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2-Benzoyl-1,3-Indanedione

    • Product Name 2-Benzoyl-1,3-Indanedione
    • Alias BDI
    • Einecs 205-067-1
    • 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

    756786

    Cas Number 606-23-5
    Molecular Formula C15H10O3
    Molecular Weight 238.24 g/mol
    Appearance Yellow crystalline powder
    Melting Point 125-128 °C
    Boiling Point 468.1 °C at 760 mmHg
    Density 1.266 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms 2-Benzoylindan-1,3-dione

    As an accredited 2-Benzoyl-1,3-Indanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing **Description:** The 100g of 2-Benzoyl-1,3-Indanedione is packaged in an amber glass bottle with a white screw cap and safety labeling.
    Shipping 2-Benzoyl-1,3-Indanedione is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous chemical, following regulations for safe transport. Packaging ensures minimal environmental exposure, and shipping documents include safety data sheets. Temperature controls may be applied to prevent product degradation during transit.
    Storage 2-Benzoyl-1,3-Indanedione should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protect from light and moisture. Store at room temperature and ensure proper chemical labeling to prevent accidental misuse. Avoid prolonged exposure to air and humidity.
    Application of 2-Benzoyl-1,3-Indanedione

    Applications of 2-Benzoyl-1,3-Indanedione in Industrial Manufacturing

    As a direct manufacturer with deep expertise in diketone chemistry, we supply 2-Benzoyl-1,3-Indanedione to specialized industrial segments worldwide. The following application scenarios focus on mature, real-world downstream uses supported by verifiable process data, regulatory environments, and product specifications from leading market participants. Each section details precise integration practices, standard compliance, formulation ratios, and finished goods exclusive to each end-use market.

    1. Synthesis of Pharmaceutical Intermediates (Anticoagulant Precursors)

    Pharmaceutical manufacturers source 2-Benzoyl-1,3-Indanedione for use as a key intermediate in the synthesis of 1,3-indandione-derived anticoagulants. In dedicated API fermentation and synthesis lines, it serves as an acylating and condensation partner during the construction of active cores for drugs used in vascular and cardiac therapy. Formulation specialists closely adjust input ratios relative to batch process scale, maintaining purity parameters demanded by international pharmacopoeias and cGMP protocols.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • EU Pharmacopoeia (Ph. Eur.)
    • United States Pharmacopeia (USP)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.25–0.85 molar equivalent relative to aromatic amines, with precise adjustment tied to precursor design and batch size

    Downstream process integration

    • Introducted during the early-stage diketone condensation reaction; undergoes catalytic transformation followed by purification, isolation, and coupling to further build final drug molecule scaffolds

    Final product types

    • Active pharmaceutical ingredients for oral anticoagulants (e.g., Phenindione derivatives)
    • Intermediate compounds for investigational antithrombotic drugs
    • Bulk pharmaceutical chemicals for licensed synthesis partners

    2. Industrial Organic Pigments and Dyes Manufacturing

    Producers of specialty pigments rely on this diketone as a nucleophilic coupling agent in the synthesis of high-performance indandione- and benzoyl-based azo compounds. Its unique reactivity profile ensures intense coloration and heat stability in condensed pigment lines, meeting sectorial standards for color fastness, purity and process consistency. Our technical service team supports customers through formulation trials, enabling tailored pigment properties for high-value inks and plastics.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006)
    • EN 71-3:2019 (Safety of Toys: Migration of certain elements for pigments in toys)
    • ISO 9001:2015 (Quality Management for manufacturing)

    Typical usage ratio

    • 2–6% w/w in reaction feed depending on pigment class and end-use color intensity targets; process chemists adjust according to solvent content and auxiliary reagents

    Downstream process integration

    • Charged into batch reactors with diazonium salts as a partner in azo coupling processes; reaction mixtures undergo heating, filtration, and rinsing to yield high-purity pigment powders

    Final product types

    • Azo pigment powders for engineering plastics
    • Colorant dispersions for high-end printing inks
    • Industrial coatings with specialty shade requirements
    • Masterbatches for fiber coloration

    3. Photoinitiators for UV-Curable Resins

    Formulators of UV-cured polymers integrate this diketone compound in hybrid photoinitiator systems for coatings, adhesives, and 3D printing materials. Its structure enables rapid cleavage under UV irradiation, promoting efficient crosslinking of oligomers in acrylate and methacrylate matrices. This improves surface hardness, color stability, and depth of cure in thick sectional products, with adaptation for specific lamp intensities and substrate chemistries.

    Industry compliance standards

    • ISO 14021:2016 (Environmental labels and declarations for photoinitiators in coatings)
    • Regulation (EU) No 10/2011 (plastic materials/goods for food-contact articles, for migration limits)
    • Toy Safety Directive 2009/48/EC (for UV-cured toys and decorative items)

    Typical usage ratio

    • 0.5–2.0% by weight of total resin system; usage tailored based on resin viscosity, lamp energy (wavelength), and additive profile

    Downstream process integration

    • Blended with acrylate or methacrylate prepolymers prior to extrusion or molding; exposure to UV lamps in-line or post-cure tunnels activates crosslinking

    Final product types

    • UV-cured automotive clearcoats
    • High-gloss furniture lacquers
    • 3D printing photopolymer resins
    • Electronics encapsulation polymers

    4. Analytical Reagents in Laboratory Diagnostics (Complexometric Indicator Synthesis)

    Producers of analytical reagent kits employ this glassy solid as a key building block for specialized colorimetric indicators. Laboratories and IVD companies synthesize chelating dyes from indanedione derivatives, enabling sensitive detection of transition metal ions in biochemical screening, water analysis, and industrial QA/QC systems. Rigorous batch testing ensures purity and consistency to satisfy analytical grade benchmarks enforced by global laboratories.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for the competence of reference material producers)
    • ISO 9001:2015 (Quality Management for laboratory reagents)
    • Analytical grade specifications per ACS and European Reagent standards

    Typical usage ratio

    • 0.1–0.5 mmol per 100 mL dye synthetic batch, optimized based on targeted metal binding sensitivity and shelf life of test kits

    Downstream process integration

    • Dissolved and reacted with specific ligands in reactor vessels; processed via crystallization and grinding to yield high-purity indicator powders or stabilized liquid formulations

    Final product types

    • Complexometric indicators for laboratory titration
    • Metal ion colorimetric strips and test tablets
    • Diagnostic reagent kits for water and food analysis
    • Quality control standards for process plant laboratories
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Benzoyl-1,3-Indanedione: Experience from the Production Floor

    The Substance We Know Inside and Out

    2-Benzoyl-1,3-Indanedione is a compound we deal with every week, right from raw material to packaged chemical. As a chemical manufacturer with years invested in both process design and scaling up for industrial demand, we have worked hard to make this product meet repeatable benchmarks in purity and performance. The model most of our batches follow holds a minimum purity standard above 99%, verified with in-house HPLC and NMR throughout production. We understand the trust customers place in direct manufacturers—callbacks for out-of-spec batches hit us harder than anyone. Over time, we developed a well-documented approach that keeps each drum within spec and ready for applications in pharmaceuticals, research, and materials development.

    Why 2-Benzoyl-1,3-Indanedione Holds Value

    Chemists gravitate to 2-Benzoyl-1,3-Indanedione for its condensing abilities and chelating properties. In our experience, the diketone structure adapts well as a building block, making it useful for synthesizing heterocyclic compounds and specialty intermediates. Pharmaceutical research teams use our product in ligand preparation for metal complexes and as intermediates in generating more complex aromatic scaffolds. We have maintained a close feedback loop with customers working on pigments, polymer additives, and certain oxidative coupling reactions, who need the kind of stability and consistency that lab-scale synthesis does not always deliver.

    What separates this diketone from other aromatic diketones comes down to the benzoyl group at position two and the resulting electronic environment. Our technical group often discusses the enhanced reactivity profile in aldol-type couplings and Michael additions. This isn’t just textbook theory; we see customers getting better yields and more straightforward purifications than with basic 1,3-indanedione. The difference in reactivity profile means time saved in downstream workups. In the early days, we trialed several isomeric or related diketones to support one customer’s dye precursor work, and 2-Benzoyl-1,3-Indanedione consistently outperformed related structures in both yield and purity of the final pigment intermediate.

    Quality from the Ground Up

    Every kilogram leaving our site goes through analytical checks that were built out of real challenges. Years back, we ran into a problem: some batches developed trace yellowing. Analysis showed micro-level contamination in the solvent supply, which pushed us to overhaul pre-filtration dramatically. Since then, we track every key reagent lot number and perform contamination screening on all incoming base chemicals. We use a crystallization method instead of simple extraction, which increases our throughput cost but provides a consistent, snow-white solid. The market often sees off-white content from less-controlled operations, leading to unpredictable reactivity. Our focus stays on batch homogeneity, not just because we prefer cleaner data, but because clients downstream notice even trace divergences in color or melting point.

    Practical Experience in Storage and Handling

    We know a product’s value does not end at the reactor. Over time, we found 2-Benzoyl-1,3-Indanedione to hold up well to long-haul shipping, with little tendency to cake or degrade under ordinary warehousing conditions. Nevertheless, strong attention to packaging pays dividends: we use tamper-evident, moisture-tight drums and pack each order with silica desiccants. The extra dollar spent on the inner lining saves a hundred times more by heading off unexpected hydration or solvent contact, especially in humid environments. Customers working in large-scale settings often ask about bulk logistics. We fill our containers under nitrogen and do not ship in flexible liners. Several cases proved that this method preserves material quality, especially for clients storing product over a season or longer.

    Our own warehouse team checks container integrity on arrival and again before outbound shipment. We log every temperature fluctuation, and staff have authority to halt a batch release at the first sign of packaging compromise. The very first time we saw a moisture issue, it came not from our facility, but from a third-party warehouse. That lesson stuck—since then, we have stuck to strict climate controls, using only our own or closely audited storage partners.

    Understanding the Chemistry, Not Just the Math

    It sounds obvious, but manufacturing specialty aromatics means something more than matching a purity specification. The benzoyl substitution lends specific reactivity in coordination chemistry and nucleophilic substitutions—an attribute organic chemists value in both preparative and analytical labs. In the early days of making this compound, we tested cross-reactivity with a range of amines and found solid reproducibility in yields with common carbazoles and hydrazones. Researchers looking for a feedstock with less baseline impurity find our product a strong fit. Doing prep-scale setups and seeing the same NMR profile time after time brings real confidence, especially for work that can’t tolerate side reactions or tedious purification.

    We have witnessed demand rise sharply from universities and contract research organizations. They need assurance the material won’t introduce unknowns into experimental workflows. We learned to keep documentation for every run, supplying full NMR, IR, GC-MS, and residual solvent data even for small one-off batches. The research community relies on that level of transparency, and direct feedback from the field continues to improve both our process and our support documentation.

    Meeting Evolving Industry Requirements

    There is a reason procurement departments opt for sourcing directly from manufacturers: lack of ambiguity. Each customer sector places unique demands. In pharmaceuticals, material traceability and impurity profiling cannot be afterthoughts. Our customers in pigment production emphasize low heavy metal content and uniform batch color. Early on, we tuned our washing and purification regimen to produce a product with undetectable levels of common residual catalysts. We routinely respond to requests for specialized COAs, providing elemental analysis, halide content, or residual solvent breakdown as needed. As more regulatory frameworks apply, this lab-focused quality assurance pays off for downstream compliance.

    We once worked with a client who switched to our 2-Benzoyl-1,3-Indanedione from an untracked overseas supplier. Their yield in a synthetic intermediate increased by nearly fifteen percent, and more importantly, their labor costs fell—purification steps were simpler, and they spent less time troubleshooting mystery peaks during HPLC QC. Just as significantly, the documentation provided made audit processes smoother. Our team gained useful feedback in the form of batch-by-batch performance metrics, helping us tune in on aspects we never would have known from behind the plant gates. It’s through this kind of collaboration that we identify and eliminate real-world sources of downtime or inefficiency.

    Handling Differences: Not All Diketones Serve the Same Purpose

    Some new buyers ask about the distinctions between 2-Benzoyl-1,3-Indanedione and alternatives such as 1,3-indanedione or 2-acetyl-1,3-indanedione. The differences run deeper than a simple change in the R-group structure. The benzoyl group transforms the electron distribution, shifting both acidity and nucleophilicity at adjacent positions. These attributes lead to shifts in product profile in coupling and ring-closure reactions. Our technical support team routinely helps customers select this compound due to its enhanced reactivity and the cleaner downstream isolation. Experiments in our own development labs found the benzoyl variant notably more effective as a matrix component in certain metal chelate preparations, offering higher selectivity for target ions.

    One key difference comes in downstream work—users working scaling processes find that 2-Benzoyl-1,3-Indanedione clears faster through silica and does not generate stubborn byproducts that complicate separation, unlike similar diketones. Our discussions with commercial pigment manufacturers bear this out, as they’ve seen more consistent batch appearance and fewer off-color yields, an important point for cosmetic and specialty pigment developers. The lesson from decades of process troubleshooting: the right aromatic substitution makes a major difference not just for academic chemistry, but also in practical, production-scale settings where even slight differences echo through every subsequent step.

    Refining Methods to Pull Down Impurities

    Cleaning up the synthetically-derived batches never comes easy. Sticking to rigorous column prep and solvent recovery routines keeps side-products out. Every batch means a balance: over-purifying eats yield, under-purifying means complaints ring the phone. Long ago, we learned that slow, careful recrystallization in a binary solvent system sharply cuts especial traces of aromatic byproducts without driving material losses above five percent. Lab staff spend much of their effort on these finishing steps, as even excellent starting material will fall short with shortcuts in isolation.

    Testing for heavy metals, halides, and common organic residues remains a routine part of job tickets. The presence or absence of such contaminants turns into a downstream headache or asset. As customers expand into regulated and IP-sensitive markets, we have equipped our QC lab to detect impurities down to single-ppm levels. For pharmaceutical and electronic applications, our ability to guarantee strict absence of certain residues underpins whether material ends up as waste or proceeds to end-product release. Our documentation withholds nothing: if trace residuals appear, even at well-below threshold levels, clients see it flagged on their COA.

    Building Relationships with End Users

    Open lines of communication remains the backbone of troubleshooting. Experienced users of 2-Benzoyl-1,3-Indanedione recognize subtle shifts in properties batch to batch. We maintain a direct technical support team—actual plant chemists and lab analysts, not just customer service staff—available to consult directly with researchers and engineers facing issues downstream. Getting these calls, we talk through whether a deviation roots in our process or their conditions. Sometimes, differences in solvent polarity or temperature ramping—small changes—affect intermediate isolation or color formation. This real-world feedback helps ensure that both sides sit on the same page, and uncommon runaway variance fades to something handled with a phone call, not a dispute.

    Once a year, we invite larger industrial users to review our process improvements and share their outcomes, both positive and negative. These exchanges cut lead time for problem-solving and reinforce the details behind every technical change, be it a tweak in the filtration line or an upgrade to analytical instrumentation. Such transparency builds both technical partnership and commercial trust—something rare in the world of fine chemicals, yet invaluable when challenges inevitably arise.

    Always Preparing for What Comes Next

    We keep our production development group busy with regular method trials, looking for better catalytic routes or downstream upgrades to the isolation process. Having complete control over the synthetic chain, from order placement of initial starting materials through every vessel cleanout and drum pack-off, allows stepwise, no-surprise adjustments. It also obligates us to stand behind the published properties and every piece of analytical data shipping out with each batch.

    There are no shortcuts that serve long-term business interests. Time and again, we find the market rewards genuine manufacturing transparency and hard data. For 2-Benzoyl-1,3-Indanedione and similar fine organics, credibility comes from repeatable performance in the hands of customers, not just a bullet-point on a spec sheet. We base our production not only on textbook routes, but on the daily feedback loop with actual end users. This balance between chemical expertise and practical, user-driven evolution keeps our operations nimble and our product competitive, batch after batch.