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5-Chloroindole-3-Carboxaldehyde

    • Product Name 5-Chloroindole-3-Carboxaldehyde
    • Alias 5-Chloro-1H-indole-3-carbaldehyde
    • Einecs 629-522-5
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    702590

    Product Name 5-Chloroindole-3-Carboxaldehyde
    Cas Number 6124-65-2
    Molecular Formula C9H6ClNO
    Molecular Weight 179.60 g/mol
    Appearance Off-white to yellow crystalline powder
    Melting Point 174-177°C
    Purity Typically ≥98%
    Boiling Point No data available
    Solubility Soluble in DMSO and DMF; slightly soluble in water
    Smiles C1=CC2=C(C=C1Cl)NC=C2C=O
    Inchi InChI=1S/C9H6ClNO/c10-7-1-2-8-9(3-7)11-4-6(8)5-12/h1-5H,(H,11,12)
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Refractive Index No data available
    Synonyms 5-Chloro-1H-indole-3-carboxaldehyde

    As an accredited 5-Chloroindole-3-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Chloroindole-3-Carboxaldehyde, 10 grams, is supplied in a tightly sealed amber glass bottle with a chemical-resistant screw cap.
    Shipping 5-Chloroindole-3-Carboxaldehyde is shipped in tightly sealed containers, protected from light, moisture, and heat. Typically dispatched as a solid, it is packed following regulations for hazardous chemicals, often with secondary containment and proper labeling. Transport is handled by certified couriers with documentation to ensure safe and compliant delivery.
    Storage 5-Chloroindole-3-Carboxaldehyde should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed to prevent moisture and air exposure. Store separately from strong oxidizing agents, acids, and bases. Use appropriate, labeled containers, and ensure that storage complies with relevant chemical safety regulations.
    Application of 5-Chloroindole-3-Carboxaldehyde

    Applications of 5-Chloroindole-3-Carboxaldehyde in Industrial Manufacturing

    5-Chloroindole-3-Carboxaldehyde plays a strategic role as a key intermediate in the synthesis of advanced pharmaceutical molecules, specialty agrochemicals, dye constituents, and fine chemical research products. As an integrated chemical manufacturer, we focus on supplying consistent quality at scale to ensure efficient downstream processing across high-value industries.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use this indole derivative in the synthesis of selective serotonin reuptake inhibitor (SSRI) precursors, kinase inhibitor scaffolds, and specialty heterocyclic APIs. Our production supports multi-step syntheses where the aldehyde group serves as the crucial point for coupling, cyclization, or reductive amination. Assurance of minimal impurities, documented elemental analyses, and traceability to raw batch allow for reliable scale-up in GMP environments.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, and JP monograph alignment for related substances and residual solvents
    • Data integrity and change control under 21 CFR Part 210/211
    • REACH Annex VII for human health hazard assessment

    Typical usage ratio

    • 10–25 mol% relative to target molecule, adjusted according to specific API pathway and desired yield
    • Final batch scale determined by required API output and regulatory validation batches

    Downstream process integration

    • Direct input in condensation or reductive amination reactions using automated reactors
    • Intermediary in Grignard or Suzuki coupling steps for heterocycle extension
    • Purification via prep HPLC or crystallization monitored by HPLC/GC-MS
    • Handled in dedicated cleanroom suites to reduce cross-contamination risk

    Final product types

    • Kinase inhibitor APIs
    • Serotonin-modulating compounds
    • Specialty indole drugs for oncology or CNS therapy
    • Regulatory compliant GMP intermediates

    2. Agrochemical Active Ingredient Development

    Leading agrochemical formulators use 5-chloroindole-3-carboxaldehyde as a nucleophilic building block during the synthesis of novel indole-based fungicides, insecticides, or plant growth regulators. Structural substitution at the indole ring allows precise biological activity targeting through further functionalization or quaternization in pilot and commercial lots. Batch traceability and environmental compliance are crucial for market registration dossiers.

    Industry compliance standards

    • OECD GLP for safety and efficacy testing
    • FAO/WHO pesticide specification protocols
    • ISO 9001 quality management systems for production and QC release
    • EU Regulation 1107/2009 relating to plant protection product registration

    Typical usage ratio

    • 5–15 mol% in actives synthesis, fine-tuned by target molecule and batch size
    • Process variation based on bioactivity trial outcomes and impurity profiles

    Downstream process integration

    • First-step condensation with other indole or aromatic feedstocks in jacketed glass reactors
    • Further halogenation, oxidation or amination under controlled temperature and pH
    • Filtration, solvent switching, and drying to isolate agrochemical actives
    • Incorporation into final microgranules, SC or EC formulations by downstream partners

    Final product types

    • Novel fungicidal actives (e.g., for cereal or rice protection)
    • Indole-based insecticide intermediates
    • Plant growth modulation additives for specialty crops
    • Test batches for regulatory registration of new active molecules

    3. Advanced Dye and Pigment Development

    Colorant and pigment producers incorporate this indole-aldehyde intermediate in the creation of high-stability chromophores and dye precursors, particularly where halogen substituents drive color intensity or chemical resistance. The product's reactivity enables controlled condensation with aromatic amines or phenols, forming core indole-based pigments for plastics, inks, and coatings. QC of spectral purity and residual solvent content ensures compliance for downstream blending.

    Industry compliance standards

    • EN 71-3:2019 for pigment migration in toys
    • REACH SVHC surveillance on halogenated dye substances
    • ISO 787 for standardized pigment analysis
    • European Printing Ink Association (EuPIA) guidelines for ink formulation

    Typical usage ratio

    • 1–8 wt% in masterbatch dye synthesis, chosen based on color depth and fastness requirements
    • Ratio varies with co-reactant structure and solvent system employed

    Downstream process integration

    • Input at first condensation or Mannich reaction for indole base construction
    • Intermediate in azo dye coupling or sulfonation reactions for enhanced solubility
    • Batch filtration, pH neutralization, and thermal drying for pigment isolation
    • QC release based on absorbance, hue, and dispersibility parameters

    Final product types

    • Indole-derived synthetic pigments for thermoplastics
    • Specialty dyes for security inks and high-performance coatings
    • Color concentrates for polymer compounding
    • Lab-scale pigment blocks for formulation R&D

    4. Fine Chemicals and Specialty Synthesis

    Chemical research and custom synthesis operations rely on our reliable supply for bench-scale or pilot-scale manufacture of advanced heterocyclic synthons, photoactive probes, and specialty analytical reagents. Reactivity of the carboxaldehyde moiety makes it valuable in complex aromatic extensions or cyclization routes. Control of impurity levels and moisture content supports reproducible reactions in high-value chemical libraries or reference standard development.

    Industry compliance standards

    • ISO 17025 laboratory standard for analytical verification
    • Sigma-Aldrich internal testing protocols for small molecule reference standards
    • GLP/ISO 9001 quality standards for specialty chemical supply
    • GHS/CLP hazard labeling and SDS documentation for lab-scale raw materials

    Typical usage ratio

    • 0.5–10 mmol per reaction, depending on target molecule, route complexity, and library design
    • Stock solution concentrations tailored for automated workstation dosing

    Downstream process integration

    • Stocking in 0.5–5 kg lot sizes for laboratory reagent set-up or pathway development
    • Input at key halogenation, aromatic extension, or cyclization stages
    • Purification by reversed-phase HPLC or prep chromatography for research-grade output
    • Batch-specific certificate of analysis to support documentation and reproducibility

    Final product types

    • Structure-activity relationship (SAR) synthesis libraries
    • Specialty chromophores for analytical instrument calibration
    • Fine chemical synthons for custom R&D
    • Stabilized derivatives for physical property measurements
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    Certification & Compliance
    More Introduction

    5-Chloroindole-3-Carboxaldehyde: A Practical Perspective from the Manufacturer

    Introduction to 5-Chloroindole-3-Carboxaldehyde

    Among the various indole derivatives that cross our production lines, 5-Chloroindole-3-Carboxaldehyde stands out due to its unique role as a building block in specialty chemistry. From the beginning, we do not lose sight of its importance to customers working in pharmaceuticals, agrochemicals, and material science research. The model designation aligns with its molecular formula, C9H6ClNO, and its CAS number, which researchers and purchasing agents turn to for proper sourcing. Over the years of making indole intermediates, each batch of this compound highlights the differences that careful synthesis and refined process control can make compared to bulk, lower-grade counterparts.

    Manufacturing Experience and Craftsmanship

    We have spent years developing practical know-how in indole chemistry. 5-Chloroindole-3-Carboxaldehyde, with its chlorinated aromatic ring and reactive aldehyde, doesn't allow room for shortcuts. In the early days, we struggled with side-reactions at the ring and aldehyde, which meant inconsistent purity or color. Through investment in controlled chlorination and strict temperature profiling, we now ensure a reproducible product that consistently achieves high purity. Minor impurities, even below 0.5%, can wreak havoc in sensitive syntheses downstream, especially for those designing new drug candidates or fine-tuning catalysts. We monitor every batch by HPLC and NMR, sharing full analytical data upon request. Clear crystal formation and uniform pale yellow coloring reflect the care we put into drying and packaging, and customers have noticed that stability improves through moisture-tight containers and rapid, hands-free bottling.

    Specifications Rooted in Real-World Application

    For 5-Chloroindole-3-Carboxaldehyde, most customers ask for purity levels above 98%. We have set our internal targets higher. Repeat orders come from those who need reliable lot-to-lot consistency for structure-activity relationship studies in medicinal chemistry. Our GC and HPLC results typically show fewer than five identifiable impurities, none of which exceed 0.2%. The melting point stays in the expected 130–133°C range and we have seen, through stability trials, that the product holds up to normal storage conditions for at least two years. Bulk material keeps well in high-density polyethylene drums with nitrogen overlay, and we fill small glass bottles under inert atmosphere for bench-scale users.

    Whenever requests come for alternative grades, we discuss the actual end use. Some research teams require higher water content tolerance, so we offer both standard (moisture less than 0.5%) and ultra-dry grades (moisture below 0.1%). Particle size hasn't been a sticking point here: most users dissolve the compound straight into organic solvents for reactions or chromatographic separations. Our experience has shown that additional milling doesn't improve performance, so we avoid unnecessary steps that might add costs or risk contamination.

    Usage and Insights from Customer Collaboration

    The main demand for this indole aldehyde centers on synthesis of pharmaceuticals and crop protection agents. Medicinal chemists favor it when creating analogues of auxin-related scaffolds. Crop protection researchers often use it to craft new herbicide leads by modifying the indole ring. We had one customer in Japan who needed extremely low halogen impurities due to sensitive downstream reactions, so we revised our washing protocol, switching to multi-stage extraction using precisely controlled solvent mixtures. Now, every batch meets the strictest halide limits, and this protocol has carried over to all orders, raising the bar for purity.

    Collaborations with university labs revealed another insight: when scaling up a particular Suzuki-Miyaura coupling, impurities in commercially available starting materials led to low yields and hard-to-remove byproducts. When our 5-Chloroindole-3-Carboxaldehyde batches were tested head-to-head, theirs yielded a single, sharp product peak; ours consistently delivered higher conversion rates and cleaner extractions, saving time in both purifications and analytical verifications. These improvements come only from actually running experiments, not generic claims or sales pitches.

    Comparing with Other Indole Derivatives

    Our lineup includes several indole-3-carboxaldehyde analogues with different substituents such as methyl or bromo groups. Each brings different reactivity and stability in lab or process settings. In practical terms, the addition of chlorine at the 5-position raises both the electron-withdrawing effect and the capacity for further functionalization on the aromatic ring. For those synthesizing drugs with enhanced metabolic stability, this minor structural change offers a significant difference over the parent indole-3-carboxaldehyde.

    Other manufacturers, especially those operating with lower overhead or less advanced equipment, occasionally produce indole derivatives that contain excess starting material or chlorinated byproducts, because chlorine chemistry can run wild without precisely tuned conditions. Complaints about off-color, sticky residues, or unexpected side-product peaks in customer product reports remind us of the importance of methodical process control. From our side, we never blend various grades to hit a specification – we manufacture to a target, confirm composition, and discard out-of-spec batches. In an industry where a single contaminant can mean a failed kilogram-scale synthesis or even a failed clinical batch, these steps are essential, not optional.

    Why Purity and Traceability Matter

    Pharmaceutical and specialty chemical manufacturers depend on traceability as much as raw quality. The European customers, even more so than our domestic ones, require batch records that stretch from starting material through final drying and packing. Our digital ledger follows every lot through each synthetic step, linking chromatography runs, spectral data, and operator logs. On the rare occasion we receive a customer callback over a questionable peak in an LC trace, we can review exact manufacturing conditions, raw material lots, and even storage environment. These checks lead to continual process improvements. Our staff recall two batches from 2019, where an early-stage solvent change led to increased yellowing. The documentation allowed us to identify and address the issue before it became a widespread problem; we switched back to the original protocol, restoring color and clarity of each subsequent batch.

    Trace elements and heavy metal content remain a point of focus, not only for regulatory reasons but for practical application. We developed an ICP-OES workflow to quantify chlorine, lead, cadmium, and iron at sub-ppm levels. Most users expect these data now, especially those in advanced synthesis settings where even low metal contamination impedes catalytic chemistry. Years ago, some labs accepted only rudimentary purity checks; today, audits and supplier qualification demand the extra assurance that only direct, in-house analysis can provide.

    Challenges Unique to 5-Chloroindole-3-Carboxaldehyde

    Raw material sourcing presents ongoing challenges. High-purity indole and chlorination reagents come from a shrinking set of specialty chemical suppliers due to increasing REACH and local environmental regulations. We now qualify each new supply lot with full COA and independent NMR analysis, since trace residuals in raw materials quickly propagate through to the finished product. For instance, we found that one supplier's lot introduced a faint sulfur smell in one batch; a closer look at the upstream synthesis revealed trace thioether carry-over. We excluded that supplier, absorbing higher costs to maintain the standards we and our customers expect.

    Waste stream management accompanies each kilogram of production, especially with chlorinated intermediates. By rerouting aqueous byproducts through an in-house neutralization system and performing solvent recycling, we have cut our halogenated waste output. Only the most resilient manufacturing management avoids regulatory fines and community relations issues. Our team partners with local agencies to ensure responsible chemical handling and reporting.

    Addressing Problems and Finding Solutions

    Each year brings a new round of questions: Can you guarantee ultra-low metals? Will this pass European import checks? Do you use sustainable manufacturing practices? For the metals, we repeat batch-level third-party testing. Our packaging lines have changed to include tamper-proof seals and QR codes for instant traceability, which builds confidence during import inspections. Sustainability is a journey, not a checklist. We source greener solvents and install energy-efficient reactors and LED lighting in our unit operations. The learning curve runs steep but necessary, as customer and government demands continually rise.

    Packaging sometimes presents overlooked problems. One of our longest-standing clients noticed occasional clumping in large drums during summer months, especially after ocean transit. After listening to their feedback, we overhauled the drying step, lowered water content limits, and transitioned to improved vacuum sealing. These steps led to better product pouring, less need for manual chip-out, and fewer complaints at reception labs. Experience tells us that little touches—a stable container, a visible lot label, easy-to-cut seals—matter to the chemists using the product as much as any advertised spec.

    Why 5-Chloroindole-3-Carboxaldehyde Remains a Key Intermediate

    Research groups and commercial manufacturers keep coming back for this intermediate not just for its chemistry, but for the reliability that skilled manufacturing brings. In pharmaceutical development, it provides a platform for arylation, halogen exchange, and ring-closing reactions. Each of these paths demands predictability. For crop chemistry, the same indole backbone leads to diversity in lead compound creation, helping stay ahead of disease resistance patterns in fields. Material scientists occasionally push the limits, using it in functional dye synthesis or surface modification work. Through all these uses, reproducible quality underpins ongoing innovation.

    Our technical staff meets directly with users when questions arise. We often conduct joint troubleshooting calls, even joining lab video calls to see how the compound behaves at their benches. These partnerships foster a feedback loop: if a procedure calls for a modification, we adapt the process; if dry-down leaves particulates, we re-examine filtration protocols; if shelf life seems too short, we run real-time and accelerated stability studies and share the unvarnished results. We believe that no sales pitch or technical data sheet matches candid communication supported by actual lab results.

    Continuous Improvement and Looking Ahead

    In a field where regulatory requirements evolve and customer innovation keeps accelerating, complacency means falling behind. We run quarterly reviews of product quality parameters, not only by studying complaint reports, but through proactive process audits and outside consultant input. These steps reveal where raw materials might drift, where a reactor or filter may need service, or where staff need refresher training. We see continuous improvement as more than just a principle; it is essential to keeping pace with both customer needs and external oversight.

    Upcoming regulatory shifts, such as possible reclassification of chlorinated compounds under stricter controls, drive us to consider greener alternatives and process substitutions. We collaborate with academic partners and industry groups, not only to anticipate rules but to encourage safer and less wasteful chemistry. At the same time, performance cannot yield to bureaucracy; our responsibility is to maintain high purity at practical scale, while reducing footprint and supporting customers through compliance changes.

    Conclusion: The Manufacturer’s Role in Chemistry Progress

    Making and delivering 5-Chloroindole-3-Carboxaldehyde isn't just a matter of running reactors and shipping powders. It involves ongoing investment in equipment, training, problem-solving, and, above all, clear, honest two-way communication with those who rely on the material. Having handled and improved this product throughout its journey allows us to see, on a daily basis, that trust grows with each successful experiment or trouble-free kilo batch. We do not treat this compound as a generic commodity; we view it as a living part of scientific advancement—one that benefits from both relentless attention to detail and a willingness to listen and adjust based on real laboratory experience. This mindset has built enduring relationships with research and manufacturing partners, creating success stories measured in both scientific progress and mutual respect.