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HS Code |
777715 |
| Cas Number | 3879-83-8 |
| Iupac Name | 6-hydroxy-1H-indole |
| Molecular Formula | C8H7NO |
| Molecular Weight | 133.15 |
| Appearance | Off-white to light brown crystalline powder |
| Melting Point | 174-177°C |
| Solubility In Water | Slightly soluble |
| Pka | 9.89 |
| Pubchem Id | 11301 |
| Smiles | C1=CC2=C(C=C1O)NC=C2 |
| Synonyms | Indol-6-ol; 6-Hydroxy-1H-indole |
| Storage Conditions | Store at 2-8°C |
As an accredited 6-Hydroxyindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 6-Hydroxyindole, labeled with chemical name, structure, CAS number, and hazard warnings. |
| Shipping | 6-Hydroxyindole is shipped in tightly sealed containers to prevent exposure to air and moisture. It is handled as a chemical substance requiring standard precautions, including labeling for safe transport. Shipping complies with regulatory guidelines, and the package includes safety documentation for handling, storage, and emergency procedures during transit. |
| Storage | 6-Hydroxyindole should be stored in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed and protected from light and moisture. Store separately from incompatible substances such as strong oxidizing agents. Use appropriate labeling and ensure proper chemical containment to prevent contamination or accidental release. |
Applications of 6-Hydroxyindole in Industrial ManufacturingAs a primary manufacturer of 6-Hydroxyindole, we supply specialized grades supporting precise production needs across several demanding industrial sectors. The following sections illustrate real application scenarios, highlighting integration, compliance, and process design at the heart of modern formulation and material science industries. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis6-Hydroxyindole acts as a critical building block in chemical syntheses for various API classes, especially indole-based compounds with neurological and metabolic indications. In GMP-compliant facilities, chemists react 6-Hydroxyindole via acylation, alkylation, or condensation for target molecule elaboration. Its purity directly affects yield and impurity profile in these multi-stage syntheses, and strict in-process controls monitor the transition through the intermediate phase. Process integration relies on maintaining batch-to-batch consistency, tailored by each partner’s target pharmacological structure. We ensure consistent reactivity for smooth transition into subsequent coupling or cyclization stages. Industry compliance standards
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2. Dye and Pigment Synthesis for Specialty PrintingManufacturers in colorant industries employ 6-Hydroxyindole as a heterocyclic aromatic core to construct complex azo and indigoid dye structures. Its hydroxyl substitution enables regiocontrolled coupling or oxidation for deep blue and violet hues, valued in solvent-resistant and high-fastness applications. Quality requirements focus on elemental and trace metal content, safeguarding against color deviation and batch variability. Due to its intrinsic reactivity, precise process design chooses point-of-addition and stirring regimes based on solvent systems and target pigment crystallinity. Our supply ensures low-ash, filtered grades for reduced aggregation and uniform chromophore generation. Industry compliance standards
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3. Biochemical Reagent Production for DiagnosticsDiagnostic reagent manufacturers utilize 6-Hydroxyindole in synthesis of fluorescence and chromogenic substrates for clinical assay kits. The indolic structure’s electron-rich environment readily couples with enzymatic or peroxidase-based detection systems, enabling accurate quantification in ELISA and colorimetric tests. Each batch requires low UV-active impurities and maximum traceability, directly impacting final assay background and calibration curves. Application methods tightly control aliquot concentration and sequence, as excessive addition leads to background interference while underdosing limits sensitivity. The material enters downstream process during late-stage conjugation steps and is analyzed by HPLC or LC-MS to confirm reagent integrity. Industry compliance standards
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4. Research Chemical Supply for Neurotransmitter Pathway StudiesResearch institutions and specialized chemical suppliers employ 6-Hydroxyindole for in vitro investigation and metabolic pathway elucidation of indole-derived neurotransmitters, especially for serotonin, melatonin, and tryptophan research. Laboratories require the raw material free from trace solvents, N-oxides, and polymeric residues to ensure reproducible findings in mass spectrometry, NMR, and enzyme assay systems. Formulation varies by experiment, with microgram- to gram-scale usage, but always under controlled concentration and diluent protocols, essential for kinetic and inhibition studies. Material is introduced during standard or isotopic enrichment labeling, often as a direct addition to buffered biological models or as a synthetic handle for analog preparation. Industry compliance standards
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Over the years, our team has handled a wide array of fine chemicals, but few intermediates spark the same level of interest among research chemists as 6-hydroxyindole. While many analogues cluster around pharmaceutical labs and dye synthesis, 6-hydroxyindole roots itself squarely in the workbenches where breakthroughs happen. Considering daily conversations with formulation chemists and process engineers, it’s clear this product responds directly to the need for clean, reliable building blocks in specialized synthesis.
Produced through our own controlled hydrolysis and purification routes, our 6-hydroxyindole (CAS No. 2380-94-1) offers high-purity grades in both small research-scale quantities and scaled-up batches. The fine, off-white crystalline powder remains stable under proper storage, and our lot-to-lot consistency traces back to careful selection of precursors, routine in-process testing, and feedback from downstream users. We know firsthand that unpredictable intermediates make for headaches at the next step, so we pay attention where it counts—particle size, purity, and residual moisture especially.
Specification sheets follow the practical needs of synthesis rather than fixed standards etched in stone. Our current offering sits at ≥98% purity HPLC, with moisture content consistently below 0.5%. Typical package sizes range from 25 grams up to multi-kilogram pails, and we maintain inventory for rapid turnaround. This approach grew out of repeated requests from R&D chemists, who often need small-batch consistency for medicinal chemistry rounds before scaling for pilot work.
What sets our product apart has less to do with high-gloss marketing and more with the way our production technicians monitor color and throughput from each batch. Consistent morphology improves wettability and handling—indispensable when transferring 6-hydroxyindole from jar to reaction flask. Few things slow down a project more than unreliable flow or unpredictable clumping, so we run in-house quality checks on every lot before shipment.
Over twenty seasons in the chemical manufacturing sector have shown that certain heterocycles crop up over and over in the most interesting projects. 6-Hydroxyindole falls into that category for good reason. Its unique position on the indole skeleton—hydroxylated at position six—makes it a go-to intermediate for producing pharmacologically relevant compounds and agricultural research materials. The electron-donating hydroxyl group presents new functionalization points, streamlining downstream chemistry compared to unsubstituted indole or other isomers.
Feedback from our regular clients—university researchers, pharmaceutical startups, and dye chemistry labs—suggests ongoing preference for this particular hydroxy derivative. Not only does it offer a path to diversified substitutions through electrophilic aromatic substitutions, but it also supports selective oxidation and alkylation processes. Our in-house technical team has observed that routine procedures sometimes need tweaking, especially in electrophilic substitution reactions, where regioselectivity can drift with subtle purity shifts in the starting material. This reinforced our decision to produce and test each batch with end-use in mind.
The organic market contains a broad range of indole analogues—3-hydroxyindole, 5-hydroxyindole, and more. Working alongside bench chemists and watching application trends, certain contrasts emerge. 3-Hydroxy and 5-hydroxy derivatives remain heavily used in neurotransmitter and natural product research. Their mainstay comes from closer resemblance to known biological products. In contrast, the fewer natural derivatives of 6-hydroxyindole mean it serves more as a synthetic “tool molecule”—less common, but all the more crucial in routes where standard isomers aren’t practical.
We’ve seen several synthetic sequences benefit from 6-hydroxyindole as a key intermediate, especially in constructing expanded heterocyclic rings, specialized pigments, or drug libraries. One notable advantage rests in its lower tendency for side condensation compared to more electron-rich positions—this means less by-product removal, tighter product profiles, and higher overall yields downstream. Technical teams confirm that while 3- and 5- substitutions bring value in their own right, 6-hydroxyindole opens up space for synthetic imagination by circumventing common pitfalls like competitive oxidation or undesired by-product formation.
A modern chemical manufacturer doesn’t operate in isolation. Years of practice have taught us that diligent waste management starts by minimizing unreacted residues and side-products from early steps onward. For each batch of 6-hydroxyindole, we recycle solvents and recover valuable minerals—not because compliance manuals say so, but because it’s the practical way to run a cost-effective operation with reduced disposal needs. Our process engineers push continuous improvements, using real-world data from energy meters and discharge records to tighten up yields and reduce resource intensity every season.
Colleagues working in European and North American research settings sometimes express concern about contaminants and trace impurities in imported intermediates. We listen closely and respond by deploying modern chromatographic and spectroscopic methods at several points in the production line. Years of dialogue with analytical chemists convinced us that transparency, traceability, and responsive support lay the groundwork for lasting partnerships. Our willingness to provide detailed batch analyses—and to discuss technical limitations without hiding behind jargon—sets us apart from larger, more transactional suppliers.
Rigorous control over source material cascades into reliable outcomes in end-use applications. Some of the most rewarding collaborations stem from sharing data on how 6-hydroxyindole behaves in exploratory syntheses. Routine alkylation, acylation, or diazotization processes depend on tight control of functional group reactivity. The electron-rich aromatic nucleus remains accessible for directed transformations, and the hydroxyl at position six serves as a versatile handle.
Development chemists working on fluorescent dyes, serotonin analogues, or extended pi-conjugation systems turn to our product for reproducible starting points. Experience shows that reliable melting points, consistent UV profiles, and minimal trace-metal content often spell the difference between unsuccessful and successful multi-step programs. We tailor isolation and drying protocols based on honest discussions with users—each new project feedback loop directly improves the next batch.
No chemical product is perfect. Over the past decade, our own R&D teams and external collaborators documented quirks that sometimes arise during the handling and use of 6-hydroxyindole. Extended exposure to air or moisture prompts gradual oxidation, leading to subtle color changes or decreased assay value. Proper storage in tightly sealed containers under inert atmosphere, away from direct light, practically eliminates this issue. On rare occasions, batches shipped during humid monsoon months needed repackaging or additional drying—a direct result of feedback from customers rather than ambitions for tighter specs on paper.
Some end-users raise technical questions concerning downstream compatibility with enzymatic or metal-catalyzed transformations. We keep open lines with academic and industrial groups testing our 6-hydroxyindole in applications as diverse as photochemically induced cyclizations to C–H bond activation. This collaboration approach drives our ongoing work on improved analytical support and batch traceability. Our strength as a manufacturer lies in quick response, whether that means additional documentation for regulatory review or technical troubleshooting for a stuck reaction.
Producing specialty chemicals like 6-hydroxyindole involves more than running a clean synthesis. Raw material prices, energy costs, and transportation challenges all affect final product availability and turnaround. Familiarity with international shipping and evolving regulations—like REACH compliance or customs declarations—arises from years of hard-earned experience. We routinely advise users on how best to store and handle shipments, drawing from real stories of customs holdups or temperature excursions en route. As a manufacturer, clear communication and practical packaging solutions create fewer headaches and lower hidden costs.
For many biopharma and materials research clients, the traceability of intermediates influences project viability. Our documentation standards grew out of real regulatory requests—full batch histories, analytical reports from independent laboratories, and detailed COA data attached to every lot. We encourage feedback on any unexpected findings, knowing that open dialogue sharpens trust over the long term.
Direct knowledge from our shipping and storage crews proved invaluable over time. The crystalline nature of 6-hydroxyindole minimizes dusting, and the relatively low vapor pressure simplifies handling. Still, prolonged exposure to ambient conditions leads to slow degradation—something we learned by examining returned samples from long-distance shipments. Keeping containers airtight and protected from humidity pays off. Based on customer input, we developed better moisture-barrier packaging, reducing product complaints and saving time for lab managers who used to worry about spoilage.
On the floor, clean transfer with minimal static and clumping helps experienced chemists avoid unnecessary waste. Most of our repeat customers now request smaller vials for sensitive projects, knowing that opening one batch at a time avoids extended air contact. This routine grew out of practical conversations rather than written protocols—a perfect example of how manufacturing insights improve end-user outcomes.
Discussions with medicinal chemists, pigment formulators, and academic research groups shape our priorities more than marketing trend reports. Every reported issue—whether trace impurities, packaging weaknesses, or documentation gaps—feeds back into internal process reviews. Small changes in the recrystallization step or drying cycle, suggested by frontline technical staff, often yield outsized benefits in purity and shelf-life. Now and then, we conduct joint trials with select partners, sharing production data and receiving real-time feedback on practical performance in synthetic pathways.
The openness of our operations reflects a belief in shared progress. We invest in continuous training for line technicians, emphasize transparency with analytical partners, and encourage user input at every stage. Minor tweaks in raw material sourcing or purification protocols may take time, but they prove their worth as repeat orders roll in accompanied by fewer support requests or technical complaints.
Our long history as a direct manufacturer of 6-hydroxyindole means we witness recurring marketplace confusion between true synthetic intermediates and less reliable commercial samples. Some researchers encounter off-specification material from secondary sources—leading to inconsistent yields, contaminated product, or stalled projects. These issues rarely make headlines, but they show up in project delays and budget overruns. By producing in-house, adopting rigorous quality review, and interacting directly with bench scientists, we sharpen our offering against mass-market alternatives.
For laboratories looking to scale up successful routes, batch-to-batch reproducibility becomes a real concern. Differences in minor impurity levels, particle morphology, or trace element content all play tangible roles in multi-kilogram syntheses. We address this through redundant process controls, thorough documentation, and willingness to answer technical queries without delay. Trust builds not from price alone, but from the demonstrated performance and reliability under real-world laboratory and pilot plant conditions.
In the last decade, several medicinal chemistry groups reported significant time savings and improved reliability after switching to our material. In one case, an oncology project team saw a marked reduction in side-product formation—something traced directly to the consistent, low-impurity profiles of our batches. Similarly, a dye manufacturer reduced purification steps when scaling from grams to kilograms, thanks to minimal colored by-products and low trace metals. Instead of vague satisfaction ratings, we receive emails detailing reaction improvements, fewer column purifications, and accelerated progress through the screening phase. These results stem directly from tight control over raw materials and willingness to tweak production parameters based on honest technical dialogue.
On-site visits to client labs provide some of the best learning opportunities. For one major university user, troubleshooting poor reaction yields prompted us to analyze and rework drying protocols, resulting in measurable improvements for both our process and their synthetic routes. That kind of back-and-forth drives small innovations year after year—cementing the value of practical partnerships in chemical manufacturing.
6-Hydroxyindole remains a niche specialty for a broad field of applications—each new user brings unique challenges and opportunities. Our factory teams, technical sales staff, and R&D chemists work together to refine both product and support, drawing from real-world lessons rather than remote standardization targets. We stay close to actual users not because it makes for slick marketing, but because each successful outcome builds the reputation and reliability of our manufacturing team.
As novel synthetic applications and advanced materials research expand the frontier, demand for consistent, high-quality chemicals continues to rise. By responding quickly to user feedback, supporting clear documentation needs, and backing every lot with thorough testing, our 6-hydroxyindole helps researchers and developers take confident steps into new scientific territory. Our perspective as a producer, rooted in practical experience rather than distance, equips us to advocate for continuous improvement where it matters most—at the junction of chemistry, practical need, and shared progress.