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3-(Trifluoroacetyl)Indole

    • Product Name 3-(Trifluoroacetyl)Indole
    • Alias TFAI
    • Einecs 623-110-1
    • 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
    VTB
    Specifications

    HS Code

    650137

    Productname 3-(Trifluoroacetyl)Indole
    Casnumber 111902-57-9
    Molecularformula C10H6F3NO
    Molecularweight 213.16
    Appearance Light yellow solid
    Meltingpoint 61-63°C
    Purity Typically >98%
    Solubility Soluble in DMSO, slightly soluble in water
    Storagetemperature 2-8°C
    Smiles C1=CC=C2C(=C1)C=CN2C(=O)C(F)(F)F
    Inchikey AETJYIQDISMNRE-UHFFFAOYSA-N

    As an accredited 3-(Trifluoroacetyl)Indole 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 5 grams of 3-(Trifluoroacetyl)Indole; labeled with hazard warnings, CAS number, and lot information.
    Shipping **Shipping Description for 3-(Trifluoroacetyl)Indole:** This chemical is shipped in sealed containers under ambient or refrigerated conditions, protected from moisture and light. Complies with standard laboratory chemical transport regulations. Labelled as a research chemical; not classified as hazardous for shipping, but appropriate handling and protective equipment are recommended upon receipt.
    Storage 3-(Trifluoroacetyl)indole should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature or refrigerated as specified by the manufacturer. Proper labeling and secure shelving are essential to prevent accidental access or spills.
    Application of 3-(Trifluoroacetyl)Indole

    Applications of 3-(Trifluoroacetyl)Indole in Industrial Manufacturing

    As the direct producer of 3-(Trifluoroacetyl)Indole, we deliver high-purity raw material for specialized downstream applications primarily in pharmaceutical synthesis, agrochemical intermediate manufacturing, advanced materials research, and fine fragrance ingredient production. Our technical and quality teams support customers in process integration to achieve consistently high yield and traceable compliance within regulated environments.

    1. Pharmaceutical Intermediate for Antineoplastic API Synthesis

    Major oncology drug manufacturers use this material as a structural building block in the synthesis of indole-derived antineoplastic actives. Its electron-withdrawing trifluoroacetyl group facilitates regioselective reactivity during heterocycle formation, supporting late-stage functionalization steps under controlled environment protocols. Integration occurs in multi-step batch synthesis lines, where critical impurity and residual solvent control is required to meet stringent regulatory filings.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) monographs applicable to API quality
    • EU GMP Part II for API production
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 0.5–3% w/w of total reaction mixture (final proportion varies with synthetic route optimization and molar ratios in target API production)

    Downstream process integration

    • Charged during initial indolization or positioned for late-stage acylation in multi-step organic synthesis; handled in sealed vessels with in-process QC monitoring for moisture and byproduct formation

    Final product types

    • Small molecule antineoplastic active pharmaceutical ingredients (APIs)
    • Complex, fluorinated indole scaffolds for clinical trial batch manufacturing

    2. Agrochemical Active Intermediate Production

    Indole derivatives featuring trifluoroacetyl substitution serve as key intermediates in the downstream manufacture of high-potency crop protection agents, especially next-generation herbicides and insecticides. The material participates in early condensation, cyclization, and selective halogenation, enabling downstream firms to construct molecules with improved field stability and biological activity. Backward integration allows producers to align traceability with the EU and U.S. agrochemical approval processes for large-scale campaigns.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • OECD Principles of Good Laboratory Practice (GLP) for test item traceability
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA 40 CFR Part 160 (GLP compliance in pesticide studies)

    Typical usage ratio

    • 1–8% w/w of stage-wise batch inputs; tailored depending on the required depth of trifluoromethylation and target molecule yield per hectare-use registration studies

    Downstream process integration

    • Added at the condensation or acylation stage in heterocycle core formation; downstream automated reactors support in-line monitoring of fluorine incorporation rates for regulatory batch records

    Final product types

    • Herbicide technical concentrates (TCs) with indole backbone
    • Insecticide intermediates for solid and liquid formulation pre-mixes

    3. Advanced Materials and Specialty Polymer Research

    Research organizations and polymer producers incorporate this indole derivative in the synthesis of specialty fluorinated polymers, where its structure drives unique dielectric or thermal stability profiles. It serves in the initial monomer pool or as a functional linker, influencing polymer chain propagation and final mechanical properties. Quality assurance teams in downstream firms rely on precise handling of this compound to meet rigorous test protocols for defense, aerospace, and electronics development programs.

    Industry compliance standards

    • ASTM International Polymer Standards (e.g., ASTM D638 for tensile properties)
    • ISO 9001:2015 certified R&D and pilot-scale production protocols
    • Restriction of Hazardous Substances (RoHS) Directive for electronic materials
    • Internal company-specific advanced materials test protocols

    Typical usage ratio

    • 2–5 mol% based on total monomer content; precise ratio set according to targeted molecular weight and fluorine distribution in final chain architecture

    Downstream process integration

    • Dosed into bulk reactors with continuous or semi-batch polymerization set-ups; monitored for conversion rates using NMR and GPC characterization

    Final product types

    • Functionalized fluorinated co-polymers for dielectric films
    • Specialty resins for electronics encapsulation and high-performance coatings

    4. Aroma Ingredient Synthesis for Fine Fragrance Sector

    Fragrance compound manufacturers value the reactivity and olfactive influence of this indole variant when producing specialty aroma molecules. Its presence in proprietary aldehyde and musk constructions imparts floral, powdery, and animalic character notes. Inclusion is guided by IFRA guidelines and IFRA-QRA limits. Downstream blending engineers control its introduction during early-stage molecule assembly, using sealed reactors to avoid contaminant profiles readily detected in finished fragrance evaluations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards (current amendment)
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9235:2013 for aroma chemical identity and purity
    • Company-internal allergen and purity screening SOPs for fragrance division

    Typical usage ratio

    • 0.01–0.2% w/w in aroma isolation protocols; proportion adjusted depending on overall perfume concentrate compliance with IFRA QRA intake scenarios

    Downstream process integration

    • Employed in early-stage aroma chemical construction, typically through Grignard or Friedel–Crafts acylation catalysts; subsequent purification and GC-olfactometry-based quality controls standard for IFRA-compliant output

    Final product types

    • Fine fragrance concentrate solutions
    • Specialty aroma ingredients for luxury perfumery and personal care compounding
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    Certification & Compliance
    More Introduction

    3-(Trifluoroacetyl)Indole: A Closer Look from the Manufacturer's Perspective

    As long-term chemical manufacturers, dealing with indole derivatives has become second nature in daily production. Among the range, 3-(Trifluoroacetyl)Indole stands out as one of our most requested products from pharmaceutical labs and research institutions. In manufacturing, even small details in the way an indole comes together make a real difference in the finished product’s purity, reliability, and performance in reactions. This commentary aims to explain our approach to this compound, highlight its role in modern synthetic applications, and reflect on what sets our material apart based on years of hands-on experience.

    What Defines 3-(Trifluoroacetyl)Indole

    3-(Trifluoroacetyl)Indole can be recognized by its unique trifluoroacetyl group at the 3-position on the indole ring. Most professionals looking for this compound want a reliable building block for synthesizing drugs, agrochemicals, or other fine chemicals where trifluoromethyl groups are in high demand. The presence of fluoro groups influences both the electronic and steric properties dramatically, meaning even small impurities or isomeric contamination can ruin a downstream process.

    Our approach starts with careful sourcing of raw materials—our indole core, trifluoroacetic anhydride, and other reagents pass multiple rounds of in-house purity and identity checks. Mistakes are costly, so each step of synthesis and isolation gets extra attention from technical staff. Years of troubleshooting have refined our protocols, cutting down side-product formation and improving both yield and repeatability.

    Specifications That Matter in Real World Use

    Not all 3-(Trifluoroacetyl)Indole on the market behaves the same in lab or pilot-scale settings. Our standard production lot delivers content above 98 percent by HPLC analysis, with typical batches hitting 99+ percent. Moisture content remains consistently below 0.5 percent thanks to vacuum drying. We know from customer feedback that wet or degraded stock causes problems. Detailed records for each batch allow us to track and troubleshoot even years later, and our experienced staff double-checks the product for residual solvents and non-volatile impurities. Purity is one thing; consistency is another. Over the past decade, we have achieved lot-to-lot reproducibility—something that direct users value far more than impressive but inconsistent laboratory results.

    Our physical process creates a white to off-white powder, free-flowing and easy to handle for weighing and transfer. Particle size falls within a window tight enough to allow accurate dosing, so researchers and production chemists are not hampered by clumping or dust. Packaging uses airtight HDPE bottles or jars, purged with an inert atmosphere to keep out atmospheric moisture and prevent slow hydrolysis. We started purging packaging years back after a few customers reported discoloration, so now every container in storage sits protected from both air and light. Shelf-life routinely reaches over 12 months under these storage conditions with no loss of integrity.

    Meeting Laboratory and Industrial Demands

    Medicinal chemists appreciate the degree of flexibility that 3-(Trifluoroacetyl)Indole offers. A key draw lies in late-stage functionalization—reactions such as Friedel-Crafts acylations, alkylations, cross-couplings, or reductions proceed more smoothly when starting materials are free from unknown byproducts. Our product enables cleaner downstream chemistry, which saves time and troubleshooting. Many clients use our material directly for library synthesis without further purification. They return because data consistently match their reference spectra.

    We also get orders from agricultural companies synthesizing test molecules with fluorinated moieties, knowing our process controls residual chlorine or bromine species effectively. On top of this, process chemists in scale-up settings comment that our product’s low residual acidity preserves expensive catalysts downstream, avoiding the costly replacements seen with lower quality stock. We welcome feedback, using it to guide process adjustments and quality priorities that benefit the entire community relying on us.

    Comparing With Other Indole Derivatives

    Compared to standard indole or 3-acetylindole, the trifluoroacetyl group bestows much higher metabolic stability and unique biological properties. Some competitors offer cheaper 3-acetylindole, but for end uses where metabolic profile or electronic effects are decisive, nothing substitutes for the trifluoromethylated version. We see a clear trend in global pharmaceutical pipelines moving towards fluorinated scaffolds to overcome metabolic liabilities. The difference impacts not just biological data but also regulatory approvals, since many regulatory bodies now expect the reduction or elimination of metabolites prone to further modification in vivo.

    From the synthetic point of view, those working with standard acetyl groups often run into problems with hydrolytic stability and side reactions, particularly in aqueous or slightly basic media. The trifluoroacetyl group resists hydrolysis and oxidation, making our compound less prone to degradation and loss of activity in reactions that require robust functional group protection. By keeping impurity profiles tight and supporting detailed analytical data—including NMR, mass spectrometry, and elemental analysis—we allow users to meet publication or submission standards without extra work on their end.

    Supporting Innovation Through Reliability

    Manufacturers making indole intermediates have a silent but central role in the medicinal and fine chemical value chain. Chemists in R&D, scale-up, or process development settings choose suppliers based on who delivers problem-solving and not just a bottle of white powder. Our position as direct producers means we learn quickly from the real issues our customers encounter. For example, a pandemic-induced raw material shortage forced us to test and validate several second-source precursors. That project highlighted the difference that a slight change in starting indole source makes on color and assay—after a few failed lots, we didn’t ship a thing until controls and analytics matched the old standard.

    Real users need answers right away when something goes wrong. Many of our returning clients reach out with questions on solubility or safety that haven’t turned up in standard literature. Our team, most of whom have run chemical reactions for years, can usually spot the issue based on pattern recognition and years of troubleshooting common lab problems. Sometimes, we’re asked about extra analytical support for batches heading into preclinical work—a call that typically means we add extra NMR or GC-MS details to reassure the project managers or quality teams down the line.

    Learning from Market Trends

    Shifts in market demand ripple back to the factory floor. An uptick in requests for trifluoromethylated indoles followed several high-profile papers on kinase inhibitors and CNS-active agents with these substituents. Meeting this demand required scaling our process without losing control. In practice, this often meant re-optimizing purification routes, addressing waste handling regulations for fluorinated solvents, and investing in updated analytical equipment to keep up with specifications required by multinational clients.

    Cost pressure affects everyone—drug developers, research labs, and manufacturers alike. For us, bulk pricing options have become increasingly popular over the past five years, especially among contract research organizations handling dozens of synthetic steps for discovery clients. Rather than compromise on grade, our response focused on driving down waste, leveraging process intensification, and collaborating with neighboring manufacturers to pool logistics for hard-to-handle fluorinated intermediates.

    Challenges in Handling and Regulatory Outlook

    Dealing with trifluoroacetyl compounds means attention to safety and environmental risk. Volatility of the trifluoroacetyl group demands careful control of exposure—both to operators and to the environment. While most research batches use small amounts, pilot plants and scale-up scenarios led us to implement forced-air evacuation and improved PPE training. Safety incidents in factories overseas prompted us to enhance incident recording and make our warehouse staff undergo twice-annual handling refreshers.

    On the regulatory side, the growing attention to PFAS (per- and polyfluoroalkyl substances) shapes how we manage waste streams and internal housekeeping. Even small-scale production of trifluorinated compounds faces environmental scrutiny, especially in regulated jurisdictions. To get ahead of possible changes, we made operational changes such as closed-loop solvent recycling and in-house neutralization of acidic waste streams. Regulators ask for traceability; our record-keeping covers source, batch, and downstream usage patterns—something we welcome as part of building trust with clients wary of supply chain disruptions or regulatory surprises.

    Addressing Problems and Offering Solutions

    Despite the growing sophistication of chemical manufacturing, trouble sometimes appears in unexpected places. A recent example involved a batch with subtle color staining due to an unintended impurity from a new cleaning agent used in one reactor. Instead of hiding the problem, we traced it, pulled the affected lots from stock, and set up a root-cause analysis that permanently eliminated the contaminant. As a result, we adjusted both cleaning protocols and the frequency of operator training. Trust grows each time a customer receives an apology before a complaint—an attitude we take seriously and implement in our daily routines.

    Real issues call for practical solutions. Several clients over the years have asked for more concentrated product forms to minimize solvent and material waste in large libraries or production runs. Responding to feedback, we tested denser, granular forms and made the investment in equipment that could tailor texture without losing spec control. Where possible, we innovate packaging or shipment to avoid breakage and exposure—foam lining, double sealing, and flexible secondary containment earn more repeat business than cutting pennies on materials.

    Some want insight into scaling up their own internal reactions. Direct experience with large and small vessels means we can share firsthand tips, for example, advising on phase separation during work-up or tricks to dry down the product without decomposition. One memorable case involved a customer scaling up by a factor of fifty and struggling with filtration. Our manufacturing team shared a filtration aid and pressure setting—simple knowledge passed from one group of chemists to another, saving days of lost work.

    The Road Ahead: Continuous Improvement

    Preparing 3-(Trifluoroacetyl)Indole as a reliable reagent is an ongoing challenge. As downstream industries grow more advanced, our manufacturing processes must keep pace. Routine product reviews, process audits, and investment in better analytical methods all help us catch problems before product leaves the door. Several years ago, we updated our analytical lab with higher field NMR and expanded our reference database to spot subtle byproducts that never made it to old specs sheets. No shortcut replaces the daily discipline required to keep standards rising.

    Changing environmental or consumer demands don’t upset us—they motivate us to become more thoughtful in waste handling, risk communication, and product stewardship. Partnerships with universities, government panels, or industry groups help inform our risk assessments. For instance, collaborating on green chemistry initiatives led us to reduce reliance on certain hazardous solvents and popularize safer alternatives. These changes benefit downstream users who work under tight compliance rules and elevated safety expectations.

    Supporting Science and Responsible Manufacturing

    Years of manufacturing experience bring perspective not always visible on the surface. We see the end use of 3-(Trifluoroacetyl)Indole reflected in academic papers, patent filings, and milestones in drug discovery. At the same time, we watch as users push the boundaries of synthetic methodology, combinatorial chemistry, and late-stage functionalization. Our pride as a manufacturer comes from knowing that each bottle shipped could play a small role in a new therapy, a tool for crop science, or a test system for technology yet to come.

    Manufacturing and serving as a resource to the scientific community is not about outsized claims, but about incremental gains in trust, quality, and problem-solving. No matter how routine a product seems, every lot we ship represents hundreds of small improvements, fixes, and collaborative troubleshooting moments. We value direct user feedback, rapid response, and transparent communication—all lessons learned on the floor, not just in manuals. 3-(Trifluoroacetyl)Indole, as a material, has proven worthy of careful stewardship, not simply because of its market demand, but due to its central role in helping chemists and scientists advance new knowledge.

    For those seeking a stable, reproducible, and well-characterized trifluoroacetyl indole for research and development, a commitment to manufacturing detail makes all the difference. Continuous investment in analytical capabilities, sustainable operations, and open expertise will keep driving improvements and keep the supply of this critical compound reliable. That’s the standard we set for ourselves each day on the production floor.