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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 | 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. |
Applications of 1-Boc-5-Aminoindole in Industrial ManufacturingAs 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 IntermediatesMedicinal 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
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2. Active Pharmaceutical Ingredient (API) SynthesisIn 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
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3. Peptidomimetic and Heterocyclic Building BlocksPeptidomimetic 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
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4. Fine Chemical Intermediates for Agrochemical SynthesisIn 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
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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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.