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HS Code |
255156 |
| Cas Number | 1532-46-7 |
| Molecular Formula | C9H6BrN |
| Molecular Weight | 208.06 g/mol |
| Iupac Name | 1-Bromoisoquinoline |
| Appearance | Pale yellow to brown crystalline solid |
| Melting Point | 42-45 °C |
| Boiling Point | 296-298 °C |
| Density | 1.582 g/cm3 |
| Solubility In Water | Insoluble |
| Purity | Typically ≥ 97% |
| Smiles | Brc1ncccc2ccccc12 |
| Inchi | InChI=1S/C9H6BrN/c10-9-7-5-3-1-2-4-6(5)8(9)11/h1-4,7H |
| Refractive Index | 1.677 |
| Synonyms | Isoquinoline, 1-bromo- |
| Storage Conditions | Store at 2-8 °C |
As an accredited 1-Bromoisoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Bromoisoquinoline, 25g: Supplied in an amber glass bottle with a tamper-evident cap and detailed hazard labeling for safe laboratory use. |
| Shipping | 1-Bromoisoquinoline is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It is protected from light, moisture, and incompatible substances. The package complies with applicable transport regulations for hazardous materials, including appropriate labeling and documentation. Handling instructions and safety data are provided to ensure secure delivery and storage. |
| Storage | 1-Bromoisoquinoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. It should be kept at room temperature and protected from moisture. Proper labeling and secure storage are essential to prevent accidental exposure or chemical reactions. Use appropriate safety precautions when handling. |
Applications of 1-Bromoisoquinoline in Industrial Manufacturing1-Bromoisoquinoline serves as a key intermediate in multiple chemical manufacturing sectors, providing function-specific value in the elaboration of advanced molecules. We support verified, global industrial customers in strictly regulated downstream applications where data-backed performance and traceability are essential. Below we outline the main industrial applications, each outlined with relevant standards, formulation practices, process integration, and end-product categories as observed in real-world production. 1. Pharmaceutical Intermediate for Anticancer Molecule SynthesisPharmaceutical manufacturers utilize our material for the construction of pharmaceutically active isoquinoline derivatives, especially those required in targeted small-molecule oncology drugs. The halogenated isoquinoline nucleus advances efficient scaffold elaboration via palladium-catalyzed coupling, allowing tailored structural modifications for patented chemotherapeutic APIs recognized in modern oncology protocols. Industry compliance standards
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2. Agrochemical Building Block for Novel Herbicidal CompoundsLeading agrochemical companies select 1-Bromoisoquinoline to construct core bioactive skeletons in advanced herbicides. As the bromo group activates direct arylation and further derivatization, it is especially preferred in the synthesis of isoquinoline-based weed control agents with improved soil persistence profiles, employed in regulated crop protection portfolios across the EU, South America, and APAC. Industry compliance standards
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3. Fine Chemical Intermediate for Organic Electronic MaterialsManufacturers of organic semiconductors and related optoelectronic materials utilize 1-Bromoisoquinoline as a key precursor for synthesizing specialty ligands and building blocks. The electron-rich framework facilitates the design of charge-transport materials and dopant-modified polymers for use in OLED displays and solar cells. Its role in niche aromatic substitution mechanisms affords electronic properties critical to next-generation display and energy storage devices. Industry compliance standards
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4. API Intermediate for Antiviral Isoquinoline DrugsSeveral large-scale pharmaceutical programs integrate 1-Bromoisoquinoline in multi-step synthesis of isoquinoline-functionalized antivirals, utilizing the material’s enabling reactivity in alkylation and nucleophilic substitution. Purity and precise substitution are critical here to meet stringent international quality and traceability standards throughout regulatory submissions and batch release. Industry compliance standards
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5. Custom Intermediate in Dye and Pigment ManufacturingProducers in the dye sector use 1-Bromoisoquinoline to introduce specialized structures during the synthesis of colorants for technical applications. Its selective reactivity enables formation of stable functionalized chromophores, enhancing tinting strength and solvent stability in advanced pigment and dye recipes earmarked for high-performance coatings, inks, and plastics. Industry compliance standards
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Our work as a dedicated producer of 1-Bromoisoquinoline means we approach each batch with a practical mindset and steady hands. To many chemists, this compound sounds like another routine reagent. For us, it represents years of refinement, process improvements, and close attention to the way this molecule fits into the expanding world of organic electronics, pharmaceuticals, and specialty materials.
1-Bromoisoquinoline, a pale to slightly yellow liquid at room temperature, belongs to the family of halogenated heterocycles. Its chemical structure supports diverse cross-coupling reactions, where bromine’s reactivity allows for confident downstream functionalization. We manufacture to a clarity that guarantees strong performance in Suzuki, Heck, or Sonogashira protocols. Every lot we release has to meet the same strict standards for impurity profile and residual solvent verification.
The isoquinoline backbone lends this molecule a unique blend of aromatic stability and site-selective reactivity. Unlike similar halo-nitrogen aromatics, 1-Bromoisoquinoline holds onto its integrity through robust extractions and high-temperature conditions. This isn’t accidental. The nitrogen atom on the ring improves chemical handling — compared to simple benzenes, you get better solubility in both polar and non-polar solvents. As a manufacturer, we keep solvent and temperature tolerances in mind, since researchers and process chemists worry about this every day at scale.
Compared to chlorinated cousins, the bromine atom in 1-Bromoisoquinoline strikes a middle ground. You get higher reactivity than chlorides but with better thermal and hydrolytic stability than iodides. While 1-Chloroisoquinoline costs a bit less to make in bulk and sees occasional use in classic batch reactions, most modern synthesis routes favor the bromo analog because it takes palladium-catalyzed chemistry further — with fewer side products and more straightforward crude workups.
1-Bromoisoquinoline’s primary market lives in pharmaceutical and agrochemical development. Over the years, we’ve watched emerging medicinal chemistry teams move steadily to nitrogen-containing aromatics, seeking compounds that can anchor everything from anti-viral scaffolds to kinase inhibitor libraries. The reactivity at the 1-position means scientists can couple complex moieties without risking interference from other positions on the ring.
Our compound has supported the synthesis of novel CNS-active drugs and anti-inflammatory agents. Detailed feedback from long-term customers has shown that purity matters. A single run of crude material, if not handled with proper separation, leads to byproducts that muddle interpretation in later biological screens. That’s why our control starts upstream: optimizing baths, distillation yields, and final drying steps. We invest in batch-to-batch analysis, typically maintaining residual base content below 0.2% and limiting heavy metals by using glass-lined vessels.
Process chemists tell us time and again that they value consistent melting points and chromatographic profiles. Low darkening upon standing, minimal water content, and freedom from isoquinoline hydrolysis fragments — these details matter at the bench and in pilot reactors. One R&D group shared that shifting from off-brand material to ours dropped their purification burden drastically, cutting column runs from three to one in a drug candidate series. Savings like that compound over time.
Outside the life sciences, the needs of the electronics industry have quietly shifted to emphasize reliable, high-purity intermediates. A few years ago, a customer building new OLED emitters and hole-transport agents approached us after finding material from a trader tainted with unreacted starting material. Their final organic layers sputtered and failed long-term thermal cycling.
In this sector, 1-Bromoisoquinoline acts as more than a simple node — it anchors molecular frameworks designed for electron flow and light emission. The performance of each final device links directly to the microscopic cleanliness and molecular orientation achieved in the synthetic intermediate. With that feedback, we tightened our storage, handling, and final filtration. Shortening oxygen exposure cycles and running in-house spectral monitoring on each bottle stopped trace degradation that could otherwise go unnoticed until a production line stalls.
Electrical engineers regularly cite the need for laser-focused repeatability. Our decades of solvent handling, distillation, and storage have allowed us to meet those needs and anticipate new requirements as the pace of technology pushes forward. We collaborate with key accounts, often receiving feedback directly from device testing labs. Adjusting trace sodium, iron, or magnesium content by as little as a few parts per million can make the difference between working electronics and catastrophic failures.
From time to time, we are asked how 1-Bromoisoquinoline stacks up against alternatives like 2-Bromopyridine, 1-Bromoquinoline, or the even more niche dibromo-doped structures. The answer lies in subtle shifts in electronic density, site accessibility, and ring stability. Isoquinoline — compared to quinoline or pyridine — gives a different π-electron delocalization, which chemists can leverage for more selective bond formation.
A researcher with an eye on structure-activity relationships often chooses isoquinoline because of its better metabolic stability in animal models, compared to simpler aza-arenes. Those familiar with cross-coupling know that bromo-substituted aromatics generally offer a “sweet spot” for C–C and C–N bond formation. We have tested comparable NMR spectra and reaction endpoints with related bromides, and observe that 1-Bromoisoquinoline responds more predictably across a range of ligands and catalytic bases.
During a pilot project, a customer in the specialty polymer area tried to swap in 1-Bromoisoquinoline for a pyridine analog. The result gave higher polymer weights and less discoloration, attributed to the better leaving-group qualities and reduced nitrogen oxidation. They reported an uptick in batch yields, fewer unreacted end-groups, and more robust thermal profiles in downstream extrusion.
Production of halogenated heterocycles has always drawn attention from regulators concerned about emissions and byproducts. Our path towards cleaner synthesis started years ago when we faced escalating waste disposal costs and growing local regulation. We moved away from traditional halogenation using elemental bromine in open systems toward a more enclosed, catalyst-driven process that both cuts reagent losses and limits operator exposure. Today, energy consumption per kilogram of product stands nearly 15% lower than previous years, with solvent recycling rates at nearly 90%.
In effect, the relentless demand for high-quality 1-Bromoisoquinoline forced us to become stewards of our own process emissions. Customers tell us regulatory acceptance in their own countries depends on transparent batch documentation, residual solvent disclosure, and a willingness to trace accountability down to every drum. We long ago learned that a cheap product that fails downstream safety checks or restricts registration isn’t worth anybody’s time.
By improving our isolation methods — such as switching to aqueous-organic phase separation and low-temperature crystallization — we have shrunk both total organic carbon and bromide discharge. Regular audits and annual process validation keep our team sharp and drive continuous improvement, not because it looks good on paper, but because our customers find fewer headaches at the compliance interface.
We occasionally field questions about best handling practices for 1-Bromoisoquinoline. Overstating safety accomplishments doesn’t help anyone; instead, our focus is on practical steps to keep both product and people protected. This compound has a modest vapor pressure, so sealed vessels and nitrogen blankets minimize loss and maintain integrity. We ship in amber glass or fluoropolymer, since both block UV and cut down trace leaching. To the process engineer, small details matter: minimizing agitation shear and running material through taut PTFE lines extends shelf life by months.
Over the years, we have noticed that uncontrolled acid or base exposure leads to subtle yellowing or formation of quaternary salts. These impurities complicate analysis downstream, reducing chromatographic resolution or complicating NMR interpretation. For scale-ups, adding toluene as a transfer solvent has proven useful, while evaporation under vacuum at mild temperatures preserves volatile integrity. Routine Karl Fischer testing ensures water remains below 0.2%, preventing hydrolysis.
For those adopting new synthetic methods, our technical team fields questions on compatibility with cross-coupling catalysts and bases. Experience shows that even low levels of iron or copper residues, sometimes picked up from reused glassware, can poison key reactions. We recommend running initial test scales with trace analysis and atom-balance controls so that any drift in catalyst reactivity gets caught early.
Modern R&D teams do not buy raw materials from casual traders any longer — nor should they. In our early days, we underestimated the cost of rework and quality claims. Years of feedback and troubleshooting taught us to audit every aspect of production, from raw source purity to finished product packaging. Inline spectroscopy now verifies color and clarity before a drop ever makes it into a drum. Each batch receives HPLC and GC-MS characterization, benchmarking against both international pharmacopeia standards and our own tighter internal controls.
Since 1-Bromoisoquinoline can easily co-elute with minor structural isomers in typical purification protocols, we refined our crystallization and column techniques. For customers with especially sensitive formulations, we’ll go further: making single-lot runs, or purifying well beyond standard specifications. Such hands-on attention pays dividends for innovation-driven labs where impurities could spike an entire campaign.
Our lot histories are never secret. Full traceability, including date of production, reactor used, operator logs, and third-party impurity panels, can be shared as needed for registration or audit. Particularly with advanced therapeutics or food-facing applications, regulators expect nothing less. Continuous feedback loops ensure that not only does our product improve, customer confidence builds year after year.
Our business depends on the long-term success of the teams and companies we supply. For years, we’ve watched trends rise and fall: “green chemistry” pushes, the surge of kinase-focused drug discovery, and the evolution of organic LED markets. Through all of it, the need for well-characterized, consistent building blocks such as 1-Bromoisoquinoline has only grown.
By staying closely attuned to our customers’ changing research needs, we gain early visibility into emerging concerns — whether that means tighter N-nitrosamine controls, batch-specific documentation, or custom impurity testing for complex regulatory filings. Regular collaboration makes a difference. It’s more straightforward to solve problems in real time, rather than waiting for a crisis and then scrambling for root cause analysis.
Looking ahead, the market will keep shifting. Sourcing teams now navigate an ecosystem where trust, quality, and transparency outweigh the appeal of the lowest factory price. Since we started, we have adapted our development and QA programs to stay a step ahead of both regulation and research trends. The results show up in fewer customer complaints, better reaction yields, and more successful product launches along the value chain.
Every producer faces tough calls every day. Raw material shortages, rising purification costs, and the unpredictability of shipping logistics test our systems. Yet by focusing on efficiency, sustainability, and high transparency, we weave quality into the fabric of our operation. Advanced real-time analytics help us quickly address deviations; ongoing training keeps our team ready for new demands. We invest in plant upgrades, solvent recovery, and on-site wastewater management so that our output supports not only the immediate needs of research but the future needs of our planet.
From the start, our drive has been to stay present in the chemistry without relying on buzzwords or short-term gains. We welcome feedback and thrive on open dialogue, because every interaction sharpens our understanding of what really matters: reproducibility, safety, and supporting innovation with reliable building blocks.
1-Bromoisoquinoline remains a testament to how hands-on manufacturing and steady process control can deliver more than just a reagent. For global researchers, formulation scientists, and process engineers working to develop the next generation of drugs, electronic components, or functional materials, it forms a trusted, well-understood node in the evolving landscape of organic chemistry. We take pride in each kilogram we send out the door, and in the relationships built with every customer relying on our consistency and partnership.