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7-Bromoindole

    • Product Name 7-Bromoindole
    • Alias 7-Bromo-1H-indole
    • Einecs 604-608-7
    • 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

    202888

    Productname 7-Bromoindole
    Casnumber 1532-09-8
    Molecularformula C8H6BrN
    Molecularweight 196.05
    Appearance Off-white to light brown solid
    Meltingpoint 80-84°C
    Purity Typically ≥98%
    Smiles Brc1cccc2[nH]ccc12
    Inchikey UDSRTJNYYBJQEU-UHFFFAOYSA-N
    Storagetemperature Store at room temperature
    Solubility Soluble in organic solvents such as DMSO and ethanol

    As an accredited 7-Bromoindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle labeled "7-Bromoindole," with a screw cap, hazard symbols, lot number, and supplier details.
    Shipping 7-Bromoindole is shipped in tightly sealed, chemically resistant containers to prevent moisture and light exposure. The package is labeled with appropriate hazard warnings and follows all regulatory guidelines for hazardous chemicals. During transit, it is handled as a flammable solid, with care to minimize risks of spillage, breakage, or contamination.
    Storage 7-Bromoindole should be stored in a tightly sealed container, away from direct sunlight, moisture, and incompatible substances (such as strong oxidizers). Keep it in a cool, dry, and well-ventilated area, ideally in a chemical storage cabinet for organics. Maintain temperatures at room temperature or below, and clearly label the container to prevent accidental misuse or contamination.
    Application of 7-Bromoindole

    Applications of 7-Bromoindole in Industrial Manufacturing

    7-Bromoindole serves as a key intermediate in critical synthetic routes across highly regulated chemical sectors. Its selective reactivity, electronic structure, and purity profile make it suitable for integration into advanced manufacturing chains, serving key market needs in pharmaceuticals, crop protection, specialty dyes, and advanced materials. Below are the principal downstream industrial settings utilizing this material.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers incorporate 7-Bromoindole as a core intermediate during multi-step syntheses for heterocyclic drug molecules, particularly in developing oncology drugs and CNS-targeted APIs. It undergoes cross-coupling, halogen exchange, and functional group transformations integral to imidazole and indole derivative drugs. Downstream operations rely on the controlled introduction of this intermediate in kilogram-scale, maintaining trace impurity levels in compliance with industry standards for human use. Process optimization focuses on reaction yield, stereochemistry, and batch cleanliness, as regulated by pharmacopeial and GMP conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP-NF (United States Pharmacopeia–National Formulary)
    • Ph. Eur. (European Pharmacopoeia) monographs for indole derivatives
    • 21 CFR 210/211 – FDA Current Good Manufacturing Practice

    Typical usage ratio

    • 0.5–5 molar equivalents per API batch; varies with molecular scaffold and stepwise integration; adjusted to minimize byproduct formation in scale-up reactions.

    Downstream process integration

    • Feeds Buchwald-Hartwig amination or Suzuki–Miyaura coupling reactors during N-alkylation, arylation, or cross-coupling synthesis routes in GMP API lines.

    Final product types

    • Anti-cancer drugs (e.g., kinase inhibitors)
    • Anti-inflammatory APIs
    • Novel central nervous system agents
    • Other heterocycle-based pharmaceuticals

    2. Agrochemical Intermediate Manufacturing

    Agrochemical producers employ 7-Bromoindole during the synthesis of indole-based fungicides and herbicides. It provides a brominated scaffold for introducing bioactive functional groups via palladium-catalyzed coupling or nucleophilic substitutions. Plant-protection chemical factories operate under regional and international standards for impurity control and environmental impact, requiring highly traceable raw input registration. Material flow is monitored from bromination input up to the final purification of active ingredients for crop-spraying use.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications
    • ISO 9001:2015 for quality management
    • REACH Regulation (EC 1907/2006) for chemical safety
    • EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act, US market)

    Typical usage ratio

    • 0.2–1.0 molar equivalent per formulation batch; adjusted by the number of brominated nodes in the targeted herbicide or fungicide molecular structure.

    Downstream process integration

    • Used in initial reaction stage for indole core assembly, or as a late-stage building block in advanced agrochemical synthesis, entering the process prior to final product crystallization and milling.

    Final product types

    • Indole-linked selective herbicides
    • Systemic agricultural fungicides
    • Pest control agents for high-value crops
    • Seed coating active formulations

    3. High-Performance Dye and Pigment Synthesis

    Specialty dye manufacturers utilize 7-Bromoindole for the production of high-purity indole-based dye molecules that target textiles, inkjet inks, and electronic display segments. The material permits controlled introduction of halogen-substituted chromophores, enhancing pigment light-fastness and color fastness while meeting REACH and industry colorant safety standards. Manufacturing lines employ this raw material for regioselective dye synthesis followed by purification and blending into stable finished colorant products.

    Industry compliance standards

    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU)
    • OEKO-TEX® Standard 100
    • ISO 13321:2008 Particle Sizing (in pigment dispersions)
    • EN 71-3 Safety of Toys (for pigment usage in inks)

    Typical usage ratio

    • 0.2–2.0 molar equivalent, depending on dye structure complexity and batch scale, with real-time adjustment for process color calibrations.

    Downstream process integration

    • Introduced as a principal feedstock in condensation or halogen-metal exchange stage for chromophore release, followed by downstream diazotization and color developer blending.

    Final product types

    • High-brightness indole-based textile dyes
    • Inkjet printer pigment formulations
    • Specialty inks for security printing
    • OLED colorant intermediates

    4. Advanced Materials and Organic Electronics

    Electronics materials manufacturers incorporate 7-Bromoindole as a monomer building block for next-generation organic semiconductors, OLED emitters, and hole transport layers. The chemical structure enables precise functionalization of π-conjugated systems, improving charge mobility and stability in printed electronics. Production facilities source this material for documented integration into multi-step aryl-amine and heterocycle frameworks employed in the fabrication of thin films and transistor substrates, under strict environmental and electronics-grade purity protocols.

    Industry compliance standards

    • RoHS Directive (EU Restriction of Hazardous Substances)
    • IEC 60749-20 Semiconductor Device Standards
    • ISO 14001 Green Manufacturing Certification
    • JEITA (Japan Electronics and Information Technology Industries Association) purity guidelines

    Typical usage ratio

    • 0.1–0.6 molar equivalent per monomer lot, fine-tuned to molecular orbital design and conductivity targets in each synthesis cycle.

    Downstream process integration

    • Used in Stille or Suzuki coupling as core monomer, entering material synthesis just prior to solid-state purification before device layer deposition.

    Final product types

    • Organic field-effect transistors
    • OLED panel emitters/charge transport layers
    • Photovoltaic organic semiconductors
    • Flexible sensor materials
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    Certification & Compliance
    More Introduction

    7-Bromoindole: Insights from a Chemical Manufacturer’s Bench

    Understanding 7-Bromoindole and Its Role in Fine Chemicals

    Working with indole derivatives for years, you start to develop a respect for the subtle differences each substitution brings. 7-Bromoindole isn’t the product that headlines chemical supply brochures, but users who know what they’re looking for recognize its value. This compound, with a bromo group at the seventh position of the indole ring, delivers notable flexibility in organic synthesis. That localization alters both the electronic characteristics and steric profile compared to regioisomers like 5-bromoindole or 3-bromoindole. Chemists synthesizing pharmaceuticals or advanced organics typically seek out such differences to unlock specific reactivity or tune physical properties while building more elaborate molecules.

    From the manufacturer’s bench, indoles require careful handling throughout their synthesis. Our facility uses batch-controlled halogenation, monitoring reagent addition and temperature to avoid polybromination or undesired isomers. The result is a crystalline solid that meets the purity criteria of medicinal chemists and research professionals. The product we send out places the bromo group at the seventh position—confirmed by NMR and HPLC—removing ambiguity that lower-grade material introduces. Structure certainty makes all the difference in research and pilot plant scale-ups, which always come with their own risks and tight timing.

    Product Model and Specifications in Everyday Language

    Instead of treating 7-Bromoindole as a faceless chemical, our team has learned that project success in the lab usually starts with reliable incoming material. We manufacture this indole to exceed 98 percent purity, and every lot gets full spectral analysis. In routine projects—cross-couplings, Suzuki reactions, stepwise syntheses for more advanced building blocks—such consistency saves countless hours and avoids immeasurable frustration.

    Much of what distinguishes one batch from another comes down to impurity profile and water content. Trace bromide salts or solvent residues introduce noise in analytic methods, obscure reaction endpoints, or poison sensitive catalysts. Across thousands of kilograms produced, we’ve adopted drying techniques and vacuum handling that bring the product’s water content below 0.2 percent, helping customers avoid downstream headaches. Each package leaves our site double-sealed, with silica packets for moisture control and packaging material chosen for both safety and practicality—not just regulation.

    Molecular weight is 210.05 g/mol. Appearance is uniformly off-white, never tan or gray, which speaks to the control over process side reactions. In the warehouse, everyone here can spot the difference. A pure lot looks bright, stays free-flowing, and never sticks to the bottle. With trace analyte checks, we keep the batch-to-batch identity high; for a customer scaling up a reaction, this predictability may mean the difference between a successful delivery and a waste-hauling problem nobody wants.

    Usage—from Synthesis to Application Bench

    Where does 7-Bromoindole most often end up? The answer spans from foundational lab work to late-stage pharmaceutical intermediates. Medicinal chemists use it to build molecules where the indole core serves as a pharmacophore. The bromo substituent provides a convenient handle for further modification, especially by palladium-catalyzed couplings—a mainstay in drug discovery labs. Complex molecules arise from such building blocks, so purity and positional certainty go straight into project reproducibility, overall yield, and regulatory success.

    In crop science, researchers seek subtle variations in heterocyclic cores to introduce new activity in agrochemicals. Substitution at the seventh position tweaks the molecular shape just enough to change biological recognition, creating opportunities not present with indoles brominated at other positions. Early-stage testing often proceeds gram-by-gram—not metric tons—but the lessons learned at our production scale inform even those first reactions.

    Photochemistry and material science groups sometimes look to 7-Bromoindole for its electronic effects, integrating it into polymers or studying its response under various photophysical conditions. Each of these applications prizes reliability. Materials scientists have returned to us again because the batch-to-batch consistency holds up once the methods transfer from bench to pilot runs. In almost every case, project leaders choose materials with a documented chain of custody and independent testing—the sort of accountability that defines manufacturing rather than brokerage.

    What Sets 7-Bromoindole Apart from Other Halogenated Indoles?

    Some users, especially those early in their research, ask what makes the 7-bromo derivative special compared to more widely available analogs, like 5-bromoindole or 2-bromoindole. Positioning matters for several reasons. Regioselectivity during downstream reactions—like palladium-catalyzed substitutions or electrophilic additions—shifts dramatically with even a single atom’s movement on the aromatic ring. The seventh-position bromine offers reactivity for substitution reactions that leaves the five- and three-positions untouched, supporting synthetic strategies that require late-stage diversification.

    Not every bromoindole can provide clean intermediates in complex target molecules. For instance, in bioactive structure–activity relationship studies, medicinal chemistry teams will test whole panels of indole derivatives to map out which substitution pattern gives the most promising activity with the least toxicity. A 7-bromo variant offers an option that bypasses cross-reactivity faced by other isomers; the subtle steric and electronic effects often yield molecules with unique properties, not just minor increments in activity.

    Researchers using more common indole derivatives sometimes face higher byproduct formation or sluggish couplings. Process trials in our facility have confirmed that the 7-substitution can circumvent many roadblocks seen with isomers crowded closer to the pyrrole nitrogen. That difference is more than academic: wasting days debugging an inefficient reaction only to find your starting material was the root cause leaves an impression. We focus on removing that source of error.

    Long-Term Sector Demands and Challenges in Halogenated Indole Production

    Making 7-Bromoindole to meet the growing sophistication of today’s research involves commitment to ongoing process control and adaptation. In early years, scale-up inconsistencies were common. Crystallization routines sometimes locked in trace impurities; later, switched solvents or temperature grids reduced the side-reaction footprint. Today, automated monitoring pairs with manual sampling, a balance most reliable manufacturers adopt after real-world trouble with all-digital control. These dual checks keep output matching the high-purity profile needed in advanced work.

    Demand pressure comes not from commodity buyers but from research-driven growth sectors. Pharmaceutical customers, especially, expect each shipment will fit seamlessly into regulated workflows. Quality agreements specify impurity levels below threshold ppm; regular audits drill down into everything from raw material sourcing to waste-stream management. We learned to anticipate these requests and build verification into our documentation because being caught without it delays shipments and damages reputations earned over decades.

    Environmental and safety regulations have become more exacting. Brominated aromatics draw extra scrutiny, both for safe workplace handling and responsible downstream treatment. Our teams invest heavily in closed-system reactivity, continuous ventilation improvements, and real-time emissions monitoring. Solvent recovery and waste segregation keep hazardous streams under control, reduce cost, and align with both national and international best practices. We see this not as a regulatory hoop, but as a practical way to operate safely in the long run.

    Supply Chain Considerations—A Manufacturer’s Perspective

    It is easy to underestimate the supply chain fragility behind a “routine” compound. Indole and its halo derivatives see spot shortages due to upstream supply hiccups, shifting freight lanes, or regulatory bottlenecks. Production planning happens months ahead, with buffer stocks carried in anticipation of sourcing disruption—especially for rare, high-purity precursors. Our warehouse managers regularly scrutinize vendor reliability and raw material assay data, selecting only those sources that have passed both technical and ethical reviews.

    Freight and packaging decisions balance chemical risk with customer needs: glass bottles for laboratory work, HDPE for larger volumes, both double-bagged and nestled in custom cushioning. Every shipment includes documentation that satisfies both user and regulator. Advanced tracking systems report each parcel from the loading dock to customer receipt, limiting the chance for loss, error, or delay. These systems draw from our own tough experiences after lost shipments and the need to re-make entire batches for delayed clients. Confidence is built on many years of learning and adaptation, not just standard procedures.

    Global logistics, especially for brominated aromatics, bring unique challenges. Countries implement their own import and environmental rules—our compliance group keeps current on every targeted restriction, builds documentation for seamless customs clearance, and coordinates with freight partners to avoid unnecessary delays. Customers rarely see these logistics battles, though delays from third-party traders or resellers often stem from these very issues. As a primary manufacturer, direct oversight prevents many of the common disruptions our competitors encounter.

    Project Experience: Feedback from the Lab

    Product development feedback often appears months, sometimes years, after shipment—compared to the instant recognition of commodities, this delayed gratification underscores the incremental, building nature of research. Chemists in both small firms and multinational labs tell us that the greatest value-add comes from product predictability. They recount stories of reaction runs ruined by “off” raw materials, or analytical ghosts traced to trace-level impurities not disclosed by secondary suppliers. Often, the choice of reagent—down to the position of a single halogen atom—marks the difference between a publishable success and a scrap-pile failure.

    We pay attention to these stories because they chart the real-world cost of inconsistency. Each batch of 7-Bromoindole we ship carries with it not only tested analytical sheets but the recognition that our partners rely on our vigilance. Our team keeps open lines of communication, helping troubleshoot, sharing optimized reaction protocols, even occasionally customizing particle size or packaging to suit unusual pilot runs. Shared expertise and transparency set the well-established manufacturer apart.

    Opportunities for Improving Halogenated Indole Products

    The research and commercial success seen with 7-Bromoindole provides both motivation and learning. Quality control will always remain a moving target as new uses for structurally similar molecules emerge. Our laboratory directs resources toward even lower impurity profiles, with goals to reach 99.5 percent purity on a routine basis and reduce trace elemental contaminants below evolving legal thresholds.

    Better energy management during synthesis—driven by wider adoption of real-time monitoring—saves costs and shrinks the processing footprint. Transitioning to greener halogenation chemistry, using less hazardous reagents and enabling easier waste treatment, forms another current project. Industry-wide standards will continue to climb as regulators, customers, and downstream partners tighten tolerances and expectations.

    A secondary focus involves more direct customer education. Many smaller firms approach these chemicals with less background in halogenated aromatics, and we’ve learned that sharing our application knowledge improves both safety and outcome success. Instructive protocols, recommendations for safe handling, and troubleshooting guides leave end-users more informed and set the stage for healthy long-term partnerships.

    Closing Thoughts from the Factory Floor

    As a chemical manufacturer in this sector for decades, we have seen trends come and go: outsourcing to cut corners, buying from least-cost providers, or seeking “just good enough” grade. Yet, high-precision research and production push for higher standards every year. The experience and care behind each gram of 7-Bromoindole shape not just the immediate reaction but the flow of progress in labs worldwide. We build to support that flow, adapting batch conditions, material controls, and end-user support with every cycle. There’s no substitute for deep familiarity with your own product—and the confidence earned by supplying it year after year without excuse.