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1-Boc-5-Aminoindole

    • Product Name 1-Boc-5-Aminoindole
    • Alias Boc-5-amino-1H-indole
    • 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

    332744

    Product Name 1-Boc-5-Aminoindole
    Cas Number 356783-16-9
    Molecular Formula C13H16N2O2
    Molecular Weight 232.28
    Appearance Off-white to pale yellow solid
    Purity Typically ≥98%
    Melting Point 88-92°C
    Solubility Soluble in DMSO, methanol, and ethanol
    Storage Condition Store at 2-8°C
    Smiles CC(C)(C)OC(=O)N1C=CC2=CC(N)=CC=C21
    Inchi Key FIKJKUQIGZIPMU-UHFFFAOYSA-N

    As an accredited 1-Boc-5-Aminoindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 1-Boc-5-Aminoindole is supplied in a 5-gram amber glass vial, tightly sealed, and labeled with product details and safety information.
    Shipping 1-Boc-5-Aminoindole is shipped in a tightly sealed container, protected from light and moisture. It is packaged with appropriate hazard labeling and compliant with chemical transportation regulations. The shipment is typically sent via ground or air, subject to the receiver’s site requirements and applicable safety protocols for laboratory chemicals.
    Storage 1-Boc-5-Aminoindole should be stored in a tightly sealed container, protected from light and moisture, at a temperature between 2–8°C (refrigerator). Avoid exposure to air and incompatible substances such as strong acids or oxidizers. Ensure storage in a well-ventilated, dry environment, and label clearly. Handle under appropriate safety protocols to prevent contamination or degradation.
    Application of 1-Boc-5-Aminoindole

    Applications of 1-Boc-5-Aminoindole in Industrial Manufacturing

    As the manufacturer of 1-Boc-5-Aminoindole, we supply this intermediate to global pharmaceutical and fine chemical producers who demand precise protection chemistry for their complex molecular syntheses. The following application scenarios reflect real, verified use cases across regulated downstream sectors.

    1. Small-Molecule Drug Discovery Intermediates

    Medicinal chemistry teams in pharmaceutical R&D use 1-Boc-5-Aminoindole for rapid assembly of indole-based scaffolds, particularly when building libraries targeting CNS disorders and oncology pipelines. Its protected amino group enables selective N-functionalization while safeguarding against side reactions during multi-step syntheses. Researchers rely on its purity and consistent performance for scalable parallel synthesis within compliant environments.

    Industry compliance standards

    • Good Laboratory Practice (GLP)
    • International Conference on Harmonisation (ICH) Q7 GMP for APIs
    • US FDA 21 CFR Part 211 (where used for cGMP sample lots)
    • European Pharmacopoeia monograph reference for intermediates: 2034

    Typical usage ratio

    • 0.1–1.2 molar equivalents per target indole ring, depending on functionalization steps and resin scale

    Downstream process integration

    • Introduced during initial scaffold assembly stages in solution-phase or solid-phase parallel synthesis workflows
    • Deprotection (removal of Boc group) performed post-coupling to expose the free amine for final elaboration

    Final product types

    • Hit-to-lead compound libraries for CNS, cancer, and anti-viral small molecules
    • Fused heterocycle intermediates for GLP toxicology studies
    • Preclinical API candidates targeting serotonin receptors

    2. Active Pharmaceutical Ingredient (API) Synthesis

    In cGMP-regulated API plants, manufacturing engineers utilize 1-Boc-5-Aminoindole as a strategically protected indole nucleus, streamlining the assembly and purification of multi-substituted APIs. Its stable Boc group shields the amino position through chlorination, alkylation, or acylation stages, before enzymatic or acid cleavage exposes the reactive site for final pharmaceutical coupling.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP) per ICH Q7 and US FDA guidelines
    • EU Guideline for APIs (EudraLex Volume 4 Part II)
    • Qualified Person (QP) release for shipment into regulated markets
    • ISO 9001:2015 for Quality Management Systems

    Typical usage ratio

    • Determined by targeted synthetic route; generally 1.0–1.1 molar equivalents in stepwise assembly

    Downstream process integration

    • Charged at the initial nucleophilic substitution or arylation stage of API core assembly
    • In-process analytical monitoring to ensure complete Boc deprotection prior to terminal modifications

    Final product types

    • Regulated API intermediates for anti-cancer, anti-inflammatory, and CNS medicines
    • Final APIs submitted for regulatory filing (e.g., US DMF, EU EDMF)

    3. Peptidomimetic and Heterocyclic Building Blocks

    Peptidomimetic and anti-viral drug manufacturers incorporate protected indole amines derived from this raw material into their backbone assemblies, exploiting enhanced chemical stability during solid-phase or solution-phase peptide synthesis. The Boc group provides temporary protection during repeated coupling and deprotection cycles, especially when designing conformationally restricted or bioisosteric residues.

    Industry compliance standards

    • FDA Good Manufacturing Practices for APIs (21 CFR 210, 211)
    • Pharmacopeial monographs for peptide building blocks (USP, JP)
    • ICH Q11 for Development and Manufacture of Drug Substances
    • Controlled Substance Schedules (if applicable)

    Typical usage ratio

    • Typically 1 equivalent per peptide elongation cycle; excess may be used to ensure completeness where steric hindrance is present

    Downstream process integration

    • Integrated as a protected amino acid analog during chain extension cycles in solid-phase peptide synthesizers (SPPS)
    • Boc deprotection coincides with global deprotection and resin cleavage steps

    Final product types

    • Investigational peptidomimetic drug substances for clinical trial supply
    • Custom amino acid derivatives for peptide screening projects
    • Bioactive cyclic peptide analogs for anti-microbial studies

    4. Fine Chemical Intermediates for Agrochemical Synthesis

    In crop protection R&D, fine chemical manufacturers employ the indole scaffold for the development of novel herbicides and fungicides. The Boc-protected aminoindole unit ensures compatibility with chlorination and oxidative coupling processes, minimizing byproduct formation until its selective removal. This supports synthesis of new chemical entities with improved selectivity profiles in regulated pesticide production.

    Industry compliance standards

    • OECD Good Laboratory Practice Guidelines for Agricultural Chemicals
    • ISO 17025 for in-house analytical and QC labs
    • European Regulation (EC) No. 1107/2009 for plant protection products
    • China National Standard GB/T 35102 for pesticide intermediates

    Typical usage ratio

    • 0.9–1.3 equivalents based on target coupling efficiency and impurity profile tolerance

    Downstream process integration

    • Added at indole core derivatization stage, followed by Boc group cleavage under acidic conditions prior to final coupling
    • In-line monitoring of residue for regulatory compliance verification

    Final product types

    • Discovery-phase herbicide chemical libraries
    • Lead fungicide candidates for field trial formulation
    • Regulated pesticide intermediates under FTO analysis
    Free Quote

    Competitive 1-Boc-5-Aminoindole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-Boc-5-Aminoindole: Advancing Synthesis in Chemical Research

    Understanding 1-Boc-5-Aminoindole from a Manufacturer's Bench

    For years, we have produced a wide range of indole derivatives. 1-Boc-5-Aminoindole stands out in the lab for its versatile applications within the pharmaceutical and agrochemical industries. Our production facilities focus on delivering this compound with consistent purity, reliable particle size, and reproducible chemical properties batch after batch. The commitment to chemical reliability comes from countless hours spent handling raw materials, monitoring reaction profiles, and overseeing crystallization steps. Our team engages closely with the compound as it moves through every stage, so we know the challenges and opportunities it brings to both bench chemists and production scientists.

    Product Focus: Chemical Model and Specifications

    We produce 1-Boc-5-Aminoindole to structure the molecule with a tert-butoxycarbonyl (Boc) protection on the amino group at the fifth position of the indole ring. The choice of the Boc protecting group is not just about custom but about chemistry that holds up during multi-step syntheses. Our manufacturing lines routinely check for color, melting point, water content, and HPLC purity, sticking with clear benchmarks for purity—often exceeding 98% as a matter of method rather than marketing. We have built systems that give users quick access to both analytical and technical support, since real-world needs rarely match generic textbook scenarios. Every batch gets characterized with FTIR, NMR, and mass spectrometry, adding confidence for researchers scaling up or optimizing reaction conditions.

    Why the Boc Group Matters in Indole Chemistry

    The Boc-protecting group makes synthetic life easier. Anyone who has tried to run coupling reactions or acylations using free amines on indoles can attest to side reactions and product loss. Installing a Boc group on the 5-amino position manages these issues, letting chemists direct reactivity elsewhere on the molecule without sacrificing yields or working up messy mixtures that are hard to purify. We often hear from customers about the frustrations of standard unprotected aminoindoles, especially in crowded reaction setups. Working with 1-Boc-5-Aminoindole gives them more predictable conversions, cleaner work-ups, and better reproducibility, whether they’re assembling drug scaffolds or developing new materials.

    How 1-Boc-5-Aminoindole Fits into Modern Synthesis

    The pharmaceutical pipeline demands intermediates that withstand tough conditions. During fragment-based drug discovery or total synthesis projects, traditional aminoindole derivatives often fall short either because of their inadequate stability or because of interfering side reactions. Boc protection, just like it did in peptide chemistry, brings practical handling, solution stability, lower risk of polymerization, and trustworthy shelf life. This helps large and small-scale chemists who rely on batch-to-batch consistency for method development or regulatory submissions. In our own research collaborations, we have watched how the Boc-protected 5-amino position responds to deprotection, electrophilic aromatic substitution, and cross-coupling reactions, giving route flexibility that would not exist otherwise.

    Critical Differences from Other Aminoindole Compounds

    Comparing 1-Boc-5-Aminoindole with its non-protected or benzyl-protected cousins draws sharp distinctions. Free 5-aminoindole is usually more reactive than desired, leading to oxidative degradation or unwanted polymerization. We have seen instances where researchers lost their products during silica purification because the unprotected amine bonded irreversibly to chromatography media. Using benzyl protection goes some way toward stability, but removing benzyl groups later almost always involves catalytic hydrogenation, which not every operation can run, especially with sensitive motifs elsewhere in the molecule.
    Our Boc-aminated product can be deprotected under mild acidic conditions, usually in TFA or HCl, which circumvents the need for hydrogen gas and expensive setups. This increases process safety and opens up options for downstream functionalization, especially in labs handling a wide scope of chemical entities. Boc-deprotection proceeds smoothly and predictably, proven not just by us but by collaborating academic and industrial researchers who have tested hundreds of analogs based on this intermediate. Our technical teams regularly compare pilot-scale samples under different synthetic routes, allowing us to advise reliably on differences in reactivity, solubility, and stability against hydrolysis, oxidation, and light.

    Applications Rooted in Research and Manufacturing

    1-Boc-5-Aminoindole delivers value during hit-to-lead and lead optimization in drug design. Medicinal chemists looking to modify the indole scaffold recognize the importance of orthogonally protected intermediates. With the Boc group in place, functionalization elsewhere proceeds without risk of deactivating the amine, which remains shielded until final-stage modifications. We know from customer feedback that this enables access to a wider set of analog libraries, particularly for kinase inhibitors, receptor modulators, and CNS-active molecules. Agrochemical development also benefits, since structure-activity studies demand subtle side-chain changes without losing core skeletons.

    Beyond pharma, 1-Boc-5-Aminoindole finds roles in specialty dyes, fluorescent probes, and advanced material monomers. Facility managers at research organizations report easier batch controls, less handling loss, and lower risks when swapping from free amines to Boc-protected intermediates. We support these users by providing thorough batch records, material safety data, and route troubleshooting, not just a shipment of material. Our scientists field questions about solvent compatibility, downstream reactivity, and impurity control based on both customer and in-house experiences.

    Manufacturing Approach: Quality from Raw Materials to Packing

    Success in synthesizing 1-Boc-5-Aminoindole begins with raw material selection—high-purity indole and tert-butoxycarbonylating agents without non-volatile residues or problematic trace metals. Our reactors operate under close monitoring; temperature, pressure, and pH are logged at every step to avoid decomposition. Unlike vendors selling repackaged or sourced material, we have line-of-sight to each manufacturing variable. Reactor operators check end-point completion by TLC and HPLC, and no intermediate reaches packaging before double-checking by NMR for target signals. Crystallization protocols target consistent polymorphs, which reduces issues with variable solubility at the user end. Packing under dry nitrogen and validated storage conditions further secure material integrity during shipment.

    We regularly examine process waste streams and minimize side-product formation—using feedback from our own process analytics. That approach lets us cut both material costs and environmental burden involved in synthesizing Boc-protected aminoindoles. Every kilogram we ship carries a low-impurity signature because our team reviews solvent recovery, cleaning validation, and line clearance to avoid cross-contamination.

    Supporting Chemists: Real-World Input

    Every chemist encounters hurdles not described in method journals. We know firsthand the frustration of solvents not behaving, reagents acting up with subtle color changes, and analytical signals not matching expectations. Having a clear, well-characterized 1-Boc-5-Aminoindole lessens those troubleshooting headaches. Our technical support team consists of scientists with years of lab experience, most of whom have run peptide coupling, Suzuki reactions, or late-stage aromatic substitutions in the same way users do. Guidance doesn’t stop with shipping; we often provide detailed reactivity comparisons if a customer is switching from another vendor or trying to optimize their own process.

    We welcome audits and qualification runs involving our batches, since transparency enhances all sides. Our R&D group holds regular workshops with industrial partners, walking through real yields, work-up procedures, and common stumbling blocks when handling not just our compound but the next stage in their pathway. Attention to these details, gained from hands-on operations, builds trust and long-term partnerships.

    Sustainability and Supply Chain Transparency

    Sustainability rises to the top of priority lists for many end-users. Running a dedicated synthesis facility places a unique burden on us to minimize environmental impact at scale. We select waste treatment processes based on actual hazards, not theoretical toxicity tables, and we design batch records to enable both backward and forward traceability in our supply chain. Our facility audits have reduced both energy and solvent consumption over the last three years, with more efficient distillation and scrubbing units. Supply risk monitoring lets us support customers with advance notice for any shortages or delays, especially as regulatory scrutiny on certain chemicals tightens globally.

    End-users benefit directly from this approach. Downstream processors, particularly those in regulated markets, find our material supply both predictable and responsive. Our established internal logistics help buffer demand spikes, and we work hard to avoid the late delivery or batch inconsistency that can sideline whole project teams. Every improvement in sustainability flows through to long-term price stability and reduced environmental liability for our customers.

    Building Trust through Data and Experience

    We base our technical claims on data, not just marketing. For 1-Boc-5-Aminoindole, regular publication of analytical results and manufacturing protocols supports user confidence. Each batch goes out the door with a real, validated certificate—not recycled, not templated for every shipment—detailing specific manufacturing lots and analytical outcomes. We build in room for customer-driven additional testing, knowing that no facility is the same and every synthesis may push our chemistry in new directions.

    Research partners push our material to its boundaries, probing stability in mixed solvent systems, reactivity in novel substitution reactions, or trace impurity profiles under heat and light stress. Instead of defending product specs, we treat every technical inquiry as a chance to learn and refine both our process and user support.

    Conclusion: Connecting Proven Chemistry to New Advances

    1-Boc-5-Aminoindole bridges the gap between traditional indole chemistry and the latest demands of medicinal chemistry and materials science. Direct experience with production, user troubleshooting, and process optimization stands behind every gram shipped. Our facility remains committed to supporting ongoing innovation—one batch, one user, and one challenge at a time.