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HS Code |
631984 |
| Cas Number | 580-16-5 |
| Molecular Formula | C9H7NO |
| Molar Mass | 145.16 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | 222-226 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.266 g/cm3 |
| Synonyms | 6-Quinolol, 6-Quinolinol |
| Iupac Name | quinolin-6-ol |
| Pka | 9.44 (for the phenolic OH) |
| Pubchem Cid | 11718 |
As an accredited 6-Hydroxyquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 6-Hydroxyquinoline is supplied in a sealed 25g amber glass bottle with a tamper-evident cap and clear labeling for safety. |
| Shipping | 6-Hydroxyquinoline is shipped in tightly sealed containers, protected from light and moisture. It should be transported in compliance with relevant regulations for hazardous chemicals, typically as a non-flammable solid. Ensure handling by trained personnel, with appropriate labeling and documentation. Storage during transit should be cool and well-ventilated to prevent degradation. |
| Storage | 6-Hydroxyquinoline should be stored in a tightly closed container, away from light, moisture, and incompatibles such as strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to excessive heat. Label containers clearly and ensure safe, secure storage to prevent accidental spills or contamination. |
Applications of 6-Hydroxyquinoline in Industrial ManufacturingAs a manufacturer with a dedicated synthesis and quality management platform, we supply 6-hydroxyquinoline (6-HQ) to downstream industries that leverage its unique chelating and functional group properties. The following sections highlight specialized industrial applications and integration routes across key sectors where this raw material demonstrates proven value, with all information rooted in direct market and production feedback. 1. Agrochemical Formulations: Synthesis of Fungicidal Active IngredientsAgrochemical producers incorporate 6-hydroxyquinoline as an intermediate for the synthesis of crop protection compounds, specifically systemic fungicides designed to combat plant pathogens in high-value crops. The phenolic and nitrogen moieties of 6-HQ facilitate ring modification reactions necessary for producing active molecules with targeted antifungal properties. Downstream formulators adjust dosing according to target actives and desired agricultural performance, subjecting production batches to batch-wise composition and residue controls throughout the process. The active compounds synthesized are critical for ensuring crop yield in regulated markets, and integration of 6-HQ directly impacts product compliance and efficacy. Industry compliance standards
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2. Pharmaceutical Manufacturing: Active Pharmaceutical Ingredient (API) SynthesisIn pharmaceutical manufacturing, 6-hydroxyquinoline serves as a building block for the synthesis of key APIs, particularly within antibacterial, antimalarial, and chelating formulations. The compound's structure allows for selective substitution, enabling the construction of novel pharmaceutical scaffolds. QC teams monitor raw material purity and batch consistency, aligning with ICH guidelines, as downstream processes demand high reproducibility during multi-step synthesis and purification of finished APIs. Manufacturers incorporate 6-HQ strategically depending on the final API pharmacophore, integrating the material with meticulous stoichiometric control according to validated cGMP protocols. Industry compliance standards
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3. Analytical Chemistry Reagents: Metal Ion Detection SolutionsProducers of analytical reagents deploy 6-hydroxyquinoline for the formulation of complexometric agents used in trace metal analysis. The compound’s binding affinity enables endpoint detection in volumetric and spectrophotometric assays employed in laboratory and industrial QC settings. Formulators adjust concentration levels for standardized solutions, balancing chelation strength for various analytical matrix requirements. The raw material is introduced during the reagent preparation phase, and all production adheres to traceability and purity requirements outlined by reagent-specific guidelines, ensuring consistency in calibration and detection limits. Industry compliance standards
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4. Corrosion Inhibitor Additives: Metalworking and Water Treatment BlendsManufacturers of water treatment formulations and metalworking fluids utilize 6-hydroxyquinoline as a specialty chelating agent and biocide booster to improve corrosion inhibition efficacy in both ferrous and non-ferrous systems. Its role is to interrupt oxidative chain reactions, thereby extending the service life of machinery and infrastructure exposed to aggressive water chemistries. Formulation chemists optimize the additive range based on system pH, temperature, and compatibility with existing inhibitors. The integration of this additive occurs directly during formulation blending stages, and downstream processes comply with industry standards for corrosion performance and safe application in technical installations. Industry compliance standards
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5. Luminescent Material Precursors: Synthesis of Organic Photoluminescent CompoundsIn the specialty materials sector, downstream manufacturers use 6-hydroxyquinoline for the production of organic ligands that serve as core components in light-emitting materials. The compound’s structural motif allows precise tuning of emission properties, resulting in advanced photophysical characteristics critical to device application. The production process requires careful control over substituent modification and purification to achieve necessary intensity and wavelength stability for end-use scenarios in optoelectronics. The concentration of 6-HQ in precursor solutions is fine-tuned to optimize device performance, and end-to-end traceability is maintained in compliance with materials specification standards. Industry compliance standards
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Over the years spent at the production site, working through batches and troubleshooting process improvements, 6-Hydroxyquinoline has become one of those dependable intermediates that season after season keeps drawing technical interest. This compound, often abbreviated as 6-HQ or by its CAS number 580-16-7, continues to play a practical role in complex synthesis for both research and large-scale applications. The appeal of 6-Hydroxyquinoline doesn’t start and end at raw specifications on a datasheet. As the team responsible for its synthesis, we understand firsthand that the tight controls and reliable consistency in each lot matter more to our customers than just purity numbers.
Manufacturing starts at procurement. Consistent quality begins with the choice of raw materials and doesn’t waiver through the end of the distillation column. Our main model of 6-Hydroxyquinoline is supplied as a pale yellow crystalline powder, rarely deviating from this appearance. Purity usually exceeds 99% by HPLC, and water content remains under 0.3%. The melting range stays in check at 225-229°C. More than certificates, these values reflect what we see batch after batch, with our process tuning focused on reproducibility rather than claims on a page.
Laboratory users often request 6-HQ in 25 kg fiber drums for safety and ease of weighing. For smaller scale, we prepare 1 kg and 5 kg options with double sealed liners to protect from trace moisture. Our experience has taught us that moisture plays a disproportionate role in downstream reactions, especially where salts risk forming or where subtle oxidation can impact the next synthetic step. That’s why we maintain rigorous granularity and tailoring—not for marketing purposes but because those details push reactions to completion the way chemists want. A batch that fails on color or texture means lost time and trust, so we keep these parameters tight.
Each batch gets tested for residual solvents, with results well below ICH guidelines, since downstream compatibility is rarely negotiable with customers requiring 6-HQ for API intermediates. At our scale, it’s not about volume churn; it’s about every sack giving the exact performance researchers expect once they commit process capital.
Those who have tried 6-Hydroxyquinoline from multiple sources notice the batch-to-batch differences that creep in—soft off odors, marginal solubility shifts, or even unplanned reactivity in sensitive syntheses. By controlling reaction environment parameters (precise temperature control, solvent quality, and rigorous pH adjustments), we have gradually eliminated the mysterious side reactions that plagued initial small-batch suppliers.
Our team has learned from direct troubleshooting with customers. Once, a research group observed trace pink coloration in their final product, traced back to an upstream impurity from a sub-par batch of 6-HQ. It wasn’t enough to fix the immediate lot—they needed tight feedback and assurance that the plant floor was adjusting practices rather than pushing the problem down the line. Over time, investing in additional crystallization steps and deeper filtration checks, we’ve locked down the issue. This process shaped how we view the business: it’s a partnership grounded in technical transparency.
So much focus inside chemical manufacturing falls on the big capital projects—yet, for specialties like 6-Hydroxyquinoline, the true difference comes from attention to detail and the willingness to act on customer feedback at the operational level.
At the plant, we map out demand patterns by hearing directly from both researchers and production chemists using this molecule. The most common usage for 6-Hydroxyquinoline remains as a key intermediate in the synthesis of pharmaceuticals, especially for antimalarial and antitubercular drugs, agrochemicals, dyes, and corrosion inhibitors. The hydroxyl group at the sixth position is a crucial functional handle, making it possible to pursue site-selective transformations with high yields.
In pharmaceutical synthesis, 6-HQ works as a starting point for compounds like clioquinol and certain antiprotozoal agents. Its structure allows for targeted modification at the quinoline ring, creating derivatives that act with superior selectivity and lower side effects. For customers in crop science, the same reactivity is harnessed to develop new phyto-regulators and fungicides.
Research institutions rely on our 6-HQ for metal ion complexation studies. Its chelating properties—originating from the proximity of the hydroxyl and nitrogen atoms—give a practical edge in analyzing trace metals. Sometimes, end users need help understanding why a result fails to replicate published findings, and more often than not, the solution lies in the purity of the starting 6-HQ or control of trace ions. As manufacturers, we’ve developed targeted grades for researchers requiring ultra-low heavy metals, adjusting both synthesis and post-processing.
Industrial dye houses leverage 6-Hydroxyquinoline for its chromophoric properties, improving stability in acidic and basic media. The demand for reproducible shades through multiple dyeing cycles means trace oxidative impurities can’t be tolerated. We’ve honed the process to ensure the final powder meets fixed UV absorbance profiles, with regular feedback from textile technologists.
It’s tempting for traders to group all quinolines together and treat them as swappable. Production experience shows the gaps between them are not just theoretical; they have real downstream impact. Take 8-Hydroxyquinoline as an example—useful in chelation but with different solubility and reactivity due to the position of the hydroxyl group. 6-HQ reacts less at the nitrogen site and provides a better leaving group in some stepwise syntheses, avoiding excessive side reactions.
Another case occurs with simple quinolines lacking hydroxyl substitution. These are often cheaper but don’t achieve the same level of reactivity in palladium-catalyzed coupling, or fail to anchor substituents for specialty dyes. We routinely explain to clients why switching to a superficially similar intermediate can risk lower product yields or introduce purification problems they hadn’t budgeted for.
6-Hydroxyquinoline sets itself apart by offering a balance between functional group reactivity and molecular stability. The para arrangement between the nitrogen and hydroxyl creates a unique electron distribution, supporting transformations that other isomers can’t match without additional steps. This becomes evident in chiral catalysis, selective methylation, or the development of ligands for asymmetric synthesis.
We’ve also seen customers ask whether to switch entirely to the more readily available 5- or 7-hydroxy derivatives to save on lead time. In practice, such decisions bring on new process controls, revalidation work, and the risk of costly delays when the chemistry doesn’t translate as anticipated. Over years of manufacturing, it has proven more cost-effective to source dedicated 6-HQ produced for purpose than to retrofit existing methods for other, less specific building blocks.
The chemistry world today expects sustainability from all levels of industry, and rightly so. On the manufacturing floor, we’ve moved step by step toward greener synthesis routes. Early production methods for 6-Hydroxyquinoline generated significant organic solvent waste and left purification as a major bottleneck. After several years of process optimization, we now capture and reuse more than 80% of solvents on site and have reduced aqueous effluent chlorides by over half. This shift emerged not from external pressure but from the practical recognition that sustainable practices cut costs and improve safety for our operators.
Applying catalytic hydrogenation to precursor steps, we reduced batch reaction times and toxic byproducts. Heat integration between reactors has helped repurpose waste heat, improving energy efficiency and keeping plant emissions down. Our analytical lab tracks every input and output, with GC and LC-MS monitoring set up to pinpoint minor impurities and guide waste stream segregation.
Compliance comes from a deep understanding of local and global expectations—REACH registration, up-to-date SDS, and tightly monitored transportation protocols. We work in partnership with regulators and client EHS specialists, not only to tick boxes but to adapt real practices for safer downstream handling. Ultimately, these efforts show in cleaner, safer finished products for labs and industrial users. Customers continue to prefer suppliers who demonstrate an actionable record on safety and the environment, and we see positive feedback reflected in long-term purchasing relationships.
Japanese and European customers occasionally report delays due to international shipping snarls, demanding tighter lead-time management from our team. Shortages of certain precursor chemicals during global supply chain stress test everyone’s ability to maintain steady production. We’ve responded by building dual-source options for critical raw materials and running buffer inventories, all visible from our central resource planner instead of leaving it to chance.
Some customers—especially in pharmaceutical and agrochemical sectors—need documentary support for audits at short notice, or batch-specific impurity maps to accompany every shipment. Our records management is set up so every lot, however small, comes with tracked synthesis details and full COA transparency. The more demanding the application, the more detailed support required. One practical improvement was digitizing all release paperwork, speeding up audit responses for customers under regulatory pressure.
A project involving custom particle sizing for a client in high-performance coating brought new challenges. Standard 6-HQ granulation proved too coarse, creating suspension instabilities and process fouling. Our team modified grinding and sieving protocols alongside fine-tuned solvent crystallization, successfully delivering a lot that matched both their mesh requirement and avoided dusting losses. Feedback from that project led to wider adoption of similar particle size controls in future batches. These lessons transferred to other specialty clients, opening opportunities in areas like optical brighteners and catalyst supports.
Sometimes, a customer will design a new route based on lab-scale 6-Hydroxyquinoline, only to find the reaction profile changes on plant scale—conversion rates slow, impurities spike, or yields drop. We’ve found solutions start with honest dialogue, open sharing of analytical data, and, when possible, joint trouble-shooting over weeks rather than quick-fixes offered by third parties. Our iterative approach, grounded in lab-to-pilot batch feedback, solves more problems than one-off sales can. Clients remember the hands-on technical input, which often tip the balance toward successful commercial scaling.
Our plant isn’t simply a chemical pipeline. Over the years, nearly a third of the clients we support bring projects that need adjustments—a change in particle size, a non-standard package, or an experimental purification protocol for a new research direction. Accommodating these requests builds a relationship of technical trust, and also keeps our in-house process team sharp. We track internal katas—documenting every process adjustment with results and pitfalls—so we don’t just reinvent the wheel each time, but refine our procedures and keep learnings accessible.
Recently, we assisted a startup working in OLED materials, who found trace levels of a specific halogenated impurity crippled their emission performance. We coordinated real-time analysis, scrubbed the process, and provided small-scale lots for iterative testing, culminating in a product that met their functional requirements. This type of iterative collaboration turns standard 6-HQ production from a commodity task into a continuous, customer-focused improvement cycle.
The push for low heavy-metal grades in catalyst research speaks to the evolving industry landscape. Simple tweaks at the purification stage—additional passes over chelating resins, filters, and distillation integrity checks—translate to batches with metal content often ten-fold lower than before. Every technical success feeds into the broader momentum toward more selective catalysts, better drug intermediates, and new materials for emerging fields.
Looking forward, the demand trajectory for high-purity 6-Hydroxyquinoline grows alongside advanced synthesis techniques in pharmaceuticals, electronics, and materials research. The challenge is not only in producing greater volumes, but in pushing the boundaries on batch-to-batch reproducibility and adaptability to stricter impurity profiles.
From our vantage working inside the production loop, the road ahead will involve blending core manufacturing discipline with rapid technical feedback from customers. Integrating digital tracking, predictive quality control, and sustainability initiatives feels less like a trend and more a baseline for doing business. Real progress happens not with slogans, but with ongoing investments in both plant infrastructure and technical staff who understand the finer points of organic synthesis and industrial logistics.
We see every kilogram of 6-Hydroxyquinoline leaving the plant floor as a reflection of cumulative experience. Beyond specs and sheets, it carries with it the trust built with customers facing high-stakes chemistry. As markets change and new applications emerge—from quantum electronics to molecular imaging—our mission remains adapting our practices so clients can rely on each batch, project after project.
In the end, the story of 6-Hydroxyquinoline is a story of craft—a constant interplay of chemistry, teamwork, and technical curiosity. While lab books and production records document the process, it’s the day-to-day effort behind every batch that sets the real foundation for long-term value.