|
HS Code |
338681 |
| Chemical Name | 5,6-Benzoquinoline |
| Molecular Formula | C13H9N |
| Molar Mass | 179.22 g/mol |
| Cas Number | 85-02-9 |
| Appearance | Yellow crystalline solid |
| Melting Point | 76-78 °C |
| Boiling Point | 359 °C |
| Density | 1.19 g/cm³ |
| Solubility In Water | Insoluble |
| Pubchem Cid | 7046 |
| Iupac Name | benzo[h]quinoline |
| Smiles | c1ccc2c(c1)cccn2 |
| Synonyms | 5,6-benzoquinoline, benzo[h]quinoline |
As an accredited 5,6-Benzoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5,6-Benzoquinoline, 25g: Supplied in an amber glass bottle with tamper-evident cap, labeled with hazard warnings, product, and supplier details. |
| Shipping | 5,6-Benzoquinoline is typically shipped in tightly sealed containers made of compatible materials to prevent leaks and contamination. It should be labeled according to hazardous material regulations and transported under controlled conditions, avoiding heat, ignition sources, and moisture. Shipping documentation must comply with local and international chemical transport guidelines. |
| Storage | 5,6-Benzoquinoline should be stored in a tightly closed container in a cool, dry, well-ventilated area. Keep away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature and ensure proper labeling. Use appropriate containment to prevent environmental release. Handle with gloves and protective equipment when accessing or transferring the chemical. |
Applications of 5,6-Benzoquinoline in Industrial ManufacturingOur 5,6-Benzoquinoline is produced to meet the stringent requirements of multiple industrial sectors where precise molecular features enable advanced product functionalities. Below, we present the most significant downstream applications, breaking down key aspects for each scenario to assist technical teams and procurement managers in their evaluation and formulation decision-making. 1. Organic Light-Emitting Diode (OLED) Emissive LayersMajor display panel and lighting manufacturers use 5,6-Benzoquinoline as a ligand in the synthesis of iridium-based phosphorescent complexes, which are crucial in green and yellow emitting layers for OLED devices. The intricate coordination chemistry enhances emission efficiency and extends device lifetimes, addressing demands for high color purity and operational stability in consumer electronics and professional displays. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Heterocyclic Intermediate for Pharmaceutical SynthesisActive substance manufacturers utilize 5,6-Benzoquinoline as a building block in synthesizing advanced heterocyclic structures required for late-stage pharmaceutical intermediates. Its chemical profile enables efficient substitution and condensation reactions, shortening synthetic routes for molecules targeting anticancer and anti-infective therapies in preclinical and clinical development. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Photoluminescent Sensor DyesAnalytical instrument and sensor manufacturers value 5,6-Benzoquinoline derivatives for use as fluorescent probes and sensor dyes in environmental and medical diagnostics. The molecule’s electronic properties allow tuning of emission wavelengths, enhancing detection selectivity for metal ions and volatile organic compounds across a range of analyte concentrations under robust operating conditions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Ligand Agent for Homogeneous CatalysisFine chemical and specialty polymer producers employ 5,6-Benzoquinoline as a chelating ligand in transition-metal catalyzed C–C and C–N coupling reactions. Its nitrogen-rich aromatic core stabilizes catalytically active metal centers, increasing catalyst lifetime and conversion rates in processes demanding high selectivity and minimal impurity formation, particularly in custom API or monomer synthesis. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 5,6-Benzoquinoline prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
From years of hands-on experience in chemical synthesis, certain molecules stand out not just for the technical challenge they present, but for the real utility they offer throughout various applications. 5,6-Benzoquinoline is one of those specialty intermediates our team has been producing for advanced materials and fine chemicals projects that demand reliability. Recognized chemically as a fused aromatic heterocycle, this compound brings together the potency of a quinoline backbone with a unique positioning of its benzene ring, forming the structure C13H9N. Instead of focusing on textbook properties or copy-paste datasheet lines, it’s more helpful to share what this compound means in practice—to those actually making, handling, and relying on it from batch to batch.
In actual day-to-day manufacturing, purity isn’t just a number to publish—it’s often the difference between a successful reaction and a costly reset. Our 5,6-benzoquinoline batches typically reach purities above 99% by HPLC, going well beyond what’s found through many other commercial channels. Several years back, we tackled persistent side-product contamination until repeated recrystallization and the use of carefully staged distillation lines finally allowed us to lock in a high-purity standard. For partners building up OLED materials, pharmaceutical intermediates, or specialty ligands, low impurity content translates to greater reproducibility in the next synthesis steps.
Unlike commodity grade quinolines, which often carry residual tars and other fused ring contaminants, 5,6-benzoquinoline requires strict inert-atmosphere processing to prevent uncontrolled side reactions, especially during cyclization. Our process control systems are built around this need. Trying to cut corners on nitrogen blanketing or workstation cleanliness quickly becomes evident, as yields and spectral purity drop off. Technicians often notice the difference during column chromatography much earlier than any instrument detection—more color, more tailing, stickier residues. Attention at each step produces a product suited for further coupling, metal complexation, or electronic device fabrication.
Benzoquinolines occupy a somewhat niche space in fine chemical synthesis, but those who work in molecular electronics, ligand synthesis, or photophysical research value them for their performance and reliability. In our collaboration with research groups developing OLEDs and NIR photoluminescent materials, 5,6-benzoquinoline acts as a core building block. Its extended conjugation and nitrogen insertion enable both electron-affinity and metal-binding capabilities not found in simpler quinolines.
Some customers approach us to compare 5,6-benzoquinoline with the more common 2- or 8-quinoline derivatives. Reference samples make the differences clear. 5,6-Benzoquinoline displays a distinct UV-vis absorption pattern, which researchers utilize for targeted energy transfer in device layers. Its nitrogen lone pair sits in a different spatial orientation, impacting both electronic effects and downstream functionalization. When we replaced 2-quinoline in a coordination complex with 5,6-benzoquinoline as a test, the resulting iridium complex showed improved emission characteristics—all thanks to that small tweak in ring fusion.
In pharmaceutical intermediate work, this molecular scaffold offers a fresh approach. We’ve seen projects adopt it for synthesizing molecules that require enhanced aromatic stacking interactions, or for introducing selectivity in metal-catalyzed transformations. Customers have relayed that attempts to use isomeric or homologous quinolines didn’t offer the same chelating profile or stability, especially when pushing reactions under harsher conditions.
Producing 5,6-benzoquinoline on a consistent scale requires attention to detail—not just in theoretical process design, but in every kilogram produced. Lab-scale glassware tests taught us how sensitive the reaction is to solvent purity and temperature gradients. Scaling that up meant redesigning heat transfer surfaces and optimizing our agitation systems. The compound is typically supplied as a pale yellow crystalline solid, melting around 78-80°C, and shows negligible vapor pressure at room temperature. Moisture sensitivity remains low under standard warehouse conditions, though we recommend storing it under desiccant for any work above a few months. Not all manufacturers can match both analytical (HPLC, GC-MS) and synthetic lot-to-lot consistency. Our in-house QA/QC team checks every drum before dispatch, ensuring the color, odor, and melting point meet strict acceptance criteria.
The particle size distribution often affects downstream handling, especially for those working in automated weighing or feed systems. Through feedback from customers in catalyst synthesis, we tuned our grinding and sieving process to minimize dust and agglomeration—a small adjustment that cut down on both loss and static electric charge issues. Attributes like solution clarity and filterability might sound trivial, but for those in scale-up process development, they make a difference between smooth operation and unplanned cleanup.
Manufacturing brings direct exposure to all the quirks of each chemical. 5,6-Benzoquinoline rarely presents acute risk with routine lab handling, yet its mild skin and mucous membrane irritation remains worth mentioning. New team members receive PPE protocols, and we always keep spill kits and eyewash stations ready during charging and transfer steps. On a few occasions, improper ventilation in scale-up rooms led to persistent aromatic odors, so our facilities continuously upgrade air handling systems to keep workplace exposure well below recommended limits.
Transport remains comparatively straightforward, as 5,6-benzoquinoline does not fall under any major hazardous material regulations. Proper drum sealing and moisture-resistant lining prevent both product loss and label degradation. For customers repackaging into smaller vials, we recommend using PTFE-lined caps and avoiding prolonged light exposure, as the compound retains optical activity suitable for photophysical characterization.
Chemists sometimes group quinolines together, yet structural differences can mean pronounced changes in reactivity and utility. 5,6-Benzoquinoline, with its unique fusion point, offers higher pi-conjugation than, say, 2-quinoline or 8-quinoline. This produces a deeper color, as seen by its faintly greenish-yellow tinge, and stronger electron-donating characteristics. As a ligand, it binds metals with both greater selectivity and altered electron density, which matters especially in synthesizing transition-metal complexes for light-emitting applications.
Working in dye and pigment synthesis, researchers report that using 5,6-benzoquinoline opens up new chromaticity ranges compared to using the standard quinoline ring. Its presence can shift emission maxima, letting formulators fine-tune color coordinates. In our own QC analytics, introducing 5,6-benzoquinoline into structure-activity studies highlights how subtle changes in ring fusion directly translate into stability, solubility, or reactivity differences. Looking at TLC and HPLC profiles, the retention times stand apart from other isomers, showing real separation in both chemical behavior and end use.
Certain batch customers ask about differences in trace metal content, as many downstream reactions use benzoquinoline as a ligand. Our process employs steel-free synthesis vessels for this reason, which keeps transition and heavy metal levels below the practical detection threshold of 10 ppm. Feedback from catalysis specialists indicates a clear preference for such low-background products, which allow tighter experimental control. Alternative synthetic routes, especially those relying on cheaper starting materials or less careful purification, struggle to achieve reagent-grade specifications suitable for demanding research.
Achieving material that consistently meets premium specifications is not simply about following SOPs—it’s a continuous process of troubleshooting and improvement. Over a decade of pilot and manufacturing experience has taught us that crude benzoquinoline synthesis invariably throws up issues: incomplete cyclization, unexpected dark impurities, and difficult crystallizations. Our R&D and production chemistry teams collaborate closely, using both analytical chemistry advances and practical hardware upgrades (e.g., better jacketed reactors, inline filtration) to keep each lot within spec.
Trace impurities can greatly affect photophysical research, leading to spectral background or unwanted side reactivity. Early on, a few lots failed in customer OLED tests due to trace phenanthridine contamination, which was only spotted after collaborative troubleshooting with university partners. To fix the issue, we invested in targeted GC-MS screening and closely tracked our upstream solvent sources, cutting unwanted side products to the lowest practical levels. Later on, switching to fully inertized transfer lines reduced oxygen and moisture ingress, driving up both yield and product shelf life.
Some end users need highly customized particle size or specific solution concentrations. Rather than producing generic lots for bulk resale, we fine-tune grinding, packing, or dissolving steps on request. In several cases, supplying freshly ground or pre-dissolved product led to fewer failed reactions and less batch-to-batch adjustment for customers. Situations like these highlight the benefit of working with a truly hands-on manufacturer, who has skin in the game and adjusts their process to real feedback.
Synthesizing advanced molecules like 5,6-benzoquinoline puts us in constant contact with R&D scientists, scale-up engineers, and exploratory project leaders. These partnerships don’t just drive sales—they inform our process optimization and new applications. In one collaboration, university chemists testing new ruthenium catalysts called us to discuss batch variance they had observed in competitive samples. Comparing their spectral data to ours, we helped them pinpoint a minor N-oxide impurity present in a rival supplier's lot. In the process, our own QC was strengthened and their research work accelerated.
A similar case arose with a pharmaceutical company seeking unique benzo-fused heterocycles for kinase inhibitor scaffolds. We worked together to deliver extra-pure 5,6-benzoquinoline and customized the batch history to trace the exact solvent and raw material origins. These projects pushed us to tighten traceability and batch documentation protocols—not some one-off marketing ploy, but in response to real needs from industry innovators working at the frontier.
Many new customers initially come from commercial distributors with little familiarity with the hands-on realities of specialty chemical manufacture. Some expect standard answers or only want to hear about general specifications. We find that the real value comes in discussing concrete process or application details: how long the material can be stored unopened, how it behaves in specific solvents, how best to filter or blend it, or what to expect if minor discoloration occurs over time.
For those used to lab-scale purchasing, questions about upstream raw material traceability, impurity profiles, or lot-to-lot variation become central as projects move into pilot or full-scale production. Our approach favors open communication, grounded in decades spent running both small glassware and multi-ton reactors. Experienced chemists on both sides save time and cost by talking frankly about observed issues—whether it's a clumping problem during storage or a small but persistent baseline drift on analytical HPLC runs. Working directly with a manufacturer, instead of through multiple middlemen, keeps both troubleshooting and product improvements moving forward efficiently.
Those who invest in research or production using fine chemicals rely on consistent, transparent supply. Our ongoing experience producing 5,6-benzoquinoline reflects this commitment. From raw material selection, through validated synthesis protocols, to final QC release, each batch passes through multiple skilled hands and detailed checks. This approach allows users to focus on discovery and innovation, not sourcing uncertainty or unexpected technical roadblocks.
Years of direct feedback and problem-solving have shaped both our product and our process. Modifications driven by real-life application experience—from improved powder handling to enhanced traceability—stand as proof that thoughtful manufacturing adds value beyond simple technical minimums. Tellingly, repeat customers often cite not just purity or technical data, but the practical reliability and openness our team offers at every stage of sourcing and application.
5,6-Benzoquinoline will continue finding new roles as a building block for advanced optical materials, specialty catalysts, pharmaceutical scaffolds, and functional dyes. As device architecture and molecular design become more sophisticated, subtle ring-fusion differences matter even more. Our ongoing process R&D investigates alternative synthetic routes, greener reagents, and further scale-up improvements to support both established and growing markets.
We welcome ongoing input and challenge from the scientific and industrial community, as every partnership brings a new perspective and often better solutions. By continually refining both product and process based on actual user feedback, we make sure our 5,6-benzoquinoline remains a reliable and well-understood option for specialists pushing at the edge of what these molecules can offer. For us, it’s not about resting on technical capability, but about supporting progress in ways only a dedicated manufacturer can.