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2-Chloro-1H-Indole-3-Carbaldehyde

    • Product Name 2-Chloro-1H-Indole-3-Carbaldehyde
    • Alias 2-Chloro-3-formylindole
    • Einecs 629-616-9
    • 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

    810028

    Productname 2-Chloro-1H-Indole-3-Carbaldehyde
    Molecularformula C9H6ClNO
    Molecularweight 179.61 g/mol
    Casnumber 136054-22-5
    Appearance Off-white to light yellow solid
    Boilingpoint No data available
    Meltingpoint 154-158 °C
    Solubility Slightly soluble in organic solvents
    Purity Typically >97%
    Density No data available
    Storagecondition Store at room temperature, in a dry and cool place
    Synonyms 2-Chloroindole-3-carboxaldehyde
    Iupacname 2-chloro-1H-indole-3-carbaldehyde
    Smiles C1=CC2=C(NC=C2C(=O)C1)Cl
    Inchi InChI=1S/C9H6ClNO/c10-9-7-2-1-3-8(6(7)4-11)5-12-9/h1-5,12H

    As an accredited 2-Chloro-1H-Indole-3-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Chloro-1H-Indole-3-Carbaldehyde, tightly sealed, with hazard labeling and product details.
    Shipping 2-Chloro-1H-Indole-3-Carbaldehyde is typically shipped in securely sealed containers to prevent moisture and contamination. It must be labeled as a hazardous organic compound and transported according to local and international chemical safety regulations. Ensure protective packaging to prevent breakage, and include necessary documentation such as MSDS and hazard warnings.
    Storage 2-Chloro-1H-Indole-3-carbaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature or as specified by the manufacturer. Proper labeling and handling precautions should be maintained to ensure chemical stability and safety.
    Application of 2-Chloro-1H-Indole-3-Carbaldehyde

    Applications of 2-Chloro-1H-Indole-3-Carbaldehyde in Industrial Manufacturing

    2-Chloro-1H-Indole-3-Carbaldehyde serves as a critical intermediate in complex synthesis routes for high-value specialty chemicals. Below, we detail key application pipelines where our material integrates directly into downstream manufacturing, covering compliance, dosage, process stages, and resulting end-products.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate Production

    Pharmaceutical manufacturers leverage this intermediate primarily for synthesizing tryptamine-based API structures. It forms part of multi-step routes targeting targeted therapies and neurological drug classes. Our high-purity specification enables reduced purification overhead for subsequent condensation and cyclization reactions, ensuring batch consistency for GMP-compliant drug production.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP Pharmacopeia general chapters on API synthesis
    • EU GMP Vol. 4: GMP Guidelines for Pharmaceuticals
    • US FDA 21 CFR Part 211

    Typical usage ratio

    • 1–4% w/w in pre-final intermediate synthesis, adjusted according to yield optimization and target API molecular structure

    Downstream process integration

    • Integrated into indole-functionalization stages, entering post-nitration and pre-cyclization steps; charged into closed reaction systems under nitrogen with dry solvents to ensure impurity control

    Final product types

    • Neuroactive compounds (e.g., serotonin reuptake inhibitors, peptide mimetics)
    • Anticancer API scaffolds
    • Psychoactive research chemicals
    • Advanced pharmaceutical research intermediates

    2. Agrochemical Synthesis (Herbicide and Insecticide Precursors)

    The indole core structure and chloro substitution pattern support effective construction of bioactive molecules for crop protection. Agrochemical plants use our material in combination and substitution reactions, allowing tuning of functional groups to access registered active ingredients. High lot consistency limits batch-to-batch variability in downstream efficacy and regulatory profiling.

    Industry compliance standards

    • FAO/WHO: Specification and evaluations for agricultural pesticides
    • ISO 9001:2015 for process quality management
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH (EC) No 1907/2006 compliance for substance registration and safe use

    Typical usage ratio

    • 0.5–2% w/w in synthesis reactant mixture, calculated according to the intended active moiety’s desired halogenation profile

    Downstream process integration

    • Dosed into electrophilic aromatic substitution and subsequent alkylation steps; utilized in semi-batch reactors under controlled temperature to prevent side-product formation

    Final product types

    • Pyrrole and indole-based pre-emergent herbicides
    • Chlorinated insecticidal intermediates
    • Novel fungicidal lead compounds
    • Registered agrochemical actives for government-regulated applications

    3. Fine Chemical Synthesis for Dye and Pigment Intermediates

    Specialty dye and pigment manufacturers employ 2-chloro-1H-indole-3-carbaldehyde in constructing highly conjugated aromatic systems. The precise substitution enables targeted colorant development, particularly for high-stability organic pigments and industrial polymers. Controlled addition enables predictable hue, solubility, and fastness properties in the final pigment backbone.

    Industry compliance standards

    • EN 71-3: Safety of toys part 3 for heavy metal migration (dyes for plastics)
    • ISO 9001:2015 for QMS in pigment production
    • Oeko-Tex® Standard 100 for restricted substances in textiles
    • RoHS Directive 2011/65/EU compliance for electronic colorants

    Typical usage ratio

    • 0.1–1.2% w/w in aromatic coupling preparations, refined according to the target pigment molecular mass and desired chromophore complexity

    Downstream process integration

    • Fed into condensation polymerization or azo coupling stages; subjected to temperature-controlled conditions to promote chromogenic core formation

    Final product types

    • High-performance industrial dyes for automotive coatings
    • Textile colorants for apparel
    • Plastics additives (masterbatches)
    • Organic pigments for digital printing inks

    4. Synthesis of Advanced Electronic Materials

    Manufacturers of advanced organic electronic materials utilize the indole-aldehyde intermediate to engineer electron-donating and -accepting units in semiconducting polymers and organic light-emitting diode (OLED) precursors. Its reactivity profile permits precise customization of optoelectronic characteristics. All batches meet stringent spectroscopic and trace impurity thresholds, pivotal for device integration.

    Industry compliance standards

    • IEC 62321: Determination of certain substances in electronic and electrical products
    • ISO 14001:2015 Environmental management systems (for handling and disposal)
    • JEDEC JESD 625B for handling in cleanroom environments
    • IPC-1752A for material declaration in the electronics sector

    Typical usage ratio

    • 0.2–0.7% w/w in monomer feed, modulated by desired electronic bandgap and charge mobility targets

    Downstream process integration

    • Incorporated into Suzuki or Stille coupling stages for polymer backbone extension, executed in solvent-free or low-polarity media to ensure high molecular weight

    Final product types

    • OLED materials for display fabrication
    • Organic semiconducting polymers for flexible electronics
    • Photoactive layers for organic solar cells
    • Sensor active layers in analytical devices

    5. Veterinary Drug Intermediate Manufacturing

    Veterinary pharmaceutical producers integrate 2-chloro-1H-indole-3-carbaldehyde into synthetic routes for indole-based veterinary drugs, commonly targeting antiparasitic or anti-inflammatory indications. The molecule supports rapid access to derivatives with specific activity profiles, while our production guarantees low residual solvent and controlled impurity levels for VMP regulatory submissions.

    Industry compliance standards

    • VICH GL2: Good Manufacturing Practice for veterinary pharmaceutical ingredients
    • Ph. Eur. (European Pharmacopoeia) monographs for animal health
    • US FDA Guidance for Industry #256: Veterinary drug residues
    • China Veterinary Pharmacopoeia (latest edition)

    Typical usage ratio

    • 0.8–2.8% w/w in animal drug precursor synthesis, fine-tuned per target molecule’s indole content and process yield analysis

    Downstream process integration

    • Added to functional group derivatization stages, enabling targeted modification prior to final API formation, often under reflux and inert gas protection

    Final product types

    • Veterinary antiparasitics
    • Anti-inflammatory injectables and oral suspensions
    • Livestock feed additives requiring regulatory monograph attestation
    • Veterinary research intermediates
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    Certification & Compliance
    More Introduction

    Introducing 2-Chloro-1H-Indole-3-Carbaldehyde: Precision in Indole Chemistry

    Years of Experience in Manufacturing Specialty Aldehydes

    Our team has dedicated decades to the craft of producing high-purity indole derivatives for demanding chemical research and industry projects. In the landscape of organic synthesis, 2-Chloro-1H-Indole-3-Carbaldehyde commands attention among indole molecular tools. The unique profile stems from a precise molecular structure: a chloro substituent at the two-position of the indole ring paired with a reactive carbaldehyde group at the three-position. We control each parameter during synthesis—reagent quality, atmospheric conditions, reaction timing, and purification approach—so each batch meets strict analytical specifications. NMR, IR, and HPLC data back every shipment. Labs that rely on our material rarely struggle with downstream purification headaches and convoluted reaction monitoring, and this peace of mind has become an expected norm among our long-term partners.

    Model and Specifications

    The compound, recognized widely under CAS number 117433-62-0, appears as an off-white solid under ambient conditions. Typical melting point ranges from 114°C to 117°C. Moisture and oxygen levels in our process rooms remain tightly controlled, lowering the risk of hydrolysis or oxidation during sensitive stages. This attention pays off: finished material consistently exceeds 98% by HPLC area. Elemental analysis supports real-world batch consistency. Though indole chemistry introduces subtle instability risks because of the electron-rich ring, our purification system removes nearly all byproducts and residual solvents. Routine GC-MS screening highlights batch-to-batch reproducibility, especially for trace-level contaminants—something synthetic chemists and medicinal chemistry researchers appreciate when tracing compound origins in screening cascades.

    Usages Across Industries

    Pharmaceutical developers turn to 2-Chloro-1H-Indole-3-Carbaldehyde as a versatile intermediate for small molecule drug synthesis. The molecule’s specific patterning, with both a reactive aldehyde and electron-withdrawing chloro group, offers synthetic access to a wide array of heterocyclic scaffolds. In medicinal chemistry, researchers use the compound in condensation reactions, such as the construction of substituted indoles, carbazoles, or pyrroloindoles. Some groups further derivatize the aldehyde to create advanced building blocks for kinase inhibitors or anti-inflammatory candidates. Agrochemical labs also pursue modifications around the indole structure, investigating plant-growth regulators or new crop protection actives. Where high-throughput screening involves structural elaboration on indole rings, reliable batch purity remains vital. Even small shifts in impurity profiles can skew biological assay results, leading to unreliable SAR trends. We have worked hand-in-hand with project scientists to troubleshoot scale-ups and eliminate impurities, especially chlorinated byproducts, that sometimes evade detection in less strictly-controlled production environments.

    What Sets Our 2-Chloro-1H-Indole-3-Carbaldehyde Apart

    Several factors and practices distinguish our output from off-the-shelf or trader-supplied options. We build our process knowledge on years of method development, from pilot runs through full-scale production. Reaction vessels stay calibrated, and regular equipment maintenance eliminates the risk of trace metal leaching. Glassware suited specifically to indolic intermediates minimizes potential side reactions, which often occur with less robust reactor setups. Sourcing our starting materials from vetted suppliers means we are less likely to see cryptic polymeric side products or unknown halogen exchange artifacts. After optimizing isolation and drying, we test random batch samples for polymorph analysis and desk stability.

    Customers who come to us after experiencing operational hiccups elsewhere often mention either inconsistency in physical properties or unexplained byproducts during formulation. In our labs, such issues receive full analytical attention. We dig beyond routine purity reports, looking at minor impurity drift across batches over several years. This long-term data-guided focus enables clearer troubleshooting, such as identifying whether off-color solids come from uro-indole tars, common during poorly controlled oxidations. A hands-on troubleshooting approach enables faster pilot project success, sometimes shaving weeks off the transition from milligram samples to kilo-scale lots.

    Supply continuity matters just as much as technical consistency. Some manufacturing groups rely on stock already on hand, which may age in variable storage settings. We refresh our inventory regularly and control local environmental conditions—resulting in samples that resist unwanted polymerization and hydrolysis. With regular customer feedback, we adapt packaging so researchers don’t waste material during transfer. Vacuum-sealed glass vials or multi-layered drums protect against atmospheric attack without excessive headspace, reducing both losses and contamination risk.

    Working Closely With Downstream Users

    Success in specialty chemical manufacturing means more than pushing powders or crystals out the door. Projects regularly demand more than technical data sheets or bulk availability. We work directly with scientists during early project planning stages, especially for custom modifications or larger-scale campaigns. Our technical team hosts annual workshops, interacting with customers’ research chemists to refine application-specific protocols. For example, our work with radiolabeling specialists uncovered specific storage modifications to further limit micro-impurity growth, improvement that pays off during intricate peptide coupling reactions. We routinely share our lessons and also keep an eye on user feedback about color, texture, or flowability changes over project timescales.

    As collaborative partners, we track the evolution of indole-based drug analogs and agrochemical templates. Small changes in the indole ring system or aldehyde substitution pattern can lead to dramatic property shifts. Our in-house chemists attended several global symposia, helping drive consensus on optimal reaction partners for 2-Chloro-1H-Indole-3-Carbaldehyde during indole ring functionalization. These forums provide ongoing insights into new protection and activation strategies, which we fold back into our process control modules. By understanding application-specific performance issues, from catalyst compatibility to photostability under assay conditions, we can suggest tweaks to purification flow, batch weight, or packaging choices. In a recent project, a European customer demonstrated that our higher-purity intermediate enabled several downstream cyclizations without extra purification, reducing overall solvent use and waste by over 20%.

    Examining the Challenges of Indole Intermediate Sourcing

    Labs entering indole chemistry for the first time regularly navigate a crowded supplier landscape. Sourcing intermediates like 2-Chloro-1H-Indole-3-Carbaldehyde once meant risk: vendor-to-vendor variation, off-spec deliveries, and poor documentation sometimes forced researchers to rerun pilot experiments. Our experience taught us early that it’s not enough to simply post a purity certificate. Years ago, we encountered a case in which misleading claims led a research partner to spend months rerunning assays because TLC-pure material masked non-chromophoric contamination. Analytical transparency remains not just a promise but embedded practice at every stage—before customer delivery and long after the project concludes.

    We’ve also seen how process scale can magnify small changes or shortcuts. At plant scale, a minor temperature swing or insufficient inert gas coverage will generate decarbonylated or polymeric byproducts uncommon at bench scale. Rather than shifting blame to batch variability, we log operational parameters and historical runs, isolating sources of drift with dedicated process analytics. This quality-first approach shifts our batch reworks from crisis-fixing toward a system of gradual, informed improvement. Over the years, this approach has yielded dramatic reductions in end-of-line purification waste, improved reproducibility, and shortened delivery timelines during seasonal demand spikes.

    Putting Stable Supplies First

    A synthetic lab’s productivity depends not just on specifications, but true, dependable physical quality. From the molecular perspective, indole-3-carbaldehyde can frustrate chemists with its tendency to yellow or darken if exposed to light or air. Substitution with a chlorine at the two-position further affects reactivity and shelf behavior. Years back, one pharmaceutical R&D group reported progressive discoloration of similar materials from another supplier—tracing the root cause to improper inert packaging and post-synthesis handling. We responded by improving both our nitrogen-purged assembly lines and the selection of tamper-proof, low-adsorption containers.

    Laboratory application has shown real, practical advantages to this approach. Stored under controlled conditions, our 2-Chloro-1H-Indole-3-Carbaldehyde holds color and maintains analytical value over extended shelf life. We provide guidance on optimizing cold-room storage, reducing sample transfer steps, and tracking batch turnover—all designed to let technical teams start every experiment with full confidence.

    What Can Go Wrong: Addressing Real-World Issues

    Some challenges stem less from manufacturing art and more from logistical realities. International clients sometimes face customs delays, creating temperature and humidity excursions no warehouse can fully anticipate. To counter these unpredictabilities, we ship with full support documents, including real-time tracking and integrity seals. On rare occasions, we have directly replaced shipments that arrived compromised, learning how differing climates affect product behavior. Feedback from those projects feeds back into enhancements to both materials management systems and our customer support frameworks.

    Product stability is only one concern. Analytical discrepancies between customer labs and our own equipment, often due to reference standard drift or differing calibration curves, can prompt pauses in development pipelines. Real-time communication between analytical teams helps clarify where the error sits—be it solvent traces, column bleed, or genuine off-spec product. Over the years, mutual trust built up from solving these puzzles forms the backbone of repeat business and ongoing process optimization.

    Differences Compared to Other Indole Derivatives and Intermediates

    2-Chloro-1H-Indole-3-Carbaldehyde shares a close kinship with other indole carbaldehydes or halogenated derivatives, but a few structural and practical details set it apart. The presence of a chlorine atom directly at the two-position changes both electronic character and steric properties. Nucleophilic substitutions run cleaner, and certain cross-coupling reactions display higher regioselectivity with this intermediate. Some related 2-unsubstituted indole aldehydes, often used in indole-3-acetic acid analogs, show unwanted dimerization during either storage or subsequent reactions. The 2-chloro variant avoids some of these risks, producing less polymeric material during downstream processing.

    During recent scale-up projects, partners using 2-chloro-1H-indole-3-carbaldehyde as a feedstock often highlighted shorter purification times and increased overall yield compared to analogous bromo- or iodo-indole derivatives. Chlorine atoms tend to be less prone to unwanted elimination or cross-reactivity, offering more forgiving handling and longer shelf life. While chloro substituents can slow down some aromatic substitution reactions, the higher selectivity this introduces benefits applications where positional fidelity matters most. Medicinal chemists targeting kinase inhibitor scaffolds regularly cite this intermediate as a robust, convenient precursor because it avoids common side reactions seen with aldehyde-only indole compounds.

    Some commercial projects speculated early on about potential environmental impacts from halogenated intermediates. Our sustainable process effort includes solvent recapture, waste stream minimization, and downstream partner engagement on disposal or recycling protocols. Detailed impurity mapping helps identify and reduce potentially persistent trace contaminants. This work enables our lab partners to design greener processes around our materials—something that sets us apart in contract development conversations where regulatory and environmental frameworks evolve quickly.

    Practical Support for Every Use Case

    We offer more than a catalog listing. Many collaborations span years, often moving from preliminary research through to commercial pilot stage. Academic projects receive the same attention to analytical clarity and shipment details as full-scale pharmaceutical or agrochemical pursuits. Our technical liaisons regularly help teams adapt to new experimental systems or changing regulatory demands. If unique packaging or alternate forms (microcrystalline vs. granular) better suit a project, we adjust process and fill accordingly—these decisions come from careful dialogue with end users, not just internal convenience.

    Those in radiochemistry or tracer molecule synthesis rely especially on batch-to-batch reproducibility. Even minor deviations in physical or chemical behavior can produce devastating downstream costs. Over the years, several isotope-labeled compound producers have worked closely with our team, jointly validating kinetics and side-product formation under mild or accelerated conditions. By maintaining open channels for results reporting and troubleshooting, we reduce research bottlenecks and enable more rapid discoveries.

    Proactive Quality—Rooted in Hard-Won Experience

    Chemical manufacturing trends tend to swing between cost leadership and value-based differentiation. In specialty synthesis, process mastery and long-term relationship building tip the balance. Our approach to 2-Chloro-1H-Indole-3-Carbaldehyde mirrors the rest of our advanced building-block portfolio: maintain absolute clarity in communication, acknowledge—and fix—mistakes in real time, and invest in analytical talent, not just new reactors. Every new partnership, whether a single-vial early stage order or a standing industrial-scale contract, receives this same commitment.

    We learned the critical value of true supply chain transparency while managing rapid demand surges during recent global disruptions. No buyer benefits from glossy brochures if a shipment never clears customs, or a technical rep cannot explain a trace impurity. Regular site audits, published stability studies, and ongoing protocol modifications all stem from these hard lessons learned by weathering real market swings. Our documentation tells a story—a record of batch histories, method changes, real-world failures, and practical, science-driven improvements.

    Ongoing Innovation and the Road Ahead

    Future development in indole chemistry promises new synthetic challenges, whether tackling chiral building blocks, photoreactive analogs, or increasingly tailored bioactive compounds. We invest in both process upgrades and staff training, sending intact teams to regional and global symposia for continued chemical education. Field reports from diverse customer bases—medicinal, agro, electronic specialty chemicals—reveal evolving technical and regulatory requirements. We fold these insights into routine plant operations, retaining the flexibility to add new analytical endpoints, storage protocols, or reaction modules as market expectations shift.

    End users often request documented data on scalability or adaptability to non-standard solvents. In response, pilot lines trial new reaction conditions (anhydrous, low-temperature, or high-dilution regimes) to stretch the limits of applicability for 2-Chloro-1H-Indole-3-Carbaldehyde. These development sprints sometimes uncover hidden side reactions—knowledge we share openly in user meetings or technical bulletins. Scientific progress relies not just on the material itself, but on honest, ongoing professional dialogue. Each inquiry, complaint, or commendation drives the next cycle of process improvement.

    Concluding Thoughts on 2-Chloro-1H-Indole-3-Carbaldehyde

    In our hands, 2-Chloro-1H-Indole-3-Carbaldehyde stands not as a commodity, but as a carefully constructed intermediate. Evidence traces back through batch records, laboratory analysis, and most importantly, the practical success of projects using our output. Our years at the bench taught us several lessons: respect process control, stay transparent with customers, and view every technical challenge as a source for future insight. Researchers and process developers count on a supply that matches both their scientific rigour and real-world production needs. We remain committed to manufacturing at this intersection—the point where technical reliability, safety, and innovation meet to support the next generation of indole-based chemistry.