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4,6-Difluoro-1-Indanone

    • Product Name 4,6-Difluoro-1-Indanone
    • Alias 4,6-Difluoro-2,3-dihydro-1H-inden-1-one
    • Einecs 643-021-3
    • 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

    292943

    Productname 4,6-Difluoro-1-Indanone
    Casnumber 885273-72-9
    Molecularformula C9H6F2O
    Molecularweight 168.14
    Appearance White to off-white powder
    Meltingpoint 67-70 °C
    Purity Typically ≥98%
    Smiles O=C1CCc2c1ccc(c2F)F
    Inchi InChI=1S/C9H6F2O/c10-6-1-2-7-4-5-8(12)3-9(7)11/h1-2H,3-5H2
    Synonyms 4,6-Difluoroindan-1-one
    Storagetemperature Store at 2-8 °C
    Solubility Soluble in organic solvents

    As an accredited 4,6-Difluoro-1-Indanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with secure cap, safety label, and hazard symbols; contains 5 grams of 4,6-Difluoro-1-Indanone powder.
    Shipping **4,6-Difluoro-1-Indanone** is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with chemical safety regulations, using UN-certified bottles placed in cushioned secondary containment. Shipping is done via licensed carriers, labeled with hazard information, and accompanied by a Safety Data Sheet (SDS) to ensure safe handling and compliance.
    Storage 4,6-Difluoro-1-Indanone should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong acids, bases, and oxidizers. Keep the container tightly closed and protected from direct sunlight and moisture. Store at room temperature, and ensure proper labeling and secure containment to prevent leaks or spills. Follow all relevant safety guidelines and regulations.
    Application of 4,6-Difluoro-1-Indanone

    Applications of 4,6-Difluoro-1-Indanone in Industrial Manufacturing

    As a manufacturer specializing in 4,6-Difluoro-1-Indanone, we provide high-purity material for established downstream sectors. Our production supports critical intermediates in the synthesis of advanced pharmaceuticals, agrochemicals, electronic chemicals, and specialty materials. Below, we outline main application fields with compliance details, typical formulation ranges, integration steps, and final product examples.

    1. Pharmaceutical API Synthesis—Fluorinated Drug Intermediates

    4,6-Difluoro-1-Indanone serves as a building block in the synthesis of fluorine-containing heterocycles for small molecule APIs targeting central nervous system and oncology indications. Leading drug makers incorporate it in multi-step syntheses to enhance metabolic stability and binding affinity of their candidate molecules, especially in kinase inhibitor development pipelines. Strict documentation controls traceability throughout QC and GMP operations to meet the regulatory threshold for impurity levels in pharmaceutical manufacturing.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210 and 211 (US FDA)
    • Ph. Eur. Monographs on related substances and solvents
    • EDQM and US Pharmacopeia ingredient documentation guidelines

    Typical usage ratio

    • 5–15% molar basis in the intermediate fragment condensation step; adjustment based on target compound scaffold and process yield requirements

    Downstream process integration

    • Introduced in Grignard, Suzuki, or Buchwald amination reactions during advanced intermediate synthesis
    • Isolated by crystallization or distillation prior to downstream deprotection or alkylation stages

    Final product types

    • Kinase inhibitors for clinical trials
    • Fluorinated CNS active pharmaceutical ingredients
    • Patent-protected investigational new drug molecules

    2. Agrochemical Intermediate for Controlled-Release Herbicides

    Industrial formulators use 4,6-Difluoro-1-Indanone during the synthesis of novel herbicidal actives that require stable aromatic fluorination. It functions as a reactant in cyclization and further alkylation processes, conferring environment-resistant properties to the molecule. Stringent compliance with agrochemical registration and safety evaluation protocols is maintained throughout the material lifecycle, from inbound QC to final packaging and submission batches.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO Quality Control Standard for Pesticide Ingredients
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • ISO 17025 for test laboratory accreditation

    Typical usage ratio

    • 8–12 wt% in the formation of the herbicidal core, with adjustments depending on the required target load and downstream substitution extent

    Downstream process integration

    • Added to batch reactors for nucleophilic substitution or cyclization, often with chlorinated co-monomers
    • Product purified prior to microencapsulation or controlled-release formulation steps

    Final product types

    • Fluorinated pre-emergence herbicides
    • Active ingredients for slow-release weed control granules
    • Selectivity-enhanced cereal crop protection agents

    3. Organic Electronics—Functionalized Building Blocks for OLED Materials

    Chemical manufacturers leverage 4,6-Difluoro-1-Indanone to introduce electron-withdrawing fluorine atoms in the synthesis of conjugated small molecules and polymers used in OLED emitter layers. Its controlled reactivity allows formation of high-purity n-type acceptor materials, essential for the charge balance and lifetime of commercial luminescent displays. Rigorous adherence to electronic grade raw material specifications ensures suitability for microelectronic assembly environments.

    Industry compliance standards

    • IPC-4101B specification for base materials in electronic assemblies
    • REACH Annex XVII (EU hazardous substance limits)
    • RoHS Directive 2011/65/EU
    • SEMI C3 standards for chemical purity

    Typical usage ratio

    • 3–10% by mass, calculated relative to total organic semiconducting input; customized per formulation for emission wavelength tuning

    Downstream process integration

    • Reacted under anhydrous conditions during Suzuki coupling or Friedel–Crafts acylation for oligomer or polymer backbone modification
    • Intermediate products further processed into spin-coatable solutions or vapor deposition precursors

    Final product types

    • OLED blue and green emitter molecules
    • Electron transport materials for flat-panel displays
    • Thin film transistor (TFT) component materials

    4. Specialty Fine Chemicals—Raw Material for Advanced Photoinitiators

    4,6-Difluoro-1-Indanone acts as a critical precursor for synthesizing organofluorine photoinitiators enabling low-energy UV curing in high-resolution coatings and 3D printing resins. Its double-fluorinated aromatic ring enhances photoreactivity and stability under intense light sources, supporting product formulations that must comply with strict standards for polymerization speed, migration limits, and residual solvent levels.

    Industry compliance standards

    • GMP for specialty chemicals (ISO 9001:2015 certified lines)
    • EN 14627 for photoinitiator migration in food packaging inks
    • SWISS Ordinance on Materials and Articles in Contact with Food
    • JEDEC purity and contamination control for microelectronics

    Typical usage ratio

    • 6–18% in custom blending for photoinitiator formulations, set according to polymerization wavelength and curing depth target

    Downstream process integration

    • Enters the formulation during the diketone condensation stage, prior to blending with co-initiators and UV stabilizers
    • Final initiator purified and directly incorporated in liquid resin or ink concentrate

    Final product types

    • Low-migration UV-curable printing inks
    • Photocurable 3D printing resin systems
    • Specialty coatings for high-definition electronic circuits

    5. Chemical Research—Synthesis Scaffold for Fluorinated Reference Compounds

    Leading chemical research institutes and commercial catalog suppliers use 4,6-Difluoro-1-Indanone as a core scaffold in the creation of custom fluorinated aromatic standards and labeled isotopologues. It provides stable ^19F and ^13C tracer positions, essential for quantitation in NMR and MS-based analytical method development. Batch documentation and handling align with research chemical quality standards, including strict cross-contamination prevention and chain-of-custody.

    Industry compliance standards

    • ISO 17034:2016 for reference material producers
    • GLP protocols for chemical synthesis traceability
    • Material safety compliance under GHS/CLP regulations
    • NIST and ERM reference material requirements

    Typical usage ratio

    • Variable, typically 1–5 mmol per synthesis run; exact quantity set according to desired molecular scale and labeling ratio

    Downstream process integration

    • Condensation, halogen exchange, or reductive amination with labeled reactants during analytical standard preparation
    • Purification by column chromatography prior to calibration curve verification and distribution

    Final product types

    • Fluorinated NMR standards
    • Stable isotope-labeled internal standards for mass spectrometry assays
    • Analytical control samples for regulatory laboratory testing
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    Certification & Compliance
    More Introduction

    4,6-Difluoro-1-Indanone: Practical Insights from the Manufacturer’s Perspective

    Understanding 4,6-Difluoro-1-Indanone

    As a chemical manufacturer, we find 4,6-Difluoro-1-Indanone to be an unusual but rewarding compound to produce. This molecule, known for its two fluorine atoms strategically located on the aromatic ring of the indanone core, offers more than a tweak in structure compared to its non-fluorinated relatives. The presence of fluorine changes how the product behaves not only in the lab but also down the line in finished APIs and specialty materials.

    The structure of 4,6-Difluoro-1-Indanone, which most chemists will recognize as 4,6-difluoro-2,3-dihydro-1H-inden-1-one, features a bicyclic backbone fused from a benzene ring and a cyclopentanone. Through years of production, we've learned that even substitutions at seemingly less dramatic positions—like the 4 and 6 fluorines—transform its reactivity and end-use potential. Fluorine’s small size and extreme electronegativity account for much of that shift. Batch after batch, the purity matters, because downstream reactions react sensitively to even trace contaminants or small byproduct peaks.

    Approaching Manufacturing and Purity

    From behind the reactor walls, controlling exotherms and moisture still play a more practical role than theoretical chemistry suggests. Producing high-purity 4,6-Difluoro-1-Indanone means getting the fluorination step clean, running the condensation with a steady hand, and finishing with a resilience to the small but persistent challenges that come with a fluorinated intermediate. Some manufacturers struggle with corrosive HF or with the selectivity of direct fluorination. We’ve leaned on a selective halogen exchange and old-fashioned patience, choosing routes that dodge difficult waste streams while yielding a consistent fluorination at the desired positions.

    Customers ask about our product’s USP and chemical specification figures every month. In practice, purity over 98% measured by GC is what most advanced applications demand. Crude batches with less than 95% purity may look similar but behave very differently, whether in pharmaceutical development or materials synthesis. Trace byproducts stemming from incomplete fluorination or starting material residues can cripple scale-up. We set our specs to keep those down in the low impurity range, recognizing that a few parts per hundred get amplified downstream.

    How Our Product Gets Used

    Conversations with R&D groups reveal where 4,6-Difluoro-1-Indanone has proven itself. This isn’t a commodity sold in drums across continents but rather a building block, culminating in progress at the molecular level. Medicinal chemists pick it up to build fluorinated indane-based scaffolds, exploring improved bioavailability or metabolic resistance. Fluorinated indanones make their way into kinase inhibitor development, often as central moieties. Some groups report enhanced CNS penetration for certain classes of drug candidates, pointing directly to the effect of fluorine at these sites.

    Beyond the medical pipeline, our technical customers experiment with this indanone in OLED precursors and specialty polymer backbones. Working directly with materials scientists, we’ve had hands-on exposure to their need for batch-to-batch consistency. While their target molecules often go through several synthesis steps, every link depends on reliable monomer supply. The bond-donating character of fluorine has become key in modulating electron transport within these specialty frameworks.

    Without regulatory barriers standing in the way of its sale, our 4,6-Difluoro-1-Indanone moves more quickly to pilot and production scale. No schedule controls and a clear hazard profile speed up procurement, but the specialized handling of fluorinated organics remains crucial. We ship it in glass bottles with PTFE caps, not metal, after seeing too many small batch corrosion issues in transit.

    What Makes This Compound Different?

    It’s tempting to see 4,6-Difluoro-1-Indanone as an analog of simpler indanones or even 2,3-difluoro-1-indanone, but practical tests dismiss that comparison. Fluorination pattern changes both electronic effect and crystal habit. Direct feedback from formulation chemists taught us that the 4,6-fluoro variant brings unique solubility and reactivity shifts. Compared with monofluorinated indanones, you notice sharper melting points and less volatility—a real benefit during scale-up, since volatility often causes headaches for both yield and containment.

    Historically, non-fluorinated 1-indanone found a home in fragrances and bulk fine chemicals, typically outside the pharmaceutical sphere. Adding fluorines at 4 and 6 goes beyond the moderate changes found with halogenation: the ring system becomes more robust under oxidative and thermal conditions. This helps researchers who need high-yield coupling in late-stage syntheses. In multiple collaborations, drug hunters have returned to say a single swap from 1-indanone or 4-fluoro-1-indanone to the 4,6-difluoro version prevented product degradation during downstream functionalization.

    As a manufacturer, we also see the changes at the shelf-life level. Unsubstituted indanones yellow or decompose faster in open air, but the difluoro product resists many of these aging processes. That residue and discoloration issue on stored samples tells a story that’s easy to overlook from purely analytic purity reporting. While others may downplay visible storage effects, we get the phone calls about false positives and sticky residues on benchtops. Choosing the right grade, keeping water rigorously excluded, and watching containers for leaching or interaction are our practical solutions.

    Managing Safety and Handling on the Production Floor

    Producing and packing 4,6-Difluoro-1-Indanone brings a very practical set of safety considerations. Many of our relatively young operators expect fluorinated compounds to behave just like their non-halogenated kin. Reality proves different. We make sure that our operators know about the specific reactivity of this molecule with strong bases and nucleophiles, as well as its volatility over time. Precaution means running all steps in closed systems, checking glove integrity, and never skipping fume hood work, even for seemingly benign preps.

    Thermal behavior also differs from similar molecules. The difluoro indanone resists ignition, but puts out fumes that demand good room air turnover during even small spills or transfers. In the early years, lax protocols led to one or two exposure incidents—minor, but enough to keep us on policy for double containment during both charging and decanting. Tetrafluoroboric acid and similar byproducts show up if upstream control isn’t sharp, so we test lots not just for purity, but for process-specific residues.

    As a hands-on manufacturer, we don’t confuse the needs of analytical chemists with those of scale-up engineers. The latter report recurring caking and clogging issues when moisture gets into the product. Handling lots in humidity-controlled rooms has reduced batch rejection rates by about 10%. We don’t advertise this as a feature, but each improvement saves real waste and headaches at the kilo scale. This attention to detail forms much of what our returning customers value.

    Technical Challenges and Continuous Improvement

    Producing a tight specification for 4,6-Difluoro-1-Indanone means more than just targeting a number on a COA. The quality variability in global offerings shows up starkly in chromatograms, both here and at customer sites. We regularly receive feedback about prior disappointments with “off-the-shelf” supply from non-specialist traders. High molecular purity alone doesn’t guarantee user satisfaction. False peaks, tars, and traces of hydrolyzed acid forms can show up even from stable-looking samples.

    Our process team revisits isolation and drying steps each quarter. Simple tweaks, like switching to argon backfilling instead of nitrogen, or adding a dedicated filtration skid, have trimmed loss rates. More than half the complaints we used to receive centered on batches smelling "wrong" or turning brown over a few months in storage. Roll up your sleeves and test small modifications—outcomes in product color and shelf-stability speak louder than running standard number reports.

    Reinvesting in analytical methods has paid dividends too. Our in-house LC/MS and NMR profiling lets us see hidden impurities and double-check that each lot really matches structural expectations. We test not only finished product but critical intermediates, and never rely on vendor-claimed purities alone for outsourced raw materials. Any batch not matching our target spectra gets held back, period.

    Handling packaging for global shipment taught us the hard way that some plastic liners leach unwanted plasticizers into the product. Moving to certified PTFE liners eliminated outgassing issues and improved product freshness on arrival. It’s tempting to look for cost savings here, but this is one area where buyer feedback and returns history urge us to invest, not skimp. In the end, chemical consistency comes from process control and real-world learning, not paperwork alone.

    Trends, Regulatory Landscape, and Market Insights

    Interest in 4,6-Difluoro-1-Indanone has grown steadily with the surge of fluorinated pharmaceuticals and the rapid pace of specialty electronics research. Governmental and industry focus on greener, more sustainable chemistry puts pressure on all sides to minimize hazardous waste streams. We view this challenge as both necessity and opportunity. Limiting halogenated byproducts during synthesis, recapturing solvents efficiently, and sending out product with clean hazardous declarations keep our process up to today’s expectations.

    Customers often ask about REACH and TSCA status before moving to bulk orders. As a product that does not trigger the most severe regulatory measures, it fits into ongoing discovery projects with fewer paperwork delays. That said, each new geography brings its own packaging, labeling, and safety-training requirements. Our team keeps up by cross-checking lot tracking, batch-specific labeling, and regional labeling laws, giving everyone on the supply chain confidence that product details meet or exceed what’s mandated.

    From the manufacturing floor, the biggest near-term bottleneck remains reliable raw material sourcing, especially for the precursor aromatics. We keep buffer stocks to minimize disruptions from supply chain hiccups. Unlike high-volume basic chemicals, small changes in the indanone market ripple quickly to end-users developing new IP. Open communication with customers saves time and reduces the number of “fire-drill” deliveries or compromised batches. Most have told us they value regular status updates over blanket guarantees, so that’s been our answer.

    The Human Side: What We've Learned by Listening

    Having spent years interacting with end-users and development chemists, we've gotten a sense of the genuine problems faced outside the conference room. R&D teams want reliable, clean, and straightforward material—every deviation from the norm ends up costing them precious time. We now host yearly feedback calls, not just relying on forms or survey responses, but speaking person-to-person about issues that don’t get captured in specification sheets. Several improvements, like switching to heavier-duty bottles or retooling our drying train, have come directly out of these conversations.

    Manufacturing this product has taught us the difference between “good enough” and “failure proof.” Good enough might get a one-time order; failure proof earns repeat business from scientists trying to solve bigger scientific problems. Tolerance for failure at the bench drops sharply as projects near regulatory submissions or pilot batch deadlines. Our role isn’t to oversell the product but to make sure nobody gets tripped up by overlooked trace impurities, off-odors, or mishandled storage.

    Moving Forward: Manufacturer’s Perspective on Solutions

    Practical production of 4,6-Difluoro-1-Indanone keeps teaching us humility and demands for continuous improvement. Scalability and reproducibility will always come before chasing short-term cost targets. In the future, we see our efforts turning to lower-waste synthesis platforms and more efficient recycling of byproducts—a necessity not only for operational cost but for the satisfaction of customers increasingly held to tighter environmental and safety regulations.

    Automation has cut error rates in the packing and labeling end of our workflow, but human attention makes the difference with this product. Eyes on every decanting operation, hands checking for trace water or off-odors, and routine batch note reviews are part of our solution to reliability. On the technical front, we are experimenting with new catalysts that cut down byproduct formation at the initial cyclization stage. Early trials point to a 20% decrease in waste with no obvious compromise in selectivity.

    Collaboration with both large and small customers remains key to practical innovation. Some of our most successful process improvements have come from custom requests by API project leads or specialty materials startups willing to share their data in exchange for better performing lots. We consider both technical feedback and narrative reports—batch log details, process notes, or even post-mortem problem summaries—just as vital as HPLC certificates. This flow of experience brings a reality check to the abstraction of molecular structure diagrams and academic yield tables.

    From our point of view on the manufacturing floor, the success of 4,6-Difluoro-1-Indanone is rooted in the details: how it’s made, how it’s tested, and how it’s used in the world’s labs. Every kilogram sent out reflects choices in synthesis, purification, and customer communication built up over years, not a solitary number on a purity report. Our direct line to problem solvers in labs and plants shapes not only our product, but the full cycle of innovation that depends on building blocks like this one.