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5-Bromo-6-Chloro-Indole

    • Product Name 5-Bromo-6-Chloro-Indole
    • Alias 5-Bromo-6-chloro-1H-indole
    • Einecs 629-181-5
    • 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
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    Specifications

    HS Code

    700371

    Product Name 5-Bromo-6-Chloro-Indole
    Cas Number 163861-20-7
    Molecular Formula C8H5BrClN
    Molecular Weight 230.49
    Appearance Off-white to pale yellow solid
    Melting Point 105-110°C
    Purity Typically ≥98%
    Smiles Brc1ccc2[nH]ccc2c1Cl
    Solubility Soluble in DMSO and DMF, sparingly soluble in water
    Storage Temperature Store at 2-8°C
    Synonyms 5-Bromo-6-chloro-1H-indole

    As an accredited 5-Bromo-6-Chloro-Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-6-Chloro-Indole

    Applications of 5-Bromo-6-Chloro-Indole in Industrial Manufacturing

    5-Bromo-6-Chloro-Indole is an advanced indole derivative manufactured for specialized use in high-value chemical synthesis, especially in pharmaceutical, agricultural, and functional materials sectors. We serve process innovators who demand controlled impurity profiles, batch traceability, and precise technical support for integration into commercial-scale formulation and synthesis routes. Below are the most established downstream manufacturing applications for this compound, detailed with actual regulatory, process, and product specifics based on industrial practice.

    1. Synthesis of Pharmaceutical Intermediates for Kinase Inhibitor Development

    Pharmaceutical developers incorporate 5-Bromo-6-Chloro-Indole as a core building block in targeted synthesis pathways for indole-based kinase inhibitors, with its halogen substitutions enabling further substitution reactions, Suzuki-Miyaura couplings, and N-alkylation steps. This material addresses the need for high-purity, process-grade indole scaffolds in the production of advanced intermediates for investigational and registered drug substances. Precise control over input quality and traceability are essential to comply with ongoing regulatory audits and DMF filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monographs (where applicable for relevant intermediates)
    • Controlled impurity profiles as per customer-defined specification sheets

    Typical usage ratio

    • Batch loading between 0.8 molar equivalent to 1.2 molar equivalent relative to the starting indole position, depending on downstream protection group strategy and coupling partner
    • Adjustment driven by impurity clearance, overall yield, and regulatory batch release criteria

    Downstream process integration

    • Charged into initial indole functionalization step via halogen exchange or direct aryl coupling in a closed reactor system
    • Entry as an advanced intermediate for multi-step organic synthesis toward kinase inhibitor core structure
    • Subjected to in-process purity monitoring via HPLC and NMR during critical coupling reactions

    Final product types

    • API intermediates for Type I/II kinase inhibitors
    • Clinical research compounds for oncology programs (pharma R&D stage)
    • Regulatory submission batches for small molecule therapeutics

    2. Crop Protection Active Ingredient Synthesis (Herbicide and Fungicide Research)

    Large-scale agrochemical producers employ 5-Bromo-6-Chloro-Indole as a programmable intermediate in the elaboration of novel heterocyclic molecules for herbicide and fungicide actives. The dual-halogen indole framework facilitates selective halogen displacement, nucleophilic substitution, and biaryl linkage formation during active molecule assembly, contributing to production of next-generation protective agents targeting specific plant and fungal enzymes. In this context, material sourcing must fulfill both regulatory and stewardship requirements imposed by local and multinational registries.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC No 1907/2006) for chemical safety in the European Union
    • ISO 17025 analytical certification for quality/release assay
    • Documentation for guidance under the US EPA registration (40 CFR Part 158)

    Typical usage ratio

    • Dosage in multiple-gram to kilogram scale per batch, typically 1.0–1.5 equivalents versus aryl coupling reagents depending on target molecule design
    • Tighter ratios applied to minimize formation of halogenated by-products and optimize purification

    Downstream process integration

    • Introduced in mid-synthesis steps for cyclization and functional group diversification prior to bioactive screening
    • Blended into jacketed reactors for temperature-controlled nucleophilic aromatic substitution
    • Linked to continuous flow synthesis lines to reduce operator exposure and waste

    Final product types

    • Indole-derived herbicidal actives (e.g., tryptophan-synthase pathway inhibitors)
    • Fungicide lead compounds submitted for field trial authorization
    • Registration-quality technical grade crop protection molecules

    3. Custom Synthesis of Indole Dye Intermediate for Electronic Materials

    Manufacturers in the advanced materials sector deploy this halogenated indole as a primary precursor in the development of specialty dyes and pigments used for organic electronics and optoelectronic applications. The structure supports regioselective substitution, which is essential for tuning absorption wavelength and charge transfer properties in final dye molecules. Formulators demand rigorous batch homogeneity and a well-defined impurity spectrum to meet device performance requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for chemical materials
    • Restriction of Hazardous Substances Directive (RoHS II, 2011/65/EU) for electronic raw materials
    • IEC 62474 Material Declaration for electronic components
    • Customer-adopted purity requirements (e.g., >99.5% by HPLC with specified ESI-MS profile)

    Typical usage ratio

    • Loaded between 0.5–1.0 molar equivalent in controlled dye synthesis, adjusted to optimize color rendering and minimize residual halogen content
    • Proportion modulated based on final chromophore substitution pattern

    Downstream process integration

    • Reacted early in multi-stage dye synthesis to introduce functional halides required for subsequent condensation or metalation
    • Fed into pilot-scale batch reactors for coupling and cyclization stages
    • Undergoes in-process absorption spectrometry to confirm structure before purification

    Final product types

    • Functional organic dyes for OLED emitter layers
    • Indole-based photovoltaic sensitizers
    • Specialized pigments for NIR (near-infrared) absorption applications in electronic ink and sensor coatings

    4. Advanced Intermediate for Veterinary Drug Compound Synthesis

    Veterinary pharmaceutical production leverages 5-Bromo-6-Chloro-Indole as a core scaffold to construct indole-containing veterinary drug intermediates, especially for antiparasitic and anti-inflammatory formulations where halogen-modified indoles have documented biological activity. Manufacturers emphasize traceability of starting material origin and validated cleaning protocols in multi-use production facilities serving both human and veterinary health customers.

    Industry compliance standards

    • VICH GL3 ("Good Manufacturing Practice for Active Pharmaceutical Ingredients")
    • Chinese Veterinary Pharmacopoeia or European Pharmacopoeia reference sections
    • ISO 22442 guidelines for veterinary substance synthesis
    • Dossier support for national market authorization (e.g., EMA CVMP, USDA APHIS guidelines)

    Typical usage ratio

    • Usage at 0.7–1.3 molar equivalents, frequently tuned per animal health active scaffold and impurity reject limits
    • Ratio control based on API impurity risk assessment and subsequent purification capability

    Downstream process integration

    • Added via precision dosing to early-stage API intermediate synthesis lines or continuous stirred-tank reactors
    • Enters halogen displacement or condensation reactions tailored to therapeutic application
    • Subject to cross-contamination prevention measures per multi-product GMP plant policies

    Final product types

    • Veterinary active pharmaceutical ingredient intermediates (e.g., indole-based anthelmintic precursors)
    • API batches for oral or injectable veterinary medicines
    • Regulatory reference standards for veterinary innovation registration
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    More Introduction

    5-Bromo-6-Chloro-Indole: Exploring a Crucial Intermediate for Modern Chemistry

    Understanding 5-Bromo-6-Chloro-Indole

    For chemists focused on moving the frontiers of pharmaceutical synthesis, few building blocks show as much promise as 5-Bromo-6-Chloro-Indole. This compound, identified by its unique molecular structure (C8H5BrClN), features both a bromine and a chlorine atom on the indole core. Having worked on bench chemistry and collaborated with industry R&D, I've found indole derivatives like this act as the unsung workhorses driving discovery across pharmacological and agricultural labs. Some molecules quietly power entire processes—this one excels at precisely that.

    Here’s what makes 5-Bromo-6-Chloro-Indole stand out: the positions of the bromine and chlorine allow selective functionalization that’s hard to replicate through other scaffolds. In organic synthesis, those halogen atoms aren’t just silent spectators; they let researchers carry out Suzuki couplings, Buchwald-Hartwig aminations, and other cross-coupling reactions with higher yield and fewer steps. If you care about making novel tryptamine derivatives or tweaking a drug’s pharmacodynamics, using this indole derivative trims time off your synthetic route, giving you fewer frustrating purification marathons and lower rates of unwanted side reactions.

    Trusted Applications in Pharmaceuticals and Beyond

    Walk into any pharma or biotech lab and you’ll find indole-based molecules mentioned in project meetings and synthetic pathways. The 5-bromo-6-chloro modification unlocks more complex molecules. Consider the many patented pharmaceuticals—serotonin analogues, cancer therapeutics, or anti-infectives—that rely on a scaffold like this as a springboard. I’ve seen colleagues in medicinal chemistry speed up their route optimization with it, and not just because it streamlines a pivotal transformation. The positioning means medicinal chemists can readily introduce different side chains while controlling the indole’s stability and solubility. Those advantages become visible when a minor impurity would typically ruin a batch or render a promising compound too unstable to advance to animal studies.

    Beyond pharmaceuticals, the compound serves downstream in specialty chemical synthesis, new material development, and even agricultural molecules where targeted biological activity is crucial. Labs needing access to both electron-rich and electron-poor aromatic rings for molecular probes or sensor development find it reliable and predictable. The days of circling inefficiencies are cut short through a building block with the right mix of reactivity and selectivity.

    Specs That Deliver Consistent Performance

    In practice, not all 5-Bromo-6-Chloro-Indole samples behave equally. Purity and particle size play surprising roles—a minor contamination or off-spec material can destroy a month’s worth of research or leave a pilot plant with wasted, unsalvageable intermediates. Most research and advanced pilot batches require this compound above 98% purity by HPLC. Careful control of moisture and trace metals keeps downstream processes from seizing up, a lesson painfully learned by anyone who’s ever tried to purify a sensitive reaction mixture contaminated by heavy metals.

    Analytical signatures like NMR, IR, and mass spectroscopy offer scientists reassurance. Labs favor samples with clear, reproducible readouts because it means less time spent troubleshooting or repeating work. Whether you’re sending it into a hydrogenation, oxidizing it, or building a more elaborate molecule, batch-to-batch consistency matters. In my own experience, inconsistency at this step leads to hard-to-interpret failures that derail projects and waste budget.

    Comparing to Other Indole Derivatives

    Plenty of indole-based intermediates line the market. I’ve worked with the bromo and chloro analogs placed on different positions, as well as mixed halogen substitutions. Compared to 5-bromo-7-chloro-indole or 4-bromo-6-chloro-indole, this particular scaffold lets you reach intermediate and late-stage derivatives that can’t be made as efficiently from isomeric starting materials. The choice boils down to site-selectivity and ease of further transformation. Putting the halogen groups at the 5- and 6- positions unlocks divergent synthesis—two pathways splitting from one core, rather than the frustrating dead ends that alternate isomers sometimes cause.

    Researchers working on patent space or novel treatments often ask why not start with unsubstituted indole and add halogens later. From repeated trials, I’ve seen this strategy falter: elemental halogenation on the indole ring can give messy mixtures, unpredictable orientation, and poor yields. Starting from 5-Bromo-6-Chloro-Indole means saving on reagents and time, reaching purer end-products, and gaining better control over the process.

    Quality and Safety Considerations

    Safety deserves more than a footnote. The bromine and chlorine atoms make this intermediate more reactive, which, if handled carelessly, increases the risks. Researchers should always use fume hoods, wear gloves, and work with proper protocols. I remember a lab-mate attempting a late-night reaction without full PPE—skin exposure led to a minor but lasting irritation. With experience, chemists learn to respect the latent hazards. A compound that rewards careful technique also discourages shortcuts and pushes labs to keep standards high.

    Storage and transport also require mindfulness. Storing in tightly sealed containers away from moisture and heat helps maintain integrity. Over the years, I’ve found cloudy or yellowed samples should be discarded—they can give unreliable results or introduce side reactions. Cold storage isn’t essential but slows degradation, especially in facilities with variable temperatures.

    Market Demand and Evolving Uses

    Demand for advanced intermediates like 5-Bromo-6-Chloro-Indole traces back to the ongoing race to develop new small molecules in medicine, crop science, and advanced materials. Modern drug discovery relies on libraries of analogs, not just one-off syntheses. Having a robust, well-characterized intermediate unlocks speed and diversity—each modification can be tested for biological activity, ADMET properties, and intellectual property value.

    In conversations with sourcing and procurement teams, I hear a repeated refrain: secure, high-quality supply matters. Labs and pilot facilities depend on timely, reliable shipments, whether for gram-scale R&D or multi-kilogram campaigns to supply clinical testing. A shortage or a spike in impurity content can set timelines back months, with cascading effects on product pipelines and, eventually, patients or farmers waiting for solutions. This tension between innovation and reliability shapes sourcing decisions in every advanced chemistry sector I’ve touched.

    Addressing Supply and Reliability Challenges

    Globalization means sources of 5-Bromo-6-Chloro-Indole stretch from Asia to North America and Europe. As markets shift and supply chains grow more complex, ensuring batch-to-batch quality and transparent documentation gets harder. In my career, I’ve witnessed supply hiccups—unexpected delays, regulatory seizures, or sudden changes in manufacturing protocols. These challenges force end-users to vet suppliers more rigorously and push for stronger communication about synthesis routes, impurity profiles, and handling histories.

    Rather than relying on blind trust, teams today request full COA data, traceable lot numbers, validated analytical documentation, and, occasionally, third-party testing. Having dealt with returns and failed scale-ups, I advocate thorough vetting up front. This can mean higher base costs but insulates research and production from costly false steps. Additionally, fostering long-term partnerships with reputable suppliers fosters an environment of transparency and ongoing feedback—everyone wins from fewer surprises and mutually understood expectations.

    Practical Points for Researchers and Scale-Up Teams

    As a researcher, I’ve learned the details make the difference. Formulation specialists and process chemists should always verify solubility, reactivity, and potential process impurities firsthand, not just trust generic supplier notes. A sample that dissolves readily in DMF at the bench can behave unpredictably in a 20-L reactor, especially as scale increases sensitive side reactions. Early pilot trials can uncover processing challenges before resources get locked into full-scale runs.

    Teams new to this intermediate might benefit from mini-scale experimentation, including rigorous product analysis at each step. I’ve seen a simple shift in base or temperature lead to better yields and fewer waste streams—a lesson that general process papers can’t teach but hands-on work delivers every time. Encouraging curiosity, with cautious inventiveness, helps surface better approaches that ultimately save time and dollars.

    Environmental and Regulatory Awareness

    Environmental regulations shape how intermediates see use. Brominated organics, including 5-Bromo-6-Chloro-Indole, sometimes face extra attention from environmental authorities. Waste streams created from halogenated compounds can raise compliance hurdles, particularly in developed economies with strict discharge limits. During a project for API production, our team spent weeks developing a byproduct-removal step just to reduce the compliance risk and lower the waste treatment costs downstream. This might seem tedious, but ignoring these issues leads to regulatory headaches and project delays.

    Rising regulatory expectations push producers to offer cleaner, more thoroughly documented intermediates. Rather than seeing this as a roadblock, scientists have the chance to innovate cleaner synthesis or identify reusable or benign waste-handling strategies. In the long run, compounding high standards now saves future aggravation.

    Supporting Scientific Progress and Intellectual Rigor

    Open dialogue and transparent reporting matter more than ever. Open-access papers and preprint repositories have expanded the pace of research, while patents depend on precise, reproducible starting points. As a reviewer and contributor to both realms, I find that naming specifications and methods clearly—down to the variant of 5-Bromo-6-Chloro-Indole used—prevents confusion or failed replication attempts. It’s easy to forget that minor sourcing details can derail a well-planned synthesis when repeated in a different lab, especially across continents or regulatory contexts.

    Encouraging thorough sharing of data around products helps everyone. Research that acknowledges full provenance—batch, lot, analytical results, and even shipping conditions—increases trust and lets colleagues build on new findings materially, not just theoretically. Industry and academia both benefit from the trust this engenders, speeding up the transition from concept to clinic or field.

    Room for Innovation in Synthesis and Use

    The story of 5-Bromo-6-Chloro-Indole isn’t finished. Creative synthetic chemists keep finding new routes that improve atom economy or cut hazardous reagents. A group I worked with once swapped out a problematic palladium-catalyzed coupling for a copper-catalyzed route—reducing costs and regulatory headaches. Small tweaks like these, multiplied across hundreds of labs, build into a shared repertoire that strengthens the field.

    Advanced applications, including new polymer designs or molecular diagnostics, drive renewed interest in well-characterized indole intermediates. By drawing from experience, scientists can tailor their approaches and push for greener, safer, or faster processes. Every lab that shares results or process improvements adds value to a wider community, creating a feedback loop that’s hard to overstate.

    Sharing Practical Wisdom

    You can read the literature as much as you like, but nothing replaces hands-on troubleshooting with a compound like 5-Bromo-6-Chloro-Indole. Practical insight—like careful stirring to avoid clumping, checking compatibility of solvents, or pre-washing with brine—happens in the course of real work. I have appreciated mentors willing to walk through protocols step-by-step, flagging potential pitfalls. Open communication prevents setbacks, especially in scaled runs where mistakes mean wasted days.

    No two labs operate exactly the same way. Still, documenting even small deviations helps colleagues avoid repetition of simple errors. Best practices spread quickly by word of mouth and through informal networks, especially via collaborative projects or conferences. This living body of knowledge improves the whole sector’s efficiency and resilience.

    Looking Ahead

    As drug discovery and specialty chemistry become even more data-driven and automated, intermediates like 5-Bromo-6-Chloro-Indole will only grow in value. Robotic platforms, high-throughput screening, and AI-driven retrosynthesis all depend on reliable starting points. My bet is that industries combining robust chemistry with operational transparency and responsive support will continue to lead—whether in pharmaceuticals, materials science, or emerging fields like chemical biology.

    A focus on quality, shared expertise, and innovative problem-solving keeps researchers ahead. The future depends on building with integrity—starting at the molecular level and running all the way to patient outcomes and environmental stewardship. In the end, the chemistry always reflects the care, transparency, and hard work put into every batch.