    We noticed, starting about four years ago, an uptick in demand from specialty electronics and materials labs. The unique fluoro group at the 5-position proved vital in tuning dielectric properties for researchers developing new polymers and resins. The methyl group, meanwhile, reduced unwanted side reactions during high-temperature processing, compared with base indanones that tend to oxidize or fragment. These practical lessons drove us to invest in application trials before releasing each new batch, collecting performance data and tweaking upstream synthesis for optimal downstream value.

    What Makes 5-Fluoro-2-Methylindan-1-One Stand Out?

    Real product value comes out in the hands of the end users. In pharmaceutical R&D, speed and reliability drive everything. A recent project partner in Europe clocked faster synthesis cycles and better yields in a lead optimization run—a 15% improvement over previous cycles using more basic indanones. Teams trying to dial in a molecule’s logP or binding affinity convince themselves quickly of the importance of properly substituted indanone intermediates. The product reads like a modular piece ready to accept a wide range of transformations, from Suzuki-Miyaura coupling to organometallic alkylation, without risk of unexpected rearrangement.

    The combination of methyl and fluoro substitutions allows for a tailored approach in late-stage functionalization. Too many intermediates on the market force medicinal chemists to add halogens or methyls at great effort, risking overreaction or order-of-addition headaches. We see researchers grateful to have a pre-made indanone where the toughest steps are already handled, letting them invest more time in discovery than in basic synthesis.

    Sustainability Considerations in Manufacturing

    Today, sustainability is more than a buzzword, and our shop floor discussions often focus on waste minimization and process yield. 5-Fluoro-2-Methylindan-1-One requires reagents that must be handled with respect—especially during fluorination. We have spent years refining waste capture and run solvent recovery stations at every synthesis step, minimizing our contribution to perfluorinated emissions. By tightening reagent handling and investing in analytical byproduct tracking, we’ve lowered hazardous waste per batch to less than 3% of gross output.

    Production-grade 5-Fluoro-2-Methylindan-1-One leaves our site with a batch record often twice as detailed as for simpler analogs. Our customers find comfort knowing every lot comes documented with full synthetic traceability, from raw material in-take to the recycled solvents used. We owe much of our improved carbon footprint to process modifications learned through long-term partnerships with industry clients who share their own process metrics.

    Safety and Regulatory Experience

    Many users ask about safe handling across research and pilot lines. Our production sites log zero safety incidents involving 5-Fluoro-2-Methylindan-1-One in five years, thanks to strict air quality monitoring and PPE compliance. As a specialty intermediate, it falls under advanced QA scrutiny—requiring not only purity but traceability of every batch. Regulatory audits emphasize the control of halogenated byproduct content; we keep full data ready to support customer filings from lab projects to IND applications.

    The product rarely runs afoul of existing regional restrictions but comes with the in-depth paperwork, trace heavy-metal content confirmations, and impurity mapping that the pharmaceutical and electronics sectors appreciate. Our technical documentation team supports client regulatory submissions with data and experience drawn from actual plant runs—not just textbook references, but real-world lessons on response to process upsets or raw material switches.

    Logistics and Customer-Centric Strategies

    Shipping indanone derivatives across borders brings challenges—customs checks on halogenated compounds grow stricter each year. Our logistics division learned through tough lessons that every container must be packed for temperature swings, moisture ingress, and vibration. We moved to thicker, static-resistant liners for long-haul shipments and trace every route through batch-level affidavits. Not every manufacturer can claim on-time, uncompromised delivery; that’s why our customers—from small biotech teams to global material science labs—trust our documentation and dedicated cold-chain processes.

    Direct technical support matters as much as the package. Every year, our staff fields technical calls covering process compatibility, spectral verification, and run-specific yield improvement. We encourage direct plant visits so customer chemists can see firsthand the controls in place, supporting trust in every delivered kilogram.

    Continuous Learning and Innovation

    Chemical manufacturing doesn’t stand still, and neither does the science behind 5-Fluoro-2-Methylindan-1-One. We keep lines open with academic partners driving the next wave of functionalized indanones. Recent collaboration with a university in Asia led to new data on how different crystallization rates affect product solubility in organic formulations, leading us to adjust our drying and sieving processes. Every tweak in the plant comes with hard-won results—sometimes shaving only a fraction off the impurity profile, but every improvement counts in client hands.

    We invest in new plant automation so every part of the process can be monitored in real time. The experience we gained from years on the floor means we can spot a bad run before an impurity ever hits the chromatograph. Continuous dialogue between production, QA, and R&D ensures 5-Fluoro-2-Methylindan-1-One doesn’t just meet standards at one time, but advances them year after year.

    Looking Ahead

    Clients chase the next breakthrough; as producers, our job is to remove pain points. The world of indanone chemistry keeps evolving, and the two-fold substituent strategy—methyl and fluoro—shows up more in custom molecules chasing everything from neurological targets to advanced materials. 5-Fluoro-2-Methylindan-1-One has set new expectations for what a simple intermediate should offer, not only to specialists but to anyone serious about quality, consistency, and downstream reliability.

    Every batch of 5-Fluoro-2-Methylindan-1-One reflects our commitment to experience-led manufacturing. It is not just about what’s in the drum or the bag—it’s about making each subsequent transformation smoother for the chemists who rely on it. As chemistry keeps discovering new ground, we stand with our customers, ensuring that each molecule offers a solid starting point for the next idea.