Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
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4-Hydroxyindole

    • Product Name 4-Hydroxyindole
    • Alias Indolin-4-ol
    • Einecs 210-519-7
    • 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

    606577

    Cas Number 2380-94-1
    Molecular Formula C8H7NO
    Molar Mass 133.15 g/mol
    Iupac Name 1H-Indol-4-ol
    Appearance Off-white to light brown solid
    Melting Point 216-218 °C
    Solubility In Water Slightly soluble
    Smiles c1cc2c(c(c1)O)cc[nH]2

    As an accredited 4-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, 25 grams, white label with chemical name, formula, hazard pictogram, batch number, and storage instructions.
    Shipping 4-Hydroxyindole is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is packed according to regulations for hazardous chemicals, ensuring safe transport. Appropriate labeling and documentation are included. Shipments comply with international standards to prevent leaks, contamination, and ensure safe delivery to the destination.
    Storage 4-Hydroxyindole should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it separate from strong oxidizing agents and acids. Store at room temperature or as specified by the manufacturer. Appropriate chemical storage procedures must be followed to prevent contamination and ensure safety.
    Application of 4-Hydroxyindole

    Applications of 4-Hydroxyindole in Industrial Manufacturing

    4-Hydroxyindole is predominantly utilized in several specialized industrial sectors due to its unique chemical properties, mainly acting as an intermediate for high-value syntheses. As the original manufacturer, we support manufacturers in optimizing process consistency, product purity, and compliance for a range of application-specific production environments.

    1. Pharmaceutical Intermediates for Serotonin Analog Synthesis

    In pharmaceutical ingredient manufacturing, 4-Hydroxyindole serves as a direct building block for the synthesis of serotonin analogs and related compounds, which are further modified into active pharmaceutical ingredients (APIs) for central nervous system medications. Downstream processors extract, purify, and derivatize to meet bioactivity requirements, which necessitate precise input quality and trace-level impurity control. Sourcing consistency directly affects batch reproducibility and pharmacopoeia compliance within regulated GMP facilities.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP)
    • United States Pharmacopoeia (USP)
    • Good Laboratory Practice (GLP) guidelines

    Typical usage ratio

    • Ranged between 0.8% to 4.5% by molar ratio in stepwise condensation reactions, tuned based on desired analog yield and downstream process scaling

    Downstream process integration

    • Input during the indole nucleus formation stage followed by hydroxy group positioning for subsequent alkylation, acylation, or amination steps

    Final product types

    • API intermediates for antidepressants
    • Precursors to tryptamine derivatives
    • Serotonin agonist compounds
    • Reference standard materials for pharmaceutical QC labs

    2. Dye Precursors in Specialty Pigment Manufacturing

    Specialty dye manufacturers employ 4-Hydroxyindole as a targeted precursor for indole-based dyes used in technical textile and inkjet applications. Its hydroxyl functionality provides reactivity for controlled coupling or further functionalization, delivering end colors with shade stability and high-performance fastness. In pigment processing, precise feed amounts impact hue consistency and finished dye solubility, which drives downstream batch certification requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile safety
    • REACH Regulation (EC) No 1907/2006
    • EN ISO 105 series for color fastness
    • ISO 9001 Quality Management System

    Typical usage ratio

    • Used at 0.2%–1.1% by total dye batch weight, adjusted to achieve target chroma without causing polymerization during high-temperature stages

    Downstream process integration

    • Entering the azo coupling or oxidative dye precursor step, reacting with aromatic diamines to form indole-based pigment frameworks in aqueous or solvent-based reactors

    Final product types

    • Indole-based textile dyes
    • Specialty inkjet colorants
    • Technical pigment dispersions for plastics and coatings
    • Analytical color standards

    3. Aroma Compound Synthesis in Flavor and Fragrance Manufacture

    Manufacturers in the flavors and fragrances sector value 4-Hydroxyindole as a key intermediate in the synthesis of high-purity indole derivatives, which impart earthy, floral, and animalic notes to fine fragrance and food flavor blends. Precision in precursor qualtity and purity is essential for downstream organoleptic quality and compliance with global additive frameworks, as final blends must pass trace-level impurity and allergen analysis prior to commercialization.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • EU Regulation (EC) No 1334/2008 on flavorings
    • ISO 9235 for natural aroma substances

    Typical usage ratio

    • Ranging from 0.05%–0.18% by total batch weight during synthesis, with dose level determined by GC-MS feedback for target sensorial profile

    Downstream process integration

    • Charged into the heterocyclic core generation stage before methylation, esterification, or final distillation for aroma compounding

    Final product types

    • Indole-derived fragrance bases
    • Flavoring agents for food and beverages
    • Aromatics for cosmetic and personal care products
    • Standard references in analytical labs

    4. Agrochemical Intermediate for Plant Growth Regulator Synthesis

    Agrochemical manufacturers utilize 4-Hydroxyindole as a precursor in synthesizing plant growth regulators—primarily indole-based auxins—used to optimize root formation and shoot development in commercial horticulture and agriculture. Input quality influences yield and downstream bioactivity of finished formulations, with strict attention to environmental residue standards and trace contaminant control.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 (EU pesticides)
    • US EPA 40 CFR Part 180 (Tolerances and exemptions for pesticide residues)
    • ISO 17025 for analytical laboratory competence

    Typical usage ratio

    • 0.4%–2.2% by total mass in synthetic conversion batches, modulated by auxin class and targeted field activity levels

    Downstream process integration

    • Added in the arylation or side-chain functionalization phase within multi-step synthesis protocols for plant hormone analogs

    Final product types

    • Indole-3-acetic acid (IAA) and derivatives
    • Plant growth stimulant concentrate formulations
    • Rooting agent liquids and powders
    • Foliar application premixes

    5. Research and Diagnostics Reference Material Production

    Chemical and biochemical research suppliers integrate 4-Hydroxyindole as a controlled standard for analytical method development, in-vitro testing, and neurochemical assays. Laboratories require reliable lot-to-lot performance with low residual solvents and by-product levels, due to direct impacts on result traceability and sensitivity in both clinical and non-clinical studies.

    Industry compliance standards

    • ISO 17034 Reference Material Producers
    • PIC/S GMP Guide for Pharmaceutical Quality Systems
    • GLP (Good Laboratory Practice)
    • OECD Principles of Good Laboratory Practice

    Typical usage ratio

    • Prepared and diluted on-site to 1–50 μg/mL for HPLC/GC/MS, or solid aliquots ranging from 0.2–2 mg per test depending on protocol sensitivity requirements

    Downstream process integration

    • Packaged after batch-level analytical verification, delivered as pre-weighed vials or solution ampoules for direct use in assay calibration or test method validation

    Final product types

    • Certified reference materials for serotonin pathway studies
    • Quantitative in-vitro assay standards
    • Analytical method validation kits
    • Neurochemical diagnostic reagents
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    Certification & Compliance
    More Introduction

    4-Hydroxyindole: Experience from the Manufacturer’s Floor

    A Closer Look at 4-Hydroxyindole Production

    Working in chemical manufacturing teaches you quickly which molecules stand apart for real-world value and reliability. 4-Hydroxyindole, with CAS number 2380-94-1 and molecular formula C8H7NO, draws interest for more than just its chemistry. Its structure—an indole ring with a hydroxyl group on the fourth carbon—shapes the kind of precision synthesis that’s become customary in our plant. Our process follows strict guidelines from raw material selection through the multi-step synthesis, constantly monitored to limit by-products.

    Experience with batch trails makes it clear that minor fluctuations in temperature and pH during the reaction stage can influence yield and purity. We invest in automation where it enhances consistency, but a skilled operator’s eye still picks up shifts in color or viscosity before the sensors catch up. The crude product forms a yellowish powder, which we purify by controlled crystallization and repeated washing. We test every lot using HPLC and NMR to verify that purity meets or exceeds 98%. Only batches that pass every checkpoint move forward, promising customers the reliable performance expected in laboratory and industrial synthesis.

    The Role of 4-Hydroxyindole in Research and Beyond

    We see steady demand for 4-Hydroxyindole from research institutions, pharmaceutical innovators, and specialty chemical houses. Its main attraction comes from the way it bridges simple heterocycles and more complex tryptamine derivatives. Many researchers use it to build serotonin analogs, melatonin derivatives, and other indole-based compounds. The hydroxyl group at position 4 enables targeted modifications through etherification, acylation, or Suzuki coupling. Pharmaceutical groups source our material to support drug discovery projects aimed at serotonergic signaling, pursuing treatments for depression and anxiety.

    Teams exploring agrochemical leads often pick up our 4-Hydroxyindole to leverage the indole core’s history in plant signal transduction research. Its reactivity, compared to 5- or 6-hydroxyindole, creates unique scaffolds not accessible from isomeric feedstocks. Every year, we field requests for custom quantities, even as small as tens of grams for method development or kilograms for larger screening runs. Experience in toll manufacturing helps us respond to shifting requirements, from grams for university screening efforts to industrial-scale runs needed for pilot plant campaigns.

    Physical Properties and Handling Observations

    There’s a lot you learn by handling the real material, beyond data sheets. 4-Hydroxyindole pours as a tan to light brown crystalline powder. It’s slightly less prone to clumping than indole, but open air exposure soon draws in moisture due to the phenolic hydroxyl. Shelf-life checks show it stands up well with proper desiccation, maintaining appearance and purity for over a year in airtight packaging. Storage at ambient temperature works, but colder, low-humidity storage rooms extend shelf stability.

    Its solubility mirrors structural relatives: easily disperses in ethanol, methanol, and DMSO, less so in hexane or ether. For synthetic work, small-scale dissolutions go quickly. At scale, we blend under nitrogen to minimize oxidation, as prolonged air contact can lead to slow darkening. For our process engineers, batch size up to 50 kilograms has shown manageable dusting and flow for both bagged and drum deliveries. Most customers request double-bagged polyethylene liners inside fiber drums, as this packaging resists static buildup and ensures a clean transfer.

    Differences Between 4-Hydroxyindole and Other Indole Derivatives

    Chemists working in this field don’t confuse the nuances between simple indole, hydroxyindoles, and more substituted analogs. Comparing 4-hydroxyindole to its 5- and 6-hydroxy siblings, the main difference appears in both electronic properties and subsequent synthetic versatility. 5-Hydroxyindole (also known as serotonin) supports immediate biological assay work, but its regulatory handling becomes complex due to its relationship with neuroactive compounds. 6-Hydroxyindole changes the resonance behavior on the indole ring, shifting the reactivity profile. By contrast, 4-hydroxyindole resists direct auto-oxidation better and offers unique sites for further substitution, especially for cross-coupling chemistry.

    From our point of view as a manufacturer, the synthesis routes for 4-hydroxyindole use milder conditions than 3-substituted isomers. This translates into fewer hazardous intermediates and lower pressure for by-product recycling. Labs seeking versatility and fewer regulatory or storage headaches often return to the 4-hydroxy isomer. We like to remind buyers that clear labeling and separate storage from strong acids or light-exposed materials preserves the quality and lowers reject rates.

    The Value of Consistent Quality in Chemical Supply

    Operating a manufacturing line means taking responsibility for the consistency that research and development depends on. We’ve lived through periods where markets tighten due to upstream shortages—sometimes a single precursor supplier halts production and the whole chain feels the pinch. We lay in raw material reserves for at least six months’ ongoing production, not just for peace of mind but to guarantee supply. Customers often share feedback about their past experiences with off-grade material from less rigorous outfits—issues like residual solvents, high ash content, or color contaminants that throw off sensitive synthesis or skew bioassay results.

    By establishing in-house reference standards, running weekly equipment calibrations, and cross-verifying purity with outside labs, we take practical steps to back up quality claims. Every lot ships with a detailed certificate of analysis, including assay, moisture content, and trace impurity profiles delivered by both HPLC and GC-MS where needed. Our technical staff welcomes direct conversations about lot-specific needs, because we know that a project sometimes succeeds or fails on the analytical subtleties. If readings ever fall outside customer-defined limits, we call attention to it and arrange rapid reprocessing rather than risk a tainted supply.

    Supporting Academic and Industrial Research

    University chemists often visit our plant to review analytical reports or tour the production hall. Collaborating with academic groups gives us a window into new methods that could boost selectivity or reduce environmental impact. We’ve supported multi-department projects that rely on kilogram lots for combinatorial chemistry, or just a few grams to confirm a mass spectrometric assay. The dialog with research labs helps us anticipate demand: when a major publication describes a breakthrough using 4-hydroxyindole as a key building block, we know to increase production for the coming year.

    On the industry side, pharmaceutical and agricultural companies expect fast turnaround, thorough documentation, and responsive technical support. Shifts in demand sometimes mean ramping up semi-batch operations or switching to a continuous flow protocol to meet tighter lead times. Product stewardship means sharing best practices for safe handling and waste minimization, as we’ve seen how oversight in bulk storage or transfer can lead to quality loss or contamination. Workshops and webinars help clients new to the compound understand hazards, best storage conditions, and simple tests to confirm compound integrity.

    Environmental and Safety Considerations

    Our environmental, health, and safety teams emphasize minimizing exposure and waste across each step. 4-Hydroxyindole is sparingly toxic, but its phenolic group means gloves, goggles, and chemical aprons stay on during handling. Solvent management forms a major part of our environmental plan. We recover and recycle polar solvents used in crystallization, reclaiming up to 85% for further use. Filtration residues pass to a licensed waste processor, never to landfill.

    Internal audits push us to search for improvements each year—tighter exhaust filtering, lower rinse water discharge, and active monitoring for any air- or water-borne byproducts. We also invest in closed-offloading and transfer equipment to limit operator exposure and keep quality at a premium. Employees undergo regular training in hazard communication, and new protocols roll out as soon as we spot chances to step up worker safety or emissions control.

    Fielding Market Changes and Customer Challenges

    Over several production cycles, market shifts kept us on our toes. Two years back, a surge in pharmaceutical demand forced us to partner with an upstream supplier to lock in key intermediary stocks. Early in the pandemic, logistics disruptions tested our inventory practices—maintaining raw material flow under shipping restrictions took constant phone calls and express courier workarounds. By strengthening talks with freight handlers and building alternate shipping documents, we kept outbound deliveries predictable.

    Developing flexibility with batch sizing matters, especially for clients experimenting with 4-hydroxyindole in new applications. Scientists working in dye development, polymer additives, or specialty sensor design often need trial runs before large-scale commitment. We offer pilot batch quantities and counsel on storage, dilution, or derivatization based on direct handling experience. Requests for custom milling, particle size control, or special purity are met in-house, leveraging both manual and semi-automated finishing systems. This responsiveness helps customers avoid downtime waiting for hard-to-source intermediates.

    Troubleshooting and Continual Improvement

    We embrace customer feedback as part of daily operations. Analytical labs sometimes point out a faint impurity registered by mass trace or unexpected retention on a chromatography column. Reviewing these results directly with customers and diving into our synthesis records lets us make corrections at the source, be it retuning a reaction temperature or switching to a different grade of catalyst. The improvements carry through in clearer product, higher yields, and fewer non-conforming lots.

    Technical support includes walking clients through solution protocols. Solubility questions arise with nearly every batch, especially for those unfamiliar with the slight differences among indole derivatives. Our process chemists suggest solvent regimes and relay tips observed on the production floor, such as gentle warming or staged addition, which help the compound dissolve smoothly.

    Continuous investment in pilot-scale reactors and new analytical equipment gives us the tools needed for repeat improvement. Our staff regularly publishes findings on method development, impurity traceability, and shelf-life studies for 4-hydroxyindole. This culture of openness and exchange brings a steady flow of process improvements and helps our clients stay ahead of regulatory or scientific hurdles.

    Commitment to Reliable Partnerships

    Real partnerships stand out in this business by the way they handle inevitable hiccups. Shipment delays, spec adjustments, or last-minute orders don’t just affect the bottom line; they can set back months of downstream research. We’ve found that clear communication and willingness to rerun or split-batch production builds trust. Contract customers benefit from priority scheduling, shared access to analytical archives, and early notifications of process changes.

    For those in new fields or unfamiliar with indole chemistry, we provide hands-on consultation. Direct conversations with our technical and production leads make all the difference in application troubleshooting. From the first sample through full order fulfillment and post-delivery feedback, each step prioritizes the client’s process reliability.

    The Evolving Place of 4-Hydroxyindole

    As research pushes indole derivatives into new therapeutic and technical fields, 4-hydroxyindole’s role continues to evolve. Sustainable production, reliable supply, and proven purity earn repeat orders and positive referrals. Labor spent refining our process translates directly to more stable and adaptable supply chains for clients tackling new challenges. With every batch released, it’s the practical needs of chemists, research planners, and process engineers that shape how we deliver this compound.

    Our work with 4-hydroxyindole stands as an example of how experience, rigorous process control, and careful partnership meet the needs of modern science. Knowledge built from years on the factory floor brings confidence to our customers, letting them focus on innovation, rather than worry about the reliability of their starting materials. Consistency, clarity, and willingness to listen—these values drive how we manufacture, package, and support every order of 4-hydroxyindole, today and in the years ahead.