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5-Hydroxy-1-Indanone

    • Product Name 5-Hydroxy-1-Indanone
    • Einecs 214-971-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    711282

    Chemical Name 5-Hydroxy-1-indanone
    Cas Number 491-36-1
    Molecular Formula C9H8O2
    Molecular Weight 148.16
    Appearance White to off-white solid
    Melting Point 121-125°C
    Boiling Point Unknown
    Density 1.269 g/cm3
    Solubility In Water Slightly soluble
    Smiles C1CC2=C(C1=O)C=C(C=C2)O

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

    Packing & Storage
    Packing The 5-Hydroxy-1-Indanone is supplied in a 25-gram amber glass bottle, sealed and labeled with product details and safety information.
    Shipping 5-Hydroxy-1-Indanone is shipped in tightly sealed containers, protected from light and moisture. It is classified as a chemical substance and should follow all applicable shipping regulations, including labeling and documentation requirements. Handle with care, ensuring compatibility with other materials, and store at controlled room temperature during transit.
    Storage 5-Hydroxy-1-Indanone should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from light and moisture to prevent degradation. Store at room temperature and avoid exposure to heat or direct sunlight. Proper labeling and handling procedures should be followed to ensure safety.
    Application of 5-Hydroxy-1-Indanone

    Applications of 5-Hydroxy-1-Indanone in Industrial Manufacturing

    As an established upstream producer, we provide 5-Hydroxy-1-Indanone meeting high-purity standards for specialized downstream manufacturing. This compound serves key roles in targeted fine chemical synthesis, pharmaceutical intermediate preparation, agrochemical production, pigment formulation, and specialized research-scale manufacturing. Below we outline real-world industrial scenarios, detailing compliance, usage ratios, integration points, and finished product types.

    1. Pharmaceutical Intermediate for Selective Serotonin Reuptake Inhibitors (SSRIs)

    Our plant-grade 5-Hydroxy-1-Indanone supports the synthesis of SSRI intermediates—particularly in multi-step reactions to obtain active pharmaceutical ingredients (APIs) such as sertraline and related indanone-based compounds. Downstream pharmaceutical agents rely on precise conversion and strict impurity profiles, demanding high-grade input for yields and safety.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) for intermediates
    • European Pharmacopeia (EP) guidance where applicable
    • FDA 21 CFR Part 211 (if exporting to US market)

    Typical usage ratio

    • 0.15–0.45 molar equivalents per reaction cycle depending on the targeted API yield and downstream step purity requirements

    Downstream process integration

    • Direct input to the first or second synthetic step for indanone core functionalization
    • Reacts via catalytic hydrogenation or halogenation to generate substituted intermediates
    • Material handling under clean-room or cGMP-controlled conditions

    Final product types

    • Pharmaceutical grade sertraline base
    • Secondary amine-containing antidepressant APIs
    • Regulated pharmaceutical intermediates for CNS drug synthesis

    2. Agrochemical Synthesis – Plant Growth Regulator Precursors

    Manufacturers in the agrochemical sector employ 5-Hydroxy-1-Indanone for the targeted synthesis of indanone-based plant growth regulators and herbicide intermediates. The controlled functional group allows for further transformation and coupling reactions in batch or semi-continuous processes. Downstream products must meet tight impurity tolerances for agricultural formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 laboratory testing compliance
    • REACH Registration (Europe) for allowed precursor chemicals
    • Local pesticide registration requirements (for country of final product use)

    Typical usage ratio

    • 10–25% by weight in the active synthesis step, adjusted according to targeted precursor chain length and conversion efficiency

    Downstream process integration

    • Reactant in oxidative coupling or Mannich-type synthesis for functionalized indanone frameworks
    • Entry step for side-chain modification in dedicated agrochemical reactors
    • Quality control by HPLC after each batch to monitor purgeable impurities

    Final product types

    • Indanone-derivative plant growth regulators
    • Precursor compounds for herbicides with selective crop activity
    • Intermediate bulk active for formulation in technical-grade agrochemicals

    3. Fine Chemical Manufacture – Dye and Pigment Precursors

    5-Hydroxy-1-Indanone serves the specialty colorant and pigment manufacturing industry as a precursor for indanone-based dye families. It offers controlled reactivity for subsequent condensation and alkylation methods, promoting stable colorant backbones for downstream organic pigments and specialty printing dyes. Manufacturers require tailored grade and batch testing for these sensitive syntheses.

    Industry compliance standards

    • ISO 9001 quality management for fine chemical production
    • REACH compliance for dye and pigment raw material registration
    • Transparency with downstream SDS compliance for shipment
    • Local safety and colorant purity standards (e.g., EN 71-3 for toy safety in Europe if applicable)

    Typical usage ratio

    • 5–18% by mass in core pigment synthesis, modulated according to final color depth and solubility requirements

    Downstream process integration

    • Reaction with aldehydes or amine derivatives in closed-vessel syntheses
    • Intermediate in Friedel-Crafts or Knoevenagel condensation processes
    • Downstream batch filtering and purification for colorant grade

    Final product types

    • Specialty printing inks
    • Indanone-based organic pigments
    • Colorant masterbatches for plastic processing

    4. Research and Development – Chemical Probe and Scaffold Synthesis

    Academic laboratories and industrial R&D groups source high-purity 5-Hydroxy-1-Indanone for the synthesis of chemical probes, molecular scaffolds, and tool compounds used to investigate biochemical pathways. The aromatic hydroxy function enables regioselective derivatization, supporting the construction of diverse indanone libraries for screening and early-stage drug discovery.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for regulated research applications
    • Institutional quality assurance for reagent tracing and purity
    • Toxicological approval as per local and institutional requirements
    • Material Transfer Agreement (MTA) stipulations for collaborative research

    Typical usage ratio

    • 0.1–1 mmol scale per reaction, often adjusted as per synthetic route and required structural analog screening batch size

    Downstream process integration

    • Initial scaffold input in library construction for new molecule discovery
    • Used in parallel synthesis and combinatorial chemistry workflows
    • Direct conjugation or protection group chemistry to generate probe toolkits

    Final product types

    • Chemical biology probe compounds
    • Molecular scaffolds for high-throughput screening
    • Unpublished tool molecules for research studies
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    Competitive 5-Hydroxy-1-Indanone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    5-Hydroxy-1-Indanone: A Key Intermediate from the Manufacturer’s Bench

    Introduction to 5-Hydroxy-1-Indanone

    Inside every drum, every bag, and every fresh batch of 5-Hydroxy-1-indanone we produce, there’s a story of chemical precision, experience, and real-world application. Over decades in the specialty chemicals market, we have worked with countless researchers and formulators who rely on this compound, often described by its CAS number 703-59-3, for its indispensable role in both small molecule pharmaceutical and agrochemical development.

    5-Hydroxy-1-indanone, also called indan-1-one-5-ol, carries the indanone nucleus with a hydroxyl group positioned at the 5-position. Chemists who work at the bench recognize the specific reactivity this placement brings, especially for downstream transformations like alkylations, condensations, and cyclizations. Out in the lab, this molecular motif is not rare by chance. Its synthetic flexibility and stability under a wide range of conditions keep it directly useful, whether you’re scaling up a kilogram batch or testing new building blocks in assay development.

    Product Model, Purity, and Physical Specifications

    Every production run starts with the same demands: consistent purity and reliable batch-to-batch performance. We provide 5-Hydroxy-1-indanone in crystalline form with a specification typical at ≥98% GC purity, though our analytical team keeps a close eye on each lot using a tight set of standards. Its appearance — pale yellow or off-white crystals — signals proper synthesis and controlled storage, since the tiniest impurity or moisture shifts color and stability even during short-term handling.

    Melting points stay tight, usually falling between 162°C and 167°C. This characteristic gives our partners quick physical validation and fits well with the compound’s handling profile during scale-up or formulation. Crystals dissolve in many common solvents: ethanol, acetone, DMSO, and methanol are often preferred for both small vial sample work and larger pilot projects. Chemists respect this property when designing protocols for downstream transformations or extractions.

    What Sets Our 5-Hydroxy-1-Indanone Apart

    Every experienced synthetic chemist will tell you that raw numbers on a certificate of analysis only tell part of the story. Customers who buy directly from our factory benefit from two things rarely seen in bulk reselling: full transparency on source and process, and the ability to tailor the production scheme to specific impurities.

    We have refined our oxidation and cyclization approach over the years, minimizing side-reactions that lead to off-product isomers. By selecting the right conditions — whether that means tuning the oxidant concentration, reaction temperatures, or using proprietary solvent systems — we ensure each kilo offers maximum yield of the target compound without accumulating by-products that complicate purification.

    Shelf stability matters as well. New users often ask about degradation or discoloration over time. Air-sensitive or hygroscopic compounds invite unexpected headaches. Our manufacturing controls focus on low residual water, tight packaging, and validated storage to preserve both appearance and chemical reactivity all the way from our site to your bench.

    Application Experience: Why 5-Hydroxy-1-Indanone Remains Essential

    Each week, we ship this compound to pharmaceutical R&D labs, fine chemical houses, and even university research groups. In the pharmaceutical sector, 5-Hydroxy-1-indanone frequently serves as a core building block for synthesizing heterocyclic derivatives and extends to custom compound libraries. The hydroxy group on the aromatic ring opens many doors for custom chemistry. It unlocks hydrogen-bonding sites in receptor studies, and provides an anchor point for O-alkylation or further functionalization — about as close to a “blank canvas” as a medicinal chemist gets in aromatic chemistry.

    Customers involved in agrochemical development come to us for the same reason. The indanone skeleton matches structural themes in a number of active crop protection agents. Whether they’re after new fungicides, insecticides, or herbicidal derivatives, the functionalization options that start with 5-Hydroxy-1-indanone speed up SAR studies, hit optimization, and lead candidate synthesis.

    We watch our product’s value in emerging sectors as well. In fine fragrance and flavor chemistry, certain indanone derivatives tie directly into essential oil motifs, and our manufacturing team has consulted with perfumers on batch-specific purities tied to olfactory thresholds. Research teams exploring new material science applications, such as organic electronic materials, have also turned to the indanone core, drawn by its rigidity, electron-rich ring, and tunable sites for further modification.

    Comparing to Other Indanone Derivatives

    It surprises many newcomers that even a single moved functional group — for example, shifting the hydroxy group away from the 5-position — often leads to thoroughly different reactivity and handling profiles. We often work with both 5-hydroxy and 6-hydroxy indanone variants, and the contrast extends far past paper specifications.

    5-Hydroxy-1-indanone tends to participate more predictably in electrophilic substitution and Mannich-type reactions than its isomeric cousins. The orientation influences resonance effects and alters interaction with catalysts or acids during secondary transformations. Users pursuing phenolic protection strategies or careful regioselective functionalization tend to experience more straightforward results with the 5-hydroxy variant — a fact supported by both academic literature and feedback from synthetic teams in the field.

    There are other “simple” indanone derivatives on the market, too. For example, unsubstituted 1-indanone offers fewer options for direct modification, while multi-substituted indanones might bring steric hindrance that limits their usefulness in certain coupling reactions. Some customers reach out to us after frustrated attempts using 4-hydroxy or 7-hydroxy analogues, coming to appreciate the balance between synthetic accessibility and downstream compatibility provided by the 5-hydroxy position.

    Manufacturing Insights: Navigating Batch Variability and Quality

    Few things frustrate chemists more than batch variability. From the manufacturer's side, we work to limit crystal polymorphism and trace contamination with each campaign. One lesson learned over the years: solvent residues not only affect product performance but can trip up automated weighing and dosing equipment in high-throughput settings.

    Large customers often make a site visit to review our QC approach. Our team regularly conducts cross-analyses for common organic solvent traces — ethanol, acetonitrile, even trace toluene — to limit interference in sensitive bioassay screens. We use validated HPLC and NMR methods, and ESI-MS for difficult impurity profiling. All this targets a simple goal: making sure the chemist who opens our bottle tomorrow experiences the same reactivity and product flow as the one who used it last year.

    Safety, Handling, and Storage Lessons from Practice

    Over time, feedback from partners has shaped how we ship, pack, and label this compound. 5-Hydroxy-1-indanone needs basic PPE — gloves, goggles, and a hood — during weighing and dissolving. Fine crystals should never float around a benchtop; minimizing static and avoiding open weighing in drafty conditions helps protect both product and people.

    Our QC data show that 5-Hydroxy-1-indanone stays stable under standard ambient conditions, but humidity has a subtle effect. We use moisture-tight polyethylene liners packed inside steel or HDPE drums for larger shipments, and recommendations always include keeping containers well-sealed. Sampling for multi-site use works best using short tongs or dedicated spatulas — even small cross-contamination between batches can influence results in sensitive applications.

    We’ve supported teams facing scale-up challenges, where melting and solidification cycles during bulk transfer created unexpected clumping. For those who need larger quantities, gentle warming in a dry oven (below 60°C) re-crystallizes material without degradation.

    Real-World Problem-Solving: Purification, Scale-Up, and Formulation Advice

    Chemists in the field often ask about purification or isolation tips to optimize yield and maintain high purity, especially in multi-gram to kilogram projects. Our experience supports selective recrystallization from mixed solvent systems — ethanol/water, acetone/hexane blends — as a way to enhance removal of colored or volatile organic impurities.

    Handling a batch destined for further derivatization? Flash chromatography can work when precise isolation of closely related analogs is needed, but for most applications, gentle filtration and a controlled temperature drying step suffice. Over-drying at high temperature sometimes leads to partial discoloration, so we coach to favor moderate vacuum drying as a safe solution.

    In pilot plant settings, we work closely with process engineers to streamline conversion steps. This means collaborating on solvent savings, catalyst choice, and even on downstream routing of waste streams. We recommend setting aside a reference aliquot for each large-scale run—later analytical checks help explain any unexpected results, making troubleshooting more effective for both QC and R&D teams.

    Regulatory and Supply Considerations: The View from Manufacturing

    Quality-driven customers watch not just purity but also regulatory traceability. We supply 5-Hydroxy-1-indanone that meets national and international transport regulations for non-hazardous organic intermediates, providing complete lot documentation and audit trails as required by both pharma and agrochemical partners.

    Supply chain interruptions happen—raw materials, solvent shortages, logistics blockages. Our facility keeps a buffer stock of key precursors and has established alternative sourcing agreements. Over time, we’ve learned to document alternate processing conditions, so customers get advance warning if any aspect of the synthesis route must change. Transparency remains central, and we are quick to provide retrospective batch analysis or stability data for regulatory filings.

    Supporting Researchers and Industry Partners

    Behind every batch, there is ongoing dialogue with formulation chemists, plant operators, process engineers, and senior scientists. A common request centers on detailed impurity data and reactivity notes—our lab team remains on call to provide technical backup, even for less common pathways or probe modifications.

    We share best practices from years of technical troubleshooting and scale-up support: sample the final powder or crystal for moisture content on arrival; If formulation into tablets or complex solid dispersions follows, pre-dispersion in a small solvent volume often improves wetting and subsequent mixing. We also recognize that every step counts when margins and yields drive economic decisions at commercial scale.

    Looking Ahead: Continuing Innovation in 5-Hydroxy-1-Indanone Production

    The research landscape keeps shifting, and we invest in both greener process development and analytical method improvement to keep up. Market feedback has prompted us to trial new catalysts for lower-temperature oxidations and to experiment with more sustainable solvent systems. Our R&D team continues to explore downstream valorization of process by-products, looking for cross-over applications in industrial and academic settings.

    As end-users chase ever tighter specs for regulated markets, we anticipate the need for even cleaner, more rigorously documented batches. We have begun cross-validating new analytical techniques, including advanced mass spectrometry and ultra-fast GC, to better characterize both the main compound and minor impurities. This effort goes hand-in-hand with real-world conversations — practical feedback from you, the users, guides our next steps.

    Conclusion: Putting Experience to Work

    Manufacturing 5-Hydroxy-1-indanone is more than a technical exercise—years of listening to chemists, testing new approaches in the pilot plant, and tracking product through real-world projects underline its value. By focusing on both the precise science and the diverse everyday needs of our customers, we keep this core intermediate reliable for the next round of discovery, production, or complex molecular synthesis. Our role is about more than supply; it’s about open collaboration and continual improvement, making sure what's inside every drum meets the standards and drives the breakthroughs that keep chemistry moving forward.