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6-Hydroxyindole

    • Product Name 6-Hydroxyindole
    • Alias 6-Hydroxy-1H-indole
    • Einecs 210-030-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 6-Hydroxyindole

    Applications of 6-Hydroxyindole in Industrial Manufacturing

    As 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) Synthesis

    6-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

    • ICH Q7 GMP for APIs
    • EU EudraLex Volume 4
    • US FDA 21 CFR Part 210/211
    • JP Pharmacopoeia for starting materials

    Typical usage ratio

    • Ranges from 5–30% w/w of total early-stage reaction mass, adjusted according to target product’s synthetic complexity and intermediate yield optimization studies.

    Downstream process integration

    • Direct charged as key precursor during initial synthetic step in batch or semi-batch reactors.
    • Subject to analytical QC before transition to further derivatization steps.
    • Intermediate isolation and purification before API coupling/condensation.

    Final product types

    • Tryptamine-derived APIs (e.g., sumatriptan, pinoline intermediates)
    • Indole-based anti-cancer and CNS active pharmaceutical ingredients
    • Serotonin receptor modulators for clinical use
    • High-value research compounds for CNS pipeline development

    2. Dye and Pigment Synthesis for Specialty Printing

    Manufacturers 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

    • EN 71-3 (Toy safety migration limits for colorants)
    • ISO 18314-1 (Analytical colorimetry)
    • REACH (EC No 1907/2006) for dye precursors
    • General Purity Specifications (DIN EN ISO 28706 for pigments)

    Typical usage ratio

    • 10–40% of total pigment precursor mix, tailored to target dye strength, substrate compatibility, and desired hue intensity.

    Downstream process integration

    • Introduced as core aromatic during nucleophilic coupling phase in high-shear or glass-lined reactors.
    • Solubilized or suspended depending on pigment process (solution-based or dispersion-based).
    • Pre-filtered before crystal aging and final grinding/fixation units.

    Final product types

    • Azo and indigoid synthetic dyes
    • Industrial printing pigments (textile, plastic, ink formulations)
    • Color masterbatches for polymer processing
    • Security and anti-counterfeit pigment preparations

    3. Biochemical Reagent Production for Diagnostics

    Diagnostic 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

    • ISO 13485:2016 (Quality systems for medical device manufacturing)
    • CLSI EP06 (Linearity evaluation for diagnostic reagents)
    • FDA 21 CFR Part 820 (Quality System Regulation for diagnostics)
    • USP/NF analytical standards for biochemical reagents

    Typical usage ratio

    • 0.01–2% w/v in assay substrate formulations; exact dosage determined by LOD/LOQ and kinetic evaluation with enzyme systems.

    Downstream process integration

    • Added after major buffer and stabilizer integration, at late synthesis or direct kit filling step.
    • Filtered and QC tested for background activity and stability under cold storage.
    • Filled into reagent vials or strip wells under ISO cleanroom conditions.

    Final product types

    • ELISA chromogenic and fluorogenic substrates
    • Urinary indole measurement test kits
    • Diagnostic buffer additives for clinical chemistry
    • Molecular biology quantitative assay reagents

    4. Research Chemical Supply for Neurotransmitter Pathway Studies

    Research 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

    • ISO 9001:2015 for laboratory reagent traceability
    • OECD GLP for chemical test substances (where relevant)
    • Chemical safety protocols (GHS, SDS requirements)
    • Institutional Review Board (IRB) standards for chemical sourcing in preclinical projects

    Typical usage ratio

    • Typically 1–50 mg per reaction, depending on pathway under investigation; concentrations are prepared in µM-mM range for enzymatic studies.

    Downstream process integration

    • Dissolved or suspended into biological assay buffers just prior to experimental run.
    • Used for click-chemistry conjugation, isotopic tagging, or direct interaction studies in in vitro models.
    • Subject to direct LC/MS, GC/MS, or NMR validation pre-use.

    Final product types

    • Research-use-only metabolic pathway probes
    • Stable isotope-labeled neurotransmitter precursors
    • Standard reference materials for biological quantification
    • Experimental serotonin/melatonin analogs for university and pharma R&D
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    Certification & Compliance
    More Introduction

    6-Hydroxyindole: Bringing Practicality to Aromatic Chemistry

    Grounded in Experience: Why 6-Hydroxyindole Matters

    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.

    Specifications Shaped by Chemist Feedback

    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.

    Where 6-Hydroxyindole Finds Purpose

    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.

    Practical Differences from Other Indole Derivatives

    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.

    Manufacturing Footprint and Sustainability in Focus

    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.

    Usage: Translating Intermediates Into Results

    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.

    Technical Challenges in the Field

    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.

    Beyond the Lab: Commercial and Regulatory Considerations

    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.

    Handling and Storage: Sharing Lessons Learned

    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.

    Continuous Improvement: Acting on Feedback

    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.

    Comparative Value in a Crowded Market

    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.

    Real World Examples: Why Our 6-Hydroxyindole Works for Users

    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.

    Looking Ahead: Supporting Innovation and Reliability

    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.