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HS Code |
661426 |
| Productname | 8-Bromoisoquinoline |
| Casnumber | 1532-97-6 |
| Molecularformula | C9H6BrN |
| Molecularweight | 208.06 |
| Appearance | Off-white to light yellow solid |
| Meltingpoint | 58-62°C |
| Boilingpoint | 310°C at 760 mmHg |
| Purity | Typically ≥97% |
| Solubility | Soluble in organic solvents like DMSO and dichloromethane |
| Smiles | Brc1cccc2ncccc12 |
| Inchikey | OUDHJXDVHIXCPP-UHFFFAOYSA-N |
| Storagetemperature | Store at room temperature |
| Refractiveindex | 1.649 (predicted) |
As an accredited 8-Bromoisoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle labeled "8-Bromoisoquinoline," featuring hazard symbols, product details, lot number, and tightly sealed with a screw cap. |
| Shipping | 8-Bromoisoquinoline is shipped in compliance with all relevant chemical safety regulations. The compound is securely packaged in sealed containers, cushioned to prevent breakage, and clearly labeled with hazard information. Shipping is handled via certified carriers, and accompanies detailed safety documentation, including Material Safety Data Sheets (MSDS) for safe handling and transport. |
| Storage | 8-Bromoisoquinoline should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. It should be kept in a cool, dry, and well-ventilated area, ideally at room temperature. Proper labeling and adherence to safety protocols are essential to prevent contamination, degradation, or hazardous reactions during storage. |
Applications of 8-Bromoisoquinoline in Industrial ManufacturingAs the manufacturer of 8-Bromoisoquinoline, we support advanced sectors where this intermediate enables high-value downstream products. Below we detail use cases in pharmaceutical synthesis, OLED material fabrication, agrochemical production, specialty dye manufacturing, and heterocyclic catalyst preparation. 1. Pharmaceutical Intermediate for Anticancer and CNS Drug SynthesisPharmaceutical companies use 8-Bromoisoquinoline as a core scaffold for developing novel heterocyclic compounds targeting cancer and central nervous system disorders. Medicinal chemists leverage the compound’s reactivity in Suzuki and Buchwald-Hartwig coupling reactions. It gets introduced at early or intermediate stages to form isoquinoline-based motifs present in investigational and approved API structures. This raw material enables customization at later synthetic stages to optimize pharmacokinetics and safety, meeting regulatory demands for traceability and impurity control. Industry compliance standards
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2. Intermediate for OLED and Display Material ProductionIn the electronics industry, 8-Bromoisoquinoline acts as an essential building block for synthesizing high-performance organic semiconductors. Manufacturers apply it in the multi-step preparation of advanced emitter and electron transport layers in OLED devices. The compound’s selective reactivity and ability to deliver isoquinoline-containing ligands support the precise doping and tuning of optoelectronic material properties, benefiting display contrast, lifespan, and energy efficiency. Careful upstream quality control ensures material compatibility and defect minimization in cleanroom OLED fabrication settings. Industry compliance standards
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3. Synthesis of Isoquinoline-Based Agrochemical Active IngredientsAgrochemical R&D divisions rely on 8-Bromoisoquinoline for the modular design of insecticidal and fungicidal compounds. Chemists exploit its reactivity to introduce isoquinoline units via palladium-catalyzed C–C and C–N bond formation. This approach tailors molecular scaffolds for bioactivity against targeted crop pests and pathogens. Final actives undergo formulation into water-dispersible granules or wettable powders, considering safety and toxicology requirements supporting regulatory dossiers worldwide. Industry compliance standards
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4. Manufacture of Specialty Dyes and PigmentsProducers of high-performance colorants employ 8-Bromoisoquinoline as a precursor for synthesizing lightfast and heat-stable isoquinoline-derived dyes. The compound reacts with diverse substituents in controlled multi-step syntheses, producing pigments for specialty textiles, security inks, and plastic coloration. Strict monitoring of trace metals and halide residues is critical to avoid hue shifts and instability in end-use conditions. Industry compliance standards
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5. Precursor for Heterocyclic Ligand and Catalysis SynthesisChemical and material science companies utilize 8-Bromoisoquinoline in the synthesis of complex ligands for transition metal catalysis and functional material development. It serves as a core aromatic ring allowing the introduction of donor atoms or additional fused rings, vital for ligand field strength and selectivity in homogeneous and heterogeneous catalysis. The compound’s purity and trace impurity profile directly influence catalyst activity and reproducibility, making strict QC essential before downstream immobilization or complexation steps. Industry compliance standards
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As manufacturers who know every step that brings a new compound from a glass reactor to a bottle ready to ship, we see the real picture behind every molecule we produce. 8-Bromoisoquinoline has occupied a unique spot for us in the ever-growing toolbox of heterocyclic building blocks. There’s a story behind why this compound continues to find itself on the benches of research labs and pilot plants, despite so many other substituted isoquinolines on the market. Every single batch we produce offers a new lesson: the little details—from bromination reactions to final purity—matter, both for our process and for the results our customers expect.
Every load of 8-Bromoisoquinoline we ship has taken a predictable yet demanding journey. The core structure, with a bromine atom attached to the eighth position, makes a difference in reactivity and downstream functionalization. Each run in our reactor gets the same careful monitoring: temperature, solvent choice, and reaction time. Years of hands-on adjustments have taught us that small changes impact impurity profiles and ultimately the ease with which downstream users can work with the material.
Our own experience has made two priorities clear. First, batch consistency sits at the foundation. In our early years, inconsistent color, solubility, or lingering byproducts led to headaches for customers working in pharmaceutical research and materials development. We took those complaints seriously and doubled down on process controls—not to brag, but when a batch hits our minimum purity specification, it means a minimum of 98%—and real-world reliability test results. Many distributors can show you a datasheet; we show you batch records and stand behind the chemistry.
Laboratory chemists and process development teams choose 8-Bromoisoquinoline for its distinctive role in synthesis. Its bromo-isoquinoline core opens doors to Suzuki couplings, Buchwald-Hartwig reactions, and other common transformations. Our production targets specific particle size distributions based on customer needs. Sometimes, maintaining a certain fine powder result allows for better dissolution and reactivity in solution-phase chemistry. Other customers want larger crystals for ease of handling and storage.
Moisture content, residual solvent traces, and trace metal analysis are not optional extras—they translate directly into higher yields or cleaner separation in follow-up steps. These factors affect both small milligram lots bound for an academic group and large batches slated for pharmaceutical development. By keeping these technical aspects a daily priority, we address purity-related demands up front rather than leaving them as problems for someone else down the line.
Most calls we get for 8-Bromoisoquinoline come from teams working in medicinal chemistry, crop protection research, or advanced materials. Its utility centers on the ability to introduce a reactive handle at a defined position, giving chemists flexibility in modifying the isoquinoline scaffold. This is not a molecule where “close enough” works. Your synthesis might demand a pure, well-characterized reagent so you can build libraries of candidate compounds. We have seen too many projects derailed when a building block didn’t deliver what was promised—so our staff checks for trace levels of isomeric or over-brominated contaminants, because isoquinoline chemistry loves surprises nobody wants.
Pharmaceutical innovators use it as a starting point for novel kinase inhibitor design or for tweaking core structures in lead optimization. Agrochemical developers value its role in scaffolds for novel herbicidal or fungicidal leads. In each case, the bromine provides a functional point for cross-coupling or nucleophilic substitution without the harsher conditions required by chloro analogues. Research clients tell us that ease of substitution at the 8-position helps streamline synthetic sequences, save time, and reduce reagent waste.
What does that look like at the bench? Imagine a medicinal chemist at a hood, assembling a panel of candidate molecules. The difference between a clean reaction and a mess of side products often comes down to building block quality. When we talk with synthetic chemists, feedback centers on minimizing downstream purifications and unexpected TLC spots. We hear stories of rival compounds, especially brominated aromatics purchased through trading intermediaries, unloading as off-colored solids or carrying persistent byproducts that resist removal. Our production staff feels satisfaction knowing each package meets an analytical profile that can stand up to scrutiny, not just an internal release standard.
Halogenated isoquinolines might appear interchangeable at a glance, but chemists working daily at scale or in high-value R&D know this is not the case. Chlorinated analogs, like 8-chloroisoquinoline, usually cost less per kilo due to lower raw material prices and sometimes simpler production. Yet, when conversion efficiency and downstream ease-of-use enter the calculations, 8-Bromoisoquinoline often justifies its higher up-front cost. The better leaving group properties of bromide facilitate smoother coupling reactions, allowing use of milder base and catalysts, increasing the chance of good selectivity and manageable side products.
We have responded to requests for both 5-bromo- and 8-bromo derivatives. Substituent position isn’t just an academic detail—it influences everything from reactivity to the kinds of interactions possible in a final compound. Some competitive suppliers attempt one-pot halogenation, accepting a mix of isomers to get higher yield, but we’ve seen too many customers waste time sorting these messes out later. Our plant design prioritizes regioselective bromination, giving us a consistent 8-bromo isomer.
There’s also the reality of purity. Any seasoned chemist who’s worked with impure halogenated heterocycles knows that even two or three percent of polysubstituted or isomeric byproducts can disrupt development work, especially when moving from small-scale exploratory runs to gram quantities or more. Lab experience in the trenches—where you don’t have time to re-purify every single bottle—teaches you that source matters. Our direct-from-manufacturer approach means you aren’t left guessing about how the powder in your vial was made or whether it will behave the same from order to order.
As technical staff, we’ve seen the inside of our own reactors and the reality on the plant floor. You get to know which solvents facilitate clean bromination, which purification steps best remove stubborn colored impurities, and which finished product specs really matter once the compound leaves the manufacturing site. We openly discuss our raw material sourcing. Since the global bromine supply chain offers risks—price spikes, quality swings, both environmental and regulatory pressure—we invest in long-term supplier relationships, stock buffer, and real-time QC on inbound shipments. We see no value in hiding this part of the process because our customers have too much at stake to buy blindly.
With more specialized chemicals, buyers sometimes navigate a world crowded with trading intermediaries or “gray market” resellers. Many such vendors repackage bulk material or source batches from several original manufacturers, rebranding them under their own labels. End-users tell us horror stories of lots varying dramatically from bottle to bottle or year to year. Because we control every stage of production—from raw material selection to finished product analysis—we can provide a reliable, reproducible product every time. Our chemists and operators take pride in each run’s output, knowing we’re sending out a building block, not just another commodity.
We often get feedback from research partners that access to reliable 8-Bromoisoquinoline speeds their timelines. A researcher running repeated transformations needs to avoid project delays due to inconsistent material or surprise impurities. Our analytical lab monitors each lot by HPLC, mass spectrometry, elemental analysis, and selects NMR for conclusive fingerprinting. These are not optional frills, but core requirements for driving real progress in pharmaceutical, agrochemical, or materials science fields. Regulatory teams in pharmaceutical discovery or manufacturing regularly request detailed impurity profiles and stability data—something trading companies rarely can provide directly.
For scale-up applications, we listen to process chemists who describe everything from filtration issues caused by trace insoluble residues to product isolation complications when unknown by-products slip through. By holding ourselves to a tight quality margin, we minimize surprises later—so grams scale smoothly to tens, hundreds, or thousands. When companies approach us with custom requirements or specific impurity thresholds, our process and analytical teams work in tandem to fine-tune production runs and ensure every critical detail matches project needs.
Over years of shipping building blocks and intermediates worldwide, we’ve learned the importance of detail in packaging and storage instructions. 8-Bromoisoquinoline, like many heteroaromatics, benefits from cool, dry storage and tightly sealed containers. Our plant has seen issues before—in hot, humid conditions or with poorly sealed drums, material can pick up enough moisture to impact precise formulations or influence solubility. We learned that packaging integrity and clear labeling are not small details; they make the difference between frustration and smooth workflow for the end user. We consistently monitor stability and conduct shelf-life studies for our inventories, so those relying on our stock can expect consistency throughout their research or production campaign.
Crafting quality 8-Bromoisoquinoline is far more than following a written procedure. We recruit operators who know how to troubleshoot reactor foaming or adjust parameters to avoid side-product formation. Our technical staff walks the floor during distillation and purification, not just sitting in office cubicles. Each batch becomes a collection of the knowledge and insight gathered from what worked—just as much as what didn’t. Bringing 8-Bromoisoquinoline to those who depend on it takes attention to detail that stretches from raw material inspection to the last screw-on seal for a glass bottle.
We understand the challenges synthetic chemists and formulation scientists face. The pressures of patent timelines, grant deadlines, and industrial scale-up leave little margin for uncertainty caused by off-spec reagents. In pharma development, we’ve seen first-hand how a single inconsistent batch can cascade into lost weeks or failed pilot studies. Academic partners report funding wasted by unpredictable batch-to-batch differences when buying from less transparent sources. These experiences feed back into our production priorities: consistency, reliability, and open communication at every turn.
Our customers continually push the boundaries of what heterocyclic chemistry can deliver. We’ve responded to custom requests for higher purities, alternative particle sizes, low-residual metal specifications, and alternate packaging formats to suit automated dispensing or micro-scale screening. Staying close to the research community—attending industry meetings, collaborating on analytical best practices, and soliciting direct process feedback—fuels improvements in how we approach manufacturing.
We monitor regulatory trends, project demand, and emerging synthetic methodologies so that production can adapt before users hit unexpected speed bumps. As stricter environmental and worker safety rules take shape in our industry, we invest in cleaner workups, improved waste management, and continuous training for production staff. The transition to greener solvents or lower-energy bromination chemistry remains a topic of internal research, reflecting both customer demands and the broader push toward more sustainable fine chemical production.
Every batch of 8-Bromoisoquinoline that leaves our plant reflects years of refinement, adaptation, and an unfiltered look at what chemists genuinely require. We treat every shipment as part of a larger conversation between bench scientist, process developer, and the plant floor. Transparency, hands-on expertise, and relentless attention to quality are not just slogans but a necessity for anyone working in fields where the details of molecular structure and impurity content make or break projects.
From countless conversations with R&D chemists, formulation scientists, and production engineers, we know that quality is not just a line on a specification sheet—it is the sum total of cumulative experience, process dedication, and a relentless drive for improvement. Our team takes pride in shipping building blocks like 8-Bromoisoquinoline, confident in the knowledge that what leaves our plant enables real innovation around the world.