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HS Code |
988010 |
| Chemicalname | 2-Bromo-1-indanone |
| Casnumber | 23082-29-1 |
| Molecularformula | C9H7BrO |
| Molecularweight | 211.06 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 58-62°C |
| Boilingpoint | 360°C at 760 mmHg |
| Purity | Typically ≥98% |
| Density | 1.636 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | Brc1ccc2c(c1)CCC2=O |
| Inchi | InChI=1S/C9H7BrO/c10-7-3-1-2-6-4-5-8(11)9(6)7/h1-3H,4-5H2 |
| Storagetemperature | 2-8°C, protect from light |
| Synonyms | 2-Bromoindan-1-one |
As an accredited 2-Bromo-1-Indanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Bromo-1-Indanone (5 grams) is packaged in a sealed amber glass bottle with a tamper-evident screw cap and hazard labeling. |
| Shipping | 2-Bromo-1-Indanone is shipped in specialized, tightly sealed containers to ensure safety and prevent moisture or contamination. The shipment complies with local and international transportation regulations for hazardous chemicals. Proper labeling, documentation, and handling procedures are strictly followed. It is typically shipped under ambient conditions unless otherwise specified by the manufacturer. |
| Storage | 2-Bromo-1-Indanone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizing agents. Protect it from moisture and direct sunlight. Use chemical-resistant storage and clearly label the container to prevent accidental misuse or exposure. Store according to local regulations. |
Applications of 2-Bromo-1-Indanone in Industrial ManufacturingAs a dedicated manufacturer of 2-Bromo-1-Indanone, we support specialized industrial users across advanced chemical sectors, focusing exclusively on well-established downstream applications. Below, we detail segmentation by real-world usage environments, including application-specific compliance frameworks, process integration guidance, and practical formulation data directly relevant to each end-use production scenario. 1. Pharmaceutical Intermediate Synthesis for CNS Drug Development2-Bromo-1-Indanone serves as a critical building block for the preparation of substituted indanone derivatives, widely employed in the synthesis of central nervous system (CNS) active pharmaceutical ingredients (APIs) such as monoamine oxidase inhibitors and neuroprotective agents. This intermediate enables control over regioselectivity and functionalization patterns required in multi-step route design by process chemists. Manufacturing partners leverage our consistent supply in scale-up batches to ensure regulatory-compliant, reproducible synthesis yields. Industry compliance standards
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2. Agrochemical Active Ingredient IntermediateLeading agrochemical manufacturers incorporate this indanone derivative in structurally precise crop protection molecule synthesis. It provides an essential framework in the creation of brominated indanone-containing herbicide and insecticide actives, allowing fine-tuning of electron density for enhanced field activity, and supports consistent reactivity within multi-component reaction sequences. Adoption in these sectors depends on traceability and compliance with active ingredient purity demands. Industry compliance standards
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3. Synthesis of Advanced Electronics and OLED MaterialsWithin the specialty electronics industry, R&D and mass production facilities utilize 2-Bromo-1-Indanone as a key precursor in the creation of indanone-based ligands and dopant materials for OLED (organic light-emitting diode) devices. Its controlled reactivity during subsequent arylation and cyclization steps fosters high-purity materials suitable for emissive and transport layer incorporation, with batch-specific documentation to support strict electronics quality and trace-level contamination standards. Industry compliance standards
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4. Fine and Specialty Chemicals – Synthesis of Chiral Ligands and OrganocatalystsChemical research and fine chemicals production companies select our material as a vital intermediate in the synthesis of chiral indanone ligands and organocatalysts for asymmetric transformations. The molecular structure supports the construction of complex chiral centers by serving as a brominated template, particularly for the generation of enantioselective catalyst scaffolds used in pharmaceutical and material science R&D. Repeat customers require batch-level analytical support for catalyst performance validation. Industry compliance standards
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Every day on our production floor, we work hands-on with 2-Bromo-1-Indanone, a building block in the world of fine chemicals. The molecule’s structure, featuring an indanone core brominated at the 2-position, gives it versatility that synthetic chemists appreciate. Over years of development, our facility has refined the process to deliver a consistently high-purity product. We control every stage of the synthesis, from the first raw feedstock to final purification, because reliability matters most in organic synthesis. Some customers come from pharmaceutical R&D, others from material science labs, yet all rely on the product’s reproducibility for successful downstream transformations.
Sourcing 2-Bromo-1-Indanone directly from a manufacturer means dealing with the people who see the process all the way from start to finish. Our chemists understand where bottlenecks appear and solve them at the source. For this compound, we use a well-established halogenation route starting from 1-Indanone. Reaction conditions have been optimized continuously, cutting down side-reactions and streamlining purification. The process produces a crystalline product, with batch-to-batch variation controlled so precisely you can expect the same reactivity every time.
Knowing the actual chemistry behind this compound shapes a different perspective on what makes a difference in quality. If an excess of the brominating agent remains, the crude product can hold on to impurities that show up during further synthesis. We lab-test every lot using established chromatography and spectroscopy methods: thin-layer chromatography, NMR, and GC-MS results are reviewed in-house by chemists who know what a clean spectrum should look like. Speculatively produced product, or material repackaged by third-parties, simply cannot provide that level of consistency or traceability.
Our current product line lists a model for 2-Bromo-1-Indanone as an off-white to light tan crystalline solid. Most produced material meets assay standards above 98%. The melting point, routinely checked at 82–85°C, acts as a straightforward marker of purity. Small batch runs enable us to respond to special requests for ultra-high purity if your downstream work demands it. Solubility matches what laboratory chemists expect: this indanone dissolves well in dichloromethane, ethyl acetate, and acetone, showing only limited solubility in water, which aligns with its structure and functionality. Because our team performs every step, we can provide details and practical guidance for specific lab setups based on how we’ve handled this compound ourselves.
After years of packaging and handling 2-Bromo-1-Indanone, we’ve learned that it stores best in tightly sealed containers, away from moisture and direct light. The crystalline form resists degradation, but open air or excess heat encourages breakdown and color change. Factory protocols include desiccated storage, and shipments go out in high-barrier or amber glass bottles, not just the cheapest available jar. Staff receive training to avoid cross-contamination. Real-life production runs have taught us how improper storage causes avoidable reactions, especially for a brominated compound. By shipping direct, we can maintain those standards until the product reaches your laboratory.
Small differences in the purity of 2-Bromo-1-Indanone can mean major differences in a downstream ketone reduction or cross-coupling reaction. Our technical specialists routinely troubleshoot syntheses that fail using off-spec material sourced from brokers. Samples straight from our reactors often outperform others, particularly in Sc(OTf)3-catalyzed alkylations and Suzuki-Miyaura couplings, where side impurities generate unwanted byproducts. The product’s crystalline particle size, often glossed over by brokers, shapes how quickly it dissolves, making it easier to handle in scale-up and improving yield on successive steps.
We have supported clients through gram and kilo-scale batches, with thorough technical documentation available for each run. As a manufacturer, our research and QA teams collaborate, keeping each lot within tight purity and performance parameters. We have learned by responding directly to user feedback. Early on, some customers reported problems with slow dissolution. Since then, we switched to controlled milling right before packaging, which reduced agglomerates and improved dissolution dramatically.
As chemists working in manufacturing, we see firsthand the many faces of 2-Bromo-1-Indanone in organic synthesis. Teams in drug discovery, agrochemical R&D, or even custom polymer work, all value reliable coupling partners. The molecule’s bromide substituent is activated enough for transition-metal catalyzed reactions, and sometimes direct nucleophilic substitution. Chemists tell us they appreciate how predictably it reacts with organometallic reagents—after all, our internal team uses the same material to make higher-order derivatives for customer-specific projects.
We regularly field questions about differences among brominated indanone analogues. For instance, 2-Bromo-1-Indanone stands apart from 3-Bromo-1-Indanone and 2-Chloro-1-Indanone in several ways. Its position-2 bromine offers a unique handle for functionalization right next to the carbonyl, enhancing reactivity for selective transformations. Compared to the chloro variant, the bromide is less stable but more reactive in most cross-coupling reactions. The positional isomers (like 3-Bromo-1-Indanone) show noticeably different properties—a simple shift in the halogen’s location makes them much less effective for several palladium-catalyzed reactions. Years of comparative data from both our customers and our own lab team confirm these differences in performance.
We see fewer side products during halogen/lithium exchange with 2-Bromo-1-Indanone versus its chloro cousins, a fact that translates to improved downstream reaction profiles. Material scientists sometimes favor the bromo variant for custom ligand design due to this clean reactivity. We have collaborated with university and industrial groups who need precisely this feature, and in each case, the direct manufacturer’s input allowed for tailored process suggestions that improved both safety and outcome.
Direct feedback from the laboratory helps us recommend sensible uses for 2-Bromo-1-Indanone. Synthetically, it excels as an intermediate for molecules with extended conjugation – for example, certain heterocyclic dyes or precursor frameworks in pharmaceutical scaffolding. Students and researchers often look for advice about optimal conditions, and we offer guidance based on our own production and derivative synthesis work. Our internal R&D has put this compound to use in Suzuki coupling, Stille reactions, and other transformations, and along the way, we identified common pitfalls: controlling moisture during reaction setup, selecting suitable solvents, and preventing unwanted side-reactions with excess base.
We have taken requests from chemists working on proprietary targets, who need a reliable bromo-indanone for stepwise synthesis. Sometimes those projects shift as research evolves. Supporting iterative optimization has taught us that flexibility in batch size and delivery time makes a difference, and keeping communication flowing avoids wasted time. As the team manufacturing the actual material, our insight reaches beyond product sheets and theory. We have tested, failed, re-optimized, and succeeded with this compound across different applications.
Working directly with those who make 2-Bromo-1-Indanone offers multiple practical advantages. Our facility can adjust synthesis to accommodate scale, special purity demands, or pressing delivery deadlines. We have supported pharmaceutical process development, resin chemistry, and university research, all with access to the chemists and production specialists actually making the product. Traceability is another point: knowing exactly the synthetic route, the timeline, and the analytical results of every batch helps labs avoid costly troubleshooting later. From the moment we receive an order, scheduling, safety documentation, and quality assessment become straightforward conversations rather than guessing games.
With direct oversight, impurity levels remain precisely monitored. Structural integrity, especially for sensitive brominated aromatics like this, depends on aging time, raw material grade, and purification protocol. We test for hydrolysis and debromination, which sometimes occur in poorly managed inventories handled by third-party distributers. As the people actually making and bagging this product, we maintain both the motivation and the expertise to address these details promptly and transparently.
Quality is not merely a selling point but a matter of practice in chemical manufacturing. Our facility’s production follows written SOPs for each stage, documenting everything from raw material loading to final bottling. Every worker signs off on each batch they handle, and we cross-check every analytical printout. We align with industry expectations and can supply supporting documents, including certificates of analysis, residual solvent results, and safety guidance. Regulatory compliance is enforced with direct oversight, ensuring that materials leaving our site meet the required standards for their intended R&D, pilot, or small-scale production roles.
Long-term customers appreciate the transparency. Whenever a research group or process engineer needs clarification, we answer with hands-on knowledge. For those concerned with scale-up or environmental health and safety, we give real-world advice—from selecting the right personal protective equipment to optimizing solvent usage. Only direct manufacturing experience can supply that level of detail.
Scaling up for kilo or tens-of-kilo orders introduces a set of challenges we have addressed many times. Logistics, storage, and batch consistency require close coordination between manufacturing and packing teams. Our track record includes fulfilling urgent projects for time-sensitive research and meeting the needs of commercial pilot plants. A direct manufacturer can tweak everything—crystallization rates, drying times, container sizes—so customers receive material that is not only chemically right, but logistically practical.
We have supported clients where confidentiality matters. Custom packaging, blind-labeling, or integration with a manufacturer’s own systems—this is only possible because we run the process in-house. Handling paperwork, clearing customs for export, or managing safe transport for hazardous labels, our experience bridges regulatory and commercial needs, avoiding delays that occur when a third-party handles things piecemeal.
Our work producing 2-Bromo-1-Indanone has improved by drawing on years of customer feedback. Early missteps taught us that small process changes can yield significant improvements in performance. We have responded by updating purification columns, adding extra QA steps at release, and adapting packaging to resist moisture. Every time a client reported unexpected performance in their downstream process, we dug deep to investigate. That collaborative approach shaped our procedures and products. Small adjustments build over time, reinforcing the value of a manufacturer who listens and adapts.
We have seen the industry shift: more companies want solid documentation and real-time support. Third-party distributors rarely provide troubleshooting or explanations for unusual spectral features—they simply cannot, since they have no direct control over synthesis. Direct partnerships with manufacturers shorten the feedback loop between chemists and suppliers, leading to better, more reproducible research outcomes.
As producers, we recognize the responsibility in handling, synthesizing, and disposing of brominated aromatics. Waste management, emission control, and efficiency enter every production run. Over the years, our plant has reduced solvent use in the final stages, transitioned to greener solvent alternatives, and improved the yield per batch, lowering raw material waste. Seeing the day-to-day impact that direct practices have—not just on cost, but on worker safety—has motivated ongoing investment in these improvements.
Sustainability efforts impact our downstream users too. Cleaner batches mean less solvent and labor needed to remove trace impurities. Communicating openly with research groups about our production improvements has led to better collaborations on lifecycle and environmental profiles.
Manufacturing 2-Bromo-1-Indanone requires controlling all variables—raw material sourcing, handling, reaction timing, and purification. Over time, we learned that certain supply chains for precursors fluctuate, so we maintain multi-source agreements to keep production uninterrupted. Our technicians check even minor equipment changes because vessels with lingering residue from previous runs can catalyze side reactions. On the rare occasion a batch falls short, we catch and address it on-site, rather than passing along inferior product. Each solution comes from direct, on-the-ground learning.
Shipping and export bring risks unique to this molecule. The correct paperwork for regulated intermediates prevents material from sitting at customs or facing unnecessary fees. By directly managing preparation and documentation, we keep orders moving efficiently to their destinations. That’s a benefit customers see in reliable arrival times and fewer logistics headaches.
What sets direct manufacturers apart is the hands-on knowledge of real chemists and plant workers. Our understanding comes from putting thousands of liters of solvent to use, working on tight timelines, and continuous hands-on troubleshooting. The 2-Bromo-1-Indanone leaving our facility reflects decades of process refinement and the dedication of the operators and chemists making it. The conversations we have with clients about technical problems, supply chain hiccups, and even about the quirks of lab-scale reactivity come from daily production and not just reading a sales sheet.
Researchers, process developers, and laboratory chemists stand to gain from that experience. Every specification, every document, and every shipment draw from our collective expertise. We take pride in giving more than a commodity; we provide technical partnership based on actual practice.
2-Bromo-1-Indanone sits at the intersection of fine chemical innovation and practical manufacturing. As we continue to refine our process and adapt to new research demands, our commitment stays rooted in what we learn on the production floor. Scientists working on proprietary syntheses, process chemists at scale, or academic researchers can reach out to discuss challenges, request custom lots, or ask about technical details. The value of direct manufacture reaches far beyond price—it means honest answers, support from real people, and the technical insight that comes only from those who make the product themselves.