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HS Code |
729680 |
| Cas Number | 387-44-0 |
| Molecular Formula | C8H6FN |
| Molecular Weight | 135.14 g/mol |
| Iupac Name | 7-fluoro-1H-indole |
| Appearance | Off-white to pale yellow solid |
| Boiling Point | 262-263°C |
| Melting Point | 65-67°C |
| Density | 1.282 g/cm³ |
| Solubility | Soluble in organic solvents like DMSO and ethanol |
| Smiles | C1=CC2=C(C=C1F)NC=C2 |
As an accredited 7-Fluoroindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a secure screw cap; labeled with "7-Fluoroindole," chemical formula, hazard warnings, and supplier information. |
| Shipping | 7-Fluoroindole is shipped in tightly sealed containers, protected from light and moisture. It should be transported in accordance with local, national, and international regulations for hazardous chemicals. Proper labeling and documentation are required, and the chemical must be handled by trained personnel using suitable protective equipment. Store in a cool, well-ventilated area. |
| Storage | 7-Fluoroindole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure that the storage area is equipped with appropriate spill containment and complies with relevant chemical safety regulations. Proper labeling and secure storage are essential. |
Applications of 7-Fluoroindole in Industrial Manufacturing7-Fluoroindole serves as a key intermediate in specialized chemical synthesis for high-value industries. Our production quality enables precise integration into various downstream operations, supporting controlled formulation and end-use safety at every stage. Below, we present specific industrial applications based on actual market practices and regulatory standards. 1. Pharmaceutical API Synthesis (Selective Serotonin Modulator Precursors)Pharmaceutical manufacturers use 7-Fluoroindole as a strategic starting material when constructing fluoro-substituted indole cores for active pharmaceutical ingredients (APIs), especially in drugs targeting CNS disorders and oncology. During the early-phase synthesis, 7-Fluoroindole undergoes site-specific functionalization and coupling reactions, forming the molecular backbone for compounds such as SSRIs and kinase inhibitors. Control over fluorine positioning supports both targeted activity and pharmacokinetic optimization in the resulting drugs. Industry compliance standards
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2. Agrochemical Discovery and Formulation (Crop Protection Molecules)Agrochemical R&D groups employ 7-Fluoroindole as a heterocyclic building block in the discovery and scale-up of new crop protection agents, including fungicides and plant-growth regulators. Its unique substitution pattern allows directed synthesis of active ingredients with improved pesticidal or bio-stimulant properties, often resulting in more persistent and selective actives. The raw material typically enters the process during the preparation of indole-based lead compounds, with successive derivatization steps adapted for field efficacy and environmental safety. Industry compliance standards
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3. Specialty Dye and Pigment Synthesis (Functional Colorants)Producers of high-performance dyes integrate 7-Fluoroindole into their pipeline to engineer specialty colorants exhibiting enhanced lightfastness, wash resistance, and substrate specificity, especially for electronic display films and technical textiles. The fluorinated indole core imparts desired chromophoric shifts and improved stability under extreme pH and UV conditions. Manufacturing batches employ the compound in precise coupling reactions linked with azo- or anthraquinone derivatives to achieve sharp coloration profiles and narrow absorption bands. Industry compliance standards
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4. Chemical Reference and Standards Manufacturing (Analytical Reagents)Producers of pharmaceutical and food analysis standards utilize 7-Fluoroindole as a calibration reference and as an intermediate for generating traceable analytical compounds. The compound’s defined fluorine position and consistent impurity profile provide reliable quantification in high-resolution mass spectrometry, NMR, and chromatographic applications. QC labs demand high-purity grades and certified reference preparations for regulatory submissions and analytical method validation. Industry compliance standards
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Our team has worked with heterocyclic fluorinated compounds for many years, and 7-Fluoroindole stands out for reliable quality and predictable performance in chemical synthesis. With a molecular formula C8H6FN and CAS number 387-44-0, 7-Fluoroindole plays a central role in labs looking for adaptability and purity in their indole intermediates. This compound features a single fluorine atom substituted at the 7-position of the indole ring, giving it distinct reactivity compared to unsubstituted indole or indoles carrying halogens at other positions.
Fluorinated building blocks have attracted attention in biomedical research and pharmaceutical manufacturing. The presence of fluorine in organic molecules can transform biological properties, influencing metabolic stability, lipophilicity, and hydrogen bonding characteristics. We have seen, from direct industry feedback and internal testing, that when using 7-Fluoroindole as a starting material, synthetic routes often require fewer downstream purification steps than those using other similarly halogenated indoles.
Developers in medicinal chemistry constantly search for ways to improve existing molecules, aiming for better potency, selectivity, or pharmacokinetics. We supply 7-Fluoroindole primarily to R&D groups and manufacturers designing tryptamine-based structures, kinase inhibitors, and advanced heterocyclic scaffolds. What we notice is that substituting fluorine at the 7-position tends not to disrupt the core aromaticity of the ring, yet still delivers the electron-donating or withdrawing effects needed for fine-tuning activity. Many customers use this intermediate as the foundation for synthesis of active pharmaceutical ingredients, bioconjugates, and custom ligands.
Handling and storage require the same precautions as other indoles: the compound remains stable under dry conditions, away from light and heat. We package material in amber glass with secure seals, minimizing any risk of contamination. QC consistently produces batches with solid-state purity exceeding 98%. That comes from both monitoring recrystallization and confirming structural integrity by NMR and mass spectrometry — processes we insist on before shipping. Over the last decade, requests for this compound have grown, driven by innovations in drug discovery and academic inquiry into electron-rich arenes.
Organic chemists value precision. Knowing this, we dedicate resources to understand the practical differences between 7-Fluoroindole and other related molecules. Compared with plain indole, the presence of a 7-fluoro substituent influences both reactivity and downstream synthesis. For instance, we have seen that nucleophilic aromatic substitution on the fluoro position rarely occurs under standard conditions, lending the molecule a stability profile that suits multi-step synthetic schemes. In comparison, chloro- or bromoindole analogs often show increased reactivity at the halogen position, which can sometimes complicate synthetic planning.
Our partners frequently ask about the distinction between 5-fluoro-, 6-fluoro-, and 7-fluoroindole. Experience tells us that the regioisomer employed can change not just chemical behavior, but biological outcomes. For some serotonin receptor studies, only the 7-fluoro group provides the receptor affinity profile needed, possibly due to its electronic influence on the pyrrole and benzene rings. Meanwhile, the steric effect at the 7-position sometimes hinders oxidation or other electrophilic aromatic substitution reactions, a difference well-understood by those designing libraries for high-throughput screening.
We first began producing this compound for use in agrochemical R&D and then expanded to supply pharmaceutical customers. Today, most of our shipments go to labs working in targeted drug discovery and advanced material development. Synthetic chemists prize the indole nucleus for its modular nature, and our version offers both reliability and consistency, eliminating headaches in batch production.
Our technical support team fields many inquiries about applications. A popular use remains as a precursor for selective serotonergic agents, especially those mimicking or modifying endogenous tryptamines. Research into tryptamine analogs for central nervous system disorders honestly seems to climb every year, and our customers regularly publish findings citing our materials. Some dive into the synthesis of kinase inhibitors for oncology, leveraging the 7-fluoro group's effects on hydrogen bonding and π-stacking interactions, which can boost inhibitor efficacy. Materials scientists also make use of our 7-Fluoroindole to design functional dyes and pigments, as the fluoro group can fine-tune optical properties.
Despite increased demand from biotech and pharma, we have also shipped to specialty chemical companies developing new photoresponsive or electroactive polymers. Often, performance of these polymers ties directly to detailed molecular tweaking—7-Fluoroindole helps there thanks to its clean substitution pattern and electronic properties.
Manufacturing fluorinated indoles differs from other indole derivatizations. We synthesize 7-Fluoroindole via established protocols involving selective lithiation, electrophilic fluoro introduction, and careful workup to avoid polymeric by-products. This process, while robust, requires tight process control; residual protic solvents, variation in reaction temperature, or trace metal contamination will hamper product quality. We see our role as more than a vendor—chemists in our plant pay attention at every stage, from raw materials to final packaging.
Meeting the needs of medicinal chemistry often means producing quantities from grams for academic labs to multi-kilogram lots for medicinal chemistry scale-up. Our plant can supply a range of lot sizes without the variability common in third-party or trader-sourced samples. Every batch gets analytical verification by NMR, GC-MS, and HPLC, and retains a sample in our archive for at least two years in case a project requires later investigation. Over hundreds of batches, our chromatographic data reflect remarkable lot-to-lot uniformity. Our direct experience shows that minor impurities—especially those arising from incomplete fluorination or side-chain oxidations—can derail downstream syntheses, so every step gets tailored for selective reactivity and minimal by-product formation.
Global regulations for pharmaceutical ingredients and intermediates grow more stringent year by year. We make it a point to avoid restricted solvents, manage waste streams, and document process adjustments thoroughly. This is crucial not only for compliance but to provide partners with predictable timelines and minimal surprises. Our customers rely on clear, accurate certificates of analysis, unrestricted data sharing, and honest timelines—a practice forged by realizing how much small synthesis labs and contract manufacturing projects stand to lose with unreliable supply.
Chemists in academic and industrial settings often request modifications or support with scaling up bespoke intermediates derived from 7-Fluoroindole. Our production lines maintain flexibility for downstream customization: whether a researcher desires N-protected variants, isotopically labeled forms, or high-purity material for analytical reference, we engage our R&D chemists directly with customer teams. Over the years, we have refined recrystallization solvents and conditions to suit evolving customer needs, responding to trends in reaction scale, downstream transformations, or new analytical methods.
Feedback from colleagues in medicinal chemistry often highlights the need for responsiveness and shared problem-solving. Our technical team routinely helps troubleshoot unexpected chromatographic issues or guides adjustments in purification strategies. For researchers working on proprietary scaffolds, we preserve confidentiality of results and provide honest feedback regarding synthetic feasibility. Partnerships grounded in collaborative troubleshooting bring better outcomes for all involved. Having handled thousands of customer projects, we know transparency and technical engagement can help customers get the yield, purity, and performance they need to move projects forward.
Fluoroindole derivatives enjoy growing attention because placing fluorine in precise positions can fundamentally alter binding to protein pockets, interaction with metabolic enzymes, and physical properties. Selection of a 7-fluoro derivative, over 5- or 6-fluoro analogs, often comes from structure-activity studies or lead optimization campaigns. In our experience, many medicinal chemists report enhanced metabolic stability and better pharmacokinetic profiles from fluoro-indole frameworks, which in turn fuels richer SAR (structure activity relationship) explorations.
We also see our 7-Fluoroindole used beyond pharmaceuticals. Research into advanced materials turns often to heterocycles for molecular electronics, organic LEDs, and photovoltaic devices. For example, substitution at the 7-position of indole can shift HOMO-LUMO energy levels, affecting material band gaps and charge mobility. We have seen a steady rise in customers purchasing 7-Fluoroindole for pre-polymer preparation, organic field-effect transistor prototyping, and dye-sensitized solar cell projects.
Within our own labs, we evaluate not only product purity but also applications in Suzuki cross-coupling, Buchwald–Hartwig amination, and indole-to-tryptophan derivatization. 7-Fluoroindole demonstrates robust coupling yields and clean product isolation in many of these routes, offering benefits that other fluoro-substituted indoles may not deliver. This direct hands-on experience shapes our understanding of real-world performance.
The volume of demand for 7-Fluoroindole illustrates a broader shift in how researchers design molecules for biological and material innovation. Small and large labs alike increasingly favor substituents that can confer metabolic stability without undermining target affinity or reactivity. Our yearly production data reflect this shift: the compound started as a niche chemical, but as more medicinal chemists publish on fluorinated indoles, orders grow both in size and variety.
Some organizations request dual fluorinated indoles, or look to experiment with halogen patterns that require custom synthesis. Our plant adapts production accordingly, gaining valuable process insights while ensuring traceability and consistency. These interactions sharpen our perspective, as we work to supply chemicals that keep pace with a rapidly evolving landscape in synthetic and medicinal chemistry.
We also grapple with logistical realities. Seasonal fluctuations in demand, raw material sourcing challenges, and occasional shifts in chemical regulation mean planning production windows with care. We keep safety as a top priority; fluoro-containing compounds demand proper ventilation and controlled reagent addition, something we never compromise in our operations.
Manufacturing 7-Fluoroindole at scale poses challenges. The fluorination step requires precise stoichiometry and temperature control, as stray by-products or residual starting material can carry over into downstream chemistry. Some years ago, process improvement efforts cut cycle times and reduced solvent use, helping both the environment and production costs. Many competitors struggle at scale, especially when purity specs tighten or when orders fluctuate quickly — experience has taught us to maintain inventory buffers and build adaptable process schedules.
Innovation continues. Feedback from industry partners and academic groups shapes how we refine synthesis and purification. Investing in analytical technology brings payoffs: real-time HPLC monitoring and rapid NMR screening spot deviations early, keeping quality consistent from batch to batch. Process safety and green chemistry principles remain our cornerstone—creating products that satisfy both industry standards and internal responsibility to people and planet.
Our role, as actual producers of 7-Fluoroindole, means we witness firsthand how innovation is driven by detail. Researchers need not only access to this building block, but assurance that what arrives matches expectations batch after batch. Consistency, communications, and technical partnership—these make an actual difference in real-world chemistry, from discovery to scale-up.
Whether a team investigates new CNS-active drugs, pioneers advanced materials, or optimizes agrochemicals, the familiarity and reliability of our fluorinated indole supply removes obstacles. By engineering our process around the unique characteristics of 7-Fluoroindole and responding to evolving research trends, we contribute a trusted foundation to customers pushing scientific boundaries.
Each bottle of 7-Fluoroindole carries the work and experience of our production crew, analysts, and the daily feedback loop with those developing the next generation of life-changing molecules. Industry moves fast, and new frontiers require dependable partners. Decades of hands-on manufacturing, shared problem-solving, and adapting to new demands inform how we make and supply 7-Fluoroindole. We believe this direct experience matters more than any specification sheet could suggest, keeping research moving forward with both confidence and creativity.