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HS Code |
963651 |
| Chemical Name | 4,6-Dichloro-1H-Indole-2-Carboxylic Acid |
| Cas Number | 39512-49-3 |
| Molecular Formula | C9H4Cl2N2O2 |
| Molecular Weight | 243.05 g/mol |
| Appearance | Off-white to light yellow solid |
| Melting Point | ≥210°C (decomposition) |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in DMSO and methanol |
| Storage Conditions | Store at 2-8°C, in a dry place |
| Inchi Key | DLUJXNCOFSGYES-UHFFFAOYSA-N |
As an accredited 4,6-Dichloro-1H-Indole-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, tamper-evident plastic bottle containing 25 grams of 4,6-Dichloro-1H-Indole-2-Carboxylic Acid, labeled with hazard warnings and product details. |
| Shipping | 4,6-Dichloro-1H-Indole-2-Carboxylic Acid is shipped in tightly sealed, chemical-resistant containers under ambient conditions. The package includes hazard labeling if required, accompanied by a safety data sheet. Transport complies with local and international regulations to prevent exposure, spills, or environmental contamination. Handle with appropriate protective equipment upon receipt. |
| Storage | 4,6-Dichloro-1H-Indole-2-Carboxylic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Protect from moisture and incompatible substances such as strong oxidizers. Label the container clearly, and ensure it is kept out of reach of unauthorized personnel and properly segregated in a chemical storage cabinet. |
Applications of 4,6-Dichloro-1H-Indole-2-Carboxylic Acid in Industrial ManufacturingAs a direct manufacturer, we supply 4,6-Dichloro-1H-Indole-2-Carboxylic Acid to specialized downstream industries that leverage its indole scaffold for complex chemical synthesis. The following sections outline key industrial application scenarios with process-critical details on compliance, formulation, workflow integration, and the nature of their end products. 1. Pharmaceutical Intermediate for Kinase Inhibitor SynthesisInnovator and generic drug manufacturers utilize this compound as an advanced intermediate in the synthesis of indole-core kinase inhibitors for oncology. Process chemists value its chlorinated indole ring for controlled halogenation in heterocyclic coupling steps specific to active pharmaceutical ingredient (API) constructs. Industry compliance standards
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2. Agrochemical Active Ingredient PrecursorMajor crop protection manufacturers employ the material in the multi-step synthesis of chlorinated indole-based herbicide or fungicide actives. Agrochemical R&D teams select it for its substitution pattern, which aligns with structure-activity relationship requirements in biological screening. Industry compliance standards
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3. Advanced Materials Synthesis for OLED and Organic ElectronicsManufacturers in organic light-emitting diodes (OLEDs) and electronic display sectors incorporate this compound as a functional group precursor in the synthesis of high-purity indole moieties for blue or green-emitting polymers and small molecules. Its defined halogen pattern leads to targeted photophysical properties for next-generation screen materials. Industry compliance standards
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4. Building Block for Fine Chemical Synthesis in Research ReagentsProducers of high-purity research chemicals and diagnostic reference standards formulate this material as a core building-block within custom synthesis protocols, leveraging its dual chlorine functionalization for downstream diversification. It is favored in libraries for biological assay work due to reproducible purity and reactivity. Industry compliance standards
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Our experience working on 4,6-Dichloro-1H-Indole-2-Carboxylic Acid goes further than laboratory testing or technical documentation. Every batch reflects a long line of practical problem-solving in real manufacturing environments. This compound—routinely abbreviated as DCI-2CA—plays a specialized role for customers stepping beyond standardized indole derivatives. We have been synthesizing indole-based products for years. Through hands-on adjustments, pilot trials, and strict process control, we have come to appreciate the unique strengths and challenges this molecule presents.
DCI-2CA shares the core indole structure common across much of our chemistry portfolio. Chlorination at the 4 and 6 positions produces significant changes. The resulting functionality impacts both reactivity and downstream compatibility. Its carboxylic acid group at the 2-position remains robust—it doesn't hydrolyze easily under mild conditions. These features matter to scientists and scaling teams alike. Compared with non-chlorinated indole-2-carboxylic acids, DCI-2CA offers altered electronic effects, which open doors to new chemistry and different product behavior in final applications.
We know purity isn’t an optional feature—process variation gets magnified as volumes rise. Our product typically offers assay levels over 98%. The crystalline powder flows well, making it amenable for both small-batch and multi-ton scale production. Brightness, particle size distribution, and moisture content get monitored on every outgoing lot. During development, we encountered trickiness with color consistency and trace impurities. Incremental upgrades in filtration, solvent exchange, and drying helped tackle these hurdles, bringing the lot-to-lot color variation within tight tolerances.
The synthetic value of 4,6-dichloro-1H-indole-2-carboxylic acid shows up most clearly in pharmaceutical intermediate work. Chemists rely on its scaffold to build targeted bioactive molecules. Besides drug development, this compound sees use in specialty agrochemical preparation and fine chemical research. Over several years, we’ve seen it integrated into advanced, structure-activity optimization projects. In some industrial pathways, the extra chlorine atoms allow new cross-coupling or substitution reactions that would be awkward or impossible with unmodified indoles.
One of the recurring topics we hear from partners: how does this molecule behave differently from close cousins such as 5-chloro or unsubstituted indole-2-carboxylic acid? The change is not just incremental. DCI-2CA’s double chlorination shifts the electron density, affecting how reactions proceed—especially when performing further halogenation, acylation, or Suzuki couplings downstream. Its solubility profile also diverges from single-substituted analogs, since increased halogen content lowers polarity and impacts dissolution in common solvents.
A practical example springs from a recent collaboration with a medicinal chemistry team: with other indole acids, yields for a set of advanced amide couplings ran up against persistent byproduct formation and slow conversion. After introducing DCI-2CA to the sequence, those same couplings hit cleaner, higher yields thanks to altered reactivity pathways. These results don’t always translate neatly across all projects, but the trend stands out over a decade of direct feedback.
Making dichlorinated indole derivatives requires real attention to solvent management, temperature control, and impurity removal. During early syntheses, we grappled with chlorination step selectivity and residual solvent carryover. Minor tweaks with chlorinating agent stoichiometry and extended phase separation cycles solved much of this. Today, our plant uses modern glass-lined reactors with automated feed control—improving yields and reducing cycle time year over year.
Dealing with waste streams from halogenated chemistry brings a second layer of responsibility. Our site adheres to local environmental regulations for effluent and air releases. Years of investing in onsite solvent reclamation and halide scrubbing have reduced our disposal volume and costs. These upgrades came partly in response to customer audits, which increasingly prioritize lifecycle management for specialty chemicals.
In this industry, traceability and transparency count. With DCI-2CA, customers often have commercial deadlines depending on reliable material supply and consistent characteristics. By controlling every stage, from chlorination through crystallization and packaging, we’ve been able to resolve scale-up surprises quickly. There have been times—especially early on—when our direct troubleshooting has kept critical projects on track for our partners, where a mere intermediary couldn’t dig into root causes.
As upstream chemical raw material shortages continue to shape global markets, we maintain a buffer of strategic supplies for essential inputs such as indole, phosphorus oxychloride, and select catalysts. Our direct purchasing relationships and in-house storage lower the risk of unexpected delays. With every major batch we validate, our team cross-checks spectral and chromatographic profiles against a multi-year library of reference samples, ensuring continuity for product development teams and routine users.
DCI-2CA requires knowledgeable handling. Workers at our facility follow a training regimen based on prior near-miss events as well as regulatory best practices. Some indole derivatives can irritate skin or mucous membranes, and we have evolved our process enclosures, dust collection, and personal protection guidance to reflect those risks. No commercial operation achieves zero incident risk, but by embedding lessons from real operations, we act faster if future issues surface.
We engage with synthesis teams at universities, start-ups, and multinationals. Many of our longtime customers found us through word of mouth, based on our willingness to tailor delivery forms or help troubleshoot their particular protocols. For instance, some groups requested extra drying steps for moisture-sensitive work—so we set up a two-stage vacuum bake process. Others needed micro-lots for high-throughput screening; our plant can flex between kilo- and gram-scale supply without cutting corners or tacking on unneeded distributors.
We strive to share technical notes and observations as they accumulate. Analytical support—ranging from IR fingerprints to impurity tracking—flows from our QC labs to our customers. As DCI-2CA continues to make its way into emerging research directions, such as heterocycle-based fluorescent probes or complex natural product synthesis, we follow these trends and adapt offerings accordingly.
We have weathered disruptions caused by logistics bottlenecks, export controls, and shutdowns. Each incident shaped improvements in how we hold safety stocks, qualify raw material sources, and ramp up or scale down lines as needed. During past indole upstream shortages, we worked with partners to forecast their true needs and prevent avoidable overstocking or waste. Our production team holds regular reviews for all narrow-use compounds to head off issues before they ripple downstream.
No process ever stops evolving, even with a mature molecule like DCI-2CA. In the last few years, we implemented stepped cooling in crystallization tanks; this dropped crystal clumping and sped up filtration times. Our QA staff have pushed for tighter residual solvent targets, and we invested in better headspace GC screening as a direct result. Candidate green chemistry approaches—such as reduced-chlorine waste and recyclable solvents—are under ongoing trials in collaboration with material scientists and plant engineers.
Legal and environmental requirements for dichlorinated indoles aren’t uniform across regions. A few jurisdictions restrict maximum residual solvent content more stringently than others. Our documentation and batch history are ready for third-party review, and past audits have confirmed our adherence to both REACH and other market-specific regulations. Customer conversations increasingly focus on sustainability—so every ton produced gets cataloged for energy and water use, and summaries flow up to company-level CSR reporting. By keeping these figures current, our buyers can transparently report environmental data to their own stakeholders.
More than once, project managers from pharmaceutical and specialty chemical firms have told us that the difference between product launch and delay came down to quick access to this exact compound, with full records and the ability to custom-match previous batches. Our response system relies on experienced chemists, not just a help desk. This real-world backup shortens downtime when bottlenecks or deviations arise.
Cost always matters in specialty chemistry. Larger customers benefit from our scale but smaller or exploratory users find our minimums reachable as well. By handling logistics in-house and managing export/import compliance directly, we smooth out the kinks that appear in regions with fast-changing regulatory climates or shifting customs priorities.
Advice given here stems directly from user and in-house lab feedback. DCI-2CA should be stored tightly sealed, with temperature and light exposure minimized. This avoids unnecessary degradation or color changes over time. Many customers ask about mixing with polar or apolar solvents. DCI-2CA dissolves cleanly in DMF, DMSO, or dichloromethane. Non-halogenated indole acids show better water solubility, but we have seen users obtain strong results with DCI-2CA by pre-dissolving in a small amount of warm solvent before dilution for reactions or formulations.
For users needing consistent bulk flow, we advise against long-term storage in high-humidity environments—caking or clumping may result over months. Running a small batch trial can identify any custom handling quirks before shifting to full production mode. If questions pop up about compatibility, we have a direct line to the process engineers and QC team who have lived with these issues in day-to-day work.
Repeat business tells us more than any single testimonial. A portfolio of tracked customer projects—ranging from early-stage R&D to global commercial launches—demonstrates DCI-2CA’s reliability when produced at source. Long-term buyers help set priorities on batch sizes, assay standards, and even logistics adaptations such as container types or shipment scheduling. These direct channels foster innovation and cut out delays that come with third-party middlemen or under-informed trading houses.
Sometimes, specifications need tightening or subtle tweaks as chemistry evolves. By keeping open communication, technical files, and retained samples, we adapt quickly to these shifting benchmarks. Trust in material consistency stems from this direct contact, not from generic assurances. Problems do arise—a minor off-color or an odd IR signal now and then—but tackling these issues quickly and openly, without passing the buck, keeps customers returning year after year.
Our manufacturing journey with 4,6-dichloro-1H-indole-2-carboxylic acid tracks ongoing chemical innovation. As pharmaceutical and fine chemical research pushes boundaries, we see demand shifting toward more tailored, functionally unique building blocks. Each step, from the core indole platform to these highly substituted derivatives, required us to rethink processes, quality checkpoints, and supply chain strategies. The lessons learned here inform other products and collaborations in our pipeline.
Customers are demanding more than a catalog number; they seek evidence, transparency, and proven performance in daily operations. We bring our factory floor perspective and detailed product understanding to every order for DCI-2CA. The product lines may change, and regulations may tighten, but our hands-on approach—grounded in experience and mutual trust—remains our strongest asset.