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5-Bromoindole

    • Product Name 5-Bromoindole
    • Alias 5-Bromo-1H-indole
    • Einecs 606-044-6
    • 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
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    Specifications

    HS Code

    879649

    Chemical Name 5-Bromoindole
    Cas Number 10075-50-0
    Molecular Formula C8H6BrN
    Molecular Weight 196.05 g/mol
    Appearance White to pale yellow solid
    Melting Point 61-65 °C
    Density 1.68 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles Brc1ccc2[nH]ccc2c1
    Inchi InChI=1S/C8H6BrN/c9-6-1-2-7-5(3-6)4-8(10-7)11/h1-4,10H

    As an accredited 5-Bromoindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "5-Bromoindole, 25g", with hazard symbols, manufacturer information, CAS number, and tightly sealed screw cap.
    Shipping **5-Bromoindole** is shipped in tightly sealed containers, protected from light and moisture. It is transported as a hazardous chemical, often via ground or air freight, following all regulatory guidelines. Proper labeling ensures safe handling, and Material Safety Data Sheets (MSDS) accompany the shipment to inform handlers of necessary precautions.
    Storage 5-Bromoindole should be stored in a tightly closed container, protected from light and moisture. It should be kept in a cool, dry, and well-ventilated area, away from sources of ignition, strong oxidizers, and incompatible materials. Ensure proper labeling and follow all safety protocols for handling organic chemicals. Use secondary containment to prevent spills or leaks.
    Application of 5-Bromoindole

    Applications of 5-Bromoindole in Industrial Manufacturing

    We supply 5-Bromoindole directly from our manufacturing facility for specialized downstream industries, supporting advanced organic synthesis, pharmaceutical intermediates, crop protection active development, industrial dyes, and academic research. Below are key approved and widely practiced industrial applications where 5-Bromoindole plays a critical role, along with industry-specific compliance, formulation requirements, process details, and the types of final products manufactured.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Antineoplastic Drugs

    5-Bromoindole serves as a core starting material in the multi-step synthesis of antineoplastic APIs, especially indole-based kinase inhibitors and other heterocyclic therapeutics. Manufactured lots must meet established pharmaceutical impurity profiles due to their direct conversion into regulated drug substances. Production teams integrate this compound in initial or mid-stage alkylation, acylation, or Suzuki coupling reactions, depending on the specific API. Each customer establishes their preferred equivalents and reaction conditions based on the downstream impurity and yield requirements outlined in their DMFs and regulatory dossiers.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EU GMP Annex 1 and 13
    • Ph. Eur. and USP monograph requirements for related substances (when applicable downstream)

    Typical usage ratio

    • 0.85–1.2 molar equivalents per target reaction step; may be adjusted for process scale and impurity control

    Downstream process integration

    • Introduced in early or intermediate coupling reaction after precursor halogenation step, followed by purification and further derivatization towards final API structure

    Final product types

    • Anticancer drugs: kinase inhibitors, proteasome modulators, and other heterocycle-based therapies

    2. Agrochemical Intermediate in Crop Protection Synthesis

    Major crop protection companies utilize this material in the manufacture of indole-derived fungicide and insecticide actives. Tight lot-to-lot consistency and trace contaminant limits are critical for safe field application and regulatory approval. Technical teams employ this intermediate in ring-substitution and cross-coupling reactions to introduce brominated indole moieties in the core structure of active compounds. Analytical QC confirms target molecular conversion before downstream formulation of the technical active.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 for Quality Management Systems
    • REACH registration and compliance for European markets
    • Chinese ICAMA registration for domestic pesticide actives

    Typical usage ratio

    • 0.95–1.10 molar equivalent depending on reaction specifics and downstream active ingredient demand

    Downstream process integration

    • Charged into the initial cyclization or Suzuki coupling step to build brominated indole scaffold, often followed by formulation into a dispersible concentrate or wettable powder

    Final product types

    • Registered fungicides containing indole moieties
    • New mode-of-action insecticidal actives

    3. Organic Synthesis Research and Fine Chemical Building Block

    Advanced research institutes, contract synthesis organizations, and specialty chemical producers use this raw material in the customized assembly of libraries of heterocyclic compounds for discovery and screening programs. Demand includes both academic and industrial R&D sectors, where structural precision and analytical documentation are closely monitored to meet project-specific requirements. Scientists introduce the compound as a coupling partner or fragment donor in liquid or solid-phase synthesis cycles, with process adaptation to new reaction pathways as required by the research protocol.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for regulated discovery projects
    • ISO 17025 for analytical reproducibility and documentation
    • RoHS/REACH statement when applicable for exported research chemicals

    Typical usage ratio

    • 0.8–1.5 equivalents per synthesis, adjusted for target structure, yield studies, and excess management

    Downstream process integration

    • Enters as a substrate in initial condensation or late-stage functionalization steps during compound library assembly

    Final product types

    • Indole-based screening libraries
    • Custom organic molecules for lead optimization

    4. Specialty Dye Intermediate for Electronic and Functional Materials

    Manufacturers of high-performance dyes and optoelectronic materials employ 5-Bromoindole for constructing indole chromophores that impart stability and unique spectral properties in display and sensor applications. The material’s halogenated position allows precise substitution and extension during dye synthesis, particularly via palladium-catalyzed coupling or condensation with electron donor/acceptor units. End users set impurity control and batch documentation standards to ensure homogeneous color and electronic properties in final articles.

    Industry compliance standards

    • ISO 9001 Quality Management Systems for specialty dye manufacturing
    • RoHS compliance for electronic applications
    • OEKO-TEX Standard 100 Class I/II for textile-related dye precursors (when applicable)

    Typical usage ratio

    • 0.95–1.20 molar equivalents relative to final dye chromophore backbone; ratio can vary for color tuning and purity requirements

    Downstream process integration

    • Added to main reaction vessel during cross-coupling or cyclization step to create indole-based dye structures, followed by purification and functionalization for desired application

    Final product types

    • Photoluminescent dyes for OLED and sensor applications
    • Specialty pigments for polymer or electronic coatings
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    Certification & Compliance
    More Introduction

    5-Bromoindole: Experience at the Source

    Understanding 5-Bromoindole and Its Practical Value

    5-Bromoindole carries a reputation for stability and performance in the world of organic synthesis. We have spent years refining the process, blending technical control with chemical insight to create a product that meets demanding lab and industrial needs. The core of 5-Bromoindole lies in its simplicity: an indole ring with a bromine atom at the 5-position. This small structural change delivers a range of benefits, from controlled reactivity to solid purity, valued in scale-up pharmaceutical projects and ongoing academic research.

    Our direct hands-on expertise with brominated indoles shows that not every sample behaves the same. Trace impurities, moisture, and even slight batch inconsistency can ruin a reaction’s outcome or skew biological testing. Through years of practice, we tuned our methods for recrystallization and purification, which results in a product that stays within tight purity specifications and exhibits stable handling characteristics in both small and large-scale operations. Each step, from raw material selection through to final drying, benefits from our experience working at the chemical’s source.

    We consistently see 5-Bromoindole used in the early stages of synthesizing biologically active compounds and advanced building blocks. Researchers depend on reliable supply to probe enzymatic pathways, modify lead compounds, and explore the synthesis of dyes, inhibitors, and heterocyclic scaffolds. Our team noticed that some of the world's best progress in tryptamine analog synthesis, kinase inhibitor research, and custom dye production came from projects that started with a well-made 5-Bromoindole input. Every lot reflects the cumulative learning from recent synthesis runs—yield optimization, thermal stability improvements, and feedback from partners who use the material in downstream transformations.

    Molecular Structure and Production Experience

    Structurally, 5-Bromoindole belongs to the indole family—aromatic, nitrogen-containing compounds. Bromination at the 5-position makes this product more versatile in certain halogen substitution reactions, especially Suzuki-Miyaura coupling and related cross-coupling chemistry. The electron-withdrawing nature of bromine at this site impacts both reactivity and downstream functionalization, delivering options for selective transformations that wouldn’t work with standard indole or with halogenated isomers at other positions.

    In the lab, we observe that 5-Bromoindole’s behavior differs noticeably from its isomeric relatives such as 2-bromoindole or 7-bromoindole. 5-position substitution changes the electronics of the indole ring, which, from practical synthesis trials, means altered reactivity in electrophilic aromatic substitution or metal-catalyzed coupling. This feature shapes the type of scaffolds built from it, drawing the interest of medicinal chemists and advanced material scientists. During manufacturing, the bromination step always requires careful thermal management and post-reaction workup to avoid byproducts. Our specialized distillation and crystallization protocols minimize colored impurities and deliver a solid suitable for advanced chemical transformation.

    Throughout the years, we observed that ambient humidity—so often ignored—can be the difference between a clumpy, inconsistent product and a free-flowing, easily handled solid. Extra care with vacuum drying and inert packaging translates directly into cleaner downstream conversions for our partners. These details, learned through repeated practice, separate merely adequate product from material that drives innovation.

    Specifications Shaped by Production Realities

    Typical 5-Bromoindole, fresh from our reactors, presents as a pale solid with noticeable aromatic odor. On the bench, it melts within a precise range—an indicator for chemists checking batch quality. In production, melt point can fluctuate if trace solvents or impurities sneak through. Our ongoing investments in batch analytics, from GC-MS to melting point probes and elemental analysis, help ensure each lot hits the right window. In daily lab application, this translates to a sample that dissolves as expected—crucial for portions destined for further coupling reactions or analytical testing.

    We maintain a purity standard that meets or exceeds 98 percent by HPLC, supporting both gram-scale and multi-kilogram requests. Lower grades that can result from shortcut processing have shown poor reproducibility in downstream work; feedback from partners tackling custom synthesis supports our drive for greater purity. Since indole derivatives sometimes carry over subtle halide impurities, we regularly test for unwanted halogenated byproducts, sulfated ash, and residual water.

    Odor and color, while minor, sometimes act as indicators of batch consistency. Yellowing, for example, suggests oxidative degradation or incomplete purification—issues we tackle by optimizing both bromination and workup. Experience makes a difference in recognizing small deviations and their root causes, whether it means a quick tweak to solvent mixture or a full revision of the purification protocol.

    Applications from the Factory Floor to Research Labs

    Applications for 5-Bromoindole bridge both exploratory research and scaled-up production. We saw this molecule serve as a backbone for making new active pharmaceutical ingredients, library intermediates, and tailored research compounds. It plays a recurring role in tryptamine synthesis, where position-specific bromination makes it possible to engineer compounds with unique activity profiles. Partners involved in CNS-active molecules, anticancer scaffolds, and biochemical pathway probes increasingly ask for reliable supplies on strict timelines. Our inventory management reflects these needs—frequent small-lot requests and larger, campaign-based orders get tailored from a core batch to minimize holding time and keep product fresh on arrival.

    In materials science, research surfaced on using 5-Bromoindole as a core unit in fluorescent dye synthesis and organic semiconductors. Production-grade material with minimal colored impurities brings out the best in these applications, where a subtle color or trace contaminant can influence device performance or introduce unwanted background signals. Regular communication with collaborators in advanced materials and dyes highlights the value of attention to packaging, storage, and rapid shipment.

    Over the last few years, we observed a jump in interest from groups exploring halogen dance rearrangements, site-selective functionalization techniques, and new cross-coupling catalysts. Each advance underscores the importance of a reliable, reactive 5-Bromoindole—small variations in substituent purity or isomer content spell the difference between success and weeks of troubleshooting. Sharing our firsthand production stories—batches that worked, batches that struggled—contributes to building strong, solution-based relationships with our partners.

    Comparing 5-Bromoindole to Other Indoles

    Comparing 5-Bromoindole with its close relatives reveals distinct differences in chemical behavior and application focus. Standard indole offers a neutral platform, open to modification at multiple positions, but delivering less selectivity in modern cross-coupling or halogenation projects. Other halogenated indoles, like 3-bromoindole or 7-bromoindole, perform best in syntheses that require reactivity at a different ring position. Our experience shows that even slight shifts in halogen placement influence chemical reactivity, solubility, and the physical nature of the product.

    For example, in situ cross-coupling reactions reveal the difference at the bench: 5-bromoindole produces cleaner product profiles and higher yields in select Suzuki coupling reactions compared to 2-bromo or 7-bromo analogs. In biological screening, the position of the bromine alters binding to critical enzymes and receptors, a detail that medicinal discovery programs now capture with increasing precision. Researchers who tried to substitute one isomer for another ended up repeating purification runs or altering catalyst systems with mixed results. Years of feedback looped into our own process improvement—getting the selectivity and purity right pays off at every turn.

    We also see differences in downstream handling. 2-bromo and 3-bromoindole often show more pronounced instability, with batch color changes during storage leading to purification headaches and inconsistent results. By contrast, 5-Bromoindole, stored as a dry, sealed solid, holds up well against air, light, and modest changes in temperature. We reinforce this with proper packaging, drawing on real shipment and storage history rather than theoretical shelf-life claims. Consistent product, reliably delivered, cuts through a lot of the hassle faced by chemists racing project timelines or fine-tuning complex molecule synthesis.

    Lessons from Real-World Manufacturing

    Manufacturing 5-Bromoindole at scale means managing multiple variables that never appear in standard texts. Raw material quality, choice of bromine source, and post-bromination purification each impact the end product. Early on, switching between halogen sources produced inconsistent yields and variable impurity profiles—errors that cost us time and forced revision of our supply chain strategy. Diligence at each step, verified by hands-on batch sampling, made the biggest difference.

    Scaling from grams to several kilograms, we discovered that localized heating and over-bromination create oxidative byproducts difficult to remove. Controlling exotherms and using mechanical stirring helped avoid these issues. Operators learned to read subtle clues—change in the smell, viscosity, or visible crystal structure during workup. These cues, reinforced by QC test data, inform adjustments in real time. Personnel training—based on repetitive, trial-and-error lessons—forms the backbone of our process stability.

    Incorporating automation brought its own set of challenges. Some critical steps, especially final drying and sieving, still call for experienced intervention. Machines check consistency, but only a trained eye spots the early signs of color change or clumping that signal a release problem downstream. This human touch—integrated into an analytical-heavy process—guarantees each lot of 5-Bromoindole meets performance expectations in real-world labs and pilot plants.

    Supporting Customers through Each Batch

    Chemists and researchers rarely have time to repeat projects because a reagent failed silently. We treat every order as a test of our reputation, tracking customer outcomes and incorporating their process feedback into both upstream manufacturing and packaging. Improvements sometimes come from a single phone call—one partner’s observation that a new batch appeared faintly yellow led us to trace back shipping conditions, tighten post-production drying, and test packaging upgrades to lock out humidity.

    Because end use varies—from high-throughput medicinal chemistry to pilot-scale intermediates—the texture and purity of the 5-Bromoindole absolutely matter. Pharmaceutical groups report higher synthesis yields and fewer purification steps when using consistently made 5-Bromoindole. Academic teams focused on reaction methodology benefit from predictable reactivity and fewer unexplained variables. We see these results mirrored in our own technical support history—queries around solubility, color, or impurity thresholds receive real data, not generic answers.

    We commit to transparency and technical collaboration. By sharing manufacturing details, batch CoAs, and run histories where possible, we help customers diagnose issues upstream rather than react to problems late. Supporting every stage of the research and production process requires more than standard certificates—it calls for open dialogue and a willingness to adjust based on hands-on laboratory experience.

    Risks, Solutions, and Continuous Improvement

    Production entails its own hazards—bromine, even in small amounts, presents safety risks that demand respect. Personnel training, closed-system addition, and properly vented reaction setups all grew from years of hands-on incident response, guided by a genuine concern for workforce health. Waste handling became a focus early on, as brominated byproducts challenge disposal protocols. Through consultation with environmental experts and repeated audits, we lowered waste levels and developed safe, compliant handling across every facility.

    Long-term product quality remains a living target. Climate, raw material supplier changes, and evolving regulatory requirements occasionally challenge our process. Real case feedback—product that worked better or worse in a new catalyst system—guides adjustments far better than guessing from literature or vendor claims. Investment in real-time production analytics now provides batch-to-batch monitoring, catching variances early and keeping our product at the highest standard achievable from a manufacturing standpoint.

    From dozens of production runs, technical failures, and customer successes, we learned the value of consistency over any claim of “best specification.” Durable, predictable performance in application always outweighs incremental gains in numerical purity or theoretical batch size. Collaborators return because the product does what they expect, again and again, not because of a glossy data sheet.

    Outlook: The Future of 5-Bromoindole Manufacture

    Research and applied demand continue to shift toward more sophisticated indole building blocks and derivatives. Applications grow each year, with more fields—green chemistry, photonics, targeted pharmaceuticals—calling for improved 5-Bromoindole standards and timely supply. We meet this challenge by investing in process refinement, batch traceability, and ongoing dialogue with users at the research, pilot, and full production scales.

    Increasing pressure for green processes shapes new runs. We see an emerging expectation for cleaner production, minimal solvent use, and greater attention to lifecycle impact. Already, our facilities incorporate solvent recovery and upgraded PPE to balance both environmental cost and practical safety. Insisting on regular operator feedback keeps us grounded in real-world application, far from the abstractions of supplier catalogs.

    In sum, 5-Bromoindole production isn’t just another process—it's a daily exercise in adaptation and attention. Each batch carries the lessons of its predecessors, shaped by practical realities rather than by-the-book standards. Our deepest progress came from repeated collaboration with scientists in pharmaceuticals, materials, and academic labs. These relationships push us toward smarter production, higher quality, and stronger, more reliable bonds with those who depend on our work.