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HS Code |
803471 |
| Chemicalname | 3-Amino-2-Phenylindenone |
| Molecularformula | C15H11NO |
| Molecularweight | 221.26 g/mol |
| Casnumber | 82459-06-9 |
| Appearance | Yellow to brown solid |
| Meltingpoint | 196-198 °C |
| Solubility | Slightly soluble in organic solvents |
| Purity | Typically >98% |
| Storagecondition | Store at room temperature, away from light and moisture |
| Smiles | N[C@@H]1C(=O)c2ccccc2C1c3ccccc3 |
| Iupacname | 3-amino-2-phenyl-1H-inden-1-one |
As an accredited 3-Amino-2-Phenylindenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-Amino-2-Phenylindenone is packaged in a sealed, amber glass bottle containing 10 grams, labeled with hazard warnings and details. |
| Shipping | 3-Amino-2-Phenylindenone is shipped in secure, chemical-resistant containers to prevent leaks or contamination. Transport complies with relevant regulations for hazardous substances, using clearly labeled packaging. Proper documentation accompanies each shipment, and temperature control may be applied if required to ensure chemical stability during transit. Handle with appropriate safety precautions. |
| Storage | Store 3-Amino-2-Phenylindenone in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Ensure the storage area is free from moisture and sources of ignition. Clearly label the container, and keep it away from food and drink. Handle using appropriate personal protective equipment (PPE). |
Applications of 3-Amino-2-Phenylindenone in Industrial ManufacturingAs the original manufacturer of 3-Amino-2-Phenylindenone, we support enterprise clients with precisely controlled, high-purity grades for advanced synthesis. Below are verified downstream use cases where this specialty intermediate plays a crucial role in manufacturing value-added products. Each application section details relevant compliance frameworks, industrial usage levels, integration steps, and typical end products. 1. Active Pharmaceutical Ingredient Synthesis for Oncology Drugs3-Amino-2-Phenylindenone forms a core building block in several heterocyclic compound syntheses for small-molecule oncology APIs. Fine chemical manufacturers leverage its indene structure in multistep reactions—specifically palladium-catalyzed amination and cyclization steps—leading toward novel kinase inhibitors or synthetic alkaloid backbones under stringent GMP oversight. Our material’s ultra-low impurity profile and batch reproducibility ensure compliance with validated drug substance routes, supporting robust quality data packages for regulatory submission. Industry compliance standards
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2. Advanced Organic Pigment Intermediate ManufacturingSpecialty pigment producers use 3-Amino-2-Phenylindenone as a structural amine donor in high-performance pigment and dye syntheses. The aromatic amine moiety serves as a reactive site during azo coupling or condensation, enabling production of pigments with tailored chromatic strength and chemical stability for plastics, coatings, and digital ink applications. Our highly consistent particle size and colored stability are validated through robust batch-to-batch analytical testing protocols required by major pigment consumers. Industry compliance standards
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3. Electronic Material Intermediate in Organic Semiconductor SynthesisLeading electronic material manufacturers employ 3-Amino-2-Phenylindenone as a precursor for constructing π-conjugated systems in organic semiconductors. Its rigid indenone scaffold facilitates the synthesis of electron-transporting layers and hole-transporting materials used in organic field-effect transistors (OFET) and OLED engineering. Ensuring high purity and proven low metal trace levels is essential for downstream device reliability and process yield in cleanroom operations. Industry compliance standards
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4. Agrochemical Synthesis—Intermediate for Insecticide FormulationsAgrochemical synthesis pathways utilize 3-Amino-2-Phenylindenone for constructing specific pyrazole and indene-based insecticidal agents, which are valued for potency and environmental stability. Manufacturers require tight control over incoming material’s residual solvents, water content, and batch consistency, as residues carry over into technical concentrate production. Our integrated QC and tailored lot sizes meet large-scale formulator demands within compliant industrial environments. Industry compliance standards
Typical usage ratio
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Every day, people outside our labs rarely think about the intricacies behind discovery work in pharmaceuticals and advanced materials. Here, that’s all we think about. One compound that keeps appearing in project requests and synthesis challenges is 3-Amino-2-Phenylindenone. Our team first encountered it while chasing candidate scaffolds for several heterocyclic intermediates in the early aughts. Since then, its place in our catalog has grown not just in quantity, but in the pivotal role it fills for researchers scaling from milligram trials to industrial kilo lots.
Chemists use 3-Amino-2-Phenylindenone for its precise reactivity when assembling particular fused ring systems. This molecule’s bridged structure, anchored by a phenyl ring and activated by an amino group, lets it drive transformations that simpler ketones or anilines can’t handle directly. The difference shows up during electrophilic substitutions or cyclizations — an area where selectivity often determines project success or failure. Across custom orders over the past several years, we’ve watched how teams in medicinal chemistry and fine chemical manufacturing turn to this compound to clear roadblocks in their synthetic schemes.
Too often, project delays trace back to inconsistent quality of starting materials. Having worked with dozens of batches in our pilot and commercial-scale reactors, our chemists take pride in delivering 3-Amino-2-Phenylindenone that maintains reliable purity, color, and particle characteristics. The material comes as a consistent yellow to pale orange crystalline powder, and we check every batch for residual solvents and starting impurities. Our analytical team tracks key markers — HPLC area percentage, melting point, and elemental analysis — informed by over a decade of internal batch records.
One point stands out. Many buyers notice rapid performance shifts when switching between sources. We saw this problem firsthand during a joint development project with a partner where off-the-shelf material led to byproduct issues in a Suzuki coupling. Fixing it meant tightening moisture specs, ensuring no amide contamination, and pinpointing the right recrystallization solvent. Since then, we have flagged single-digit ppm levels of trace byproducts and included these controls as our baseline. Feedback from several clients indicates this attention to detail shortens troubleshooting cycles at their own benches, saving time and frustration compared to dealing with off-spec lots.
Plenty of ketones enter the market, from simple acetophenones to indanones, but few match the unique profile given by the amino and phenyl substitution on the indenone core. The amino group at position 3 is a key position for routes involving nucleophilic aromatic substitution, amidation, or the attachment of labeling reagents. We have observed, especially in custom peptide and library builds, that the ortho-positioned phenyl ring doesn’t just act as a spectator — it creates valuable steric effects that guide selectivity through multi-step syntheses.
When compared head-to-head against related molecules like 3-Amino-1-indanone or other aminophenyl analogues, the advantages become clear in cyclization and condensation reactions. Chemists working on dye intermediates and sensory materials praise the compound for its clean, repeatable formation of larger ring systems without byproduct tar formation common to less substituted scaffolds. This isn’t theoretical; we’ve witnessed kilo-scale processes run to completion without major chromatography, relying entirely on crystallization and simple filtration, thanks to this product’s reactivity and profile.
We also field regular calls from groups working on early-stage pharmaceutical leads, especially those trying to tweak framework rigidity and polarity in lead optimization. 3-Amino-2-Phenylindenone often appears as a supporting actor when developing core scaffolds for kinase inhibitors, anti-inflammatory prototypes, and imaging agent cores. The combination of a conjugated system and an amino functionality helps teams tune binding and solubility without sacrificing synthetic accessibility. What’s more, this structure resists air and light degradation better than many of its cousins, lending stability when stored properly in standard lab packaging.
Our typical lot of 3-Amino-2-Phenylindenone features a molecular formula of C15H11NO, with a molecular weight that lands at 221.26 g/mol. Batch certificates routinely show purity levels over 98% by HPLC and very low moisture by Karl Fischer analysis. The melting point falls in the 210-215 °C range, and we keep samples available for repeat analysis up to three years from production, as part of our internal accountability protocol.
This sounds dry to outsiders, but reaching these benchmarks reflects years of method refinement. Many chemists can relate to losing weeks of R&D to tracking down impurities originating from previous synthetic steps. Early on, we ran into purification bottlenecks due to the product’s tendency to co-crystallize with residual palladium or iron from catalyst runs. In response, we overhauled workup protocols to rout out metal traces — using advanced chelation processes and an extra round of charcoal polishing. Our scale-up chemists implemented these changes, and reprocessing requests from customers dropped by 80% within a year. The difference between a standard product and one designed by persistent problem-solving becomes obvious over time.
As a direct manufacturer, we build flexibility into our operations to support requests for substitutions or related analogues. This often means running customized campaigns for groups needing either higher-purity research lots or tailored packaging — from grams in glass to multi-kilo drums with moisture-barrier liners. Several times, customer collaboration has spurred adjustments in isolation and drying steps to better suit specific downstream applications, such as solid-phase synthesis, fragment-based drug discovery, or semiconductor research. We welcome these technical conversations; it keeps us tied to practical outcomes, rather than just serving as a commodity source.
Many users come to us after struggling with inconsistent supplies or hesitant third parties. Because we control every step, from raw material sourcing to final QC (quality control), our inventory doesn’t vanish overnight due to upstream shortages or fluctuating margins. We keep real material on the shelves and offer regular reserves for long-term partners — a practice rooted in experience rather than theory. This approach reduces the risk of delays on urgent projects, whether for a small startup or a global pharmaceutical group.
As synthetic chemists ourselves, we know the frustration when vendors treat orders like commodities. Over the years, researchers from Japan, Europe, and North America shared stories about “mystery batches” arriving with unpredictable solubility or color. These lessons pressed us into building out robust documentation for each lot and running supplemental analyses upon request, allowing users to check their own data against ours before scaling up. We have supported both rush samples shipped overnight and multi-ton runs scheduled out months in advance. Not only do we ship on time — we stay prepared to offer process samples, retention material for regulatory submissions, and direct answers to technical queries from real chemists, not call center scripts.
One group working on catalyst development faced recurring inconsistencies from brokered material, leading to product failures in gram-scale test runs. After switching to our lot, they reported reproducible catalytic cycles and purity profiles that matched their reference standards. This story matches feedback from manufacturers in pigment synthesis, specialty polymers, and NCE (New Chemical Entities) evaluation, showing the ripple effects of supply reliability in scientific work.
Producing specialty chemicals creates waste streams, but we aim to minimize the impact from day one. In the early days, we struggled with solvent recycling issues and high energy input during crystallization. Over time, we invested in closed-loop solvent handling and heat reclamation equipment, reducing both waste generation and power draw. Our plant operators transitioned from reactive controls to proactive maintenance routines, tracking emissions and solvent losses tied to each production campaign.
Feedback from the factory floor shaped many updates in our process. Operators pressed for safer material handling guidelines and more ergonomic packaging, especially for drum-scale shipments. In response, we switched to lighter liners, implemented vacuum transfer for powder handling, and revamped labeling for rapid hazard identification. These changes didn’t just boost safety metrics — they sped up order turnaround and allowed for more flexible scheduling across shifts.
Our central goal remains to deliver quality building blocks, not just chase volume. We welcome audit teams and client site visits, knowing no third-party distributor can replace the first-hand insight gained by seeing a real operation in motion. Seeing the blend of automation, human oversight, and collaborative problem solving throughout daily production showcases the pride we take in our people and facilities. Each batch of 3-Amino-2-Phenylindenone represents this ongoing push for cleaner output, better documentation, and safer handling from receiving dock to customer bench.
These days, requests for technical documentation outpace order forms. Many of our customers ask detailed questions about reactivity with certain acyl donors, photostability under strong light, or compatibility with new polymer matrices. Drawing on data from internal experiments and partner collaborations, we maintain an archive of real-world procedures and validated references for the compound. This resource pool doesn’t sit behind paywalls — we want to support both new researchers and long-time chemists troubleshooting tricky syntheses.
We’ve worked closely with academic labs investigating applications in both medicinal chemistry and materials science. For instance, a university group recently explored photoinitiated cycloaddition reactions with 3-Amino-2-Phenylindenone, and our technical team helped optimize their solvent selection and isolations. In industry, customers building high-density data storage materials rely on this product’s clean reactivity profile. They share back results, and we use them to fine-tune our production protocols and suggest handling tips to future users.
Training sessions and open lines of communication shrink the learning curve for teams testing this compound for the first time. By sharing real case studies — both successes and failures — we collectively push toward more efficient research and scale-up. Instead of hiding behind generic datasheets, we field direct calls and email threads, reviewing chromatograms, NMR traces, or isolation Q&A in real time. This exchange improves not only user outcomes, but also shapes the next iteration of our internal procedures.
In a world awash in resellers and anonymous brokers, working directly with a manufacturer matters. We have witnessed too often the confusion caused by compound relabeling, questionable lot histories, and ever-shifting supply chains. Our ethos rests on transparent production, detailed documentation, and a refusal to compromise batch integrity — even under pricing pressure. That means all 3-Amino-2-Phenylindenone leaving our facility comes with batch-level traceability, full analytical records, and technical support direct from our team.
Supply chain volatility is not some abstract threat. Global disruptions, raw material price swings, and increased regulatory scrutiny test the resilience of every chemical producer. Because we live in this environment, every year brings process reviews, supplier audits, and investment in backup inventory. Clients rely on us for secure access to critical intermediates, knowing surprises and excuses have no place here. Backup plans exist for energy outages, transport delays, and even geopolitical shifts, reflecting the hands-on flexibility that comes from direct manufacturing experience.
No chemical exists in a vacuum. Each user who invests in 3-Amino-2-Phenylindenone expects more than powder in a bottle. They look for reliability, peer-like support, and ongoing engagement as new challenges emerge at the lab bench or reactor scale. We design our business to fit this expectation, from the way we qualify suppliers and train plant staff to how we answer after-hours queries from researchers with tight deadlines. The goal isn’t mere compliance — it’s long-term partnership and mutual progress.
Our history with this compound taught us that experienced chemists seek more than the basics. Routinely, customers approach us for process optimization advice — whether on solvent swaps, reaction temperature tweaks, or downstream crystallization tactics. Even the most sophisticated operations hit speedbumps, and having a responsive manufacturing partner turns logistical headaches into manageable technical puzzles.
Sometimes, groups need custom derivatives — methyl, halogen, or alkoxy substitutions, for example — built on the same indenone backbone. Our R&D team stands ready to prototype limited campaigns, monitoring both analytical results and process feasibility. Through such targeted efforts, we stay attuned to changing market needs and evolving research trajectories, making our support more than checkbox fulfillment.
Hand-in-hand with service comes honest communication about what works, what doesn’t, and which long-shot ideas have a fighting chance in the real world. Feedback loops between production chemists, technical sales, and end users foster a shared knowledge base. This fuels faster troubleshooting, creative problem solving, and steady improvements with each lot released. Our approach puts real faces and hands behind every shipment, anchoring each compound’s place in research or industrial progress.
Producing 3-Amino-2-Phenylindenone isn’t just about satisfying a line on a catalog. It’s a continual process of learning, improving, and meeting evolving demands from colleagues pushing the boundaries of science and technology. The challenges we’ve faced, from purification hurdles to shipment logistics during global slowdowns, only deepen our commitment. By anchoring everything in solid hands-on experience, transparent operations, and active technical support, we strive to set a standard that goes beyond the chemical’s structure or price.
As you develop your next synthesis pathway, troubleshoot an unexpected result, or explore a brand-new research direction, know that every vial and drum of our 3-Amino-2-Phenylindenone draws on real expertise and continuous partnership. We invite you to connect with our team — whether to solve immediate problems, learn from our journey, or build longer-term solutions for tomorrow’s projects.